MSH2 | AFIPNDVTL | ENDOMETRIUM | 649 | p.Y656fs | c.1966_1966delT | Frame_Shift_Del | 2 | 0.11 | HEC108 | Y | 8 | 10 | 0 | N |
MSH2 | APIWEVNQH | ENDOMETRIUM | 669 | p.Y656fs | c.1966_1966delT | Frame_Shift_Del | 6 | 0.11 | HEC108 | N | 0 | 0 | 0 | N |
MSH2 | ATHFHELSL | SOFT_TISSUE | 781 | p.T788fs | c.2363_2364delCT | Frame_Shift_Del | 2 | 0.11 | SKUT1 | Y | 6 | 12 | 0 | N |
MSH2 | CSTSLLAPI | ENDOMETRIUM | 663 | p.Y656fs | c.1966_1966delT | Frame_Shift_Del | 5 | 0.11 | HEC108 | N | 5 | 0 | 0 | N |
MSH2 | DTTGSQSGC | ENDOMETRIUM | 319 | p.S325fs | c.973_974delTC | Frame_Shift_Del | 2 | 0.11 | JHUEM1 | N | 0 | 0 | 0 | N |
MSH2 | DVTLKKINR | ENDOMETRIUM | 654 | p.Y656fs | c.1966_1966delT | Frame_Shift_Del | 5 | 0.11 | HEC108 | Y | 5 | 9 | 0 | N |
MSH2 | EDTTGSQSG | ENDOMETRIUM | 318 | p.S325fs | c.973_974delTC | Frame_Shift_Del | 1 | 0.11 | JHUEM1 | N | 0 | 0 | 0 | N |
MSH2 | ELSLGQSDT | SOFT_TISSUE | 786 | p.T788fs | c.2363_2364delCT | Frame_Shift_Del | 5 | 0.11 | SKUT1 | N | 1 | 0 | 0 | N |
MSH2 | EVNQHIFDK | ENDOMETRIUM | 673 | p.Y656fs | c.1966_1966delT | Frame_Shift_Del | 5 | 0.11 | HEC108 | Y | 5 | 11 | 0 | N |
MSH2 | FATHFHELS | SOFT_TISSUE | 780 | p.T788fs | c.2363_2364delCT | Frame_Shift_Del | 1 | 0.11 | SKUT1 | N | 3 | 0 | 0 | N |
MSH2 | FHELSLGQS | SOFT_TISSUE | 784 | p.T788fs | c.2363_2364delCT | Frame_Shift_Del | 5 | 0.11 | SKUT1 | N | 4 | 0 | 2 | N |
MSH2 | FIPNDVTLK | ENDOMETRIUM | 650 | p.Y656fs | c.1966_1966delT | Frame_Shift_Del | 3 | 0.11 | HEC108 | N | 5 | 0 | 9 | N |
MSH2 | GSQSGCLAE | ENDOMETRIUM | 322 | p.S325fs | c.973_974delTC | Frame_Shift_Del | 5 | 0.11 | JHUEM1 | N | 0 | 0 | 0 | N |
MSH2 | HELSLGQSD | SOFT_TISSUE | 785 | p.T788fs | c.2363_2364delCT | Frame_Shift_Del | 5 | 0.11 | SKUT1 | N | 0 | 0 | 0 | N |
MSH2 | HFHELSLGQ | SOFT_TISSUE | 783 | p.T788fs | c.2363_2364delCT | Frame_Shift_Del | 4 | 0.11 | SKUT1 | N | 0 | 0 | 0 | N |
MSH2 | IAFIPNDVT | ENDOMETRIUM | 648 | p.Y656fs | c.1966_1966delT | Frame_Shift_Del | 1 | 0.11 | HEC108 | N | 5 | 0 | 0 | N |
MSH2 | INRCSTSLL | ENDOMETRIUM | 660 | p.Y656fs | c.1966_1966delT | Frame_Shift_Del | 5 | 0.11 | HEC108 | N | 7 | 0 | 8 | N |
MSH2 | IPNDVTLKK | ENDOMETRIUM | 651 | p.Y656fs | c.1966_1966delT | Frame_Shift_Del | 3 | 0.11 | HEC108 | Y | 4 | 12 | 10 | N |
MSH2 | IWEVNQHIF | ENDOMETRIUM | 671 | p.Y656fs | c.1966_1966delT | Frame_Shift_Del | 5 | 0.11 | HEC108 | N | 4 | 0 | 0 | N |
MSH2 | KASPGNLSV | OVARY | 122 | p.N127fs | c.381_382delTC | Frame_Shift_Del | 1 | 0.11 | EFO27 | N | 6 | 0 | 0 | N |
MSH2 | KINRCSTSL | ENDOMETRIUM | 659 | p.Y656fs | c.1966_1966delT | Frame_Shift_Del | 5 | 0.11 | HEC108 | Y | 10 | 10 | 0 | N |
MSH2 | KKINRCSTS | ENDOMETRIUM | 658 | p.Y656fs | c.1966_1966delT | Frame_Shift_Del | 5 | 0.11 | HEC108 | N | 2 | 0 | 0 | N |
MSH2 | LAPIWEVNQ | ENDOMETRIUM | 668 | p.Y656fs | c.1966_1966delT | Frame_Shift_Del | 6 | 0.11 | HEC108 | N | 0 | 0 | 0 | N |
MSH2 | LKKINRCST | ENDOMETRIUM | 657 | p.Y656fs | c.1966_1966delT | Frame_Shift_Del | 5 | 0.11 | HEC108 | N | 1 | 0 | 1 | N |
MSH2 | LLAPIWEVN | ENDOMETRIUM | 667 | p.Y656fs | c.1966_1966delT | Frame_Shift_Del | 5 | 0.11 | HEC108 | N | 0 | 0 | 0 | N |
MSH2 | LSLGQSDTN | SOFT_TISSUE | 787 | p.T788fs | c.2363_2364delCT | Frame_Shift_Del | 5 | 0.11 | SKUT1 | N | 0 | 0 | 0 | N |
MSH2 | NDVTLKKIN | ENDOMETRIUM | 653 | p.Y656fs | c.1966_1966delT | Frame_Shift_Del | 5 | 0.11 | HEC108 | N | 2 | 0 | 0 | N |
MSH2 | NQHIFDKLG | ENDOMETRIUM | 675 | p.Y656fs | c.1966_1966delT | Frame_Shift_Del | 5 | 0.11 | HEC108 | N | 0 | 0 | 0 | N |
MSH2 | NRCSTSLLA | ENDOMETRIUM | 661 | p.Y656fs | c.1966_1966delT | Frame_Shift_Del | 5 | 0.11 | HEC108 | N | 2 | 0 | 0 | N |
MSH2 | PIWEVNQHI | ENDOMETRIUM | 670 | p.Y656fs | c.1966_1966delT | Frame_Shift_Del | 5 | 0.11 | HEC108 | N | 2 | 0 | 0 | N |
MSH2 | PNDVTLKKI | ENDOMETRIUM | 652 | p.Y656fs | c.1966_1966delT | Frame_Shift_Del | 4 | 0.11 | HEC108 | N | 0 | 0 | 0 | N |
MSH2 | RCSTSLLAP | ENDOMETRIUM | 662 | p.Y656fs | c.1966_1966delT | Frame_Shift_Del | 5 | 0.11 | HEC108 | N | 0 | 0 | 0 | N |
MSH2 | SLGQSDTNC | SOFT_TISSUE | 788 | p.T788fs | c.2363_2364delCT | Frame_Shift_Del | 6 | 0.11 | SKUT1 | N | 2 | 0 | 0 | N |
MSH2 | SLLAPIWEV | ENDOMETRIUM | 666 | p.Y656fs | c.1966_1966delT | Frame_Shift_Del | 5 | 0.11 | HEC108 | Y | 8 | 9 | 0 | N |
MSH2 | STSLLAPIW | ENDOMETRIUM | 664 | p.Y656fs | c.1966_1966delT | Frame_Shift_Del | 5 | 0.11 | HEC108 | N | 1 | 0 | 0 | N |
MSH2 | TGSQSGCLA | ENDOMETRIUM | 321 | p.S325fs | c.973_974delTC | Frame_Shift_Del | 4 | 0.11 | JHUEM1 | N | 1 | 0 | 0 | N |
MSH2 | THFHELSLG | SOFT_TISSUE | 782 | p.T788fs | c.2363_2364delCT | Frame_Shift_Del | 3 | 0.11 | SKUT1 | N | 0 | 0 | 0 | N |
MSH2 | TLKKINRCS | ENDOMETRIUM | 656 | p.Y656fs | c.1966_1966delT | Frame_Shift_Del | 5 | 0.11 | HEC108 | N | 1 | 0 | 0 | N |
MSH2 | TSLLAPIWE | ENDOMETRIUM | 665 | p.Y656fs | c.1966_1966delT | Frame_Shift_Del | 5 | 0.11 | HEC108 | N | 0 | 0 | 0 | N |
MSH2 | TTGSQSGCL | ENDOMETRIUM | 320 | p.S325fs | c.973_974delTC | Frame_Shift_Del | 3 | 0.11 | JHUEM1 | N | 4 | 0 | 0 | N |
MSH2 | VNQHIFDKL | ENDOMETRIUM | 674 | p.Y656fs | c.1966_1966delT | Frame_Shift_Del | 4 | 0.11 | HEC108 | N | 11 | 0 | 0 | N |
MSH2 | VTLKKINRC | ENDOMETRIUM | 655 | p.Y656fs | c.1966_1966delT | Frame_Shift_Del | 5 | 0.11 | HEC108 | N | 1 | 0 | 13 | N |
MSH2 | WEVNQHIFD | ENDOMETRIUM | 672 | p.Y656fs | c.1966_1966delT | Frame_Shift_Del | 5 | 0.11 | HEC108 | N | 3 | 0 | 1 | N |
MSH2 | DPNLSELSK | ENDOMETRIUM | 475 | p.L481fs | c.1441_1442insTAAG | Frame_Shift_Ins | 2 | 0.11 | HEC59 | N | 1 | 0 | 0 | Y |
MSH2 | FDPNLSELS | ENDOMETRIUM | 474 | p.L481fs | c.1441_1442insTAAG | Frame_Shift_Ins | 1 | 0.11 | HEC59 | N | 5 | 0 | 2 | N |
MSH2 | LSELSKRNN | ENDOMETRIUM | 478 | p.L481fs | c.1441_1442insTAAG | Frame_Shift_Ins | 4 | 0.11 | HEC59 | N | 1 | 0 | 0 | N |
MSH2 | NLSELSKRN | ENDOMETRIUM | 477 | p.L481fs | c.1441_1442insTAAG | Frame_Shift_Ins | 4 | 0.11 | HEC59 | N | 0 | 0 | 0 | N |
MSH2 | PNLSELSKR | ENDOMETRIUM | 476 | p.L481fs | c.1441_1442insTAAG | Frame_Shift_Ins | 3 | 0.11 | HEC59 | N | 0 | 0 | 0 | Y |
MSH2 | SELSKRNNE | ENDOMETRIUM | 479 | p.L481fs | c.1441_1442insTAAG | Frame_Shift_Ins | 4 | 0.11 | HEC59 | N | 1 | 0 | 0 | N |
MSH2 | AAEVGLVRF | LUNG | 14 | p.F19L | c.57C>A | Missense_Mutation | 1 | 0.11 | NCIH596 | N | 4 | 0 | 0 | N |
MSH2 | AAVKALNLF | LARGE_INTESTINE | 305 | p.R308K | c.923G>A | Missense_Mutation | 1 | 0.11 | KM12 | N | 6 | 0 | 0 | N |
MSH2 | AELANFTKH | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 831 | p.P837T | c.2509C>A | Missense_Mutation | 1 | 0.11 | MOLM13 | N | 3 | 0 | 0 | N |
MSH2 | AEVGLVRFF | LUNG | 15 | p.F19L | c.57C>A | Missense_Mutation | 1 | 0.11 | NCIH596 | Y | 7 | 10 | 0 | N |
MSH2 | AGANNLQSV | ENDOMETRIUM | 70 | p.K73N | c.219G>T | Missense_Mutation | 1 | 0.11 | HEC251 | N | 7 | 0 | 0 | N |
MSH2 | AKKFQRQTA | ENDOMETRIUM | 391 | p.A398T | c.1192G>A | Missense_Mutation | 1 | 0.11 | HEC108 | N | 2 | 0 | 0 | Y |
MSH2 | ALNLFQVSV | LIVER | 309 | p.G315V | c.944G>T | Missense_Mutation | 1 | 0.11 | SKHEP1 | Y | 6 | 10 | 0 | N |
MSH2 | ANFTKHVIE | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 834 | p.P837T | c.2509C>A | Missense_Mutation | 1 | 0.11 | MOLM13 | N | 0 | 0 | 0 | N |
MSH2 | ANNLQSVVL | ENDOMETRIUM | 72 | p.K73N | c.219G>T | Missense_Mutation | 1 | 0.11 | HEC251 | Y | 4 | 15 | 0 | N |
MSH2 | AQIGCSVPC | PANCREAS | 689 | p.F694S | c.2081T>C | Missense_Mutation | 1 | 0.11 | SNU324 | N | 2 | 0 | 0 | N |
MSH2 | AQLDAVASF | LARGE_INTESTINE | 600 | p.V606A | c.1817T>C | Missense_Mutation | 1 | 0.11 | SNU175 | Y | 10 | 9 | 0 | N |
MSH2 | ASFAHVSNG | LARGE_INTESTINE | 606 | p.V606A | c.1817T>C | Missense_Mutation | 1 | 0.11 | SNU175 | Y | 0 | 12 | 0 | N |
MSH2 | ASIIRSATK | PROSTATE | 733 | p.L736I | c.2206C>A | Missense_Mutation | 1 | 0.11 | DU145 | Y | 2 | 11 | 0 | N |
MSH2 | AVASFAHVS | LARGE_INTESTINE | 604 | p.V606A | c.1817T>C | Missense_Mutation | 1 | 0.11 | SNU175 | N | 0 | 0 | 0 | N |
MSH2 | AVKALNLFQ | LARGE_INTESTINE | 306 | p.R308K | c.923G>A | Missense_Mutation | 1 | 0.11 | KM12 | N | 0 | 0 | 0 | N |
MSH2 | AVQQKETLQ | STOMACH | 2 | p.P5Q | c.14C>A | Missense_Mutation | 1 | 0.11 | SNU601 | N | 0 | 0 | 0 | N |
MSH2 | CMGPAGAKN | ENDOMETRIUM | 66 | p.Y66C | c.197A>G | Missense_Mutation | 1 | 0.11 | HEC251 | N | 0 | 0 | 0 | N |
MSH2 | CSVPCESAE | PANCREAS | 693 | p.F694S | c.2081T>C | Missense_Mutation | 1 | 0.11 | SNU324 | N | 0 | 0 | 0 | N |
MSH2 | DAVASFAHV | LARGE_INTESTINE | 603 | p.V606A | c.1817T>C | Missense_Mutation | 1 | 0.11 | SNU175 | Y | 5 | 10 | 0 | N |
MSH2 | DIAAVKALN | LARGE_INTESTINE | 303 | p.R308K | c.923G>A | Missense_Mutation | 1 | 0.11 | KM12 | N | 0 | 0 | 0 | N |
MSH2 | DLEKKIQST | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 487 | p.M492I | c.1476G>A | Missense_Mutation | 1 | 0.11 | SR786 | N | 0 | 0 | 0 | N |
MSH2 | DMDQVENHK | BREAST | 459 | p.E467K | c.1399G>A | Missense_Mutation | 1 | 0.11 | HCC2218 | N | 5 | 0 | 0 | N |
MSH2 | DQVENHKFL | BREAST | 461 | p.E467K | c.1399G>A | Missense_Mutation | 1 | 0.11 | HCC2218 | N | 15 | 0 | 0 | N |
MSH2 | DSIQRKLGP | LARGE_INTESTINE | 167 | p.L175P | c.524T>C | Missense_Mutation | 1 | 0.11 | CCK81 | N | 0 | 0 | 0 | N |
MSH2 | DSQLKGVFT | SKIN | 716 | p.S723F | c.2168C>T | Missense_Mutation | 1 | 0.11 | SKMEL2 | N | 1 | 0 | 0 | N |
MSH2 | DVLVQLDAV | LARGE_INTESTINE | 597 | p.A600V | c.1799C>T | Missense_Mutation | 1 | 0.11 | HRT18 | Y | 4 | 10 | 0 | N |
MSH2 | EEFQYIGEL | LIVER | 852 | p.S860L | c.2579C>T | Missense_Mutation | 1 | 0.11 | ALEXANDERCELLS | Y | 11 | 11 | 0 | N |
MSH2 | EFQYIGELQ | LIVER | 853 | p.S860L | c.2579C>T | Missense_Mutation | 1 | 0.11 | ALEXANDERCELLS | N | 0 | 0 | 0 | N |
MSH2 | EKKIQSTLI | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 489 | p.M492I | c.1476G>A | Missense_Mutation | 1 | 0.11 | SR786 | N | 2 | 0 | 0 | N |
MSH2 | ELANFTKHV | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 832 | p.P837T | c.2509C>A | Missense_Mutation | 1 | 0.11 | MOLM13 | N | 4 | 0 | 0 | N |
MSH2 | ELQGYDIME | LIVER | 859 | p.S860L | c.2579C>T | Missense_Mutation | 1 | 0.11 | ALEXANDERCELLS | N | 0 | 0 | 0 | N |
MSH2 | EMLETASII | PROSTATE | 728 | p.L736I | c.2206C>A | Missense_Mutation | 1 | 0.11 | DU145 | N | 12 | 0 | 0 | N |
MSH2 | ENHKFLVKP | BREAST | 464 | p.E467K | c.1399G>A | Missense_Mutation | 1 | 0.11 | HCC2218 | N | 0 | 0 | 0 | N |
MSH2 | ESAAEVGLV | LUNG | 12 | p.F19L | c.57C>A | Missense_Mutation | 1 | 0.11 | NCIH596 | N | 3 | 0 | 0 | N |
MSH2 | ETASIIRSA | PROSTATE | 731 | p.L736I | c.2206C>A | Missense_Mutation | 1 | 0.11 | DU145 | N | 3 | 0 | 0 | N |
MSH2 | EVGLVRFFQ | LUNG | 16 | p.F19L | c.57C>A | Missense_Mutation | 1 | 0.11 | NCIH596 | N | 1 | 0 | 0 | N |
MSH2 | FKTQGVIKC | ENDOMETRIUM | 58 | p.Y66C | c.197A>G | Missense_Mutation | 1 | 0.11 | HEC251 | N | 3 | 0 | 18 | N |
MSH2 | FQRQTANLQ | ENDOMETRIUM | 394 | p.A398T | c.1192G>A | Missense_Mutation | 1 | 0.11 | HEC108 | N | 2 | 0 | 22 | Y |
MSH2 | FQVSVEDTT | LIVER | 313 | p.G315V | c.944G>T | Missense_Mutation | 1 | 0.11 | SKHEP1 | N | 4 | 0 | 0 | N |
MSH2 | FQYIGELQG | LIVER | 854 | p.S860L | c.2579C>T | Missense_Mutation | 1 | 0.11 | ALEXANDERCELLS | N | 2 | 0 | 6 | N |
MSH2 | FTFMAEMLE | SKIN | 723 | p.S723F | c.2168C>T | Missense_Mutation | 1 | 0.11 | SKMEL2 | N | 2 | 0 | 4 | N |
MSH2 | FTKHVIECA | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 836 | p.P837T | c.2509C>A | Missense_Mutation | 1 | 0.11 | MOLM13 | N | 5 | 0 | 0 | N |
MSH2 | GANNLQSVV | ENDOMETRIUM | 71 | p.K73N | c.219G>T | Missense_Mutation | 1 | 0.11 | HEC251 | N | 6 | 0 | 0 | N |
MSH2 | GCSVPCESA | PANCREAS | 692 | p.F694S | c.2081T>C | Missense_Mutation | 1 | 0.11 | SNU324 | N | 1 | 0 | 0 | N |
MSH2 | GDSQLKGVF | SKIN | 715 | p.S723F | c.2168C>T | Missense_Mutation | 1 | 0.11 | SKMEL2 | N | 6 | 0 | 0 | N |
MSH2 | GELQGYDIM | LIVER | 858 | p.S860L | c.2579C>T | Missense_Mutation | 1 | 0.11 | ALEXANDERCELLS | N | 10 | 0 | 0 | N |
MSH2 | GKHQKLLLV | CENTRAL_NERVOUS_SYSTEM | 426 | p.A434V | c.1301C>T | Missense_Mutation | 1 | 0.11 | SW1783 | N | 4 | 0 | 0 | N |
MSH2 | GLVRFFQGM | LUNG | 18 | p.F19L | c.57C>A | Missense_Mutation | 1 | 0.11 | NCIH596 | N | 11 | 0 | 0 | N |
MSH2 | GPAGANNLQ | ENDOMETRIUM | 68 | p.K73N | c.219G>T | Missense_Mutation | 1 | 0.11 | HEC251 | N | 0 | 0 | 0 | N |
MSH2 | GPCEFPDND | LARGE_INTESTINE | 174 | p.L175P | c.524T>C | Missense_Mutation | 1 | 0.11 | CCK81 | N | 0 | 0 | 0 | N |
MSH2 | GVFTFMAEM | SKIN | 721 | p.S723F | c.2168C>T | Missense_Mutation | 1 | 0.11 | SKMEL2 | Y | 10 | 10 | 0 | N |
MSH2 | GVIKCMGPA | ENDOMETRIUM | 62 | p.Y66C | c.197A>G | Missense_Mutation | 1 | 0.11 | HEC251 | N | 2 | 0 | 0 | N |
MSH2 | HKFLVKPSF | BREAST | 466 | p.E467K | c.1399G>A | Missense_Mutation | 1 | 0.11 | HCC2218 | N | 4 | 0 | 0 | N |
MSH2 | HKNRIEERL | LUNG | 352 | p.D352H | c.1054G>C | Missense_Mutation | 1 | 0.11 | NCIH522 | N | 4 | 0 | 0 | N |
MSH2 | HQKLLLVVF | CENTRAL_NERVOUS_SYSTEM | 428 | p.A434V | c.1301C>T | Missense_Mutation | 1 | 0.11 | SW1783 | N | 7 | 0 | 0 | N |
MSH2 | HVAELANFT | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 829 | p.P837T | c.2509C>A | Missense_Mutation | 1 | 0.11 | MOLM13 | N | 2 | 0 | 0 | N |
MSH2 | IAAVKALNL | LARGE_INTESTINE | 304 | p.R308K | c.923G>A | Missense_Mutation | 1 | 0.11 | KM12 | Y | 13 | 9 | 3 | N |
MSH2 | IGCSVPCES | PANCREAS | 691 | p.F694S | c.2081T>C | Missense_Mutation | 1 | 0.11 | SNU324 | N | 0 | 0 | 5 | N |
MSH2 | IGELQGYDI | LIVER | 857 | p.S860L | c.2579C>T | Missense_Mutation | 1 | 0.11 | ALEXANDERCELLS | N | 7 | 0 | 1 | N |
MSH2 | IIRSATKDS | PROSTATE | 735 | p.L736I | c.2206C>A | Missense_Mutation | 1 | 0.11 | DU145 | N | 0 | 0 | 31 | N |
MSH2 | IKCMGPAGA | ENDOMETRIUM | 64 | p.Y66C | c.197A>G | Missense_Mutation | 1 | 0.11 | HEC251 | N | 2 | 0 | 21 | N |
MSH2 | IKQPLMHKN | LUNG | 346 | p.D352H | c.1054G>C | Missense_Mutation | 1 | 0.11 | NCIH522 | N | 1 | 0 | 0 | N |
MSH2 | IMNDLEKKI | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 484 | p.M492I | c.1476G>A | Missense_Mutation | 1 | 0.11 | SR786 | N | 8 | 0 | 0 | N |
MSH2 | IQRKLGPCE | LARGE_INTESTINE | 169 | p.L175P | c.524T>C | Missense_Mutation | 1 | 0.11 | CCK81 | N | 1 | 0 | 4 | N |
MSH2 | IQSTLISAA | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 492 | p.M492I | c.1476G>A | Missense_Mutation | 1 | 0.11 | SR786 | N | 4 | 0 | 0 | N |
MSH2 | IRSATKDSL | PROSTATE | 736 | p.L736I | c.2206C>A | Missense_Mutation | 1 | 0.11 | DU145 | N | 6 | 0 | 6 | N |
MSH2 | KALNLFQGS | LARGE_INTESTINE | 308 | p.R308K | c.923G>A | Missense_Mutation | 1 | 0.11 | KM12 | N | 3 | 0 | 0 | N |
MSH2 | KCMGPAGAK | ENDOMETRIUM | 65 | p.Y66C | c.197A>G | Missense_Mutation | 1 | 0.11 | HEC251 | N | 4 | 0 | 0 | N |
MSH2 | KFLVKPSFD | BREAST | 467 | p.E467K | c.1399G>A | Missense_Mutation | 1 | 0.11 | HCC2218 | N | 0 | 0 | 0 | N |
MSH2 | KFQRQTANL | ENDOMETRIUM | 393 | p.A398T | c.1192G>A | Missense_Mutation | 1 | 0.11 | HEC108 | Y | 9 | 11 | 0 | N |
MSH2 | KGVFTFMAE | SKIN | 720 | p.S723F | c.2168C>T | Missense_Mutation | 1 | 0.11 | SKMEL2 | N | 0 | 0 | 0 | N |
MSH2 | KHQKLLLVV | CENTRAL_NERVOUS_SYSTEM | 427 | p.A434V | c.1301C>T | Missense_Mutation | 1 | 0.11 | SW1783 | N | 4 | 0 | 0 | N |
MSH2 | KIQSTLISA | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 491 | p.M492I | c.1476G>A | Missense_Mutation | 1 | 0.11 | SR786 | Y | 5 | 9 | 0 | N |
MSH2 | KKFQRQTAN | ENDOMETRIUM | 392 | p.A398T | c.1192G>A | Missense_Mutation | 1 | 0.11 | HEC108 | N | 1 | 0 | 0 | Y |
MSH2 | KKIQSTLIS | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 490 | p.M492I | c.1476G>A | Missense_Mutation | 1 | 0.11 | SR786 | N | 1 | 0 | 0 | N |
MSH2 | KLDIAAVKA | LARGE_INTESTINE | 301 | p.R308K | c.923G>A | Missense_Mutation | 1 | 0.11 | KM12 | N | 3 | 0 | 0 | N |
MSH2 | KLGPCEFPD | LARGE_INTESTINE | 172 | p.L175P | c.524T>C | Missense_Mutation | 1 | 0.11 | CCK81 | N | 0 | 0 | 0 | Y |
MSH2 | KLLLVVFVT | CENTRAL_NERVOUS_SYSTEM | 430 | p.A434V | c.1301C>T | Missense_Mutation | 1 | 0.11 | SW1783 | N | 5 | 0 | 0 | N |
MSH2 | KQPLMHKNR | LUNG | 347 | p.D352H | c.1054G>C | Missense_Mutation | 1 | 0.11 | NCIH522 | N | 5 | 0 | 0 | N |
MSH2 | KTQGVIKCM | ENDOMETRIUM | 59 | p.Y66C | c.197A>G | Missense_Mutation | 1 | 0.11 | HEC251 | Y | 4 | 9 | 0 | N |
MSH2 | KYMGPAGAN | ENDOMETRIUM | 65 | p.K73N | c.219G>T | Missense_Mutation | 1 | 0.11 | HEC251 | N | 2 | 0 | 0 | N |
MSH2 | LAKKFQRQT | ENDOMETRIUM | 390 | p.A398T | c.1192G>A | Missense_Mutation | 1 | 0.11 | HEC108 | N | 4 | 0 | 0 | N |
MSH2 | LANFTKHVI | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 833 | p.P837T | c.2509C>A | Missense_Mutation | 1 | 0.11 | MOLM13 | N | 7 | 0 | 13 | N |
MSH2 | LAQLDAVAS | LARGE_INTESTINE | 599 | p.V606A | c.1817T>C | Missense_Mutation | 1 | 0.11 | SNU175 | N | 1 | 0 | 2 | N |
MSH2 | LDAVASFAH | LARGE_INTESTINE | 602 | p.V606A | c.1817T>C | Missense_Mutation | 1 | 0.11 | SNU175 | N | 0 | 0 | 0 | N |
MSH2 | LDIAAVKAL | LARGE_INTESTINE | 302 | p.R308K | c.923G>A | Missense_Mutation | 1 | 0.11 | KM12 | N | 7 | 0 | 0 | N |
MSH2 | LEKKIQSTL | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 488 | p.M492I | c.1476G>A | Missense_Mutation | 1 | 0.11 | SR786 | N | 10 | 0 | 0 | N |
MSH2 | LESAAEVGL | LUNG | 11 | p.F19L | c.57C>A | Missense_Mutation | 1 | 0.11 | NCIH596 | N | 8 | 0 | 0 | N |
MSH2 | LETASIIRS | PROSTATE | 730 | p.L736I | c.2206C>A | Missense_Mutation | 1 | 0.11 | DU145 | N | 4 | 0 | 4 | N |
MSH2 | LFQVSVEDT | LIVER | 312 | p.G315V | c.944G>T | Missense_Mutation | 1 | 0.11 | SKHEP1 | N | 1 | 0 | 0 | N |
MSH2 | LGPCEFPDN | LARGE_INTESTINE | 173 | p.L175P | c.524T>C | Missense_Mutation | 1 | 0.11 | CCK81 | N | 1 | 0 | 0 | N |
MSH2 | LKGVFTFMA | SKIN | 719 | p.S723F | c.2168C>T | Missense_Mutation | 1 | 0.11 | SKMEL2 | N | 4 | 0 | 15 | N |
MSH2 | LLLVVFVTP | CENTRAL_NERVOUS_SYSTEM | 431 | p.A434V | c.1301C>T | Missense_Mutation | 1 | 0.11 | SW1783 | N | 0 | 0 | 0 | N |
MSH2 | LLVVFVTPL | CENTRAL_NERVOUS_SYSTEM | 432 | p.A434V | c.1301C>T | Missense_Mutation | 1 | 0.11 | SW1783 | N | 20 | 0 | 8 | N |
MSH2 | LMAQIGCSV | PANCREAS | 687 | p.F694S | c.2081T>C | Missense_Mutation | 1 | 0.11 | SNU324 | N | 6 | 0 | 2 | N |
MSH2 | LMHKNRIEE | LUNG | 350 | p.D352H | c.1054G>C | Missense_Mutation | 1 | 0.11 | NCIH522 | N | 1 | 0 | 8 | N |
MSH2 | LNDVLVQLD | LARGE_INTESTINE | 595 | p.A600V | c.1799C>T | Missense_Mutation | 1 | 0.11 | HRT18 | N | 0 | 0 | 0 | N |
MSH2 | LNLFQVSVE | LIVER | 310 | p.G315V | c.944G>T | Missense_Mutation | 1 | 0.11 | SKHEP1 | N | 0 | 0 | 12 | N |
MSH2 | LQGYDIMEP | LIVER | 860 | p.S860L | c.2579C>T | Missense_Mutation | 1 | 0.11 | ALEXANDERCELLS | N | 0 | 0 | 9 | N |
MSH2 | LVQLDAVVS | LARGE_INTESTINE | 599 | p.A600V | c.1799C>T | Missense_Mutation | 1 | 0.11 | HRT18 | N | 0 | 0 | 42 | N |
MSH2 | LVRFFQGMP | LUNG | 19 | p.F19L | c.57C>A | Missense_Mutation | 1 | 0.11 | NCIH596 | N | 0 | 0 | 2 | N |
MSH2 | LVVFVTPLT | CENTRAL_NERVOUS_SYSTEM | 433 | p.A434V | c.1301C>T | Missense_Mutation | 1 | 0.11 | SW1783 | N | 2 | 0 | 30 | N |
MSH2 | MAQIGCSVP | PANCREAS | 688 | p.F694S | c.2081T>C | Missense_Mutation | 1 | 0.11 | SNU324 | N | 0 | 0 | 0 | N |
MSH2 | MAVQQKETL | STOMACH | 1 | p.P5Q | c.14C>A | Missense_Mutation | 1 | 0.11 | SNU601 | Y | 16 | 10 | 0 | N |
MSH2 | MDQVENHKF | BREAST | 460 | p.E467K | c.1399G>A | Missense_Mutation | 1 | 0.11 | HCC2218 | N | 4 | 0 | 0 | N |
MSH2 | MGPAGANNL | ENDOMETRIUM | 67 | p.K73N | c.219G>T | Missense_Mutation | 1 | 0.11 | HEC251 | N | 12 | 0 | 4 | Y |
MSH2 | MHKNRIEER | LUNG | 351 | p.D352H | c.1054G>C | Missense_Mutation | 1 | 0.11 | NCIH522 | N | 1 | 0 | 0 | N |
MSH2 | MKLDIAAVK | LARGE_INTESTINE | 300 | p.R308K | c.923G>A | Missense_Mutation | 1 | 0.11 | KM12 | N | 1 | 0 | 11 | N |
MSH2 | MLETASIIR | PROSTATE | 729 | p.L736I | c.2206C>A | Missense_Mutation | 1 | 0.11 | DU145 | N | 7 | 0 | 2 | N |
MSH2 | MNDLEKKIQ | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 485 | p.M492I | c.1476G>A | Missense_Mutation | 1 | 0.11 | SR786 | N | 0 | 0 | 5 | N |
MSH2 | MQTLNDVLV | LARGE_INTESTINE | 592 | p.A600V | c.1799C>T | Missense_Mutation | 1 | 0.11 | HRT18 | N | 12 | 0 | 0 | N |
MSH2 | NDLEKKIQS | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 486 | p.M492I | c.1476G>A | Missense_Mutation | 1 | 0.11 | SR786 | N | 2 | 0 | 0 | N |
MSH2 | NDVLVQLDA | LARGE_INTESTINE | 596 | p.A600V | c.1799C>T | Missense_Mutation | 1 | 0.11 | HRT18 | N | 4 | 0 | 0 | N |
MSH2 | NFTKHVIEC | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 835 | p.P837T | c.2509C>A | Missense_Mutation | 1 | 0.11 | MOLM13 | N | 1 | 0 | 0 | N |
MSH2 | NHKFLVKPS | BREAST | 465 | p.E467K | c.1399G>A | Missense_Mutation | 1 | 0.11 | HCC2218 | N | 0 | 0 | 0 | N |
MSH2 | NLFQVSVED | LIVER | 311 | p.G315V | c.944G>T | Missense_Mutation | 1 | 0.11 | SKHEP1 | N | 0 | 0 | 0 | N |
MSH2 | NNLQSVVLS | ENDOMETRIUM | 73 | p.K73N | c.219G>T | Missense_Mutation | 1 | 0.11 | HEC251 | N | 0 | 0 | 0 | N |
MSH2 | PAGANNLQS | ENDOMETRIUM | 69 | p.K73N | c.219G>T | Missense_Mutation | 1 | 0.11 | HEC251 | N | 0 | 0 | 0 | N |
MSH2 | PCEFPDNDQ | LARGE_INTESTINE | 175 | p.L175P | c.524T>C | Missense_Mutation | 1 | 0.11 | CCK81 | N | 0 | 0 | 0 | N |
MSH2 | PLMHKNRIE | LUNG | 349 | p.D352H | c.1054G>C | Missense_Mutation | 1 | 0.11 | NCIH522 | N | 0 | 0 | 0 | N |
MSH2 | QGVIKCMGP | ENDOMETRIUM | 61 | p.Y66C | c.197A>G | Missense_Mutation | 1 | 0.11 | HEC251 | N | 0 | 0 | 0 | N |
MSH2 | QIGCSVPCE | PANCREAS | 690 | p.F694S | c.2081T>C | Missense_Mutation | 1 | 0.11 | SNU324 | N | 0 | 0 | 0 | N |
MSH2 | QKETLQLES | STOMACH | 5 | p.P5Q | c.14C>A | Missense_Mutation | 1 | 0.11 | SNU601 | N | 1 | 0 | 0 | N |
MSH2 | QKLLLVVFV | CENTRAL_NERVOUS_SYSTEM | 429 | p.A434V | c.1301C>T | Missense_Mutation | 1 | 0.11 | SW1783 | N | 6 | 0 | 0 | N |
MSH2 | QLDAVASFA | LARGE_INTESTINE | 601 | p.V606A | c.1817T>C | Missense_Mutation | 1 | 0.11 | SNU175 | N | 2 | 0 | 0 | N |
MSH2 | QLKGVFTFM | SKIN | 718 | p.S723F | c.2168C>T | Missense_Mutation | 1 | 0.11 | SKMEL2 | N | 6 | 0 | 0 | N |
MSH2 | QPLMHKNRI | LUNG | 348 | p.D352H | c.1054G>C | Missense_Mutation | 1 | 0.11 | NCIH522 | N | 14 | 0 | 0 | N |
MSH2 | QQKETLQLE | STOMACH | 4 | p.P5Q | c.14C>A | Missense_Mutation | 1 | 0.11 | SNU601 | N | 0 | 0 | 0 | N |
MSH2 | QRKLGPCEF | LARGE_INTESTINE | 170 | p.L175P | c.524T>C | Missense_Mutation | 1 | 0.11 | CCK81 | Y | 2 | 9 | 0 | N |
MSH2 | QRQTANLQD | ENDOMETRIUM | 395 | p.A398T | c.1192G>A | Missense_Mutation | 1 | 0.11 | HEC108 | N | 1 | 0 | 0 | N |
MSH2 | QTANLQDCY | ENDOMETRIUM | 397 | p.A398T | c.1192G>A | Missense_Mutation | 1 | 0.11 | HEC108 | N | 6 | 0 | 0 | N |
MSH2 | QTLNDVLVQ | LARGE_INTESTINE | 593 | p.A600V | c.1799C>T | Missense_Mutation | 1 | 0.11 | HRT18 | N | 0 | 0 | 0 | N |
MSH2 | QVENHKFLV | BREAST | 462 | p.E467K | c.1399G>A | Missense_Mutation | 1 | 0.11 | HCC2218 | N | 2 | 0 | 0 | N |
MSH2 | QVSVEDTTG | LIVER | 314 | p.G315V | c.944G>T | Missense_Mutation | 1 | 0.11 | SKHEP1 | N | 0 | 0 | 0 | N |
MSH2 | QWIKQPLMH | LUNG | 344 | p.D352H | c.1054G>C | Missense_Mutation | 1 | 0.11 | NCIH522 | N | 0 | 0 | 0 | N |
MSH2 | QYIGELQGY | LIVER | 855 | p.S860L | c.2579C>T | Missense_Mutation | 1 | 0.11 | ALEXANDERCELLS | N | 5 | 0 | 0 | N |
MSH2 | RALNLFQVS | LIVER | 308 | p.G315V | c.944G>T | Missense_Mutation | 1 | 0.11 | SKHEP1 | N | 3 | 0 | 0 | N |
MSH2 | RKLGPCEFP | LARGE_INTESTINE | 171 | p.L175P | c.524T>C | Missense_Mutation | 1 | 0.11 | CCK81 | N | 0 | 0 | 0 | Y |
MSH2 | RQTANLQDC | ENDOMETRIUM | 396 | p.A398T | c.1192G>A | Missense_Mutation | 1 | 0.11 | HEC108 | N | 5 | 0 | 0 | N |
MSH2 | SAAEVGLVR | LUNG | 13 | p.F19L | c.57C>A | Missense_Mutation | 1 | 0.11 | NCIH596 | N | 4 | 0 | 0 | N |
MSH2 | SIIRSATKD | PROSTATE | 734 | p.L736I | c.2206C>A | Missense_Mutation | 1 | 0.11 | DU145 | N | 0 | 0 | 0 | N |
MSH2 | SIQRKLGPC | LARGE_INTESTINE | 168 | p.L175P | c.524T>C | Missense_Mutation | 1 | 0.11 | CCK81 | N | 0 | 0 | 0 | N |
MSH2 | SQLKGVFTF | SKIN | 717 | p.S723F | c.2168C>T | Missense_Mutation | 1 | 0.11 | SKMEL2 | Y | 10 | 9 | 0 | N |
MSH2 | SVPCESAEV | PANCREAS | 694 | p.F694S | c.2081T>C | Missense_Mutation | 1 | 0.11 | SNU324 | Y | 3 | 11 | 0 | N |
MSH2 | TANLQDCYR | ENDOMETRIUM | 398 | p.A398T | c.1192G>A | Missense_Mutation | 1 | 0.11 | HEC108 | N | 3 | 0 | 0 | N |
MSH2 | TASIIRSAT | PROSTATE | 732 | p.L736I | c.2206C>A | Missense_Mutation | 1 | 0.11 | DU145 | N | 3 | 0 | 0 | N |
MSH2 | TKHVIECAK | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 837 | p.P837T | c.2509C>A | Missense_Mutation | 1 | 0.11 | MOLM13 | N | 1 | 0 | 0 | N |
MSH2 | TLNDVLVQL | LARGE_INTESTINE | 594 | p.A600V | c.1799C>T | Missense_Mutation | 1 | 0.11 | HRT18 | Y | 17 | 12 | 0 | N |
MSH2 | TQGVIKCMG | ENDOMETRIUM | 60 | p.Y66C | c.197A>G | Missense_Mutation | 1 | 0.11 | HEC251 | N | 0 | 0 | 0 | N |
MSH2 | VAELANFTK | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 830 | p.P837T | c.2509C>A | Missense_Mutation | 1 | 0.11 | MOLM13 | N | 3 | 0 | 0 | N |
MSH2 | VASFAHVSN | LARGE_INTESTINE | 605 | p.V606A | c.1817T>C | Missense_Mutation | 1 | 0.11 | SNU175 | N | 1 | 0 | 0 | N |
MSH2 | VENHKFLVK | BREAST | 463 | p.E467K | c.1399G>A | Missense_Mutation | 1 | 0.11 | HCC2218 | Y | 1 | 14 | 0 | N |
MSH2 | VFTFMAEML | SKIN | 722 | p.S723F | c.2168C>T | Missense_Mutation | 1 | 0.11 | SKMEL2 | N | 9 | 0 | 3 | N |
MSH2 | VGLVRFFQG | LUNG | 17 | p.F19L | c.57C>A | Missense_Mutation | 1 | 0.11 | NCIH596 | N | 0 | 0 | 0 | N |
MSH2 | VIKCMGPAG | ENDOMETRIUM | 63 | p.Y66C | c.197A>G | Missense_Mutation | 1 | 0.11 | HEC251 | N | 0 | 0 | 0 | N |
MSH2 | VKALNLFQG | LARGE_INTESTINE | 307 | p.R308K | c.923G>A | Missense_Mutation | 1 | 0.11 | KM12 | N | 0 | 0 | 4 | N |
MSH2 | VLAQLDAVA | LARGE_INTESTINE | 598 | p.V606A | c.1817T>C | Missense_Mutation | 1 | 0.11 | SNU175 | N | 4 | 0 | 0 | N |
MSH2 | VLMAQIGCS | PANCREAS | 686 | p.F694S | c.2081T>C | Missense_Mutation | 1 | 0.11 | SNU324 | N | 0 | 0 | 30 | N |
MSH2 | VLVQLDAVV | LARGE_INTESTINE | 598 | p.A600V | c.1799C>T | Missense_Mutation | 1 | 0.11 | HRT18 | Y | 8 | 13 | 0 | N |
MSH2 | VQLDAVVSF | LARGE_INTESTINE | 600 | p.A600V | c.1799C>T | Missense_Mutation | 1 | 0.11 | HRT18 | Y | 12 | 9 | 14 | N |
MSH2 | VQQKETLQL | STOMACH | 3 | p.P5Q | c.14C>A | Missense_Mutation | 1 | 0.11 | SNU601 | N | 14 | 0 | 21 | N |
MSH2 | VRALNLFQV | LIVER | 307 | p.G315V | c.944G>T | Missense_Mutation | 1 | 0.11 | SKHEP1 | Y | 7 | 9 | 25 | N |
MSH2 | VSVEDTTGS | LIVER | 315 | p.G315V | c.944G>T | Missense_Mutation | 1 | 0.11 | SKHEP1 | N | 0 | 0 | 5 | N |
MSH2 | VVFVTPLTD | CENTRAL_NERVOUS_SYSTEM | 434 | p.A434V | c.1301C>T | Missense_Mutation | 1 | 0.11 | SW1783 | N | 0 | 0 | 25 | N |
MSH2 | WIKQPLMHK | LUNG | 345 | p.D352H | c.1054G>C | Missense_Mutation | 1 | 0.11 | NCIH522 | Y | 5 | 11 | 6 | N |
MSH2 | YIGELQGYD | LIVER | 856 | p.S860L | c.2579C>T | Missense_Mutation | 1 | 0.11 | ALEXANDERCELLS | N | 2 | 0 | 0 | N |
MSH2 | YMGPAGANN | ENDOMETRIUM | 66 | p.K73N | c.219G>T | Missense_Mutation | 1 | 0.11 | HEC251 | N | 2 | 0 | 0 | N |
MSH2 | AEMLETTSI | LUNG | 727 | p.A733T | c.2197G>A | Missense_Mutation | 1 | 0.22 | RERFLCMS | N | 6 | 0 | 0 | N |
MSH2 | AEMLETTSI | LIVER | 727 | p.A733T | c.2197G>A | Missense_Mutation | 1 | 0.22 | SNU886 | N | 6 | 0 | 0 | N |
MSH2 | AQFGYYFPV | OVARY | 517 | p.R524P | c.1571G>C | Missense_Mutation | 1 | 0.22 | OC316 | Y | 13 | 11 | 0 | Y |
MSH2 | AQFGYYFPV | ENDOMETRIUM | 517 | p.R524P | c.1571G>C | Missense_Mutation | 1 | 0.22 | RL952 | Y | 13 | 11 | 0 | Y |
MSH2 | EMLETTSIL | LUNG | 728 | p.A733T | c.2197G>A | Missense_Mutation | 1 | 0.22 | RERFLCMS | N | 19 | 0 | 0 | N |
MSH2 | EMLETTSIL | LIVER | 728 | p.A733T | c.2197G>A | Missense_Mutation | 1 | 0.22 | SNU886 | N | 19 | 0 | 0 | N |
MSH2 | ESFVKYLLL | ENDOMETRIUM | 86 | p.D91Y | c.271G>T | Missense_Mutation | 1 | 0.22 | HEC251 | Y | 16 | 10 | 0 | N |
MSH2 | ESFVKYLLL | ENDOMETRIUM | 86 | p.D91Y | c.271G>T | Missense_Mutation | 1 | 0.22 | JHUEM7 | Y | 16 | 10 | 0 | N |
MSH2 | ETTSILRSA | LUNG | 731 | p.A733T | c.2197G>A | Missense_Mutation | 1 | 0.22 | RERFLCMS | N | 1 | 0 | 0 | N |
MSH2 | ETTSILRSA | LIVER | 731 | p.A733T | c.2197G>A | Missense_Mutation | 1 | 0.22 | SNU886 | N | 1 | 0 | 0 | N |
MSH2 | FESFVKYLL | ENDOMETRIUM | 85 | p.D91Y | c.271G>T | Missense_Mutation | 1 | 0.22 | HEC251 | Y | 12 | 9 | 5 | N |
MSH2 | FESFVKYLL | ENDOMETRIUM | 85 | p.D91Y | c.271G>T | Missense_Mutation | 1 | 0.22 | JHUEM7 | Y | 12 | 9 | 5 | N |
MSH2 | FGYYFPVTC | OVARY | 519 | p.R524P | c.1571G>C | Missense_Mutation | 1 | 0.22 | OC316 | N | 7 | 0 | 12 | N |
MSH2 | FGYYFPVTC | ENDOMETRIUM | 519 | p.R524P | c.1571G>C | Missense_Mutation | 1 | 0.22 | RL952 | N | 7 | 0 | 12 | N |
MSH2 | FMAEMLETT | LUNG | 725 | p.A733T | c.2197G>A | Missense_Mutation | 1 | 0.22 | RERFLCMS | N | 4 | 0 | 0 | N |
MSH2 | FMAEMLETT | LIVER | 725 | p.A733T | c.2197G>A | Missense_Mutation | 1 | 0.22 | SNU886 | N | 4 | 0 | 0 | N |
MSH2 | FPVTCKEEK | OVARY | 523 | p.R524P | c.1571G>C | Missense_Mutation | 1 | 0.22 | OC316 | N | 5 | 0 | 0 | N |
MSH2 | FPVTCKEEK | ENDOMETRIUM | 523 | p.R524P | c.1571G>C | Missense_Mutation | 1 | 0.22 | RL952 | N | 5 | 0 | 0 | N |
MSH2 | FVKYLLLVR | ENDOMETRIUM | 88 | p.D91Y | c.271G>T | Missense_Mutation | 1 | 0.22 | HEC251 | N | 8 | 0 | 20 | N |
MSH2 | FVKYLLLVR | ENDOMETRIUM | 88 | p.D91Y | c.271G>T | Missense_Mutation | 1 | 0.22 | JHUEM7 | N | 8 | 0 | 20 | N |
MSH2 | GYYFPVTCK | OVARY | 520 | p.R524P | c.1571G>C | Missense_Mutation | 1 | 0.22 | OC316 | Y | 3 | 11 | 0 | N |
MSH2 | GYYFPVTCK | ENDOMETRIUM | 520 | p.R524P | c.1571G>C | Missense_Mutation | 1 | 0.22 | RL952 | Y | 3 | 11 | 0 | N |
MSH2 | KYLLLVRQY | ENDOMETRIUM | 90 | p.D91Y | c.271G>T | Missense_Mutation | 1 | 0.22 | HEC251 | Y | 7 | 10 | 0 | N |
MSH2 | KYLLLVRQY | ENDOMETRIUM | 90 | p.D91Y | c.271G>T | Missense_Mutation | 1 | 0.22 | JHUEM7 | Y | 7 | 10 | 0 | N |
MSH2 | LETTSILRS | LUNG | 730 | p.A733T | c.2197G>A | Missense_Mutation | 1 | 0.22 | RERFLCMS | N | 4 | 0 | 4 | N |
MSH2 | LETTSILRS | LIVER | 730 | p.A733T | c.2197G>A | Missense_Mutation | 1 | 0.22 | SNU886 | N | 4 | 0 | 4 | N |
MSH2 | MAEMLETTS | LUNG | 726 | p.A733T | c.2197G>A | Missense_Mutation | 1 | 0.22 | RERFLCMS | N | 2 | 0 | 0 | N |
MSH2 | MAEMLETTS | LIVER | 726 | p.A733T | c.2197G>A | Missense_Mutation | 1 | 0.22 | SNU886 | N | 2 | 0 | 0 | N |
MSH2 | MLETTSILR | LUNG | 729 | p.A733T | c.2197G>A | Missense_Mutation | 1 | 0.22 | RERFLCMS | N | 7 | 0 | 2 | N |
MSH2 | MLETTSILR | LIVER | 729 | p.A733T | c.2197G>A | Missense_Mutation | 1 | 0.22 | SNU886 | N | 7 | 0 | 2 | N |
MSH2 | MNFESFVKY | ENDOMETRIUM | 83 | p.D91Y | c.271G>T | Missense_Mutation | 1 | 0.22 | HEC251 | N | 8 | 0 | 0 | N |
MSH2 | MNFESFVKY | ENDOMETRIUM | 83 | p.D91Y | c.271G>T | Missense_Mutation | 1 | 0.22 | JHUEM7 | N | 8 | 0 | 0 | N |
MSH2 | NFESFVKYL | ENDOMETRIUM | 84 | p.D91Y | c.271G>T | Missense_Mutation | 1 | 0.22 | HEC251 | N | 8 | 0 | 0 | N |
MSH2 | NFESFVKYL | ENDOMETRIUM | 84 | p.D91Y | c.271G>T | Missense_Mutation | 1 | 0.22 | JHUEM7 | N | 8 | 0 | 0 | N |
MSH2 | PVTCKEEKV | OVARY | 524 | p.R524P | c.1571G>C | Missense_Mutation | 1 | 0.22 | OC316 | N | 1 | 0 | 0 | N |
MSH2 | PVTCKEEKV | ENDOMETRIUM | 524 | p.R524P | c.1571G>C | Missense_Mutation | 1 | 0.22 | RL952 | N | 1 | 0 | 0 | N |
MSH2 | QFGYYFPVT | OVARY | 518 | p.R524P | c.1571G>C | Missense_Mutation | 1 | 0.22 | OC316 | N | 1 | 0 | 0 | N |
MSH2 | QFGYYFPVT | ENDOMETRIUM | 518 | p.R524P | c.1571G>C | Missense_Mutation | 1 | 0.22 | RL952 | N | 1 | 0 | 0 | N |
MSH2 | SAQFGYYFP | OVARY | 516 | p.R524P | c.1571G>C | Missense_Mutation | 1 | 0.22 | OC316 | N | 0 | 0 | 0 | N |
MSH2 | SAQFGYYFP | ENDOMETRIUM | 516 | p.R524P | c.1571G>C | Missense_Mutation | 1 | 0.22 | RL952 | N | 0 | 0 | 0 | N |
MSH2 | SFVKYLLLV | ENDOMETRIUM | 87 | p.D91Y | c.271G>T | Missense_Mutation | 1 | 0.22 | HEC251 | Y | 4 | 10 | 0 | N |
MSH2 | SFVKYLLLV | ENDOMETRIUM | 87 | p.D91Y | c.271G>T | Missense_Mutation | 1 | 0.22 | JHUEM7 | Y | 4 | 10 | 0 | N |
MSH2 | TSILRSATK | LUNG | 733 | p.A733T | c.2197G>A | Missense_Mutation | 1 | 0.22 | RERFLCMS | N | 2 | 0 | 0 | N |
MSH2 | TSILRSATK | LIVER | 733 | p.A733T | c.2197G>A | Missense_Mutation | 1 | 0.22 | SNU886 | N | 2 | 0 | 0 | N |
MSH2 | TTSILRSAT | LUNG | 732 | p.A733T | c.2197G>A | Missense_Mutation | 1 | 0.22 | RERFLCMS | N | 1 | 0 | 0 | N |
MSH2 | TTSILRSAT | LIVER | 732 | p.A733T | c.2197G>A | Missense_Mutation | 1 | 0.22 | SNU886 | N | 1 | 0 | 0 | N |
MSH2 | VKYLLLVRQ | ENDOMETRIUM | 89 | p.D91Y | c.271G>T | Missense_Mutation | 1 | 0.22 | HEC251 | N | 0 | 0 | 28 | N |
MSH2 | VKYLLLVRQ | ENDOMETRIUM | 89 | p.D91Y | c.271G>T | Missense_Mutation | 1 | 0.22 | JHUEM7 | N | 0 | 0 | 28 | N |
MSH2 | YFPVTCKEE | OVARY | 522 | p.R524P | c.1571G>C | Missense_Mutation | 1 | 0.22 | OC316 | N | 2 | 0 | 4 | N |
MSH2 | YFPVTCKEE | ENDOMETRIUM | 522 | p.R524P | c.1571G>C | Missense_Mutation | 1 | 0.22 | RL952 | N | 2 | 0 | 4 | N |
MSH2 | YLLLVRQYR | ENDOMETRIUM | 91 | p.D91Y | c.271G>T | Missense_Mutation | 1 | 0.22 | HEC251 | Y | 7 | 9 | 15 | N |
MSH2 | YLLLVRQYR | ENDOMETRIUM | 91 | p.D91Y | c.271G>T | Missense_Mutation | 1 | 0.22 | JHUEM7 | Y | 7 | 9 | 15 | N |
MSH2 | YYFPVTCKE | OVARY | 521 | p.R524P | c.1571G>C | Missense_Mutation | 1 | 0.22 | OC316 | N | 2 | 0 | 4 | N |
MSH2 | YYFPVTCKE | ENDOMETRIUM | 521 | p.R524P | c.1571G>C | Missense_Mutation | 1 | 0.22 | RL952 | N | 2 | 0 | 4 | N |
MSH2 | IKALEKHEG | LIVER | 418 | p.Q419K | c.1255C>A | Missense_Mutation | 1 | 0.66 | JHH7 | N | 0 | 0 | 18 | N |
MSH2 | IKALEKHEG | STOMACH | 418 | p.Q419K | c.1255C>A | Missense_Mutation | 1 | 0.66 | NCCSTCK140 | N | 0 | 0 | 18 | N |
MSH2 | IKALEKHEG | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 418 | p.Q419K | c.1255C>A | Missense_Mutation | 1 | 0.66 | SKM1 | N | 0 | 0 | 18 | N |
MSH2 | IKALEKHEG | LARGE_INTESTINE | 418 | p.Q419K | c.1255C>A | Missense_Mutation | 1 | 0.66 | SNU283 | N | 0 | 0 | 18 | N |
MSH2 | IKALEKHEG | CENTRAL_NERVOUS_SYSTEM | 418 | p.Q419K | c.1255C>A | Missense_Mutation | 1 | 0.66 | SNU738 | N | 0 | 0 | 18 | N |
MSH2 | IKALEKHEG | OVARY | 418 | p.Q419K | c.1255C>A | Missense_Mutation | 1 | 0.66 | TYKNU | N | 0 | 0 | 18 | N |
MSH2 | INQLPNVIK | LIVER | 411 | p.Q419K | c.1255C>A | Missense_Mutation | 1 | 0.66 | JHH7 | N | 0 | 0 | 5 | Y |
MSH2 | INQLPNVIK | STOMACH | 411 | p.Q419K | c.1255C>A | Missense_Mutation | 1 | 0.66 | NCCSTCK140 | N | 0 | 0 | 5 | Y |
MSH2 | INQLPNVIK | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 411 | p.Q419K | c.1255C>A | Missense_Mutation | 1 | 0.66 | SKM1 | N | 0 | 0 | 5 | Y |
MSH2 | INQLPNVIK | LARGE_INTESTINE | 411 | p.Q419K | c.1255C>A | Missense_Mutation | 1 | 0.66 | SNU283 | N | 0 | 0 | 5 | Y |
MSH2 | INQLPNVIK | CENTRAL_NERVOUS_SYSTEM | 411 | p.Q419K | c.1255C>A | Missense_Mutation | 1 | 0.66 | SNU738 | N | 0 | 0 | 5 | Y |
MSH2 | INQLPNVIK | OVARY | 411 | p.Q419K | c.1255C>A | Missense_Mutation | 1 | 0.66 | TYKNU | N | 0 | 0 | 5 | Y |
MSH2 | KALEKHEGK | LIVER | 419 | p.Q419K | c.1255C>A | Missense_Mutation | 1 | 0.66 | JHH7 | N | 4 | 0 | 0 | N |
MSH2 | KALEKHEGK | STOMACH | 419 | p.Q419K | c.1255C>A | Missense_Mutation | 1 | 0.66 | NCCSTCK140 | N | 4 | 0 | 0 | N |
MSH2 | KALEKHEGK | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 419 | p.Q419K | c.1255C>A | Missense_Mutation | 1 | 0.66 | SKM1 | N | 4 | 0 | 0 | N |
MSH2 | KALEKHEGK | LARGE_INTESTINE | 419 | p.Q419K | c.1255C>A | Missense_Mutation | 1 | 0.66 | SNU283 | N | 4 | 0 | 0 | N |
MSH2 | KALEKHEGK | CENTRAL_NERVOUS_SYSTEM | 419 | p.Q419K | c.1255C>A | Missense_Mutation | 1 | 0.66 | SNU738 | N | 4 | 0 | 0 | N |
MSH2 | KALEKHEGK | OVARY | 419 | p.Q419K | c.1255C>A | Missense_Mutation | 1 | 0.66 | TYKNU | N | 4 | 0 | 0 | N |
MSH2 | LPNVIKALE | LIVER | 414 | p.Q419K | c.1255C>A | Missense_Mutation | 1 | 0.66 | JHH7 | N | 2 | 0 | 2 | N |
MSH2 | LPNVIKALE | STOMACH | 414 | p.Q419K | c.1255C>A | Missense_Mutation | 1 | 0.66 | NCCSTCK140 | N | 2 | 0 | 2 | N |
MSH2 | LPNVIKALE | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 414 | p.Q419K | c.1255C>A | Missense_Mutation | 1 | 0.66 | SKM1 | N | 2 | 0 | 2 | N |
MSH2 | LPNVIKALE | LARGE_INTESTINE | 414 | p.Q419K | c.1255C>A | Missense_Mutation | 1 | 0.66 | SNU283 | N | 2 | 0 | 2 | N |
MSH2 | LPNVIKALE | CENTRAL_NERVOUS_SYSTEM | 414 | p.Q419K | c.1255C>A | Missense_Mutation | 1 | 0.66 | SNU738 | N | 2 | 0 | 2 | N |
MSH2 | LPNVIKALE | OVARY | 414 | p.Q419K | c.1255C>A | Missense_Mutation | 1 | 0.66 | TYKNU | N | 2 | 0 | 2 | N |
MSH2 | NQLPNVIKA | LIVER | 412 | p.Q419K | c.1255C>A | Missense_Mutation | 1 | 0.66 | JHH7 | Y | 7 | 9 | 0 | N |
MSH2 | NQLPNVIKA | STOMACH | 412 | p.Q419K | c.1255C>A | Missense_Mutation | 1 | 0.66 | NCCSTCK140 | Y | 7 | 9 | 0 | N |
MSH2 | NQLPNVIKA | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 412 | p.Q419K | c.1255C>A | Missense_Mutation | 1 | 0.66 | SKM1 | Y | 7 | 9 | 0 | N |
MSH2 | NQLPNVIKA | LARGE_INTESTINE | 412 | p.Q419K | c.1255C>A | Missense_Mutation | 1 | 0.66 | SNU283 | Y | 7 | 9 | 0 | N |
MSH2 | NQLPNVIKA | CENTRAL_NERVOUS_SYSTEM | 412 | p.Q419K | c.1255C>A | Missense_Mutation | 1 | 0.66 | SNU738 | Y | 7 | 9 | 0 | N |
MSH2 | NQLPNVIKA | OVARY | 412 | p.Q419K | c.1255C>A | Missense_Mutation | 1 | 0.66 | TYKNU | Y | 7 | 9 | 0 | N |
MSH2 | NVIKALEKH | LIVER | 416 | p.Q419K | c.1255C>A | Missense_Mutation | 1 | 0.66 | JHH7 | N | 1 | 0 | 0 | N |
MSH2 | NVIKALEKH | STOMACH | 416 | p.Q419K | c.1255C>A | Missense_Mutation | 1 | 0.66 | NCCSTCK140 | N | 1 | 0 | 0 | N |
MSH2 | NVIKALEKH | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 416 | p.Q419K | c.1255C>A | Missense_Mutation | 1 | 0.66 | SKM1 | N | 1 | 0 | 0 | N |
MSH2 | NVIKALEKH | LARGE_INTESTINE | 416 | p.Q419K | c.1255C>A | Missense_Mutation | 1 | 0.66 | SNU283 | N | 1 | 0 | 0 | N |
MSH2 | NVIKALEKH | CENTRAL_NERVOUS_SYSTEM | 416 | p.Q419K | c.1255C>A | Missense_Mutation | 1 | 0.66 | SNU738 | N | 1 | 0 | 0 | N |
MSH2 | NVIKALEKH | OVARY | 416 | p.Q419K | c.1255C>A | Missense_Mutation | 1 | 0.66 | TYKNU | N | 1 | 0 | 0 | N |
MSH2 | PNVIKALEK | LIVER | 415 | p.Q419K | c.1255C>A | Missense_Mutation | 1 | 0.66 | JHH7 | N | 0 | 0 | 0 | N |
MSH2 | PNVIKALEK | STOMACH | 415 | p.Q419K | c.1255C>A | Missense_Mutation | 1 | 0.66 | NCCSTCK140 | N | 0 | 0 | 0 | N |
MSH2 | PNVIKALEK | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 415 | p.Q419K | c.1255C>A | Missense_Mutation | 1 | 0.66 | SKM1 | N | 0 | 0 | 0 | N |
MSH2 | PNVIKALEK | LARGE_INTESTINE | 415 | p.Q419K | c.1255C>A | Missense_Mutation | 1 | 0.66 | SNU283 | N | 0 | 0 | 0 | N |
MSH2 | PNVIKALEK | CENTRAL_NERVOUS_SYSTEM | 415 | p.Q419K | c.1255C>A | Missense_Mutation | 1 | 0.66 | SNU738 | N | 0 | 0 | 0 | N |
MSH2 | PNVIKALEK | OVARY | 415 | p.Q419K | c.1255C>A | Missense_Mutation | 1 | 0.66 | TYKNU | N | 0 | 0 | 0 | N |
MSH2 | QLPNVIKAL | LIVER | 413 | p.Q419K | c.1255C>A | Missense_Mutation | 1 | 0.66 | JHH7 | Y | 15 | 12 | 0 | N |
MSH2 | QLPNVIKAL | STOMACH | 413 | p.Q419K | c.1255C>A | Missense_Mutation | 1 | 0.66 | NCCSTCK140 | Y | 15 | 12 | 0 | N |
MSH2 | QLPNVIKAL | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 413 | p.Q419K | c.1255C>A | Missense_Mutation | 1 | 0.66 | SKM1 | Y | 15 | 12 | 0 | N |
MSH2 | QLPNVIKAL | LARGE_INTESTINE | 413 | p.Q419K | c.1255C>A | Missense_Mutation | 1 | 0.66 | SNU283 | Y | 15 | 12 | 0 | N |
MSH2 | QLPNVIKAL | CENTRAL_NERVOUS_SYSTEM | 413 | p.Q419K | c.1255C>A | Missense_Mutation | 1 | 0.66 | SNU738 | Y | 15 | 12 | 0 | N |
MSH2 | QLPNVIKAL | OVARY | 413 | p.Q419K | c.1255C>A | Missense_Mutation | 1 | 0.66 | TYKNU | Y | 15 | 12 | 0 | N |
MSH2 | VIKALEKHE | LIVER | 417 | p.Q419K | c.1255C>A | Missense_Mutation | 1 | 0.66 | JHH7 | N | 0 | 0 | 0 | N |
MSH2 | VIKALEKHE | STOMACH | 417 | p.Q419K | c.1255C>A | Missense_Mutation | 1 | 0.66 | NCCSTCK140 | N | 0 | 0 | 0 | N |
MSH2 | VIKALEKHE | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 417 | p.Q419K | c.1255C>A | Missense_Mutation | 1 | 0.66 | SKM1 | N | 0 | 0 | 0 | N |
MSH2 | VIKALEKHE | LARGE_INTESTINE | 417 | p.Q419K | c.1255C>A | Missense_Mutation | 1 | 0.66 | SNU283 | N | 0 | 0 | 0 | N |
MSH2 | VIKALEKHE | CENTRAL_NERVOUS_SYSTEM | 417 | p.Q419K | c.1255C>A | Missense_Mutation | 1 | 0.66 | SNU738 | N | 0 | 0 | 0 | N |
MSH2 | VIKALEKHE | OVARY | 417 | p.Q419K | c.1255C>A | Missense_Mutation | 1 | 0.66 | TYKNU | N | 0 | 0 | 0 | N |