MYLK | AHLVPLTFG | STOMACH | 1336 | p.P1334fs | c.4001_4001delC | Frame_Shift_Del | 5 | 0.11 | 2313287 | N | 0 | 0 | 0 | N |
MYLK | APRHLRRQQ | ENDOMETRIUM | 1227 | p.P1228fs | c.3684_3684delC | Frame_Shift_Del | 6 | 0.11 | HEC108 | N | 2 | 0 | 0 | N |
MYLK | AQESQWSCL | ENDOMETRIUM | 1250 | p.P1228fs | c.3684_3684delC | Frame_Shift_Del | 5 | 0.11 | HEC108 | N | 6 | 0 | 0 | N |
MYLK | CPLRSSSSL | ENDOMETRIUM | 1236 | p.P1228fs | c.3684_3684delC | Frame_Shift_Del | 5 | 0.11 | HEC108 | N | 18 | 0 | 0 | N |
MYLK | DKPDPQLAH | STOMACH | 1329 | p.P1334fs | c.4001_4001delC | Frame_Shift_Del | 4 | 0.11 | 2313287 | N | 1 | 0 | 0 | N |
MYLK | DPQLAHLVP | STOMACH | 1332 | p.P1334fs | c.4001_4001delC | Frame_Shift_Del | 5 | 0.11 | 2313287 | N | 0 | 0 | 0 | N |
MYLK | ESQWSCLAK | ENDOMETRIUM | 1252 | p.P1228fs | c.3684_3684delC | Frame_Shift_Del | 5 | 0.11 | HEC108 | N | 3 | 0 | 0 | N |
MYLK | HLRRQQCPL | ENDOMETRIUM | 1230 | p.P1228fs | c.3684_3684delC | Frame_Shift_Del | 5 | 0.11 | HEC108 | N | 8 | 0 | 0 | N |
MYLK | HLVPLTFGA | STOMACH | 1337 | p.P1334fs | c.4001_4001delC | Frame_Shift_Del | 5 | 0.11 | 2313287 | N | 4 | 0 | 0 | N |
MYLK | KKKPAPRHL | ENDOMETRIUM | 1223 | p.P1228fs | c.3684_3684delC | Frame_Shift_Del | 3 | 0.11 | HEC108 | Y | 3 | 12 | 0 | N |
MYLK | KKPAPRHLR | ENDOMETRIUM | 1224 | p.P1228fs | c.3684_3684delC | Frame_Shift_Del | 4 | 0.11 | HEC108 | N | 1 | 0 | 0 | N |
MYLK | KPAPRHLRR | ENDOMETRIUM | 1225 | p.P1228fs | c.3684_3684delC | Frame_Shift_Del | 5 | 0.11 | HEC108 | Y | 6 | 11 | 0 | N |
MYLK | KPDPQLAHL | STOMACH | 1330 | p.P1334fs | c.4001_4001delC | Frame_Shift_Del | 5 | 0.11 | 2313287 | Y | 20 | 10 | 0 | N |
MYLK | LAHLVPLTF | STOMACH | 1335 | p.P1334fs | c.4001_4001delC | Frame_Shift_Del | 5 | 0.11 | 2313287 | N | 7 | 0 | 8 | N |
MYLK | LRRQQCPLR | ENDOMETRIUM | 1231 | p.P1228fs | c.3684_3684delC | Frame_Shift_Del | 5 | 0.11 | HEC108 | N | 3 | 0 | 16 | N |
MYLK | LRSSSSLRT | ENDOMETRIUM | 1238 | p.P1228fs | c.3684_3684delC | Frame_Shift_Del | 5 | 0.11 | HEC108 | N | 2 | 0 | 18 | Y |
MYLK | LRTRRYAQE | ENDOMETRIUM | 1244 | p.P1228fs | c.3684_3684delC | Frame_Shift_Del | 6 | 0.11 | HEC108 | N | 1 | 0 | 3 | N |
MYLK | LVPLTFGAP | STOMACH | 1338 | p.P1334fs | c.4001_4001delC | Frame_Shift_Del | 5 | 0.11 | 2313287 | N | 0 | 0 | 0 | N |
MYLK | PAPRHLRRQ | ENDOMETRIUM | 1226 | p.P1228fs | c.3684_3684delC | Frame_Shift_Del | 6 | 0.11 | HEC108 | N | 0 | 0 | 0 | N |
MYLK | PDPQLAHLV | STOMACH | 1331 | p.P1334fs | c.4001_4001delC | Frame_Shift_Del | 5 | 0.11 | 2313287 | N | 1 | 0 | 0 | N |
MYLK | PLRSSSSLR | ENDOMETRIUM | 1237 | p.P1228fs | c.3684_3684delC | Frame_Shift_Del | 5 | 0.11 | HEC108 | N | 0 | 0 | 0 | Y |
MYLK | PQLAHLVPL | STOMACH | 1333 | p.P1334fs | c.4001_4001delC | Frame_Shift_Del | 5 | 0.11 | 2313287 | N | 5 | 0 | 0 | N |
MYLK | PRHLRRQQC | ENDOMETRIUM | 1228 | p.P1228fs | c.3684_3684delC | Frame_Shift_Del | 6 | 0.11 | HEC108 | N | 2 | 0 | 0 | N |
MYLK | QCPLRSSSS | ENDOMETRIUM | 1235 | p.P1228fs | c.3684_3684delC | Frame_Shift_Del | 5 | 0.11 | HEC108 | N | 1 | 0 | 0 | N |
MYLK | QESQWSCLA | ENDOMETRIUM | 1251 | p.P1228fs | c.3684_3684delC | Frame_Shift_Del | 5 | 0.11 | HEC108 | N | 6 | 0 | 0 | N |
MYLK | QLAHLVPLT | STOMACH | 1334 | p.P1334fs | c.4001_4001delC | Frame_Shift_Del | 5 | 0.11 | 2313287 | N | 3 | 0 | 0 | N |
MYLK | QQCPLRSSS | ENDOMETRIUM | 1234 | p.P1228fs | c.3684_3684delC | Frame_Shift_Del | 5 | 0.11 | HEC108 | N | 0 | 0 | 0 | N |
MYLK | RHLRRQQCP | ENDOMETRIUM | 1229 | p.P1228fs | c.3684_3684delC | Frame_Shift_Del | 5 | 0.11 | HEC108 | N | 0 | 0 | 0 | N |
MYLK | RQQCPLRSS | ENDOMETRIUM | 1233 | p.P1228fs | c.3684_3684delC | Frame_Shift_Del | 5 | 0.11 | HEC108 | N | 0 | 0 | 0 | N |
MYLK | RRQQCPLRS | ENDOMETRIUM | 1232 | p.P1228fs | c.3684_3684delC | Frame_Shift_Del | 5 | 0.11 | HEC108 | N | 2 | 0 | 0 | N |
MYLK | RRYAQESQW | ENDOMETRIUM | 1247 | p.P1228fs | c.3684_3684delC | Frame_Shift_Del | 5 | 0.11 | HEC108 | N | 4 | 0 | 0 | N |
MYLK | RSSSSLRTR | ENDOMETRIUM | 1239 | p.P1228fs | c.3684_3684delC | Frame_Shift_Del | 5 | 0.11 | HEC108 | N | 3 | 0 | 0 | Y |
MYLK | RTRRYAQES | ENDOMETRIUM | 1245 | p.P1228fs | c.3684_3684delC | Frame_Shift_Del | 5 | 0.11 | HEC108 | N | 1 | 0 | 0 | N |
MYLK | RYAQESQWS | ENDOMETRIUM | 1248 | p.P1228fs | c.3684_3684delC | Frame_Shift_Del | 6 | 0.11 | HEC108 | N | 1 | 0 | 0 | N |
MYLK | SLRTRRYAQ | ENDOMETRIUM | 1243 | p.P1228fs | c.3684_3684delC | Frame_Shift_Del | 5 | 0.11 | HEC108 | Y | 1 | 15 | 0 | N |
MYLK | SSLRTRRYA | ENDOMETRIUM | 1242 | p.P1228fs | c.3684_3684delC | Frame_Shift_Del | 5 | 0.11 | HEC108 | Y | 2 | 9 | 0 | N |
MYLK | SSSLRTRRY | ENDOMETRIUM | 1241 | p.P1228fs | c.3684_3684delC | Frame_Shift_Del | 4 | 0.11 | HEC108 | Y | 5 | 12 | 0 | Y |
MYLK | SSSSLRTRR | ENDOMETRIUM | 1240 | p.P1228fs | c.3684_3684delC | Frame_Shift_Del | 5 | 0.11 | HEC108 | Y | 3 | 9 | 0 | Y |
MYLK | TRRYAQESQ | ENDOMETRIUM | 1246 | p.P1228fs | c.3684_3684delC | Frame_Shift_Del | 5 | 0.11 | HEC108 | N | 1 | 0 | 0 | N |
MYLK | TVKKKPAPR | ENDOMETRIUM | 1221 | p.P1228fs | c.3684_3684delC | Frame_Shift_Del | 1 | 0.11 | HEC108 | N | 5 | 0 | 0 | N |
MYLK | TVVDKPDPQ | STOMACH | 1326 | p.P1334fs | c.4001_4001delC | Frame_Shift_Del | 1 | 0.11 | 2313287 | N | 0 | 0 | 0 | N |
MYLK | VDKPDPQLA | STOMACH | 1328 | p.P1334fs | c.4001_4001delC | Frame_Shift_Del | 3 | 0.11 | 2313287 | N | 4 | 0 | 0 | N |
MYLK | VKKKPAPRH | ENDOMETRIUM | 1222 | p.P1228fs | c.3684_3684delC | Frame_Shift_Del | 2 | 0.11 | HEC108 | N | 1 | 0 | 6 | N |
MYLK | VPLTFGAPH | STOMACH | 1339 | p.P1334fs | c.4001_4001delC | Frame_Shift_Del | 5 | 0.11 | 2313287 | N | 2 | 0 | 0 | Y |
MYLK | VVDKPDPQL | STOMACH | 1327 | p.P1334fs | c.4001_4001delC | Frame_Shift_Del | 2 | 0.11 | 2313287 | N | 7 | 0 | 0 | N |
MYLK | YAQESQWSC | ENDOMETRIUM | 1249 | p.P1228fs | c.3684_3684delC | Frame_Shift_Del | 6 | 0.11 | HEC108 | N | 7 | 0 | 0 | N |
MYLK | AAMPPSDHP | ENDOMETRIUM | 1234 | p.P1238fs | c.3713_3714insC | Frame_Shift_Ins | 4 | 0.11 | HEC1A | N | 0 | 0 | 0 | N |
MYLK | AMPPSDHPV | ENDOMETRIUM | 1235 | p.P1238fs | c.3713_3714insC | Frame_Shift_Ins | 5 | 0.11 | HEC1A | N | 5 | 0 | 0 | Y |
MYLK | KAAMPPSDH | ENDOMETRIUM | 1233 | p.P1238fs | c.3713_3714insC | Frame_Shift_Ins | 3 | 0.11 | HEC1A | N | 0 | 0 | 0 | N |
MYLK | MPPSDHPVP | ENDOMETRIUM | 1236 | p.P1238fs | c.3713_3714insC | Frame_Shift_Ins | 5 | 0.11 | HEC1A | N | 2 | 0 | 0 | Y |
MYLK | PKAAMPPSD | ENDOMETRIUM | 1232 | p.P1238fs | c.3713_3714insC | Frame_Shift_Ins | 2 | 0.11 | HEC1A | N | 0 | 0 | 0 | N |
MYLK | PPKAAMPPS | ENDOMETRIUM | 1231 | p.P1238fs | c.3713_3714insC | Frame_Shift_Ins | 1 | 0.11 | HEC1A | N | 1 | 0 | 0 | N |
MYLK | ACQVTVELT | ENDOMETRIUM | 114 | p.R115C | c.343C>T | Missense_Mutation | 1 | 0.11 | HEC151 | N | 0 | 0 | 0 | N |
MYLK | ADSHYLCLL | CENTRAL_NERVOUS_SYSTEM | 467 | p.G468D | c.1403G>A | Missense_Mutation | 1 | 0.11 | CAS1 | N | 5 | 0 | 0 | N |
MYLK | ADVSQAFLE | AUTONOMIC_GANGLIA | 1790 | p.E1790A | c.5369A>C | Missense_Mutation | 1 | 0.11 | NB1 | N | 1 | 0 | 0 | Y |
MYLK | AEKLESEAD | AUTONOMIC_GANGLIA | 1783 | p.E1790A | c.5369A>C | Missense_Mutation | 1 | 0.11 | NB1 | N | 0 | 0 | 0 | N |
MYLK | AETLNAKTV | PANCREAS | 1000 | p.A1007T | c.3019G>A | Missense_Mutation | 1 | 0.11 | PK45H | Y | 7 | 11 | 0 | N |
MYLK | AFNEISDDA | LARGE_INTESTINE | 1684 | p.D1686N | c.5056G>A | Missense_Mutation | 1 | 0.11 | SNU175 | N | 1 | 0 | 0 | N |
MYLK | AGDPFPKVH | STOMACH | 745 | p.T751K | c.2252_2253CC>AA | Missense_Mutation | 1 | 0.11 | TGBC11TKB | N | 1 | 0 | 0 | N |
MYLK | AHVSVSEKN | LIVER | 205 | p.R206H | c.617G>A | Missense_Mutation | 1 | 0.11 | SNU182 | N | 1 | 0 | 0 | N |
MYLK | AIAGDPFPK | STOMACH | 743 | p.T751K | c.2252_2253CC>AA | Missense_Mutation | 1 | 0.11 | TGBC11TKB | N | 4 | 0 | 0 | N |
MYLK | AIGRLSSMV | CENTRAL_NERVOUS_SYSTEM | 1754 | p.A1762V | c.5285C>T | Missense_Mutation | 1 | 0.11 | U87MG | N | 3 | 0 | 0 | N |
MYLK | AINVYGTSK | BREAST | 1406 | p.E1414K | c.4240G>A | Missense_Mutation | 1 | 0.11 | ZR751 | N | 2 | 0 | 0 | N |
MYLK | AKPAKTLKP | SKIN | 1041 | p.E1045K | c.3133G>A | Missense_Mutation | 1 | 0.11 | COLO829 | N | 0 | 0 | 0 | N |
MYLK | AKQMDFRAN | LUNG | 920 | p.E921K | c.2761G>A | Missense_Mutation | 1 | 0.11 | NCIH1092 | N | 1 | 0 | 0 | N |
MYLK | AKTLKPMGN | SKIN | 1044 | p.E1045K | c.3133G>A | Missense_Mutation | 1 | 0.11 | COLO829 | N | 1 | 0 | 0 | N |
MYLK | AKTVESSKP | PANCREAS | 1005 | p.A1007T | c.3019G>A | Missense_Mutation | 1 | 0.11 | PK45H | N | 0 | 0 | 0 | N |
MYLK | AMISGPSGR | LARGE_INTESTINE | 1762 | p.L1767P | c.5300T>C | Missense_Mutation | 1 | 0.11 | SNUC5 | N | 6 | 0 | 0 | N |
MYLK | APAVETHPS | LIVER | 146 | p.R152H | c.455G>A | Missense_Mutation | 1 | 0.11 | SNU449 | N | 3 | 0 | 0 | N |
MYLK | APPRSATFP | ENDOMETRIUM | 375 | p.P379S | c.1135C>T | Missense_Mutation | 1 | 0.11 | HEC59 | N | 0 | 0 | 0 | N |
MYLK | APSKPTGPI | BONE | 616 | p.A622G | c.1865C>G | Missense_Mutation | 1 | 0.11 | U2OS | N | 12 | 0 | 0 | Y |
MYLK | AQCVDAFEE | UPPER_AERODIGESTIVE_TRACT | 1522 | p.V1522A | c.4565T>C | Missense_Mutation | 1 | 0.11 | CAL33 | N | 0 | 0 | 0 | N |
MYLK | AQVTLTVVD | OVARY | 1321 | p.N1324T | c.3971A>C | Missense_Mutation | 1 | 0.11 | OVK18 | N | 0 | 0 | 0 | N |
MYLK | ARPSGPLKP | UPPER_AERODIGESTIVE_TRACT | 1017 | p.Q1018R | c.3053A>G | Missense_Mutation | 1 | 0.11 | DETROIT562 | N | 1 | 0 | 0 | Y |
MYLK | ARQYEILLK | LIVER | 789 | p.G790R | c.2368G>C | Missense_Mutation | 1 | 0.11 | ALEXANDERCELLS | N | 2 | 0 | 0 | N |
MYLK | ARRKWQKMG | LARGE_INTESTINE | 1741 | p.T1748M | c.5243C>T | Missense_Mutation | 1 | 0.11 | HT115 | N | 0 | 0 | 0 | N |
MYLK | ARTRDSGIY | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 477 | p.T484I | c.1451C>T | Missense_Mutation | 1 | 0.11 | SUDHL1 | N | 2 | 0 | 0 | N |
MYLK | ASAFKQKLQ | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1097 | p.P1098S | c.3292C>T | Missense_Mutation | 1 | 0.11 | DB | N | 0 | 0 | 0 | N |
MYLK | ASDIQSSSL | CENTRAL_NERVOUS_SYSTEM | 1340 | p.R1344Q | c.4031G>A | Missense_Mutation | 1 | 0.11 | SNU201 | N | 7 | 0 | 0 | N |
MYLK | ATDKFEGRV | AUTONOMIC_GANGLIA | 48 | p.A50D | c.149C>A | Missense_Mutation | 1 | 0.11 | NB1 | Y | 3 | 13 | 0 | N |
MYLK | ATGRSTSFN | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1382 | p.C1384G | c.4150T>G | Missense_Mutation | 1 | 0.11 | KIJK | N | 0 | 0 | 0 | N |
MYLK | ATNGSGACQ | ENDOMETRIUM | 108 | p.R115C | c.343C>T | Missense_Mutation | 1 | 0.11 | HEC151 | N | 0 | 0 | 0 | N |
MYLK | ATPDFCSVL | SKIN | 977 | p.R982C | c.2944C>T | Missense_Mutation | 1 | 0.11 | G361 | Y | 14 | 11 | 0 | N |
MYLK | ATVKMKPAP | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1220 | p.K1224M | c.3671A>T | Missense_Mutation | 1 | 0.11 | KIJK | N | 0 | 0 | 0 | N |
MYLK | AVETHPSIW | LIVER | 148 | p.R152H | c.455G>A | Missense_Mutation | 1 | 0.11 | SNU449 | N | 1 | 0 | 0 | N |
MYLK | CASDIQSSS | CENTRAL_NERVOUS_SYSTEM | 1339 | p.R1344Q | c.4031G>A | Missense_Mutation | 1 | 0.11 | SNU201 | N | 1 | 0 | 0 | N |
MYLK | CIKEGATDK | AUTONOMIC_GANGLIA | 43 | p.A50D | c.149C>A | Missense_Mutation | 1 | 0.11 | NB1 | N | 2 | 0 | 0 | N |
MYLK | CLHHPKLAQ | UPPER_AERODIGESTIVE_TRACT | 1515 | p.V1522A | c.4565T>C | Missense_Mutation | 1 | 0.11 | CAL33 | N | 0 | 0 | 0 | N |
MYLK | CQVSSDPPT | ENDOMETRIUM | 1119 | p.A1127T | c.3379G>A | Missense_Mutation | 1 | 0.11 | SNGM | N | 2 | 0 | 0 | Y |
MYLK | CQVTVELTV | ENDOMETRIUM | 115 | p.R115C | c.343C>T | Missense_Mutation | 1 | 0.11 | HEC151 | N | 8 | 0 | 0 | N |
MYLK | CSVLGGKKK | SKIN | 982 | p.R982C | c.2944C>T | Missense_Mutation | 1 | 0.11 | G361 | N | 1 | 0 | 0 | N |
MYLK | DADSHYLCL | CENTRAL_NERVOUS_SYSTEM | 466 | p.G468D | c.1403G>A | Missense_Mutation | 1 | 0.11 | CAS1 | N | 11 | 0 | 0 | N |
MYLK | DATVKMKPA | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1219 | p.K1224M | c.3671A>T | Missense_Mutation | 1 | 0.11 | KIJK | N | 4 | 0 | 0 | N |
MYLK | DDEAFNEIS | LARGE_INTESTINE | 1681 | p.D1686N | c.5056G>A | Missense_Mutation | 1 | 0.11 | SNU175 | N | 3 | 0 | 0 | N |
MYLK | DDLKEIPAK | LUNG | 913 | p.E921K | c.2761G>A | Missense_Mutation | 1 | 0.11 | NCIH1092 | N | 0 | 0 | 0 | N |
MYLK | DEAFNEISD | LARGE_INTESTINE | 1682 | p.D1686N | c.5056G>A | Missense_Mutation | 1 | 0.11 | SNU175 | N | 2 | 0 | 0 | N |
MYLK | DFCSVLGGK | SKIN | 980 | p.R982C | c.2944C>T | Missense_Mutation | 1 | 0.11 | G361 | N | 0 | 0 | 0 | N |
MYLK | DFDDEAFNE | LARGE_INTESTINE | 1679 | p.D1686N | c.5056G>A | Missense_Mutation | 1 | 0.11 | SNU175 | N | 0 | 0 | 0 | N |
MYLK | DFHSVLAKK | LARGE_INTESTINE | 952 | p.R954H | c.2861G>A | Missense_Mutation | 1 | 0.11 | HT115 | Y | 0 | 10 | 0 | N |
MYLK | DFRDLLVKK | OVARY | 896 | p.G902V | c.2705G>T | Missense_Mutation | 1 | 0.11 | OVCAR8 | N | 0 | 0 | 0 | N |
MYLK | DFRDPLGKK | LARGE_INTESTINE | 896 | p.L900P | c.2699T>C | Missense_Mutation | 1 | 0.11 | CW2 | N | 0 | 0 | 0 | Y |
MYLK | DGGGSDRYV | ENDOMETRIUM | 839 | p.G847V | c.2540G>T | Missense_Mutation | 1 | 0.11 | SNGM | Y | 4 | 9 | 0 | N |
MYLK | DGNALCKDT | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 757 | p.K759N | c.2277A>C | Missense_Mutation | 1 | 0.11 | HT | N | 1 | 0 | 0 | N |
MYLK | DIQSSSLTL | CENTRAL_NERVOUS_SYSTEM | 1342 | p.R1344Q | c.4031G>A | Missense_Mutation | 1 | 0.11 | SNU201 | N | 5 | 0 | 0 | N |
MYLK | DIRSSSLTQ | SKIN | 1342 | p.L1350Q | c.4049T>A | Missense_Mutation | 1 | 0.11 | MELJUSO | N | 1 | 0 | 0 | N |
MYLK | DKFEGRVRG | AUTONOMIC_GANGLIA | 50 | p.A50D | c.149C>A | Missense_Mutation | 1 | 0.11 | NB1 | N | 0 | 0 | 0 | Y |
MYLK | DLKEIPAKQ | LUNG | 914 | p.E921K | c.2761G>A | Missense_Mutation | 1 | 0.11 | NCIH1092 | N | 0 | 0 | 0 | N |
MYLK | DLLVKKVST | OVARY | 899 | p.G902V | c.2705G>T | Missense_Mutation | 1 | 0.11 | OVCAR8 | N | 1 | 0 | 0 | N |
MYLK | DPFPKVHWL | STOMACH | 747 | p.T751K | c.2252_2253CC>AA | Missense_Mutation | 1 | 0.11 | TGBC11TKB | Y | 23 | 9 | 0 | N |
MYLK | DPLGKKVST | LARGE_INTESTINE | 899 | p.L900P | c.2699T>C | Missense_Mutation | 1 | 0.11 | CW2 | N | 6 | 0 | 0 | N |
MYLK | DPLQPSARV | LARGE_INTESTINE | 199 | p.V199D | c.596T>A | Missense_Mutation | 1 | 0.11 | RKO | Y | 12 | 9 | 0 | N |
MYLK | DPPTTIIWT | ENDOMETRIUM | 1124 | p.A1127T | c.3379G>A | Missense_Mutation | 1 | 0.11 | SNGM | N | 6 | 0 | 0 | N |
MYLK | DRGKYTYEA | PROSTATE | 100 | p.C106Y | c.317G>A | Missense_Mutation | 1 | 0.11 | 22RV1 | N | 1 | 0 | 0 | N |
MYLK | DRYVSLRPG | ENDOMETRIUM | 844 | p.G847V | c.2540G>T | Missense_Mutation | 1 | 0.11 | SNGM | N | 1 | 0 | 0 | N |
MYLK | DSGIYSCTA | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 481 | p.T484I | c.1451C>T | Missense_Mutation | 1 | 0.11 | SUDHL1 | N | 1 | 0 | 0 | N |
MYLK | DSHYLCLLK | CENTRAL_NERVOUS_SYSTEM | 468 | p.G468D | c.1403G>A | Missense_Mutation | 1 | 0.11 | CAS1 | N | 3 | 0 | 0 | N |
MYLK | DVENDVNCK | LUNG | 1070 | p.K1072E | c.3214A>G | Missense_Mutation | 1 | 0.11 | CORL24 | N | 5 | 0 | 0 | N |
MYLK | DVRKEVTNL | LUNG | 270 | p.V278L | c.832G>T | Missense_Mutation | 1 | 0.11 | NCIH23 | Y | 6 | 11 | 0 | N |
MYLK | EADVSQAFL | AUTONOMIC_GANGLIA | 1789 | p.E1790A | c.5369A>C | Missense_Mutation | 1 | 0.11 | NB1 | Y | 9 | 9 | 0 | N |
MYLK | EAFNEISDD | LARGE_INTESTINE | 1683 | p.D1686N | c.5056G>A | Missense_Mutation | 1 | 0.11 | SNU175 | N | 0 | 0 | 0 | N |
MYLK | EATNGSGAC | ENDOMETRIUM | 107 | p.R115C | c.343C>T | Missense_Mutation | 1 | 0.11 | HEC151 | N | 2 | 0 | 0 | N |
MYLK | EDADSHYLC | CENTRAL_NERVOUS_SYSTEM | 465 | p.G468D | c.1403G>A | Missense_Mutation | 1 | 0.11 | CAS1 | N | 2 | 0 | 0 | N |
MYLK | EDRGKYTYE | PROSTATE | 99 | p.C106Y | c.317G>A | Missense_Mutation | 1 | 0.11 | 22RV1 | N | 0 | 0 | 0 | N |
MYLK | EEDRGKYTY | PROSTATE | 98 | p.C106Y | c.317G>A | Missense_Mutation | 1 | 0.11 | 22RV1 | Y | 6 | 13 | 0 | N |
MYLK | EEERKVHSS | LUNG | 940 | p.P948S | c.2842C>T | Missense_Mutation | 1 | 0.11 | NCIH2172 | N | 3 | 0 | 0 | N |
MYLK | EELKKDVEN | LUNG | 1065 | p.K1072E | c.3214A>G | Missense_Mutation | 1 | 0.11 | CORL24 | N | 5 | 0 | 0 | N |
MYLK | EERKVHSSQ | LUNG | 941 | p.P948S | c.2842C>T | Missense_Mutation | 1 | 0.11 | NCIH2172 | N | 0 | 0 | 0 | N |
MYLK | EGATDKFEG | AUTONOMIC_GANGLIA | 46 | p.A50D | c.149C>A | Missense_Mutation | 1 | 0.11 | NB1 | N | 0 | 0 | 0 | N |
MYLK | EIPAKQMDF | LUNG | 917 | p.E921K | c.2761G>A | Missense_Mutation | 1 | 0.11 | NCIH1092 | N | 3 | 0 | 0 | Y |
MYLK | EISIVNCLH | OVARY | 1509 | p.M1513V | c.4537A>G | Missense_Mutation | 1 | 0.11 | OV90 | N | 1 | 0 | 0 | N |
MYLK | EKLESEADV | AUTONOMIC_GANGLIA | 1784 | p.E1790A | c.5369A>C | Missense_Mutation | 1 | 0.11 | NB1 | N | 3 | 0 | 0 | N |
MYLK | EKPHVKPYL | ENDOMETRIUM | 1803 | p.F1811L | c.5433C>A | Missense_Mutation | 1 | 0.11 | JHUEM7 | N | 5 | 0 | 0 | Y |
MYLK | ELATGRSTS | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1380 | p.C1384G | c.4150T>G | Missense_Mutation | 1 | 0.11 | KIJK | N | 0 | 0 | 0 | N |
MYLK | ELKKDVEND | LUNG | 1066 | p.K1072E | c.3214A>G | Missense_Mutation | 1 | 0.11 | CORL24 | N | 0 | 0 | 0 | N |
MYLK | EMKSRRPNS | ENDOMETRIUM | 1200 | p.K1207N | c.3621G>T | Missense_Mutation | 1 | 0.11 | HEC251 | N | 3 | 0 | 0 | N |
MYLK | ENDVNCKRG | LUNG | 1072 | p.K1072E | c.3214A>G | Missense_Mutation | 1 | 0.11 | CORL24 | N | 0 | 0 | 0 | N |
MYLK | EPHYGTQPW | OESOPHAGUS | 714 | p.D717Y | c.2149G>T | Missense_Mutation | 1 | 0.11 | KYSE180 | N | 8 | 0 | 0 | N |
MYLK | EPIRYATDM | PANCREAS | 1636 | p.G1639R | c.4915G>C | Missense_Mutation | 1 | 0.11 | HPAFII | N | 12 | 0 | 0 | N |
MYLK | EPRVTWHRN | LARGE_INTESTINE | 61 | p.Q63R | c.188A>G | Missense_Mutation | 1 | 0.11 | CCK81 | N | 6 | 0 | 0 | Y |
MYLK | EQLDFRDPL | LARGE_INTESTINE | 893 | p.L900P | c.2699T>C | Missense_Mutation | 1 | 0.11 | CW2 | N | 16 | 0 | 0 | N |
MYLK | ERKVHSSQQ | LUNG | 942 | p.P948S | c.2842C>T | Missense_Mutation | 1 | 0.11 | NCIH2172 | N | 0 | 0 | 0 | N |
MYLK | ESDATVKMK | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1217 | p.K1224M | c.3671A>T | Missense_Mutation | 1 | 0.11 | KIJK | N | 3 | 0 | 0 | N |
MYLK | ESEADVSQA | AUTONOMIC_GANGLIA | 1787 | p.E1790A | c.5369A>C | Missense_Mutation | 1 | 0.11 | NB1 | N | 2 | 0 | 0 | Y |
MYLK | ESPTSPLNA | ENDOMETRIUM | 1775 | p.G1775E | c.5324G>A | Missense_Mutation | 1 | 0.11 | AN3CA | N | 3 | 0 | 0 | N |
MYLK | ESQGTASAF | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1092 | p.P1098S | c.3292C>T | Missense_Mutation | 1 | 0.11 | DB | N | 5 | 0 | 0 | N |
MYLK | ETHPSIWGE | LIVER | 150 | p.R152H | c.455G>A | Missense_Mutation | 1 | 0.11 | SNU449 | N | 0 | 0 | 0 | N |
MYLK | ETLNAKTVE | PANCREAS | 1001 | p.A1007T | c.3019G>A | Missense_Mutation | 1 | 0.11 | PK45H | N | 0 | 0 | 0 | N |
MYLK | EVINYEPIR | PANCREAS | 1631 | p.G1639R | c.4915G>C | Missense_Mutation | 1 | 0.11 | HPAFII | N | 6 | 0 | 0 | N |
MYLK | EVTNLISKE | LUNG | 274 | p.V278L | c.832G>T | Missense_Mutation | 1 | 0.11 | NCIH23 | N | 0 | 0 | 0 | N |
MYLK | EVYEDADSH | CENTRAL_NERVOUS_SYSTEM | 462 | p.G468D | c.1403G>A | Missense_Mutation | 1 | 0.11 | CAS1 | N | 2 | 0 | 0 | N |
MYLK | FCSVLGGKK | SKIN | 981 | p.R982C | c.2944C>T | Missense_Mutation | 1 | 0.11 | G361 | N | 3 | 0 | 2 | N |
MYLK | FDDEAFNEI | LARGE_INTESTINE | 1680 | p.D1686N | c.5056G>A | Missense_Mutation | 1 | 0.11 | SNU175 | N | 5 | 0 | 0 | N |
MYLK | FGKVTGTQS | ENDOMETRIUM | 1258 | p.P1266S | c.3796C>T | Missense_Mutation | 1 | 0.11 | HEC265 | N | 2 | 0 | 2 | N |
MYLK | FHSVLAKKG | LARGE_INTESTINE | 953 | p.R954H | c.2861G>A | Missense_Mutation | 1 | 0.11 | HT115 | N | 2 | 0 | 2 | N |
MYLK | FISNLLKKN | LARGE_INTESTINE | 1695 | p.D1703N | c.5107G>A | Missense_Mutation | 1 | 0.11 | SW48 | N | 2 | 0 | 0 | Y |
MYLK | FNEISDDAK | LARGE_INTESTINE | 1685 | p.D1686N | c.5056G>A | Missense_Mutation | 1 | 0.11 | SNU175 | N | 2 | 0 | 0 | N |
MYLK | FPKVHWLRD | STOMACH | 749 | p.T751K | c.2252_2253CC>AA | Missense_Mutation | 1 | 0.11 | TGBC11TKB | N | 4 | 0 | 0 | N |
MYLK | FRDLLVKKV | OVARY | 897 | p.G902V | c.2705G>T | Missense_Mutation | 1 | 0.11 | OVCAR8 | Y | 8 | 11 | 15 | N |
MYLK | FRDPLGKKV | LARGE_INTESTINE | 897 | p.L900P | c.2699T>C | Missense_Mutation | 1 | 0.11 | CW2 | Y | 7 | 10 | 0 | Y |
MYLK | FSAPAVETH | LIVER | 144 | p.R152H | c.455G>A | Missense_Mutation | 1 | 0.11 | SNU449 | N | 2 | 0 | 0 | Y |
MYLK | FSKTIHDLE | LARGE_INTESTINE | 1811 | p.R1816H | c.5447G>A | Missense_Mutation | 1 | 0.11 | SNU1040 | N | 2 | 0 | 0 | N |
MYLK | GACQVTVEL | ENDOMETRIUM | 113 | p.R115C | c.343C>T | Missense_Mutation | 1 | 0.11 | HEC151 | Y | 13 | 10 | 0 | N |
MYLK | GATDKFEGR | AUTONOMIC_GANGLIA | 47 | p.A50D | c.149C>A | Missense_Mutation | 1 | 0.11 | NB1 | N | 4 | 0 | 0 | N |
MYLK | GDPFPKVHW | STOMACH | 746 | p.T751K | c.2252_2253CC>AA | Missense_Mutation | 1 | 0.11 | TGBC11TKB | N | 3 | 0 | 0 | N |
MYLK | GGGSDRYVS | ENDOMETRIUM | 840 | p.G847V | c.2540G>T | Missense_Mutation | 1 | 0.11 | SNGM | N | 0 | 0 | 0 | N |
MYLK | GGSDRYVSL | ENDOMETRIUM | 841 | p.G847V | c.2540G>T | Missense_Mutation | 1 | 0.11 | SNGM | Y | 15 | 10 | 0 | N |
MYLK | GIYSCTASN | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 483 | p.T484I | c.1451C>T | Missense_Mutation | 1 | 0.11 | SUDHL1 | N | 0 | 0 | 0 | N |
MYLK | GKVTGTQSI | ENDOMETRIUM | 1259 | p.P1266S | c.3796C>T | Missense_Mutation | 1 | 0.11 | HEC265 | N | 2 | 0 | 0 | N |
MYLK | GKYTYEATN | PROSTATE | 102 | p.C106Y | c.317G>A | Missense_Mutation | 1 | 0.11 | 22RV1 | N | 1 | 0 | 0 | N |
MYLK | GLGSQHVVS | SALIVARY_GLAND | 388 | p.D393H | c.1177G>C | Missense_Mutation | 1 | 0.11 | YD15 | N | 0 | 0 | 0 | N |
MYLK | GNAKPAKTL | SKIN | 1039 | p.E1045K | c.3133G>A | Missense_Mutation | 1 | 0.11 | COLO829 | N | 5 | 0 | 0 | N |
MYLK | GNALCKDTG | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 758 | p.K759N | c.2277A>C | Missense_Mutation | 1 | 0.11 | HT | N | 0 | 0 | 0 | N |
MYLK | GNDPLQPSA | LARGE_INTESTINE | 197 | p.V199D | c.596T>A | Missense_Mutation | 1 | 0.11 | RKO | N | 1 | 0 | 0 | Y |
MYLK | GNPPPKVIW | LUNG | 648 | p.E653K | c.1957G>A | Missense_Mutation | 1 | 0.11 | NCIH1703 | N | 2 | 0 | 0 | N |
MYLK | GNVPLQQSA | LUNG | 197 | p.P203Q | c.608C>A | Missense_Mutation | 1 | 0.11 | NCIH2405 | N | 2 | 0 | 0 | Y |
MYLK | GPIFLQGLS | BONE | 622 | p.A622G | c.1865C>G | Missense_Mutation | 1 | 0.11 | U2OS | N | 4 | 0 | 0 | N |
MYLK | GPPTSPLNA | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1775 | p.S1776P | c.5326T>C | Missense_Mutation | 1 | 0.11 | PF382 | N | 9 | 0 | 0 | N |
MYLK | GPSGRKSST | LARGE_INTESTINE | 1766 | p.L1767P | c.5300T>C | Missense_Mutation | 1 | 0.11 | SNUC5 | N | 6 | 0 | 0 | N |
MYLK | GQPITSRGR | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 70 | p.G76R | c.226G>A | Missense_Mutation | 1 | 0.11 | MOLT13 | N | 4 | 0 | 0 | N |
MYLK | GRKSSTESP | ENDOMETRIUM | 1769 | p.G1775E | c.5324G>A | Missense_Mutation | 1 | 0.11 | AN3CA | N | 1 | 0 | 0 | N |
MYLK | GRKSSTGPP | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1769 | p.S1776P | c.5326T>C | Missense_Mutation | 1 | 0.11 | PF382 | N | 1 | 0 | 0 | N |
MYLK | GRLSSMVMI | CENTRAL_NERVOUS_SYSTEM | 1756 | p.A1762V | c.5285C>T | Missense_Mutation | 1 | 0.11 | U87MG | Y | 7 | 11 | 0 | N |
MYLK | GRSTSFNVQ | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1384 | p.C1384G | c.4150T>G | Missense_Mutation | 1 | 0.11 | KIJK | N | 1 | 0 | 0 | N |
MYLK | GSDRYVSLR | ENDOMETRIUM | 842 | p.G847V | c.2540G>T | Missense_Mutation | 1 | 0.11 | SNGM | Y | 5 | 10 | 0 | N |
MYLK | GSGACQVTV | ENDOMETRIUM | 111 | p.R115C | c.343C>T | Missense_Mutation | 1 | 0.11 | HEC151 | Y | 3 | 10 | 0 | N |
MYLK | GSQHVVSKA | SALIVARY_GLAND | 390 | p.D393H | c.1177G>C | Missense_Mutation | 1 | 0.11 | YD15 | N | 1 | 0 | 0 | N |
MYLK | GSRQAQVTL | OVARY | 1317 | p.N1324T | c.3971A>C | Missense_Mutation | 1 | 0.11 | OVK18 | Y | 6 | 10 | 0 | N |
MYLK | GTASAFKQK | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1095 | p.P1098S | c.3292C>T | Missense_Mutation | 1 | 0.11 | DB | Y | 3 | 11 | 0 | N |
MYLK | GTPCASDIQ | CENTRAL_NERVOUS_SYSTEM | 1336 | p.R1344Q | c.4031G>A | Missense_Mutation | 1 | 0.11 | SNU201 | N | 0 | 0 | 0 | N |
MYLK | GTQSITCTW | ENDOMETRIUM | 1263 | p.P1266S | c.3796C>T | Missense_Mutation | 1 | 0.11 | HEC265 | N | 1 | 0 | 0 | N |
MYLK | GTSKPSQES | BREAST | 1411 | p.E1414K | c.4240G>A | Missense_Mutation | 1 | 0.11 | ZR751 | N | 0 | 0 | 0 | N |
MYLK | GYPEPRVTW | LARGE_INTESTINE | 58 | p.Q63R | c.188A>G | Missense_Mutation | 1 | 0.11 | CCK81 | Y | 3 | 10 | 0 | N |
MYLK | HARQYEILL | LIVER | 788 | p.G790R | c.2368G>C | Missense_Mutation | 1 | 0.11 | ALEXANDERCELLS | Y | 10 | 10 | 0 | N |
MYLK | HDLEVVEGS | LARGE_INTESTINE | 1816 | p.R1816H | c.5447G>A | Missense_Mutation | 1 | 0.11 | SNU1040 | N | 2 | 0 | 0 | N |
MYLK | HHPKLAQCV | UPPER_AERODIGESTIVE_TRACT | 1517 | p.V1522A | c.4565T>C | Missense_Mutation | 1 | 0.11 | CAL33 | N | 4 | 0 | 0 | N |
MYLK | HPKLAQCVD | UPPER_AERODIGESTIVE_TRACT | 1518 | p.V1522A | c.4565T>C | Missense_Mutation | 1 | 0.11 | CAL33 | N | 1 | 0 | 0 | N |
MYLK | HPSIWGECP | LIVER | 152 | p.R152H | c.455G>A | Missense_Mutation | 1 | 0.11 | SNU449 | N | 1 | 0 | 0 | N |
MYLK | HSPQQVDFH | LARGE_INTESTINE | 946 | p.R954H | c.2861G>A | Missense_Mutation | 1 | 0.11 | HT115 | N | 0 | 0 | 0 | N |
MYLK | HSSQQVDFR | LUNG | 946 | p.P948S | c.2842C>T | Missense_Mutation | 1 | 0.11 | NCIH2172 | N | 3 | 0 | 0 | N |
MYLK | HSVLAKKGT | LARGE_INTESTINE | 954 | p.R954H | c.2861G>A | Missense_Mutation | 1 | 0.11 | HT115 | N | 1 | 0 | 0 | N |
MYLK | HVKPYLSKT | ENDOMETRIUM | 1806 | p.F1811L | c.5433C>A | Missense_Mutation | 1 | 0.11 | JHUEM7 | N | 1 | 0 | 0 | N |
MYLK | HVSVSEKNG | LIVER | 206 | p.R206H | c.617G>A | Missense_Mutation | 1 | 0.11 | SNU182 | N | 0 | 0 | 0 | N |
MYLK | HVVSKAANR | SALIVARY_GLAND | 393 | p.D393H | c.1177G>C | Missense_Mutation | 1 | 0.11 | YD15 | Y | 6 | 9 | 0 | N |
MYLK | HWLRDGNAL | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 753 | p.K759N | c.2277A>C | Missense_Mutation | 1 | 0.11 | HT | N | 7 | 0 | 0 | N |
MYLK | HYGTQPWFI | OESOPHAGUS | 716 | p.D717Y | c.2149G>T | Missense_Mutation | 1 | 0.11 | KYSE180 | Y | 6 | 11 | 0 | N |
MYLK | IAGDPFPKV | STOMACH | 744 | p.T751K | c.2252_2253CC>AA | Missense_Mutation | 1 | 0.11 | TGBC11TKB | Y | 7 | 10 | 0 | Y |
MYLK | IEVYEDADS | CENTRAL_NERVOUS_SYSTEM | 461 | p.G468D | c.1403G>A | Missense_Mutation | 1 | 0.11 | CAS1 | N | 4 | 0 | 0 | N |
MYLK | IGRLSSMVM | CENTRAL_NERVOUS_SYSTEM | 1755 | p.A1762V | c.5285C>T | Missense_Mutation | 1 | 0.11 | U87MG | N | 8 | 0 | 25 | N |
MYLK | IHDLEVVEG | LARGE_INTESTINE | 1815 | p.R1816H | c.5447G>A | Missense_Mutation | 1 | 0.11 | SNU1040 | N | 0 | 0 | 0 | N |
MYLK | IKEGATDKF | AUTONOMIC_GANGLIA | 44 | p.A50D | c.149C>A | Missense_Mutation | 1 | 0.11 | NB1 | N | 3 | 0 | 0 | N |
MYLK | INVYGTSKP | BREAST | 1407 | p.E1414K | c.4240G>A | Missense_Mutation | 1 | 0.11 | ZR751 | N | 0 | 0 | 4 | N |
MYLK | INYEPIRYA | PANCREAS | 1633 | p.G1639R | c.4915G>C | Missense_Mutation | 1 | 0.11 | HPAFII | N | 5 | 0 | 5 | N |
MYLK | IPAKQMDFR | LUNG | 918 | p.E921K | c.2761G>A | Missense_Mutation | 1 | 0.11 | NCIH1092 | N | 5 | 0 | 0 | Y |
MYLK | IQSSSLTLS | CENTRAL_NERVOUS_SYSTEM | 1343 | p.R1344Q | c.4031G>A | Missense_Mutation | 1 | 0.11 | SNU201 | N | 0 | 0 | 7 | N |
MYLK | IRQEISIVN | OVARY | 1506 | p.M1513V | c.4537A>G | Missense_Mutation | 1 | 0.11 | OV90 | N | 2 | 0 | 4 | N |
MYLK | IRSSSLTQS | SKIN | 1343 | p.L1350Q | c.4049T>A | Missense_Mutation | 1 | 0.11 | MELJUSO | N | 3 | 0 | 14 | N |
MYLK | IRYATDMWS | PANCREAS | 1638 | p.G1639R | c.4915G>C | Missense_Mutation | 1 | 0.11 | HPAFII | N | 3 | 0 | 20 | N |
MYLK | ISGPSGRKS | LARGE_INTESTINE | 1764 | p.L1767P | c.5300T>C | Missense_Mutation | 1 | 0.11 | SNUC5 | N | 1 | 0 | 0 | N |
MYLK | ISIVNCLHH | OVARY | 1510 | p.M1513V | c.4537A>G | Missense_Mutation | 1 | 0.11 | OV90 | N | 2 | 0 | 13 | N |
MYLK | ISNLLKKNM | LARGE_INTESTINE | 1696 | p.D1703N | c.5107G>A | Missense_Mutation | 1 | 0.11 | SW48 | N | 5 | 0 | 9 | Y |
MYLK | ITSRGRFLL | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 73 | p.G76R | c.226G>A | Missense_Mutation | 1 | 0.11 | MOLT13 | Y | 9 | 9 | 4 | N |
MYLK | IVNCLHHPK | OVARY | 1512 | p.M1513V | c.4537A>G | Missense_Mutation | 1 | 0.11 | OV90 | N | 3 | 0 | 17 | N |
MYLK | IYSCTASNA | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 484 | p.T484I | c.1451C>T | Missense_Mutation | 1 | 0.11 | SUDHL1 | Y | 3 | 11 | 1 | N |
MYLK | KARTRDSGI | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 476 | p.T484I | c.1451C>T | Missense_Mutation | 1 | 0.11 | SUDHL1 | N | 8 | 0 | 0 | N |
MYLK | KDVENDVNC | LUNG | 1069 | p.K1072E | c.3214A>G | Missense_Mutation | 1 | 0.11 | CORL24 | N | 3 | 0 | 0 | N |
MYLK | KEELKKDVE | LUNG | 1064 | p.K1072E | c.3214A>G | Missense_Mutation | 1 | 0.11 | CORL24 | N | 0 | 0 | 0 | N |
MYLK | KEGATDKFE | AUTONOMIC_GANGLIA | 45 | p.A50D | c.149C>A | Missense_Mutation | 1 | 0.11 | NB1 | N | 0 | 0 | 0 | N |
MYLK | KEIPAKQMD | LUNG | 916 | p.E921K | c.2761G>A | Missense_Mutation | 1 | 0.11 | NCIH1092 | N | 2 | 0 | 0 | N |
MYLK | KELATGRST | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1379 | p.C1384G | c.4150T>G | Missense_Mutation | 1 | 0.11 | KIJK | N | 5 | 0 | 0 | N |
MYLK | KEVTNLISK | LUNG | 273 | p.V278L | c.832G>T | Missense_Mutation | 1 | 0.11 | NCIH23 | N | 4 | 0 | 0 | N |
MYLK | KGNDPLQPS | LARGE_INTESTINE | 196 | p.V199D | c.596T>A | Missense_Mutation | 1 | 0.11 | RKO | N | 1 | 0 | 0 | N |
MYLK | KGNVPLQQS | LUNG | 196 | p.P203Q | c.608C>A | Missense_Mutation | 1 | 0.11 | NCIH2405 | N | 1 | 0 | 0 | N |
MYLK | KKDVENDVN | LUNG | 1068 | p.K1072E | c.3214A>G | Missense_Mutation | 1 | 0.11 | CORL24 | N | 1 | 0 | 0 | N |
MYLK | KKNMKNRLD | LARGE_INTESTINE | 1701 | p.D1703N | c.5107G>A | Missense_Mutation | 1 | 0.11 | SW48 | N | 0 | 0 | 0 | N |
MYLK | KKVQPWHAR | LIVER | 782 | p.G790R | c.2368G>C | Missense_Mutation | 1 | 0.11 | ALEXANDERCELLS | N | 1 | 0 | 0 | N |
MYLK | KLAQCVDAF | UPPER_AERODIGESTIVE_TRACT | 1520 | p.V1522A | c.4565T>C | Missense_Mutation | 1 | 0.11 | CAL33 | N | 9 | 0 | 0 | N |
MYLK | KLESEADVS | AUTONOMIC_GANGLIA | 1785 | p.E1790A | c.5369A>C | Missense_Mutation | 1 | 0.11 | NB1 | N | 1 | 0 | 0 | N |
MYLK | KMGNAVRAI | LARGE_INTESTINE | 1747 | p.T1748M | c.5243C>T | Missense_Mutation | 1 | 0.11 | HT115 | N | 6 | 0 | 0 | N |
MYLK | KMKPAPKTP | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1223 | p.K1224M | c.3671A>T | Missense_Mutation | 1 | 0.11 | KIJK | N | 0 | 0 | 0 | N |
MYLK | KNMKNRLDC | LARGE_INTESTINE | 1702 | p.D1703N | c.5107G>A | Missense_Mutation | 1 | 0.11 | SW48 | N | 2 | 0 | 0 | N |
MYLK | KPAKTLKPM | SKIN | 1042 | p.E1045K | c.3133G>A | Missense_Mutation | 1 | 0.11 | COLO829 | N | 11 | 0 | 0 | N |
MYLK | KPATPDFCS | SKIN | 975 | p.R982C | c.2944C>T | Missense_Mutation | 1 | 0.11 | G361 | N | 4 | 0 | 0 | Y |
MYLK | KPHVKPYLS | ENDOMETRIUM | 1804 | p.F1811L | c.5433C>A | Missense_Mutation | 1 | 0.11 | JHUEM7 | N | 3 | 0 | 0 | N |
MYLK | KPLSNARPS | UPPER_AERODIGESTIVE_TRACT | 1012 | p.Q1018R | c.3053A>G | Missense_Mutation | 1 | 0.11 | DETROIT562 | N | 4 | 0 | 0 | N |
MYLK | KPSQESELT | BREAST | 1414 | p.E1414K | c.4240G>A | Missense_Mutation | 1 | 0.11 | ZR751 | N | 4 | 0 | 0 | N |
MYLK | KPTGPIFLQ | BONE | 619 | p.A622G | c.1865C>G | Missense_Mutation | 1 | 0.11 | U2OS | N | 1 | 0 | 0 | N |
MYLK | KPYFSKTIH | LARGE_INTESTINE | 1808 | p.R1816H | c.5447G>A | Missense_Mutation | 1 | 0.11 | SNU1040 | N | 3 | 0 | 0 | N |
MYLK | KPYLSKTIR | ENDOMETRIUM | 1808 | p.F1811L | c.5433C>A | Missense_Mutation | 1 | 0.11 | JHUEM7 | N | 8 | 0 | 0 | N |
MYLK | KQMDFRANL | LUNG | 921 | p.E921K | c.2761G>A | Missense_Mutation | 1 | 0.11 | NCIH1092 | Y | 20 | 11 | 0 | N |
MYLK | KRPAPPRSA | ENDOMETRIUM | 372 | p.P379S | c.1135C>T | Missense_Mutation | 1 | 0.11 | HEC59 | N | 4 | 0 | 0 | N |
MYLK | KSRRPNSSL | ENDOMETRIUM | 1202 | p.K1207N | c.3621G>T | Missense_Mutation | 1 | 0.11 | HEC251 | Y | 8 | 12 | 0 | N |
MYLK | KSSLPPLLG | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1207 | p.V1213L | c.3637G>C | Missense_Mutation | 1 | 0.11 | HDLM2 | N | 0 | 0 | 0 | N |
MYLK | KSSTESPTS | ENDOMETRIUM | 1771 | p.G1775E | c.5324G>A | Missense_Mutation | 1 | 0.11 | AN3CA | N | 1 | 0 | 0 | N |
MYLK | KSSTGPPTS | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1771 | p.S1776P | c.5326T>C | Missense_Mutation | 1 | 0.11 | PF382 | N | 1 | 0 | 0 | N |
MYLK | KTIHDLEVV | LARGE_INTESTINE | 1813 | p.R1816H | c.5447G>A | Missense_Mutation | 1 | 0.11 | SNU1040 | N | 5 | 0 | 0 | N |
MYLK | KTLKPMGNA | SKIN | 1045 | p.E1045K | c.3133G>A | Missense_Mutation | 1 | 0.11 | COLO829 | N | 3 | 0 | 0 | N |
MYLK | KTVESSKPL | PANCREAS | 1006 | p.A1007T | c.3019G>A | Missense_Mutation | 1 | 0.11 | PK45H | N | 17 | 0 | 0 | N |
MYLK | KTWKELATG | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1376 | p.C1384G | c.4150T>G | Missense_Mutation | 1 | 0.11 | KIJK | N | 1 | 0 | 0 | N |
MYLK | KVHSSQQVD | LUNG | 944 | p.P948S | c.2842C>T | Missense_Mutation | 1 | 0.11 | NCIH2172 | N | 0 | 0 | 0 | N |
MYLK | KVHWLRDGK | STOMACH | 751 | p.T751K | c.2252_2253CC>AA | Missense_Mutation | 1 | 0.11 | TGBC11TKB | N | 6 | 0 | 0 | N |
MYLK | KVIWLHNGN | LUNG | 653 | p.E653K | c.1957G>A | Missense_Mutation | 1 | 0.11 | NCIH1703 | N | 0 | 0 | 0 | N |
MYLK | KVQPWHARQ | LIVER | 783 | p.G790R | c.2368G>C | Missense_Mutation | 1 | 0.11 | ALEXANDERCELLS | N | 0 | 0 | 0 | N |
MYLK | KVTGTQSIT | ENDOMETRIUM | 1260 | p.P1266S | c.3796C>T | Missense_Mutation | 1 | 0.11 | HEC265 | N | 1 | 0 | 0 | N |
MYLK | KWQKMGNAV | LARGE_INTESTINE | 1744 | p.T1748M | c.5243C>T | Missense_Mutation | 1 | 0.11 | HT115 | N | 3 | 0 | 0 | N |
MYLK | KYTYEATNG | PROSTATE | 103 | p.C106Y | c.317G>A | Missense_Mutation | 1 | 0.11 | 22RV1 | N | 0 | 0 | 0 | N |
MYLK | LAQCVDAFE | UPPER_AERODIGESTIVE_TRACT | 1521 | p.V1522A | c.4565T>C | Missense_Mutation | 1 | 0.11 | CAL33 | N | 0 | 0 | 0 | N |
MYLK | LATGRSTSF | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1381 | p.C1384G | c.4150T>G | Missense_Mutation | 1 | 0.11 | KIJK | N | 7 | 0 | 0 | N |
MYLK | LCIKEGATD | AUTONOMIC_GANGLIA | 42 | p.A50D | c.149C>A | Missense_Mutation | 1 | 0.11 | NB1 | N | 0 | 0 | 4 | N |
MYLK | LDFRDLLVK | OVARY | 895 | p.G902V | c.2705G>T | Missense_Mutation | 1 | 0.11 | OVCAR8 | N | 0 | 0 | 0 | N |
MYLK | LDFRDPLGK | LARGE_INTESTINE | 895 | p.L900P | c.2699T>C | Missense_Mutation | 1 | 0.11 | CW2 | N | 0 | 0 | 1 | N |
MYLK | LESEADVSQ | AUTONOMIC_GANGLIA | 1786 | p.E1790A | c.5369A>C | Missense_Mutation | 1 | 0.11 | NB1 | N | 0 | 0 | 0 | N |
MYLK | LGSQHVVSK | SALIVARY_GLAND | 389 | p.D393H | c.1177G>C | Missense_Mutation | 1 | 0.11 | YD15 | N | 0 | 0 | 3 | N |
MYLK | LGSRQAQVT | OVARY | 1316 | p.N1324T | c.3971A>C | Missense_Mutation | 1 | 0.11 | OVK18 | N | 1 | 0 | 0 | N |
MYLK | LHHPKLAQC | UPPER_AERODIGESTIVE_TRACT | 1516 | p.V1522A | c.4565T>C | Missense_Mutation | 1 | 0.11 | CAL33 | N | 1 | 0 | 0 | N |
MYLK | LISKESKLD | LUNG | 278 | p.V278L | c.832G>T | Missense_Mutation | 1 | 0.11 | NCIH23 | N | 0 | 0 | 4 | N |
MYLK | LKEIPAKQM | LUNG | 915 | p.E921K | c.2761G>A | Missense_Mutation | 1 | 0.11 | NCIH1092 | N | 3 | 0 | 0 | N |
MYLK | LKGNDPLQP | LARGE_INTESTINE | 195 | p.V199D | c.596T>A | Missense_Mutation | 1 | 0.11 | RKO | N | 0 | 0 | 3 | N |
MYLK | LKGNVPLQQ | LUNG | 195 | p.P203Q | c.608C>A | Missense_Mutation | 1 | 0.11 | NCIH2405 | N | 0 | 0 | 26 | N |
MYLK | LKKDVENDV | LUNG | 1067 | p.K1072E | c.3214A>G | Missense_Mutation | 1 | 0.11 | CORL24 | N | 2 | 0 | 0 | N |
MYLK | LKKNMKNRL | LARGE_INTESTINE | 1700 | p.D1703N | c.5107G>A | Missense_Mutation | 1 | 0.11 | SW48 | N | 4 | 0 | 5 | N |
MYLK | LLGTESDAT | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1213 | p.V1213L | c.3637G>C | Missense_Mutation | 1 | 0.11 | HDLM2 | N | 2 | 0 | 0 | N |
MYLK | LLKKNMKNR | LARGE_INTESTINE | 1699 | p.D1703N | c.5107G>A | Missense_Mutation | 1 | 0.11 | SW48 | Y | 5 | 11 | 0 | N |
MYLK | LLVKKVSTK | OVARY | 900 | p.G902V | c.2705G>T | Missense_Mutation | 1 | 0.11 | OVCAR8 | N | 6 | 0 | 10 | N |
MYLK | LNAKTVESS | PANCREAS | 1003 | p.A1007T | c.3019G>A | Missense_Mutation | 1 | 0.11 | PK45H | N | 0 | 0 | 12 | N |
MYLK | LPPLLGTES | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1210 | p.V1213L | c.3637G>C | Missense_Mutation | 1 | 0.11 | HDLM2 | N | 4 | 0 | 0 | N |
MYLK | LQPSAHVSV | LIVER | 201 | p.R206H | c.617G>A | Missense_Mutation | 1 | 0.11 | SNU182 | N | 10 | 0 | 2 | N |
MYLK | LQQSARVSV | LUNG | 201 | p.P203Q | c.608C>A | Missense_Mutation | 1 | 0.11 | NCIH2405 | N | 9 | 0 | 9 | N |
MYLK | LRDGNALCK | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 755 | p.K759N | c.2277A>C | Missense_Mutation | 1 | 0.11 | HT | N | 3 | 0 | 0 | Y |
MYLK | LSGRKSSTE | ENDOMETRIUM | 1767 | p.G1775E | c.5324G>A | Missense_Mutation | 1 | 0.11 | AN3CA | N | 0 | 0 | 0 | N |
MYLK | LSKTIRDLE | ENDOMETRIUM | 1811 | p.F1811L | c.5433C>A | Missense_Mutation | 1 | 0.11 | JHUEM7 | N | 0 | 0 | 0 | N |
MYLK | LSNARPSGP | UPPER_AERODIGESTIVE_TRACT | 1014 | p.Q1018R | c.3053A>G | Missense_Mutation | 1 | 0.11 | DETROIT562 | N | 0 | 0 | 0 | N |
MYLK | LSSMVMISG | CENTRAL_NERVOUS_SYSTEM | 1758 | p.A1762V | c.5285C>T | Missense_Mutation | 1 | 0.11 | U87MG | N | 0 | 0 | 0 | N |
MYLK | LSWSGSSYD | LUNG | 1350 | p.Y1353S | c.4058A>C | Missense_Mutation | 1 | 0.11 | PC14 | N | 0 | 0 | 0 | N |
MYLK | LTLSWSGSS | LUNG | 1348 | p.Y1353S | c.4058A>C | Missense_Mutation | 1 | 0.11 | PC14 | N | 0 | 0 | 1 | N |
MYLK | LTQSWYGSS | SKIN | 1348 | p.L1350Q | c.4049T>A | Missense_Mutation | 1 | 0.11 | MELJUSO | N | 1 | 0 | 0 | N |
MYLK | LTVQEPHYG | OESOPHAGUS | 710 | p.D717Y | c.2149G>T | Missense_Mutation | 1 | 0.11 | KYSE180 | N | 0 | 0 | 0 | N |
MYLK | LVKKVSTKT | OVARY | 901 | p.G902V | c.2705G>T | Missense_Mutation | 1 | 0.11 | OVCAR8 | N | 0 | 0 | 2 | N |
MYLK | MAMISGPSG | LARGE_INTESTINE | 1761 | p.L1767P | c.5300T>C | Missense_Mutation | 1 | 0.11 | SNUC5 | N | 0 | 0 | 1 | N |
MYLK | MARRKWQKM | LARGE_INTESTINE | 1740 | p.T1748M | c.5243C>T | Missense_Mutation | 1 | 0.11 | HT115 | N | 9 | 0 | 0 | N |
MYLK | MGNAKPAKT | SKIN | 1038 | p.E1045K | c.3133G>A | Missense_Mutation | 1 | 0.11 | COLO829 | N | 1 | 0 | 0 | N |
MYLK | MGNAVRAIG | LARGE_INTESTINE | 1748 | p.T1748M | c.5243C>T | Missense_Mutation | 1 | 0.11 | HT115 | N | 0 | 0 | 0 | N |
MYLK | MISGPSGRK | LARGE_INTESTINE | 1763 | p.L1767P | c.5300T>C | Missense_Mutation | 1 | 0.11 | SNUC5 | N | 2 | 0 | 0 | N |
MYLK | MKPAPKTPP | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1224 | p.K1224M | c.3671A>T | Missense_Mutation | 1 | 0.11 | KIJK | N | 0 | 0 | 0 | N |
MYLK | MKSRRPNSS | ENDOMETRIUM | 1201 | p.K1207N | c.3621G>T | Missense_Mutation | 1 | 0.11 | HEC251 | N | 1 | 0 | 22 | N |
MYLK | MVMISGLSG | CENTRAL_NERVOUS_SYSTEM | 1761 | p.A1762V | c.5285C>T | Missense_Mutation | 1 | 0.11 | U87MG | N | 0 | 0 | 40 | N |
MYLK | NAEKLESEA | AUTONOMIC_GANGLIA | 1782 | p.E1790A | c.5369A>C | Missense_Mutation | 1 | 0.11 | NB1 | N | 3 | 0 | 0 | N |
MYLK | NAKPAKTLK | SKIN | 1040 | p.E1045K | c.3133G>A | Missense_Mutation | 1 | 0.11 | COLO829 | N | 1 | 0 | 0 | N |
MYLK | NAKTVESSK | PANCREAS | 1004 | p.A1007T | c.3019G>A | Missense_Mutation | 1 | 0.11 | PK45H | N | 1 | 0 | 0 | N |
MYLK | NALCKDTGH | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 759 | p.K759N | c.2277A>C | Missense_Mutation | 1 | 0.11 | HT | N | 0 | 0 | 0 | N |
MYLK | NARPSGPLK | UPPER_AERODIGESTIVE_TRACT | 1016 | p.Q1018R | c.3053A>G | Missense_Mutation | 1 | 0.11 | DETROIT562 | Y | 1 | 11 | 0 | Y |
MYLK | NCLHHPKLA | UPPER_AERODIGESTIVE_TRACT | 1514 | p.V1522A | c.4565T>C | Missense_Mutation | 1 | 0.11 | CAL33 | N | 0 | 0 | 0 | N |
MYLK | NDPLQPSAR | LARGE_INTESTINE | 198 | p.V199D | c.596T>A | Missense_Mutation | 1 | 0.11 | RKO | N | 0 | 0 | 0 | N |
MYLK | NEISDDAKD | LARGE_INTESTINE | 1686 | p.D1686N | c.5056G>A | Missense_Mutation | 1 | 0.11 | SNU175 | N | 2 | 0 | 0 | N |
MYLK | NGQPITSRG | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 69 | p.G76R | c.226G>A | Missense_Mutation | 1 | 0.11 | MOLT13 | N | 0 | 0 | 0 | N |
MYLK | NGSGACQVT | ENDOMETRIUM | 110 | p.R115C | c.343C>T | Missense_Mutation | 1 | 0.11 | HEC151 | N | 1 | 0 | 0 | N |
MYLK | NIRQEISIV | OVARY | 1505 | p.M1513V | c.4537A>G | Missense_Mutation | 1 | 0.11 | OV90 | Y | 0 | 9 | 0 | N |
MYLK | NLISKESKL | LUNG | 277 | p.V278L | c.832G>T | Missense_Mutation | 1 | 0.11 | NCIH23 | N | 13 | 0 | 0 | N |
MYLK | NLLKKNMKN | LARGE_INTESTINE | 1698 | p.D1703N | c.5107G>A | Missense_Mutation | 1 | 0.11 | SW48 | N | 0 | 0 | 0 | N |
MYLK | NMKNRLDCT | LARGE_INTESTINE | 1703 | p.D1703N | c.5107G>A | Missense_Mutation | 1 | 0.11 | SW48 | N | 1 | 0 | 0 | N |
MYLK | NPPPKVIWL | LUNG | 649 | p.E653K | c.1957G>A | Missense_Mutation | 1 | 0.11 | NCIH1703 | Y | 21 | 9 | 0 | N |
MYLK | NSSLPPVLG | ENDOMETRIUM | 1207 | p.K1207N | c.3621G>T | Missense_Mutation | 1 | 0.11 | HEC251 | N | 0 | 0 | 0 | N |
MYLK | NVPLQPSAH | LIVER | 198 | p.R206H | c.617G>A | Missense_Mutation | 1 | 0.11 | SNU182 | N | 0 | 0 | 0 | N |
MYLK | NVPLQQSAR | LUNG | 198 | p.P203Q | c.608C>A | Missense_Mutation | 1 | 0.11 | NCIH2405 | Y | 5 | 9 | 0 | Y |
MYLK | NVYGTSKPS | BREAST | 1408 | p.E1414K | c.4240G>A | Missense_Mutation | 1 | 0.11 | ZR751 | N | 0 | 0 | 0 | N |
MYLK | NYEPIRYAT | PANCREAS | 1634 | p.G1639R | c.4915G>C | Missense_Mutation | 1 | 0.11 | HPAFII | N | 4 | 0 | 0 | N |
MYLK | PAKQMDFRA | LUNG | 919 | p.E921K | c.2761G>A | Missense_Mutation | 1 | 0.11 | NCIH1092 | N | 0 | 0 | 0 | N |
MYLK | PAKTLKPMG | SKIN | 1043 | p.E1045K | c.3133G>A | Missense_Mutation | 1 | 0.11 | COLO829 | N | 0 | 0 | 0 | N |
MYLK | PAPPRSATF | ENDOMETRIUM | 374 | p.P379S | c.1135C>T | Missense_Mutation | 1 | 0.11 | HEC59 | N | 2 | 0 | 0 | N |
MYLK | PATPDFCSV | SKIN | 976 | p.R982C | c.2944C>T | Missense_Mutation | 1 | 0.11 | G361 | N | 3 | 0 | 0 | Y |
MYLK | PAVETHPSI | LIVER | 147 | p.R152H | c.455G>A | Missense_Mutation | 1 | 0.11 | SNU449 | N | 3 | 0 | 0 | N |
MYLK | PCASDIQSS | CENTRAL_NERVOUS_SYSTEM | 1338 | p.R1344Q | c.4031G>A | Missense_Mutation | 1 | 0.11 | SNU201 | N | 0 | 0 | 0 | N |
MYLK | PDFCSVLGG | SKIN | 979 | p.R982C | c.2944C>T | Missense_Mutation | 1 | 0.11 | G361 | N | 0 | 0 | 0 | N |
MYLK | PEMKSRRPN | ENDOMETRIUM | 1199 | p.K1207N | c.3621G>T | Missense_Mutation | 1 | 0.11 | HEC251 | N | 0 | 0 | 0 | Y |
MYLK | PEPRVTWHR | LARGE_INTESTINE | 60 | p.Q63R | c.188A>G | Missense_Mutation | 1 | 0.11 | CCK81 | N | 0 | 0 | 0 | Y |
MYLK | PFPKVHWLR | STOMACH | 748 | p.T751K | c.2252_2253CC>AA | Missense_Mutation | 1 | 0.11 | TGBC11TKB | N | 1 | 0 | 0 | N |
MYLK | PGLGSQHVV | SALIVARY_GLAND | 387 | p.D393H | c.1177G>C | Missense_Mutation | 1 | 0.11 | YD15 | N | 4 | 0 | 0 | N |
MYLK | PHVKPYLSK | ENDOMETRIUM | 1805 | p.F1811L | c.5433C>A | Missense_Mutation | 1 | 0.11 | JHUEM7 | N | 0 | 0 | 0 | N |
MYLK | PHYGTQPWF | OESOPHAGUS | 715 | p.D717Y | c.2149G>T | Missense_Mutation | 1 | 0.11 | KYSE180 | N | 2 | 0 | 0 | N |
MYLK | PIRYATDMW | PANCREAS | 1637 | p.G1639R | c.4915G>C | Missense_Mutation | 1 | 0.11 | HPAFII | N | 0 | 0 | 0 | N |
MYLK | PITSRGRFL | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 72 | p.G76R | c.226G>A | Missense_Mutation | 1 | 0.11 | MOLT13 | N | 0 | 0 | 0 | N |
MYLK | PKLAQCVDA | UPPER_AERODIGESTIVE_TRACT | 1519 | p.V1522A | c.4565T>C | Missense_Mutation | 1 | 0.11 | CAL33 | N | 1 | 0 | 0 | N |
MYLK | PKPATPDFC | SKIN | 974 | p.R982C | c.2944C>T | Missense_Mutation | 1 | 0.11 | G361 | N | 0 | 0 | 0 | Y |
MYLK | PKSSLPPLL | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1206 | p.V1213L | c.3637G>C | Missense_Mutation | 1 | 0.11 | HDLM2 | N | 3 | 0 | 0 | N |
MYLK | PKVHWLRDG | STOMACH | 750 | p.T751K | c.2252_2253CC>AA | Missense_Mutation | 1 | 0.11 | TGBC11TKB | N | 0 | 0 | 0 | N |
MYLK | PKVIWLHNG | LUNG | 652 | p.E653K | c.1957G>A | Missense_Mutation | 1 | 0.11 | NCIH1703 | N | 0 | 0 | 0 | N |
MYLK | PLGKKVSTK | LARGE_INTESTINE | 900 | p.L900P | c.2699T>C | Missense_Mutation | 1 | 0.11 | CW2 | N | 1 | 0 | 0 | N |
MYLK | PLLGTESDA | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1212 | p.V1213L | c.3637G>C | Missense_Mutation | 1 | 0.11 | HDLM2 | N | 1 | 0 | 0 | N |
MYLK | PLQPSAHVS | LIVER | 200 | p.R206H | c.617G>A | Missense_Mutation | 1 | 0.11 | SNU182 | N | 0 | 0 | 0 | N |
MYLK | PLQQSARVS | LUNG | 200 | p.P203Q | c.608C>A | Missense_Mutation | 1 | 0.11 | NCIH2405 | N | 0 | 0 | 0 | N |
MYLK | PLSNARPSG | UPPER_AERODIGESTIVE_TRACT | 1013 | p.Q1018R | c.3053A>G | Missense_Mutation | 1 | 0.11 | DETROIT562 | N | 0 | 0 | 0 | N |
MYLK | PMGNAKPAK | SKIN | 1037 | p.E1045K | c.3133G>A | Missense_Mutation | 1 | 0.11 | COLO829 | N | 1 | 0 | 0 | N |
MYLK | PNSSLPPVL | ENDOMETRIUM | 1206 | p.K1207N | c.3621G>T | Missense_Mutation | 1 | 0.11 | HEC251 | N | 0 | 0 | 0 | N |
MYLK | PPKVIWLHN | LUNG | 651 | p.E653K | c.1957G>A | Missense_Mutation | 1 | 0.11 | NCIH1703 | N | 0 | 0 | 0 | N |
MYLK | PPLLGTESD | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1211 | p.V1213L | c.3637G>C | Missense_Mutation | 1 | 0.11 | HDLM2 | N | 0 | 0 | 0 | N |
MYLK | PPPKVIWLH | LUNG | 650 | p.E653K | c.1957G>A | Missense_Mutation | 1 | 0.11 | NCIH1703 | N | 0 | 0 | 0 | N |
MYLK | PPRSATFPT | ENDOMETRIUM | 376 | p.P379S | c.1135C>T | Missense_Mutation | 1 | 0.11 | HEC59 | N | 1 | 0 | 0 | N |
MYLK | PPTSPLNAE | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1776 | p.S1776P | c.5326T>C | Missense_Mutation | 1 | 0.11 | PF382 | N | 0 | 0 | 0 | N |
MYLK | PPTTIIWTL | ENDOMETRIUM | 1125 | p.A1127T | c.3379G>A | Missense_Mutation | 1 | 0.11 | SNGM | N | 10 | 0 | 0 | N |
MYLK | PQQVDFHSV | LARGE_INTESTINE | 948 | p.R954H | c.2861G>A | Missense_Mutation | 1 | 0.11 | HT115 | N | 1 | 0 | 0 | Y |
MYLK | PRSATFPTR | ENDOMETRIUM | 377 | p.P379S | c.1135C>T | Missense_Mutation | 1 | 0.11 | HEC59 | N | 1 | 0 | 0 | N |
MYLK | PRVTWHRNG | LARGE_INTESTINE | 62 | p.Q63R | c.188A>G | Missense_Mutation | 1 | 0.11 | CCK81 | N | 0 | 0 | 0 | Y |
MYLK | PSAHVSVSE | LIVER | 203 | p.R206H | c.617G>A | Missense_Mutation | 1 | 0.11 | SNU182 | N | 0 | 0 | 0 | N |
MYLK | PSGRKSSTG | LARGE_INTESTINE | 1767 | p.L1767P | c.5300T>C | Missense_Mutation | 1 | 0.11 | SNUC5 | N | 0 | 0 | 0 | N |
MYLK | PSKPTGPIF | BONE | 617 | p.A622G | c.1865C>G | Missense_Mutation | 1 | 0.11 | U2OS | Y | 1 | 10 | 0 | N |
MYLK | PTGPIFLQG | BONE | 620 | p.A622G | c.1865C>G | Missense_Mutation | 1 | 0.11 | U2OS | N | 0 | 0 | 0 | N |
MYLK | PTTIIWTLN | ENDOMETRIUM | 1126 | p.A1127T | c.3379G>A | Missense_Mutation | 1 | 0.11 | SNGM | N | 0 | 0 | 0 | N |
MYLK | PVAPSKPTG | BONE | 614 | p.A622G | c.1865C>G | Missense_Mutation | 1 | 0.11 | U2OS | N | 0 | 0 | 0 | Y |
MYLK | PWHARQYEI | LIVER | 786 | p.G790R | c.2368G>C | Missense_Mutation | 1 | 0.11 | ALEXANDERCELLS | N | 0 | 0 | 0 | N |
MYLK | PYFSKTIHD | LARGE_INTESTINE | 1809 | p.R1816H | c.5447G>A | Missense_Mutation | 1 | 0.11 | SNU1040 | N | 0 | 0 | 0 | N |
MYLK | PYLSKTIRD | ENDOMETRIUM | 1809 | p.F1811L | c.5433C>A | Missense_Mutation | 1 | 0.11 | JHUEM7 | N | 0 | 0 | 0 | N |
MYLK | QAQVTLTVV | OVARY | 1320 | p.N1324T | c.3971A>C | Missense_Mutation | 1 | 0.11 | OVK18 | N | 5 | 0 | 0 | N |
MYLK | QEISIVNCL | OVARY | 1508 | p.M1513V | c.4537A>G | Missense_Mutation | 1 | 0.11 | OV90 | Y | 11 | 11 | 0 | N |
MYLK | QEPHYGTQP | OESOPHAGUS | 713 | p.D717Y | c.2149G>T | Missense_Mutation | 1 | 0.11 | KYSE180 | N | 0 | 0 | 0 | N |
MYLK | QGTASAFKQ | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1094 | p.P1098S | c.3292C>T | Missense_Mutation | 1 | 0.11 | DB | N | 0 | 0 | 0 | N |
MYLK | QHVVSKAAN | SALIVARY_GLAND | 392 | p.D393H | c.1177G>C | Missense_Mutation | 1 | 0.11 | YD15 | N | 1 | 0 | 0 | N |
MYLK | QKMGNAVRA | LARGE_INTESTINE | 1746 | p.T1748M | c.5243C>T | Missense_Mutation | 1 | 0.11 | HT115 | N | 2 | 0 | 0 | N |
MYLK | QLDFRDLLV | OVARY | 894 | p.G902V | c.2705G>T | Missense_Mutation | 1 | 0.11 | OVCAR8 | Y | 4 | 12 | 0 | N |
MYLK | QLDFRDPLG | LARGE_INTESTINE | 894 | p.L900P | c.2699T>C | Missense_Mutation | 1 | 0.11 | CW2 | N | 0 | 0 | 0 | N |
MYLK | QPGLGSQHV | SALIVARY_GLAND | 386 | p.D393H | c.1177G>C | Missense_Mutation | 1 | 0.11 | YD15 | Y | 11 | 11 | 0 | N |
MYLK | QPITSRGRF | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 71 | p.G76R | c.226G>A | Missense_Mutation | 1 | 0.11 | MOLT13 | N | 11 | 0 | 0 | N |
MYLK | QPSAHVSVS | LIVER | 202 | p.R206H | c.617G>A | Missense_Mutation | 1 | 0.11 | SNU182 | N | 2 | 0 | 0 | N |
MYLK | QPWHARQYE | LIVER | 785 | p.G790R | c.2368G>C | Missense_Mutation | 1 | 0.11 | ALEXANDERCELLS | N | 1 | 0 | 0 | N |
MYLK | QQSARVSVS | LUNG | 202 | p.P203Q | c.608C>A | Missense_Mutation | 1 | 0.11 | NCIH2405 | N | 0 | 0 | 0 | N |
MYLK | QQVDFHSVL | LARGE_INTESTINE | 949 | p.R954H | c.2861G>A | Missense_Mutation | 1 | 0.11 | HT115 | N | 18 | 0 | 0 | N |
MYLK | QSARVSVSE | LUNG | 203 | p.P203Q | c.608C>A | Missense_Mutation | 1 | 0.11 | NCIH2405 | N | 0 | 0 | 0 | N |
MYLK | QSITCTWMK | ENDOMETRIUM | 1265 | p.P1266S | c.3796C>T | Missense_Mutation | 1 | 0.11 | HEC265 | N | 2 | 0 | 0 | N |
MYLK | QSSSLTLSW | CENTRAL_NERVOUS_SYSTEM | 1344 | p.R1344Q | c.4031G>A | Missense_Mutation | 1 | 0.11 | SNU201 | N | 3 | 0 | 0 | N |
MYLK | QSWYGSSYD | SKIN | 1350 | p.L1350Q | c.4049T>A | Missense_Mutation | 1 | 0.11 | MELJUSO | N | 0 | 0 | 0 | N |
MYLK | QVDFHSVLA | LARGE_INTESTINE | 950 | p.R954H | c.2861G>A | Missense_Mutation | 1 | 0.11 | HT115 | N | 0 | 0 | 0 | N |
MYLK | QVSGNPPPK | LUNG | 645 | p.E653K | c.1957G>A | Missense_Mutation | 1 | 0.11 | NCIH1703 | N | 4 | 0 | 0 | N |
MYLK | QVSSDPPTT | ENDOMETRIUM | 1120 | p.A1127T | c.3379G>A | Missense_Mutation | 1 | 0.11 | SNGM | N | 1 | 0 | 0 | N |
MYLK | QVTLTVVDK | OVARY | 1322 | p.N1324T | c.3971A>C | Missense_Mutation | 1 | 0.11 | OVK18 | Y | 4 | 14 | 0 | N |
MYLK | QVTWLKGND | LARGE_INTESTINE | 191 | p.V199D | c.596T>A | Missense_Mutation | 1 | 0.11 | RKO | N | 0 | 0 | 0 | N |
MYLK | RDGNALCKD | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 756 | p.K759N | c.2277A>C | Missense_Mutation | 1 | 0.11 | HT | N | 0 | 0 | 0 | N |
MYLK | RDLLVKKVS | OVARY | 898 | p.G902V | c.2705G>T | Missense_Mutation | 1 | 0.11 | OVCAR8 | N | 2 | 0 | 0 | N |
MYLK | RDPLGKKVS | LARGE_INTESTINE | 898 | p.L900P | c.2699T>C | Missense_Mutation | 1 | 0.11 | CW2 | N | 1 | 0 | 0 | Y |
MYLK | RDSGIYSCT | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 480 | p.T484I | c.1451C>T | Missense_Mutation | 1 | 0.11 | SUDHL1 | N | 2 | 0 | 0 | N |
MYLK | RGKYTYEAT | PROSTATE | 101 | p.C106Y | c.317G>A | Missense_Mutation | 1 | 0.11 | 22RV1 | N | 2 | 0 | 0 | N |
MYLK | RGRFLLDCG | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 76 | p.G76R | c.226G>A | Missense_Mutation | 1 | 0.11 | MOLT13 | N | 0 | 0 | 0 | N |
MYLK | RGYPEPRVT | LARGE_INTESTINE | 57 | p.Q63R | c.188A>G | Missense_Mutation | 1 | 0.11 | CCK81 | N | 3 | 0 | 0 | N |
MYLK | RKEVTNLIS | LUNG | 272 | p.V278L | c.832G>T | Missense_Mutation | 1 | 0.11 | NCIH23 | N | 1 | 0 | 0 | N |
MYLK | RKRPAPPRS | ENDOMETRIUM | 371 | p.P379S | c.1135C>T | Missense_Mutation | 1 | 0.11 | HEC59 | N | 1 | 0 | 0 | N |
MYLK | RKSSTESPT | ENDOMETRIUM | 1770 | p.G1775E | c.5324G>A | Missense_Mutation | 1 | 0.11 | AN3CA | N | 1 | 0 | 0 | N |
MYLK | RKSSTGPPT | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1770 | p.S1776P | c.5326T>C | Missense_Mutation | 1 | 0.11 | PF382 | N | 1 | 0 | 0 | N |
MYLK | RKVHSSQQV | LUNG | 943 | p.P948S | c.2842C>T | Missense_Mutation | 1 | 0.11 | NCIH2172 | N | 3 | 0 | 0 | N |
MYLK | RKWQKMGNA | LARGE_INTESTINE | 1743 | p.T1748M | c.5243C>T | Missense_Mutation | 1 | 0.11 | HT115 | N | 3 | 0 | 0 | N |
MYLK | RLSSMVMIS | CENTRAL_NERVOUS_SYSTEM | 1757 | p.A1762V | c.5285C>T | Missense_Mutation | 1 | 0.11 | U87MG | N | 1 | 0 | 0 | N |
MYLK | RNGQPITSR | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 68 | p.G76R | c.226G>A | Missense_Mutation | 1 | 0.11 | MOLT13 | N | 3 | 0 | 0 | N |
MYLK | RPAPPRSAT | ENDOMETRIUM | 373 | p.P379S | c.1135C>T | Missense_Mutation | 1 | 0.11 | HEC59 | N | 5 | 0 | 0 | N |
MYLK | RPKSSLPPL | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1205 | p.V1213L | c.3637G>C | Missense_Mutation | 1 | 0.11 | HDLM2 | Y | 16 | 11 | 0 | N |
MYLK | RPNSSLPPV | ENDOMETRIUM | 1205 | p.K1207N | c.3621G>T | Missense_Mutation | 1 | 0.11 | HEC251 | N | 12 | 0 | 0 | N |
MYLK | RPSGPLKPV | UPPER_AERODIGESTIVE_TRACT | 1018 | p.Q1018R | c.3053A>G | Missense_Mutation | 1 | 0.11 | DETROIT562 | Y | 12 | 9 | 0 | Y |
MYLK | RQAQVTLTV | OVARY | 1319 | p.N1324T | c.3971A>C | Missense_Mutation | 1 | 0.11 | OVK18 | Y | 9 | 12 | 0 | N |
MYLK | RQEISIVNC | OVARY | 1507 | p.M1513V | c.4537A>G | Missense_Mutation | 1 | 0.11 | OV90 | N | 2 | 0 | 0 | N |
MYLK | RQPGLGSQH | SALIVARY_GLAND | 385 | p.D393H | c.1177G>C | Missense_Mutation | 1 | 0.11 | YD15 | N | 2 | 0 | 0 | N |
MYLK | RQYEILLKN | LIVER | 790 | p.G790R | c.2368G>C | Missense_Mutation | 1 | 0.11 | ALEXANDERCELLS | N | 3 | 0 | 0 | N |
MYLK | RRKWQKMGN | LARGE_INTESTINE | 1742 | p.T1748M | c.5243C>T | Missense_Mutation | 1 | 0.11 | HT115 | N | 3 | 0 | 0 | N |
MYLK | RRPNSSLPP | ENDOMETRIUM | 1204 | p.K1207N | c.3621G>T | Missense_Mutation | 1 | 0.11 | HEC251 | N | 2 | 0 | 0 | N |
MYLK | RSATFPTRQ | ENDOMETRIUM | 378 | p.P379S | c.1135C>T | Missense_Mutation | 1 | 0.11 | HEC59 | N | 1 | 0 | 0 | N |
MYLK | RSESQGTAS | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1090 | p.P1098S | c.3292C>T | Missense_Mutation | 1 | 0.11 | DB | N | 2 | 0 | 0 | N |
MYLK | RSSSLTQSW | SKIN | 1344 | p.L1350Q | c.4049T>A | Missense_Mutation | 1 | 0.11 | MELJUSO | N | 5 | 0 | 0 | N |
MYLK | RTRDSGIYS | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 478 | p.T484I | c.1451C>T | Missense_Mutation | 1 | 0.11 | SUDHL1 | N | 1 | 0 | 0 | N |
MYLK | RVRGYPEPR | LARGE_INTESTINE | 55 | p.Q63R | c.188A>G | Missense_Mutation | 1 | 0.11 | CCK81 | N | 7 | 0 | 0 | N |
MYLK | RVTWHRNGQ | LARGE_INTESTINE | 63 | p.Q63R | c.188A>G | Missense_Mutation | 1 | 0.11 | CCK81 | N | 0 | 0 | 0 | N |
MYLK | RYATDMWSI | PANCREAS | 1639 | p.G1639R | c.4915G>C | Missense_Mutation | 1 | 0.11 | HPAFII | Y | 4 | 13 | 0 | N |
MYLK | RYVSLRPGW | ENDOMETRIUM | 845 | p.G847V | c.2540G>T | Missense_Mutation | 1 | 0.11 | SNGM | N | 5 | 0 | 0 | N |
MYLK | SAETLNAKT | PANCREAS | 999 | p.A1007T | c.3019G>A | Missense_Mutation | 1 | 0.11 | PK45H | N | 4 | 0 | 0 | N |
MYLK | SAFKQKLQD | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1098 | p.P1098S | c.3292C>T | Missense_Mutation | 1 | 0.11 | DB | N | 0 | 0 | 0 | N |
MYLK | SAHVSVSEK | LIVER | 204 | p.R206H | c.617G>A | Missense_Mutation | 1 | 0.11 | SNU182 | N | 2 | 0 | 0 | N |
MYLK | SAPAVETHP | LIVER | 145 | p.R152H | c.455G>A | Missense_Mutation | 1 | 0.11 | SNU449 | N | 0 | 0 | 0 | N |
MYLK | SATFPTRQP | ENDOMETRIUM | 379 | p.P379S | c.1135C>T | Missense_Mutation | 1 | 0.11 | HEC59 | N | 0 | 0 | 0 | N |
MYLK | SDATVKMKP | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1218 | p.K1224M | c.3671A>T | Missense_Mutation | 1 | 0.11 | KIJK | N | 0 | 0 | 0 | N |
MYLK | SDIQSSSLT | CENTRAL_NERVOUS_SYSTEM | 1341 | p.R1344Q | c.4031G>A | Missense_Mutation | 1 | 0.11 | SNU201 | N | 3 | 0 | 0 | N |
MYLK | SDPPTTIIW | ENDOMETRIUM | 1123 | p.A1127T | c.3379G>A | Missense_Mutation | 1 | 0.11 | SNGM | Y | 5 | 11 | 0 | N |
MYLK | SDRYVSLRP | ENDOMETRIUM | 843 | p.G847V | c.2540G>T | Missense_Mutation | 1 | 0.11 | SNGM | N | 0 | 0 | 0 | N |
MYLK | SEADVSQAF | AUTONOMIC_GANGLIA | 1788 | p.E1790A | c.5369A>C | Missense_Mutation | 1 | 0.11 | NB1 | Y | 8 | 9 | 0 | Y |
MYLK | SESQGTASA | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1091 | p.P1098S | c.3292C>T | Missense_Mutation | 1 | 0.11 | DB | N | 5 | 0 | 0 | N |
MYLK | SGACQVTVE | ENDOMETRIUM | 112 | p.R115C | c.343C>T | Missense_Mutation | 1 | 0.11 | HEC151 | N | 0 | 0 | 0 | N |
MYLK | SGIYSCTAS | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 482 | p.T484I | c.1451C>T | Missense_Mutation | 1 | 0.11 | SUDHL1 | N | 2 | 0 | 0 | N |
MYLK | SGNPPPKVI | LUNG | 647 | p.E653K | c.1957G>A | Missense_Mutation | 1 | 0.11 | NCIH1703 | Y | 7 | 10 | 0 | N |
MYLK | SGPSGRKSS | LARGE_INTESTINE | 1765 | p.L1767P | c.5300T>C | Missense_Mutation | 1 | 0.11 | SNUC5 | N | 1 | 0 | 0 | N |
MYLK | SGRKSSTES | ENDOMETRIUM | 1768 | p.G1775E | c.5324G>A | Missense_Mutation | 1 | 0.11 | AN3CA | N | 1 | 0 | 0 | N |
MYLK | SGRKSSTGP | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1768 | p.S1776P | c.5326T>C | Missense_Mutation | 1 | 0.11 | PF382 | N | 0 | 0 | 0 | N |
MYLK | SGSSYDGGS | LUNG | 1353 | p.Y1353S | c.4058A>C | Missense_Mutation | 1 | 0.11 | PC14 | N | 0 | 0 | 0 | N |
MYLK | SIEVYEDAD | CENTRAL_NERVOUS_SYSTEM | 460 | p.G468D | c.1403G>A | Missense_Mutation | 1 | 0.11 | CAS1 | N | 0 | 0 | 0 | N |
MYLK | SITCTWMKF | ENDOMETRIUM | 1266 | p.P1266S | c.3796C>T | Missense_Mutation | 1 | 0.11 | HEC265 | N | 2 | 0 | 0 | N |
MYLK | SIVNCLHHP | OVARY | 1511 | p.M1513V | c.4537A>G | Missense_Mutation | 1 | 0.11 | OV90 | N | 0 | 0 | 0 | N |
MYLK | SKPLSNARP | UPPER_AERODIGESTIVE_TRACT | 1011 | p.Q1018R | c.3053A>G | Missense_Mutation | 1 | 0.11 | DETROIT562 | N | 0 | 0 | 0 | N |
MYLK | SKPSQESEL | BREAST | 1413 | p.E1414K | c.4240G>A | Missense_Mutation | 1 | 0.11 | ZR751 | N | 6 | 0 | 0 | N |
MYLK | SKPTGPIFL | BONE | 618 | p.A622G | c.1865C>G | Missense_Mutation | 1 | 0.11 | U2OS | Y | 7 | 10 | 0 | N |
MYLK | SKTIHDLEV | LARGE_INTESTINE | 1812 | p.R1816H | c.5447G>A | Missense_Mutation | 1 | 0.11 | SNU1040 | N | 1 | 0 | 0 | N |
MYLK | SLPPLLGTE | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1209 | p.V1213L | c.3637G>C | Missense_Mutation | 1 | 0.11 | HDLM2 | N | 0 | 0 | 0 | N |
MYLK | SLTLSWSGS | LUNG | 1347 | p.Y1353S | c.4058A>C | Missense_Mutation | 1 | 0.11 | PC14 | N | 0 | 0 | 0 | N |
MYLK | SLTQSWYGS | SKIN | 1347 | p.L1350Q | c.4049T>A | Missense_Mutation | 1 | 0.11 | MELJUSO | N | 0 | 0 | 0 | N |
MYLK | SMAMISGPS | LARGE_INTESTINE | 1760 | p.L1767P | c.5300T>C | Missense_Mutation | 1 | 0.11 | SNUC5 | N | 0 | 0 | 0 | N |
MYLK | SMVMISGLS | CENTRAL_NERVOUS_SYSTEM | 1760 | p.A1762V | c.5285C>T | Missense_Mutation | 1 | 0.11 | U87MG | N | 0 | 0 | 0 | N |
MYLK | SNARPSGPL | UPPER_AERODIGESTIVE_TRACT | 1015 | p.Q1018R | c.3053A>G | Missense_Mutation | 1 | 0.11 | DETROIT562 | N | 5 | 0 | 0 | Y |
MYLK | SNLLKKNMK | LARGE_INTESTINE | 1697 | p.D1703N | c.5107G>A | Missense_Mutation | 1 | 0.11 | SW48 | N | 0 | 0 | 0 | N |
MYLK | SPQQVDFHS | LARGE_INTESTINE | 947 | p.R954H | c.2861G>A | Missense_Mutation | 1 | 0.11 | HT115 | N | 3 | 0 | 0 | N |
MYLK | SQGTASAFK | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1093 | p.P1098S | c.3292C>T | Missense_Mutation | 1 | 0.11 | DB | N | 4 | 0 | 0 | N |
MYLK | SQHVVSKAA | SALIVARY_GLAND | 391 | p.D393H | c.1177G>C | Missense_Mutation | 1 | 0.11 | YD15 | N | 2 | 0 | 0 | N |
MYLK | SQQVDFRSV | LUNG | 948 | p.P948S | c.2842C>T | Missense_Mutation | 1 | 0.11 | NCIH2172 | N | 4 | 0 | 0 | N |
MYLK | SRGRFLLDC | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 75 | p.G76R | c.226G>A | Missense_Mutation | 1 | 0.11 | MOLT13 | N | 3 | 0 | 0 | N |
MYLK | SRQAQVTLT | OVARY | 1318 | p.N1324T | c.3971A>C | Missense_Mutation | 1 | 0.11 | OVK18 | N | 2 | 0 | 0 | N |
MYLK | SRRPNSSLP | ENDOMETRIUM | 1203 | p.K1207N | c.3621G>T | Missense_Mutation | 1 | 0.11 | HEC251 | N | 1 | 0 | 0 | N |
MYLK | SSDPPTTII | ENDOMETRIUM | 1122 | p.A1127T | c.3379G>A | Missense_Mutation | 1 | 0.11 | SNGM | N | 5 | 0 | 0 | N |
MYLK | SSKPLSNAR | UPPER_AERODIGESTIVE_TRACT | 1010 | p.Q1018R | c.3053A>G | Missense_Mutation | 1 | 0.11 | DETROIT562 | Y | 3 | 9 | 0 | N |
MYLK | SSLPPLLGT | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1208 | p.V1213L | c.3637G>C | Missense_Mutation | 1 | 0.11 | HDLM2 | N | 3 | 0 | 0 | N |
MYLK | SSLTLSWSG | LUNG | 1346 | p.Y1353S | c.4058A>C | Missense_Mutation | 1 | 0.11 | PC14 | N | 0 | 0 | 0 | N |
MYLK | SSLTQSWYG | SKIN | 1346 | p.L1350Q | c.4049T>A | Missense_Mutation | 1 | 0.11 | MELJUSO | N | 0 | 0 | 0 | N |
MYLK | SSMAMISGP | LARGE_INTESTINE | 1759 | p.L1767P | c.5300T>C | Missense_Mutation | 1 | 0.11 | SNUC5 | N | 0 | 0 | 0 | N |
MYLK | SSMVMISGL | CENTRAL_NERVOUS_SYSTEM | 1759 | p.A1762V | c.5285C>T | Missense_Mutation | 1 | 0.11 | U87MG | N | 14 | 0 | 0 | N |
MYLK | SSQQVDFRS | LUNG | 947 | p.P948S | c.2842C>T | Missense_Mutation | 1 | 0.11 | NCIH2172 | N | 0 | 0 | 0 | Y |
MYLK | SSSLTLSWS | LUNG | 1345 | p.Y1353S | c.4058A>C | Missense_Mutation | 1 | 0.11 | PC14 | N | 0 | 0 | 0 | N |
MYLK | SSSLTQSWY | SKIN | 1345 | p.L1350Q | c.4049T>A | Missense_Mutation | 1 | 0.11 | MELJUSO | N | 6 | 0 | 0 | N |
MYLK | SSTESPTSP | ENDOMETRIUM | 1772 | p.G1775E | c.5324G>A | Missense_Mutation | 1 | 0.11 | AN3CA | N | 0 | 0 | 0 | N |
MYLK | SSTGPPTSP | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1772 | p.S1776P | c.5326T>C | Missense_Mutation | 1 | 0.11 | PF382 | N | 0 | 0 | 0 | N |
MYLK | STESPTSPL | ENDOMETRIUM | 1773 | p.G1775E | c.5324G>A | Missense_Mutation | 1 | 0.11 | AN3CA | N | 6 | 0 | 0 | N |
MYLK | STGPPTSPL | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1773 | p.S1776P | c.5326T>C | Missense_Mutation | 1 | 0.11 | PF382 | N | 7 | 0 | 0 | N |
MYLK | SWSGSSYDG | LUNG | 1351 | p.Y1353S | c.4058A>C | Missense_Mutation | 1 | 0.11 | PC14 | N | 0 | 0 | 0 | N |
MYLK | TASAFKQKL | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1096 | p.P1098S | c.3292C>T | Missense_Mutation | 1 | 0.11 | DB | Y | 12 | 9 | 0 | N |
MYLK | TDKFEGRVR | AUTONOMIC_GANGLIA | 49 | p.A50D | c.149C>A | Missense_Mutation | 1 | 0.11 | NB1 | N | 0 | 0 | 0 | N |
MYLK | TESDATVKM | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1216 | p.K1224M | c.3671A>T | Missense_Mutation | 1 | 0.11 | KIJK | Y | 7 | 9 | 0 | Y |
MYLK | TESPTSPLN | ENDOMETRIUM | 1774 | p.G1775E | c.5324G>A | Missense_Mutation | 1 | 0.11 | AN3CA | N | 5 | 0 | 0 | N |
MYLK | TGPIFLQGL | BONE | 621 | p.A622G | c.1865C>G | Missense_Mutation | 1 | 0.11 | U2OS | Y | 15 | 9 | 0 | N |
MYLK | TGPPTSPLN | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1774 | p.S1776P | c.5326T>C | Missense_Mutation | 1 | 0.11 | PF382 | N | 1 | 0 | 0 | N |
MYLK | TGRSTSFNV | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1383 | p.C1384G | c.4150T>G | Missense_Mutation | 1 | 0.11 | KIJK | N | 4 | 0 | 0 | N |
MYLK | TGTQSITCT | ENDOMETRIUM | 1262 | p.P1266S | c.3796C>T | Missense_Mutation | 1 | 0.11 | HEC265 | N | 2 | 0 | 0 | N |
MYLK | THPSIWGEC | LIVER | 151 | p.R152H | c.455G>A | Missense_Mutation | 1 | 0.11 | SNU449 | N | 1 | 0 | 0 | N |
MYLK | TIHDLEVVE | LARGE_INTESTINE | 1814 | p.R1816H | c.5447G>A | Missense_Mutation | 1 | 0.11 | SNU1040 | N | 0 | 0 | 0 | N |
MYLK | TLNAKTVES | PANCREAS | 1002 | p.A1007T | c.3019G>A | Missense_Mutation | 1 | 0.11 | PK45H | N | 0 | 0 | 0 | N |
MYLK | TLSWSGSSY | LUNG | 1349 | p.Y1353S | c.4058A>C | Missense_Mutation | 1 | 0.11 | PC14 | N | 5 | 0 | 0 | N |
MYLK | TLTVVDKPD | OVARY | 1324 | p.N1324T | c.3971A>C | Missense_Mutation | 1 | 0.11 | OVK18 | N | 0 | 0 | 0 | N |
MYLK | TNGSGACQV | ENDOMETRIUM | 109 | p.R115C | c.343C>T | Missense_Mutation | 1 | 0.11 | HEC151 | Y | 0 | 16 | 0 | N |
MYLK | TNLISKESK | LUNG | 276 | p.V278L | c.832G>T | Missense_Mutation | 1 | 0.11 | NCIH23 | N | 0 | 0 | 0 | N |
MYLK | TPCASDIQS | CENTRAL_NERVOUS_SYSTEM | 1337 | p.R1344Q | c.4031G>A | Missense_Mutation | 1 | 0.11 | SNU201 | N | 3 | 0 | 0 | N |
MYLK | TPDFCSVLG | SKIN | 978 | p.R982C | c.2944C>T | Missense_Mutation | 1 | 0.11 | G361 | N | 0 | 0 | 0 | N |
MYLK | TQSITCTWM | ENDOMETRIUM | 1264 | p.P1266S | c.3796C>T | Missense_Mutation | 1 | 0.11 | HEC265 | Y | 6 | 12 | 0 | N |
MYLK | TQSWYGSSY | SKIN | 1349 | p.L1350Q | c.4049T>A | Missense_Mutation | 1 | 0.11 | MELJUSO | N | 6 | 0 | 0 | N |
MYLK | TRDSGIYSC | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 479 | p.T484I | c.1451C>T | Missense_Mutation | 1 | 0.11 | SUDHL1 | Y | 2 | 9 | 0 | N |
MYLK | TSKPSQESE | BREAST | 1412 | p.E1414K | c.4240G>A | Missense_Mutation | 1 | 0.11 | ZR751 | N | 0 | 0 | 0 | N |
MYLK | TSRGRFLLD | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 74 | p.G76R | c.226G>A | Missense_Mutation | 1 | 0.11 | MOLT13 | N | 0 | 0 | 0 | N |
MYLK | TTIIWTLNG | ENDOMETRIUM | 1127 | p.A1127T | c.3379G>A | Missense_Mutation | 1 | 0.11 | SNGM | N | 0 | 0 | 0 | N |
MYLK | TVESSKPLS | PANCREAS | 1007 | p.A1007T | c.3019G>A | Missense_Mutation | 1 | 0.11 | PK45H | N | 1 | 0 | 0 | N |
MYLK | TVHWLRDGN | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 751 | p.K759N | c.2277A>C | Missense_Mutation | 1 | 0.11 | HT | N | 0 | 0 | 0 | N |
MYLK | TVKMKPAPK | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1221 | p.K1224M | c.3671A>T | Missense_Mutation | 1 | 0.11 | KIJK | N | 3 | 0 | 0 | N |
MYLK | TVQEPHYGT | OESOPHAGUS | 711 | p.D717Y | c.2149G>T | Missense_Mutation | 1 | 0.11 | KYSE180 | N | 1 | 0 | 0 | Y |
MYLK | TWKELATGR | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1377 | p.C1384G | c.4150T>G | Missense_Mutation | 1 | 0.11 | KIJK | N | 1 | 0 | 0 | N |
MYLK | TWLKGNDPL | LARGE_INTESTINE | 193 | p.V199D | c.596T>A | Missense_Mutation | 1 | 0.11 | RKO | N | 6 | 0 | 0 | N |
MYLK | TYEATNGSG | PROSTATE | 105 | p.C106Y | c.317G>A | Missense_Mutation | 1 | 0.11 | 22RV1 | N | 0 | 0 | 0 | N |
MYLK | VAPSKPTGP | BONE | 615 | p.A622G | c.1865C>G | Missense_Mutation | 1 | 0.11 | U2OS | N | 0 | 0 | 0 | Y |
MYLK | VDFHSVLAK | LARGE_INTESTINE | 951 | p.R954H | c.2861G>A | Missense_Mutation | 1 | 0.11 | HT115 | N | 1 | 0 | 6 | N |
MYLK | VENDVNCKR | LUNG | 1071 | p.K1072E | c.3214A>G | Missense_Mutation | 1 | 0.11 | CORL24 | Y | 1 | 9 | 1 | N |
MYLK | VEQLDFRDP | LARGE_INTESTINE | 892 | p.L900P | c.2699T>C | Missense_Mutation | 1 | 0.11 | CW2 | N | 0 | 0 | 0 | N |
MYLK | VETHPSIWG | LIVER | 149 | p.R152H | c.455G>A | Missense_Mutation | 1 | 0.11 | SNU449 | N | 0 | 0 | 1 | N |
MYLK | VHSSQQVDF | LUNG | 945 | p.P948S | c.2842C>T | Missense_Mutation | 1 | 0.11 | NCIH2172 | N | 4 | 0 | 2 | N |
MYLK | VHWLRDGNA | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 752 | p.K759N | c.2277A>C | Missense_Mutation | 1 | 0.11 | HT | N | 2 | 0 | 0 | N |
MYLK | VINYEPIRY | PANCREAS | 1632 | p.G1639R | c.4915G>C | Missense_Mutation | 1 | 0.11 | HPAFII | Y | 6 | 11 | 11 | N |
MYLK | VKKVSTKTL | OVARY | 902 | p.G902V | c.2705G>T | Missense_Mutation | 1 | 0.11 | OVCAR8 | N | 4 | 0 | 4 | N |
MYLK | VKMKPAPKT | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1222 | p.K1224M | c.3671A>T | Missense_Mutation | 1 | 0.11 | KIJK | N | 1 | 0 | 5 | N |
MYLK | VKPYLSKTI | ENDOMETRIUM | 1807 | p.F1811L | c.5433C>A | Missense_Mutation | 1 | 0.11 | JHUEM7 | N | 4 | 0 | 7 | N |
MYLK | VLTVQEPHY | OESOPHAGUS | 709 | p.D717Y | c.2149G>T | Missense_Mutation | 1 | 0.11 | KYSE180 | N | 6 | 0 | 0 | N |
MYLK | VMISGLSGR | CENTRAL_NERVOUS_SYSTEM | 1762 | p.A1762V | c.5285C>T | Missense_Mutation | 1 | 0.11 | U87MG | N | 6 | 0 | 9 | N |
MYLK | VNCLHHPKL | OVARY | 1513 | p.M1513V | c.4537A>G | Missense_Mutation | 1 | 0.11 | OV90 | N | 4 | 0 | 0 | N |
MYLK | VPLQPSAHV | LIVER | 199 | p.R206H | c.617G>A | Missense_Mutation | 1 | 0.11 | SNU182 | Y | 14 | 10 | 0 | N |
MYLK | VPLQQSARV | LUNG | 199 | p.P203Q | c.608C>A | Missense_Mutation | 1 | 0.11 | NCIH2405 | N | 13 | 0 | 0 | N |
MYLK | VQEPHYGTQ | OESOPHAGUS | 712 | p.D717Y | c.2149G>T | Missense_Mutation | 1 | 0.11 | KYSE180 | N | 1 | 0 | 0 | N |
MYLK | VQPWHARQY | LIVER | 784 | p.G790R | c.2368G>C | Missense_Mutation | 1 | 0.11 | ALEXANDERCELLS | N | 7 | 0 | 12 | N |
MYLK | VRGYPEPRV | LARGE_INTESTINE | 56 | p.Q63R | c.188A>G | Missense_Mutation | 1 | 0.11 | CCK81 | N | 4 | 0 | 3 | N |
MYLK | VRKEVTNLI | LUNG | 271 | p.V278L | c.832G>T | Missense_Mutation | 1 | 0.11 | NCIH23 | Y | 5 | 9 | 20 | N |
MYLK | VSGNPPPKV | LUNG | 646 | p.E653K | c.1957G>A | Missense_Mutation | 1 | 0.11 | NCIH1703 | N | 3 | 0 | 0 | N |
MYLK | VSLRPGWPA | ENDOMETRIUM | 847 | p.G847V | c.2540G>T | Missense_Mutation | 1 | 0.11 | SNGM | N | 4 | 0 | 0 | Y |
MYLK | VSSDPPTTI | ENDOMETRIUM | 1121 | p.A1127T | c.3379G>A | Missense_Mutation | 1 | 0.11 | SNGM | N | 6 | 0 | 6 | N |
MYLK | VTGTQSITC | ENDOMETRIUM | 1261 | p.P1266S | c.3796C>T | Missense_Mutation | 1 | 0.11 | HEC265 | N | 1 | 0 | 0 | N |
MYLK | VTLTVVDKP | OVARY | 1323 | p.N1324T | c.3971A>C | Missense_Mutation | 1 | 0.11 | OVK18 | N | 0 | 0 | 0 | N |
MYLK | VTNLISKES | LUNG | 275 | p.V278L | c.832G>T | Missense_Mutation | 1 | 0.11 | NCIH23 | N | 0 | 0 | 7 | N |
MYLK | VTWLKGNDP | LARGE_INTESTINE | 192 | p.V199D | c.596T>A | Missense_Mutation | 1 | 0.11 | RKO | N | 0 | 0 | 0 | N |
MYLK | VYEDADSHY | CENTRAL_NERVOUS_SYSTEM | 463 | p.G468D | c.1403G>A | Missense_Mutation | 1 | 0.11 | CAS1 | N | 5 | 0 | 0 | N |
MYLK | VYGTSKPSQ | BREAST | 1409 | p.E1414K | c.4240G>A | Missense_Mutation | 1 | 0.11 | ZR751 | N | 0 | 0 | 5 | N |
MYLK | WDFDDEAFN | LARGE_INTESTINE | 1678 | p.D1686N | c.5056G>A | Missense_Mutation | 1 | 0.11 | SNU175 | N | 3 | 0 | 0 | N |
MYLK | WHARQYEIL | LIVER | 787 | p.G790R | c.2368G>C | Missense_Mutation | 1 | 0.11 | ALEXANDERCELLS | N | 8 | 0 | 0 | N |
MYLK | WKELATGRS | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1378 | p.C1384G | c.4150T>G | Missense_Mutation | 1 | 0.11 | KIJK | N | 3 | 0 | 10 | N |
MYLK | WLKGNDPLQ | LARGE_INTESTINE | 194 | p.V199D | c.596T>A | Missense_Mutation | 1 | 0.11 | RKO | N | 2 | 0 | 0 | N |
MYLK | WLRDGNALC | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 754 | p.K759N | c.2277A>C | Missense_Mutation | 1 | 0.11 | HT | N | 6 | 0 | 11 | N |
MYLK | WQKMGNAVR | LARGE_INTESTINE | 1745 | p.T1748M | c.5243C>T | Missense_Mutation | 1 | 0.11 | HT115 | N | 8 | 0 | 11 | N |
MYLK | WSGSSYDGG | LUNG | 1352 | p.Y1353S | c.4058A>C | Missense_Mutation | 1 | 0.11 | PC14 | N | 2 | 0 | 0 | N |
MYLK | YEATNGSGA | PROSTATE | 106 | p.C106Y | c.317G>A | Missense_Mutation | 1 | 0.11 | 22RV1 | N | 9 | 0 | 0 | N |
MYLK | YEDADSHYL | CENTRAL_NERVOUS_SYSTEM | 464 | p.G468D | c.1403G>A | Missense_Mutation | 1 | 0.11 | CAS1 | N | 11 | 0 | 0 | N |
MYLK | YEPIRYATD | PANCREAS | 1635 | p.G1639R | c.4915G>C | Missense_Mutation | 1 | 0.11 | HPAFII | Y | 2 | 9 | 0 | N |
MYLK | YFSKTIHDL | LARGE_INTESTINE | 1810 | p.R1816H | c.5447G>A | Missense_Mutation | 1 | 0.11 | SNU1040 | N | 8 | 0 | 8 | N |
MYLK | YGTQPWFIS | OESOPHAGUS | 717 | p.D717Y | c.2149G>T | Missense_Mutation | 1 | 0.11 | KYSE180 | N | 3 | 0 | 0 | N |
MYLK | YGTSKPSQE | BREAST | 1410 | p.E1414K | c.4240G>A | Missense_Mutation | 1 | 0.11 | ZR751 | N | 2 | 0 | 0 | N |
MYLK | YLSKTIRDL | ENDOMETRIUM | 1810 | p.F1811L | c.5433C>A | Missense_Mutation | 1 | 0.11 | JHUEM7 | Y | 12 | 9 | 17 | N |
MYLK | YPEPRVTWH | LARGE_INTESTINE | 59 | p.Q63R | c.188A>G | Missense_Mutation | 1 | 0.11 | CCK81 | Y | 4 | 13 | 0 | N |
MYLK | YTYEATNGS | PROSTATE | 104 | p.C106Y | c.317G>A | Missense_Mutation | 1 | 0.11 | 22RV1 | N | 3 | 0 | 10 | N |
MYLK | YVSLRPGWP | ENDOMETRIUM | 846 | p.G847V | c.2540G>T | Missense_Mutation | 1 | 0.11 | SNGM | N | 2 | 0 | 11 | N |
MYLK | AGDPFSTVH | SKIN | 745 | p.P750S | c.2248C>T | Missense_Mutation | 1 | 0.22 | IGR37 | N | 1 | 0 | 0 | N |
MYLK | AGDPFSTVH | SKIN | 745 | p.P750S | c.2248C>T | Missense_Mutation | 1 | 0.22 | IGR39 | N | 1 | 0 | 0 | N |
MYLK | AIAGDPFST | SKIN | 743 | p.P750S | c.2248C>T | Missense_Mutation | 1 | 0.22 | IGR37 | N | 1 | 0 | 0 | N |
MYLK | AIAGDPFST | SKIN | 743 | p.P750S | c.2248C>T | Missense_Mutation | 1 | 0.22 | IGR39 | N | 1 | 0 | 0 | N |
MYLK | CAIAGDPFS | SKIN | 742 | p.P750S | c.2248C>T | Missense_Mutation | 1 | 0.22 | IGR37 | N | 2 | 0 | 0 | N |
MYLK | CAIAGDPFS | SKIN | 742 | p.P750S | c.2248C>T | Missense_Mutation | 1 | 0.22 | IGR39 | N | 2 | 0 | 0 | N |
MYLK | CEVSGIPKT | OVARY | 435 | p.P443T | c.1327C>A | Missense_Mutation | 1 | 0.22 | OVMANA | N | 5 | 0 | 0 | N |
MYLK | CEVSGIPKT | LUNG | 435 | p.P443T | c.1327C>A | Missense_Mutation | 1 | 0.22 | RERFLCSQ1 | N | 5 | 0 | 0 | N |
MYLK | CVNQTGTRI | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1593 | p.K1596Q | c.4786A>C | Missense_Mutation | 1 | 0.22 | KMS26 | N | 4 | 0 | 0 | N |
MYLK | CVNQTGTRI | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1593 | p.K1596Q | c.4786A>C | Missense_Mutation | 1 | 0.22 | MOTN1 | N | 4 | 0 | 0 | N |
MYLK | DPFSTVHWL | SKIN | 747 | p.P750S | c.2248C>T | Missense_Mutation | 1 | 0.22 | IGR37 | Y | 22 | 10 | 0 | N |
MYLK | DPFSTVHWL | SKIN | 747 | p.P750S | c.2248C>T | Missense_Mutation | 1 | 0.22 | IGR39 | Y | 22 | 10 | 0 | N |
MYLK | EIYGVNQDD | ENDOMETRIUM | 219 | p.H221Y | c.661C>T | Missense_Mutation | 1 | 0.22 | COLO684 | N | 0 | 0 | 0 | Y |
MYLK | EIYGVNQDD | OVARY | 219 | p.H221Y | c.661C>T | Missense_Mutation | 1 | 0.22 | COLO704 | N | 0 | 0 | 0 | Y |
MYLK | ENIMCVNQT | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1589 | p.K1596Q | c.4786A>C | Missense_Mutation | 1 | 0.22 | KMS26 | N | 1 | 0 | 0 | N |
MYLK | ENIMCVNQT | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1589 | p.K1596Q | c.4786A>C | Missense_Mutation | 1 | 0.22 | MOTN1 | N | 1 | 0 | 0 | N |
MYLK | EVSGIPKTE | OVARY | 436 | p.P443T | c.1327C>A | Missense_Mutation | 1 | 0.22 | OVMANA | N | 0 | 0 | 0 | N |
MYLK | EVSGIPKTE | LUNG | 436 | p.P443T | c.1327C>A | Missense_Mutation | 1 | 0.22 | RERFLCSQ1 | N | 0 | 0 | 0 | N |
MYLK | FSTVHWLRD | SKIN | 749 | p.P750S | c.2248C>T | Missense_Mutation | 1 | 0.22 | IGR37 | N | 2 | 0 | 0 | N |
MYLK | FSTVHWLRD | SKIN | 749 | p.P750S | c.2248C>T | Missense_Mutation | 1 | 0.22 | IGR39 | N | 2 | 0 | 0 | N |
MYLK | GDPFSTVHW | SKIN | 746 | p.P750S | c.2248C>T | Missense_Mutation | 1 | 0.22 | IGR37 | N | 3 | 0 | 0 | N |
MYLK | GDPFSTVHW | SKIN | 746 | p.P750S | c.2248C>T | Missense_Mutation | 1 | 0.22 | IGR39 | N | 3 | 0 | 0 | N |
MYLK | GIPKTEVAW | OVARY | 439 | p.P443T | c.1327C>A | Missense_Mutation | 1 | 0.22 | OVMANA | N | 1 | 0 | 0 | N |
MYLK | GIPKTEVAW | LUNG | 439 | p.P443T | c.1327C>A | Missense_Mutation | 1 | 0.22 | RERFLCSQ1 | N | 1 | 0 | 0 | N |
MYLK | GMQVLEIYG | ENDOMETRIUM | 214 | p.H221Y | c.661C>T | Missense_Mutation | 1 | 0.22 | COLO684 | N | 0 | 0 | 0 | N |
MYLK | GMQVLEIYG | OVARY | 214 | p.H221Y | c.661C>T | Missense_Mutation | 1 | 0.22 | COLO704 | N | 0 | 0 | 0 | N |
MYLK | IAGDPFSTV | SKIN | 744 | p.P750S | c.2248C>T | Missense_Mutation | 1 | 0.22 | IGR37 | Y | 8 | 9 | 0 | N |
MYLK | IAGDPFSTV | SKIN | 744 | p.P750S | c.2248C>T | Missense_Mutation | 1 | 0.22 | IGR39 | Y | 8 | 9 | 0 | N |
MYLK | IMCVNQTGT | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1591 | p.K1596Q | c.4786A>C | Missense_Mutation | 1 | 0.22 | KMS26 | N | 4 | 0 | 0 | N |
MYLK | IMCVNQTGT | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1591 | p.K1596Q | c.4786A>C | Missense_Mutation | 1 | 0.22 | MOTN1 | N | 4 | 0 | 0 | N |
MYLK | IPKTEVAWF | OVARY | 440 | p.P443T | c.1327C>A | Missense_Mutation | 1 | 0.22 | OVMANA | Y | 10 | 9 | 0 | N |
MYLK | IPKTEVAWF | LUNG | 440 | p.P443T | c.1327C>A | Missense_Mutation | 1 | 0.22 | RERFLCSQ1 | Y | 10 | 9 | 0 | N |
MYLK | IYGVNQDDV | ENDOMETRIUM | 220 | p.H221Y | c.661C>T | Missense_Mutation | 1 | 0.22 | COLO684 | N | 4 | 0 | 0 | N |
MYLK | IYGVNQDDV | OVARY | 220 | p.H221Y | c.661C>T | Missense_Mutation | 1 | 0.22 | COLO704 | N | 4 | 0 | 0 | N |
MYLK | KTEVAWFLE | OVARY | 442 | p.P443T | c.1327C>A | Missense_Mutation | 1 | 0.22 | OVMANA | N | 1 | 0 | 0 | N |
MYLK | KTEVAWFLE | LUNG | 442 | p.P443T | c.1327C>A | Missense_Mutation | 1 | 0.22 | RERFLCSQ1 | N | 1 | 0 | 0 | N |
MYLK | LEIYGVNQD | ENDOMETRIUM | 218 | p.H221Y | c.661C>T | Missense_Mutation | 1 | 0.22 | COLO684 | N | 2 | 0 | 12 | Y |
MYLK | LEIYGVNQD | OVARY | 218 | p.H221Y | c.661C>T | Missense_Mutation | 1 | 0.22 | COLO704 | N | 2 | 0 | 12 | Y |
MYLK | MCVNQTGTR | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1592 | p.K1596Q | c.4786A>C | Missense_Mutation | 1 | 0.22 | KMS26 | N | 4 | 0 | 0 | N |
MYLK | MCVNQTGTR | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1592 | p.K1596Q | c.4786A>C | Missense_Mutation | 1 | 0.22 | MOTN1 | N | 4 | 0 | 0 | N |
MYLK | MQVLEIYGV | ENDOMETRIUM | 215 | p.H221Y | c.661C>T | Missense_Mutation | 1 | 0.22 | COLO684 | N | 11 | 0 | 18 | Y |
MYLK | MQVLEIYGV | OVARY | 215 | p.H221Y | c.661C>T | Missense_Mutation | 1 | 0.22 | COLO704 | N | 11 | 0 | 18 | Y |
MYLK | NGMQVLEIY | ENDOMETRIUM | 213 | p.H221Y | c.661C>T | Missense_Mutation | 1 | 0.22 | COLO684 | N | 6 | 0 | 0 | N |
MYLK | NGMQVLEIY | OVARY | 213 | p.H221Y | c.661C>T | Missense_Mutation | 1 | 0.22 | COLO704 | N | 6 | 0 | 0 | N |
MYLK | NIMCVNQTG | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1590 | p.K1596Q | c.4786A>C | Missense_Mutation | 1 | 0.22 | KMS26 | N | 0 | 0 | 0 | N |
MYLK | NIMCVNQTG | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1590 | p.K1596Q | c.4786A>C | Missense_Mutation | 1 | 0.22 | MOTN1 | N | 0 | 0 | 0 | N |
MYLK | NQTGTRIKL | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1595 | p.K1596Q | c.4786A>C | Missense_Mutation | 1 | 0.22 | KMS26 | Y | 10 | 10 | 0 | N |
MYLK | NQTGTRIKL | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1595 | p.K1596Q | c.4786A>C | Missense_Mutation | 1 | 0.22 | MOTN1 | Y | 10 | 10 | 0 | N |
MYLK | PENIMCVNQ | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1588 | p.K1596Q | c.4786A>C | Missense_Mutation | 1 | 0.22 | KMS26 | N | 0 | 0 | 0 | N |
MYLK | PENIMCVNQ | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1588 | p.K1596Q | c.4786A>C | Missense_Mutation | 1 | 0.22 | MOTN1 | N | 0 | 0 | 0 | N |
MYLK | PFSTVHWLR | SKIN | 748 | p.P750S | c.2248C>T | Missense_Mutation | 1 | 0.22 | IGR37 | N | 1 | 0 | 0 | N |
MYLK | PFSTVHWLR | SKIN | 748 | p.P750S | c.2248C>T | Missense_Mutation | 1 | 0.22 | IGR39 | N | 1 | 0 | 0 | N |
MYLK | PKTEVAWFL | OVARY | 441 | p.P443T | c.1327C>A | Missense_Mutation | 1 | 0.22 | OVMANA | N | 3 | 0 | 0 | N |
MYLK | PKTEVAWFL | LUNG | 441 | p.P443T | c.1327C>A | Missense_Mutation | 1 | 0.22 | RERFLCSQ1 | N | 3 | 0 | 0 | N |
MYLK | QTGTRIKLI | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1596 | p.K1596Q | c.4786A>C | Missense_Mutation | 1 | 0.22 | KMS26 | Y | 6 | 12 | 0 | N |
MYLK | QTGTRIKLI | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1596 | p.K1596Q | c.4786A>C | Missense_Mutation | 1 | 0.22 | MOTN1 | Y | 6 | 12 | 0 | N |
MYLK | QVLEIYGVN | ENDOMETRIUM | 216 | p.H221Y | c.661C>T | Missense_Mutation | 1 | 0.22 | COLO684 | N | 0 | 0 | 0 | Y |
MYLK | QVLEIYGVN | OVARY | 216 | p.H221Y | c.661C>T | Missense_Mutation | 1 | 0.22 | COLO704 | N | 0 | 0 | 0 | Y |
MYLK | SGIPKTEVA | OVARY | 438 | p.P443T | c.1327C>A | Missense_Mutation | 1 | 0.22 | OVMANA | N | 4 | 0 | 0 | N |
MYLK | SGIPKTEVA | LUNG | 438 | p.P443T | c.1327C>A | Missense_Mutation | 1 | 0.22 | RERFLCSQ1 | N | 4 | 0 | 0 | N |
MYLK | STVHWLRDG | SKIN | 750 | p.P750S | c.2248C>T | Missense_Mutation | 1 | 0.22 | IGR37 | N | 0 | 0 | 0 | N |
MYLK | STVHWLRDG | SKIN | 750 | p.P750S | c.2248C>T | Missense_Mutation | 1 | 0.22 | IGR39 | N | 0 | 0 | 0 | N |
MYLK | TEVAWFLEG | OVARY | 443 | p.P443T | c.1327C>A | Missense_Mutation | 1 | 0.22 | OVMANA | N | 1 | 0 | 0 | N |
MYLK | TEVAWFLEG | LUNG | 443 | p.P443T | c.1327C>A | Missense_Mutation | 1 | 0.22 | RERFLCSQ1 | N | 1 | 0 | 0 | N |
MYLK | VLEIYGVNQ | ENDOMETRIUM | 217 | p.H221Y | c.661C>T | Missense_Mutation | 1 | 0.22 | COLO684 | N | 2 | 0 | 0 | Y |
MYLK | VLEIYGVNQ | OVARY | 217 | p.H221Y | c.661C>T | Missense_Mutation | 1 | 0.22 | COLO704 | N | 2 | 0 | 0 | Y |
MYLK | VNQTGTRIK | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1594 | p.K1596Q | c.4786A>C | Missense_Mutation | 1 | 0.22 | KMS26 | N | 0 | 0 | 3 | N |
MYLK | VNQTGTRIK | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1594 | p.K1596Q | c.4786A>C | Missense_Mutation | 1 | 0.22 | MOTN1 | N | 0 | 0 | 3 | N |
MYLK | VSGIPKTEV | OVARY | 437 | p.P443T | c.1327C>A | Missense_Mutation | 1 | 0.22 | OVMANA | N | 3 | 0 | 0 | N |
MYLK | VSGIPKTEV | LUNG | 437 | p.P443T | c.1327C>A | Missense_Mutation | 1 | 0.22 | RERFLCSQ1 | N | 3 | 0 | 0 | N |
MYLK | YGVNQDDVG | ENDOMETRIUM | 221 | p.H221Y | c.661C>T | Missense_Mutation | 1 | 0.22 | COLO684 | N | 2 | 0 | 0 | N |
MYLK | YGVNQDDVG | OVARY | 221 | p.H221Y | c.661C>T | Missense_Mutation | 1 | 0.22 | COLO704 | N | 2 | 0 | 0 | N |
MYLK | AHQVTVELT | LUNG | 114 | p.R115H | c.344G>A | Missense_Mutation | 1 | 0.33 | HCC1588 | N | 1 | 0 | 0 | N |
MYLK | AHQVTVELT | LARGE_INTESTINE | 114 | p.R115H | c.344G>A | Missense_Mutation | 1 | 0.33 | LS513 | N | 1 | 0 | 0 | N |
MYLK | AHQVTVELT | LARGE_INTESTINE | 114 | p.R115H | c.344G>A | Missense_Mutation | 1 | 0.33 | SNU1040 | N | 1 | 0 | 0 | N |
MYLK | ATNGSGAHQ | LUNG | 108 | p.R115H | c.344G>A | Missense_Mutation | 1 | 0.33 | HCC1588 | N | 0 | 0 | 0 | N |
MYLK | ATNGSGAHQ | LARGE_INTESTINE | 108 | p.R115H | c.344G>A | Missense_Mutation | 1 | 0.33 | LS513 | N | 0 | 0 | 0 | N |
MYLK | ATNGSGAHQ | LARGE_INTESTINE | 108 | p.R115H | c.344G>A | Missense_Mutation | 1 | 0.33 | SNU1040 | N | 0 | 0 | 0 | N |
MYLK | EATNGSGAH | LUNG | 107 | p.R115H | c.344G>A | Missense_Mutation | 1 | 0.33 | HCC1588 | N | 0 | 0 | 0 | N |
MYLK | EATNGSGAH | LARGE_INTESTINE | 107 | p.R115H | c.344G>A | Missense_Mutation | 1 | 0.33 | LS513 | N | 0 | 0 | 0 | N |
MYLK | EATNGSGAH | LARGE_INTESTINE | 107 | p.R115H | c.344G>A | Missense_Mutation | 1 | 0.33 | SNU1040 | N | 0 | 0 | 0 | N |
MYLK | GAHQVTVEL | LUNG | 113 | p.R115H | c.344G>A | Missense_Mutation | 1 | 0.33 | HCC1588 | Y | 15 | 11 | 0 | N |
MYLK | GAHQVTVEL | LARGE_INTESTINE | 113 | p.R115H | c.344G>A | Missense_Mutation | 1 | 0.33 | LS513 | Y | 15 | 11 | 0 | N |
MYLK | GAHQVTVEL | LARGE_INTESTINE | 113 | p.R115H | c.344G>A | Missense_Mutation | 1 | 0.33 | SNU1040 | Y | 15 | 11 | 0 | N |
MYLK | GSGAHQVTV | LUNG | 111 | p.R115H | c.344G>A | Missense_Mutation | 1 | 0.33 | HCC1588 | N | 3 | 0 | 0 | N |
MYLK | GSGAHQVTV | LARGE_INTESTINE | 111 | p.R115H | c.344G>A | Missense_Mutation | 1 | 0.33 | LS513 | N | 3 | 0 | 0 | N |
MYLK | GSGAHQVTV | LARGE_INTESTINE | 111 | p.R115H | c.344G>A | Missense_Mutation | 1 | 0.33 | SNU1040 | N | 3 | 0 | 0 | N |
MYLK | HQVTVELTV | LUNG | 115 | p.R115H | c.344G>A | Missense_Mutation | 1 | 0.33 | HCC1588 | N | 7 | 0 | 0 | N |
MYLK | HQVTVELTV | LARGE_INTESTINE | 115 | p.R115H | c.344G>A | Missense_Mutation | 1 | 0.33 | LS513 | N | 7 | 0 | 0 | N |
MYLK | HQVTVELTV | LARGE_INTESTINE | 115 | p.R115H | c.344G>A | Missense_Mutation | 1 | 0.33 | SNU1040 | N | 7 | 0 | 0 | N |
MYLK | NGSGAHQVT | LUNG | 110 | p.R115H | c.344G>A | Missense_Mutation | 1 | 0.33 | HCC1588 | N | 1 | 0 | 0 | N |
MYLK | NGSGAHQVT | LARGE_INTESTINE | 110 | p.R115H | c.344G>A | Missense_Mutation | 1 | 0.33 | LS513 | N | 1 | 0 | 0 | N |
MYLK | NGSGAHQVT | LARGE_INTESTINE | 110 | p.R115H | c.344G>A | Missense_Mutation | 1 | 0.33 | SNU1040 | N | 1 | 0 | 0 | N |
MYLK | SGAHQVTVE | LUNG | 112 | p.R115H | c.344G>A | Missense_Mutation | 1 | 0.33 | HCC1588 | N | 0 | 0 | 0 | Y |
MYLK | SGAHQVTVE | LARGE_INTESTINE | 112 | p.R115H | c.344G>A | Missense_Mutation | 1 | 0.33 | LS513 | N | 0 | 0 | 0 | Y |
MYLK | SGAHQVTVE | LARGE_INTESTINE | 112 | p.R115H | c.344G>A | Missense_Mutation | 1 | 0.33 | SNU1040 | N | 0 | 0 | 0 | Y |
MYLK | TNGSGAHQV | LUNG | 109 | p.R115H | c.344G>A | Missense_Mutation | 1 | 0.33 | HCC1588 | Y | 0 | 17 | 0 | N |
MYLK | TNGSGAHQV | LARGE_INTESTINE | 109 | p.R115H | c.344G>A | Missense_Mutation | 1 | 0.33 | LS513 | Y | 0 | 17 | 0 | N |
MYLK | TNGSGAHQV | LARGE_INTESTINE | 109 | p.R115H | c.344G>A | Missense_Mutation | 1 | 0.33 | SNU1040 | Y | 0 | 17 | 0 | N |