MET | ANLGHQRVA | STOMACH | 453 | p.G456fs | c.1366_1366delG | Frame_Shift_Del | 5 | 0.11 | MKN74 | N | 1 | 0 | 0 | N |
MET | ASCRLWFLD | STOMACH | 461 | p.G456fs | c.1366_1366delG | Frame_Shift_Del | 6 | 0.11 | MKN74 | N | 0 | 0 | 0 | N |
MET | CRLWFLDQD | STOMACH | 463 | p.G456fs | c.1366_1366delG | Frame_Shift_Del | 6 | 0.11 | MKN74 | N | 1 | 0 | 0 | N |
MET | DLTIANLGH | STOMACH | 449 | p.G456fs | c.1366_1366delG | Frame_Shift_Del | 1 | 0.11 | MKN74 | N | 0 | 0 | 0 | N |
MET | DQSYIDVYL | LARGE_INTESTINE | 231 | p.V237fs | c.710_710delT | Frame_Shift_Del | 2 | 0.11 | HCT116 | N | 7 | 0 | 0 | N |
MET | DVYLSSEIL | LARGE_INTESTINE | 236 | p.V237fs | c.710_710delT | Frame_Shift_Del | 5 | 0.11 | HCT116 | N | 10 | 0 | 0 | N |
MET | EILTPLSMS | LARGE_INTESTINE | 242 | p.V237fs | c.710_710delT | Frame_Shift_Del | 6 | 0.11 | HCT116 | N | 1 | 0 | 0 | N |
MET | FLDQDHQPL | STOMACH | 467 | p.G456fs | c.1366_1366delG | Frame_Shift_Del | 6 | 0.11 | MKN74 | N | 14 | 0 | 0 | N |
MET | GHQRVASCR | STOMACH | 456 | p.G456fs | c.1366_1366delG | Frame_Shift_Del | 6 | 0.11 | MKN74 | N | 1 | 0 | 0 | N |
MET | HQRVASCRL | STOMACH | 457 | p.G456fs | c.1366_1366delG | Frame_Shift_Del | 6 | 0.11 | MKN74 | N | 8 | 0 | 0 | N |
MET | IANLGHQRV | STOMACH | 452 | p.G456fs | c.1366_1366delG | Frame_Shift_Del | 4 | 0.11 | MKN74 | N | 5 | 0 | 0 | N |
MET | IDVYLSSEI | LARGE_INTESTINE | 235 | p.V237fs | c.710_710delT | Frame_Shift_Del | 5 | 0.11 | HCT116 | N | 7 | 0 | 2 | N |
MET | ILTPLSMSM | LARGE_INTESTINE | 243 | p.V237fs | c.710_710delT | Frame_Shift_Del | 6 | 0.11 | HCT116 | N | 7 | 0 | 0 | N |
MET | LDQDHQPLM | STOMACH | 468 | p.G456fs | c.1366_1366delG | Frame_Shift_Del | 6 | 0.11 | MKN74 | N | 5 | 0 | 0 | N |
MET | LGHQRVASC | STOMACH | 455 | p.G456fs | c.1366_1366delG | Frame_Shift_Del | 5 | 0.11 | MKN74 | N | 1 | 0 | 5 | N |
MET | LKATILFTS | LARGE_INTESTINE | 253 | p.V237fs | c.710_710delT | Frame_Shift_Del | 5 | 0.11 | HCT116 | N | 1 | 0 | 0 | N |
MET | LSMSMPLKA | LARGE_INTESTINE | 247 | p.V237fs | c.710_710delT | Frame_Shift_Del | 5 | 0.11 | HCT116 | N | 4 | 0 | 11 | N |
MET | LSSEILTPL | LARGE_INTESTINE | 239 | p.V237fs | c.710_710delT | Frame_Shift_Del | 5 | 0.11 | HCT116 | N | 16 | 0 | 0 | N |
MET | LTIANLGHQ | STOMACH | 450 | p.G456fs | c.1366_1366delG | Frame_Shift_Del | 2 | 0.11 | MKN74 | N | 0 | 0 | 4 | N |
MET | LTPLSMSMP | LARGE_INTESTINE | 244 | p.V237fs | c.710_710delT | Frame_Shift_Del | 6 | 0.11 | HCT116 | N | 0 | 0 | 0 | N |
MET | LWFLDQDHQ | STOMACH | 465 | p.G456fs | c.1366_1366delG | Frame_Shift_Del | 6 | 0.11 | MKN74 | N | 0 | 0 | 0 | N |
MET | MPLKATILF | LARGE_INTESTINE | 251 | p.V237fs | c.710_710delT | Frame_Shift_Del | 5 | 0.11 | HCT116 | N | 13 | 0 | 4 | N |
MET | MSMPLKATI | LARGE_INTESTINE | 249 | p.V237fs | c.710_710delT | Frame_Shift_Del | 5 | 0.11 | HCT116 | N | 9 | 0 | 0 | N |
MET | NLGHQRVAS | STOMACH | 454 | p.G456fs | c.1366_1366delG | Frame_Shift_Del | 5 | 0.11 | MKN74 | N | 0 | 0 | 0 | N |
MET | PLKATILFT | LARGE_INTESTINE | 252 | p.V237fs | c.710_710delT | Frame_Shift_Del | 5 | 0.11 | HCT116 | N | 0 | 0 | 0 | N |
MET | PLSMSMPLK | LARGE_INTESTINE | 246 | p.V237fs | c.710_710delT | Frame_Shift_Del | 5 | 0.11 | HCT116 | N | 1 | 0 | 0 | N |
MET | QRVASCRLW | STOMACH | 458 | p.G456fs | c.1366_1366delG | Frame_Shift_Del | 6 | 0.11 | MKN74 | N | 2 | 0 | 0 | N |
MET | QSYIDVYLS | LARGE_INTESTINE | 232 | p.V237fs | c.710_710delT | Frame_Shift_Del | 3 | 0.11 | HCT116 | N | 0 | 0 | 0 | N |
MET | RLWFLDQDH | STOMACH | 464 | p.G456fs | c.1366_1366delG | Frame_Shift_Del | 6 | 0.11 | MKN74 | N | 2 | 0 | 0 | N |
MET | RVASCRLWF | STOMACH | 459 | p.G456fs | c.1366_1366delG | Frame_Shift_Del | 6 | 0.11 | MKN74 | Y | 5 | 10 | 0 | N |
MET | SCRLWFLDQ | STOMACH | 462 | p.G456fs | c.1366_1366delG | Frame_Shift_Del | 6 | 0.11 | MKN74 | N | 0 | 0 | 0 | N |
MET | SEILTPLSM | LARGE_INTESTINE | 241 | p.V237fs | c.710_710delT | Frame_Shift_Del | 5 | 0.11 | HCT116 | N | 7 | 0 | 0 | N |
MET | SMPLKATIL | LARGE_INTESTINE | 250 | p.V237fs | c.710_710delT | Frame_Shift_Del | 6 | 0.11 | HCT116 | N | 13 | 0 | 0 | N |
MET | SMSMPLKAT | LARGE_INTESTINE | 248 | p.V237fs | c.710_710delT | Frame_Shift_Del | 5 | 0.11 | HCT116 | N | 2 | 0 | 0 | N |
MET | SSEILTPLS | LARGE_INTESTINE | 240 | p.V237fs | c.710_710delT | Frame_Shift_Del | 5 | 0.11 | HCT116 | N | 1 | 0 | 0 | N |
MET | SYIDVYLSS | LARGE_INTESTINE | 233 | p.V237fs | c.710_710delT | Frame_Shift_Del | 4 | 0.11 | HCT116 | N | 3 | 0 | 0 | N |
MET | TDQSYIDVY | LARGE_INTESTINE | 230 | p.V237fs | c.710_710delT | Frame_Shift_Del | 1 | 0.11 | HCT116 | N | 3 | 0 | 0 | N |
MET | TIANLGHQR | STOMACH | 451 | p.G456fs | c.1366_1366delG | Frame_Shift_Del | 3 | 0.11 | MKN74 | N | 4 | 0 | 0 | N |
MET | TPLSMSMPL | LARGE_INTESTINE | 245 | p.V237fs | c.710_710delT | Frame_Shift_Del | 5 | 0.11 | HCT116 | N | 21 | 0 | 0 | N |
MET | VASCRLWFL | STOMACH | 460 | p.G456fs | c.1366_1366delG | Frame_Shift_Del | 6 | 0.11 | MKN74 | Y | 18 | 10 | 0 | N |
MET | VYLSSEILT | LARGE_INTESTINE | 237 | p.V237fs | c.710_710delT | Frame_Shift_Del | 5 | 0.11 | HCT116 | N | 3 | 0 | 0 | N |
MET | WFLDQDHQP | STOMACH | 466 | p.G456fs | c.1366_1366delG | Frame_Shift_Del | 6 | 0.11 | MKN74 | N | 2 | 0 | 0 | N |
MET | YIDVYLSSE | LARGE_INTESTINE | 234 | p.V237fs | c.710_710delT | Frame_Shift_Del | 5 | 0.11 | HCT116 | N | 2 | 0 | 0 | N |
MET | YLSSEILTP | LARGE_INTESTINE | 238 | p.V237fs | c.710_710delT | Frame_Shift_Del | 5 | 0.11 | HCT116 | N | 3 | 0 | 5 | N |
MET | AAIQSEVHC | STOMACH | 152 | p.D153A | c.458A>C | Missense_Mutation | 1 | 0.11 | SNU719 | N | 3 | 0 | 0 | N |
MET | ACQHHSNSE | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 807 | p.R811H | c.2432G>A | Missense_Mutation | 1 | 0.11 | SUPHD1 | N | 0 | 0 | 0 | N |
MET | ACQHRSNSD | OESOPHAGUS | 807 | p.E815D | c.2445G>C | Missense_Mutation | 1 | 0.11 | TE5 | N | 0 | 0 | 0 | N |
MET | ADCVVSALG | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 173 | p.P173A | c.517C>G | Missense_Mutation | 1 | 0.11 | BCP1 | N | 1 | 0 | 0 | N |
MET | AEYKIGPVL | LARGE_INTESTINE | 82 | p.T86I | c.257C>T | Missense_Mutation | 1 | 0.11 | LS411N | N | 15 | 0 | 0 | N |
MET | AFFMLDRIL | ENDOMETRIUM | 837 | p.G843R | c.2527G>A | Missense_Mutation | 1 | 0.11 | EN | N | 8 | 0 | 0 | N |
MET | AFLCTVPND | LUNG | 909 | p.V910F | c.2728G>T | Missense_Mutation | 1 | 0.11 | DMS273 | N | 0 | 0 | 0 | N |
MET | AIQSEVHCI | STOMACH | 153 | p.D153A | c.458A>C | Missense_Mutation | 1 | 0.11 | SNU719 | N | 3 | 0 | 0 | N |
MET | ANFGLARDM | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1239 | p.D1240N | c.3718G>A | Missense_Mutation | 1 | 0.11 | KMM1 | N | 4 | 0 | 0 | N |
MET | ANIGTSEGR | LARGE_INTESTINE | 453 | p.L455I | c.1363C>A | Missense_Mutation | 1 | 0.11 | HT115 | N | 2 | 0 | 0 | N |
MET | ANLSRGVWK | ENDOMETRIUM | 105 | p.G109R | c.325G>A | Missense_Mutation | 1 | 0.11 | TEN | Y | 0 | 18 | 0 | N |
MET | ARSISPTTE | OESOPHAGUS | 1004 | p.V1007I | c.3019G>A | Missense_Mutation | 1 | 0.11 | OE33 | N | 1 | 0 | 0 | N |
MET | ARSVSSTTE | STOMACH | 1004 | p.P1009S | c.3025C>T | Missense_Mutation | 1 | 0.11 | ECC12 | N | 1 | 0 | 0 | N |
MET | CADCVVSAL | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 172 | p.P173A | c.517C>G | Missense_Mutation | 1 | 0.11 | BCP1 | Y | 10 | 10 | 0 | N |
MET | CDARVHTPH | LUNG | 989 | p.Y989C | c.2966A>G | Missense_Mutation | 1 | 0.11 | NCIH1869 | N | 0 | 0 | 0 | N |
MET | CGNVNRGTC | ENDOMETRIUM | 133 | p.S135N | c.404G>A | Missense_Mutation | 1 | 0.11 | MFE319 | N | 2 | 0 | 0 | N |
MET | CGWDFGFWR | LARGE_INTESTINE | 584 | p.R591W | c.1771C>T | Missense_Mutation | 1 | 0.11 | SNU81 | N | 1 | 0 | 0 | N |
MET | CIFSPQIEK | LUNG | 160 | p.E168K | c.502G>A | Missense_Mutation | 1 | 0.11 | NCIH2342 | Y | 5 | 10 | 0 | N |
MET | CLQSEGSPL | ENDOMETRIUM | 1164 | p.R1166Q | c.3497G>A | Missense_Mutation | 1 | 0.11 | JHUEM7 | N | 12 | 0 | 0 | N |
MET | CQHHSNSEI | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 808 | p.R811H | c.2432G>A | Missense_Mutation | 1 | 0.11 | SUPHD1 | N | 6 | 0 | 0 | N |
MET | CQHRSNSDI | OESOPHAGUS | 808 | p.E815D | c.2445G>C | Missense_Mutation | 1 | 0.11 | TE5 | N | 6 | 0 | 0 | N |
MET | CSQCVSAPP | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 526 | p.L530V | c.1588C>G | Missense_Mutation | 1 | 0.11 | MC116 | N | 0 | 0 | 0 | Y |
MET | CSSKANLSR | ENDOMETRIUM | 101 | p.G109R | c.325G>A | Missense_Mutation | 1 | 0.11 | TEN | N | 3 | 0 | 0 | N |
MET | CVSAPPFVQ | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 529 | p.L530V | c.1588C>G | Missense_Mutation | 1 | 0.11 | MC116 | N | 0 | 0 | 0 | Y |
MET | DDILFRVFA | ENDOMETRIUM | 339 | p.G344R | c.1030G>A | Missense_Mutation | 1 | 0.11 | AN3CA | N | 4 | 0 | 0 | N |
MET | DDQLISCGN | ENDOMETRIUM | 127 | p.S135N | c.404G>A | Missense_Mutation | 1 | 0.11 | MFE319 | N | 2 | 0 | 0 | N |
MET | DEKFTVKIA | KIDNEY | 1231 | p.V1238I | c.3712G>A | Missense_Mutation | 1 | 0.11 | CAKI1 | Y | 5 | 10 | 0 | N |
MET | DFFNKIINK | BONE | 372 | p.V378I | c.1132G>A | Missense_Mutation | 1 | 0.11 | OUMS27 | Y | 2 | 11 | 0 | N |
MET | DFGFWRNNK | LARGE_INTESTINE | 587 | p.R591W | c.1771C>T | Missense_Mutation | 1 | 0.11 | SNU81 | Y | 0 | 10 | 0 | Y |
MET | DFSHPNVFS | LUNG | 1151 | p.L1158F | c.3472C>T | Missense_Mutation | 1 | 0.11 | HCC15 | N | 0 | 0 | 0 | N |
MET | DFSHPNVLL | LARGE_INTESTINE | 1151 | p.S1159L | c.3476C>T | Missense_Mutation | 1 | 0.11 | SNUC5 | Y | 6 | 9 | 0 | N |
MET | DHVNATYVN | ENDOMETRIUM | 1368 | p.V1368D | c.4103T>A | Missense_Mutation | 1 | 0.11 | HEC1A | N | 1 | 0 | 0 | N |
MET | DIICCTTPS | OESOPHAGUS | 815 | p.E815D | c.2445G>C | Missense_Mutation | 1 | 0.11 | TE5 | N | 1 | 0 | 0 | N |
MET | DILFRVFAQ | ENDOMETRIUM | 340 | p.G344R | c.1030G>A | Missense_Mutation | 1 | 0.11 | AN3CA | N | 1 | 0 | 0 | N |
MET | DLFYVHNPV | LUNG | 850 | p.I852F | c.2554A>T | Missense_Mutation | 1 | 0.11 | NCIH1339 | N | 11 | 0 | 0 | N |
MET | DLGSELVRC | LUNG | 981 | p.Y989C | c.2966A>G | Missense_Mutation | 1 | 0.11 | NCIH1869 | N | 1 | 0 | 0 | N |
MET | DLIHVHNPV | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 850 | p.Y853H | c.2557T>C | Missense_Mutation | 1 | 0.11 | HUNS1 | Y | 5 | 9 | 0 | N |
MET | DLKKTRVVL | CENTRAL_NERVOUS_SYSTEM | 597 | p.L604V | c.1810C>G | Missense_Mutation | 1 | 0.11 | BECKER | Y | 7 | 10 | 0 | N |
MET | DLQNFIRNE | ENDOMETRIUM | 1182 | p.R1184Q | c.3551G>A | Missense_Mutation | 1 | 0.11 | HEC251 | N | 0 | 0 | 0 | N |
MET | DLTIANIGT | LARGE_INTESTINE | 449 | p.L455I | c.1363C>A | Missense_Mutation | 1 | 0.11 | HT115 | N | 1 | 0 | 0 | N |
MET | DQLISCGNV | ENDOMETRIUM | 128 | p.S135N | c.404G>A | Missense_Mutation | 1 | 0.11 | MFE319 | Y | 3 | 9 | 0 | N |
MET | DRILSKYFD | ENDOMETRIUM | 842 | p.G843R | c.2527G>A | Missense_Mutation | 1 | 0.11 | EN | N | 0 | 0 | 0 | N |
MET | DRLVSARSI | OESOPHAGUS | 999 | p.V1007I | c.3019G>A | Missense_Mutation | 1 | 0.11 | OE33 | N | 5 | 0 | 0 | N |
MET | DVLPEFRDY | LIVER | 236 | p.S244Y | c.731C>A | Missense_Mutation | 1 | 0.11 | C3A | N | 5 | 0 | 0 | N |
MET | DYYPIKYVH | LIVER | 243 | p.S244Y | c.731C>A | Missense_Mutation | 1 | 0.11 | C3A | N | 1 | 0 | 0 | N |
MET | EAFLCTVPN | LUNG | 908 | p.V910F | c.2728G>T | Missense_Mutation | 1 | 0.11 | DMS273 | N | 3 | 0 | 0 | N |
MET | EEPSQCADC | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 167 | p.P173A | c.517C>G | Missense_Mutation | 1 | 0.11 | BCP1 | N | 5 | 0 | 0 | N |
MET | EFRDYYPIK | LIVER | 240 | p.S244Y | c.731C>A | Missense_Mutation | 1 | 0.11 | C3A | N | 0 | 0 | 0 | N |
MET | EHYDHVNAT | ENDOMETRIUM | 1365 | p.V1368D | c.4103T>A | Missense_Mutation | 1 | 0.11 | HEC1A | N | 3 | 0 | 0 | N |
MET | EIHPTKYFI | ENDOMETRIUM | 746 | p.S752Y | c.2255C>A | Missense_Mutation | 1 | 0.11 | JHUEM7 | N | 4 | 0 | 0 | N |
MET | EKFTVKIAD | KIDNEY | 1232 | p.V1238I | c.3712G>A | Missense_Mutation | 1 | 0.11 | CAKI1 | N | 0 | 0 | 0 | N |
MET | EKFTVKVAN | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1232 | p.D1240N | c.3718G>A | Missense_Mutation | 1 | 0.11 | KMM1 | N | 1 | 0 | 0 | N |
MET | EKPSQCPDC | LUNG | 167 | p.E168K | c.502G>A | Missense_Mutation | 1 | 0.11 | NCIH2342 | N | 1 | 0 | 0 | Y |
MET | ELVRCDARV | LUNG | 985 | p.Y989C | c.2966A>G | Missense_Mutation | 1 | 0.11 | NCIH1869 | Y | 4 | 11 | 0 | N |
MET | EPSQCADCV | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 168 | p.P173A | c.517C>G | Missense_Mutation | 1 | 0.11 | BCP1 | N | 11 | 0 | 0 | N |
MET | ESLNIVSFL | SKIN | 760 | p.P761S | c.2281C>T | Missense_Mutation | 1 | 0.11 | CHL1 | Y | 16 | 11 | 0 | N |
MET | ETHNPTVKH | BREAST | 1190 | p.D1198H | c.3592G>C | Missense_Mutation | 1 | 0.11 | HCC202 | N | 0 | 0 | 0 | N |
MET | EYKIGPVLE | LARGE_INTESTINE | 83 | p.T86I | c.257C>T | Missense_Mutation | 1 | 0.11 | LS411N | N | 0 | 0 | 0 | Y |
MET | FDLFYVHNP | LUNG | 849 | p.I852F | c.2554A>T | Missense_Mutation | 1 | 0.11 | NCIH1339 | N | 2 | 0 | 0 | N |
MET | FDLIHVHNP | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 849 | p.Y853H | c.2557T>C | Missense_Mutation | 1 | 0.11 | HUNS1 | N | 2 | 0 | 0 | N |
MET | FDLKKTRVV | CENTRAL_NERVOUS_SYSTEM | 596 | p.L604V | c.1810C>G | Missense_Mutation | 1 | 0.11 | BECKER | N | 8 | 0 | 6 | N |
MET | FFLWLKKTK | LARGE_INTESTINE | 969 | p.R976T | c.2927G>C | Missense_Mutation | 1 | 0.11 | NCIH508 | N | 3 | 0 | 17 | N |
MET | FFMLDRILS | ENDOMETRIUM | 838 | p.G843R | c.2527G>A | Missense_Mutation | 1 | 0.11 | EN | N | 2 | 0 | 41 | N |
MET | FFNKIINKN | BONE | 373 | p.V378I | c.1132G>A | Missense_Mutation | 1 | 0.11 | OUMS27 | N | 1 | 0 | 9 | N |
MET | FGFWRNNKF | LARGE_INTESTINE | 588 | p.R591W | c.1771C>T | Missense_Mutation | 1 | 0.11 | SNU81 | N | 11 | 0 | 6 | N |
MET | FIGEHYDHV | ENDOMETRIUM | 1362 | p.V1368D | c.4103T>A | Missense_Mutation | 1 | 0.11 | HEC1A | N | 6 | 0 | 0 | N |
MET | FILVQRSNG | SKIN | 16 | p.T17I | c.50C>T | Missense_Mutation | 1 | 0.11 | RPMI7951 | N | 2 | 0 | 10 | N |
MET | FISTWWKES | SKIN | 753 | p.P761S | c.2281C>T | Missense_Mutation | 1 | 0.11 | CHL1 | N | 2 | 0 | 0 | N |
MET | FLCTVPNDL | LUNG | 910 | p.V910F | c.2728G>T | Missense_Mutation | 1 | 0.11 | DMS273 | N | 14 | 0 | 5 | N |
MET | FLWLKKTKQ | LARGE_INTESTINE | 970 | p.R976T | c.2927G>C | Missense_Mutation | 1 | 0.11 | NCIH508 | N | 3 | 0 | 10 | Y |
MET | FMLDRILSK | ENDOMETRIUM | 839 | p.G843R | c.2527G>A | Missense_Mutation | 1 | 0.11 | EN | Y | 8 | 10 | 17 | N |
MET | FNKIINKNN | BONE | 374 | p.V378I | c.1132G>A | Missense_Mutation | 1 | 0.11 | OUMS27 | N | 2 | 0 | 1 | N |
MET | FNMSLIISN | LUNG | 634 | p.I638L | c.1912A>T | Missense_Mutation | 1 | 0.11 | NCIH838 | N | 3 | 0 | 12 | N |
MET | FPHNHTAAI | STOMACH | 146 | p.D153A | c.458A>C | Missense_Mutation | 1 | 0.11 | SNU719 | N | 13 | 0 | 3 | N |
MET | FQSCSQCVS | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 523 | p.L530V | c.1588C>G | Missense_Mutation | 1 | 0.11 | MC116 | N | 2 | 0 | 11 | Y |
MET | FRDYYPIKY | LIVER | 241 | p.S244Y | c.731C>A | Missense_Mutation | 1 | 0.11 | C3A | Y | 7 | 10 | 7 | N |
MET | FRVFAQSKP | ENDOMETRIUM | 343 | p.G344R | c.1030G>A | Missense_Mutation | 1 | 0.11 | AN3CA | N | 3 | 0 | 3 | N |
MET | FSHPNVFSL | LUNG | 1152 | p.L1158F | c.3472C>T | Missense_Mutation | 1 | 0.11 | HCC15 | Y | 17 | 10 | 2 | Y |
MET | FSHPNVLLL | LARGE_INTESTINE | 1152 | p.S1159L | c.3476C>T | Missense_Mutation | 1 | 0.11 | SNUC5 | Y | 18 | 12 | 2 | N |
MET | FSLLGICLR | LUNG | 1158 | p.L1158F | c.3472C>T | Missense_Mutation | 1 | 0.11 | HCC15 | Y | 5 | 9 | 9 | N |
MET | FSPQIEKPS | LUNG | 162 | p.E168K | c.502G>A | Missense_Mutation | 1 | 0.11 | NCIH2342 | N | 2 | 0 | 0 | N |
MET | FTVACQHHS | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 804 | p.R811H | c.2432G>A | Missense_Mutation | 1 | 0.11 | SUPHD1 | N | 2 | 0 | 0 | N |
MET | FTVKIADFG | KIDNEY | 1234 | p.V1238I | c.3712G>A | Missense_Mutation | 1 | 0.11 | CAKI1 | N | 2 | 0 | 0 | N |
MET | FTVKVANFG | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1234 | p.D1240N | c.3718G>A | Missense_Mutation | 1 | 0.11 | KMM1 | N | 2 | 0 | 2 | N |
MET | FWRNNKFDL | LARGE_INTESTINE | 590 | p.R591W | c.1771C>T | Missense_Mutation | 1 | 0.11 | SNU81 | N | 9 | 0 | 5 | N |
MET | FYVHNPVFK | LUNG | 852 | p.I852F | c.2554A>T | Missense_Mutation | 1 | 0.11 | NCIH1339 | Y | 3 | 16 | 13 | N |
MET | GDLQNFIRN | ENDOMETRIUM | 1181 | p.R1184Q | c.3551G>A | Missense_Mutation | 1 | 0.11 | HEC251 | N | 2 | 0 | 0 | N |
MET | GDLTIANIG | LARGE_INTESTINE | 448 | p.L455I | c.1363C>A | Missense_Mutation | 1 | 0.11 | HT115 | N | 0 | 0 | 0 | N |
MET | GEHYDHVNA | ENDOMETRIUM | 1364 | p.V1368D | c.4103T>A | Missense_Mutation | 1 | 0.11 | HEC1A | N | 6 | 0 | 0 | N |
MET | GFFLWLKKT | LARGE_INTESTINE | 968 | p.R976T | c.2927G>C | Missense_Mutation | 1 | 0.11 | NCIH508 | N | 1 | 0 | 0 | N |
MET | GFWRNNKFD | LARGE_INTESTINE | 589 | p.R591W | c.1771C>T | Missense_Mutation | 1 | 0.11 | SNU81 | N | 1 | 0 | 0 | N |
MET | GICLQSEGS | ENDOMETRIUM | 1162 | p.R1166Q | c.3497G>A | Missense_Mutation | 1 | 0.11 | JHUEM7 | N | 0 | 0 | 0 | N |
MET | GILVLLFIL | SKIN | 10 | p.T17I | c.50C>T | Missense_Mutation | 1 | 0.11 | RPMI7951 | N | 16 | 0 | 0 | N |
MET | GKKITKIPM | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 507 | p.L515M | c.1543T>A | Missense_Mutation | 1 | 0.11 | KIJK | N | 3 | 0 | 0 | N |
MET | GKLIVQPDQ | LUNG | 939 | p.V941L | c.2821G>T | Missense_Mutation | 1 | 0.11 | NCIH1838 | N | 0 | 0 | 0 | N |
MET | GNVNRGTCQ | ENDOMETRIUM | 134 | p.S135N | c.404G>A | Missense_Mutation | 1 | 0.11 | MFE319 | N | 0 | 0 | 0 | N |
MET | GSELVRCDA | LUNG | 983 | p.Y989C | c.2966A>G | Missense_Mutation | 1 | 0.11 | NCIH1869 | N | 2 | 0 | 0 | N |
MET | GWDFGFWRN | LARGE_INTESTINE | 585 | p.R591W | c.1771C>T | Missense_Mutation | 1 | 0.11 | SNU81 | N | 0 | 0 | 0 | N |
MET | HFNMSLIIS | LUNG | 633 | p.I638L | c.1912A>T | Missense_Mutation | 1 | 0.11 | NCIH838 | N | 0 | 0 | 0 | N |
MET | HFQSCSQCV | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 522 | p.L530V | c.1588C>G | Missense_Mutation | 1 | 0.11 | MC116 | N | 3 | 0 | 0 | N |
MET | HGDLQNFIR | ENDOMETRIUM | 1180 | p.R1184Q | c.3551G>A | Missense_Mutation | 1 | 0.11 | HEC251 | N | 2 | 0 | 0 | N |
MET | HHSNSEIIC | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 810 | p.R811H | c.2432G>A | Missense_Mutation | 1 | 0.11 | SUPHD1 | N | 1 | 0 | 0 | N |
MET | HLHSEAFLC | LUNG | 904 | p.V910F | c.2728G>T | Missense_Mutation | 1 | 0.11 | DMS273 | N | 2 | 0 | 0 | N |
MET | HLIGFGLQV | BREAST | 1198 | p.D1198H | c.3592G>C | Missense_Mutation | 1 | 0.11 | HCC202 | N | 7 | 0 | 0 | N |
MET | HNHTAAIQS | STOMACH | 148 | p.D153A | c.458A>C | Missense_Mutation | 1 | 0.11 | SNU719 | N | 0 | 0 | 0 | N |
MET | HNPTVKHLI | BREAST | 1192 | p.D1198H | c.3592G>C | Missense_Mutation | 1 | 0.11 | HCC202 | N | 5 | 0 | 0 | N |
MET | HPNVFSLLG | LUNG | 1154 | p.L1158F | c.3472C>T | Missense_Mutation | 1 | 0.11 | HCC15 | N | 1 | 0 | 0 | N |
MET | HPNVLLLLG | LARGE_INTESTINE | 1154 | p.S1159L | c.3476C>T | Missense_Mutation | 1 | 0.11 | SNUC5 | N | 1 | 0 | 0 | N |
MET | HPTKYFIST | ENDOMETRIUM | 748 | p.S752Y | c.2255C>A | Missense_Mutation | 1 | 0.11 | JHUEM7 | N | 5 | 0 | 0 | N |
MET | HRSNSDIIC | OESOPHAGUS | 810 | p.E815D | c.2445G>C | Missense_Mutation | 1 | 0.11 | TE5 | N | 2 | 0 | 0 | N |
MET | HSEAFLCTV | LUNG | 906 | p.V910F | c.2728G>T | Missense_Mutation | 1 | 0.11 | DMS273 | N | 5 | 0 | 0 | N |
MET | HSNSEIICC | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 811 | p.R811H | c.2432G>A | Missense_Mutation | 1 | 0.11 | SUPHD1 | N | 1 | 0 | 0 | N |
MET | HTAAIQSEV | STOMACH | 150 | p.D153A | c.458A>C | Missense_Mutation | 1 | 0.11 | SNU719 | N | 2 | 0 | 0 | N |
MET | HVHNPVFKP | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 853 | p.Y853H | c.2557T>C | Missense_Mutation | 1 | 0.11 | HUNS1 | N | 0 | 0 | 0 | N |
MET | HYDHVNATY | ENDOMETRIUM | 1366 | p.V1368D | c.4103T>A | Missense_Mutation | 1 | 0.11 | HEC1A | Y | 6 | 11 | 0 | N |
MET | IANIGTSEG | LARGE_INTESTINE | 452 | p.L455I | c.1363C>A | Missense_Mutation | 1 | 0.11 | HT115 | N | 0 | 0 | 6 | N |
MET | ICGWDFGFW | LARGE_INTESTINE | 583 | p.R591W | c.1771C>T | Missense_Mutation | 1 | 0.11 | SNU81 | N | 3 | 0 | 0 | N |
MET | ICLQSEGSP | ENDOMETRIUM | 1163 | p.R1166Q | c.3497G>A | Missense_Mutation | 1 | 0.11 | JHUEM7 | N | 0 | 0 | 0 | N |
MET | IEEPSQCAD | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 166 | p.P173A | c.517C>G | Missense_Mutation | 1 | 0.11 | BCP1 | N | 0 | 0 | 0 | N |
MET | IEKPSQCPD | LUNG | 166 | p.E168K | c.502G>A | Missense_Mutation | 1 | 0.11 | NCIH2342 | N | 0 | 0 | 0 | N |
MET | IFSPQIEKP | LUNG | 161 | p.E168K | c.502G>A | Missense_Mutation | 1 | 0.11 | NCIH2342 | N | 0 | 0 | 0 | N |
MET | IGEHYDHVN | ENDOMETRIUM | 1363 | p.V1368D | c.4103T>A | Missense_Mutation | 1 | 0.11 | HEC1A | N | 0 | 0 | 0 | N |
MET | IGPVLEHPD | LARGE_INTESTINE | 86 | p.T86I | c.257C>T | Missense_Mutation | 1 | 0.11 | LS411N | N | 0 | 0 | 0 | N |
MET | IGTSEGRFM | LARGE_INTESTINE | 455 | p.L455I | c.1363C>A | Missense_Mutation | 1 | 0.11 | HT115 | N | 6 | 0 | 0 | N |
MET | IHLHSEAFL | LUNG | 903 | p.V910F | c.2728G>T | Missense_Mutation | 1 | 0.11 | DMS273 | N | 10 | 0 | 0 | N |
MET | IHPTKYFIS | ENDOMETRIUM | 747 | p.S752Y | c.2255C>A | Missense_Mutation | 1 | 0.11 | JHUEM7 | N | 3 | 0 | 0 | N |
MET | IHVHNPVFK | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 852 | p.Y853H | c.2557T>C | Missense_Mutation | 1 | 0.11 | HUNS1 | N | 0 | 0 | 9 | N |
MET | IINKNNVRC | BONE | 377 | p.V378I | c.1132G>A | Missense_Mutation | 1 | 0.11 | OUMS27 | N | 1 | 0 | 4 | N |
MET | ILFRVFAQS | ENDOMETRIUM | 341 | p.G344R | c.1030G>A | Missense_Mutation | 1 | 0.11 | AN3CA | N | 4 | 0 | 6 | N |
MET | ILSKYFDLF | LUNG | 844 | p.I852F | c.2554A>T | Missense_Mutation | 1 | 0.11 | NCIH1339 | N | 9 | 0 | 0 | N |
MET | ILVLLFILV | SKIN | 11 | p.T17I | c.50C>T | Missense_Mutation | 1 | 0.11 | RPMI7951 | Y | 9 | 10 | 4 | N |
MET | ILVQRSNGE | SKIN | 17 | p.T17I | c.50C>T | Missense_Mutation | 1 | 0.11 | RPMI7951 | N | 0 | 0 | 4 | N |
MET | INKNNVRCL | BONE | 378 | p.V378I | c.1132G>A | Missense_Mutation | 1 | 0.11 | OUMS27 | Y | 9 | 14 | 12 | N |
MET | IPMNGLGCR | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 513 | p.L515M | c.1543T>A | Missense_Mutation | 1 | 0.11 | KIJK | N | 6 | 0 | 0 | N |
MET | ISCGNVNRG | ENDOMETRIUM | 131 | p.S135N | c.404G>A | Missense_Mutation | 1 | 0.11 | MFE319 | N | 0 | 0 | 0 | N |
MET | ISPTTEMVS | OESOPHAGUS | 1007 | p.V1007I | c.3019G>A | Missense_Mutation | 1 | 0.11 | OE33 | N | 0 | 0 | 0 | N |
MET | ISSTVLGKL | LUNG | 933 | p.V941L | c.2821G>T | Missense_Mutation | 1 | 0.11 | NCIH1838 | Y | 11 | 10 | 0 | N |
MET | ISTWWKESL | SKIN | 754 | p.P761S | c.2281C>T | Missense_Mutation | 1 | 0.11 | CHL1 | N | 10 | 0 | 0 | Y |
MET | ITKIPMNGL | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 510 | p.L515M | c.1543T>A | Missense_Mutation | 1 | 0.11 | KIJK | Y | 6 | 12 | 2 | N |
MET | KAFFMLDRI | ENDOMETRIUM | 836 | p.G843R | c.2527G>A | Missense_Mutation | 1 | 0.11 | EN | Y | 12 | 10 | 0 | N |
MET | KANLSRGVW | ENDOMETRIUM | 104 | p.G109R | c.325G>A | Missense_Mutation | 1 | 0.11 | TEN | N | 4 | 0 | 0 | N |
MET | KDFSHPNVF | LUNG | 1150 | p.L1158F | c.3472C>T | Missense_Mutation | 1 | 0.11 | HCC15 | N | 9 | 0 | 0 | N |
MET | KESLNIVSF | SKIN | 759 | p.P761S | c.2281C>T | Missense_Mutation | 1 | 0.11 | CHL1 | Y | 10 | 9 | 0 | N |
MET | KFTVKIADF | KIDNEY | 1233 | p.V1238I | c.3712G>A | Missense_Mutation | 1 | 0.11 | CAKI1 | N | 6 | 0 | 0 | N |
MET | KFTVKVANF | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1233 | p.D1240N | c.3718G>A | Missense_Mutation | 1 | 0.11 | KMM1 | Y | 6 | 9 | 0 | N |
MET | KGDLTIANI | LARGE_INTESTINE | 447 | p.L455I | c.1363C>A | Missense_Mutation | 1 | 0.11 | HT115 | Y | 6 | 9 | 0 | N |
MET | KHFNMSLII | LUNG | 632 | p.I638L | c.1912A>T | Missense_Mutation | 1 | 0.11 | NCIH838 | N | 8 | 0 | 0 | N |
MET | KHGDLQNFI | ENDOMETRIUM | 1179 | p.R1184Q | c.3551G>A | Missense_Mutation | 1 | 0.11 | HEC251 | N | 4 | 0 | 0 | N |
MET | KHLIGFGLQ | BREAST | 1197 | p.D1198H | c.3592G>C | Missense_Mutation | 1 | 0.11 | HCC202 | N | 0 | 0 | 0 | N |
MET | KIGPVLEHP | LARGE_INTESTINE | 85 | p.T86I | c.257C>T | Missense_Mutation | 1 | 0.11 | LS411N | N | 0 | 0 | 0 | N |
MET | KIINKNNVR | BONE | 376 | p.V378I | c.1132G>A | Missense_Mutation | 1 | 0.11 | OUMS27 | N | 6 | 0 | 0 | N |
MET | KIPMNGLGC | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 512 | p.L515M | c.1543T>A | Missense_Mutation | 1 | 0.11 | KIJK | N | 2 | 0 | 0 | N |
MET | KITKIPMNG | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 509 | p.L515M | c.1543T>A | Missense_Mutation | 1 | 0.11 | KIJK | N | 0 | 0 | 0 | N |
MET | KKITKIPMN | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 508 | p.L515M | c.1543T>A | Missense_Mutation | 1 | 0.11 | KIJK | N | 1 | 0 | 0 | N |
MET | KKTKQIKDL | LARGE_INTESTINE | 974 | p.R976T | c.2927G>C | Missense_Mutation | 1 | 0.11 | NCIH508 | N | 6 | 0 | 0 | N |
MET | KKTRVVLGN | CENTRAL_NERVOUS_SYSTEM | 599 | p.L604V | c.1810C>G | Missense_Mutation | 1 | 0.11 | BECKER | N | 1 | 0 | 0 | N |
MET | KLIVQPDQN | LUNG | 940 | p.V941L | c.2821G>T | Missense_Mutation | 1 | 0.11 | NCIH1838 | N | 0 | 0 | 0 | N |
MET | KPSQCPDCV | LUNG | 168 | p.E168K | c.502G>A | Missense_Mutation | 1 | 0.11 | NCIH2342 | N | 11 | 0 | 0 | N |
MET | KTKQIKDLG | LARGE_INTESTINE | 975 | p.R976T | c.2927G>C | Missense_Mutation | 1 | 0.11 | NCIH508 | N | 2 | 0 | 0 | N |
MET | KTRVVLGNE | CENTRAL_NERVOUS_SYSTEM | 600 | p.L604V | c.1810C>G | Missense_Mutation | 1 | 0.11 | BECKER | Y | 1 | 12 | 0 | N |
MET | KVAEYKIGP | LARGE_INTESTINE | 80 | p.T86I | c.257C>T | Missense_Mutation | 1 | 0.11 | LS411N | N | 0 | 0 | 0 | N |
MET | KVANFGLAR | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1237 | p.D1240N | c.3718G>A | Missense_Mutation | 1 | 0.11 | KMM1 | Y | 6 | 10 | 0 | N |
MET | KYFDLFYVH | LUNG | 847 | p.I852F | c.2554A>T | Missense_Mutation | 1 | 0.11 | NCIH1339 | N | 1 | 0 | 0 | N |
MET | KYFDLIHVH | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 847 | p.Y853H | c.2557T>C | Missense_Mutation | 1 | 0.11 | HUNS1 | N | 0 | 0 | 0 | N |
MET | KYFISTWWK | ENDOMETRIUM | 751 | p.S752Y | c.2255C>A | Missense_Mutation | 1 | 0.11 | JHUEM7 | Y | 3 | 15 | 0 | N |
MET | LDEKFTVKI | KIDNEY | 1230 | p.V1238I | c.3712G>A | Missense_Mutation | 1 | 0.11 | CAKI1 | N | 5 | 0 | 0 | N |
MET | LDRILSKYF | ENDOMETRIUM | 841 | p.G843R | c.2527G>A | Missense_Mutation | 1 | 0.11 | EN | N | 5 | 0 | 0 | N |
MET | LFILVQRSN | SKIN | 15 | p.T17I | c.50C>T | Missense_Mutation | 1 | 0.11 | RPMI7951 | N | 0 | 0 | 9 | N |
MET | LFRVFAQSK | ENDOMETRIUM | 342 | p.G344R | c.1030G>A | Missense_Mutation | 1 | 0.11 | AN3CA | N | 1 | 0 | 2 | N |
MET | LFYVHNPVF | LUNG | 851 | p.I852F | c.2554A>T | Missense_Mutation | 1 | 0.11 | NCIH1339 | N | 8 | 0 | 0 | N |
MET | LGICLQSEG | ENDOMETRIUM | 1161 | p.R1166Q | c.3497G>A | Missense_Mutation | 1 | 0.11 | JHUEM7 | N | 0 | 0 | 0 | N |
MET | LGKLIVQPD | LUNG | 938 | p.V941L | c.2821G>T | Missense_Mutation | 1 | 0.11 | NCIH1838 | N | 0 | 0 | 3 | N |
MET | LGSELVRCD | LUNG | 982 | p.Y989C | c.2966A>G | Missense_Mutation | 1 | 0.11 | NCIH1869 | N | 0 | 0 | 1 | N |
MET | LHSEAFLCT | LUNG | 905 | p.V910F | c.2728G>T | Missense_Mutation | 1 | 0.11 | DMS273 | N | 1 | 0 | 0 | N |
MET | LIHVHNPVF | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 851 | p.Y853H | c.2557T>C | Missense_Mutation | 1 | 0.11 | HUNS1 | N | 5 | 0 | 0 | N |
MET | LIISNGHGT | LUNG | 638 | p.I638L | c.1912A>T | Missense_Mutation | 1 | 0.11 | NCIH838 | N | 3 | 0 | 3 | N |
MET | LISCGNVNR | ENDOMETRIUM | 130 | p.S135N | c.404G>A | Missense_Mutation | 1 | 0.11 | MFE319 | N | 4 | 0 | 1 | N |
MET | LIVQPDQNF | LUNG | 941 | p.V941L | c.2821G>T | Missense_Mutation | 1 | 0.11 | NCIH1838 | N | 4 | 0 | 0 | N |
MET | LKKTKQIKD | LARGE_INTESTINE | 973 | p.R976T | c.2927G>C | Missense_Mutation | 1 | 0.11 | NCIH508 | N | 0 | 0 | 0 | N |
MET | LKKTRVVLG | CENTRAL_NERVOUS_SYSTEM | 598 | p.L604V | c.1810C>G | Missense_Mutation | 1 | 0.11 | BECKER | N | 0 | 0 | 0 | N |
MET | LLFILVQRS | SKIN | 14 | p.T17I | c.50C>T | Missense_Mutation | 1 | 0.11 | RPMI7951 | N | 1 | 0 | 42 | N |
MET | LLGICLQSE | ENDOMETRIUM | 1160 | p.R1166Q | c.3497G>A | Missense_Mutation | 1 | 0.11 | JHUEM7 | N | 0 | 0 | 0 | N |
MET | LLLGICLRS | LARGE_INTESTINE | 1159 | p.S1159L | c.3476C>T | Missense_Mutation | 1 | 0.11 | SNUC5 | N | 0 | 0 | 17 | N |
MET | LLLLGICLR | LARGE_INTESTINE | 1158 | p.S1159L | c.3476C>T | Missense_Mutation | 1 | 0.11 | SNUC5 | Y | 5 | 9 | 23 | N |
MET | LNDDILFRV | ENDOMETRIUM | 337 | p.G344R | c.1030G>A | Missense_Mutation | 1 | 0.11 | AN3CA | N | 6 | 0 | 0 | N |
MET | LPEFRDYYP | LIVER | 238 | p.S244Y | c.731C>A | Missense_Mutation | 1 | 0.11 | C3A | N | 2 | 0 | 0 | N |
MET | LQKVAEYKI | LARGE_INTESTINE | 78 | p.T86I | c.257C>T | Missense_Mutation | 1 | 0.11 | LS411N | N | 8 | 0 | 0 | N |
MET | LQNFIRNET | ENDOMETRIUM | 1183 | p.R1184Q | c.3551G>A | Missense_Mutation | 1 | 0.11 | HEC251 | N | 2 | 0 | 14 | N |
MET | LQSEGSPLV | ENDOMETRIUM | 1165 | p.R1166Q | c.3497G>A | Missense_Mutation | 1 | 0.11 | JHUEM7 | N | 8 | 0 | 3 | N |
MET | LSKYFDLFY | LUNG | 845 | p.I852F | c.2554A>T | Missense_Mutation | 1 | 0.11 | NCIH1339 | N | 7 | 0 | 0 | N |
MET | LSKYFDLIH | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 845 | p.Y853H | c.2557T>C | Missense_Mutation | 1 | 0.11 | HUNS1 | N | 0 | 0 | 0 | N |
MET | LSLLGICLQ | ENDOMETRIUM | 1158 | p.R1166Q | c.3497G>A | Missense_Mutation | 1 | 0.11 | JHUEM7 | N | 0 | 0 | 19 | N |
MET | LSRGVWKDN | ENDOMETRIUM | 107 | p.G109R | c.325G>A | Missense_Mutation | 1 | 0.11 | TEN | N | 0 | 0 | 0 | N |
MET | LTIANIGTS | LARGE_INTESTINE | 450 | p.L455I | c.1363C>A | Missense_Mutation | 1 | 0.11 | HT115 | N | 0 | 0 | 12 | N |
MET | LVLLFILVQ | SKIN | 12 | p.T17I | c.50C>T | Missense_Mutation | 1 | 0.11 | RPMI7951 | N | 0 | 0 | 47 | N |
MET | LVRCDARVH | LUNG | 986 | p.Y989C | c.2966A>G | Missense_Mutation | 1 | 0.11 | NCIH1869 | N | 0 | 0 | 30 | N |
MET | LVSARSISP | OESOPHAGUS | 1001 | p.V1007I | c.3019G>A | Missense_Mutation | 1 | 0.11 | OE33 | N | 0 | 0 | 7 | N |
MET | LVSARSVSS | STOMACH | 1001 | p.P1009S | c.3025C>T | Missense_Mutation | 1 | 0.11 | ECC12 | N | 0 | 0 | 36 | N |
MET | LWLKKTKQI | LARGE_INTESTINE | 971 | p.R976T | c.2927G>C | Missense_Mutation | 1 | 0.11 | NCIH508 | N | 8 | 0 | 13 | N |
MET | MKHGDLQNF | ENDOMETRIUM | 1178 | p.R1184Q | c.3551G>A | Missense_Mutation | 1 | 0.11 | HEC251 | N | 3 | 0 | 0 | N |
MET | MLDRILSKY | ENDOMETRIUM | 840 | p.G843R | c.2527G>A | Missense_Mutation | 1 | 0.11 | EN | N | 7 | 0 | 0 | N |
MET | MNGLGCRHF | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 515 | p.L515M | c.1543T>A | Missense_Mutation | 1 | 0.11 | KIJK | Y | 3 | 13 | 9 | N |
MET | MNKHFNMSL | LUNG | 630 | p.I638L | c.1912A>T | Missense_Mutation | 1 | 0.11 | NCIH838 | Y | 9 | 15 | 9 | N |
MET | MSLIISNGH | LUNG | 636 | p.I638L | c.1912A>T | Missense_Mutation | 1 | 0.11 | NCIH838 | N | 0 | 0 | 8 | N |
MET | NDDILFRVF | ENDOMETRIUM | 338 | p.G344R | c.1030G>A | Missense_Mutation | 1 | 0.11 | AN3CA | N | 4 | 0 | 0 | N |
MET | NDFFNKIIN | BONE | 371 | p.V378I | c.1132G>A | Missense_Mutation | 1 | 0.11 | OUMS27 | N | 1 | 0 | 0 | N |
MET | NFGLARDMY | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1240 | p.D1240N | c.3718G>A | Missense_Mutation | 1 | 0.11 | KMM1 | N | 2 | 0 | 0 | N |
MET | NFTVACQHH | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 803 | p.R811H | c.2432G>A | Missense_Mutation | 1 | 0.11 | SUPHD1 | N | 0 | 0 | 0 | N |
MET | NHTAAIQSE | STOMACH | 149 | p.D153A | c.458A>C | Missense_Mutation | 1 | 0.11 | SNU719 | N | 0 | 0 | 0 | N |
MET | NIGTSEGRF | LARGE_INTESTINE | 454 | p.L455I | c.1363C>A | Missense_Mutation | 1 | 0.11 | HT115 | N | 2 | 0 | 0 | N |
MET | NIHLHSEAF | LUNG | 902 | p.V910F | c.2728G>T | Missense_Mutation | 1 | 0.11 | DMS273 | N | 3 | 0 | 0 | N |
MET | NKHFNMSLI | LUNG | 631 | p.I638L | c.1912A>T | Missense_Mutation | 1 | 0.11 | NCIH838 | Y | 4 | 10 | 0 | N |
MET | NKIINKNNV | BONE | 375 | p.V378I | c.1132G>A | Missense_Mutation | 1 | 0.11 | OUMS27 | N | 3 | 0 | 0 | N |
MET | NLSRGVWKD | ENDOMETRIUM | 106 | p.G109R | c.325G>A | Missense_Mutation | 1 | 0.11 | TEN | N | 0 | 0 | 0 | N |
MET | NMSLIISNG | LUNG | 635 | p.I638L | c.1912A>T | Missense_Mutation | 1 | 0.11 | NCIH838 | Y | 0 | 9 | 0 | N |
MET | NPTVKHLIG | BREAST | 1193 | p.D1198H | c.3592G>C | Missense_Mutation | 1 | 0.11 | HCC202 | N | 0 | 0 | 0 | N |
MET | NSDIICCTT | OESOPHAGUS | 813 | p.E815D | c.2445G>C | Missense_Mutation | 1 | 0.11 | TE5 | N | 2 | 0 | 0 | N |
MET | NVFSLLGIC | LUNG | 1156 | p.L1158F | c.3472C>T | Missense_Mutation | 1 | 0.11 | HCC15 | N | 2 | 0 | 0 | N |
MET | NVLLLLGIC | LARGE_INTESTINE | 1156 | p.S1159L | c.3476C>T | Missense_Mutation | 1 | 0.11 | SNUC5 | N | 1 | 0 | 0 | N |
MET | NVNRGTCQR | ENDOMETRIUM | 135 | p.S135N | c.404G>A | Missense_Mutation | 1 | 0.11 | MFE319 | Y | 5 | 9 | 0 | N |
MET | PEFRDYYPI | LIVER | 239 | p.S244Y | c.731C>A | Missense_Mutation | 1 | 0.11 | C3A | N | 5 | 0 | 0 | N |
MET | PGILVLLFI | SKIN | 9 | p.T17I | c.50C>T | Missense_Mutation | 1 | 0.11 | RPMI7951 | N | 5 | 0 | 0 | N |
MET | PHNHTAAIQ | STOMACH | 147 | p.D153A | c.458A>C | Missense_Mutation | 1 | 0.11 | SNU719 | N | 0 | 0 | 0 | N |
MET | PMNGLGCRH | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 514 | p.L515M | c.1543T>A | Missense_Mutation | 1 | 0.11 | KIJK | N | 0 | 0 | 0 | N |
MET | PNVFSLLGI | LUNG | 1155 | p.L1158F | c.3472C>T | Missense_Mutation | 1 | 0.11 | HCC15 | N | 0 | 0 | 0 | N |
MET | PNVLLLLGI | LARGE_INTESTINE | 1155 | p.S1159L | c.3476C>T | Missense_Mutation | 1 | 0.11 | SNUC5 | N | 0 | 0 | 0 | N |
MET | PQIEKPSQC | LUNG | 164 | p.E168K | c.502G>A | Missense_Mutation | 1 | 0.11 | NCIH2342 | N | 0 | 0 | 0 | N |
MET | PSQCADCVV | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 169 | p.P173A | c.517C>G | Missense_Mutation | 1 | 0.11 | BCP1 | N | 0 | 0 | 0 | N |
MET | PTKYFISTW | ENDOMETRIUM | 749 | p.S752Y | c.2255C>A | Missense_Mutation | 1 | 0.11 | JHUEM7 | N | 1 | 0 | 0 | N |
MET | PTVKHLIGF | BREAST | 1194 | p.D1198H | c.3592G>C | Missense_Mutation | 1 | 0.11 | HCC202 | N | 1 | 0 | 0 | N |
MET | PYMKHGDLQ | ENDOMETRIUM | 1176 | p.R1184Q | c.3551G>A | Missense_Mutation | 1 | 0.11 | HEC251 | N | 0 | 0 | 0 | N |
MET | QCADCVVSA | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 171 | p.P173A | c.517C>G | Missense_Mutation | 1 | 0.11 | BCP1 | Y | 0 | 13 | 0 | N |
MET | QCVSAPPFV | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 528 | p.L530V | c.1588C>G | Missense_Mutation | 1 | 0.11 | MC116 | N | 2 | 0 | 0 | N |
MET | QHHSNSEII | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 809 | p.R811H | c.2432G>A | Missense_Mutation | 1 | 0.11 | SUPHD1 | N | 5 | 0 | 0 | N |
MET | QHRSNSDII | OESOPHAGUS | 809 | p.E815D | c.2445G>C | Missense_Mutation | 1 | 0.11 | TE5 | N | 5 | 0 | 0 | N |
MET | QIEEPSQCA | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 165 | p.P173A | c.517C>G | Missense_Mutation | 1 | 0.11 | BCP1 | N | 1 | 0 | 0 | N |
MET | QIEKPSQCP | LUNG | 165 | p.E168K | c.502G>A | Missense_Mutation | 1 | 0.11 | NCIH2342 | N | 0 | 0 | 0 | N |
MET | QKVAEYKIG | LARGE_INTESTINE | 79 | p.T86I | c.257C>T | Missense_Mutation | 1 | 0.11 | LS411N | N | 0 | 0 | 0 | N |
MET | QLISCGNVN | ENDOMETRIUM | 129 | p.S135N | c.404G>A | Missense_Mutation | 1 | 0.11 | MFE319 | N | 0 | 0 | 0 | N |
MET | QNFIRNETH | ENDOMETRIUM | 1184 | p.R1184Q | c.3551G>A | Missense_Mutation | 1 | 0.11 | HEC251 | N | 0 | 0 | 0 | N |
MET | QSCSQCVSA | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 524 | p.L530V | c.1588C>G | Missense_Mutation | 1 | 0.11 | MC116 | N | 1 | 0 | 0 | N |
MET | QSEGSPLVV | ENDOMETRIUM | 1166 | p.R1166Q | c.3497G>A | Missense_Mutation | 1 | 0.11 | JHUEM7 | N | 3 | 0 | 0 | N |
MET | RCDARVHTP | LUNG | 988 | p.Y989C | c.2966A>G | Missense_Mutation | 1 | 0.11 | NCIH1869 | N | 0 | 0 | 0 | N |
MET | RDYYPIKYV | LIVER | 242 | p.S244Y | c.731C>A | Missense_Mutation | 1 | 0.11 | C3A | N | 8 | 0 | 0 | N |
MET | RGVWKDNIN | ENDOMETRIUM | 109 | p.G109R | c.325G>A | Missense_Mutation | 1 | 0.11 | TEN | N | 1 | 0 | 0 | N |
MET | RILSKYFDL | ENDOMETRIUM | 843 | p.G843R | c.2527G>A | Missense_Mutation | 1 | 0.11 | EN | Y | 17 | 9 | 0 | N |
MET | RLVSARSIS | OESOPHAGUS | 1000 | p.V1007I | c.3019G>A | Missense_Mutation | 1 | 0.11 | OE33 | N | 0 | 0 | 0 | N |
MET | RSISPTTEM | OESOPHAGUS | 1005 | p.V1007I | c.3019G>A | Missense_Mutation | 1 | 0.11 | OE33 | Y | 8 | 9 | 0 | N |
MET | RSNSDIICC | OESOPHAGUS | 811 | p.E815D | c.2445G>C | Missense_Mutation | 1 | 0.11 | TE5 | N | 1 | 0 | 0 | N |
MET | RSVSSTTEM | STOMACH | 1005 | p.P1009S | c.3025C>T | Missense_Mutation | 1 | 0.11 | ECC12 | N | 8 | 0 | 0 | N |
MET | RVFAQSKPD | ENDOMETRIUM | 344 | p.G344R | c.1030G>A | Missense_Mutation | 1 | 0.11 | AN3CA | N | 0 | 0 | 0 | N |
MET | RVVLGNESC | CENTRAL_NERVOUS_SYSTEM | 602 | p.L604V | c.1810C>G | Missense_Mutation | 1 | 0.11 | BECKER | N | 0 | 0 | 0 | N |
MET | SARSISPTT | OESOPHAGUS | 1003 | p.V1007I | c.3019G>A | Missense_Mutation | 1 | 0.11 | OE33 | N | 4 | 0 | 0 | N |
MET | SARSVSSTT | STOMACH | 1003 | p.P1009S | c.3025C>T | Missense_Mutation | 1 | 0.11 | ECC12 | N | 4 | 0 | 0 | N |
MET | SCGNVNRGT | ENDOMETRIUM | 132 | p.S135N | c.404G>A | Missense_Mutation | 1 | 0.11 | MFE319 | N | 0 | 0 | 0 | N |
MET | SCSQCVSAP | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 525 | p.L530V | c.1588C>G | Missense_Mutation | 1 | 0.11 | MC116 | N | 0 | 0 | 0 | N |
MET | SDIICCTTP | OESOPHAGUS | 814 | p.E815D | c.2445G>C | Missense_Mutation | 1 | 0.11 | TE5 | N | 0 | 0 | 0 | N |
MET | SEAFLCTVP | LUNG | 907 | p.V910F | c.2728G>T | Missense_Mutation | 1 | 0.11 | DMS273 | N | 1 | 0 | 0 | N |
MET | SELVRCDAR | LUNG | 984 | p.Y989C | c.2966A>G | Missense_Mutation | 1 | 0.11 | NCIH1869 | Y | 1 | 10 | 0 | N |
MET | SHPNVFSLL | LUNG | 1153 | p.L1158F | c.3472C>T | Missense_Mutation | 1 | 0.11 | HCC15 | Y | 8 | 10 | 0 | N |
MET | SHPNVLLLL | LARGE_INTESTINE | 1153 | p.S1159L | c.3476C>T | Missense_Mutation | 1 | 0.11 | SNUC5 | Y | 9 | 11 | 0 | N |
MET | SISPTTEMV | OESOPHAGUS | 1006 | p.V1007I | c.3019G>A | Missense_Mutation | 1 | 0.11 | OE33 | N | 2 | 0 | 0 | N |
MET | SKANLSRGV | ENDOMETRIUM | 103 | p.G109R | c.325G>A | Missense_Mutation | 1 | 0.11 | TEN | N | 1 | 0 | 0 | N |
MET | SKYFDLFYV | LUNG | 846 | p.I852F | c.2554A>T | Missense_Mutation | 1 | 0.11 | NCIH1339 | N | 5 | 0 | 0 | N |
MET | SKYFDLIHV | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 846 | p.Y853H | c.2557T>C | Missense_Mutation | 1 | 0.11 | HUNS1 | N | 3 | 0 | 0 | N |
MET | SLIISNGHG | LUNG | 637 | p.I638L | c.1912A>T | Missense_Mutation | 1 | 0.11 | NCIH838 | N | 0 | 0 | 0 | N |
MET | SLLGICLQS | ENDOMETRIUM | 1159 | p.R1166Q | c.3497G>A | Missense_Mutation | 1 | 0.11 | JHUEM7 | N | 0 | 0 | 0 | N |
MET | SLNDDILFR | ENDOMETRIUM | 336 | p.G344R | c.1030G>A | Missense_Mutation | 1 | 0.11 | AN3CA | Y | 6 | 9 | 0 | N |
MET | SLNIVSFLF | SKIN | 761 | p.P761S | c.2281C>T | Missense_Mutation | 1 | 0.11 | CHL1 | N | 5 | 0 | 0 | N |
MET | SNSDIICCT | OESOPHAGUS | 812 | p.E815D | c.2445G>C | Missense_Mutation | 1 | 0.11 | TE5 | N | 0 | 0 | 0 | N |
MET | SPQIEKPSQ | LUNG | 163 | p.E168K | c.502G>A | Missense_Mutation | 1 | 0.11 | NCIH2342 | N | 0 | 0 | 0 | N |
MET | SQCADCVVS | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 170 | p.P173A | c.517C>G | Missense_Mutation | 1 | 0.11 | BCP1 | N | 0 | 0 | 0 | N |
MET | SQCVSAPPF | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 527 | p.L530V | c.1588C>G | Missense_Mutation | 1 | 0.11 | MC116 | N | 7 | 0 | 0 | N |
MET | SRGVWKDNI | ENDOMETRIUM | 108 | p.G109R | c.325G>A | Missense_Mutation | 1 | 0.11 | TEN | N | 2 | 0 | 0 | N |
MET | SSKANLSRG | ENDOMETRIUM | 102 | p.G109R | c.325G>A | Missense_Mutation | 1 | 0.11 | TEN | Y | 0 | 9 | 0 | N |
MET | SSTTEMVSN | STOMACH | 1008 | p.P1009S | c.3025C>T | Missense_Mutation | 1 | 0.11 | ECC12 | N | 0 | 0 | 0 | N |
MET | SSTVLGKLI | LUNG | 934 | p.V941L | c.2821G>T | Missense_Mutation | 1 | 0.11 | NCIH1838 | N | 5 | 0 | 0 | N |
MET | STFIGEHYD | ENDOMETRIUM | 1360 | p.V1368D | c.4103T>A | Missense_Mutation | 1 | 0.11 | HEC1A | N | 0 | 0 | 0 | N |
MET | STTEMVSNE | STOMACH | 1009 | p.P1009S | c.3025C>T | Missense_Mutation | 1 | 0.11 | ECC12 | N | 0 | 0 | 0 | N |
MET | STVLGKLIV | LUNG | 935 | p.V941L | c.2821G>T | Missense_Mutation | 1 | 0.11 | NCIH1838 | Y | 4 | 10 | 0 | N |
MET | STWWKESLN | SKIN | 755 | p.P761S | c.2281C>T | Missense_Mutation | 1 | 0.11 | CHL1 | N | 0 | 0 | 0 | Y |
MET | SVSSTTEMV | STOMACH | 1006 | p.P1009S | c.3025C>T | Missense_Mutation | 1 | 0.11 | ECC12 | N | 1 | 0 | 0 | N |
MET | TAAIQSEVH | STOMACH | 151 | p.D153A | c.458A>C | Missense_Mutation | 1 | 0.11 | SNU719 | N | 0 | 0 | 0 | N |
MET | TFIGEHYDH | ENDOMETRIUM | 1361 | p.V1368D | c.4103T>A | Missense_Mutation | 1 | 0.11 | HEC1A | N | 0 | 0 | 0 | N |
MET | THNPTVKHL | BREAST | 1191 | p.D1198H | c.3592G>C | Missense_Mutation | 1 | 0.11 | HCC202 | Y | 4 | 11 | 0 | N |
MET | TIANIGTSE | LARGE_INTESTINE | 451 | p.L455I | c.1363C>A | Missense_Mutation | 1 | 0.11 | HT115 | N | 0 | 0 | 0 | N |
MET | TKAFFMLDR | ENDOMETRIUM | 835 | p.G843R | c.2527G>A | Missense_Mutation | 1 | 0.11 | EN | N | 1 | 0 | 0 | N |
MET | TKIPMNGLG | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 511 | p.L515M | c.1543T>A | Missense_Mutation | 1 | 0.11 | KIJK | N | 0 | 0 | 0 | N |
MET | TKQIKDLGS | LARGE_INTESTINE | 976 | p.R976T | c.2927G>C | Missense_Mutation | 1 | 0.11 | NCIH508 | N | 1 | 0 | 0 | N |
MET | TKYFISTWW | ENDOMETRIUM | 750 | p.S752Y | c.2255C>A | Missense_Mutation | 1 | 0.11 | JHUEM7 | N | 3 | 0 | 0 | N |
MET | TRVVLGNES | CENTRAL_NERVOUS_SYSTEM | 601 | p.L604V | c.1810C>G | Missense_Mutation | 1 | 0.11 | BECKER | N | 2 | 0 | 0 | N |
MET | TVACQHHSN | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 805 | p.R811H | c.2432G>A | Missense_Mutation | 1 | 0.11 | SUPHD1 | N | 0 | 0 | 0 | N |
MET | TVKHLIGFG | BREAST | 1195 | p.D1198H | c.3592G>C | Missense_Mutation | 1 | 0.11 | HCC202 | N | 0 | 0 | 0 | N |
MET | TVKIADFGL | KIDNEY | 1235 | p.V1238I | c.3712G>A | Missense_Mutation | 1 | 0.11 | CAKI1 | N | 5 | 0 | 0 | N |
MET | TVKVANFGL | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1235 | p.D1240N | c.3718G>A | Missense_Mutation | 1 | 0.11 | KMM1 | N | 4 | 0 | 0 | N |
MET | TVLGKLIVQ | LUNG | 936 | p.V941L | c.2821G>T | Missense_Mutation | 1 | 0.11 | NCIH1838 | N | 0 | 0 | 0 | N |
MET | TWWKESLNI | SKIN | 756 | p.P761S | c.2281C>T | Missense_Mutation | 1 | 0.11 | CHL1 | N | 6 | 0 | 0 | N |
MET | VACQHHSNS | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 806 | p.R811H | c.2432G>A | Missense_Mutation | 1 | 0.11 | SUPHD1 | N | 1 | 0 | 0 | N |
MET | VAEYKIGPV | LARGE_INTESTINE | 81 | p.T86I | c.257C>T | Missense_Mutation | 1 | 0.11 | LS411N | N | 9 | 0 | 0 | N |
MET | VANFGLARD | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1238 | p.D1240N | c.3718G>A | Missense_Mutation | 1 | 0.11 | KMM1 | N | 0 | 0 | 0 | N |
MET | VFPHNHTAA | STOMACH | 145 | p.D153A | c.458A>C | Missense_Mutation | 1 | 0.11 | SNU719 | N | 3 | 0 | 0 | N |
MET | VFSLLGICL | LUNG | 1157 | p.L1158F | c.3472C>T | Missense_Mutation | 1 | 0.11 | HCC15 | N | 8 | 0 | 8 | N |
MET | VKHLIGFGL | BREAST | 1196 | p.D1198H | c.3592G>C | Missense_Mutation | 1 | 0.11 | HCC202 | N | 8 | 0 | 8 | N |
MET | VKIADFGLA | KIDNEY | 1236 | p.V1238I | c.3712G>A | Missense_Mutation | 1 | 0.11 | CAKI1 | N | 3 | 0 | 0 | N |
MET | VKVANFGLA | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1236 | p.D1240N | c.3718G>A | Missense_Mutation | 1 | 0.11 | KMM1 | N | 4 | 0 | 0 | N |
MET | VLGKLIVQP | LUNG | 937 | p.V941L | c.2821G>T | Missense_Mutation | 1 | 0.11 | NCIH1838 | N | 0 | 0 | 1 | N |
MET | VLGNESCTL | CENTRAL_NERVOUS_SYSTEM | 604 | p.L604V | c.1810C>G | Missense_Mutation | 1 | 0.11 | BECKER | N | 9 | 0 | 2 | N |
MET | VLLFILVQR | SKIN | 13 | p.T17I | c.50C>T | Missense_Mutation | 1 | 0.11 | RPMI7951 | N | 5 | 0 | 10 | N |
MET | VLLLLGICL | LARGE_INTESTINE | 1157 | p.S1159L | c.3476C>T | Missense_Mutation | 1 | 0.11 | SNUC5 | N | 19 | 0 | 15 | N |
MET | VLPEFRDYY | LIVER | 237 | p.S244Y | c.731C>A | Missense_Mutation | 1 | 0.11 | C3A | Y | 9 | 12 | 0 | N |
MET | VNDFFNKII | BONE | 370 | p.V378I | c.1132G>A | Missense_Mutation | 1 | 0.11 | OUMS27 | N | 7 | 0 | 0 | N |
MET | VRCDARVHT | LUNG | 987 | p.Y989C | c.2966A>G | Missense_Mutation | 1 | 0.11 | NCIH1869 | N | 3 | 0 | 8 | N |
MET | VSAPPFVQC | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 530 | p.L530V | c.1588C>G | Missense_Mutation | 1 | 0.11 | MC116 | Y | 1 | 9 | 0 | N |
MET | VSARSISPT | OESOPHAGUS | 1002 | p.V1007I | c.3019G>A | Missense_Mutation | 1 | 0.11 | OE33 | N | 1 | 0 | 0 | N |
MET | VSARSVSST | STOMACH | 1002 | p.P1009S | c.3025C>T | Missense_Mutation | 1 | 0.11 | ECC12 | N | 1 | 0 | 0 | N |
MET | VSSTTEMVS | STOMACH | 1007 | p.P1009S | c.3025C>T | Missense_Mutation | 1 | 0.11 | ECC12 | N | 0 | 0 | 0 | N |
MET | VVLGNESCT | CENTRAL_NERVOUS_SYSTEM | 603 | p.L604V | c.1810C>G | Missense_Mutation | 1 | 0.11 | BECKER | N | 5 | 0 | 0 | N |
MET | VYEIHPTKY | ENDOMETRIUM | 744 | p.S752Y | c.2255C>A | Missense_Mutation | 1 | 0.11 | JHUEM7 | N | 5 | 0 | 0 | N |
MET | WDFGFWRNN | LARGE_INTESTINE | 586 | p.R591W | c.1771C>T | Missense_Mutation | 1 | 0.11 | SNU81 | N | 3 | 0 | 0 | Y |
MET | WKESLNIVS | SKIN | 758 | p.P761S | c.2281C>T | Missense_Mutation | 1 | 0.11 | CHL1 | N | 4 | 0 | 4 | N |
MET | WLKKTKQIK | LARGE_INTESTINE | 972 | p.R976T | c.2927G>C | Missense_Mutation | 1 | 0.11 | NCIH508 | Y | 5 | 13 | 8 | N |
MET | WRNNKFDLK | LARGE_INTESTINE | 591 | p.R591W | c.1771C>T | Missense_Mutation | 1 | 0.11 | SNU81 | Y | 4 | 11 | 2 | N |
MET | WWKESLNIV | SKIN | 757 | p.P761S | c.2281C>T | Missense_Mutation | 1 | 0.11 | CHL1 | N | 6 | 0 | 0 | N |
MET | YDHVNATYV | ENDOMETRIUM | 1367 | p.V1368D | c.4103T>A | Missense_Mutation | 1 | 0.11 | HEC1A | Y | 7 | 9 | 0 | N |
MET | YEIHPTKYF | ENDOMETRIUM | 745 | p.S752Y | c.2255C>A | Missense_Mutation | 1 | 0.11 | JHUEM7 | N | 9 | 0 | 20 | N |
MET | YFDLFYVHN | LUNG | 848 | p.I852F | c.2554A>T | Missense_Mutation | 1 | 0.11 | NCIH1339 | N | 2 | 0 | 0 | N |
MET | YFDLIHVHN | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 848 | p.Y853H | c.2557T>C | Missense_Mutation | 1 | 0.11 | HUNS1 | N | 2 | 0 | 0 | N |
MET | YFISTWWKE | ENDOMETRIUM | 752 | p.S752Y | c.2255C>A | Missense_Mutation | 1 | 0.11 | JHUEM7 | N | 3 | 0 | 1 | N |
MET | YKIGPVLEH | LARGE_INTESTINE | 84 | p.T86I | c.257C>T | Missense_Mutation | 1 | 0.11 | LS411N | N | 3 | 0 | 31 | N |
MET | YMKHGDLQN | ENDOMETRIUM | 1177 | p.R1184Q | c.3551G>A | Missense_Mutation | 1 | 0.11 | HEC251 | N | 2 | 0 | 0 | N |
MET | YYPIKYVHA | LIVER | 244 | p.S244Y | c.731C>A | Missense_Mutation | 1 | 0.11 | C3A | N | 7 | 0 | 1 | N |
MET | AQLARQLGA | LARGE_INTESTINE | 327 | p.I333L | c.997A>T | Missense_Mutation | 1 | 0.22 | COLO201 | N | 3 | 0 | 0 | Y |
MET | AQLARQLGA | LARGE_INTESTINE | 327 | p.I333L | c.997A>T | Missense_Mutation | 1 | 0.22 | COLO205 | N | 3 | 0 | 0 | Y |
MET | ARQLGASLN | LARGE_INTESTINE | 330 | p.I333L | c.997A>T | Missense_Mutation | 1 | 0.22 | COLO201 | N | 2 | 0 | 0 | N |
MET | ARQLGASLN | LARGE_INTESTINE | 330 | p.I333L | c.997A>T | Missense_Mutation | 1 | 0.22 | COLO205 | N | 2 | 0 | 0 | N |
MET | DFFKKIVNK | ENDOMETRIUM | 372 | p.N375K | c.1125C>G | Missense_Mutation | 1 | 0.22 | HEC108 | N | 0 | 0 | 0 | N |
MET | DFFKKIVNK | OESOPHAGUS | 372 | p.N375K | c.1125C>G | Missense_Mutation | 1 | 0.22 | TE8 | N | 0 | 0 | 0 | N |
MET | EECKEALAK | SOFT_TISSUE | 24 | p.G24E | c.71G>A | Missense_Mutation | 1 | 0.22 | TE441T | N | 0 | 0 | 0 | N |
MET | EECKEALAK | URINARY_TRACT | 24 | p.G24E | c.71G>A | Missense_Mutation | 1 | 0.22 | UMUC1 | N | 0 | 0 | 0 | N |
MET | FFKKIVNKN | ENDOMETRIUM | 373 | p.N375K | c.1125C>G | Missense_Mutation | 1 | 0.22 | HEC108 | N | 1 | 0 | 9 | N |
MET | FFKKIVNKN | OESOPHAGUS | 373 | p.N375K | c.1125C>G | Missense_Mutation | 1 | 0.22 | TE8 | N | 1 | 0 | 9 | N |
MET | FKKIVNKNN | ENDOMETRIUM | 374 | p.N375K | c.1125C>G | Missense_Mutation | 1 | 0.22 | HEC108 | N | 3 | 0 | 3 | N |
MET | FKKIVNKNN | OESOPHAGUS | 374 | p.N375K | c.1125C>G | Missense_Mutation | 1 | 0.22 | TE8 | N | 3 | 0 | 3 | N |
MET | FTLVQRSNE | SOFT_TISSUE | 16 | p.G24E | c.71G>A | Missense_Mutation | 1 | 0.22 | TE441T | N | 2 | 0 | 2 | N |
MET | FTLVQRSNE | URINARY_TRACT | 16 | p.G24E | c.71G>A | Missense_Mutation | 1 | 0.22 | UMUC1 | N | 2 | 0 | 2 | N |
MET | GAQLARQLG | LARGE_INTESTINE | 326 | p.I333L | c.997A>T | Missense_Mutation | 1 | 0.22 | COLO201 | N | 0 | 0 | 0 | Y |
MET | GAQLARQLG | LARGE_INTESTINE | 326 | p.I333L | c.997A>T | Missense_Mutation | 1 | 0.22 | COLO205 | N | 0 | 0 | 0 | Y |
MET | IKYVNDFFK | ENDOMETRIUM | 367 | p.N375K | c.1125C>G | Missense_Mutation | 1 | 0.22 | HEC108 | N | 1 | 0 | 2 | N |
MET | IKYVNDFFK | OESOPHAGUS | 367 | p.N375K | c.1125C>G | Missense_Mutation | 1 | 0.22 | TE8 | N | 1 | 0 | 2 | N |
MET | KKIVNKNNV | ENDOMETRIUM | 375 | p.N375K | c.1125C>G | Missense_Mutation | 1 | 0.22 | HEC108 | N | 4 | 0 | 0 | N |
MET | KKIVNKNNV | OESOPHAGUS | 375 | p.N375K | c.1125C>G | Missense_Mutation | 1 | 0.22 | TE8 | N | 4 | 0 | 0 | N |
MET | KYVNDFFKK | ENDOMETRIUM | 368 | p.N375K | c.1125C>G | Missense_Mutation | 1 | 0.22 | HEC108 | N | 3 | 0 | 0 | N |
MET | KYVNDFFKK | OESOPHAGUS | 368 | p.N375K | c.1125C>G | Missense_Mutation | 1 | 0.22 | TE8 | N | 3 | 0 | 0 | N |
MET | LARQLGASL | LARGE_INTESTINE | 329 | p.I333L | c.997A>T | Missense_Mutation | 1 | 0.22 | COLO201 | N | 12 | 0 | 1 | N |
MET | LARQLGASL | LARGE_INTESTINE | 329 | p.I333L | c.997A>T | Missense_Mutation | 1 | 0.22 | COLO205 | N | 12 | 0 | 1 | N |
MET | LGASLNDDI | LARGE_INTESTINE | 333 | p.I333L | c.997A>T | Missense_Mutation | 1 | 0.22 | COLO201 | N | 9 | 0 | 0 | N |
MET | LGASLNDDI | LARGE_INTESTINE | 333 | p.I333L | c.997A>T | Missense_Mutation | 1 | 0.22 | COLO205 | N | 9 | 0 | 0 | N |
MET | LVQRSNEEC | SOFT_TISSUE | 18 | p.G24E | c.71G>A | Missense_Mutation | 1 | 0.22 | TE441T | N | 0 | 0 | 2 | N |
MET | LVQRSNEEC | URINARY_TRACT | 18 | p.G24E | c.71G>A | Missense_Mutation | 1 | 0.22 | UMUC1 | N | 0 | 0 | 2 | N |
MET | NDFFKKIVN | ENDOMETRIUM | 371 | p.N375K | c.1125C>G | Missense_Mutation | 1 | 0.22 | HEC108 | N | 1 | 0 | 0 | N |
MET | NDFFKKIVN | OESOPHAGUS | 371 | p.N375K | c.1125C>G | Missense_Mutation | 1 | 0.22 | TE8 | N | 1 | 0 | 0 | N |
MET | NEECKEALA | SOFT_TISSUE | 23 | p.G24E | c.71G>A | Missense_Mutation | 1 | 0.22 | TE441T | N | 6 | 0 | 0 | N |
MET | NEECKEALA | URINARY_TRACT | 23 | p.G24E | c.71G>A | Missense_Mutation | 1 | 0.22 | UMUC1 | N | 6 | 0 | 0 | N |
MET | PGAQLARQL | LARGE_INTESTINE | 325 | p.I333L | c.997A>T | Missense_Mutation | 1 | 0.22 | COLO201 | N | 1 | 0 | 0 | N |
MET | PGAQLARQL | LARGE_INTESTINE | 325 | p.I333L | c.997A>T | Missense_Mutation | 1 | 0.22 | COLO205 | N | 1 | 0 | 0 | N |
MET | QLARQLGAS | LARGE_INTESTINE | 328 | p.I333L | c.997A>T | Missense_Mutation | 1 | 0.22 | COLO201 | N | 0 | 0 | 0 | Y |
MET | QLARQLGAS | LARGE_INTESTINE | 328 | p.I333L | c.997A>T | Missense_Mutation | 1 | 0.22 | COLO205 | N | 0 | 0 | 0 | Y |
MET | QLGASLNDD | LARGE_INTESTINE | 332 | p.I333L | c.997A>T | Missense_Mutation | 1 | 0.22 | COLO201 | N | 0 | 0 | 0 | N |
MET | QLGASLNDD | LARGE_INTESTINE | 332 | p.I333L | c.997A>T | Missense_Mutation | 1 | 0.22 | COLO205 | N | 0 | 0 | 0 | N |
MET | QRSNEECKE | SOFT_TISSUE | 20 | p.G24E | c.71G>A | Missense_Mutation | 1 | 0.22 | TE441T | N | 1 | 0 | 0 | N |
MET | QRSNEECKE | URINARY_TRACT | 20 | p.G24E | c.71G>A | Missense_Mutation | 1 | 0.22 | UMUC1 | N | 1 | 0 | 0 | N |
MET | RQLGASLND | LARGE_INTESTINE | 331 | p.I333L | c.997A>T | Missense_Mutation | 1 | 0.22 | COLO201 | N | 0 | 0 | 0 | N |
MET | RQLGASLND | LARGE_INTESTINE | 331 | p.I333L | c.997A>T | Missense_Mutation | 1 | 0.22 | COLO205 | N | 0 | 0 | 0 | N |
MET | RSNEECKEA | SOFT_TISSUE | 21 | p.G24E | c.71G>A | Missense_Mutation | 1 | 0.22 | TE441T | N | 3 | 0 | 0 | N |
MET | RSNEECKEA | URINARY_TRACT | 21 | p.G24E | c.71G>A | Missense_Mutation | 1 | 0.22 | UMUC1 | N | 3 | 0 | 0 | N |
MET | SNEECKEAL | SOFT_TISSUE | 22 | p.G24E | c.71G>A | Missense_Mutation | 1 | 0.22 | TE441T | N | 5 | 0 | 0 | N |
MET | SNEECKEAL | URINARY_TRACT | 22 | p.G24E | c.71G>A | Missense_Mutation | 1 | 0.22 | UMUC1 | N | 5 | 0 | 0 | N |
MET | TLVQRSNEE | SOFT_TISSUE | 17 | p.G24E | c.71G>A | Missense_Mutation | 1 | 0.22 | TE441T | N | 0 | 0 | 0 | N |
MET | TLVQRSNEE | URINARY_TRACT | 17 | p.G24E | c.71G>A | Missense_Mutation | 1 | 0.22 | UMUC1 | N | 0 | 0 | 0 | N |
MET | VNDFFKKIV | ENDOMETRIUM | 370 | p.N375K | c.1125C>G | Missense_Mutation | 1 | 0.22 | HEC108 | N | 5 | 0 | 0 | N |
MET | VNDFFKKIV | OESOPHAGUS | 370 | p.N375K | c.1125C>G | Missense_Mutation | 1 | 0.22 | TE8 | N | 5 | 0 | 0 | N |
MET | VQRSNEECK | SOFT_TISSUE | 19 | p.G24E | c.71G>A | Missense_Mutation | 1 | 0.22 | TE441T | N | 3 | 0 | 0 | N |
MET | VQRSNEECK | URINARY_TRACT | 19 | p.G24E | c.71G>A | Missense_Mutation | 1 | 0.22 | UMUC1 | N | 3 | 0 | 0 | N |
MET | YVNDFFKKI | ENDOMETRIUM | 369 | p.N375K | c.1125C>G | Missense_Mutation | 1 | 0.22 | HEC108 | Y | 11 | 9 | 7 | N |
MET | YVNDFFKKI | OESOPHAGUS | 369 | p.N375K | c.1125C>G | Missense_Mutation | 1 | 0.22 | TE8 | Y | 11 | 9 | 7 | N |
MET | DHPWHSISV | OVARY | 208 | p.L211W | c.632T>G | Missense_Mutation | 1 | 0.33 | JHOC5 | N | 4 | 0 | 0 | N |
MET | DHPWHSISV | PANCREAS | 208 | p.L211W | c.632T>G | Missense_Mutation | 1 | 0.33 | PK59 | N | 4 | 0 | 0 | N |
MET | DHPWHSISV | CENTRAL_NERVOUS_SYSTEM | 208 | p.L211W | c.632T>G | Missense_Mutation | 1 | 0.33 | SNU466 | N | 4 | 0 | 0 | N |
MET | FPDHPWHSI | OVARY | 206 | p.L211W | c.632T>G | Missense_Mutation | 1 | 0.33 | JHOC5 | Y | 13 | 11 | 0 | N |
MET | FPDHPWHSI | PANCREAS | 206 | p.L211W | c.632T>G | Missense_Mutation | 1 | 0.33 | PK59 | Y | 13 | 11 | 0 | N |
MET | FPDHPWHSI | CENTRAL_NERVOUS_SYSTEM | 206 | p.L211W | c.632T>G | Missense_Mutation | 1 | 0.33 | SNU466 | Y | 13 | 11 | 0 | N |
MET | HPWHSISVR | OVARY | 209 | p.L211W | c.632T>G | Missense_Mutation | 1 | 0.33 | JHOC5 | N | 7 | 0 | 0 | N |
MET | HPWHSISVR | PANCREAS | 209 | p.L211W | c.632T>G | Missense_Mutation | 1 | 0.33 | PK59 | N | 7 | 0 | 0 | N |
MET | HPWHSISVR | CENTRAL_NERVOUS_SYSTEM | 209 | p.L211W | c.632T>G | Missense_Mutation | 1 | 0.33 | SNU466 | N | 7 | 0 | 0 | N |
MET | PDHPWHSIS | OVARY | 207 | p.L211W | c.632T>G | Missense_Mutation | 1 | 0.33 | JHOC5 | N | 0 | 0 | 0 | N |
MET | PDHPWHSIS | PANCREAS | 207 | p.L211W | c.632T>G | Missense_Mutation | 1 | 0.33 | PK59 | N | 0 | 0 | 0 | N |
MET | PDHPWHSIS | CENTRAL_NERVOUS_SYSTEM | 207 | p.L211W | c.632T>G | Missense_Mutation | 1 | 0.33 | SNU466 | N | 0 | 0 | 0 | N |
MET | PWHSISVRR | OVARY | 210 | p.L211W | c.632T>G | Missense_Mutation | 1 | 0.33 | JHOC5 | N | 0 | 0 | 0 | N |
MET | PWHSISVRR | PANCREAS | 210 | p.L211W | c.632T>G | Missense_Mutation | 1 | 0.33 | PK59 | N | 0 | 0 | 0 | N |
MET | PWHSISVRR | CENTRAL_NERVOUS_SYSTEM | 210 | p.L211W | c.632T>G | Missense_Mutation | 1 | 0.33 | SNU466 | N | 0 | 0 | 0 | N |
MET | SSYFPDHPW | OVARY | 203 | p.L211W | c.632T>G | Missense_Mutation | 1 | 0.33 | JHOC5 | N | 7 | 0 | 0 | N |
MET | SSYFPDHPW | PANCREAS | 203 | p.L211W | c.632T>G | Missense_Mutation | 1 | 0.33 | PK59 | N | 7 | 0 | 0 | N |
MET | SSYFPDHPW | CENTRAL_NERVOUS_SYSTEM | 203 | p.L211W | c.632T>G | Missense_Mutation | 1 | 0.33 | SNU466 | N | 7 | 0 | 0 | N |
MET | SYFPDHPWH | OVARY | 204 | p.L211W | c.632T>G | Missense_Mutation | 1 | 0.33 | JHOC5 | N | 0 | 0 | 0 | N |
MET | SYFPDHPWH | PANCREAS | 204 | p.L211W | c.632T>G | Missense_Mutation | 1 | 0.33 | PK59 | N | 0 | 0 | 0 | N |
MET | SYFPDHPWH | CENTRAL_NERVOUS_SYSTEM | 204 | p.L211W | c.632T>G | Missense_Mutation | 1 | 0.33 | SNU466 | N | 0 | 0 | 0 | N |
MET | WHSISVRRL | OVARY | 211 | p.L211W | c.632T>G | Missense_Mutation | 1 | 0.33 | JHOC5 | Y | 6 | 10 | 16 | N |
MET | WHSISVRRL | PANCREAS | 211 | p.L211W | c.632T>G | Missense_Mutation | 1 | 0.33 | PK59 | Y | 6 | 10 | 16 | N |
MET | WHSISVRRL | CENTRAL_NERVOUS_SYSTEM | 211 | p.L211W | c.632T>G | Missense_Mutation | 1 | 0.33 | SNU466 | Y | 6 | 10 | 16 | N |
MET | YFPDHPWHS | OVARY | 205 | p.L211W | c.632T>G | Missense_Mutation | 1 | 0.33 | JHOC5 | N | 2 | 0 | 12 | N |
MET | YFPDHPWHS | PANCREAS | 205 | p.L211W | c.632T>G | Missense_Mutation | 1 | 0.33 | PK59 | N | 2 | 0 | 12 | N |
MET | YFPDHPWHS | CENTRAL_NERVOUS_SYSTEM | 205 | p.L211W | c.632T>G | Missense_Mutation | 1 | 0.33 | SNU466 | N | 2 | 0 | 12 | N |