Cancertope
In silico Platform for designing genome-based
Personalized immunotherapy or Vaccine against Cancer
Personalized immunotherapy or Vaccine against Cancer
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The result page of search shows exclusive peptide/epitopes generated due to mutation [Neoepitope], the tissue of origin [Tissue], position of peptide in protein [Position], number of mismatches counted by aligning mutated and normal protein sequence [Num Mismatch, percentage of cell lines with this peptide over total number of cell lines [Promiscuity %]. The immune information include CTL epitopes (Yes/No), MHC I binders, MHC II binders (both given as number of alleles) and B cell epitopes (Yes/No). For more information, please click |
| Result | Search: | |||||||||||||||||||||||||
| Protein | Neoepitopes | Tissue | Position | Prot Mutation | cDNA Mutation | Mutation Type | Num Mismatch | Promiscuity (%) | Cell Line | CTL | MHC I | NHLApred | MHC II | Bcell | ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| BRAF | ATPLPHYLA | ENDOMETRIUM | 400 | p.P403fs | c.1208_1208delC | Frame_Shift_Del | 6 | 0.22 | ISHIKAWAHERAKLIO02ER | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | ATPLPHYLA | ENDOMETRIUM | 400 | p.P403fs | c.1208_1208delC | Frame_Shift_Del | 6 | 0.22 | RL952 | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | GLSATPLPH | ENDOMETRIUM | 397 | p.P403fs | c.1208_1208delC | Frame_Shift_Del | 3 | 0.22 | ISHIKAWAHERAKLIO02ER | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | GLSATPLPH | ENDOMETRIUM | 397 | p.P403fs | c.1208_1208delC | Frame_Shift_Del | 3 | 0.22 | RL952 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | LSATPLPHY | ENDOMETRIUM | 398 | p.P403fs | c.1208_1208delC | Frame_Shift_Del | 4 | 0.22 | ISHIKAWAHERAKLIO02ER | N | 8 | 0 | 0 | N | ||||||||||||
| BRAF | LSATPLPHY | ENDOMETRIUM | 398 | p.P403fs | c.1208_1208delC | Frame_Shift_Del | 4 | 0.22 | RL952 | N | 8 | 0 | 0 | N | ||||||||||||
| BRAF | SATPLPHYL | ENDOMETRIUM | 399 | p.P403fs | c.1208_1208delC | Frame_Shift_Del | 5 | 0.22 | ISHIKAWAHERAKLIO02ER | Y | 12 | 10 | 0 | N | ||||||||||||
| BRAF | SATPLPHYL | ENDOMETRIUM | 399 | p.P403fs | c.1208_1208delC | Frame_Shift_Del | 5 | 0.22 | RL952 | Y | 12 | 10 | 0 | N | ||||||||||||
| BRAF | TGLSATPLP | ENDOMETRIUM | 396 | p.P403fs | c.1208_1208delC | Frame_Shift_Del | 2 | 0.22 | ISHIKAWAHERAKLIO02ER | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | TGLSATPLP | ENDOMETRIUM | 396 | p.P403fs | c.1208_1208delC | Frame_Shift_Del | 2 | 0.22 | RL952 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | TPLPHYLAH | ENDOMETRIUM | 401 | p.P403fs | c.1208_1208delC | Frame_Shift_Del | 6 | 0.22 | ISHIKAWAHERAKLIO02ER | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | TPLPHYLAH | ENDOMETRIUM | 401 | p.P403fs | c.1208_1208delC | Frame_Shift_Del | 6 | 0.22 | RL952 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | TTGLSATPL | ENDOMETRIUM | 395 | p.P403fs | c.1208_1208delC | Frame_Shift_Del | 1 | 0.22 | ISHIKAWAHERAKLIO02ER | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | TTGLSATPL | ENDOMETRIUM | 395 | p.P403fs | c.1208_1208delC | Frame_Shift_Del | 1 | 0.22 | RL952 | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | ATTVKSRWS | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 598 | p.599_599T>TT | c.1796_1797insTAC | In_Frame_Ins | 2 | 0.11 | SUDHL8 | N | 0 | 0 | 0 | Y | ||||||||||||
| BRAF | DFGLATTVK | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 594 | p.599_599T>TT | c.1796_1797insTAC | In_Frame_Ins | 3 | 0.11 | SUDHL8 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | FGLATTVKS | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 595 | p.599_599T>TT | c.1796_1797insTAC | In_Frame_Ins | 4 | 0.11 | SUDHL8 | N | 4 | 0 | 33 | N | ||||||||||||
| BRAF | GDFGLATTV | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 593 | p.599_599T>TT | c.1796_1797insTAC | In_Frame_Ins | 2 | 0.11 | SUDHL8 | N | 7 | 0 | 0 | N | ||||||||||||
| BRAF | GLATTVKSR | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 596 | p.599_599T>TT | c.1796_1797insTAC | In_Frame_Ins | 4 | 0.11 | SUDHL8 | Y | 5 | 12 | 0 | Y | ||||||||||||
| BRAF | IGDFGLATT | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 592 | p.599_599T>TT | c.1796_1797insTAC | In_Frame_Ins | 1 | 0.11 | SUDHL8 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | LATTVKSRW | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 597 | p.599_599T>TT | c.1796_1797insTAC | In_Frame_Ins | 3 | 0.11 | SUDHL8 | N | 3 | 0 | 0 | Y | ||||||||||||
| BRAF | TTVKSRWSG | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 599 | p.599_599T>TT | c.1796_1797insTAC | In_Frame_Ins | 1 | 0.11 | SUDHL8 | N | 0 | 0 | 0 | Y | ||||||||||||
| BRAF | ADEDHQNQF | LARGE_INTESTINE | 349 | p.R354Q | c.1061G>A | Missense_Mutation | 1 | 0.11 | HT115 | N | 2 | 0 | 0 | Y | ||||||||||||
| BRAF | AFTNEVGVL | ENDOMETRIUM | 497 | p.K499T | c.1496A>C | Missense_Mutation | 1 | 0.11 | JHUEM7 | N | 5 | 0 | 0 | N | ||||||||||||
| BRAF | AIVAQWCEG | LARGE_INTESTINE | 526 | p.T529A | c.1585A>G | Missense_Mutation | 1 | 0.11 | GP2D | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | APSIYLEAY | BREAST | 74 | p.P74A | c.220C>G | Missense_Mutation | 1 | 0.11 | MDAMB415 | N | 10 | 0 | 0 | N | ||||||||||||
| BRAF | AQSNPKSPQ | CENTRAL_NERVOUS_SYSTEM | 145 | p.R146Q | c.437G>A | Missense_Mutation | 1 | 0.11 | CCFSTTG1 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | AQWCEGSSL | LARGE_INTESTINE | 529 | p.T529A | c.1585A>G | Missense_Mutation | 1 | 0.11 | GP2D | N | 12 | 0 | 0 | N | ||||||||||||
| BRAF | ARSLPKIHC | LARGE_INTESTINE | 718 | p.R726C | c.2176C>T | Missense_Mutation | 1 | 0.11 | SNU407 | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | ASMDSVTSS | LARGE_INTESTINE | 115 | p.T119S | c.356C>G | Missense_Mutation | 1 | 0.11 | HT29 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | ATKKSRWSG | LARGE_INTESTINE | 598 | p.V600K | c.1798_1799GT>AA | Missense_Mutation | 1 | 0.11 | MDST8 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | ATVYKGKWH | LUNG | 469 | p.G469A | c.1406G>C | Missense_Mutation | 1 | 0.11 | NCIH1755 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | AVKMWNVTA | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 481 | p.L485W | c.1454T>G | Missense_Mutation | 1 | 0.11 | CI1 | Y | 1 | 11 | 0 | N | ||||||||||||
| BRAF | CNTEVPLMC | LARGE_INTESTINE | 272 | p.S273N | c.818G>A | Missense_Mutation | 1 | 0.11 | CCK81 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | CSASEPSLN | LARGE_INTESTINE | 726 | p.R726C | c.2176C>T | Missense_Mutation | 1 | 0.11 | SNU407 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | CSTKVPLMC | SKIN | 272 | p.E275K | c.823G>A | Missense_Mutation | 1 | 0.11 | SKMEL30 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | CVNYDQLHL | SKIN | 280 | p.D287H | c.859G>C | Missense_Mutation | 1 | 0.11 | SKMEL30 | N | 5 | 0 | 0 | N | ||||||||||||
| BRAF | DEDHQNQFG | LARGE_INTESTINE | 350 | p.R354Q | c.1061G>A | Missense_Mutation | 1 | 0.11 | HT115 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | DFGLATKKS | LARGE_INTESTINE | 594 | p.V600K | c.1798_1799GT>AA | Missense_Mutation | 1 | 0.11 | MDST8 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | DFGRATVKS | PROSTATE | 594 | p.L597R | c.1790T>G | Missense_Mutation | 1 | 0.11 | 22RV1 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | DFGVATVKS | LUNG | 594 | p.L597V | c.1789C>G | Missense_Mutation | 1 | 0.11 | NCIH2087 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | DFRLATVKS | LARGE_INTESTINE | 594 | p.G596R | c.1786G>C | Missense_Mutation | 1 | 0.11 | NCIH508 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | DFSLYVCAS | OVARY | 742 | p.A747V | c.2240C>T | Missense_Mutation | 1 | 0.11 | OC316 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | DGEKKPVGW | SKIN | 202 | p.I208V | c.622A>G | Missense_Mutation | 1 | 0.11 | LOXIMVI | N | 2 | 0 | 0 | Y | ||||||||||||
| BRAF | DHQNQFGQR | LARGE_INTESTINE | 352 | p.R354Q | c.1061G>A | Missense_Mutation | 1 | 0.11 | HT115 | N | 1 | 0 | 0 | Y | ||||||||||||
| BRAF | DKFGGEHNA | BREAST | 66 | p.P74A | c.220C>G | Missense_Mutation | 1 | 0.11 | MDAMB415 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | DLKSNKIFL | SKIN | 576 | p.N581K | c.1743T>A | Missense_Mutation | 1 | 0.11 | HS936T | Y | 9 | 11 | 0 | N | ||||||||||||
| BRAF | DLKSNYIFL | LARGE_INTESTINE | 576 | p.N581Y | c.1741A>T | Missense_Mutation | 1 | 0.11 | HT55 | Y | 8 | 10 | 0 | N | ||||||||||||
| BRAF | DLSKVRNNC | LUNG | 677 | p.S683N | c.2048G>A | Missense_Mutation | 1 | 0.11 | SW1271 | Y | 1 | 9 | 0 | N | ||||||||||||
| BRAF | DPVNIDDLI | LUNG | 375 | p.E375D | c.1125A>T | Missense_Mutation | 1 | 0.11 | NCIH1651 | N | 14 | 0 | 0 | N | ||||||||||||
| BRAF | DQLHLLFVS | SKIN | 284 | p.D287H | c.859G>C | Missense_Mutation | 1 | 0.11 | SKMEL30 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | DSNRMKTLG | LUNG | 434 | p.R435S | c.1305G>T | Missense_Mutation | 1 | 0.11 | RERFLCAD1 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | DSVTSSSSS | LARGE_INTESTINE | 118 | p.T119S | c.356C>G | Missense_Mutation | 1 | 0.11 | HT29 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | DVAQSNPKS | CENTRAL_NERVOUS_SYSTEM | 143 | p.R146Q | c.437G>A | Missense_Mutation | 1 | 0.11 | CCFSTTG1 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | DVAVKMWNV | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 479 | p.L485W | c.1454T>G | Missense_Mutation | 1 | 0.11 | CI1 | Y | 4 | 11 | 0 | N | ||||||||||||
| BRAF | EDFSLYVCA | OVARY | 741 | p.A747V | c.2240C>T | Missense_Mutation | 1 | 0.11 | OC316 | N | 8 | 0 | 0 | N | ||||||||||||
| BRAF | EDHQNQFGQ | LARGE_INTESTINE | 351 | p.R354Q | c.1061G>A | Missense_Mutation | 1 | 0.11 | HT115 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | EDSNRMKTL | LUNG | 433 | p.R435S | c.1305G>T | Missense_Mutation | 1 | 0.11 | RERFLCAD1 | Y | 7 | 9 | 0 | N | ||||||||||||
| BRAF | EELHVEMLE | OVARY | 220 | p.V226M | c.676G>A | Missense_Mutation | 1 | 0.11 | A2780 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | EHNAPSIYL | BREAST | 71 | p.P74A | c.220C>G | Missense_Mutation | 1 | 0.11 | MDAMB415 | Y | 3 | 9 | 0 | N | ||||||||||||
| BRAF | EKKPIGWGT | LARGE_INTESTINE | 204 | p.D211G | c.632A>G | Missense_Mutation | 1 | 0.11 | LS180 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | EKKPVGWDT | SKIN | 204 | p.I208V | c.622A>G | Missense_Mutation | 1 | 0.11 | LOXIMVI | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | ELHVEMLEN | OVARY | 221 | p.V226M | c.676G>A | Missense_Mutation | 1 | 0.11 | A2780 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | ELITGQLPY | URINARY_TRACT | 648 | p.M650I | c.1950G>T | Missense_Mutation | 1 | 0.11 | KMBC2 | N | 6 | 0 | 0 | N | ||||||||||||
| BRAF | EMLENVPLT | OVARY | 225 | p.V226M | c.676G>A | Missense_Mutation | 1 | 0.11 | A2780 | N | 5 | 0 | 0 | N | ||||||||||||
| BRAF | ESGSFGTVY | OVARY | 464 | p.G464E | c.1391G>A | Missense_Mutation | 1 | 0.11 | HEYA8 | N | 7 | 0 | 0 | N | ||||||||||||
| BRAF | FATVYKGKW | LUNG | 468 | p.G469A | c.1406G>C | Missense_Mutation | 1 | 0.11 | NCIH1755 | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | FGGEHNAPS | BREAST | 68 | p.P74A | c.220C>G | Missense_Mutation | 1 | 0.11 | MDAMB415 | N | 2 | 0 | 4 | N | ||||||||||||
| BRAF | FGIVLYELI | URINARY_TRACT | 642 | p.M650I | c.1950G>T | Missense_Mutation | 1 | 0.11 | KMBC2 | N | 15 | 0 | 4 | N | ||||||||||||
| BRAF | FGLATKKSR | LARGE_INTESTINE | 595 | p.V600K | c.1798_1799GT>AA | Missense_Mutation | 1 | 0.11 | MDST8 | N | 3 | 0 | 12 | N | ||||||||||||
| BRAF | FGRATVKSR | PROSTATE | 595 | p.L597R | c.1790T>G | Missense_Mutation | 1 | 0.11 | 22RV1 | N | 3 | 0 | 11 | N | ||||||||||||
| BRAF | FGVATVKSR | LUNG | 595 | p.L597V | c.1789C>G | Missense_Mutation | 1 | 0.11 | NCIH2087 | N | 3 | 0 | 6 | N | ||||||||||||
| BRAF | FHQRCNTEV | LARGE_INTESTINE | 268 | p.S273N | c.818G>A | Missense_Mutation | 1 | 0.11 | CCK81 | N | 5 | 0 | 1 | N | ||||||||||||
| BRAF | FHQRCSTKV | SKIN | 268 | p.E275K | c.823G>A | Missense_Mutation | 1 | 0.11 | SKMEL30 | N | 5 | 0 | 1 | N | ||||||||||||
| BRAF | FPQILTSIE | LARGE_INTESTINE | 707 | p.A712T | c.2134G>A | Missense_Mutation | 1 | 0.11 | KM12 | N | 3 | 0 | 3 | N | ||||||||||||
| BRAF | FQNPTDVAQ | CENTRAL_NERVOUS_SYSTEM | 138 | p.R146Q | c.437G>A | Missense_Mutation | 1 | 0.11 | CCFSTTG1 | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | FRLATVKSR | LARGE_INTESTINE | 595 | p.G596R | c.1786G>C | Missense_Mutation | 1 | 0.11 | NCIH508 | N | 5 | 0 | 39 | N | ||||||||||||
| BRAF | FRPADEDHQ | LARGE_INTESTINE | 346 | p.R354Q | c.1061G>A | Missense_Mutation | 1 | 0.11 | HT115 | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | FSLYVCASP | OVARY | 743 | p.A747V | c.2240C>T | Missense_Mutation | 1 | 0.11 | OC316 | N | 2 | 0 | 2 | N | ||||||||||||
| BRAF | FTNEVGVLR | ENDOMETRIUM | 498 | p.K499T | c.1496A>C | Missense_Mutation | 1 | 0.11 | JHUEM7 | Y | 7 | 9 | 0 | N | ||||||||||||
| BRAF | GDFGLATKK | LARGE_INTESTINE | 593 | p.V600K | c.1798_1799GT>AA | Missense_Mutation | 1 | 0.11 | MDST8 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | GDFGRATVK | PROSTATE | 593 | p.L597R | c.1790T>G | Missense_Mutation | 1 | 0.11 | 22RV1 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | GDFGVATVK | LUNG | 593 | p.L597V | c.1789C>G | Missense_Mutation | 1 | 0.11 | NCIH2087 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | GDFRLATVK | LARGE_INTESTINE | 593 | p.G596R | c.1786G>C | Missense_Mutation | 1 | 0.11 | NCIH508 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | GDVAVKMWN | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 478 | p.L485W | c.1454T>G | Missense_Mutation | 1 | 0.11 | CI1 | N | 3 | 0 | 0 | N | ||||||||||||
| BRAF | GEELHVEML | OVARY | 219 | p.V226M | c.676G>A | Missense_Mutation | 1 | 0.11 | A2780 | Y | 7 | 12 | 0 | N | ||||||||||||
| BRAF | GEHNAPSIY | BREAST | 70 | p.P74A | c.220C>G | Missense_Mutation | 1 | 0.11 | MDAMB415 | N | 6 | 0 | 0 | N | ||||||||||||
| BRAF | GEKKPIGWG | LARGE_INTESTINE | 203 | p.D211G | c.632A>G | Missense_Mutation | 1 | 0.11 | LS180 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | GEKKPVGWD | SKIN | 203 | p.I208V | c.622A>G | Missense_Mutation | 1 | 0.11 | LOXIMVI | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | GGEHNAPSI | BREAST | 69 | p.P74A | c.220C>G | Missense_Mutation | 1 | 0.11 | MDAMB415 | N | 7 | 0 | 0 | N | ||||||||||||
| BRAF | GGSTTGLSV | STOMACH | 392 | p.A400V | c.1199C>T | Missense_Mutation | 1 | 0.11 | SNU1 | N | 7 | 0 | 0 | N | ||||||||||||
| BRAF | GIVLYELIT | URINARY_TRACT | 643 | p.M650I | c.1950G>T | Missense_Mutation | 1 | 0.11 | KMBC2 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | GLATKKSRW | LARGE_INTESTINE | 596 | p.V600K | c.1798_1799GT>AA | Missense_Mutation | 1 | 0.11 | MDST8 | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | GLSVTPPAS | STOMACH | 397 | p.A400V | c.1199C>T | Missense_Mutation | 1 | 0.11 | SNU1 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | GQRIESGSF | OVARY | 460 | p.G464E | c.1391G>A | Missense_Mutation | 1 | 0.11 | HEYA8 | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | GQRIVSGSF | BREAST | 460 | p.G464V | c.1391G>T | Missense_Mutation | 1 | 0.11 | MDAMB231 | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | GRATVKSRW | PROSTATE | 596 | p.L597R | c.1790T>G | Missense_Mutation | 1 | 0.11 | 22RV1 | Y | 2 | 9 | 0 | Y | ||||||||||||
| BRAF | GSFATVYKG | LUNG | 466 | p.G469A | c.1406G>C | Missense_Mutation | 1 | 0.11 | NCIH1755 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | GSGSFATVY | LUNG | 464 | p.G469A | c.1406G>C | Missense_Mutation | 1 | 0.11 | NCIH1755 | N | 7 | 0 | 0 | N | ||||||||||||
| BRAF | GSSPSSPAS | LUNG | 315 | p.A320S | c.958G>T | Missense_Mutation | 1 | 0.11 | NCIH2227 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | GSTTGLSVT | STOMACH | 393 | p.A400V | c.1199C>T | Missense_Mutation | 1 | 0.11 | SNU1 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | GTDISWLTG | LARGE_INTESTINE | 211 | p.D211G | c.632A>G | Missense_Mutation | 1 | 0.11 | LS180 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | GVATVKSRW | LUNG | 596 | p.L597V | c.1789C>G | Missense_Mutation | 1 | 0.11 | NCIH2087 | Y | 1 | 10 | 0 | Y | ||||||||||||
| BRAF | GWGTDISWL | LARGE_INTESTINE | 209 | p.D211G | c.632A>G | Missense_Mutation | 1 | 0.11 | LS180 | N | 5 | 0 | 0 | N | ||||||||||||
| BRAF | GYKFHQRCN | LARGE_INTESTINE | 265 | p.S273N | c.818G>A | Missense_Mutation | 1 | 0.11 | CCK81 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | HCSASEPSL | LARGE_INTESTINE | 725 | p.R726C | c.2176C>T | Missense_Mutation | 1 | 0.11 | SNU407 | N | 5 | 0 | 0 | N | ||||||||||||
| BRAF | HGDVAVKMW | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 477 | p.L485W | c.1454T>G | Missense_Mutation | 1 | 0.11 | CI1 | N | 3 | 0 | 0 | N | ||||||||||||
| BRAF | HINTIDPVN | LUNG | 370 | p.E375D | c.1125A>T | Missense_Mutation | 1 | 0.11 | NCIH1651 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | HLLFVSKFF | SKIN | 287 | p.D287H | c.859G>C | Missense_Mutation | 1 | 0.11 | SKMEL30 | N | 6 | 0 | 0 | N | ||||||||||||
| BRAF | HNAPSIYLE | BREAST | 72 | p.P74A | c.220C>G | Missense_Mutation | 1 | 0.11 | MDAMB415 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | HQNQFGQRD | LARGE_INTESTINE | 353 | p.R354Q | c.1061G>A | Missense_Mutation | 1 | 0.11 | HT115 | N | 0 | 0 | 0 | Y | ||||||||||||
| BRAF | HQRCNTEVP | LARGE_INTESTINE | 269 | p.S273N | c.818G>A | Missense_Mutation | 1 | 0.11 | CCK81 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | HQRCSTKVP | SKIN | 269 | p.E275K | c.823G>A | Missense_Mutation | 1 | 0.11 | SKMEL30 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | HRDLKSNKI | SKIN | 574 | p.N581K | c.1743T>A | Missense_Mutation | 1 | 0.11 | HS936T | N | 6 | 0 | 0 | N | ||||||||||||
| BRAF | HRDLKSNYI | LARGE_INTESTINE | 574 | p.N581Y | c.1741A>T | Missense_Mutation | 1 | 0.11 | HT55 | N | 6 | 0 | 0 | N | ||||||||||||
| BRAF | HVEMLENVP | OVARY | 223 | p.V226M | c.676G>A | Missense_Mutation | 1 | 0.11 | A2780 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | IDPVNIDDL | LUNG | 374 | p.E375D | c.1125A>T | Missense_Mutation | 1 | 0.11 | NCIH1651 | N | 10 | 0 | 0 | N | ||||||||||||
| BRAF | IESGSFGTV | OVARY | 463 | p.G464E | c.1391G>A | Missense_Mutation | 1 | 0.11 | HEYA8 | Y | 7 | 10 | 0 | N | ||||||||||||
| BRAF | IGDFGLATK | LARGE_INTESTINE | 592 | p.V600K | c.1798_1799GT>AA | Missense_Mutation | 1 | 0.11 | MDST8 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | IGDFGRATV | PROSTATE | 592 | p.L597R | c.1790T>G | Missense_Mutation | 1 | 0.11 | 22RV1 | Y | 5 | 11 | 0 | N | ||||||||||||
| BRAF | IGDFGVATV | LUNG | 592 | p.L597V | c.1789C>G | Missense_Mutation | 1 | 0.11 | NCIH2087 | Y | 7 | 10 | 0 | N | ||||||||||||
| BRAF | IGDFRLATV | LARGE_INTESTINE | 592 | p.G596R | c.1786G>C | Missense_Mutation | 1 | 0.11 | NCIH508 | Y | 7 | 11 | 0 | N | ||||||||||||
| BRAF | IGSGSFATV | LUNG | 463 | p.G469A | c.1406G>C | Missense_Mutation | 1 | 0.11 | NCIH1755 | Y | 8 | 9 | 0 | N | ||||||||||||
| BRAF | IGWGTDISW | LARGE_INTESTINE | 208 | p.D211G | c.632A>G | Missense_Mutation | 1 | 0.11 | LS180 | N | 5 | 0 | 0 | N | ||||||||||||
| BRAF | IHCSASEPS | LARGE_INTESTINE | 724 | p.R726C | c.2176C>T | Missense_Mutation | 1 | 0.11 | SNU407 | N | 1 | 0 | 7 | N | ||||||||||||
| BRAF | IHRDLKSNK | SKIN | 573 | p.N581K | c.1743T>A | Missense_Mutation | 1 | 0.11 | HS936T | N | 0 | 0 | 8 | N | ||||||||||||
| BRAF | IHRDLKSNY | LARGE_INTESTINE | 573 | p.N581Y | c.1741A>T | Missense_Mutation | 1 | 0.11 | HT55 | N | 4 | 0 | 8 | N | ||||||||||||
| BRAF | ILTSIELLA | LARGE_INTESTINE | 710 | p.A712T | c.2134G>A | Missense_Mutation | 1 | 0.11 | KM12 | N | 7 | 0 | 0 | N | ||||||||||||
| BRAF | INTIDPVNI | LUNG | 371 | p.E375D | c.1125A>T | Missense_Mutation | 1 | 0.11 | NCIH1651 | N | 3 | 0 | 4 | N | ||||||||||||
| BRAF | IQDGEKKPV | SKIN | 200 | p.I208V | c.622A>G | Missense_Mutation | 1 | 0.11 | LOXIMVI | N | 5 | 0 | 0 | N | ||||||||||||
| BRAF | ITGQLPYSN | URINARY_TRACT | 650 | p.M650I | c.1950G>T | Missense_Mutation | 1 | 0.11 | KMBC2 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | ITVGQRIES | OVARY | 457 | p.G464E | c.1391G>A | Missense_Mutation | 1 | 0.11 | HEYA8 | N | 0 | 0 | 8 | N | ||||||||||||
| BRAF | ITVGQRIVS | BREAST | 457 | p.G464V | c.1391G>T | Missense_Mutation | 1 | 0.11 | MDAMB231 | N | 0 | 0 | 8 | N | ||||||||||||
| BRAF | IVAQWCEGS | LARGE_INTESTINE | 527 | p.T529A | c.1585A>G | Missense_Mutation | 1 | 0.11 | GP2D | N | 0 | 0 | 21 | N | ||||||||||||
| BRAF | IVLYELITG | URINARY_TRACT | 644 | p.M650I | c.1950G>T | Missense_Mutation | 1 | 0.11 | KMBC2 | N | 0 | 0 | 26 | N | ||||||||||||
| BRAF | IVSGSFGTV | BREAST | 463 | p.G464V | c.1391G>T | Missense_Mutation | 1 | 0.11 | MDAMB231 | Y | 2 | 10 | 0 | N | ||||||||||||
| BRAF | KFGGEHNAP | BREAST | 67 | p.P74A | c.220C>G | Missense_Mutation | 1 | 0.11 | MDAMB415 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | KFHQRCNTE | LARGE_INTESTINE | 267 | p.S273N | c.818G>A | Missense_Mutation | 1 | 0.11 | CCK81 | Y | 1 | 12 | 0 | N | ||||||||||||
| BRAF | KFHQRCSTK | SKIN | 267 | p.E275K | c.823G>A | Missense_Mutation | 1 | 0.11 | SKMEL30 | Y | 2 | 9 | 0 | Y | ||||||||||||
| BRAF | KIFLHEDLT | SKIN | 581 | p.N581K | c.1743T>A | Missense_Mutation | 1 | 0.11 | HS936T | N | 3 | 0 | 0 | N | ||||||||||||
| BRAF | KIGDFGRAT | PROSTATE | 591 | p.L597R | c.1790T>G | Missense_Mutation | 1 | 0.11 | 22RV1 | N | 3 | 0 | 0 | N | ||||||||||||
| BRAF | KIGDFGVAT | LUNG | 591 | p.L597V | c.1789C>G | Missense_Mutation | 1 | 0.11 | NCIH2087 | N | 3 | 0 | 0 | N | ||||||||||||
| BRAF | KIGDFRLAT | LARGE_INTESTINE | 591 | p.G596R | c.1786G>C | Missense_Mutation | 1 | 0.11 | NCIH508 | Y | 2 | 11 | 0 | N | ||||||||||||
| BRAF | KIHCSASEP | LARGE_INTESTINE | 723 | p.R726C | c.2176C>T | Missense_Mutation | 1 | 0.11 | SNU407 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | KKPIGWGTD | LARGE_INTESTINE | 205 | p.D211G | c.632A>G | Missense_Mutation | 1 | 0.11 | LS180 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | KKPVGWDTD | SKIN | 205 | p.I208V | c.622A>G | Missense_Mutation | 1 | 0.11 | LOXIMVI | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | KKSRWSGSH | LARGE_INTESTINE | 600 | p.V600K | c.1798_1799GT>AA | Missense_Mutation | 1 | 0.11 | MDST8 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | KMWNVTAPT | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 483 | p.L485W | c.1454T>G | Missense_Mutation | 1 | 0.11 | CI1 | N | 6 | 0 | 0 | N | ||||||||||||
| BRAF | KPIGWGTDI | LARGE_INTESTINE | 206 | p.D211G | c.632A>G | Missense_Mutation | 1 | 0.11 | LS180 | N | 14 | 0 | 0 | N | ||||||||||||
| BRAF | KPQLAIVAQ | LARGE_INTESTINE | 522 | p.T529A | c.1585A>G | Missense_Mutation | 1 | 0.11 | GP2D | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | KPVGWDTDI | SKIN | 206 | p.I208V | c.622A>G | Missense_Mutation | 1 | 0.11 | LOXIMVI | N | 13 | 0 | 0 | N | ||||||||||||
| BRAF | KSNKIFLHE | SKIN | 578 | p.N581K | c.1743T>A | Missense_Mutation | 1 | 0.11 | HS936T | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | KSNYIFLHE | LARGE_INTESTINE | 578 | p.N581Y | c.1741A>T | Missense_Mutation | 1 | 0.11 | HT55 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | KSSSSSEDS | LUNG | 427 | p.R435S | c.1305G>T | Missense_Mutation | 1 | 0.11 | RERFLCAD1 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | KVPLMCVNY | SKIN | 275 | p.E275K | c.823G>A | Missense_Mutation | 1 | 0.11 | SKMEL30 | Y | 7 | 12 | 0 | N | ||||||||||||
| BRAF | KVRNNCPKA | LUNG | 680 | p.S683N | c.2048G>A | Missense_Mutation | 1 | 0.11 | SW1271 | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | LAIVAQWCE | LARGE_INTESTINE | 525 | p.T529A | c.1585A>G | Missense_Mutation | 1 | 0.11 | GP2D | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | LATKKSRWS | LARGE_INTESTINE | 597 | p.V600K | c.1798_1799GT>AA | Missense_Mutation | 1 | 0.11 | MDST8 | N | 1 | 0 | 12 | N | ||||||||||||
| BRAF | LFPQILTSI | LARGE_INTESTINE | 706 | p.A712T | c.2134G>A | Missense_Mutation | 1 | 0.11 | KM12 | N | 11 | 0 | 0 | N | ||||||||||||
| BRAF | LHLLFVSKF | SKIN | 286 | p.D287H | c.859G>C | Missense_Mutation | 1 | 0.11 | SKMEL30 | N | 6 | 0 | 18 | N | ||||||||||||
| BRAF | LHVEMLENV | OVARY | 222 | p.V226M | c.676G>A | Missense_Mutation | 1 | 0.11 | A2780 | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | LITGQLPYS | URINARY_TRACT | 649 | p.M650I | c.1950G>T | Missense_Mutation | 1 | 0.11 | KMBC2 | N | 0 | 0 | 4 | N | ||||||||||||
| BRAF | LKSNKIFLH | SKIN | 577 | p.N581K | c.1743T>A | Missense_Mutation | 1 | 0.11 | HS936T | N | 1 | 0 | 9 | N | ||||||||||||
| BRAF | LKSNYIFLH | LARGE_INTESTINE | 577 | p.N581Y | c.1741A>T | Missense_Mutation | 1 | 0.11 | HT55 | N | 1 | 0 | 9 | N | ||||||||||||
| BRAF | LPKIHCSAS | LARGE_INTESTINE | 721 | p.R726C | c.2176C>T | Missense_Mutation | 1 | 0.11 | SNU407 | N | 5 | 0 | 2 | Y | ||||||||||||
| BRAF | LQAFTNEVG | ENDOMETRIUM | 495 | p.K499T | c.1496A>C | Missense_Mutation | 1 | 0.11 | JHUEM7 | N | 0 | 0 | 4 | N | ||||||||||||
| BRAF | LSKVRNNCP | LUNG | 678 | p.S683N | c.2048G>A | Missense_Mutation | 1 | 0.11 | SW1271 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | LSVTPPASL | STOMACH | 398 | p.A400V | c.1199C>T | Missense_Mutation | 1 | 0.11 | SNU1 | N | 15 | 0 | 0 | N | ||||||||||||
| BRAF | LTSGSSPSS | LUNG | 312 | p.A320S | c.958G>T | Missense_Mutation | 1 | 0.11 | NCIH2227 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | LTSIELLAR | LARGE_INTESTINE | 711 | p.A712T | c.2134G>A | Missense_Mutation | 1 | 0.11 | KM12 | N | 7 | 0 | 4 | N | ||||||||||||
| BRAF | LTVKIGDFR | LARGE_INTESTINE | 588 | p.G596R | c.1786G>C | Missense_Mutation | 1 | 0.11 | NCIH508 | N | 6 | 0 | 0 | N | ||||||||||||
| BRAF | LYELITGQL | URINARY_TRACT | 646 | p.M650I | c.1950G>T | Missense_Mutation | 1 | 0.11 | KMBC2 | N | 10 | 0 | 0 | N | ||||||||||||
| BRAF | LYVCASPKT | OVARY | 745 | p.A747V | c.2240C>T | Missense_Mutation | 1 | 0.11 | OC316 | N | 3 | 0 | 0 | N | ||||||||||||
| BRAF | MCVNYDQLH | SKIN | 279 | p.D287H | c.859G>C | Missense_Mutation | 1 | 0.11 | SKMEL30 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | MDSVTSSSS | LARGE_INTESTINE | 117 | p.T119S | c.356C>G | Missense_Mutation | 1 | 0.11 | HT29 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | MLENVPLTT | OVARY | 226 | p.V226M | c.676G>A | Missense_Mutation | 1 | 0.11 | A2780 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | MWNVTAPTP | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 484 | p.L485W | c.1454T>G | Missense_Mutation | 1 | 0.11 | CI1 | N | 0 | 0 | 0 | Y | ||||||||||||
| BRAF | NAPSIYLEA | BREAST | 73 | p.P74A | c.220C>G | Missense_Mutation | 1 | 0.11 | MDAMB415 | Y | 4 | 9 | 0 | N | ||||||||||||
| BRAF | NKIFLHEDL | SKIN | 580 | p.N581K | c.1743T>A | Missense_Mutation | 1 | 0.11 | HS936T | N | 6 | 0 | 0 | N | ||||||||||||
| BRAF | NNCPKAMKR | LUNG | 683 | p.S683N | c.2048G>A | Missense_Mutation | 1 | 0.11 | SW1271 | Y | 3 | 9 | 0 | N | ||||||||||||
| BRAF | NPTDVAQSN | CENTRAL_NERVOUS_SYSTEM | 140 | p.R146Q | c.437G>A | Missense_Mutation | 1 | 0.11 | CCFSTTG1 | N | 3 | 0 | 0 | N | ||||||||||||
| BRAF | NTEVPLMCV | LARGE_INTESTINE | 273 | p.S273N | c.818G>A | Missense_Mutation | 1 | 0.11 | CCK81 | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | NTIDPVNID | LUNG | 372 | p.E375D | c.1125A>T | Missense_Mutation | 1 | 0.11 | NCIH1651 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | NVHINTIDP | LUNG | 368 | p.E375D | c.1125A>T | Missense_Mutation | 1 | 0.11 | NCIH1651 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | NYDQLHLLF | SKIN | 282 | p.D287H | c.859G>C | Missense_Mutation | 1 | 0.11 | SKMEL30 | N | 5 | 0 | 0 | N | ||||||||||||
| BRAF | NYIFLHEDL | LARGE_INTESTINE | 580 | p.N581Y | c.1741A>T | Missense_Mutation | 1 | 0.11 | HT55 | Y | 9 | 9 | 0 | N | ||||||||||||
| BRAF | PADEDHQNQ | LARGE_INTESTINE | 348 | p.R354Q | c.1061G>A | Missense_Mutation | 1 | 0.11 | HT115 | N | 0 | 0 | 0 | Y | ||||||||||||
| BRAF | PDLSKVRNN | LUNG | 676 | p.S683N | c.2048G>A | Missense_Mutation | 1 | 0.11 | SW1271 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | PIGWGTDIS | LARGE_INTESTINE | 207 | p.D211G | c.632A>G | Missense_Mutation | 1 | 0.11 | LS180 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | PKIHCSASE | LARGE_INTESTINE | 722 | p.R726C | c.2176C>T | Missense_Mutation | 1 | 0.11 | SNU407 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | PLFPQILTS | LARGE_INTESTINE | 705 | p.A712T | c.2134G>A | Missense_Mutation | 1 | 0.11 | KM12 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | PNVHINTID | LUNG | 367 | p.E375D | c.1125A>T | Missense_Mutation | 1 | 0.11 | NCIH1651 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | PQILTSIEL | LARGE_INTESTINE | 708 | p.A712T | c.2134G>A | Missense_Mutation | 1 | 0.11 | KM12 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | PQLAIVAQW | LARGE_INTESTINE | 523 | p.T529A | c.1585A>G | Missense_Mutation | 1 | 0.11 | GP2D | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | PQQLQAFTN | ENDOMETRIUM | 492 | p.K499T | c.1496A>C | Missense_Mutation | 1 | 0.11 | JHUEM7 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | PSSPASDSI | LUNG | 318 | p.A320S | c.958G>T | Missense_Mutation | 1 | 0.11 | NCIH2227 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | PTDVAQSNP | CENTRAL_NERVOUS_SYSTEM | 141 | p.R146Q | c.437G>A | Missense_Mutation | 1 | 0.11 | CCFSTTG1 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | PVGWDTDIS | SKIN | 207 | p.I208V | c.622A>G | Missense_Mutation | 1 | 0.11 | LOXIMVI | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | QAFTNEVGV | ENDOMETRIUM | 496 | p.K499T | c.1496A>C | Missense_Mutation | 1 | 0.11 | JHUEM7 | N | 9 | 0 | 0 | N | ||||||||||||
| BRAF | QDGEKKPVG | SKIN | 201 | p.I208V | c.622A>G | Missense_Mutation | 1 | 0.11 | LOXIMVI | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | QILTSIELL | LARGE_INTESTINE | 709 | p.A712T | c.2134G>A | Missense_Mutation | 1 | 0.11 | KM12 | N | 12 | 0 | 0 | N | ||||||||||||
| BRAF | QITVGQRIE | OVARY | 456 | p.G464E | c.1391G>A | Missense_Mutation | 1 | 0.11 | HEYA8 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | QITVGQRIV | BREAST | 456 | p.G464V | c.1391G>T | Missense_Mutation | 1 | 0.11 | MDAMB231 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | QLAIVAQWC | LARGE_INTESTINE | 524 | p.T529A | c.1585A>G | Missense_Mutation | 1 | 0.11 | GP2D | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | QLHLLFVSK | SKIN | 285 | p.D287H | c.859G>C | Missense_Mutation | 1 | 0.11 | SKMEL30 | N | 5 | 0 | 0 | N | ||||||||||||
| BRAF | QLQAFTNEV | ENDOMETRIUM | 494 | p.K499T | c.1496A>C | Missense_Mutation | 1 | 0.11 | JHUEM7 | Y | 6 | 13 | 0 | N | ||||||||||||
| BRAF | QNPTDVAQS | CENTRAL_NERVOUS_SYSTEM | 139 | p.R146Q | c.437G>A | Missense_Mutation | 1 | 0.11 | CCFSTTG1 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | QNQFGQRDR | LARGE_INTESTINE | 354 | p.R354Q | c.1061G>A | Missense_Mutation | 1 | 0.11 | HT115 | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | QQLQAFTNE | ENDOMETRIUM | 493 | p.K499T | c.1496A>C | Missense_Mutation | 1 | 0.11 | JHUEM7 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | QRCNTEVPL | LARGE_INTESTINE | 270 | p.S273N | c.818G>A | Missense_Mutation | 1 | 0.11 | CCK81 | N | 5 | 0 | 0 | N | ||||||||||||
| BRAF | QRCSTKVPL | SKIN | 270 | p.E275K | c.823G>A | Missense_Mutation | 1 | 0.11 | SKMEL30 | N | 6 | 0 | 0 | N | ||||||||||||
| BRAF | QRIESGSFG | OVARY | 461 | p.G464E | c.1391G>A | Missense_Mutation | 1 | 0.11 | HEYA8 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | QRIGSGSFA | LUNG | 461 | p.G469A | c.1406G>C | Missense_Mutation | 1 | 0.11 | NCIH1755 | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | QRIVSGSFG | BREAST | 461 | p.G464V | c.1391G>T | Missense_Mutation | 1 | 0.11 | MDAMB231 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | QSNPKSPQK | CENTRAL_NERVOUS_SYSTEM | 146 | p.R146Q | c.437G>A | Missense_Mutation | 1 | 0.11 | CCFSTTG1 | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | QTEDFSLYV | OVARY | 739 | p.A747V | c.2240C>T | Missense_Mutation | 1 | 0.11 | OC316 | Y | 4 | 14 | 0 | N | ||||||||||||
| BRAF | RATVKSRWS | PROSTATE | 597 | p.L597R | c.1790T>G | Missense_Mutation | 1 | 0.11 | 22RV1 | N | 1 | 0 | 0 | Y | ||||||||||||
| BRAF | RCNTEVPLM | LARGE_INTESTINE | 271 | p.S273N | c.818G>A | Missense_Mutation | 1 | 0.11 | CCK81 | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | RCSTKVPLM | SKIN | 271 | p.E275K | c.823G>A | Missense_Mutation | 1 | 0.11 | SKMEL30 | N | 3 | 0 | 0 | N | ||||||||||||
| BRAF | RDLKSNKIF | SKIN | 575 | p.N581K | c.1743T>A | Missense_Mutation | 1 | 0.11 | HS936T | N | 6 | 0 | 0 | N | ||||||||||||
| BRAF | RDLKSNYIF | LARGE_INTESTINE | 575 | p.N581Y | c.1741A>T | Missense_Mutation | 1 | 0.11 | HT55 | N | 6 | 0 | 0 | N | ||||||||||||
| BRAF | RIESGSFGT | OVARY | 462 | p.G464E | c.1391G>A | Missense_Mutation | 1 | 0.11 | HEYA8 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | RIGSGSFAT | LUNG | 462 | p.G469A | c.1406G>C | Missense_Mutation | 1 | 0.11 | NCIH1755 | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | RIVSGSFGT | BREAST | 462 | p.G464V | c.1391G>T | Missense_Mutation | 1 | 0.11 | MDAMB231 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | RLATVKSRW | LARGE_INTESTINE | 596 | p.G596R | c.1786G>C | Missense_Mutation | 1 | 0.11 | NCIH508 | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | RNNCPKAMK | LUNG | 682 | p.S683N | c.2048G>A | Missense_Mutation | 1 | 0.11 | SW1271 | Y | 1 | 19 | 0 | N | ||||||||||||
| BRAF | RPADEDHQN | LARGE_INTESTINE | 347 | p.R354Q | c.1061G>A | Missense_Mutation | 1 | 0.11 | HT115 | N | 3 | 0 | 0 | N | ||||||||||||
| BRAF | RPLFPQILT | LARGE_INTESTINE | 704 | p.A712T | c.2134G>A | Missense_Mutation | 1 | 0.11 | KM12 | N | 5 | 0 | 0 | N | ||||||||||||
| BRAF | RSLPKIHCS | LARGE_INTESTINE | 719 | p.R726C | c.2176C>T | Missense_Mutation | 1 | 0.11 | SNU407 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | SASMDSVTS | LARGE_INTESTINE | 114 | p.T119S | c.356C>G | Missense_Mutation | 1 | 0.11 | HT29 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | SEDSNRMKT | LUNG | 432 | p.R435S | c.1305G>T | Missense_Mutation | 1 | 0.11 | RERFLCAD1 | N | 5 | 0 | 0 | N | ||||||||||||
| BRAF | SFATVYKGK | LUNG | 467 | p.G469A | c.1406G>C | Missense_Mutation | 1 | 0.11 | NCIH1755 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | SGSFATVYK | LUNG | 465 | p.G469A | c.1406G>C | Missense_Mutation | 1 | 0.11 | NCIH1755 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | SGSSPSSPA | LUNG | 314 | p.A320S | c.958G>T | Missense_Mutation | 1 | 0.11 | NCIH2227 | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | SKVRNNCPK | LUNG | 679 | p.S683N | c.2048G>A | Missense_Mutation | 1 | 0.11 | SW1271 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | SLPKIHCSA | LARGE_INTESTINE | 720 | p.R726C | c.2176C>T | Missense_Mutation | 1 | 0.11 | SNU407 | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | SLYVCASPK | OVARY | 744 | p.A747V | c.2240C>T | Missense_Mutation | 1 | 0.11 | OC316 | N | 5 | 0 | 0 | N | ||||||||||||
| BRAF | SMDSVTSSS | LARGE_INTESTINE | 116 | p.T119S | c.356C>G | Missense_Mutation | 1 | 0.11 | HT29 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | SNKIFLHED | SKIN | 579 | p.N581K | c.1743T>A | Missense_Mutation | 1 | 0.11 | HS936T | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | SNRMKTLGR | LUNG | 435 | p.R435S | c.1305G>T | Missense_Mutation | 1 | 0.11 | RERFLCAD1 | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | SNYIFLHED | LARGE_INTESTINE | 579 | p.N581Y | c.1741A>T | Missense_Mutation | 1 | 0.11 | HT55 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | SPASDSIGP | LUNG | 320 | p.A320S | c.958G>T | Missense_Mutation | 1 | 0.11 | NCIH2227 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | SPDLSKVRN | LUNG | 675 | p.S683N | c.2048G>A | Missense_Mutation | 1 | 0.11 | SW1271 | N | 2 | 0 | 0 | Y | ||||||||||||
| BRAF | SPSSPASDS | LUNG | 317 | p.A320S | c.958G>T | Missense_Mutation | 1 | 0.11 | NCIH2227 | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | SSASMDSVT | LARGE_INTESTINE | 113 | p.T119S | c.356C>G | Missense_Mutation | 1 | 0.11 | HT29 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | SSEDSNRMK | LUNG | 431 | p.R435S | c.1305G>T | Missense_Mutation | 1 | 0.11 | RERFLCAD1 | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | SSPASDSIG | LUNG | 319 | p.A320S | c.958G>T | Missense_Mutation | 1 | 0.11 | NCIH2227 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | SSPSSPASD | LUNG | 316 | p.A320S | c.958G>T | Missense_Mutation | 1 | 0.11 | NCIH2227 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | SSSASMDSV | LARGE_INTESTINE | 112 | p.T119S | c.356C>G | Missense_Mutation | 1 | 0.11 | HT29 | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | SSSEDSNRM | LUNG | 430 | p.R435S | c.1305G>T | Missense_Mutation | 1 | 0.11 | RERFLCAD1 | Y | 5 | 9 | 0 | N | ||||||||||||
| BRAF | SSSSEDSNR | LUNG | 429 | p.R435S | c.1305G>T | Missense_Mutation | 1 | 0.11 | RERFLCAD1 | N | 3 | 0 | 0 | N | ||||||||||||
| BRAF | SSSSSEDSN | LUNG | 428 | p.R435S | c.1305G>T | Missense_Mutation | 1 | 0.11 | RERFLCAD1 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | STKVPLMCV | SKIN | 273 | p.E275K | c.823G>A | Missense_Mutation | 1 | 0.11 | SKMEL30 | Y | 3 | 9 | 0 | N | ||||||||||||
| BRAF | STTGLSVTP | STOMACH | 394 | p.A400V | c.1199C>T | Missense_Mutation | 1 | 0.11 | SNU1 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | SVTPPASLP | STOMACH | 399 | p.A400V | c.1199C>T | Missense_Mutation | 1 | 0.11 | SNU1 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | SVTSSSSSS | LARGE_INTESTINE | 119 | p.T119S | c.356C>G | Missense_Mutation | 1 | 0.11 | HT29 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | TDVAQSNPK | CENTRAL_NERVOUS_SYSTEM | 142 | p.R146Q | c.437G>A | Missense_Mutation | 1 | 0.11 | CCFSTTG1 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | TEDFSLYVC | OVARY | 740 | p.A747V | c.2240C>T | Missense_Mutation | 1 | 0.11 | OC316 | N | 5 | 0 | 0 | N | ||||||||||||
| BRAF | TGEELHVEM | OVARY | 218 | p.V226M | c.676G>A | Missense_Mutation | 1 | 0.11 | A2780 | N | 3 | 0 | 0 | N | ||||||||||||
| BRAF | TGLSVTPPA | STOMACH | 396 | p.A400V | c.1199C>T | Missense_Mutation | 1 | 0.11 | SNU1 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | TIDPVNIDD | LUNG | 373 | p.E375D | c.1125A>T | Missense_Mutation | 1 | 0.11 | NCIH1651 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | TKKSRWSGS | LARGE_INTESTINE | 599 | p.V600K | c.1798_1799GT>AA | Missense_Mutation | 1 | 0.11 | MDST8 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | TKPQLAIVA | LARGE_INTESTINE | 521 | p.T529A | c.1585A>G | Missense_Mutation | 1 | 0.11 | GP2D | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | TKVPLMCVN | SKIN | 274 | p.E275K | c.823G>A | Missense_Mutation | 1 | 0.11 | SKMEL30 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | TNEVGVLRK | ENDOMETRIUM | 499 | p.K499T | c.1496A>C | Missense_Mutation | 1 | 0.11 | JHUEM7 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | TPQQLQAFT | ENDOMETRIUM | 491 | p.K499T | c.1496A>C | Missense_Mutation | 1 | 0.11 | JHUEM7 | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | TSGSSPSSP | LUNG | 313 | p.A320S | c.958G>T | Missense_Mutation | 1 | 0.11 | NCIH2227 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | TSIELLARS | LARGE_INTESTINE | 712 | p.A712T | c.2134G>A | Missense_Mutation | 1 | 0.11 | KM12 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | TTGLSVTPP | STOMACH | 395 | p.A400V | c.1199C>T | Missense_Mutation | 1 | 0.11 | SNU1 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | TVGQRIESG | OVARY | 458 | p.G464E | c.1391G>A | Missense_Mutation | 1 | 0.11 | HEYA8 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | TVGQRIVSG | BREAST | 458 | p.G464V | c.1391G>T | Missense_Mutation | 1 | 0.11 | MDAMB231 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | TVKIGDFGR | PROSTATE | 589 | p.L597R | c.1790T>G | Missense_Mutation | 1 | 0.11 | 22RV1 | Y | 6 | 9 | 0 | N | ||||||||||||
| BRAF | TVKIGDFGV | LUNG | 589 | p.L597V | c.1789C>G | Missense_Mutation | 1 | 0.11 | NCIH2087 | Y | 2 | 11 | 0 | N | ||||||||||||
| BRAF | TVKIGDFRL | LARGE_INTESTINE | 589 | p.G596R | c.1786G>C | Missense_Mutation | 1 | 0.11 | NCIH508 | Y | 4 | 10 | 0 | N | ||||||||||||
| BRAF | VAQSNPKSP | CENTRAL_NERVOUS_SYSTEM | 144 | p.R146Q | c.437G>A | Missense_Mutation | 1 | 0.11 | CCFSTTG1 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | VAQWCEGSS | LARGE_INTESTINE | 528 | p.T529A | c.1585A>G | Missense_Mutation | 1 | 0.11 | GP2D | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | VATVKSRWS | LUNG | 597 | p.L597V | c.1789C>G | Missense_Mutation | 1 | 0.11 | NCIH2087 | N | 1 | 0 | 1 | Y | ||||||||||||
| BRAF | VAVKMWNVT | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 480 | p.L485W | c.1454T>G | Missense_Mutation | 1 | 0.11 | CI1 | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | VCASPKTPI | OVARY | 747 | p.A747V | c.2240C>T | Missense_Mutation | 1 | 0.11 | OC316 | N | 5 | 0 | 0 | N | ||||||||||||
| BRAF | VEMLENVPL | OVARY | 224 | p.V226M | c.676G>A | Missense_Mutation | 1 | 0.11 | A2780 | N | 12 | 0 | 14 | N | ||||||||||||
| BRAF | VGQRIESGS | OVARY | 459 | p.G464E | c.1391G>A | Missense_Mutation | 1 | 0.11 | HEYA8 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | VGQRIVSGS | BREAST | 459 | p.G464V | c.1391G>T | Missense_Mutation | 1 | 0.11 | MDAMB231 | N | 1 | 0 | 6 | N | ||||||||||||
| BRAF | VGWDTDISW | SKIN | 208 | p.I208V | c.622A>G | Missense_Mutation | 1 | 0.11 | LOXIMVI | N | 5 | 0 | 0 | N | ||||||||||||
| BRAF | VHINTIDPV | LUNG | 369 | p.E375D | c.1125A>T | Missense_Mutation | 1 | 0.11 | NCIH1651 | N | 3 | 0 | 4 | N | ||||||||||||
| BRAF | VKIGDFGRA | PROSTATE | 590 | p.L597R | c.1790T>G | Missense_Mutation | 1 | 0.11 | 22RV1 | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | VKIGDFGVA | LUNG | 590 | p.L597V | c.1789C>G | Missense_Mutation | 1 | 0.11 | NCIH2087 | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | VKIGDFRLA | LARGE_INTESTINE | 590 | p.G596R | c.1786G>C | Missense_Mutation | 1 | 0.11 | NCIH508 | N | 3 | 0 | 1 | N | ||||||||||||
| BRAF | VKMWNVTAP | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 482 | p.L485W | c.1454T>G | Missense_Mutation | 1 | 0.11 | CI1 | N | 0 | 0 | 14 | N | ||||||||||||
| BRAF | VLYELITGQ | URINARY_TRACT | 645 | p.M650I | c.1950G>T | Missense_Mutation | 1 | 0.11 | KMBC2 | N | 0 | 0 | 2 | N | ||||||||||||
| BRAF | VNYDQLHLL | SKIN | 281 | p.D287H | c.859G>C | Missense_Mutation | 1 | 0.11 | SKMEL30 | N | 18 | 0 | 6 | N | ||||||||||||
| BRAF | VRNNCPKAM | LUNG | 681 | p.S683N | c.2048G>A | Missense_Mutation | 1 | 0.11 | SW1271 | N | 4 | 0 | 36 | N | ||||||||||||
| BRAF | VSGSFGTVY | BREAST | 464 | p.G464V | c.1391G>T | Missense_Mutation | 1 | 0.11 | MDAMB231 | N | 9 | 0 | 0 | N | ||||||||||||
| BRAF | VSSSASMDS | LARGE_INTESTINE | 111 | p.T119S | c.356C>G | Missense_Mutation | 1 | 0.11 | HT29 | N | 0 | 0 | 4 | N | ||||||||||||
| BRAF | VTPPASLPG | STOMACH | 400 | p.A400V | c.1199C>T | Missense_Mutation | 1 | 0.11 | SNU1 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | WGTDISWLT | LARGE_INTESTINE | 210 | p.D211G | c.632A>G | Missense_Mutation | 1 | 0.11 | LS180 | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | WNVTAPTPQ | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 485 | p.L485W | c.1454T>G | Missense_Mutation | 1 | 0.11 | CI1 | N | 2 | 0 | 6 | Y | ||||||||||||
| BRAF | YDQLHLLFV | SKIN | 283 | p.D287H | c.859G>C | Missense_Mutation | 1 | 0.11 | SKMEL30 | N | 7 | 0 | 0 | N | ||||||||||||
| BRAF | YELITGQLP | URINARY_TRACT | 647 | p.M650I | c.1950G>T | Missense_Mutation | 1 | 0.11 | KMBC2 | N | 2 | 0 | 1 | Y | ||||||||||||
| BRAF | YIFLHEDLT | LARGE_INTESTINE | 581 | p.N581Y | c.1741A>T | Missense_Mutation | 1 | 0.11 | HT55 | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | YKFHQRCNT | LARGE_INTESTINE | 266 | p.S273N | c.818G>A | Missense_Mutation | 1 | 0.11 | CCK81 | N | 4 | 0 | 16 | N | ||||||||||||
| BRAF | YVCASPKTP | OVARY | 746 | p.A747V | c.2240C>T | Missense_Mutation | 1 | 0.11 | OC316 | N | 1 | 0 | 8 | N | ||||||||||||
| BRAF | ATDKSRWSG | SKIN | 598 | p.V600D | c.1799_1800TG>AT | Missense_Mutation | 1 | 0.22 | WM115 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | ATDKSRWSG | SKIN | 598 | p.V600D | c.1799_1800TG>AT | Missense_Mutation | 1 | 0.22 | WM2664 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | ATVNSRWSG | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 598 | p.K601N | c.1803A>T | Missense_Mutation | 1 | 0.22 | JVM3 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | ATVNSRWSG | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 598 | p.K601N | c.1803A>T | Missense_Mutation | 1 | 0.22 | U266B1 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | AVYRIQDGL | LUNG | 196 | p.E204L | c.610_611GA>TT | Missense_Mutation | 1 | 0.22 | HCC1588 | N | 14 | 0 | 0 | N | ||||||||||||
| BRAF | AVYRIQDGL | LARGE_INTESTINE | 196 | p.E204L | c.610_611GA>TT | Missense_Mutation | 1 | 0.22 | LS513 | N | 14 | 0 | 0 | N | ||||||||||||
| BRAF | DFGLATDKS | SKIN | 594 | p.V600D | c.1799_1800TG>AT | Missense_Mutation | 1 | 0.22 | WM115 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | DFGLATDKS | SKIN | 594 | p.V600D | c.1799_1800TG>AT | Missense_Mutation | 1 | 0.22 | WM2664 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | DFGLATVNS | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 594 | p.K601N | c.1803A>T | Missense_Mutation | 1 | 0.22 | JVM3 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | DFGLATVNS | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 594 | p.K601N | c.1803A>T | Missense_Mutation | 1 | 0.22 | U266B1 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | DGLKKPIGW | LUNG | 202 | p.E204L | c.610_611GA>TT | Missense_Mutation | 1 | 0.22 | HCC1588 | N | 3 | 0 | 0 | N | ||||||||||||
| BRAF | DGLKKPIGW | LARGE_INTESTINE | 202 | p.E204L | c.610_611GA>TT | Missense_Mutation | 1 | 0.22 | LS513 | N | 3 | 0 | 0 | N | ||||||||||||
| BRAF | DKSRWSGSH | SKIN | 600 | p.V600D | c.1799_1800TG>AT | Missense_Mutation | 1 | 0.22 | WM115 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | DKSRWSGSH | SKIN | 600 | p.V600D | c.1799_1800TG>AT | Missense_Mutation | 1 | 0.22 | WM2664 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | DLSKVQSNC | ENDOMETRIUM | 677 | p.R682Q | c.2045G>A | Missense_Mutation | 1 | 0.22 | HEC1A | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | DLSKVQSNC | ENDOMETRIUM | 677 | p.R682Q | c.2045G>A | Missense_Mutation | 1 | 0.22 | HEC1B | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | FGLATDKSR | SKIN | 595 | p.V600D | c.1799_1800TG>AT | Missense_Mutation | 1 | 0.22 | WM115 | N | 3 | 0 | 2 | N | ||||||||||||
| BRAF | FGLATDKSR | SKIN | 595 | p.V600D | c.1799_1800TG>AT | Missense_Mutation | 1 | 0.22 | WM2664 | N | 3 | 0 | 2 | N | ||||||||||||
| BRAF | FGLATVNSR | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 595 | p.K601N | c.1803A>T | Missense_Mutation | 1 | 0.22 | JVM3 | N | 3 | 0 | 15 | N | ||||||||||||
| BRAF | FGLATVNSR | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 595 | p.K601N | c.1803A>T | Missense_Mutation | 1 | 0.22 | U266B1 | N | 3 | 0 | 15 | N | ||||||||||||
| BRAF | GDFGLATDK | SKIN | 593 | p.V600D | c.1799_1800TG>AT | Missense_Mutation | 1 | 0.22 | WM115 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | GDFGLATDK | SKIN | 593 | p.V600D | c.1799_1800TG>AT | Missense_Mutation | 1 | 0.22 | WM2664 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | GDFGLATVN | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 593 | p.K601N | c.1803A>T | Missense_Mutation | 1 | 0.22 | JVM3 | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | GDFGLATVN | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 593 | p.K601N | c.1803A>T | Missense_Mutation | 1 | 0.22 | U266B1 | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | GLATDKSRW | SKIN | 596 | p.V600D | c.1799_1800TG>AT | Missense_Mutation | 1 | 0.22 | WM115 | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | GLATDKSRW | SKIN | 596 | p.V600D | c.1799_1800TG>AT | Missense_Mutation | 1 | 0.22 | WM2664 | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | GLATVNSRW | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 596 | p.K601N | c.1803A>T | Missense_Mutation | 1 | 0.22 | JVM3 | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | GLATVNSRW | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 596 | p.K601N | c.1803A>T | Missense_Mutation | 1 | 0.22 | U266B1 | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | GLKKPIGWD | LUNG | 203 | p.E204L | c.610_611GA>TT | Missense_Mutation | 1 | 0.22 | HCC1588 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | GLKKPIGWD | LARGE_INTESTINE | 203 | p.E204L | c.610_611GA>TT | Missense_Mutation | 1 | 0.22 | LS513 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | GQRIGSVSF | LUNG | 460 | p.G466V | c.1397G>T | Missense_Mutation | 1 | 0.22 | CAL12T | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | GQRIGSVSF | LUNG | 460 | p.G466V | c.1397G>T | Missense_Mutation | 1 | 0.22 | NCIH1666 | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | GSVSFGTVY | LUNG | 464 | p.G466V | c.1397G>T | Missense_Mutation | 1 | 0.22 | CAL12T | N | 7 | 0 | 0 | N | ||||||||||||
| BRAF | GSVSFGTVY | LUNG | 464 | p.G466V | c.1397G>T | Missense_Mutation | 1 | 0.22 | NCIH1666 | N | 7 | 0 | 0 | N | ||||||||||||
| BRAF | IGDFGLATD | SKIN | 592 | p.V600D | c.1799_1800TG>AT | Missense_Mutation | 1 | 0.22 | WM115 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | IGDFGLATD | SKIN | 592 | p.V600D | c.1799_1800TG>AT | Missense_Mutation | 1 | 0.22 | WM2664 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | IGSVSFGTV | LUNG | 463 | p.G466V | c.1397G>T | Missense_Mutation | 1 | 0.22 | CAL12T | N | 6 | 0 | 0 | N | ||||||||||||
| BRAF | IGSVSFGTV | LUNG | 463 | p.G466V | c.1397G>T | Missense_Mutation | 1 | 0.22 | NCIH1666 | N | 6 | 0 | 0 | N | ||||||||||||
| BRAF | IQDGLKKPI | LUNG | 200 | p.E204L | c.610_611GA>TT | Missense_Mutation | 1 | 0.22 | HCC1588 | N | 8 | 0 | 0 | N | ||||||||||||
| BRAF | IQDGLKKPI | LARGE_INTESTINE | 200 | p.E204L | c.610_611GA>TT | Missense_Mutation | 1 | 0.22 | LS513 | N | 8 | 0 | 0 | N | ||||||||||||
| BRAF | KVQSNCPKA | ENDOMETRIUM | 680 | p.R682Q | c.2045G>A | Missense_Mutation | 1 | 0.22 | HEC1A | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | KVQSNCPKA | ENDOMETRIUM | 680 | p.R682Q | c.2045G>A | Missense_Mutation | 1 | 0.22 | HEC1B | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | LATDKSRWS | SKIN | 597 | p.V600D | c.1799_1800TG>AT | Missense_Mutation | 1 | 0.22 | WM115 | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | LATDKSRWS | SKIN | 597 | p.V600D | c.1799_1800TG>AT | Missense_Mutation | 1 | 0.22 | WM2664 | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | LATVNSRWS | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 597 | p.K601N | c.1803A>T | Missense_Mutation | 1 | 0.22 | JVM3 | N | 2 | 0 | 1 | N | ||||||||||||
| BRAF | LATVNSRWS | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 597 | p.K601N | c.1803A>T | Missense_Mutation | 1 | 0.22 | U266B1 | N | 2 | 0 | 1 | N | ||||||||||||
| BRAF | LKKPIGWDT | LUNG | 204 | p.E204L | c.610_611GA>TT | Missense_Mutation | 1 | 0.22 | HCC1588 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | LKKPIGWDT | LARGE_INTESTINE | 204 | p.E204L | c.610_611GA>TT | Missense_Mutation | 1 | 0.22 | LS513 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | LSKVQSNCP | ENDOMETRIUM | 678 | p.R682Q | c.2045G>A | Missense_Mutation | 1 | 0.22 | HEC1A | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | LSKVQSNCP | ENDOMETRIUM | 678 | p.R682Q | c.2045G>A | Missense_Mutation | 1 | 0.22 | HEC1B | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | LSPDLSKVQ | ENDOMETRIUM | 674 | p.R682Q | c.2045G>A | Missense_Mutation | 1 | 0.22 | HEC1A | N | 0 | 0 | 6 | N | ||||||||||||
| BRAF | LSPDLSKVQ | ENDOMETRIUM | 674 | p.R682Q | c.2045G>A | Missense_Mutation | 1 | 0.22 | HEC1B | N | 0 | 0 | 6 | N | ||||||||||||
| BRAF | NSRWSGSHQ | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 601 | p.K601N | c.1803A>T | Missense_Mutation | 1 | 0.22 | JVM3 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | NSRWSGSHQ | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 601 | p.K601N | c.1803A>T | Missense_Mutation | 1 | 0.22 | U266B1 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | PDLSKVQSN | ENDOMETRIUM | 676 | p.R682Q | c.2045G>A | Missense_Mutation | 1 | 0.22 | HEC1A | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | PDLSKVQSN | ENDOMETRIUM | 676 | p.R682Q | c.2045G>A | Missense_Mutation | 1 | 0.22 | HEC1B | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | QDGLKKPIG | LUNG | 201 | p.E204L | c.610_611GA>TT | Missense_Mutation | 1 | 0.22 | HCC1588 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | QDGLKKPIG | LARGE_INTESTINE | 201 | p.E204L | c.610_611GA>TT | Missense_Mutation | 1 | 0.22 | LS513 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | QRIGSVSFG | LUNG | 461 | p.G466V | c.1397G>T | Missense_Mutation | 1 | 0.22 | CAL12T | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | QRIGSVSFG | LUNG | 461 | p.G466V | c.1397G>T | Missense_Mutation | 1 | 0.22 | NCIH1666 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | QSNCPKAMK | ENDOMETRIUM | 682 | p.R682Q | c.2045G>A | Missense_Mutation | 1 | 0.22 | HEC1A | Y | 2 | 13 | 0 | N | ||||||||||||
| BRAF | QSNCPKAMK | ENDOMETRIUM | 682 | p.R682Q | c.2045G>A | Missense_Mutation | 1 | 0.22 | HEC1B | Y | 2 | 13 | 0 | N | ||||||||||||
| BRAF | RIGSVSFGT | LUNG | 462 | p.G466V | c.1397G>T | Missense_Mutation | 1 | 0.22 | CAL12T | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | RIGSVSFGT | LUNG | 462 | p.G466V | c.1397G>T | Missense_Mutation | 1 | 0.22 | NCIH1666 | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | RIQDGLKKP | LUNG | 199 | p.E204L | c.610_611GA>TT | Missense_Mutation | 1 | 0.22 | HCC1588 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | RIQDGLKKP | LARGE_INTESTINE | 199 | p.E204L | c.610_611GA>TT | Missense_Mutation | 1 | 0.22 | LS513 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | SKVQSNCPK | ENDOMETRIUM | 679 | p.R682Q | c.2045G>A | Missense_Mutation | 1 | 0.22 | HEC1A | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | SKVQSNCPK | ENDOMETRIUM | 679 | p.R682Q | c.2045G>A | Missense_Mutation | 1 | 0.22 | HEC1B | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | SPDLSKVQS | ENDOMETRIUM | 675 | p.R682Q | c.2045G>A | Missense_Mutation | 1 | 0.22 | HEC1A | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | SPDLSKVQS | ENDOMETRIUM | 675 | p.R682Q | c.2045G>A | Missense_Mutation | 1 | 0.22 | HEC1B | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | SVSFGTVYK | LUNG | 465 | p.G466V | c.1397G>T | Missense_Mutation | 1 | 0.22 | CAL12T | Y | 3 | 11 | 0 | N | ||||||||||||
| BRAF | SVSFGTVYK | LUNG | 465 | p.G466V | c.1397G>T | Missense_Mutation | 1 | 0.22 | NCIH1666 | Y | 3 | 11 | 0 | N | ||||||||||||
| BRAF | TDKSRWSGS | SKIN | 599 | p.V600D | c.1799_1800TG>AT | Missense_Mutation | 1 | 0.22 | WM115 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | TDKSRWSGS | SKIN | 599 | p.V600D | c.1799_1800TG>AT | Missense_Mutation | 1 | 0.22 | WM2664 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | TVGQRIGSV | LUNG | 458 | p.G466V | c.1397G>T | Missense_Mutation | 1 | 0.22 | CAL12T | Y | 5 | 12 | 0 | N | ||||||||||||
| BRAF | TVGQRIGSV | LUNG | 458 | p.G466V | c.1397G>T | Missense_Mutation | 1 | 0.22 | NCIH1666 | Y | 5 | 12 | 0 | N | ||||||||||||
| BRAF | TVNSRWSGS | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 599 | p.K601N | c.1803A>T | Missense_Mutation | 1 | 0.22 | JVM3 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | TVNSRWSGS | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 599 | p.K601N | c.1803A>T | Missense_Mutation | 1 | 0.22 | U266B1 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | VGQRIGSVS | LUNG | 459 | p.G466V | c.1397G>T | Missense_Mutation | 1 | 0.22 | CAL12T | N | 1 | 0 | 1 | N | ||||||||||||
| BRAF | VGQRIGSVS | LUNG | 459 | p.G466V | c.1397G>T | Missense_Mutation | 1 | 0.22 | NCIH1666 | N | 1 | 0 | 1 | N | ||||||||||||
| BRAF | VNSRWSGSH | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 600 | p.K601N | c.1803A>T | Missense_Mutation | 1 | 0.22 | JVM3 | N | 0 | 0 | 5 | N | ||||||||||||
| BRAF | VNSRWSGSH | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 600 | p.K601N | c.1803A>T | Missense_Mutation | 1 | 0.22 | U266B1 | N | 0 | 0 | 5 | N | ||||||||||||
| BRAF | VQSNCPKAM | ENDOMETRIUM | 681 | p.R682Q | c.2045G>A | Missense_Mutation | 1 | 0.22 | HEC1A | N | 4 | 0 | 7 | N | ||||||||||||
| BRAF | VQSNCPKAM | ENDOMETRIUM | 681 | p.R682Q | c.2045G>A | Missense_Mutation | 1 | 0.22 | HEC1B | N | 4 | 0 | 7 | N | ||||||||||||
| BRAF | VSFGTVYKG | LUNG | 466 | p.G466V | c.1397G>T | Missense_Mutation | 1 | 0.22 | CAL12T | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | VSFGTVYKG | LUNG | 466 | p.G466V | c.1397G>T | Missense_Mutation | 1 | 0.22 | NCIH1666 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | VYRIQDGLK | LUNG | 197 | p.E204L | c.610_611GA>TT | Missense_Mutation | 1 | 0.22 | HCC1588 | N | 1 | 0 | 2 | N | ||||||||||||
| BRAF | VYRIQDGLK | LARGE_INTESTINE | 197 | p.E204L | c.610_611GA>TT | Missense_Mutation | 1 | 0.22 | LS513 | N | 1 | 0 | 2 | N | ||||||||||||
| BRAF | YRIQDGLKK | LUNG | 198 | p.E204L | c.610_611GA>TT | Missense_Mutation | 1 | 0.22 | HCC1588 | N | 4 | 0 | 35 | N | ||||||||||||
| BRAF | YRIQDGLKK | LARGE_INTESTINE | 198 | p.E204L | c.610_611GA>TT | Missense_Mutation | 1 | 0.22 | LS513 | N | 4 | 0 | 35 | N | ||||||||||||
| BRAF | ATEKSRWSG | THYROID | 598 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | 8305C | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | ATEKSRWSG | THYROID | 598 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | 8505C | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | ATEKSRWSG | SKIN | 598 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | A101D | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | ATEKSRWSG | SKIN | 598 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | A2058 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | ATEKSRWSG | SKIN | 598 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | A375 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | ATEKSRWSG | BONE | 598 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | A673 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | ATEKSRWSG | CENTRAL_NERVOUS_SYSTEM | 598 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | AM38 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | ATEKSRWSG | THYROID | 598 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | BCPAP | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | ATEKSRWSG | SKIN | 598 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | C32 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | ATEKSRWSG | LARGE_INTESTINE | 598 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | CL34 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | ATEKSRWSG | LARGE_INTESTINE | 598 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | COLO201 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | ATEKSRWSG | LARGE_INTESTINE | 598 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | COLO205 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | ATEKSRWSG | SKIN | 598 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | COLO679 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | ATEKSRWSG | SKIN | 598 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | COLO741 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | ATEKSRWSG | SKIN | 598 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | COLO783 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | ATEKSRWSG | SKIN | 598 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | COLO818 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | ATEKSRWSG | SKIN | 598 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | COLO829 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | ATEKSRWSG | CENTRAL_NERVOUS_SYSTEM | 598 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | DBTRG05MG | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | ATEKSRWSG | BREAST | 598 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | DU4475 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | ATEKSRWSG | OVARY | 598 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | ES2 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | ATEKSRWSG | SKIN | 598 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | G361 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | ATEKSRWSG | SOFT_TISSUE | 598 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | GCT | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | ATEKSRWSG | SKIN | 598 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | HS695T | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | ATEKSRWSG | SKIN | 598 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | HT144 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | ATEKSRWSG | LARGE_INTESTINE | 598 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | HT29 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | ATEKSRWSG | SKIN | 598 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | IGR37 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | ATEKSRWSG | SKIN | 598 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | IGR39 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | ATEKSRWSG | OVARY | 598 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | JHOM2B | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | ATEKSRWSG | SKIN | 598 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | K029AX | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | ATEKSRWSG | SKIN | 598 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | LOXIMVI | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | ATEKSRWSG | LARGE_INTESTINE | 598 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | LS411N | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | ATEKSRWSG | SKIN | 598 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | MALME3M | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | ATEKSRWSG | SKIN | 598 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | MDAMB435S | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | ATEKSRWSG | SKIN | 598 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | MELHO | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | ATEKSRWSG | LUNG | 598 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | NCIH854 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | ATEKSRWSG | CENTRAL_NERVOUS_SYSTEM | 598 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | NMCG1 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | ATEKSRWSG | LARGE_INTESTINE | 598 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | OUMS23 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | ATEKSRWSG | LARGE_INTESTINE | 598 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | RKO | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | ATEKSRWSG | SKIN | 598 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | RPMI7951 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | ATEKSRWSG | SKIN | 598 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SH4 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | ATEKSRWSG | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 598 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SIGM5 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | ATEKSRWSG | LIVER | 598 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SKHEP1 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | ATEKSRWSG | SKIN | 598 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SKMEL1 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | ATEKSRWSG | SKIN | 598 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SKMEL24 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | ATEKSRWSG | SKIN | 598 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SKMEL28 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | ATEKSRWSG | SKIN | 598 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SKMEL3 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | ATEKSRWSG | SKIN | 598 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SKMEL5 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | ATEKSRWSG | LARGE_INTESTINE | 598 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SNUC5 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | ATEKSRWSG | LARGE_INTESTINE | 598 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SW1417 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | ATEKSRWSG | SKIN | 598 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | UACC257 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | ATEKSRWSG | SKIN | 598 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | UACC62 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | ATEKSRWSG | SKIN | 598 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | WM1799 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | ATEKSRWSG | SKIN | 598 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | WM793 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | ATEKSRWSG | SKIN | 598 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | WM88 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | ATEKSRWSG | SKIN | 598 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | WM983B | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | DFGLATEKS | THYROID | 594 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | 8305C | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | DFGLATEKS | THYROID | 594 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | 8505C | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | DFGLATEKS | SKIN | 594 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | A101D | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | DFGLATEKS | SKIN | 594 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | A2058 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | DFGLATEKS | SKIN | 594 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | A375 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | DFGLATEKS | BONE | 594 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | A673 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | DFGLATEKS | CENTRAL_NERVOUS_SYSTEM | 594 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | AM38 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | DFGLATEKS | THYROID | 594 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | BCPAP | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | DFGLATEKS | SKIN | 594 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | C32 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | DFGLATEKS | LARGE_INTESTINE | 594 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | CL34 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | DFGLATEKS | LARGE_INTESTINE | 594 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | COLO201 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | DFGLATEKS | LARGE_INTESTINE | 594 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | COLO205 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | DFGLATEKS | SKIN | 594 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | COLO679 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | DFGLATEKS | SKIN | 594 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | COLO741 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | DFGLATEKS | SKIN | 594 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | COLO783 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | DFGLATEKS | SKIN | 594 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | COLO818 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | DFGLATEKS | SKIN | 594 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | COLO829 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | DFGLATEKS | CENTRAL_NERVOUS_SYSTEM | 594 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | DBTRG05MG | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | DFGLATEKS | BREAST | 594 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | DU4475 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | DFGLATEKS | OVARY | 594 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | ES2 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | DFGLATEKS | SKIN | 594 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | G361 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | DFGLATEKS | SOFT_TISSUE | 594 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | GCT | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | DFGLATEKS | SKIN | 594 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | HS695T | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | DFGLATEKS | SKIN | 594 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | HT144 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | DFGLATEKS | LARGE_INTESTINE | 594 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | HT29 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | DFGLATEKS | SKIN | 594 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | IGR37 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | DFGLATEKS | SKIN | 594 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | IGR39 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | DFGLATEKS | OVARY | 594 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | JHOM2B | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | DFGLATEKS | SKIN | 594 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | K029AX | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | DFGLATEKS | SKIN | 594 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | LOXIMVI | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | DFGLATEKS | LARGE_INTESTINE | 594 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | LS411N | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | DFGLATEKS | SKIN | 594 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | MALME3M | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | DFGLATEKS | SKIN | 594 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | MDAMB435S | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | DFGLATEKS | SKIN | 594 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | MELHO | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | DFGLATEKS | LUNG | 594 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | NCIH854 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | DFGLATEKS | CENTRAL_NERVOUS_SYSTEM | 594 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | NMCG1 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | DFGLATEKS | LARGE_INTESTINE | 594 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | OUMS23 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | DFGLATEKS | LARGE_INTESTINE | 594 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | RKO | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | DFGLATEKS | SKIN | 594 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | RPMI7951 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | DFGLATEKS | SKIN | 594 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SH4 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | DFGLATEKS | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 594 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SIGM5 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | DFGLATEKS | LIVER | 594 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SKHEP1 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | DFGLATEKS | SKIN | 594 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SKMEL1 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | DFGLATEKS | SKIN | 594 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SKMEL24 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | DFGLATEKS | SKIN | 594 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SKMEL28 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | DFGLATEKS | SKIN | 594 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SKMEL3 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | DFGLATEKS | SKIN | 594 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SKMEL5 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | DFGLATEKS | LARGE_INTESTINE | 594 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SNUC5 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | DFGLATEKS | LARGE_INTESTINE | 594 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SW1417 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | DFGLATEKS | SKIN | 594 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | UACC257 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | DFGLATEKS | SKIN | 594 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | UACC62 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | DFGLATEKS | SKIN | 594 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | WM1799 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | DFGLATEKS | SKIN | 594 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | WM793 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | DFGLATEKS | SKIN | 594 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | WM88 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | DFGLATEKS | SKIN | 594 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | WM983B | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | EKSRWSGSH | THYROID | 600 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | 8305C | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | EKSRWSGSH | THYROID | 600 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | 8505C | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | EKSRWSGSH | SKIN | 600 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | A101D | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | EKSRWSGSH | SKIN | 600 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | A2058 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | EKSRWSGSH | SKIN | 600 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | A375 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | EKSRWSGSH | BONE | 600 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | A673 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | EKSRWSGSH | CENTRAL_NERVOUS_SYSTEM | 600 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | AM38 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | EKSRWSGSH | THYROID | 600 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | BCPAP | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | EKSRWSGSH | SKIN | 600 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | C32 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | EKSRWSGSH | LARGE_INTESTINE | 600 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | CL34 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | EKSRWSGSH | LARGE_INTESTINE | 600 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | COLO201 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | EKSRWSGSH | LARGE_INTESTINE | 600 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | COLO205 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | EKSRWSGSH | SKIN | 600 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | COLO679 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | EKSRWSGSH | SKIN | 600 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | COLO741 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | EKSRWSGSH | SKIN | 600 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | COLO783 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | EKSRWSGSH | SKIN | 600 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | COLO818 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | EKSRWSGSH | SKIN | 600 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | COLO829 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | EKSRWSGSH | CENTRAL_NERVOUS_SYSTEM | 600 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | DBTRG05MG | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | EKSRWSGSH | BREAST | 600 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | DU4475 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | EKSRWSGSH | OVARY | 600 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | ES2 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | EKSRWSGSH | SKIN | 600 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | G361 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | EKSRWSGSH | SOFT_TISSUE | 600 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | GCT | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | EKSRWSGSH | SKIN | 600 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | HS695T | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | EKSRWSGSH | SKIN | 600 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | HT144 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | EKSRWSGSH | LARGE_INTESTINE | 600 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | HT29 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | EKSRWSGSH | SKIN | 600 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | IGR37 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | EKSRWSGSH | SKIN | 600 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | IGR39 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | EKSRWSGSH | OVARY | 600 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | JHOM2B | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | EKSRWSGSH | SKIN | 600 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | K029AX | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | EKSRWSGSH | SKIN | 600 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | LOXIMVI | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | EKSRWSGSH | LARGE_INTESTINE | 600 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | LS411N | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | EKSRWSGSH | SKIN | 600 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | MALME3M | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | EKSRWSGSH | SKIN | 600 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | MDAMB435S | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | EKSRWSGSH | SKIN | 600 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | MELHO | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | EKSRWSGSH | LUNG | 600 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | NCIH854 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | EKSRWSGSH | CENTRAL_NERVOUS_SYSTEM | 600 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | NMCG1 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | EKSRWSGSH | LARGE_INTESTINE | 600 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | OUMS23 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | EKSRWSGSH | LARGE_INTESTINE | 600 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | RKO | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | EKSRWSGSH | SKIN | 600 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | RPMI7951 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | EKSRWSGSH | SKIN | 600 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SH4 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | EKSRWSGSH | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 600 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SIGM5 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | EKSRWSGSH | LIVER | 600 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SKHEP1 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | EKSRWSGSH | SKIN | 600 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SKMEL1 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | EKSRWSGSH | SKIN | 600 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SKMEL24 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | EKSRWSGSH | SKIN | 600 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SKMEL28 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | EKSRWSGSH | SKIN | 600 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SKMEL3 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | EKSRWSGSH | SKIN | 600 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SKMEL5 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | EKSRWSGSH | LARGE_INTESTINE | 600 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SNUC5 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | EKSRWSGSH | LARGE_INTESTINE | 600 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SW1417 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | EKSRWSGSH | SKIN | 600 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | UACC257 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | EKSRWSGSH | SKIN | 600 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | UACC62 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | EKSRWSGSH | SKIN | 600 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | WM1799 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | EKSRWSGSH | SKIN | 600 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | WM793 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | EKSRWSGSH | SKIN | 600 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | WM88 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | EKSRWSGSH | SKIN | 600 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | WM983B | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | FGLATEKSR | THYROID | 595 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | 8305C | N | 3 | 0 | 2 | N | ||||||||||||
| BRAF | FGLATEKSR | THYROID | 595 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | 8505C | N | 3 | 0 | 2 | N | ||||||||||||
| BRAF | FGLATEKSR | SKIN | 595 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | A101D | N | 3 | 0 | 2 | N | ||||||||||||
| BRAF | FGLATEKSR | SKIN | 595 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | A2058 | N | 3 | 0 | 2 | N | ||||||||||||
| BRAF | FGLATEKSR | SKIN | 595 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | A375 | N | 3 | 0 | 2 | N | ||||||||||||
| BRAF | FGLATEKSR | BONE | 595 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | A673 | N | 3 | 0 | 2 | N | ||||||||||||
| BRAF | FGLATEKSR | CENTRAL_NERVOUS_SYSTEM | 595 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | AM38 | N | 3 | 0 | 2 | N | ||||||||||||
| BRAF | FGLATEKSR | THYROID | 595 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | BCPAP | N | 3 | 0 | 2 | N | ||||||||||||
| BRAF | FGLATEKSR | SKIN | 595 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | C32 | N | 3 | 0 | 2 | N | ||||||||||||
| BRAF | FGLATEKSR | LARGE_INTESTINE | 595 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | CL34 | N | 3 | 0 | 2 | N | ||||||||||||
| BRAF | FGLATEKSR | LARGE_INTESTINE | 595 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | COLO201 | N | 3 | 0 | 2 | N | ||||||||||||
| BRAF | FGLATEKSR | LARGE_INTESTINE | 595 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | COLO205 | N | 3 | 0 | 2 | N | ||||||||||||
| BRAF | FGLATEKSR | SKIN | 595 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | COLO679 | N | 3 | 0 | 2 | N | ||||||||||||
| BRAF | FGLATEKSR | SKIN | 595 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | COLO741 | N | 3 | 0 | 2 | N | ||||||||||||
| BRAF | FGLATEKSR | SKIN | 595 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | COLO783 | N | 3 | 0 | 2 | N | ||||||||||||
| BRAF | FGLATEKSR | SKIN | 595 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | COLO818 | N | 3 | 0 | 2 | N | ||||||||||||
| BRAF | FGLATEKSR | SKIN | 595 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | COLO829 | N | 3 | 0 | 2 | N | ||||||||||||
| BRAF | FGLATEKSR | CENTRAL_NERVOUS_SYSTEM | 595 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | DBTRG05MG | N | 3 | 0 | 2 | N | ||||||||||||
| BRAF | FGLATEKSR | BREAST | 595 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | DU4475 | N | 3 | 0 | 2 | N | ||||||||||||
| BRAF | FGLATEKSR | OVARY | 595 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | ES2 | N | 3 | 0 | 2 | N | ||||||||||||
| BRAF | FGLATEKSR | SKIN | 595 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | G361 | N | 3 | 0 | 2 | N | ||||||||||||
| BRAF | FGLATEKSR | SOFT_TISSUE | 595 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | GCT | N | 3 | 0 | 2 | N | ||||||||||||
| BRAF | FGLATEKSR | SKIN | 595 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | HS695T | N | 3 | 0 | 2 | N | ||||||||||||
| BRAF | FGLATEKSR | SKIN | 595 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | HT144 | N | 3 | 0 | 2 | N | ||||||||||||
| BRAF | FGLATEKSR | LARGE_INTESTINE | 595 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | HT29 | N | 3 | 0 | 2 | N | ||||||||||||
| BRAF | FGLATEKSR | SKIN | 595 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | IGR37 | N | 3 | 0 | 2 | N | ||||||||||||
| BRAF | FGLATEKSR | SKIN | 595 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | IGR39 | N | 3 | 0 | 2 | N | ||||||||||||
| BRAF | FGLATEKSR | OVARY | 595 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | JHOM2B | N | 3 | 0 | 2 | N | ||||||||||||
| BRAF | FGLATEKSR | SKIN | 595 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | K029AX | N | 3 | 0 | 2 | N | ||||||||||||
| BRAF | FGLATEKSR | SKIN | 595 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | LOXIMVI | N | 3 | 0 | 2 | N | ||||||||||||
| BRAF | FGLATEKSR | LARGE_INTESTINE | 595 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | LS411N | N | 3 | 0 | 2 | N | ||||||||||||
| BRAF | FGLATEKSR | SKIN | 595 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | MALME3M | N | 3 | 0 | 2 | N | ||||||||||||
| BRAF | FGLATEKSR | SKIN | 595 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | MDAMB435S | N | 3 | 0 | 2 | N | ||||||||||||
| BRAF | FGLATEKSR | SKIN | 595 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | MELHO | N | 3 | 0 | 2 | N | ||||||||||||
| BRAF | FGLATEKSR | LUNG | 595 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | NCIH854 | N | 3 | 0 | 2 | N | ||||||||||||
| BRAF | FGLATEKSR | CENTRAL_NERVOUS_SYSTEM | 595 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | NMCG1 | N | 3 | 0 | 2 | N | ||||||||||||
| BRAF | FGLATEKSR | LARGE_INTESTINE | 595 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | OUMS23 | N | 3 | 0 | 2 | N | ||||||||||||
| BRAF | FGLATEKSR | LARGE_INTESTINE | 595 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | RKO | N | 3 | 0 | 2 | N | ||||||||||||
| BRAF | FGLATEKSR | SKIN | 595 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | RPMI7951 | N | 3 | 0 | 2 | N | ||||||||||||
| BRAF | FGLATEKSR | SKIN | 595 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SH4 | N | 3 | 0 | 2 | N | ||||||||||||
| BRAF | FGLATEKSR | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 595 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SIGM5 | N | 3 | 0 | 2 | N | ||||||||||||
| BRAF | FGLATEKSR | LIVER | 595 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SKHEP1 | N | 3 | 0 | 2 | N | ||||||||||||
| BRAF | FGLATEKSR | SKIN | 595 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SKMEL1 | N | 3 | 0 | 2 | N | ||||||||||||
| BRAF | FGLATEKSR | SKIN | 595 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SKMEL24 | N | 3 | 0 | 2 | N | ||||||||||||
| BRAF | FGLATEKSR | SKIN | 595 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SKMEL28 | N | 3 | 0 | 2 | N | ||||||||||||
| BRAF | FGLATEKSR | SKIN | 595 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SKMEL3 | N | 3 | 0 | 2 | N | ||||||||||||
| BRAF | FGLATEKSR | SKIN | 595 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SKMEL5 | N | 3 | 0 | 2 | N | ||||||||||||
| BRAF | FGLATEKSR | LARGE_INTESTINE | 595 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SNUC5 | N | 3 | 0 | 2 | N | ||||||||||||
| BRAF | FGLATEKSR | LARGE_INTESTINE | 595 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SW1417 | N | 3 | 0 | 2 | N | ||||||||||||
| BRAF | FGLATEKSR | SKIN | 595 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | UACC257 | N | 3 | 0 | 2 | N | ||||||||||||
| BRAF | FGLATEKSR | SKIN | 595 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | UACC62 | N | 3 | 0 | 2 | N | ||||||||||||
| BRAF | FGLATEKSR | SKIN | 595 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | WM1799 | N | 3 | 0 | 2 | N | ||||||||||||
| BRAF | FGLATEKSR | SKIN | 595 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | WM793 | N | 3 | 0 | 2 | N | ||||||||||||
| BRAF | FGLATEKSR | SKIN | 595 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | WM88 | N | 3 | 0 | 2 | N | ||||||||||||
| BRAF | FGLATEKSR | SKIN | 595 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | WM983B | N | 3 | 0 | 2 | N | ||||||||||||
| BRAF | GDFGLATEK | THYROID | 593 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | 8305C | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | GDFGLATEK | THYROID | 593 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | 8505C | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | GDFGLATEK | SKIN | 593 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | A101D | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | GDFGLATEK | SKIN | 593 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | A2058 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | GDFGLATEK | SKIN | 593 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | A375 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | GDFGLATEK | BONE | 593 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | A673 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | GDFGLATEK | CENTRAL_NERVOUS_SYSTEM | 593 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | AM38 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | GDFGLATEK | THYROID | 593 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | BCPAP | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | GDFGLATEK | SKIN | 593 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | C32 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | GDFGLATEK | LARGE_INTESTINE | 593 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | CL34 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | GDFGLATEK | LARGE_INTESTINE | 593 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | COLO201 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | GDFGLATEK | LARGE_INTESTINE | 593 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | COLO205 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | GDFGLATEK | SKIN | 593 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | COLO679 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | GDFGLATEK | SKIN | 593 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | COLO741 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | GDFGLATEK | SKIN | 593 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | COLO783 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | GDFGLATEK | SKIN | 593 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | COLO818 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | GDFGLATEK | SKIN | 593 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | COLO829 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | GDFGLATEK | CENTRAL_NERVOUS_SYSTEM | 593 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | DBTRG05MG | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | GDFGLATEK | BREAST | 593 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | DU4475 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | GDFGLATEK | OVARY | 593 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | ES2 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | GDFGLATEK | SKIN | 593 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | G361 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | GDFGLATEK | SOFT_TISSUE | 593 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | GCT | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | GDFGLATEK | SKIN | 593 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | HS695T | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | GDFGLATEK | SKIN | 593 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | HT144 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | GDFGLATEK | LARGE_INTESTINE | 593 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | HT29 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | GDFGLATEK | SKIN | 593 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | IGR37 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | GDFGLATEK | SKIN | 593 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | IGR39 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | GDFGLATEK | OVARY | 593 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | JHOM2B | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | GDFGLATEK | SKIN | 593 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | K029AX | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | GDFGLATEK | SKIN | 593 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | LOXIMVI | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | GDFGLATEK | LARGE_INTESTINE | 593 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | LS411N | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | GDFGLATEK | SKIN | 593 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | MALME3M | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | GDFGLATEK | SKIN | 593 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | MDAMB435S | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | GDFGLATEK | SKIN | 593 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | MELHO | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | GDFGLATEK | LUNG | 593 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | NCIH854 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | GDFGLATEK | CENTRAL_NERVOUS_SYSTEM | 593 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | NMCG1 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | GDFGLATEK | LARGE_INTESTINE | 593 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | OUMS23 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | GDFGLATEK | LARGE_INTESTINE | 593 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | RKO | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | GDFGLATEK | SKIN | 593 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | RPMI7951 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | GDFGLATEK | SKIN | 593 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SH4 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | GDFGLATEK | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 593 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SIGM5 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | GDFGLATEK | LIVER | 593 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SKHEP1 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | GDFGLATEK | SKIN | 593 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SKMEL1 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | GDFGLATEK | SKIN | 593 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SKMEL24 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | GDFGLATEK | SKIN | 593 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SKMEL28 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | GDFGLATEK | SKIN | 593 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SKMEL3 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | GDFGLATEK | SKIN | 593 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SKMEL5 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | GDFGLATEK | LARGE_INTESTINE | 593 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SNUC5 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | GDFGLATEK | LARGE_INTESTINE | 593 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SW1417 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | GDFGLATEK | SKIN | 593 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | UACC257 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | GDFGLATEK | SKIN | 593 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | UACC62 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | GDFGLATEK | SKIN | 593 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | WM1799 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | GDFGLATEK | SKIN | 593 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | WM793 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | GDFGLATEK | SKIN | 593 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | WM88 | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | GDFGLATEK | SKIN | 593 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | WM983B | N | 1 | 0 | 0 | N | ||||||||||||
| BRAF | GLATEKSRW | THYROID | 596 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | 8305C | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | GLATEKSRW | THYROID | 596 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | 8505C | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | GLATEKSRW | SKIN | 596 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | A101D | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | GLATEKSRW | SKIN | 596 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | A2058 | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | GLATEKSRW | SKIN | 596 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | A375 | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | GLATEKSRW | BONE | 596 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | A673 | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | GLATEKSRW | CENTRAL_NERVOUS_SYSTEM | 596 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | AM38 | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | GLATEKSRW | THYROID | 596 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | BCPAP | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | GLATEKSRW | SKIN | 596 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | C32 | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | GLATEKSRW | LARGE_INTESTINE | 596 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | CL34 | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | GLATEKSRW | LARGE_INTESTINE | 596 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | COLO201 | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | GLATEKSRW | LARGE_INTESTINE | 596 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | COLO205 | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | GLATEKSRW | SKIN | 596 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | COLO679 | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | GLATEKSRW | SKIN | 596 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | COLO741 | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | GLATEKSRW | SKIN | 596 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | COLO783 | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | GLATEKSRW | SKIN | 596 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | COLO818 | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | GLATEKSRW | SKIN | 596 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | COLO829 | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | GLATEKSRW | CENTRAL_NERVOUS_SYSTEM | 596 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | DBTRG05MG | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | GLATEKSRW | BREAST | 596 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | DU4475 | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | GLATEKSRW | OVARY | 596 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | ES2 | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | GLATEKSRW | SKIN | 596 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | G361 | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | GLATEKSRW | SOFT_TISSUE | 596 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | GCT | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | GLATEKSRW | SKIN | 596 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | HS695T | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | GLATEKSRW | SKIN | 596 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | HT144 | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | GLATEKSRW | LARGE_INTESTINE | 596 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | HT29 | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | GLATEKSRW | SKIN | 596 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | IGR37 | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | GLATEKSRW | SKIN | 596 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | IGR39 | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | GLATEKSRW | OVARY | 596 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | JHOM2B | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | GLATEKSRW | SKIN | 596 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | K029AX | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | GLATEKSRW | SKIN | 596 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | LOXIMVI | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | GLATEKSRW | LARGE_INTESTINE | 596 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | LS411N | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | GLATEKSRW | SKIN | 596 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | MALME3M | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | GLATEKSRW | SKIN | 596 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | MDAMB435S | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | GLATEKSRW | SKIN | 596 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | MELHO | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | GLATEKSRW | LUNG | 596 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | NCIH854 | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | GLATEKSRW | CENTRAL_NERVOUS_SYSTEM | 596 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | NMCG1 | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | GLATEKSRW | LARGE_INTESTINE | 596 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | OUMS23 | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | GLATEKSRW | LARGE_INTESTINE | 596 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | RKO | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | GLATEKSRW | SKIN | 596 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | RPMI7951 | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | GLATEKSRW | SKIN | 596 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SH4 | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | GLATEKSRW | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 596 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SIGM5 | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | GLATEKSRW | LIVER | 596 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SKHEP1 | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | GLATEKSRW | SKIN | 596 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SKMEL1 | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | GLATEKSRW | SKIN | 596 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SKMEL24 | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | GLATEKSRW | SKIN | 596 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SKMEL28 | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | GLATEKSRW | SKIN | 596 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SKMEL3 | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | GLATEKSRW | SKIN | 596 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SKMEL5 | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | GLATEKSRW | LARGE_INTESTINE | 596 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SNUC5 | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | GLATEKSRW | LARGE_INTESTINE | 596 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SW1417 | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | GLATEKSRW | SKIN | 596 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | UACC257 | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | GLATEKSRW | SKIN | 596 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | UACC62 | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | GLATEKSRW | SKIN | 596 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | WM1799 | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | GLATEKSRW | SKIN | 596 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | WM793 | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | GLATEKSRW | SKIN | 596 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | WM88 | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | GLATEKSRW | SKIN | 596 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | WM983B | N | 4 | 0 | 0 | N | ||||||||||||
| BRAF | IGDFGLATE | THYROID | 592 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | 8305C | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | IGDFGLATE | THYROID | 592 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | 8505C | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | IGDFGLATE | SKIN | 592 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | A101D | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | IGDFGLATE | SKIN | 592 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | A2058 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | IGDFGLATE | SKIN | 592 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | A375 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | IGDFGLATE | BONE | 592 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | A673 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | IGDFGLATE | CENTRAL_NERVOUS_SYSTEM | 592 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | AM38 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | IGDFGLATE | THYROID | 592 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | BCPAP | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | IGDFGLATE | SKIN | 592 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | C32 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | IGDFGLATE | LARGE_INTESTINE | 592 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | CL34 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | IGDFGLATE | LARGE_INTESTINE | 592 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | COLO201 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | IGDFGLATE | LARGE_INTESTINE | 592 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | COLO205 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | IGDFGLATE | SKIN | 592 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | COLO679 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | IGDFGLATE | SKIN | 592 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | COLO741 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | IGDFGLATE | SKIN | 592 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | COLO783 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | IGDFGLATE | SKIN | 592 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | COLO818 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | IGDFGLATE | SKIN | 592 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | COLO829 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | IGDFGLATE | CENTRAL_NERVOUS_SYSTEM | 592 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | DBTRG05MG | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | IGDFGLATE | BREAST | 592 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | DU4475 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | IGDFGLATE | OVARY | 592 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | ES2 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | IGDFGLATE | SKIN | 592 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | G361 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | IGDFGLATE | SOFT_TISSUE | 592 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | GCT | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | IGDFGLATE | SKIN | 592 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | HS695T | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | IGDFGLATE | SKIN | 592 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | HT144 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | IGDFGLATE | LARGE_INTESTINE | 592 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | HT29 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | IGDFGLATE | SKIN | 592 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | IGR37 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | IGDFGLATE | SKIN | 592 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | IGR39 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | IGDFGLATE | OVARY | 592 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | JHOM2B | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | IGDFGLATE | SKIN | 592 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | K029AX | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | IGDFGLATE | SKIN | 592 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | LOXIMVI | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | IGDFGLATE | LARGE_INTESTINE | 592 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | LS411N | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | IGDFGLATE | SKIN | 592 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | MALME3M | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | IGDFGLATE | SKIN | 592 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | MDAMB435S | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | IGDFGLATE | SKIN | 592 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | MELHO | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | IGDFGLATE | LUNG | 592 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | NCIH854 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | IGDFGLATE | CENTRAL_NERVOUS_SYSTEM | 592 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | NMCG1 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | IGDFGLATE | LARGE_INTESTINE | 592 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | OUMS23 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | IGDFGLATE | LARGE_INTESTINE | 592 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | RKO | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | IGDFGLATE | SKIN | 592 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | RPMI7951 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | IGDFGLATE | SKIN | 592 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SH4 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | IGDFGLATE | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 592 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SIGM5 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | IGDFGLATE | LIVER | 592 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SKHEP1 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | IGDFGLATE | SKIN | 592 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SKMEL1 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | IGDFGLATE | SKIN | 592 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SKMEL24 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | IGDFGLATE | SKIN | 592 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SKMEL28 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | IGDFGLATE | SKIN | 592 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SKMEL3 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | IGDFGLATE | SKIN | 592 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SKMEL5 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | IGDFGLATE | LARGE_INTESTINE | 592 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SNUC5 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | IGDFGLATE | LARGE_INTESTINE | 592 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SW1417 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | IGDFGLATE | SKIN | 592 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | UACC257 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | IGDFGLATE | SKIN | 592 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | UACC62 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | IGDFGLATE | SKIN | 592 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | WM1799 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | IGDFGLATE | SKIN | 592 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | WM793 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | IGDFGLATE | SKIN | 592 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | WM88 | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | IGDFGLATE | SKIN | 592 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | WM983B | N | 0 | 0 | 0 | N | ||||||||||||
| BRAF | LATEKSRWS | THYROID | 597 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | 8305C | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | LATEKSRWS | THYROID | 597 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | 8505C | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | LATEKSRWS | SKIN | 597 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | A101D | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | LATEKSRWS | SKIN | 597 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | A2058 | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | LATEKSRWS | SKIN | 597 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | A375 | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | LATEKSRWS | BONE | 597 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | A673 | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | LATEKSRWS | CENTRAL_NERVOUS_SYSTEM | 597 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | AM38 | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | LATEKSRWS | THYROID | 597 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | BCPAP | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | LATEKSRWS | SKIN | 597 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | C32 | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | LATEKSRWS | LARGE_INTESTINE | 597 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | CL34 | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | LATEKSRWS | LARGE_INTESTINE | 597 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | COLO201 | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | LATEKSRWS | LARGE_INTESTINE | 597 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | COLO205 | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | LATEKSRWS | SKIN | 597 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | COLO679 | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | LATEKSRWS | SKIN | 597 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | COLO741 | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | LATEKSRWS | SKIN | 597 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | COLO783 | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | LATEKSRWS | SKIN | 597 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | COLO818 | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | LATEKSRWS | SKIN | 597 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | COLO829 | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | LATEKSRWS | CENTRAL_NERVOUS_SYSTEM | 597 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | DBTRG05MG | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | LATEKSRWS | BREAST | 597 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | DU4475 | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | LATEKSRWS | OVARY | 597 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | ES2 | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | LATEKSRWS | SKIN | 597 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | G361 | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | LATEKSRWS | SOFT_TISSUE | 597 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | GCT | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | LATEKSRWS | SKIN | 597 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | HS695T | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | LATEKSRWS | SKIN | 597 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | HT144 | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | LATEKSRWS | LARGE_INTESTINE | 597 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | HT29 | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | LATEKSRWS | SKIN | 597 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | IGR37 | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | LATEKSRWS | SKIN | 597 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | IGR39 | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | LATEKSRWS | OVARY | 597 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | JHOM2B | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | LATEKSRWS | SKIN | 597 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | K029AX | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | LATEKSRWS | SKIN | 597 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | LOXIMVI | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | LATEKSRWS | LARGE_INTESTINE | 597 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | LS411N | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | LATEKSRWS | SKIN | 597 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | MALME3M | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | LATEKSRWS | SKIN | 597 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | MDAMB435S | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | LATEKSRWS | SKIN | 597 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | MELHO | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | LATEKSRWS | LUNG | 597 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | NCIH854 | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | LATEKSRWS | CENTRAL_NERVOUS_SYSTEM | 597 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | NMCG1 | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | LATEKSRWS | LARGE_INTESTINE | 597 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | OUMS23 | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | LATEKSRWS | LARGE_INTESTINE | 597 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | RKO | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | LATEKSRWS | SKIN | 597 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | RPMI7951 | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | LATEKSRWS | SKIN | 597 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SH4 | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | LATEKSRWS | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 597 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SIGM5 | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | LATEKSRWS | LIVER | 597 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SKHEP1 | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | LATEKSRWS | SKIN | 597 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SKMEL1 | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | LATEKSRWS | SKIN | 597 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SKMEL24 | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | LATEKSRWS | SKIN | 597 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SKMEL28 | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | LATEKSRWS | SKIN | 597 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SKMEL3 | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | LATEKSRWS | SKIN | 597 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SKMEL5 | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | LATEKSRWS | LARGE_INTESTINE | 597 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SNUC5 | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | LATEKSRWS | LARGE_INTESTINE | 597 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SW1417 | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | LATEKSRWS | SKIN | 597 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | UACC257 | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | LATEKSRWS | SKIN | 597 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | UACC62 | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | LATEKSRWS | SKIN | 597 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | WM1799 | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | LATEKSRWS | SKIN | 597 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | WM793 | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | LATEKSRWS | SKIN | 597 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | WM88 | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | LATEKSRWS | SKIN | 597 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | WM983B | N | 2 | 0 | 0 | N | ||||||||||||
| BRAF | TEKSRWSGS | THYROID | 599 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | 8305C | N | 3 | 0 | 0 | N | ||||||||||||
| BRAF | TEKSRWSGS | THYROID | 599 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | 8505C | N | 3 | 0 | 0 | N | ||||||||||||
| BRAF | TEKSRWSGS | SKIN | 599 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | A101D | N | 3 | 0 | 0 | N | ||||||||||||
| BRAF | TEKSRWSGS | SKIN | 599 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | A2058 | N | 3 | 0 | 0 | N | ||||||||||||
| BRAF | TEKSRWSGS | SKIN | 599 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | A375 | N | 3 | 0 | 0 | N | ||||||||||||
| BRAF | TEKSRWSGS | BONE | 599 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | A673 | N | 3 | 0 | 0 | N | ||||||||||||
| BRAF | TEKSRWSGS | CENTRAL_NERVOUS_SYSTEM | 599 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | AM38 | N | 3 | 0 | 0 | N | ||||||||||||
| BRAF | TEKSRWSGS | THYROID | 599 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | BCPAP | N | 3 | 0 | 0 | N | ||||||||||||
| BRAF | TEKSRWSGS | SKIN | 599 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | C32 | N | 3 | 0 | 0 | N | ||||||||||||
| BRAF | TEKSRWSGS | LARGE_INTESTINE | 599 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | CL34 | N | 3 | 0 | 0 | N | ||||||||||||
| BRAF | TEKSRWSGS | LARGE_INTESTINE | 599 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | COLO201 | N | 3 | 0 | 0 | N | ||||||||||||
| BRAF | TEKSRWSGS | LARGE_INTESTINE | 599 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | COLO205 | N | 3 | 0 | 0 | N | ||||||||||||
| BRAF | TEKSRWSGS | SKIN | 599 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | COLO679 | N | 3 | 0 | 0 | N | ||||||||||||
| BRAF | TEKSRWSGS | SKIN | 599 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | COLO741 | N | 3 | 0 | 0 | N | ||||||||||||
| BRAF | TEKSRWSGS | SKIN | 599 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | COLO783 | N | 3 | 0 | 0 | N | ||||||||||||
| BRAF | TEKSRWSGS | SKIN | 599 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | COLO818 | N | 3 | 0 | 0 | N | ||||||||||||
| BRAF | TEKSRWSGS | SKIN | 599 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | COLO829 | N | 3 | 0 | 0 | N | ||||||||||||
| BRAF | TEKSRWSGS | CENTRAL_NERVOUS_SYSTEM | 599 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | DBTRG05MG | N | 3 | 0 | 0 | N | ||||||||||||
| BRAF | TEKSRWSGS | BREAST | 599 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | DU4475 | N | 3 | 0 | 0 | N | ||||||||||||
| BRAF | TEKSRWSGS | OVARY | 599 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | ES2 | N | 3 | 0 | 0 | N | ||||||||||||
| BRAF | TEKSRWSGS | SKIN | 599 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | G361 | N | 3 | 0 | 0 | N | ||||||||||||
| BRAF | TEKSRWSGS | SOFT_TISSUE | 599 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | GCT | N | 3 | 0 | 0 | N | ||||||||||||
| BRAF | TEKSRWSGS | SKIN | 599 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | HS695T | N | 3 | 0 | 0 | N | ||||||||||||
| BRAF | TEKSRWSGS | SKIN | 599 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | HT144 | N | 3 | 0 | 0 | N | ||||||||||||
| BRAF | TEKSRWSGS | LARGE_INTESTINE | 599 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | HT29 | N | 3 | 0 | 0 | N | ||||||||||||
| BRAF | TEKSRWSGS | SKIN | 599 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | IGR37 | N | 3 | 0 | 0 | N | ||||||||||||
| BRAF | TEKSRWSGS | SKIN | 599 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | IGR39 | N | 3 | 0 | 0 | N | ||||||||||||
| BRAF | TEKSRWSGS | OVARY | 599 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | JHOM2B | N | 3 | 0 | 0 | N | ||||||||||||
| BRAF | TEKSRWSGS | SKIN | 599 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | K029AX | N | 3 | 0 | 0 | N | ||||||||||||
| BRAF | TEKSRWSGS | SKIN | 599 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | LOXIMVI | N | 3 | 0 | 0 | N | ||||||||||||
| BRAF | TEKSRWSGS | LARGE_INTESTINE | 599 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | LS411N | N | 3 | 0 | 0 | N | ||||||||||||
| BRAF | TEKSRWSGS | SKIN | 599 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | MALME3M | N | 3 | 0 | 0 | N | ||||||||||||
| BRAF | TEKSRWSGS | SKIN | 599 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | MDAMB435S | N | 3 | 0 | 0 | N | ||||||||||||
| BRAF | TEKSRWSGS | SKIN | 599 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | MELHO | N | 3 | 0 | 0 | N | ||||||||||||
| BRAF | TEKSRWSGS | LUNG | 599 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | NCIH854 | N | 3 | 0 | 0 | N | ||||||||||||
| BRAF | TEKSRWSGS | CENTRAL_NERVOUS_SYSTEM | 599 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | NMCG1 | N | 3 | 0 | 0 | N | ||||||||||||
| BRAF | TEKSRWSGS | LARGE_INTESTINE | 599 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | OUMS23 | N | 3 | 0 | 0 | N | ||||||||||||
| BRAF | TEKSRWSGS | LARGE_INTESTINE | 599 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | RKO | N | 3 | 0 | 0 | N | ||||||||||||
| BRAF | TEKSRWSGS | SKIN | 599 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | RPMI7951 | N | 3 | 0 | 0 | N | ||||||||||||
| BRAF | TEKSRWSGS | SKIN | 599 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SH4 | N | 3 | 0 | 0 | N | ||||||||||||
| BRAF | TEKSRWSGS | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 599 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SIGM5 | N | 3 | 0 | 0 | N | ||||||||||||
| BRAF | TEKSRWSGS | LIVER | 599 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SKHEP1 | N | 3 | 0 | 0 | N | ||||||||||||
| BRAF | TEKSRWSGS | SKIN | 599 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SKMEL1 | N | 3 | 0 | 0 | N | ||||||||||||
| BRAF | TEKSRWSGS | SKIN | 599 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SKMEL24 | N | 3 | 0 | 0 | N | ||||||||||||
| BRAF | TEKSRWSGS | SKIN | 599 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SKMEL28 | N | 3 | 0 | 0 | N | ||||||||||||
| BRAF | TEKSRWSGS | SKIN | 599 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SKMEL3 | N | 3 | 0 | 0 | N | ||||||||||||
| BRAF | TEKSRWSGS | SKIN | 599 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SKMEL5 | N | 3 | 0 | 0 | N | ||||||||||||
| BRAF | TEKSRWSGS | LARGE_INTESTINE | 599 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SNUC5 | N | 3 | 0 | 0 | N | ||||||||||||
| BRAF | TEKSRWSGS | LARGE_INTESTINE | 599 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | SW1417 | N | 3 | 0 | 0 | N | ||||||||||||
| BRAF | TEKSRWSGS | SKIN | 599 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | UACC257 | N | 3 | 0 | 0 | N | ||||||||||||
| BRAF | TEKSRWSGS | SKIN | 599 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | UACC62 | N | 3 | 0 | 0 | N | ||||||||||||
| BRAF | TEKSRWSGS | SKIN | 599 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | WM1799 | N | 3 | 0 | 0 | N | ||||||||||||
| BRAF | TEKSRWSGS | SKIN | 599 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | WM793 | N | 3 | 0 | 0 | N | ||||||||||||
| BRAF | TEKSRWSGS | SKIN | 599 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | WM88 | N | 3 | 0 | 0 | N | ||||||||||||
| BRAF | TEKSRWSGS | SKIN | 599 | p.V600E | c.1799T>A | Missense_Mutation | 1 | 6.08 | WM983B | N | 3 | 0 | 0 | N | ||||||||||||
|
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