FGFR2 | PHINGSVKH | ENDOMETRIUM | 814 | p.T822fs | c.2464_2464delA | Frame_Shift_Del | 1 | 0.11 | ISHIKAWAHERAKLIO02ER | N | 0 | 0 | 0 | N |
FGFR2 | ADTPHAGRG | LARGE_INTESTINE | 456 | p.P459fs | c.1377_1378insC | Frame_Shift_Ins | 5 | 0.11 | SNUC4 | N | 0 | 0 | 0 | N |
FGFR2 | DTPHAGRGL | LARGE_INTESTINE | 457 | p.P459fs | c.1377_1378insC | Frame_Shift_Ins | 6 | 0.11 | SNUC4 | N | 6 | 0 | 0 | N |
FGFR2 | LSSTADTPH | LARGE_INTESTINE | 452 | p.P459fs | c.1377_1378insC | Frame_Shift_Ins | 1 | 0.11 | SNUC4 | N | 0 | 0 | 0 | N |
FGFR2 | PHAGRGLRV | LARGE_INTESTINE | 459 | p.P459fs | c.1377_1378insC | Frame_Shift_Ins | 6 | 0.11 | SNUC4 | N | 0 | 0 | 0 | N |
FGFR2 | SSTADTPHA | LARGE_INTESTINE | 453 | p.P459fs | c.1377_1378insC | Frame_Shift_Ins | 2 | 0.11 | SNUC4 | N | 1 | 0 | 0 | Y |
FGFR2 | STADTPHAG | LARGE_INTESTINE | 454 | p.P459fs | c.1377_1378insC | Frame_Shift_Ins | 3 | 0.11 | SNUC4 | N | 0 | 0 | 0 | N |
FGFR2 | TADTPHAGR | LARGE_INTESTINE | 455 | p.P459fs | c.1377_1378insC | Frame_Shift_Ins | 4 | 0.11 | SNUC4 | N | 4 | 0 | 0 | N |
FGFR2 | TPHAGRGLR | LARGE_INTESTINE | 458 | p.P459fs | c.1377_1378insC | Frame_Shift_Ins | 6 | 0.11 | SNUC4 | N | 4 | 0 | 0 | N |
FGFR2 | AARNVLVTK | SKIN | 629 | p.E637K | c.1909G>A | Missense_Mutation | 1 | 0.11 | A375 | Y | 2 | 14 | 0 | Y |
FGFR2 | ACTASSTVD | UPPER_AERODIGESTIVE_TRACT | 106 | p.R111S | c.333G>C | Missense_Mutation | 1 | 0.11 | SNU899 | N | 0 | 0 | 0 | N |
FGFR2 | ACTQNGPLY | SKIN | 554 | p.D558N | c.1672G>A | Missense_Mutation | 1 | 0.11 | COLO679 | N | 4 | 0 | 0 | N |
FGFR2 | ADAGEYICN | ENDOMETRIUM | 333 | p.K341N | c.1023G>T | Missense_Mutation | 1 | 0.11 | HEC251 | N | 1 | 0 | 0 | N |
FGFR2 | AEVFVSENS | LARGE_INTESTINE | 140 | p.D142V | c.425A>T | Missense_Mutation | 1 | 0.11 | SNU283 | N | 5 | 0 | 0 | N |
FGFR2 | AGEYICNVS | ENDOMETRIUM | 335 | p.K341N | c.1023G>T | Missense_Mutation | 1 | 0.11 | HEC251 | N | 0 | 0 | 0 | N |
FGFR2 | AGGNPMSTM | LARGE_INTESTINE | 181 | p.P187S | c.559C>T | Missense_Mutation | 1 | 0.11 | SNU1040 | N | 5 | 0 | 0 | N |
FGFR2 | AIYRIGVFL | ENDOMETRIUM | 380 | p.C383R | c.1147T>C | Missense_Mutation | 1 | 0.11 | JHUEM2 | N | 15 | 0 | 0 | N |
FGFR2 | APGRKKEIT | LUNG | 363 | p.E367K | c.1099G>A | Missense_Mutation | 1 | 0.11 | SBC5 | N | 6 | 0 | 0 | N |
FGFR2 | ARNVLVTKN | SKIN | 630 | p.E637K | c.1909G>A | Missense_Mutation | 1 | 0.11 | A375 | N | 2 | 0 | 0 | N |
FGFR2 | ARRPLGMEY | LARGE_INTESTINE | 579 | p.P583L | c.1748C>T | Missense_Mutation | 1 | 0.11 | HCT116 | Y | 3 | 10 | 0 | N |
FGFR2 | ARRPPGMEH | ENDOMETRIUM | 579 | p.Y587H | c.1759T>C | Missense_Mutation | 1 | 0.11 | EN | Y | 2 | 11 | 0 | Y |
FGFR2 | ASSTVDSET | UPPER_AERODIGESTIVE_TRACT | 109 | p.R111S | c.333G>C | Missense_Mutation | 1 | 0.11 | SNU899 | N | 1 | 0 | 0 | N |
FGFR2 | ATGMEYLAS | LUNG | 612 | p.R613T | c.1838G>C | Missense_Mutation | 1 | 0.11 | NCIH2009 | N | 1 | 0 | 0 | N |
FGFR2 | AVHKLTKRM | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 415 | p.I423M | c.1269C>G | Missense_Mutation | 1 | 0.11 | OCIM1 | N | 3 | 0 | 0 | N |
FGFR2 | AVHKLTKRV | LARGE_INTESTINE | 415 | p.I423V | c.1267A>G | Missense_Mutation | 1 | 0.11 | GP2D | N | 2 | 0 | 0 | N |
FGFR2 | AVTVVVKML | ENDOMETRIUM | 512 | p.A516V | c.1547C>T | Missense_Mutation | 1 | 0.11 | HEC59 | Y | 7 | 10 | 0 | N |
FGFR2 | AYTPMLAGV | LARGE_INTESTINE | 456 | p.D457Y | c.1369G>T | Missense_Mutation | 1 | 0.11 | SNU175 | N | 3 | 0 | 0 | N |
FGFR2 | CIGGYKVRN | BREAST | 203 | p.R203C | c.607C>T | Missense_Mutation | 1 | 0.11 | HCC1143 | N | 0 | 0 | 0 | N |
FGFR2 | CLPQYTHIN | PANCREAS | 809 | p.P814T | c.2440C>A | Missense_Mutation | 1 | 0.11 | PSN1 | N | 2 | 0 | 0 | N |
FGFR2 | CNVSNYIGQ | ENDOMETRIUM | 340 | p.K341N | c.1023G>T | Missense_Mutation | 1 | 0.11 | HEC251 | N | 0 | 0 | 0 | Y |
FGFR2 | CPAGGNPMS | LARGE_INTESTINE | 179 | p.P187S | c.559C>T | Missense_Mutation | 1 | 0.11 | SNU1040 | N | 3 | 0 | 0 | N |
FGFR2 | CQMKNTTKK | STOMACH | 399 | p.R400Q | c.1199G>A | Missense_Mutation | 1 | 0.11 | MKN74 | N | 6 | 0 | 0 | N |
FGFR2 | CRMKNMTKK | PLEURA | 399 | p.T404M | c.1211C>T | Missense_Mutation | 1 | 0.11 | MSTO211H | N | 2 | 0 | 0 | N |
FGFR2 | CTASSTVDS | UPPER_AERODIGESTIVE_TRACT | 107 | p.R111S | c.333G>C | Missense_Mutation | 1 | 0.11 | SNU899 | N | 0 | 0 | 0 | N |
FGFR2 | CTQNGPLYV | SKIN | 555 | p.D558N | c.1672G>A | Missense_Mutation | 1 | 0.11 | COLO679 | Y | 2 | 12 | 0 | N |
FGFR2 | CTYQLATGM | LUNG | 607 | p.R613T | c.1838G>C | Missense_Mutation | 1 | 0.11 | NCIH2009 | N | 5 | 0 | 0 | N |
FGFR2 | DAGEYICNV | ENDOMETRIUM | 334 | p.K341N | c.1023G>T | Missense_Mutation | 1 | 0.11 | HEC251 | Y | 4 | 9 | 0 | N |
FGFR2 | DDTDGAEVF | LARGE_INTESTINE | 135 | p.D142V | c.425A>T | Missense_Mutation | 1 | 0.11 | SNU283 | N | 5 | 0 | 0 | N |
FGFR2 | DGAEVFVSE | LARGE_INTESTINE | 138 | p.D142V | c.425A>T | Missense_Mutation | 1 | 0.11 | SNU283 | N | 0 | 0 | 0 | Y |
FGFR2 | DGLPYLRVL | ENDOMETRIUM | 304 | p.K310R | c.929A>G | Missense_Mutation | 1 | 0.11 | AN3CA | N | 17 | 0 | 0 | N |
FGFR2 | DGPLYVVVE | BILIARY_TRACT | 558 | p.I564V | c.1690A>G | Missense_Mutation | 1 | 0.11 | SNU245 | N | 1 | 0 | 0 | N |
FGFR2 | DKDKPKETV | LARGE_INTESTINE | 505 | p.A512T | c.1534G>A | Missense_Mutation | 1 | 0.11 | SNU503 | N | 1 | 0 | 0 | N |
FGFR2 | DKPKETVTV | LARGE_INTESTINE | 507 | p.A512T | c.1534G>A | Missense_Mutation | 1 | 0.11 | SNU503 | N | 2 | 0 | 0 | N |
FGFR2 | DPMPYEPYL | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 802 | p.C809Y | c.2426G>A | Missense_Mutation | 1 | 0.11 | RCHACV | Y | 19 | 10 | 0 | N |
FGFR2 | DTDGAEVFV | LARGE_INTESTINE | 136 | p.D142V | c.425A>T | Missense_Mutation | 1 | 0.11 | SNU283 | Y | 3 | 11 | 0 | N |
FGFR2 | DYLEIAIYR | ENDOMETRIUM | 375 | p.C383R | c.1147T>C | Missense_Mutation | 1 | 0.11 | JHUEM2 | Y | 2 | 9 | 0 | N |
FGFR2 | EAVTVVVKM | ENDOMETRIUM | 511 | p.A516V | c.1547C>T | Missense_Mutation | 1 | 0.11 | HEC59 | N | 8 | 0 | 0 | N |
FGFR2 | EDDTDGAEV | LARGE_INTESTINE | 134 | p.D142V | c.425A>T | Missense_Mutation | 1 | 0.11 | SNU283 | N | 3 | 0 | 0 | N |
FGFR2 | EFKQEHCIG | BREAST | 197 | p.R203C | c.607C>T | Missense_Mutation | 1 | 0.11 | HCC1143 | N | 0 | 0 | 0 | N |
FGFR2 | EHCIGGYKV | BREAST | 201 | p.R203C | c.607C>T | Missense_Mutation | 1 | 0.11 | HCC1143 | N | 2 | 0 | 0 | N |
FGFR2 | EHSYDINRV | ENDOMETRIUM | 586 | p.Y587H | c.1759T>C | Missense_Mutation | 1 | 0.11 | EN | N | 2 | 0 | 0 | N |
FGFR2 | EIAIYRIGV | ENDOMETRIUM | 378 | p.C383R | c.1147T>C | Missense_Mutation | 1 | 0.11 | JHUEM2 | N | 1 | 0 | 0 | N |
FGFR2 | EIFTLGGLP | ENDOMETRIUM | 696 | p.S703L | c.2108C>T | Missense_Mutation | 1 | 0.11 | HEC151 | N | 0 | 0 | 0 | N |
FGFR2 | ENNVMKTAD | KIDNEY | 637 | p.I643T | c.1928T>C | Missense_Mutation | 1 | 0.11 | A498 | N | 0 | 0 | 0 | N |
FGFR2 | EPCLPQYTH | PANCREAS | 807 | p.P814T | c.2440C>A | Missense_Mutation | 1 | 0.11 | PSN1 | N | 0 | 0 | 0 | N |
FGFR2 | EPYLPQYPH | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 807 | p.C809Y | c.2426G>A | Missense_Mutation | 1 | 0.11 | RCHACV | N | 1 | 0 | 0 | N |
FGFR2 | ETVTVAVKM | LARGE_INTESTINE | 511 | p.A512T | c.1534G>A | Missense_Mutation | 1 | 0.11 | SNU503 | N | 4 | 0 | 0 | N |
FGFR2 | EVFVSENSN | LARGE_INTESTINE | 141 | p.D142V | c.425A>T | Missense_Mutation | 1 | 0.11 | SNU283 | N | 0 | 0 | 0 | N |
FGFR2 | EYICNVSNY | ENDOMETRIUM | 337 | p.K341N | c.1023G>T | Missense_Mutation | 1 | 0.11 | HEC251 | Y | 5 | 14 | 0 | N |
FGFR2 | EYLRARRPL | LARGE_INTESTINE | 575 | p.P583L | c.1748C>T | Missense_Mutation | 1 | 0.11 | HCT116 | Y | 9 | 10 | 0 | N |
FGFR2 | FISLVVVTM | KIDNEY | 7 | p.C9S | c.25T>A | Missense_Mutation | 1 | 0.11 | A498 | Y | 6 | 9 | 29 | N |
FGFR2 | FKQEHCIGG | BREAST | 198 | p.R203C | c.607C>T | Missense_Mutation | 1 | 0.11 | HCC1143 | N | 2 | 0 | 4 | N |
FGFR2 | FTLGGLPYP | ENDOMETRIUM | 698 | p.S703L | c.2108C>T | Missense_Mutation | 1 | 0.11 | HEC151 | N | 2 | 0 | 0 | N |
FGFR2 | GACTQNGPL | SKIN | 553 | p.D558N | c.1672G>A | Missense_Mutation | 1 | 0.11 | COLO679 | N | 9 | 0 | 0 | N |
FGFR2 | GAEVFVSEN | LARGE_INTESTINE | 139 | p.D142V | c.425A>T | Missense_Mutation | 1 | 0.11 | SNU283 | N | 2 | 0 | 0 | Y |
FGFR2 | GEYICNVSN | ENDOMETRIUM | 336 | p.K341N | c.1023G>T | Missense_Mutation | 1 | 0.11 | HEC251 | N | 4 | 0 | 0 | N |
FGFR2 | GGLPYPGIP | ENDOMETRIUM | 701 | p.S703L | c.2108C>T | Missense_Mutation | 1 | 0.11 | HEC151 | N | 0 | 0 | 0 | N |
FGFR2 | GGNPMSTMR | LARGE_INTESTINE | 182 | p.P187S | c.559C>T | Missense_Mutation | 1 | 0.11 | SNU1040 | N | 1 | 0 | 0 | N |
FGFR2 | GKEFKQEHC | BREAST | 195 | p.R203C | c.607C>T | Missense_Mutation | 1 | 0.11 | HCC1143 | N | 1 | 0 | 0 | N |
FGFR2 | GLPYLRVLK | ENDOMETRIUM | 305 | p.K310R | c.929A>G | Missense_Mutation | 1 | 0.11 | AN3CA | Y | 4 | 14 | 0 | N |
FGFR2 | GLPYPGIPV | ENDOMETRIUM | 702 | p.S703L | c.2108C>T | Missense_Mutation | 1 | 0.11 | HEC151 | N | 7 | 0 | 0 | N |
FGFR2 | GLYACTASS | UPPER_AERODIGESTIVE_TRACT | 103 | p.R111S | c.333G>C | Missense_Mutation | 1 | 0.11 | SNU899 | N | 2 | 0 | 0 | N |
FGFR2 | GMEHSYDIN | ENDOMETRIUM | 584 | p.Y587H | c.1759T>C | Missense_Mutation | 1 | 0.11 | EN | N | 0 | 0 | 0 | N |
FGFR2 | GNPMSTMRW | LARGE_INTESTINE | 183 | p.P187S | c.559C>T | Missense_Mutation | 1 | 0.11 | SNU1040 | N | 1 | 0 | 0 | N |
FGFR2 | GPDGLPYLR | ENDOMETRIUM | 302 | p.K310R | c.929A>G | Missense_Mutation | 1 | 0.11 | AN3CA | N | 6 | 0 | 0 | N |
FGFR2 | GPLYVVVEY | BILIARY_TRACT | 559 | p.I564V | c.1690A>G | Missense_Mutation | 1 | 0.11 | SNU245 | N | 12 | 0 | 0 | N |
FGFR2 | GRFISLVVV | KIDNEY | 5 | p.C9S | c.25T>A | Missense_Mutation | 1 | 0.11 | A498 | N | 7 | 0 | 0 | N |
FGFR2 | GRKKEITAS | LUNG | 365 | p.E367K | c.1099G>A | Missense_Mutation | 1 | 0.11 | SBC5 | N | 2 | 0 | 0 | N |
FGFR2 | HCIGGYKVR | BREAST | 202 | p.R203C | c.607C>T | Missense_Mutation | 1 | 0.11 | HCC1143 | N | 3 | 0 | 0 | N |
FGFR2 | HKLTKRMPL | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 417 | p.I423M | c.1269C>G | Missense_Mutation | 1 | 0.11 | OCIM1 | N | 5 | 0 | 0 | N |
FGFR2 | HKLTKRVPL | LARGE_INTESTINE | 417 | p.I423V | c.1267A>G | Missense_Mutation | 1 | 0.11 | GP2D | N | 5 | 0 | 0 | N |
FGFR2 | HSYDINRVP | ENDOMETRIUM | 587 | p.Y587H | c.1759T>C | Missense_Mutation | 1 | 0.11 | EN | N | 0 | 0 | 0 | N |
FGFR2 | IAIYRIGVF | ENDOMETRIUM | 379 | p.C383R | c.1147T>C | Missense_Mutation | 1 | 0.11 | JHUEM2 | N | 10 | 0 | 7 | N |
FGFR2 | ICNVSNYIG | ENDOMETRIUM | 339 | p.K341N | c.1023G>T | Missense_Mutation | 1 | 0.11 | HEC251 | N | 0 | 0 | 0 | N |
FGFR2 | IDKDKPKET | LARGE_INTESTINE | 504 | p.A512T | c.1534G>A | Missense_Mutation | 1 | 0.11 | SNU503 | N | 2 | 0 | 0 | N |
FGFR2 | IDYYKETTN | BREAST | 655 | p.K660E | c.1978A>G | Missense_Mutation | 1 | 0.11 | EFM19 | N | 1 | 0 | 0 | N |
FGFR2 | IFTLGGLPY | ENDOMETRIUM | 697 | p.S703L | c.2108C>T | Missense_Mutation | 1 | 0.11 | HEC151 | N | 4 | 0 | 1 | N |
FGFR2 | ILCQMKNTT | STOMACH | 397 | p.R400Q | c.1199G>A | Missense_Mutation | 1 | 0.11 | MKN74 | N | 2 | 0 | 4 | N |
FGFR2 | ILCRMKNMT | PLEURA | 397 | p.T404M | c.1211C>T | Missense_Mutation | 1 | 0.11 | MSTO211H | N | 2 | 0 | 5 | N |
FGFR2 | INNIDYYKE | BREAST | 652 | p.K660E | c.1978A>G | Missense_Mutation | 1 | 0.11 | EFM19 | N | 0 | 0 | 0 | N |
FGFR2 | ISLVVVTMA | KIDNEY | 8 | p.C9S | c.25T>A | Missense_Mutation | 1 | 0.11 | A498 | N | 3 | 0 | 3 | N |
FGFR2 | ITTRLSLTA | LUNG | 448 | p.S454L | c.1361C>T | Missense_Mutation | 1 | 0.11 | NCIH647 | N | 3 | 0 | 2 | N |
FGFR2 | IVEYLQIKG | LUNG | 88 | p.G89V | c.266G>T | Missense_Mutation | 1 | 0.11 | CAL12T | N | 1 | 0 | 3 | N |
FGFR2 | IYRIGVFLI | ENDOMETRIUM | 381 | p.C383R | c.1147T>C | Missense_Mutation | 1 | 0.11 | JHUEM2 | Y | 8 | 10 | 38 | N |
FGFR2 | KDKPKETVT | LARGE_INTESTINE | 506 | p.A512T | c.1534G>A | Missense_Mutation | 1 | 0.11 | SNU503 | N | 2 | 0 | 0 | N |
FGFR2 | KEAVTVVVK | ENDOMETRIUM | 510 | p.A516V | c.1547C>T | Missense_Mutation | 1 | 0.11 | HEC59 | N | 4 | 0 | 0 | N |
FGFR2 | KEFKQEHCI | BREAST | 196 | p.R203C | c.607C>T | Missense_Mutation | 1 | 0.11 | HCC1143 | Y | 10 | 9 | 0 | N |
FGFR2 | KETVTVAVK | LARGE_INTESTINE | 510 | p.A512T | c.1534G>A | Missense_Mutation | 1 | 0.11 | SNU503 | N | 3 | 0 | 0 | N |
FGFR2 | KKEITASPD | LUNG | 367 | p.E367K | c.1099G>A | Missense_Mutation | 1 | 0.11 | SBC5 | N | 0 | 0 | 0 | N |
FGFR2 | KLTKRMPLR | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 418 | p.I423M | c.1269C>G | Missense_Mutation | 1 | 0.11 | OCIM1 | Y | 7 | 9 | 0 | N |
FGFR2 | KLTKRVPLR | LARGE_INTESTINE | 418 | p.I423V | c.1267A>G | Missense_Mutation | 1 | 0.11 | GP2D | Y | 7 | 10 | 0 | N |
FGFR2 | KNMTKKPDF | PLEURA | 402 | p.T404M | c.1211C>T | Missense_Mutation | 1 | 0.11 | MSTO211H | N | 7 | 0 | 0 | N |
FGFR2 | KNNVMKIAD | SKIN | 637 | p.E637K | c.1909G>A | Missense_Mutation | 1 | 0.11 | A375 | N | 0 | 0 | 0 | N |
FGFR2 | KPKEAVTVV | ENDOMETRIUM | 508 | p.A516V | c.1547C>T | Missense_Mutation | 1 | 0.11 | HEC59 | Y | 13 | 12 | 0 | N |
FGFR2 | KPKETVTVA | LARGE_INTESTINE | 508 | p.A512T | c.1534G>A | Missense_Mutation | 1 | 0.11 | SNU503 | N | 10 | 0 | 0 | N |
FGFR2 | KQEHCIGGY | BREAST | 199 | p.R203C | c.607C>T | Missense_Mutation | 1 | 0.11 | HCC1143 | N | 7 | 0 | 0 | N |
FGFR2 | KQQAPGRKK | LUNG | 360 | p.E367K | c.1099G>A | Missense_Mutation | 1 | 0.11 | SBC5 | N | 2 | 0 | 0 | N |
FGFR2 | KRMPLRRQV | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 421 | p.I423M | c.1269C>G | Missense_Mutation | 1 | 0.11 | OCIM1 | Y | 4 | 12 | 0 | N |
FGFR2 | KRVPLRRQV | LARGE_INTESTINE | 421 | p.I423V | c.1267A>G | Missense_Mutation | 1 | 0.11 | GP2D | Y | 4 | 11 | 0 | N |
FGFR2 | KTADFGLAR | KIDNEY | 642 | p.I643T | c.1928T>C | Missense_Mutation | 1 | 0.11 | A498 | Y | 7 | 12 | 0 | Y |
FGFR2 | LATGMEYLA | LUNG | 611 | p.R613T | c.1838G>C | Missense_Mutation | 1 | 0.11 | NCIH2009 | N | 6 | 0 | 0 | N |
FGFR2 | LCQMKNTTK | STOMACH | 398 | p.R400Q | c.1199G>A | Missense_Mutation | 1 | 0.11 | MKN74 | N | 1 | 0 | 5 | N |
FGFR2 | LCRMKNMTK | PLEURA | 398 | p.T404M | c.1211C>T | Missense_Mutation | 1 | 0.11 | MSTO211H | N | 2 | 0 | 15 | N |
FGFR2 | LEIAIYRIG | ENDOMETRIUM | 377 | p.C383R | c.1147T>C | Missense_Mutation | 1 | 0.11 | JHUEM2 | N | 2 | 0 | 0 | N |
FGFR2 | LGACTQNGP | SKIN | 552 | p.D558N | c.1672G>A | Missense_Mutation | 1 | 0.11 | COLO679 | N | 0 | 0 | 0 | N |
FGFR2 | LGGLPYPGI | ENDOMETRIUM | 700 | p.S703L | c.2108C>T | Missense_Mutation | 1 | 0.11 | HEC151 | N | 8 | 0 | 0 | N |
FGFR2 | LGMEYSYDI | LARGE_INTESTINE | 583 | p.P583L | c.1748C>T | Missense_Mutation | 1 | 0.11 | HCT116 | N | 10 | 0 | 9 | Y |
FGFR2 | LIVEYLQIK | LUNG | 87 | p.G89V | c.266G>T | Missense_Mutation | 1 | 0.11 | CAL12T | N | 4 | 0 | 0 | N |
FGFR2 | LLGACTQNG | SKIN | 551 | p.D558N | c.1672G>A | Missense_Mutation | 1 | 0.11 | COLO679 | N | 0 | 0 | 6 | N |
FGFR2 | LPQYTHING | PANCREAS | 810 | p.P814T | c.2440C>A | Missense_Mutation | 1 | 0.11 | PSN1 | N | 2 | 0 | 0 | N |
FGFR2 | LPYLRVLKH | ENDOMETRIUM | 306 | p.K310R | c.929A>G | Missense_Mutation | 1 | 0.11 | AN3CA | N | 4 | 0 | 29 | N |
FGFR2 | LPYPGIPVE | ENDOMETRIUM | 703 | p.S703L | c.2108C>T | Missense_Mutation | 1 | 0.11 | HEC151 | N | 3 | 0 | 0 | N |
FGFR2 | LRARRPLGM | LARGE_INTESTINE | 577 | p.P583L | c.1748C>T | Missense_Mutation | 1 | 0.11 | HCT116 | Y | 4 | 12 | 28 | N |
FGFR2 | LRVLKHSGI | ENDOMETRIUM | 309 | p.K310R | c.929A>G | Missense_Mutation | 1 | 0.11 | AN3CA | N | 7 | 0 | 27 | N |
FGFR2 | LSLTADTPM | LUNG | 452 | p.S454L | c.1361C>T | Missense_Mutation | 1 | 0.11 | NCIH647 | N | 7 | 0 | 0 | N |
FGFR2 | LSSTAYTPM | LARGE_INTESTINE | 452 | p.D457Y | c.1369G>T | Missense_Mutation | 1 | 0.11 | SNU175 | N | 8 | 0 | 0 | N |
FGFR2 | LTADTPMLA | LUNG | 454 | p.S454L | c.1361C>T | Missense_Mutation | 1 | 0.11 | NCIH647 | N | 3 | 0 | 8 | N |
FGFR2 | LTKRMPLRR | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 419 | p.I423M | c.1269C>G | Missense_Mutation | 1 | 0.11 | OCIM1 | N | 5 | 0 | 0 | N |
FGFR2 | LTKRVPLRR | LARGE_INTESTINE | 419 | p.I423V | c.1267A>G | Missense_Mutation | 1 | 0.11 | GP2D | N | 6 | 0 | 0 | N |
FGFR2 | LVTKNNVMK | SKIN | 634 | p.E637K | c.1909G>A | Missense_Mutation | 1 | 0.11 | A375 | N | 3 | 0 | 7 | N |
FGFR2 | LYACTASST | UPPER_AERODIGESTIVE_TRACT | 104 | p.R111S | c.333G>C | Missense_Mutation | 1 | 0.11 | SNU899 | N | 1 | 0 | 0 | Y |
FGFR2 | LYVVVEYAS | BILIARY_TRACT | 561 | p.I564V | c.1690A>G | Missense_Mutation | 1 | 0.11 | SNU245 | N | 2 | 0 | 0 | N |
FGFR2 | MEHSYDINR | ENDOMETRIUM | 585 | p.Y587H | c.1759T>C | Missense_Mutation | 1 | 0.11 | EN | Y | 0 | 9 | 0 | N |
FGFR2 | MKNMTKKPD | PLEURA | 401 | p.T404M | c.1211C>T | Missense_Mutation | 1 | 0.11 | MSTO211H | N | 0 | 0 | 17 | N |
FGFR2 | MKTADFGLA | KIDNEY | 641 | p.I643T | c.1928T>C | Missense_Mutation | 1 | 0.11 | A498 | N | 2 | 0 | 0 | N |
FGFR2 | MPLRRQVTV | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 423 | p.I423M | c.1269C>G | Missense_Mutation | 1 | 0.11 | OCIM1 | Y | 15 | 9 | 0 | N |
FGFR2 | MPYEPYLPQ | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 804 | p.C809Y | c.2426G>A | Missense_Mutation | 1 | 0.11 | RCHACV | N | 4 | 0 | 0 | Y |
FGFR2 | MSTMRWLKN | LARGE_INTESTINE | 186 | p.P187S | c.559C>T | Missense_Mutation | 1 | 0.11 | SNU1040 | N | 0 | 0 | 0 | N |
FGFR2 | MTKKPDFSS | PLEURA | 404 | p.T404M | c.1211C>T | Missense_Mutation | 1 | 0.11 | MSTO211H | N | 0 | 0 | 0 | Y |
FGFR2 | MVSWGRFIS | KIDNEY | 1 | p.C9S | c.25T>A | Missense_Mutation | 1 | 0.11 | A498 | N | 0 | 0 | 32 | N |
FGFR2 | MVVTVILCQ | STOMACH | 392 | p.R400Q | c.1199G>A | Missense_Mutation | 1 | 0.11 | MKN74 | N | 0 | 0 | 35 | N |
FGFR2 | NGPLYVIVE | SKIN | 558 | p.D558N | c.1672G>A | Missense_Mutation | 1 | 0.11 | COLO679 | N | 1 | 0 | 0 | N |
FGFR2 | NIDYYKETT | BREAST | 654 | p.K660E | c.1978A>G | Missense_Mutation | 1 | 0.11 | EFM19 | N | 0 | 0 | 0 | N |
FGFR2 | NLLGACTQN | SKIN | 550 | p.D558N | c.1672G>A | Missense_Mutation | 1 | 0.11 | COLO679 | N | 0 | 0 | 0 | N |
FGFR2 | NMTKKPDFS | PLEURA | 403 | p.T404M | c.1211C>T | Missense_Mutation | 1 | 0.11 | MSTO211H | N | 0 | 0 | 0 | N |
FGFR2 | NNIDYYKET | BREAST | 653 | p.K660E | c.1978A>G | Missense_Mutation | 1 | 0.11 | EFM19 | N | 1 | 0 | 0 | N |
FGFR2 | NNRTVLIVE | LUNG | 82 | p.G89V | c.266G>T | Missense_Mutation | 1 | 0.11 | CAL12T | N | 0 | 0 | 0 | Y |
FGFR2 | NNVMKTADF | KIDNEY | 638 | p.I643T | c.1928T>C | Missense_Mutation | 1 | 0.11 | A498 | N | 3 | 0 | 0 | N |
FGFR2 | NPMSTMRWL | LARGE_INTESTINE | 184 | p.P187S | c.559C>T | Missense_Mutation | 1 | 0.11 | SNU1040 | Y | 20 | 9 | 0 | N |
FGFR2 | NRTVLIVEY | LUNG | 83 | p.G89V | c.266G>T | Missense_Mutation | 1 | 0.11 | CAL12T | N | 4 | 0 | 0 | Y |
FGFR2 | NVLVTKNNV | SKIN | 632 | p.E637K | c.1909G>A | Missense_Mutation | 1 | 0.11 | A375 | Y | 4 | 10 | 0 | N |
FGFR2 | NVMKTADFG | KIDNEY | 639 | p.I643T | c.1928T>C | Missense_Mutation | 1 | 0.11 | A498 | N | 0 | 0 | 0 | N |
FGFR2 | NVSNYIGQA | ENDOMETRIUM | 341 | p.K341N | c.1023G>T | Missense_Mutation | 1 | 0.11 | HEC251 | N | 1 | 0 | 0 | Y |
FGFR2 | PAGGNPMST | LARGE_INTESTINE | 180 | p.P187S | c.559C>T | Missense_Mutation | 1 | 0.11 | SNU1040 | N | 0 | 0 | 0 | N |
FGFR2 | PCLPQYTHI | PANCREAS | 808 | p.P814T | c.2440C>A | Missense_Mutation | 1 | 0.11 | PSN1 | N | 1 | 0 | 0 | N |
FGFR2 | PDGLPYLRV | ENDOMETRIUM | 303 | p.K310R | c.929A>G | Missense_Mutation | 1 | 0.11 | AN3CA | N | 0 | 0 | 0 | N |
FGFR2 | PDPMPYEPY | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 801 | p.C809Y | c.2426G>A | Missense_Mutation | 1 | 0.11 | RCHACV | N | 1 | 0 | 0 | N |
FGFR2 | PGMEHSYDI | ENDOMETRIUM | 583 | p.Y587H | c.1759T>C | Missense_Mutation | 1 | 0.11 | EN | N | 3 | 0 | 0 | N |
FGFR2 | PGRKKEITA | LUNG | 364 | p.E367K | c.1099G>A | Missense_Mutation | 1 | 0.11 | SBC5 | N | 1 | 0 | 0 | N |
FGFR2 | PKEAVTVVV | ENDOMETRIUM | 509 | p.A516V | c.1547C>T | Missense_Mutation | 1 | 0.11 | HEC59 | N | 1 | 0 | 0 | N |
FGFR2 | PKETVTVAV | LARGE_INTESTINE | 509 | p.A512T | c.1534G>A | Missense_Mutation | 1 | 0.11 | SNU503 | N | 1 | 0 | 0 | N |
FGFR2 | PKQQAPGRK | LUNG | 359 | p.E367K | c.1099G>A | Missense_Mutation | 1 | 0.11 | SBC5 | N | 1 | 0 | 0 | N |
FGFR2 | PLGMEYSYD | LARGE_INTESTINE | 582 | p.P583L | c.1748C>T | Missense_Mutation | 1 | 0.11 | HCT116 | N | 0 | 0 | 0 | N |
FGFR2 | PLYVVVEYA | BILIARY_TRACT | 560 | p.I564V | c.1690A>G | Missense_Mutation | 1 | 0.11 | SNU245 | N | 3 | 0 | 0 | N |
FGFR2 | PMPYEPYLP | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 803 | p.C809Y | c.2426G>A | Missense_Mutation | 1 | 0.11 | RCHACV | N | 0 | 0 | 0 | N |
FGFR2 | PMSTMRWLK | LARGE_INTESTINE | 185 | p.P187S | c.559C>T | Missense_Mutation | 1 | 0.11 | SNU1040 | N | 1 | 0 | 0 | N |
FGFR2 | PNNRTVLIV | LUNG | 81 | p.G89V | c.266G>T | Missense_Mutation | 1 | 0.11 | CAL12T | Y | 0 | 14 | 0 | Y |
FGFR2 | PPGMEHSYD | ENDOMETRIUM | 582 | p.Y587H | c.1759T>C | Missense_Mutation | 1 | 0.11 | EN | N | 0 | 0 | 0 | N |
FGFR2 | PQYTHINGS | PANCREAS | 811 | p.P814T | c.2440C>A | Missense_Mutation | 1 | 0.11 | PSN1 | N | 0 | 0 | 0 | N |
FGFR2 | PYEPYLPQY | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 805 | p.C809Y | c.2426G>A | Missense_Mutation | 1 | 0.11 | RCHACV | N | 2 | 0 | 0 | Y |
FGFR2 | PYLPQYPHI | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 808 | p.C809Y | c.2426G>A | Missense_Mutation | 1 | 0.11 | RCHACV | Y | 3 | 11 | 0 | N |
FGFR2 | PYLRVLKHS | ENDOMETRIUM | 307 | p.K310R | c.929A>G | Missense_Mutation | 1 | 0.11 | AN3CA | N | 0 | 0 | 0 | N |
FGFR2 | QAPGRKKEI | LUNG | 362 | p.E367K | c.1099G>A | Missense_Mutation | 1 | 0.11 | SBC5 | N | 7 | 0 | 0 | N |
FGFR2 | QDGPLYVVV | BILIARY_TRACT | 557 | p.I564V | c.1690A>G | Missense_Mutation | 1 | 0.11 | SNU245 | N | 6 | 0 | 0 | N |
FGFR2 | QEHCIGGYK | BREAST | 200 | p.R203C | c.607C>T | Missense_Mutation | 1 | 0.11 | HCC1143 | N | 1 | 0 | 0 | N |
FGFR2 | QLATGMEYL | LUNG | 610 | p.R613T | c.1838G>C | Missense_Mutation | 1 | 0.11 | NCIH2009 | Y | 10 | 12 | 0 | N |
FGFR2 | QMKNTTKKP | STOMACH | 400 | p.R400Q | c.1199G>A | Missense_Mutation | 1 | 0.11 | MKN74 | N | 0 | 0 | 0 | N |
FGFR2 | QNGPLYVIV | SKIN | 557 | p.D558N | c.1672G>A | Missense_Mutation | 1 | 0.11 | COLO679 | Y | 2 | 17 | 0 | N |
FGFR2 | QQAPGRKKE | LUNG | 361 | p.E367K | c.1099G>A | Missense_Mutation | 1 | 0.11 | SBC5 | N | 0 | 0 | 0 | N |
FGFR2 | QYTHINGSV | PANCREAS | 812 | p.P814T | c.2440C>A | Missense_Mutation | 1 | 0.11 | PSN1 | N | 3 | 0 | 0 | N |
FGFR2 | RARRPLGME | LARGE_INTESTINE | 578 | p.P583L | c.1748C>T | Missense_Mutation | 1 | 0.11 | HCT116 | N | 0 | 0 | 0 | N |
FGFR2 | RFISLVVVT | KIDNEY | 6 | p.C9S | c.25T>A | Missense_Mutation | 1 | 0.11 | A498 | N | 1 | 0 | 0 | N |
FGFR2 | RIGVFLIAC | ENDOMETRIUM | 383 | p.C383R | c.1147T>C | Missense_Mutation | 1 | 0.11 | JHUEM2 | Y | 3 | 10 | 0 | N |
FGFR2 | RITTRLSLT | LUNG | 447 | p.S454L | c.1361C>T | Missense_Mutation | 1 | 0.11 | NCIH647 | N | 1 | 0 | 0 | N |
FGFR2 | RKKEITASP | LUNG | 366 | p.E367K | c.1099G>A | Missense_Mutation | 1 | 0.11 | SBC5 | N | 0 | 0 | 0 | N |
FGFR2 | RLSLTADTP | LUNG | 451 | p.S454L | c.1361C>T | Missense_Mutation | 1 | 0.11 | NCIH647 | N | 0 | 0 | 0 | N |
FGFR2 | RLSSTAYTP | LARGE_INTESTINE | 451 | p.D457Y | c.1369G>T | Missense_Mutation | 1 | 0.11 | SNU175 | N | 1 | 0 | 0 | N |
FGFR2 | RMKNMTKKP | PLEURA | 400 | p.T404M | c.1211C>T | Missense_Mutation | 1 | 0.11 | MSTO211H | N | 0 | 0 | 0 | N |
FGFR2 | RMPLRRQVT | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 422 | p.I423M | c.1269C>G | Missense_Mutation | 1 | 0.11 | OCIM1 | N | 3 | 0 | 0 | N |
FGFR2 | RNVLVTKNN | SKIN | 631 | p.E637K | c.1909G>A | Missense_Mutation | 1 | 0.11 | A375 | N | 0 | 0 | 0 | N |
FGFR2 | RPLGMEYSY | LARGE_INTESTINE | 581 | p.P583L | c.1748C>T | Missense_Mutation | 1 | 0.11 | HCT116 | N | 12 | 0 | 0 | N |
FGFR2 | RPPGMEHSY | ENDOMETRIUM | 581 | p.Y587H | c.1759T>C | Missense_Mutation | 1 | 0.11 | EN | N | 11 | 0 | 0 | Y |
FGFR2 | RRPLGMEYS | LARGE_INTESTINE | 580 | p.P583L | c.1748C>T | Missense_Mutation | 1 | 0.11 | HCT116 | N | 4 | 0 | 0 | N |
FGFR2 | RRPPGMEHS | ENDOMETRIUM | 580 | p.Y587H | c.1759T>C | Missense_Mutation | 1 | 0.11 | EN | N | 4 | 0 | 0 | N |
FGFR2 | RTVLIVEYL | LUNG | 84 | p.G89V | c.266G>T | Missense_Mutation | 1 | 0.11 | CAL12T | Y | 18 | 12 | 0 | N |
FGFR2 | RVLKHSGIN | ENDOMETRIUM | 310 | p.K310R | c.929A>G | Missense_Mutation | 1 | 0.11 | AN3CA | N | 0 | 0 | 0 | N |
FGFR2 | RVPLRRQVT | LARGE_INTESTINE | 422 | p.I423V | c.1267A>G | Missense_Mutation | 1 | 0.11 | GP2D | N | 3 | 0 | 0 | N |
FGFR2 | SCTYQLATG | LUNG | 606 | p.R613T | c.1838G>C | Missense_Mutation | 1 | 0.11 | NCIH2009 | N | 0 | 0 | 0 | N |
FGFR2 | SLTADTPML | LUNG | 453 | p.S454L | c.1361C>T | Missense_Mutation | 1 | 0.11 | NCIH647 | N | 12 | 0 | 0 | N |
FGFR2 | SLVVVTMAT | KIDNEY | 9 | p.C9S | c.25T>A | Missense_Mutation | 1 | 0.11 | A498 | N | 3 | 0 | 0 | N |
FGFR2 | SSTAYTPML | LARGE_INTESTINE | 453 | p.D457Y | c.1369G>T | Missense_Mutation | 1 | 0.11 | SNU175 | N | 10 | 0 | 0 | N |
FGFR2 | SSTVDSETW | UPPER_AERODIGESTIVE_TRACT | 110 | p.R111S | c.333G>C | Missense_Mutation | 1 | 0.11 | SNU899 | N | 3 | 0 | 0 | N |
FGFR2 | STAYTPMLA | LARGE_INTESTINE | 454 | p.D457Y | c.1369G>T | Missense_Mutation | 1 | 0.11 | SNU175 | N | 1 | 0 | 0 | N |
FGFR2 | STMRWLKNG | LARGE_INTESTINE | 187 | p.P187S | c.559C>T | Missense_Mutation | 1 | 0.11 | SNU1040 | N | 0 | 0 | 0 | N |
FGFR2 | STVDSETWY | UPPER_AERODIGESTIVE_TRACT | 111 | p.R111S | c.333G>C | Missense_Mutation | 1 | 0.11 | SNU899 | N | 5 | 0 | 0 | N |
FGFR2 | SWGRFISLV | KIDNEY | 3 | p.C9S | c.25T>A | Missense_Mutation | 1 | 0.11 | A498 | Y | 3 | 9 | 0 | N |
FGFR2 | TADFGLARD | KIDNEY | 643 | p.I643T | c.1928T>C | Missense_Mutation | 1 | 0.11 | A498 | N | 0 | 0 | 0 | N |
FGFR2 | TASSTVDSE | UPPER_AERODIGESTIVE_TRACT | 108 | p.R111S | c.333G>C | Missense_Mutation | 1 | 0.11 | SNU899 | N | 0 | 0 | 0 | N |
FGFR2 | TAYTPMLAG | LARGE_INTESTINE | 455 | p.D457Y | c.1369G>T | Missense_Mutation | 1 | 0.11 | SNU175 | N | 0 | 0 | 0 | N |
FGFR2 | TDGAEVFVS | LARGE_INTESTINE | 137 | p.D142V | c.425A>T | Missense_Mutation | 1 | 0.11 | SNU283 | N | 2 | 0 | 0 | Y |
FGFR2 | TENNVMKTA | KIDNEY | 636 | p.I643T | c.1928T>C | Missense_Mutation | 1 | 0.11 | A498 | Y | 6 | 9 | 0 | N |
FGFR2 | TGMEYLASQ | LUNG | 613 | p.R613T | c.1838G>C | Missense_Mutation | 1 | 0.11 | NCIH2009 | N | 0 | 0 | 0 | N |
FGFR2 | THINGSVKT | PANCREAS | 814 | p.P814T | c.2440C>A | Missense_Mutation | 1 | 0.11 | PSN1 | N | 1 | 0 | 0 | N |
FGFR2 | TKNNVMKIA | SKIN | 636 | p.E637K | c.1909G>A | Missense_Mutation | 1 | 0.11 | A375 | N | 1 | 0 | 0 | N |
FGFR2 | TKRMPLRRQ | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 420 | p.I423M | c.1269C>G | Missense_Mutation | 1 | 0.11 | OCIM1 | N | 0 | 0 | 0 | N |
FGFR2 | TKRVPLRRQ | LARGE_INTESTINE | 420 | p.I423V | c.1267A>G | Missense_Mutation | 1 | 0.11 | GP2D | N | 0 | 0 | 0 | N |
FGFR2 | TLGGLPYPG | ENDOMETRIUM | 699 | p.S703L | c.2108C>T | Missense_Mutation | 1 | 0.11 | HEC151 | N | 0 | 0 | 0 | N |
FGFR2 | TQDGPLYVV | BILIARY_TRACT | 556 | p.I564V | c.1690A>G | Missense_Mutation | 1 | 0.11 | SNU245 | N | 4 | 0 | 0 | N |
FGFR2 | TQNGPLYVI | SKIN | 556 | p.D558N | c.1672G>A | Missense_Mutation | 1 | 0.11 | COLO679 | Y | 6 | 13 | 0 | N |
FGFR2 | TRLSLTADT | LUNG | 450 | p.S454L | c.1361C>T | Missense_Mutation | 1 | 0.11 | NCIH647 | N | 3 | 0 | 0 | N |
FGFR2 | TRLSSTAYT | LARGE_INTESTINE | 450 | p.D457Y | c.1369G>T | Missense_Mutation | 1 | 0.11 | SNU175 | N | 3 | 0 | 0 | N |
FGFR2 | TTRLSLTAD | LUNG | 449 | p.S454L | c.1361C>T | Missense_Mutation | 1 | 0.11 | NCIH647 | N | 0 | 0 | 0 | N |
FGFR2 | TTRLSSTAY | LARGE_INTESTINE | 449 | p.D457Y | c.1369G>T | Missense_Mutation | 1 | 0.11 | SNU175 | N | 6 | 0 | 0 | N |
FGFR2 | TVILCQMKN | STOMACH | 395 | p.R400Q | c.1199G>A | Missense_Mutation | 1 | 0.11 | MKN74 | N | 0 | 0 | 0 | N |
FGFR2 | TVLIVEYLQ | LUNG | 85 | p.G89V | c.266G>T | Missense_Mutation | 1 | 0.11 | CAL12T | N | 0 | 0 | 0 | Y |
FGFR2 | TVTVAVKML | LARGE_INTESTINE | 512 | p.A512T | c.1534G>A | Missense_Mutation | 1 | 0.11 | SNU503 | Y | 7 | 9 | 0 | N |
FGFR2 | TVVVKMLKD | ENDOMETRIUM | 514 | p.A516V | c.1547C>T | Missense_Mutation | 1 | 0.11 | HEC59 | N | 0 | 0 | 0 | N |
FGFR2 | TYQLATGME | LUNG | 608 | p.R613T | c.1838G>C | Missense_Mutation | 1 | 0.11 | NCIH2009 | N | 0 | 0 | 0 | N |
FGFR2 | VEYLQIKGA | LUNG | 89 | p.G89V | c.266G>T | Missense_Mutation | 1 | 0.11 | CAL12T | N | 7 | 0 | 8 | N |
FGFR2 | VFVSENSNN | LARGE_INTESTINE | 142 | p.D142V | c.425A>T | Missense_Mutation | 1 | 0.11 | SNU283 | N | 0 | 0 | 2 | Y |
FGFR2 | VHKLTKRMP | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 416 | p.I423M | c.1269C>G | Missense_Mutation | 1 | 0.11 | OCIM1 | N | 0 | 0 | 11 | N |
FGFR2 | VHKLTKRVP | LARGE_INTESTINE | 416 | p.I423V | c.1267A>G | Missense_Mutation | 1 | 0.11 | GP2D | N | 0 | 0 | 11 | N |
FGFR2 | VILCQMKNT | STOMACH | 396 | p.R400Q | c.1199G>A | Missense_Mutation | 1 | 0.11 | MKN74 | N | 2 | 0 | 0 | N |
FGFR2 | VILCRMKNM | PLEURA | 396 | p.T404M | c.1211C>T | Missense_Mutation | 1 | 0.11 | MSTO211H | N | 8 | 0 | 0 | N |
FGFR2 | VLIVEYLQI | LUNG | 86 | p.G89V | c.266G>T | Missense_Mutation | 1 | 0.11 | CAL12T | N | 15 | 0 | 15 | Y |
FGFR2 | VLVTKNNVM | SKIN | 633 | p.E637K | c.1909G>A | Missense_Mutation | 1 | 0.11 | A375 | N | 7 | 0 | 11 | N |
FGFR2 | VMKTADFGL | KIDNEY | 640 | p.I643T | c.1928T>C | Missense_Mutation | 1 | 0.11 | A498 | N | 10 | 0 | 2 | N |
FGFR2 | VPLRRQVTV | LARGE_INTESTINE | 423 | p.I423V | c.1267A>G | Missense_Mutation | 1 | 0.11 | GP2D | Y | 15 | 10 | 0 | N |
FGFR2 | VRITTRLSL | LUNG | 446 | p.S454L | c.1361C>T | Missense_Mutation | 1 | 0.11 | NCIH647 | N | 9 | 0 | 42 | N |
FGFR2 | VSCTYQLAT | LUNG | 605 | p.R613T | c.1838G>C | Missense_Mutation | 1 | 0.11 | NCIH2009 | N | 1 | 0 | 0 | N |
FGFR2 | VSWGRFISL | KIDNEY | 2 | p.C9S | c.25T>A | Missense_Mutation | 1 | 0.11 | A498 | Y | 21 | 11 | 0 | N |
FGFR2 | VTENNVMKT | KIDNEY | 635 | p.I643T | c.1928T>C | Missense_Mutation | 1 | 0.11 | A498 | N | 2 | 0 | 0 | N |
FGFR2 | VTKNNVMKI | SKIN | 635 | p.E637K | c.1909G>A | Missense_Mutation | 1 | 0.11 | A375 | N | 7 | 0 | 6 | N |
FGFR2 | VTVILCQMK | STOMACH | 394 | p.R400Q | c.1199G>A | Missense_Mutation | 1 | 0.11 | MKN74 | N | 3 | 0 | 2 | N |
FGFR2 | VTVVVKMLK | ENDOMETRIUM | 513 | p.A516V | c.1547C>T | Missense_Mutation | 1 | 0.11 | HEC59 | N | 5 | 0 | 12 | N |
FGFR2 | VVEYASKGN | BILIARY_TRACT | 564 | p.I564V | c.1690A>G | Missense_Mutation | 1 | 0.11 | SNU245 | N | 1 | 0 | 2 | N |
FGFR2 | VVKMLKDDA | ENDOMETRIUM | 516 | p.A516V | c.1547C>T | Missense_Mutation | 1 | 0.11 | HEC59 | N | 2 | 0 | 20 | N |
FGFR2 | VVTVILCQM | STOMACH | 393 | p.R400Q | c.1199G>A | Missense_Mutation | 1 | 0.11 | MKN74 | N | 5 | 0 | 14 | N |
FGFR2 | VVVEYASKG | BILIARY_TRACT | 563 | p.I564V | c.1690A>G | Missense_Mutation | 1 | 0.11 | SNU245 | N | 0 | 0 | 5 | N |
FGFR2 | VVVKMLKDD | ENDOMETRIUM | 515 | p.A516V | c.1547C>T | Missense_Mutation | 1 | 0.11 | HEC59 | N | 0 | 0 | 12 | N |
FGFR2 | WEIFTLGGL | ENDOMETRIUM | 695 | p.S703L | c.2108C>T | Missense_Mutation | 1 | 0.11 | HEC151 | Y | 13 | 11 | 7 | N |
FGFR2 | WGRFISLVV | KIDNEY | 4 | p.C9S | c.25T>A | Missense_Mutation | 1 | 0.11 | A498 | N | 9 | 0 | 20 | N |
FGFR2 | YACTASSTV | UPPER_AERODIGESTIVE_TRACT | 105 | p.R111S | c.333G>C | Missense_Mutation | 1 | 0.11 | SNU899 | N | 9 | 0 | 2 | N |
FGFR2 | YEPCLPQYT | PANCREAS | 806 | p.P814T | c.2440C>A | Missense_Mutation | 1 | 0.11 | PSN1 | N | 8 | 0 | 1 | N |
FGFR2 | YEPYLPQYP | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 806 | p.C809Y | c.2426G>A | Missense_Mutation | 1 | 0.11 | RCHACV | N | 2 | 0 | 0 | Y |
FGFR2 | YICNVSNYI | ENDOMETRIUM | 338 | p.K341N | c.1023G>T | Missense_Mutation | 1 | 0.11 | HEC251 | Y | 10 | 10 | 8 | N |
FGFR2 | YLEIAIYRI | ENDOMETRIUM | 376 | p.C383R | c.1147T>C | Missense_Mutation | 1 | 0.11 | JHUEM2 | Y | 11 | 13 | 2 | N |
FGFR2 | YLPQYPHIN | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 809 | p.C809Y | c.2426G>A | Missense_Mutation | 1 | 0.11 | RCHACV | N | 4 | 0 | 4 | N |
FGFR2 | YLRARRPLG | LARGE_INTESTINE | 576 | p.P583L | c.1748C>T | Missense_Mutation | 1 | 0.11 | HCT116 | N | 3 | 0 | 10 | N |
FGFR2 | YLRVLKHSG | ENDOMETRIUM | 308 | p.K310R | c.929A>G | Missense_Mutation | 1 | 0.11 | AN3CA | N | 2 | 0 | 16 | N |
FGFR2 | YQLATGMEY | LUNG | 609 | p.R613T | c.1838G>C | Missense_Mutation | 1 | 0.11 | NCIH2009 | N | 9 | 0 | 12 | N |
FGFR2 | YRIGVFLIA | ENDOMETRIUM | 382 | p.C383R | c.1147T>C | Missense_Mutation | 1 | 0.11 | JHUEM2 | Y | 6 | 10 | 17 | N |
FGFR2 | YTHINGSVK | PANCREAS | 813 | p.P814T | c.2440C>A | Missense_Mutation | 1 | 0.11 | PSN1 | N | 3 | 0 | 2 | N |
FGFR2 | YTPMLAGVS | LARGE_INTESTINE | 457 | p.D457Y | c.1369G>T | Missense_Mutation | 1 | 0.11 | SNU175 | N | 2 | 0 | 7 | N |
FGFR2 | YVVVEYASK | BILIARY_TRACT | 562 | p.I564V | c.1690A>G | Missense_Mutation | 1 | 0.11 | SNU245 | Y | 6 | 15 | 6 | N |
FGFR2 | DVVERWPHR | ENDOMETRIUM | 247 | p.S252W | c.755C>G | Missense_Mutation | 1 | 0.22 | MFE280 | Y | 5 | 9 | 0 | Y |
FGFR2 | DVVERWPHR | ENDOMETRIUM | 247 | p.S252W | c.755C>G | Missense_Mutation | 1 | 0.22 | MFE319 | Y | 5 | 9 | 0 | Y |
FGFR2 | ERWPHRPIL | ENDOMETRIUM | 250 | p.S252W | c.755C>G | Missense_Mutation | 1 | 0.22 | MFE280 | Y | 6 | 9 | 0 | N |
FGFR2 | ERWPHRPIL | ENDOMETRIUM | 250 | p.S252W | c.755C>G | Missense_Mutation | 1 | 0.22 | MFE319 | Y | 6 | 9 | 0 | N |
FGFR2 | GKHKNIIKL | ENDOMETRIUM | 543 | p.N550K | c.1650T>G | Missense_Mutation | 1 | 0.22 | AN3CA | Y | 6 | 11 | 0 | N |
FGFR2 | GKHKNIIKL | ENDOMETRIUM | 543 | p.N550K | c.1650T>G | Missense_Mutation | 1 | 0.22 | MFE296 | Y | 6 | 11 | 0 | N |
FGFR2 | HKNIIKLLG | ENDOMETRIUM | 545 | p.N550K | c.1650T>G | Missense_Mutation | 1 | 0.22 | AN3CA | N | 0 | 0 | 0 | N |
FGFR2 | HKNIIKLLG | ENDOMETRIUM | 545 | p.N550K | c.1650T>G | Missense_Mutation | 1 | 0.22 | MFE296 | N | 0 | 0 | 0 | N |
FGFR2 | HLDVVERWP | ENDOMETRIUM | 245 | p.S252W | c.755C>G | Missense_Mutation | 1 | 0.22 | MFE280 | N | 0 | 0 | 0 | Y |
FGFR2 | HLDVVERWP | ENDOMETRIUM | 245 | p.S252W | c.755C>G | Missense_Mutation | 1 | 0.22 | MFE319 | N | 0 | 0 | 0 | Y |
FGFR2 | IGKHKNIIK | ENDOMETRIUM | 542 | p.N550K | c.1650T>G | Missense_Mutation | 1 | 0.22 | AN3CA | N | 0 | 0 | 3 | N |
FGFR2 | IGKHKNIIK | ENDOMETRIUM | 542 | p.N550K | c.1650T>G | Missense_Mutation | 1 | 0.22 | MFE296 | N | 0 | 0 | 3 | N |
FGFR2 | IIKLLGACT | ENDOMETRIUM | 548 | p.N550K | c.1650T>G | Missense_Mutation | 1 | 0.22 | AN3CA | N | 1 | 0 | 2 | N |
FGFR2 | IIKLLGACT | ENDOMETRIUM | 548 | p.N550K | c.1650T>G | Missense_Mutation | 1 | 0.22 | MFE296 | N | 1 | 0 | 2 | N |
FGFR2 | IKLLGACTQ | ENDOMETRIUM | 549 | p.N550K | c.1650T>G | Missense_Mutation | 1 | 0.22 | AN3CA | N | 0 | 0 | 35 | N |
FGFR2 | IKLLGACTQ | ENDOMETRIUM | 549 | p.N550K | c.1650T>G | Missense_Mutation | 1 | 0.22 | MFE296 | N | 0 | 0 | 35 | N |
FGFR2 | KHKNIIKLL | ENDOMETRIUM | 544 | p.N550K | c.1650T>G | Missense_Mutation | 1 | 0.22 | AN3CA | N | 5 | 0 | 0 | N |
FGFR2 | KHKNIIKLL | ENDOMETRIUM | 544 | p.N550K | c.1650T>G | Missense_Mutation | 1 | 0.22 | MFE296 | N | 5 | 0 | 0 | N |
FGFR2 | KLLGACTQD | ENDOMETRIUM | 550 | p.N550K | c.1650T>G | Missense_Mutation | 1 | 0.22 | AN3CA | N | 0 | 0 | 0 | N |
FGFR2 | KLLGACTQD | ENDOMETRIUM | 550 | p.N550K | c.1650T>G | Missense_Mutation | 1 | 0.22 | MFE296 | N | 0 | 0 | 0 | N |
FGFR2 | KNIIKLLGA | ENDOMETRIUM | 546 | p.N550K | c.1650T>G | Missense_Mutation | 1 | 0.22 | AN3CA | Y | 3 | 13 | 0 | N |
FGFR2 | KNIIKLLGA | ENDOMETRIUM | 546 | p.N550K | c.1650T>G | Missense_Mutation | 1 | 0.22 | MFE296 | Y | 3 | 13 | 0 | N |
FGFR2 | LDVVERWPH | ENDOMETRIUM | 246 | p.S252W | c.755C>G | Missense_Mutation | 1 | 0.22 | MFE280 | N | 0 | 0 | 0 | Y |
FGFR2 | LDVVERWPH | ENDOMETRIUM | 246 | p.S252W | c.755C>G | Missense_Mutation | 1 | 0.22 | MFE319 | N | 0 | 0 | 0 | Y |
FGFR2 | NIIKLLGAC | ENDOMETRIUM | 547 | p.N550K | c.1650T>G | Missense_Mutation | 1 | 0.22 | AN3CA | N | 0 | 0 | 0 | N |
FGFR2 | NIIKLLGAC | ENDOMETRIUM | 547 | p.N550K | c.1650T>G | Missense_Mutation | 1 | 0.22 | MFE296 | N | 0 | 0 | 0 | N |
FGFR2 | RWPHRPILQ | ENDOMETRIUM | 251 | p.S252W | c.755C>G | Missense_Mutation | 1 | 0.22 | MFE280 | N | 0 | 0 | 0 | N |
FGFR2 | RWPHRPILQ | ENDOMETRIUM | 251 | p.S252W | c.755C>G | Missense_Mutation | 1 | 0.22 | MFE319 | N | 0 | 0 | 0 | N |
FGFR2 | VERWPHRPI | ENDOMETRIUM | 249 | p.S252W | c.755C>G | Missense_Mutation | 1 | 0.22 | MFE280 | N | 8 | 0 | 11 | Y |
FGFR2 | VERWPHRPI | ENDOMETRIUM | 249 | p.S252W | c.755C>G | Missense_Mutation | 1 | 0.22 | MFE319 | N | 8 | 0 | 11 | Y |
FGFR2 | VVERWPHRP | ENDOMETRIUM | 248 | p.S252W | c.755C>G | Missense_Mutation | 1 | 0.22 | MFE280 | N | 0 | 0 | 0 | Y |
FGFR2 | VVERWPHRP | ENDOMETRIUM | 248 | p.S252W | c.755C>G | Missense_Mutation | 1 | 0.22 | MFE319 | N | 0 | 0 | 0 | Y |
FGFR2 | WPHRPILQA | ENDOMETRIUM | 252 | p.S252W | c.755C>G | Missense_Mutation | 1 | 0.22 | MFE280 | Y | 9 | 9 | 5 | N |
FGFR2 | WPHRPILQA | ENDOMETRIUM | 252 | p.S252W | c.755C>G | Missense_Mutation | 1 | 0.22 | MFE319 | Y | 9 | 9 | 5 | N |
FGFR2 | YHLDVVERW | ENDOMETRIUM | 244 | p.S252W | c.755C>G | Missense_Mutation | 1 | 0.22 | MFE280 | Y | 6 | 12 | 11 | Y |
FGFR2 | YHLDVVERW | ENDOMETRIUM | 244 | p.S252W | c.755C>G | Missense_Mutation | 1 | 0.22 | MFE319 | Y | 6 | 12 | 11 | Y |
FGFR2 | DYYKETTNG | BREAST | 656 | p.K660E | c.1978A>G | Missense_Mutation | 1 | 0.33 | EFM19 | N | 0 | 0 | 0 | N |
FGFR2 | ETTNGRLPV | BREAST | 660 | p.K660E | c.1978A>G | Missense_Mutation | 1 | 0.33 | EFM19 | N | 2 | 0 | 0 | N |
FGFR2 | KETTNGRLP | BREAST | 659 | p.K660E | c.1978A>G | Missense_Mutation | 1 | 0.33 | EFM19 | N | 0 | 0 | 0 | N |
FGFR2 | YKETTNGRL | BREAST | 658 | p.K660E | c.1978A>G | Missense_Mutation | 1 | 0.33 | EFM19 | N | 7 | 0 | 2 | N |
FGFR2 | YYKETTNGR | BREAST | 657 | p.K660E | c.1978A>G | Missense_Mutation | 1 | 0.33 | EFM19 | N | 3 | 0 | 4 | N |