Mutation - TCGA Type Chromosome Start Position End Position Strand Variant Classification Variant Type Reference Allele Tumor_seq Allele 1 Tumor_seq Allele 2 Tumor Sample Barcode Matched Norm Sample Barcode Genome Change cDNA Change Codon Change Protein Change ACC 23 125298569 125298569 + Missense_Mutation SNP C C A TCGA-PK-A5HB-01A-11D-A29I-10 TCGA-PK-A5HB-11A-11D-A29L-10 g.chrX:125298569C>A c.1339G>T c.(1339-1341)Ggg>Tgg p.G447W ACC 23 125299535 125299535 + Missense_Mutation SNP C C A TCGA-OR-A5KB-01A-11D-A30A-10 TCGA-OR-A5KB-11A-11D-A30A-10 g.chrX:125299535C>A c.373G>T c.(373-375)Gtg>Ttg p.V125L BLCA 23 125298729 125298729 + Silent SNP G G A TCGA-E7-A5KE-01A-11D-A289-08 TCGA-E7-A5KE-10A-01D-A289-08 g.chrX:125298729G>A c.1179C>T c.(1177-1179)tcC>tcT p.S393S BLCA 23 125298848 125298848 + Missense_Mutation SNP G G C TCGA-K4-A3WS-01A-11D-A22Z-08 TCGA-K4-A3WS-10A-01D-A22Z-08 g.chrX:125298848G>C c.1060C>G c.(1060-1062)Cgg>Ggg p.R354G BLCA 23 125298899 125298899 + Missense_Mutation SNP G G A TCGA-BT-A20X-01A-11D-A16O-08 TCGA-BT-A20X-11A-12D-A16O-08 g.chrX:125298899G>A c.1009C>T c.(1009-1011)Cgc>Tgc p.R337C BLCA 23 125298921 125298921 + Silent SNP G G A TCGA-FD-A6TH-01A-11D-A32B-08 TCGA-FD-A6TH-10A-01D-A329-08 g.chrX:125298921G>A c.987C>T c.(985-987)gtC>gtT p.V329V BLCA 23 125299030 125299030 + Missense_Mutation SNP C C A TCGA-XF-AAN5-01A-11D-A42E-08 TCGA-XF-AAN5-10A-01D-A42H-08 g.chrX:125299030C>A c.878G>T c.(877-879)aGc>aTc p.S293I BLCA 23 125299121 125299121 + Missense_Mutation SNP G G A TCGA-FD-A62O-01A-11D-A30E-08 TCGA-FD-A62O-10A-01D-A30H-08 g.chrX:125299121G>A c.787C>T c.(787-789)Cgc>Tgc p.R263C BLCA 23 125299171 125299171 + Missense_Mutation SNP C C T TCGA-BT-A3PH-01A-11D-A21Z-08 TCGA-BT-A3PH-10A-01D-A21Z-08 g.chrX:125299171C>T c.737G>A c.(736-738)cGt>cAt p.R246H BLCA 23 125299261 125299261 + Missense_Mutation SNP G G T TCGA-GD-A3OP-01A-21D-A21Z-08 TCGA-GD-A3OP-10A-01D-A21Z-08 g.chrX:125299261G>T c.647C>A c.(646-648)aCc>aAc p.T216N BLCA 23 125299271 125299271 + Missense_Mutation SNP G G T TCGA-G2-AA3F-01A-12D-A42E-08 TCGA-G2-AA3F-10A-01D-A42H-08 g.chrX:125299271G>T c.637C>A c.(637-639)Cgc>Agc p.R213S BLCA 23 125299408 125299408 + Missense_Mutation SNP C C T TCGA-GU-A42P-01A-11D-A23U-08 TCGA-GU-A42P-10A-01D-A23U-08 g.chrX:125299408C>T c.500G>A c.(499-501)gGc>gAc p.G167D BLCA 23 125299413 125299413 + Silent SNP G G A TCGA-FD-A6TC-01A-21D-A339-08 TCGA-FD-A6TC-10A-21D-A339-08 g.chrX:125299413G>A c.495C>T c.(493-495)gcC>gcT p.A165A BLCA 23 125299590 125299590 + Silent SNP C C A TCGA-DK-A3X1-01A-12D-A22Z-08 TCGA-DK-A3X1-10A-01D-A22Z-08 g.chrX:125299590C>A c.318G>T c.(316-318)ctG>ctT p.L106L BLCA 23 125299664 125299664 + Missense_Mutation SNP T T A TCGA-FD-A3B4-01A-12D-A202-08 TCGA-FD-A3B4-10A-01D-A202-08 g.chrX:125299664T>A c.244A>T c.(244-246)Agg>Tgg p.R82W BLCA 23 125299768 125299768 + Missense_Mutation SNP G G A TCGA-ZF-A9R3-01A-11D-A38G-08 TCGA-ZF-A9R3-10A-01D-A38J-08 g.chrX:125299768G>A c.140C>T c.(139-141)aCg>aTg p.T47M BRCA 23 125298649 125298649 + Missense_Mutation SNP T T A TCGA-A8-A083-01A-21W-A019-09 TCGA-A8-A083-10A-01W-A021-09 g.chrX:125298649T>A c.1259A>T c.(1258-1260)tAc>tTc p.Y420F BRCA 23 125298656 125298656 + Missense_Mutation SNP C C G TCGA-A8-A08R-01A-11W-A050-09 TCGA-A8-A08R-10A-01W-A055-09 g.chrX:125298656C>G c.1252G>C c.(1252-1254)Gtg>Ctg p.V418L BRCA 23 125298870 125298870 + Silent SNP A A T TCGA-E2-A1IN-01A-11D-A13L-09 TCGA-E2-A1IN-10A-01D-A188-09 g.chrX:125298870A>T c.1038T>A c.(1036-1038)tcT>tcA p.S346S BRCA 23 125298898 125298898 + Missense_Mutation SNP C C T TCGA-OL-A66I-01A-21D-A29N-09 TCGA-OL-A66I-10A-01D-A29N-09 g.chrX:125298898C>T c.1010G>A c.(1009-1011)cGc>cAc p.R337H BRCA 23 125299410 125299410 + Silent SNP G G A TCGA-AO-A12H-01A-11D-A10Y-09 TCGA-AO-A12H-10A-01D-A110-09 g.chrX:125299410G>A c.498C>T c.(496-498)acC>acT p.T166T CESC 23 125298619 125298619 + Missense_Mutation SNP G G A TCGA-FU-A3HZ-01A-11D-A20U-09 TCGA-FU-A3HZ-10A-01D-A20U-09 g.chrX:125298619G>A c.1289C>T c.(1288-1290)gCg>gTg p.A430V CESC 23 125298663 125298663 + Silent SNP G G A TCGA-Q1-A6DT-01A-11D-A32I-09 TCGA-Q1-A6DT-10A-01D-A32I-09 g.chrX:125298663G>A c.1245C>T c.(1243-1245)gaC>gaT p.D415D CESC 23 125298775 125298775 + Missense_Mutation SNP C C T TCGA-IR-A3LK-01A-12D-A20U-09 TCGA-IR-A3LK-10A-01D-A20U-09 g.chrX:125298775C>T c.1133G>A c.(1132-1134)cGc>cAc p.R378H CESC 23 125299005 125299005 + Silent SNP G G A TCGA-IR-A3LK-01A-12D-A20U-09 TCGA-IR-A3LK-10A-01D-A20U-09 g.chrX:125299005G>A c.903C>T c.(901-903)atC>atT p.I301I CESC 23 125299273 125299273 + Missense_Mutation SNP G G A TCGA-EA-A3HU-01A-11D-A20U-09 TCGA-EA-A3HU-10B-01D-A20U-09 g.chrX:125299273G>A c.635C>T c.(634-636)tCc>tTc p.S212F CESC 23 125299852 125299852 + Missense_Mutation SNP C C T TCGA-C5-A1MH-01A-11D-A14W-08 TCGA-C5-A1MH-10A-01D-A14W-08 g.chrX:125299852C>T c.56G>A c.(55-57)gGa>gAa p.G19E COAD 23 125298540 125298540 + Silent SNP C C T TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chrX:125298540C>T c.1368G>A c.(1366-1368)ggG>ggA p.G456G COAD 23 125298563 125298564 + Frame_Shift_Ins INS - - C TCGA-CK-5916-01A-11D-1650-10 TCGA-CK-5916-10A-01D-1650-10 g.chrX:125298563_125298564insC c.1344_1345insG c.(1342-1347)gggcctfs p.P449fs COAD 23 125298563 125298564 + Frame_Shift_Ins INS - - C TCGA-CK-6746-01A-11D-1835-10 TCGA-CK-6746-10A-01D-1835-10 g.chrX:125298563_125298564insC c.1344_1345insG c.(1342-1347)gggcctfs p.P449fs COAD 23 125298589 125298589 + Missense_Mutation SNP T T C TCGA-AD-6901-01A-11D-1924-10 TCGA-AD-6901-10A-01D-1924-10 g.chrX:125298589T>C c.1319A>G c.(1318-1320)gAg>gGg p.E440G COAD 23 125298736 125298736 + Missense_Mutation SNP A A G TCGA-CM-5868-01A-01D-1650-10 TCGA-CM-5868-10A-01D-1650-10 g.chrX:125298736A>G c.1172T>C c.(1171-1173)cTg>cCg p.L391P COAD 23 125298736 125298736 + Missense_Mutation SNP A A G TCGA-G4-6307-01A-11D-1719-10 TCGA-G4-6307-10A-01D-1720-10 g.chrX:125298736A>G c.1172T>C c.(1171-1173)cTg>cCg p.L391P COAD 23 125298775 125298775 + Missense_Mutation SNP C C T TCGA-A6-5665-01A-01D-1650-10 TCGA-A6-5665-10A-01D-1650-10 g.chrX:125298775C>T c.1133G>A c.(1132-1134)cGc>cAc p.R378H COAD 23 125298899 125298899 + Missense_Mutation SNP G G A TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chrX:125298899G>A c.1009C>T c.(1009-1011)Cgc>Tgc p.R337C COAD 23 125298907 125298907 + Missense_Mutation SNP G G A TCGA-AA-3660-01A-01D-1719-10 TCGA-AA-3660-11A-01D-1719-10 g.chrX:125298907G>A c.1001C>T c.(1000-1002)cCg>cTg p.P334L COAD 23 125299020 125299020 + Silent SNP G G A TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chrX:125299020G>A c.888C>T c.(886-888)tcC>tcT p.S296S COAD 23 125299120 125299120 + Missense_Mutation SNP C C T TCGA-AU-6004-01A-11D-1719-10 TCGA-AU-6004-10A-01D-1719-10 g.chrX:125299120C>T c.788G>A c.(787-789)cGc>cAc p.R263H COAD 23 125299283 125299283 + Missense_Mutation SNP C C T TCGA-F4-6570-01A-11D-1771-10 TCGA-F4-6570-10A-01D-1771-10 g.chrX:125299283C>T c.625G>A c.(625-627)Gtg>Atg p.V209M COAD 23 125299314 125299314 + Silent SNP G G A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chrX:125299314G>A c.594C>T c.(592-594)ttC>ttT p.F198F COAD 23 125299408 125299408 + Missense_Mutation SNP C C A TCGA-F4-6460-01A-11D-1771-10 TCGA-F4-6460-10B-01D-1771-10 g.chrX:125299408C>A c.500G>T c.(499-501)gGc>gTc p.G167V COAD 23 125299408 125299408 + Missense_Mutation SNP C C T TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chrX:125299408C>T c.500G>A c.(499-501)gGc>gAc p.G167D COAD 23 125299440 125299440 + Silent SNP C C T TCGA-AZ-6603-01A-11D-1835-10 TCGA-AZ-6603-11A-02D-1835-10 g.chrX:125299440C>T c.468G>A c.(466-468)gaG>gaA p.E156E COAD 23 125299441 125299441 + Missense_Mutation SNP T T C TCGA-CM-5860-01A-01D-1650-10 TCGA-CM-5860-10A-01D-1650-10 g.chrX:125299441T>C c.467A>G c.(466-468)gAg>gGg p.E156G COAD 23 125299441 125299441 + Missense_Mutation SNP T T C TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chrX:125299441T>C c.467A>G c.(466-468)gAg>gGg p.E156G COAD 23 125299604 125299604 + Missense_Mutation SNP C C T TCGA-AA-3821-01A-01W-0995-10 TCGA-AA-3821-10A-01W-0995-10 g.chrX:125299604C>T c.304G>A c.(304-306)Gcg>Acg p.A102T COAD 23 125299762 125299762 + Missense_Mutation SNP C C T TCGA-A6-6654-01A-21D-1835-10 TCGA-A6-6654-10A-01D-1835-10 g.chrX:125299762C>T c.146G>A c.(145-147)cGc>cAc p.R49H COAD 23 125299782 125299782 + Missense_Mutation SNP C C A TCGA-A6-5665-01A-01D-1650-10 TCGA-A6-5665-10A-01D-1650-10 g.chrX:125299782C>A c.126G>T c.(124-126)caG>caT p.Q42H COAD 23 125299859 125299859 + Missense_Mutation SNP C C T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chrX:125299859C>T c.49G>A c.(49-51)Gag>Aag p.E17K COADREAD 23 125298540 125298540 + Silent SNP C C T TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chrX:125298540C>T c.1368G>A c.(1366-1368)ggG>ggA p.G456G COADREAD 23 125298563 125298564 + Frame_Shift_Ins INS - - C TCGA-CK-5916-01A-11D-1650-10 TCGA-CK-5916-10A-01D-1650-10 g.chrX:125298563_125298564insC c.1344_1345insG c.(1342-1347)gggcctfs p.P449fs COADREAD 23 125298563 125298564 + Frame_Shift_Ins INS - - C TCGA-CK-6746-01A-11D-1835-10 TCGA-CK-6746-10A-01D-1835-10 g.chrX:125298563_125298564insC c.1344_1345insG c.(1342-1347)gggcctfs p.P449fs COADREAD 23 125298589 125298589 + Missense_Mutation SNP T T C TCGA-AD-6901-01A-11D-1924-10 TCGA-AD-6901-10A-01D-1924-10 g.chrX:125298589T>C c.1319A>G c.(1318-1320)gAg>gGg p.E440G COADREAD 23 125298618 125298618 + Silent SNP C C T TCGA-AG-3892-01A-01W-1073-09 TCGA-AG-3892-10A-01W-1073-09 g.chrX:125298618C>T c.1290G>A c.(1288-1290)gcG>gcA p.A430A COADREAD 23 125298736 125298736 + Missense_Mutation SNP A A G TCGA-CM-5868-01A-01D-1650-10 TCGA-CM-5868-10A-01D-1650-10 g.chrX:125298736A>G c.1172T>C c.(1171-1173)cTg>cCg p.L391P COADREAD 23 125298736 125298736 + Missense_Mutation SNP A A G TCGA-G4-6307-01A-11D-1719-10 TCGA-G4-6307-10A-01D-1720-10 g.chrX:125298736A>G c.1172T>C c.(1171-1173)cTg>cCg p.L391P COADREAD 23 125298775 125298775 + Missense_Mutation SNP C C T TCGA-A6-5665-01A-01D-1650-10 TCGA-A6-5665-10A-01D-1650-10 g.chrX:125298775C>T c.1133G>A c.(1132-1134)cGc>cAc p.R378H COADREAD 23 125298899 125298899 + Missense_Mutation SNP G G A TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chrX:125298899G>A c.1009C>T c.(1009-1011)Cgc>Tgc p.R337C COADREAD 23 125298907 125298907 + Missense_Mutation SNP G G A TCGA-AA-3660-01A-01D-1719-10 TCGA-AA-3660-11A-01D-1719-10 g.chrX:125298907G>A c.1001C>T c.(1000-1002)cCg>cTg p.P334L COADREAD 23 125298991 125298991 + Missense_Mutation SNP C C A TCGA-AG-A026-01A-32W-A096-10 TCGA-AG-A026-10A-01W-A096-10 g.chrX:125298991C>A c.917G>T c.(916-918)tGc>tTc p.C306F COADREAD 23 125299020 125299020 + Silent SNP G G A TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chrX:125299020G>A c.888C>T c.(886-888)tcC>tcT p.S296S COADREAD 23 125299059 125299059 + Silent SNP G G A TCGA-AG-3909-01A-01W-1073-09 TCGA-AG-3909-10A-01W-1073-09 g.chrX:125299059G>A c.849C>T c.(847-849)gaC>gaT p.D283D COADREAD 23 125299120 125299120 + Missense_Mutation SNP C C T TCGA-AU-6004-01A-11D-1719-10 TCGA-AU-6004-10A-01D-1719-10 g.chrX:125299120C>T c.788G>A c.(787-789)cGc>cAc p.R263H COADREAD 23 125299283 125299283 + Missense_Mutation SNP C C T TCGA-F4-6570-01A-11D-1771-10 TCGA-F4-6570-10A-01D-1771-10 g.chrX:125299283C>T c.625G>A c.(625-627)Gtg>Atg p.V209M COADREAD 23 125299314 125299314 + Silent SNP G G A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chrX:125299314G>A c.594C>T c.(592-594)ttC>ttT p.F198F COADREAD 23 125299408 125299408 + Missense_Mutation SNP C C A TCGA-F4-6460-01A-11D-1771-10 TCGA-F4-6460-10B-01D-1771-10 g.chrX:125299408C>A c.500G>T c.(499-501)gGc>gTc p.G167V COADREAD 23 125299408 125299408 + Missense_Mutation SNP C C T TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chrX:125299408C>T c.500G>A c.(499-501)gGc>gAc p.G167D COADREAD 23 125299440 125299440 + Silent SNP C C T TCGA-AZ-6603-01A-11D-1835-10 TCGA-AZ-6603-11A-02D-1835-10 g.chrX:125299440C>T c.468G>A c.(466-468)gaG>gaA p.E156E COADREAD 23 125299441 125299441 + Missense_Mutation SNP T T C TCGA-CM-5860-01A-01D-1650-10 TCGA-CM-5860-10A-01D-1650-10 g.chrX:125299441T>C c.467A>G c.(466-468)gAg>gGg p.E156G COADREAD 23 125299441 125299441 + Missense_Mutation SNP T T C TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chrX:125299441T>C c.467A>G c.(466-468)gAg>gGg p.E156G COADREAD 23 125299499 125299499 + Missense_Mutation SNP G G A TCGA-EI-6506-01A-11D-1733-10 TCGA-EI-6506-10A-01D-1733-10 g.chrX:125299499G>A c.409C>T c.(409-411)Cgg>Tgg p.R137W COADREAD 23 125299604 125299604 + Missense_Mutation SNP C C T TCGA-AA-3821-01A-01W-0995-10 TCGA-AA-3821-10A-01W-0995-10 g.chrX:125299604C>T c.304G>A c.(304-306)Gcg>Acg p.A102T COADREAD 23 125299656 125299656 + Silent SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chrX:125299656G>A c.252C>T c.(250-252)ccC>ccT p.P84P COADREAD 23 125299670 125299670 + Missense_Mutation SNP C C T TCGA-AG-4007-01A-01W-1073-09 TCGA-AG-4007-10A-01W-1073-09 g.chrX:125299670C>T c.238G>A c.(238-240)Gtc>Atc p.V80I COADREAD 23 125299762 125299762 + Missense_Mutation SNP C C T TCGA-A6-6654-01A-21D-1835-10 TCGA-A6-6654-10A-01D-1835-10 g.chrX:125299762C>T c.146G>A c.(145-147)cGc>cAc p.R49H COADREAD 23 125299782 125299782 + Missense_Mutation SNP C C A TCGA-A6-5665-01A-01D-1650-10 TCGA-A6-5665-10A-01D-1650-10 g.chrX:125299782C>A c.126G>T c.(124-126)caG>caT p.Q42H COADREAD 23 125299859 125299859 + Missense_Mutation SNP C C T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chrX:125299859C>T c.49G>A c.(49-51)Gag>Aag p.E17K ESCA 23 125298723 125298723 + Silent SNP C C T TCGA-R6-A8W8-01B-11D-A37C-09 TCGA-R6-A8W8-10A-01D-A37F-09 g.chrX:125298723C>T c.1185G>A c.(1183-1185)ccG>ccA p.P395P ESCA 23 125298766 125298766 + Missense_Mutation SNP T T G TCGA-L5-A43E-01A-11D-A247-09 TCGA-L5-A43E-10A-01D-A247-09 g.chrX:125298766T>G c.1142A>C c.(1141-1143)aAg>aCg p.K381T ESCA 23 125298805 125298805 + Missense_Mutation SNP C C A TCGA-2H-A9GH-01A-11D-A37C-09 TCGA-2H-A9GH-11A-11D-A37F-09 g.chrX:125298805C>A c.1103G>T c.(1102-1104)gGc>gTc p.G368V ESCA 23 125298846 125298846 + Silent SNP C C A TCGA-JY-A93C-01A-11D-A387-09 TCGA-JY-A93C-10A-01D-A38A-09 g.chrX:125298846C>A c.1062G>T c.(1060-1062)cgG>cgT p.R354R ESCA 23 125298882 125298882 + Silent SNP C C A TCGA-VR-A8EX-01A-11D-A36J-09 TCGA-VR-A8EX-10A-01D-A36M-09 g.chrX:125298882C>A c.1026G>T c.(1024-1026)cgG>cgT p.R342R ESCA 23 125299265 125299265 + Missense_Mutation SNP C C A TCGA-LN-A49Y-01A-11D-A27G-09 TCGA-LN-A49Y-10A-01D-A27G-09 g.chrX:125299265C>A c.643G>T c.(643-645)Ggc>Tgc p.G215C ESCA 23 125299490 125299490 + Missense_Mutation SNP C C T TCGA-2H-A9GF-01A-11D-A37C-09 TCGA-2H-A9GF-11A-11D-A37F-09 g.chrX:125299490C>T c.418G>A c.(418-420)Gag>Aag p.E140K ESCA 23 125299586 125299586 + Missense_Mutation SNP C C T TCGA-VR-AA7B-01A-31D-A403-09 TCGA-VR-AA7B-10A-01D-A403-09 g.chrX:125299586C>T c.322G>A c.(322-324)Gcc>Acc p.A108T GBM 23 125298905 125298905 + Missense_Mutation SNP G G A TCGA-06-0141-01A-01D-1490-08 TCGA-06-0141-10A-01D-1490-08 g.chrX:125298905G>A c.1003C>T c.(1003-1005)Cgc>Tgc p.R335C GBM 23 125299171 125299171 + Missense_Mutation SNP C C T TCGA-06-0155-01B-01D-1492-08 TCGA-06-0155-10A-01D-1492-08 g.chrX:125299171C>T c.737G>A c.(736-738)cGt>cAt p.R246H GBM 23 125299171 125299171 + Missense_Mutation SNP C C T TCGA-06-6694-01A-12D-1845-08 TCGA-06-6694-10A-01D-1845-08 g.chrX:125299171C>T c.737G>A c.(736-738)cGt>cAt p.R246H GBM 23 125299277 125299277 + Missense_Mutation SNP C C T TCGA-14-0862-01B-01D-1845-08 TCGA-14-0862-10C-01D-1845-08 g.chrX:125299277C>T c.631G>A c.(631-633)Ggc>Agc p.G211S GBM 23 125299442 125299442 + Missense_Mutation SNP C C T TCGA-06-6697-01A-11D-1845-08 TCGA-06-6697-10A-01D-1845-08 g.chrX:125299442C>T c.466G>A c.(466-468)Gag>Aag p.E156K GBM 23 125299499 125299499 + Missense_Mutation SNP G G A TCGA-06-0132-01A-02D-1491-08 TCGA-06-0132-10A-01D-1491-08 g.chrX:125299499G>A c.409C>T c.(409-411)Cgg>Tgg p.R137W GBM 23 125299765 125299765 + Missense_Mutation SNP C C T TCGA-06-0174-01A-01D-1491-08 TCGA-06-0174-10B-01D-1491-08 g.chrX:125299765C>T c.143G>A c.(142-144)cGt>cAt p.R48H GBM 23 125299891 125299891 + Missense_Mutation SNP G G T TCGA-02-2485-01A-01D-1494-08 TCGA-02-2485-10A-01D-1494-08 g.chrX:125299891G>T c.17C>A c.(16-18)aCa>aAa p.T6K GBMLGG 23 125298550 125298550 + Missense_Mutation SNP C C T TCGA-S9-A7R8-01A-11D-A34J-08 TCGA-S9-A7R8-10A-01D-A34M-08 g.chrX:125298550C>T c.1358G>A c.(1357-1359)gGc>gAc p.G453D GBMLGG 23 125298843 125298843 + Silent SNP C C T TCGA-TQ-A7RP-01A-21D-A34A-08 TCGA-TQ-A7RP-10A-01D-A34A-08 g.chrX:125298843C>T c.1065G>A c.(1063-1065)tcG>tcA p.S355S GBMLGG 23 125298904 125298904 + Missense_Mutation SNP C C G TCGA-DU-A5TU-01A-11D-A289-08 TCGA-DU-A5TU-10A-01D-A289-08 g.chrX:125298904C>G c.1004G>C c.(1003-1005)cGc>cCc p.R335P GBMLGG 23 125298905 125298905 + Missense_Mutation SNP G G A TCGA-06-0141-01A-01D-1490-08 TCGA-06-0141-10A-01D-1490-08 g.chrX:125298905G>A c.1003C>T c.(1003-1005)Cgc>Tgc p.R335C GBMLGG 23 125298906 125298906 + Silent SNP C C T TCGA-S9-A7IZ-01A-11D-A34A-08 TCGA-S9-A7IZ-10A-01D-A34A-08 g.chrX:125298906C>T c.1002G>A c.(1000-1002)ccG>ccA p.P334P GBMLGG 23 125299120 125299120 + Missense_Mutation SNP C C T TCGA-DB-A4XH-01A-11D-A27K-08 TCGA-DB-A4XH-10A-01D-A27N-08 g.chrX:125299120C>T c.788G>A c.(787-789)cGc>cAc p.R263H GBMLGG 23 125299120 125299120 + Missense_Mutation SNP C C T TCGA-HT-7689-01A-11D-2253-08 TCGA-HT-7689-10A-01D-2253-08 g.chrX:125299120C>T c.788G>A c.(787-789)cGc>cAc p.R263H GBMLGG 23 125299171 125299171 + Missense_Mutation SNP C C T TCGA-06-0155-01B-01D-1492-08 TCGA-06-0155-10A-01D-1492-08 g.chrX:125299171C>T c.737G>A c.(736-738)cGt>cAt p.R246H GBMLGG 23 125299171 125299171 + Missense_Mutation SNP C C T TCGA-06-6694-01A-12D-1845-08 TCGA-06-6694-10A-01D-1845-08 g.chrX:125299171C>T c.737G>A c.(736-738)cGt>cAt p.R246H GBMLGG 23 125299212 125299212 + Silent SNP G G T TCGA-S9-A6U0-01A-12D-A32B-08 TCGA-S9-A6U0-10A-01D-A329-08 g.chrX:125299212G>T c.696C>A c.(694-696)gcC>gcA p.A232A GBMLGG 23 125299247 125299247 + Missense_Mutation SNP G G A TCGA-E1-A7YQ-01A-11D-A34J-08 TCGA-E1-A7YQ-10A-01D-A34M-08 g.chrX:125299247G>A c.661C>T c.(661-663)Cgg>Tgg p.R221W GBMLGG 23 125299277 125299277 + Missense_Mutation SNP C C T TCGA-14-0862-01B-01D-1845-08 TCGA-14-0862-10C-01D-1845-08 g.chrX:125299277C>T c.631G>A c.(631-633)Ggc>Agc p.G211S GBMLGG 23 125299442 125299442 + Missense_Mutation SNP C C T TCGA-06-6697-01A-11D-1845-08 TCGA-06-6697-10A-01D-1845-08 g.chrX:125299442C>T c.466G>A c.(466-468)Gag>Aag p.E156K GBMLGG 23 125299499 125299499 + Missense_Mutation SNP G G A TCGA-06-0132-01A-02D-1491-08 TCGA-06-0132-10A-01D-1491-08 g.chrX:125299499G>A c.409C>T c.(409-411)Cgg>Tgg p.R137W GBMLGG 23 125299672 125299672 + Missense_Mutation SNP G G A TCGA-HW-A5KL-01A-11D-A27K-08 TCGA-HW-A5KL-10A-01D-A27N-08 g.chrX:125299672G>A c.236C>T c.(235-237)gCc>gTc p.A79V GBMLGG 23 125299762 125299762 + Missense_Mutation SNP C C T TCGA-TQ-A7RJ-01A-11D-A33T-08 TCGA-TQ-A7RJ-10A-01D-A33W-08 g.chrX:125299762C>T c.146G>A c.(145-147)cGc>cAc p.R49H GBMLGG 23 125299765 125299765 + Missense_Mutation SNP C C T TCGA-06-0174-01A-01D-1491-08 TCGA-06-0174-10B-01D-1491-08 g.chrX:125299765C>T c.143G>A c.(142-144)cGt>cAt p.R48H GBMLGG 23 125299773 125299773 + Silent SNP C C T TCGA-WY-A85E-01A-11D-A36O-08 TCGA-WY-A85E-10A-01D-A367-08 g.chrX:125299773C>T c.135G>A c.(133-135)ccG>ccA p.P45P GBMLGG 23 125299816 125299816 + Missense_Mutation SNP G G A TCGA-TM-A84H-01A-11D-A36O-08 TCGA-TM-A84H-10A-01D-A367-08 g.chrX:125299816G>A c.92C>T c.(91-93)gCg>gTg p.A31V GBMLGG 23 125299891 125299891 + Missense_Mutation SNP G G T TCGA-02-2485-01A-01D-1494-08 TCGA-02-2485-10A-01D-1494-08 g.chrX:125299891G>T c.17C>A c.(16-18)aCa>aAa p.T6K HNSC 23 125298689 125298689 + Missense_Mutation SNP C C T TCGA-CV-A6K1-01A-11D-A31L-08 TCGA-CV-A6K1-10A-01D-A31J-08 g.chrX:125298689C>T c.1219G>A c.(1219-1221)Ggc>Agc p.G407S HNSC 23 125298719 125298719 + Missense_Mutation SNP G G T TCGA-CN-A641-01A-11D-A30E-08 TCGA-CN-A641-10A-01D-A30H-08 g.chrX:125298719G>T c.1189C>A c.(1189-1191)Ccc>Acc p.P397T HNSC 23 125298763 125298763 + Missense_Mutation SNP A A G TCGA-KU-A6H7-01A-11D-A31L-08 TCGA-KU-A6H7-10A-01D-A31J-08 g.chrX:125298763A>G c.1145T>C c.(1144-1146)tTc>tCc p.F382S HNSC 23 125298775 125298775 + Missense_Mutation SNP C C T TCGA-CV-A6JY-01A-11D-A31L-08 TCGA-CV-A6JY-10A-01D-A31J-08 g.chrX:125298775C>T c.1133G>A c.(1132-1134)cGc>cAc p.R378H HNSC 23 125298829 125298829 + Missense_Mutation SNP T T A TCGA-BA-4075-01A-01D-1434-08 TCGA-BA-4075-10A-01D-1434-08 g.chrX:125298829T>A c.1079A>T c.(1078-1080)cAg>cTg p.Q360L HNSC 23 125298830 125298830 + Missense_Mutation SNP G G T TCGA-BA-4075-01A-01D-1434-08 TCGA-BA-4075-10A-01D-1434-08 g.chrX:125298830G>T c.1078C>A c.(1078-1080)Cag>Aag p.Q360K HNSC 23 125298868 125298868 + Missense_Mutation SNP C C G TCGA-CQ-A4CD-01A-21D-A25D-08 TCGA-CQ-A4CD-10A-01D-A25E-08 g.chrX:125298868C>G c.1040G>C c.(1039-1041)cGa>cCa p.R347P HNSC 23 125298905 125298905 + Missense_Mutation SNP G G C TCGA-KU-A66S-01A-21D-A30E-08 TCGA-KU-A66S-10A-01D-A30H-08 g.chrX:125298905G>C c.1003C>G c.(1003-1005)Cgc>Ggc p.R335G HNSC 23 125299012 125299012 + Missense_Mutation SNP A A T TCGA-CR-7388-01A-11D-2012-08 TCGA-CR-7388-10A-01D-2013-08 g.chrX:125299012A>T c.896T>A c.(895-897)cTg>cAg p.L299Q HNSC 23 125299102 125299102 + Missense_Mutation SNP G G T TCGA-CV-A45Z-01A-21D-A25D-08 TCGA-CV-A45Z-10A-01D-A25E-08 g.chrX:125299102G>T c.806C>A c.(805-807)gCc>gAc p.A269D HNSC 23 125299536 125299536 + Silent SNP G G A TCGA-CV-6942-01A-21D-2012-08 TCGA-CV-6942-10A-01D-2013-08 g.chrX:125299536G>A c.372C>T c.(370-372)gaC>gaT p.D124D HNSC 23 125299776 125299776 + Silent SNP C C T TCGA-CV-7245-01A-11D-2012-08 TCGA-CV-7245-10A-01D-2013-08 g.chrX:125299776C>T c.132G>A c.(130-132)cgG>cgA p.R44R HNSC 23 125299869 125299869 + Silent SNP C C A TCGA-D6-A6EN-01A-11D-A31L-08 TCGA-D6-A6EN-10A-01D-A31J-08 g.chrX:125299869C>A c.39G>T c.(37-39)gcG>gcT p.A13A KICH 23 125299514 125299514 + Missense_Mutation SNP G G A TCGA-KN-8428-01A-11D-2310-10 TCGA-KN-8428-11A-01D-2311-10 g.chrX:125299514G>A c.394C>T c.(394-396)Cgc>Tgc p.R132C KIPAN 23 125299313 125299313 + Missense_Mutation SNP C C T TCGA-B2-3923-01A-01D-1458-08 TCGA-B2-3923-10A-01D-1458-08 g.chrX:125299313C>T c.595G>A c.(595-597)Gca>Aca p.A199T KIPAN 23 125299514 125299514 + Missense_Mutation SNP G G A TCGA-KN-8428-01A-11D-2310-10 TCGA-KN-8428-11A-01D-2311-10 g.chrX:125299514G>A c.394C>T c.(394-396)Cgc>Tgc p.R132C KIRC 23 125299313 125299313 + Missense_Mutation SNP C C T TCGA-B2-3923-01A-01D-1458-08 TCGA-B2-3923-10A-01D-1458-08 g.chrX:125299313C>T c.595G>A c.(595-597)Gca>Aca p.A199T LGG 23 125298550 125298550 + Missense_Mutation SNP C C T TCGA-S9-A7R8-01A-11D-A34J-08 TCGA-S9-A7R8-10A-01D-A34M-08 g.chrX:125298550C>T c.1358G>A c.(1357-1359)gGc>gAc p.G453D LGG 23 125298843 125298843 + Silent SNP C C T TCGA-TQ-A7RP-01A-21D-A34A-08 TCGA-TQ-A7RP-10A-01D-A34A-08 g.chrX:125298843C>T c.1065G>A c.(1063-1065)tcG>tcA p.S355S LGG 23 125298904 125298904 + Missense_Mutation SNP C C G TCGA-DU-A5TU-01A-11D-A289-08 TCGA-DU-A5TU-10A-01D-A289-08 g.chrX:125298904C>G c.1004G>C c.(1003-1005)cGc>cCc p.R335P LGG 23 125298906 125298906 + Silent SNP C C T TCGA-S9-A7IZ-01A-11D-A34A-08 TCGA-S9-A7IZ-10A-01D-A34A-08 g.chrX:125298906C>T c.1002G>A c.(1000-1002)ccG>ccA p.P334P LGG 23 125299120 125299120 + Missense_Mutation SNP C C T TCGA-DB-A4XH-01A-11D-A27K-08 TCGA-DB-A4XH-10A-01D-A27N-08 g.chrX:125299120C>T c.788G>A c.(787-789)cGc>cAc p.R263H LGG 23 125299120 125299120 + Missense_Mutation SNP C C T TCGA-HT-7689-01A-11D-2253-08 TCGA-HT-7689-10A-01D-2253-08 g.chrX:125299120C>T c.788G>A c.(787-789)cGc>cAc p.R263H LGG 23 125299212 125299212 + Silent SNP G G T TCGA-S9-A6U0-01A-12D-A32B-08 TCGA-S9-A6U0-10A-01D-A329-08 g.chrX:125299212G>T c.696C>A c.(694-696)gcC>gcA p.A232A LGG 23 125299247 125299247 + Missense_Mutation SNP G G A TCGA-E1-A7YQ-01A-11D-A34J-08 TCGA-E1-A7YQ-10A-01D-A34M-08 g.chrX:125299247G>A c.661C>T c.(661-663)Cgg>Tgg p.R221W LGG 23 125299672 125299672 + Missense_Mutation SNP G G A TCGA-HW-A5KL-01A-11D-A27K-08 TCGA-HW-A5KL-10A-01D-A27N-08 g.chrX:125299672G>A c.236C>T c.(235-237)gCc>gTc p.A79V LGG 23 125299762 125299762 + Missense_Mutation SNP C C T TCGA-TQ-A7RJ-01A-11D-A33T-08 TCGA-TQ-A7RJ-10A-01D-A33W-08 g.chrX:125299762C>T c.146G>A c.(145-147)cGc>cAc p.R49H LGG 23 125299773 125299773 + Silent SNP C C T TCGA-WY-A85E-01A-11D-A36O-08 TCGA-WY-A85E-10A-01D-A367-08 g.chrX:125299773C>T c.135G>A c.(133-135)ccG>ccA p.P45P LGG 23 125299816 125299816 + Missense_Mutation SNP G G A TCGA-TM-A84H-01A-11D-A36O-08 TCGA-TM-A84H-10A-01D-A367-08 g.chrX:125299816G>A c.92C>T c.(91-93)gCg>gTg p.A31V LIHC 23 125299293 125299293 + Missense_Mutation SNP G G T TCGA-BC-A3KG-01A-11D-A20W-10 TCGA-BC-A3KG-10A-01D-A20W-10 g.chrX:125299293G>T c.615C>A c.(613-615)gaC>gaA p.D205E LIHC 23 125299403 125299403 + Missense_Mutation SNP C C T TCGA-2Y-A9H9-01A-21D-A38X-10 TCGA-2Y-A9H9-10A-01D-A38X-10 g.chrX:125299403C>T c.505G>A c.(505-507)Gaa>Aaa p.E169K LIHC 23 125299819 125299819 + Missense_Mutation SNP G G A TCGA-DD-AACI-01A-11D-A40R-10 TCGA-DD-AACI-10A-01D-A40U-10 g.chrX:125299819G>A c.89C>T c.(88-90)gCg>gTg p.A30V LUAD 23 125298530 125298530 + Missense_Mutation SNP C C A TCGA-73-4668-01A-01D-1265-08 TCGA-73-4668-11A-01D-1265-08 g.chrX:125298530C>A c.1378G>T c.(1378-1380)Ggc>Tgc p.G460C LUAD 23 125298568 125298568 + Missense_Mutation SNP C C A TCGA-05-4427-01A-21D-1855-08 TCGA-05-4427-10A-01D-1855-08 g.chrX:125298568C>A c.1340G>T c.(1339-1341)gGg>gTg p.G447V LUAD 23 125298588 125298588 + Missense_Mutation SNP C C A TCGA-62-8399-01A-21D-2323-08 TCGA-62-8399-10A-01D-2323-08 g.chrX:125298588C>A c.1320G>T c.(1318-1320)gaG>gaT p.E440D LUAD 23 125298590 125298590 + Nonsense_Mutation SNP C C A TCGA-67-3771-01A-01D-1040-01 TCGA-67-3771-10A-01D-1040-01 g.chrX:125298590C>A c.1318G>T c.(1318-1320)Gag>Tag p.E440* LUAD 23 125298594 125298594 + Nonsense_Mutation SNP C C T TCGA-50-5045-01A-01D-1625-08 TCGA-50-5045-10A-01D-1625-08 g.chrX:125298594C>T c.1314G>A c.(1312-1314)tgG>tgA p.W438* LUAD 23 125298618 125298618 + Silent SNP C C A TCGA-38-4626-01A-01D-1553-08 TCGA-38-4626-11A-01D-1553-08 g.chrX:125298618C>A c.1290G>T c.(1288-1290)gcG>gcT p.A430A LUAD 23 125298619 125298619 + Missense_Mutation SNP G G T TCGA-05-4427-01A-21D-1855-08 TCGA-05-4427-10A-01D-1855-08 g.chrX:125298619G>T c.1289C>A c.(1288-1290)gCg>gAg p.A430E LUAD 23 125298632 125298632 + Missense_Mutation SNP C C T TCGA-05-4389-01A-01D-1265-08 TCGA-05-4389-10A-01D-1265-08 g.chrX:125298632C>T c.1276G>A c.(1276-1278)Gag>Aag p.E426K LUAD 23 125298677 125298677 + Missense_Mutation SNP G G T TCGA-78-7147-01A-11D-2036-08 TCGA-78-7147-10A-01D-2036-08 g.chrX:125298677G>T c.1231C>A c.(1231-1233)Ctc>Atc p.L411I LUAD 23 125298730 125298730 + Missense_Mutation SNP G G T TCGA-69-7979-01A-11D-2184-08 TCGA-69-7979-10A-01D-2184-08 g.chrX:125298730G>T c.1178C>A c.(1177-1179)tCc>tAc p.S393Y LUAD 23 125298753 125298753 + Silent SNP C C T TCGA-55-8208-01A-11D-2238-08 TCGA-55-8208-10A-01D-2238-08 g.chrX:125298753C>T c.1155G>A c.(1153-1155)gaG>gaA p.E385E LUAD 23 125298759 125298759 + Silent SNP C C G TCGA-55-A4DG-01A-11D-A24D-08 TCGA-55-A4DG-10A-01D-A24F-08 g.chrX:125298759C>G c.1149G>C c.(1147-1149)ctG>ctC p.L383L LUAD 23 125298774 125298774 + Silent SNP G G A TCGA-86-7954-01A-11D-2184-08 TCGA-86-7954-10A-01D-2184-08 g.chrX:125298774G>A c.1134C>T c.(1132-1134)cgC>cgT p.R378R LUAD 23 125298776 125298776 + Missense_Mutation SNP G G A TCGA-05-4430-01A-02D-1265-08 TCGA-05-4430-10A-01D-1265-08 g.chrX:125298776G>A c.1132C>T c.(1132-1134)Cgc>Tgc p.R378C LUAD 23 125298782 125298782 + Missense_Mutation SNP C C A TCGA-55-7907-01A-11D-2167-08 TCGA-55-7907-10A-01D-2167-08 g.chrX:125298782C>A c.1126G>T c.(1126-1128)Gac>Tac p.D376Y LUAD 23 125298801 125298801 + Missense_Mutation SNP A A T TCGA-49-6761-01A-31D-1945-08 TCGA-49-6761-11A-01D-1945-08 g.chrX:125298801A>T c.1107T>A c.(1105-1107)caT>caA p.H369Q LUAD 23 125298847 125298847 + Missense_Mutation SNP C C A TCGA-05-4405-01A-21D-1855-08 TCGA-05-4405-10A-01D-1855-08 g.chrX:125298847C>A c.1061G>T c.(1060-1062)cGg>cTg p.R354L LUAD 23 125298849 125298849 + Silent SNP C C G TCGA-55-8616-01A-11D-2393-08 TCGA-55-8616-10A-01D-2393-08 g.chrX:125298849C>G c.1059G>C c.(1057-1059)gtG>gtC p.V353V LUAD 23 125298852 125298852 + Silent SNP G G T TCGA-78-7161-01A-11D-2036-08 TCGA-78-7161-10A-01D-2036-08 g.chrX:125298852G>T c.1056C>A c.(1054-1056)ggC>ggA p.G352G LUAD 23 125298867 125298867 + Silent SNP T T C TCGA-55-8208-01A-11D-2238-08 TCGA-55-8208-10A-01D-2238-08 g.chrX:125298867T>C c.1041A>G c.(1039-1041)cgA>cgG p.R347R LUAD 23 125298868 125298868 + Missense_Mutation SNP C C A TCGA-44-8117-01A-11D-2238-08 TCGA-44-8117-10A-01D-2238-08 g.chrX:125298868C>A c.1040G>T c.(1039-1041)cGa>cTa p.R347L LUAD 23 125298876 125298876 + Silent SNP C C A TCGA-83-5908-01A-21D-2284-08 TCGA-83-5908-10A-01D-2284-08 g.chrX:125298876C>A c.1032G>T c.(1030-1032)ctG>ctT p.L344L LUAD 23 125298902 125298902 + Missense_Mutation SNP G G T TCGA-MN-A4N1-01A-11D-A24P-08 TCGA-MN-A4N1-10A-01D-A24P-08 g.chrX:125298902G>T c.1006C>A c.(1006-1008)Cag>Aag p.Q336K LUAD 23 125298905 125298905 + Missense_Mutation SNP G G T TCGA-17-Z021-01A-01W-0746-08 TCGA-17-Z021-11A-01W-0746-08 g.chrX:125298905G>T c.1003C>A c.(1003-1005)Cgc>Agc p.R335S LUAD 23 125298934 125298934 + Missense_Mutation SNP G G C TCGA-38-4626-01A-01D-1553-08 TCGA-38-4626-11A-01D-1553-08 g.chrX:125298934G>C c.974C>G c.(973-975)tCt>tGt p.S325C LUAD 23 125298976 125298976 + Missense_Mutation SNP C C A TCGA-55-8616-01A-11D-2393-08 TCGA-55-8616-10A-01D-2393-08 g.chrX:125298976C>A c.932G>T c.(931-933)tGc>tTc p.C311F LUAD 23 125298988 125298988 + Missense_Mutation SNP C C T TCGA-49-4512-01A-21D-1855-08 TCGA-49-4512-11A-01D-1855-08 g.chrX:125298988C>T c.920G>A c.(919-921)cGa>cAa p.R307Q LUAD 23 125298989 125298989 + Silent SNP G G T TCGA-55-8203-01A-11D-2238-08 TCGA-55-8203-10A-01D-2238-08 g.chrX:125298989G>T c.919C>A c.(919-921)Cga>Aga p.R307R LUAD 23 125298989 125298989 + Silent SNP G G T TCGA-75-5126-01A-01D-1753-08 TCGA-75-5126-10A-01D-1753-08 g.chrX:125298989G>T c.919C>A c.(919-921)Cga>Aga p.R307R LUAD 23 125299009 125299009 + Missense_Mutation SNP G G T TCGA-NJ-A4YQ-01A-11D-A25L-08 TCGA-NJ-A4YQ-10A-01D-A25L-08 g.chrX:125299009G>T c.899C>A c.(898-900)tCc>tAc p.S300Y LUAD 23 125299020 125299020 + Silent SNP G G T TCGA-73-4666-01A-01D-1265-08 TCGA-73-4666-11A-01D-1265-08 g.chrX:125299020G>T c.888C>A c.(886-888)tcC>tcA p.S296S LUAD 23 125299021 125299021 + Missense_Mutation SNP G G T TCGA-49-4494-01A-01D-1265-08 TCGA-49-4494-11A-01D-1265-08 g.chrX:125299021G>T c.887C>A c.(886-888)tCc>tAc p.S296Y LUAD 23 125299047 125299047 + Missense_Mutation SNP G G T TCGA-49-4494-01A-01D-1265-08 TCGA-49-4494-11A-01D-1265-08 g.chrX:125299047G>T c.861C>A c.(859-861)caC>caA p.H287Q LUAD 23 125299068 125299068 + Silent SNP C C A TCGA-97-A4M0-01A-11D-A24P-08 TCGA-97-A4M0-10A-01D-A24P-08 g.chrX:125299068C>A c.840G>T c.(838-840)gtG>gtT p.V280V LUAD 23 125299101 125299101 + Silent SNP G G T TCGA-75-6214-01A-41D-1945-08 TCGA-75-6214-10A-01D-1946-08 g.chrX:125299101G>T c.807C>A c.(805-807)gcC>gcA p.A269A LUAD 23 125299247 125299247 + Silent SNP G G T TCGA-64-1679-01A-21D-2063-08 TCGA-64-1679-10A-01D-2063-08 g.chrX:125299247G>T c.661C>A c.(661-663)Cgg>Agg p.R221R LUAD 23 125299249 125299249 + Missense_Mutation SNP C C A TCGA-78-8662-01A-11D-2393-08 TCGA-78-8662-10A-01D-2393-08 g.chrX:125299249C>A c.659G>T c.(658-660)tGg>tTg p.W220L LUAD 23 125299259 125299259 + Missense_Mutation SNP C C T TCGA-64-5779-01A-01D-1625-08 TCGA-64-5779-10A-01D-1625-08 g.chrX:125299259C>T c.649G>A c.(649-651)Gtg>Atg p.V217M LUAD 23 125299273 125299273 + Missense_Mutation SNP G G A TCGA-99-8033-01A-11D-2238-08 TCGA-99-8033-10A-01D-2238-08 g.chrX:125299273G>A c.635C>T c.(634-636)tCc>tTc p.S212F LUAD 23 125299276 125299276 + Missense_Mutation SNP C C A TCGA-78-8662-01A-11D-2393-08 TCGA-78-8662-10A-01D-2393-08 g.chrX:125299276C>A c.632G>T c.(631-633)gGc>gTc p.G211V LUAD 23 125299277 125299277 + Missense_Mutation SNP C C A TCGA-78-8662-01A-11D-2393-08 TCGA-78-8662-10A-01D-2393-08 g.chrX:125299277C>A c.631G>T c.(631-633)Ggc>Tgc p.G211C LUAD 23 125299290 125299290 + Silent SNP G G C TCGA-05-4427-01A-21D-1855-08 TCGA-05-4427-10A-01D-1855-08 g.chrX:125299290G>C c.618C>G c.(616-618)acC>acG p.T206T LUAD 23 125299371 125299371 + Silent SNP C C G TCGA-55-8511-01A-11D-2393-08 TCGA-55-8511-10A-01D-2393-08 g.chrX:125299371C>G c.537G>C c.(535-537)ctG>ctC p.L179L LUAD 23 125299403 125299403 + Nonsense_Mutation SNP C C A TCGA-44-8117-01A-11D-2238-08 TCGA-44-8117-10A-01D-2238-08 g.chrX:125299403C>A c.505G>T c.(505-507)Gaa>Taa p.E169* LUAD 23 125299513 125299513 + Missense_Mutation SNP C C A TCGA-49-4486-01A-01D-1265-08 TCGA-49-4486-11A-01D-1265-08 g.chrX:125299513C>A c.395G>T c.(394-396)cGc>cTc p.R132L LUAD 23 125299578 125299578 + Missense_Mutation SNP C C A TCGA-55-7910-01A-11D-2167-08 TCGA-55-7910-11A-01D-2167-08 g.chrX:125299578C>A c.330G>T c.(328-330)caG>caT p.Q110H LUAD 23 125299581 125299581 + Missense_Mutation SNP C C A TCGA-17-Z030-01A-01W-0746-08 TCGA-17-Z030-11A-01W-0746-08 g.chrX:125299581C>A c.327G>T c.(325-327)agG>agT p.R109S LUAD 23 125299602 125299602 + Silent SNP C C G TCGA-91-6848-01A-11D-1945-08 TCGA-91-6848-11A-01D-1945-08 g.chrX:125299602C>G c.306G>C c.(304-306)gcG>gcC p.A102A LUAD 23 125299717 125299717 + Missense_Mutation SNP C C A TCGA-55-8616-01A-11D-2393-08 TCGA-55-8616-10A-01D-2393-08 g.chrX:125299717C>A c.191G>T c.(190-192)gGc>gTc p.G64V LUAD 23 125299720 125299720 + Missense_Mutation SNP C C A TCGA-44-3918-01A-01D-1105-08 TCGA-44-3918-11A-01D-1105-08 g.chrX:125299720C>A c.188G>T c.(187-189)cGg>cTg p.R63L LUAD 23 125299759 125299759 + Missense_Mutation SNP C C A TCGA-64-5775-01A-01D-1625-08 TCGA-64-5775-10A-01D-1625-08 g.chrX:125299759C>A c.149G>T c.(148-150)aGg>aTg p.R50M LUAD 23 125299761 125299761 + Silent SNP G G A TCGA-49-6767-01A-11D-1855-08 TCGA-49-6767-11A-01D-1855-08 g.chrX:125299761G>A c.147C>T c.(145-147)cgC>cgT p.R49R LUAD 23 125299815 125299815 + Silent SNP C C T TCGA-55-8506-01A-11D-2393-08 TCGA-55-8506-10A-01D-2393-08 g.chrX:125299815C>T c.93G>A c.(91-93)gcG>gcA p.A31A LUAD 23 125299863 125299863 + Silent SNP C C A TCGA-55-8094-01A-11D-2238-08 TCGA-55-8094-10A-01D-2238-08 g.chrX:125299863C>A c.45G>T c.(43-45)gcG>gcT p.A15A LUAD 23 125299865 125299865 + Missense_Mutation SNP C C A TCGA-50-5931-01A-11D-1753-08 TCGA-50-5931-11A-01D-1753-08 g.chrX:125299865C>A c.43G>T c.(43-45)Gcg>Tcg p.A15S LUAD 23 125299867 125299867 + Missense_Mutation SNP G G T TCGA-MP-A5C7-01A-11D-A25L-08 TCGA-MP-A5C7-10A-01D-A25L-08 g.chrX:125299867G>T c.41C>A c.(40-42)cCc>cAc p.P14H LUAD 23 125299885 125299885 + Missense_Mutation SNP C C T TCGA-86-8358-01A-11D-2323-08 TCGA-86-8358-10A-01D-2323-08 g.chrX:125299885C>T c.23G>A c.(22-24)aGc>aAc p.S8N LUSC 23 125298566 125298566 + Missense_Mutation SNP C C G TCGA-60-2722-01A-01D-1522-08 TCGA-60-2722-11A-01D-1522-08 g.chrX:125298566C>G c.1342G>C c.(1342-1344)Ggg>Cgg p.G448R LUSC 23 125298856 125298856 + Missense_Mutation SNP G G T TCGA-34-5929-01A-11D-1817-08 TCGA-34-5929-11A-01D-1817-08 g.chrX:125298856G>T c.1052C>A c.(1051-1053)aCa>aAa p.T351K LUSC 23 125298951 125298952 + Nonsense_Mutation DNP GG GG TT TCGA-66-2770-01A-01D-1522-08 TCGA-66-2770-11A-01D-1522-08 g.chrX:125298951_125298952GG>TT c.956_957CC>AA c.(955-957)tCC>tAA p.S319* LUSC 23 125299017 125299017 + Missense_Mutation SNP C C A TCGA-66-2777-01A-01D-1267-08 TCGA-66-2777-11A-01D-1267-08 g.chrX:125299017C>A c.891G>T c.(889-891)agG>agT p.R297S LUSC 23 125299305 125299305 + Silent SNP G G C TCGA-60-2711-01A-01D-1522-08 TCGA-60-2711-11A-01D-1522-08 g.chrX:125299305G>C c.603C>G c.(601-603)gcC>gcG p.A201A LUSC 23 125299528 125299528 + Missense_Mutation SNP G G A TCGA-66-2786-01A-01D-1522-08 TCGA-66-2786-11A-01D-1522-08 g.chrX:125299528G>A c.380C>T c.(379-381)tCa>tTa p.S127L LUSC 23 125299535 125299535 + Missense_Mutation SNP C C G TCGA-43-6647-01A-11D-1817-08 TCGA-43-6647-11A-01D-1817-08 g.chrX:125299535C>G c.373G>C c.(373-375)Gtg>Ctg p.V125L OV 23 125298656 125298656 + Missense_Mutation SNP C C A TCGA-13-1510-01A-02D-0472-08 TCGA-13-1510-10A-01W-0546-08 g.chrX:125298656C>A c.1252G>T c.(1252-1254)Gtg>Ttg p.V418L OV 23 125298739 125298739 + Missense_Mutation SNP C C T TCGA-20-1687-01A-01W-0633-09 TCGA-20-1687-10A-01W-0633-09 g.chrX:125298739C>T c.1169G>A c.(1168-1170)aGc>aAc p.S390N OV 23 125298898 125298898 + Missense_Mutation SNP C C T TCGA-29-1696-01A-01W-0633-09 TCGA-29-1696-10A-01W-0633-09 g.chrX:125298898C>T c.1010G>A c.(1009-1011)cGc>cAc p.R337H OV 23 125299587 125299587 + Silent SNP G G A TCGA-29-1691-01A-01W-0633-09 TCGA-29-1691-10A-01W-0633-09 g.chrX:125299587G>A c.321C>T c.(319-321)aaC>aaT p.N107N OV 23 125299722 125299722 + Silent SNP C C A TCGA-30-1891-01A-01W-0699-08 TCGA-30-1891-10A-01W-0699-08 g.chrX:125299722C>A c.186G>T c.(184-186)gcG>gcT p.A62A PAAD 23 125299095 125299095 + Silent SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chrX:125299095G>A c.813C>T c.(811-813)agC>agT p.S271S PAAD 23 125299102 125299102 + Missense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chrX:125299102G>A c.806C>T c.(805-807)gCc>gTc p.A269V PAAD 23 125299404 125299404 + Silent SNP G G A TCGA-HV-AA8X-01A-11D-A397-08 TCGA-HV-AA8X-10A-01D-A39A-08 g.chrX:125299404G>A c.504C>T c.(502-504)ggC>ggT p.G168G PRAD 23 125298898 125298898 + Missense_Mutation SNP C C T TCGA-HI-7169-01A-11D-2114-08 TCGA-HI-7169-10A-01D-2115-08 g.chrX:125298898C>T c.1010G>A c.(1009-1011)cGc>cAc p.R337H PRAD 23 125299264 125299264 + Missense_Mutation SNP C C T TCGA-KK-A6E7-01A-11D-A31L-08 TCGA-KK-A6E7-11A-11D-A31J-08 g.chrX:125299264C>T c.644G>A c.(643-645)gGc>gAc p.G215D READ 23 125298618 125298618 + Silent SNP C C T TCGA-AG-3892-01A-01W-1073-09 TCGA-AG-3892-10A-01W-1073-09 g.chrX:125298618C>T c.1290G>A c.(1288-1290)gcG>gcA p.A430A READ 23 125298991 125298991 + Missense_Mutation SNP C C A TCGA-AG-A026-01A-32W-A096-10 TCGA-AG-A026-10A-01W-A096-10 g.chrX:125298991C>A c.917G>T c.(916-918)tGc>tTc p.C306F READ 23 125299059 125299059 + Silent SNP G G A TCGA-AG-3909-01A-01W-1073-09 TCGA-AG-3909-10A-01W-1073-09 g.chrX:125299059G>A c.849C>T c.(847-849)gaC>gaT p.D283D READ 23 125299499 125299499 + Missense_Mutation SNP G G A TCGA-EI-6506-01A-11D-1733-10 TCGA-EI-6506-10A-01D-1733-10 g.chrX:125299499G>A c.409C>T c.(409-411)Cgg>Tgg p.R137W READ 23 125299656 125299656 + Silent SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chrX:125299656G>A c.252C>T c.(250-252)ccC>ccT p.P84P READ 23 125299670 125299670 + Missense_Mutation SNP C C T TCGA-AG-4007-01A-01W-1073-09 TCGA-AG-4007-10A-01W-1073-09 g.chrX:125299670C>T c.238G>A c.(238-240)Gtc>Atc p.V80I SARC 23 125299630 125299630 + Missense_Mutation SNP T T C TCGA-3R-A8YX-01A-11D-A37C-09 TCGA-3R-A8YX-10A-01D-A37F-09 g.chrX:125299630T>C c.278A>G c.(277-279)gAc>gGc p.D93G SKCM 23 125298562 125298562 + Missense_Mutation SNP G G A TCGA-DA-A1HV-06A-21D-A196-08 TCGA-DA-A1HV-10A-01D-A198-08 g.chrX:125298562G>A c.1346C>T c.(1345-1347)cCt>cTt p.P449L SKCM 23 125298602 125298602 + Missense_Mutation SNP A A G TCGA-EE-A182-06A-11D-A196-08 TCGA-EE-A182-10A-01D-A198-08 g.chrX:125298602A>G c.1306T>C c.(1306-1308)Tac>Cac p.Y436H SKCM 23 125298627 125298627 + Silent SNP G G A TCGA-D3-A3C8-06A-12D-A19A-08 TCGA-D3-A3C8-10A-01D-A19A-08 g.chrX:125298627G>A c.1281C>T c.(1279-1281)ttC>ttT p.F427F SKCM 23 125298683 125298683 + Missense_Mutation SNP C C T TCGA-EE-A20H-06A-11D-A197-08 TCGA-EE-A20H-10A-01D-A199-08 g.chrX:125298683C>T c.1225G>A c.(1225-1227)Ggc>Agc p.G409S SKCM 23 125298729 125298729 + Silent SNP G G A TCGA-GF-A6C9-06A-11D-A30X-08 TCGA-GF-A6C9-10A-01D-A30X-08 g.chrX:125298729G>A c.1179C>T c.(1177-1179)tcC>tcT p.S393S SKCM 23 125298807 125298807 + Silent SNP G G T TCGA-D3-A51T-06A-11D-A25O-08 TCGA-D3-A51T-10A-01D-A25O-08 g.chrX:125298807G>T c.1101C>A c.(1099-1101)acC>acA p.T367T SKCM 23 125298919 125298919 + Missense_Mutation SNP G G A TCGA-ER-A19D-06A-11D-A197-08 TCGA-ER-A19D-10A-01D-A199-08 g.chrX:125298919G>A c.989C>T c.(988-990)tCc>tTc p.S330F SKCM 23 125299075 125299075 + Missense_Mutation SNP C C T TCGA-EE-A2GO-06A-11D-A196-08 TCGA-EE-A2GO-10A-01D-A198-08 g.chrX:125299075C>T c.833G>A c.(832-834)gGa>gAa p.G278E SKCM 23 125299163 125299163 + Missense_Mutation SNP C C T TCGA-D3-A2JF-06A-11D-A196-08 TCGA-D3-A2JF-10A-01D-A198-08 g.chrX:125299163C>T c.745G>A c.(745-747)Gat>Aat p.D249N SKCM 23 125299167 125299167 + Silent SNP C C T TCGA-D3-A2JH-06A-11D-A196-08 TCGA-D3-A2JH-10A-01D-A198-08 g.chrX:125299167C>T c.741G>A c.(739-741)ccG>ccA p.P247P SKCM 23 125299239 125299239 + Silent SNP G G A TCGA-EE-A2GO-06A-11D-A196-08 TCGA-EE-A2GO-10A-01D-A198-08 g.chrX:125299239G>A c.669C>T c.(667-669)gaC>gaT p.D223D SKCM 23 125299290 125299290 + Silent SNP G G A TCGA-EE-A185-06A-11D-A196-08 TCGA-EE-A185-10A-01D-A198-08 g.chrX:125299290G>A c.618C>T c.(616-618)acC>acT p.T206T SKCM 23 125299403 125299403 + Missense_Mutation SNP C C T TCGA-EE-A2GO-06A-11D-A196-08 TCGA-EE-A2GO-10A-01D-A198-08 g.chrX:125299403C>T c.505G>A c.(505-507)Gaa>Aaa p.E169K SKCM 23 125299437 125299437 + Silent SNP C C T TCGA-EE-A3JD-06A-11D-A20D-08 TCGA-EE-A3JD-10A-01D-A20D-08 g.chrX:125299437C>T c.471G>A c.(469-471)ctG>ctA p.L157L SKCM 23 125299509 125299509 + Silent SNP G G A TCGA-EE-A3JD-06A-11D-A20D-08 TCGA-EE-A3JD-10A-01D-A20D-08 g.chrX:125299509G>A c.399C>T c.(397-399)atC>atT p.I133I SKCM 23 125299644 125299644 + Silent SNP C C T TCGA-D3-A3ML-06A-11D-A21A-08 TCGA-D3-A3ML-10A-01D-A21A-08 g.chrX:125299644C>T c.264G>A c.(262-264)acG>acA p.T88T SKCM 23 125299816 125299816 + Missense_Mutation SNP G G C TCGA-EB-A44Q-06A-11D-A25O-08 TCGA-EB-A44Q-10A-01D-A25O-08 g.chrX:125299816G>C c.92C>G c.(91-93)gCg>gGg p.A31G SKCM 23 125299827 125299827 + Silent SNP A A G TCGA-GN-A262-06A-11D-A196-08 TCGA-GN-A262-10A-01D-A198-08 g.chrX:125299827A>G c.81T>C c.(79-81)ggT>ggC p.G27G

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BLCA-CN X 125298634 125298634 single base substitution C T missense_variant G425E 1274G>A BLCA-US X 125298848 125298848 single base substitution G C missense_variant R354G 1060C>G BLCA-US X 125299171 125299171 single base substitution C T missense_variant R246H 737G>A BLCA-US X 125299261 125299261 single base substitution G T missense_variant T216N 647C>A BLCA-US X 125299590 125299590 single base substitution C A synonymous_variant L106L 318G>T BRCA-EU X 125293497 125293497 single base substitution G A downstream_gene_variant BRCA-EU X 125295173 125295173 single base substitution T C downstream_gene_variant BRCA-EU X 125295329 125295329 deletion of <=200bp T - downstream_gene_variant BRCA-EU X 125295523 125295523 single base substitution C A downstream_gene_variant BRCA-EU X 125295626 125295626 single base substitution G C downstream_gene_variant BRCA-EU X 125296397 125296397 single base substitution C A downstream_gene_variant BRCA-EU X 125296472 125296472 single base substitution T C downstream_gene_variant BRCA-EU X 125296692 125296692 single base substitution T A downstream_gene_variant BRCA-EU X 125296863 125296863 single base substitution T C downstream_gene_variant BRCA-EU X 125296961 125296961 single base substitution T A downstream_gene_variant BRCA-EU X 125297351 125297351 single base substitution T C downstream_gene_variant BRCA-EU X 125297738 125297738 single base substitution G T downstream_gene_variant BRCA-EU X 125297922 125297922 single base substitution A G downstream_gene_variant BRCA-EU X 125298183 125298183 single base substitution G C downstream_gene_variant BRCA-EU X 125298905 125298905 single base substitution G A missense_variant R335C 1003C>T BRCA-EU X 125298907 125298907 single base substitution G A missense_variant P334L 1001C>T BRCA-EU X 125301592 125301592 single base substitution G T upstream_gene_variant BRCA-EU X 125301703 125301703 single base substitution G A upstream_gene_variant BRCA-EU X 125302113 125302113 single base substitution T C upstream_gene_variant BRCA-EU X 125302322 125302322 single base substitution C A upstream_gene_variant BRCA-EU X 125304016 125304016 single base substitution A G upstream_gene_variant BRCA-EU X 125304329 125304329 single base substitution T G upstream_gene_variant BRCA-EU X 125304392 125304392 single base substitution C T upstream_gene_variant BRCA-EU X 125304440 125304440 single base substitution A T upstream_gene_variant BRCA-FR X 125296692 125296692 single base substitution T A downstream_gene_variant BRCA-FR X 125297922 125297922 single base substitution A G downstream_gene_variant BRCA-FR X 125300495 125300495 single base substitution C A upstream_gene_variant BRCA-FR X 125301592 125301592 single base substitution G T upstream_gene_variant BRCA-FR X 125302113 125302113 single base substitution T C upstream_gene_variant BRCA-FR X 125304392 125304392 single base substitution C T upstream_gene_variant BRCA-KR X 125298685 125298685 single base substitution C T missense_variant R408K 1223G>A BRCA-US X 125298649 125298649 single base substitution T A missense_variant Y420F 1259A>T BRCA-US X 125298656 125298656 single base substitution C G missense_variant V418L 1252G>C BRCA-US X 125298870 125298870 single base substitution A T synonymous_variant S346S 1038T>A BRCA-US X 125298898 125298898 single base substitution C T missense_variant R337H 1010G>A BRCA-US X 125299410 125299410 single base substitution G A synonymous_variant T166T 498C>T BTCA-JP X 125298940 125298940 single base substitution A T missense_variant V323E 968T>A BTCA-JP X 125298970 125298970 single base substitution G A missense_variant T313I 938C>T BTCA-JP X 125299602 125299602 single base substitution C T synonymous_variant A102A 306G>A BTCA-JP X 125299943 125299943 single base substitution C T intron_variant BTCA-JP X 125299943 125299943 single base substitution C T upstream_gene_variant CESC-US X 125298619 125298619 single base substitution G A missense_variant A430V 1289C>T CESC-US X 125298663 125298663 single base substitution G A synonymous_variant D415D 1245C>T CESC-US X 125298775 125298775 single base substitution C T missense_variant R378H 1133G>A CESC-US X 125299005 125299005 single base substitution G A synonymous_variant I301I 903C>T CESC-US X 125299273 125299273 single base substitution G A missense_variant S212F 635C>T CESC-US X 125299852 125299852 single base substitution C T missense_variant G19E 56G>A CLLE-ES X 125295372 125295372 single base substitution T G downstream_gene_variant CLLE-ES X 125297500 125297500 single base substitution C T downstream_gene_variant CLLE-ES X 125299321 125299321 single base substitution C A missense_variant W196L 587G>T CLLE-ES X 125304954 125304954 single base substitution T C upstream_gene_variant COAD-US X 125298589 125298589 single base substitution T C missense_variant E440G 1319A>G COAD-US X 125298690 125298690 single base substitution G A synonymous_variant C406C 1218C>T COAD-US X 125298775 125298775 single base substitution C T missense_variant R378H 1133G>A COAD-US X 125298899 125298899 single base substitution G A missense_variant R337C 1009C>T COAD-US X 125298907 125298907 single base substitution G A missense_variant P334L 1001C>T COAD-US X 125299101 125299101 single base substitution G T synonymous_variant A269A 807C>A COAD-US X 125299120 125299120 single base substitution C T missense_variant R263H 788G>A COAD-US X 125299283 125299283 single base substitution C T missense_variant V209M 625G>A COAD-US X 125299314 125299314 single base substitution G A synonymous_variant F198F 594C>T COAD-US X 125299408 125299408 single base substitution C A missense_variant G167V 500G>T COAD-US X 125299423 125299423 single base substitution G A missense_variant T162M 485C>T COAD-US X 125299467 125299467 single base substitution G T missense_variant H147Q 441C>A COAD-US X 125299762 125299762 single base substitution C T missense_variant R49H 146G>A COAD-US X 125299782 125299782 single base substitution C A missense_variant Q42H 126G>T COCA-CN X 125298679 125298679 single base substitution C T stop_gained W410* 1229G>A COCA-CN X 125298869 125298869 single base substitution G A stop_gained R347* 1039C>T COCA-CN X 125298921 125298921 single base substitution G T synonymous_variant V329V 987C>A COCA-CN X 125299134 125299134 single base substitution G A synonymous_variant T258T 774C>T COCA-CN X 125299172 125299172 single base substitution G A missense_variant R246C 736C>T COCA-CN X 125299458 125299458 single base substitution G A synonymous_variant C150C 450C>T COCA-CN X 125299467 125299467 single base substitution G T missense_variant H147Q 441C>A COCA-CN X 125299694 125299694 single base substitution C T missense_variant E72K 214G>A COCA-CN X 125299818 125299818 single base substitution C T synonymous_variant A30A 90G>A GBM-US X 125298905 125298905 single base substitution G A missense_variant R335C 1003C>T GBM-US X 125299171 125299171 single base substitution C T missense_variant R246H 737G>A GBM-US X 125299277 125299277 single base substitution C T missense_variant G211S 631G>A GBM-US X 125299442 125299442 single base substitution C T missense_variant E156K 466G>A GBM-US X 125299499 125299499 single base substitution G A missense_variant R137W 409C>T GBM-US X 125299765 125299765 single base substitution C T missense_variant R48H 143G>A GBM-US X 125299891 125299891 single base substitution G T missense_variant T6K 17C>A LGG-US X 125298904 125298904 single base substitution C G missense_variant R335P 1004G>C LGG-US X 125299120 125299120 single base substitution C T missense_variant R263H 788G>A LGG-US X 125299672 125299672 single base substitution G A missense_variant A79V 236C>T LICA-FR X 125299064 125299064 single base substitution A C missense_variant L282V 844T>G LICA-FR X 125299237 125299237 single base substitution G T missense_variant P224Q 671C>A LICA-FR X 125299344 125299344 single base substitution G A synonymous_variant G188G 564C>T LIHC-US X 125298937 125298937 single base substitution C A missense_variant G324V 971G>T LIHC-US X 125298989 125298989 single base substitution G A stop_gained R307* 919C>T LIHC-US X 125299293 125299293 single base substitution G T missense_variant D205E 615C>A LINC-JP X 125298456 125298456 single base substitution A G 3_prime_UTR_variant LINC-JP X 125298456 125298456 single base substitution A G downstream_gene_variant LINC-JP X 125299313 125299313 single base substitution C T missense_variant A199T 595G>A LINC-JP X 125299367 125299367 insertion of <=200bp - T frameshift_variant T181N? LINC-JP X 125299902 125299902 single base substitution G T synonymous_variant A2A 6C>A LINC-JP X 125300179 125300179 single base substitution C T upstream_gene_variant LIRI-JP X 125293910 125293910 single base substitution C A downstream_gene_variant LIRI-JP X 125294105 125294105 single base substitution C T downstream_gene_variant LIRI-JP X 125297659 125297659 single base substitution C A downstream_gene_variant LIRI-JP X 125297980 125297980 single base substitution C A downstream_gene_variant LIRI-JP X 125298279 125298279 single base substitution C G downstream_gene_variant LIRI-JP X 125298445 125298445 single base substitution C T 3_prime_UTR_variant LIRI-JP X 125298445 125298445 single base substitution C T downstream_gene_variant LIRI-JP X 125298609 125298609 single base substitution G C synonymous_variant T433T 1299C>G LIRI-JP X 125298960 125298960 single base substitution A G synonymous_variant D316D 948T>C LIRI-JP X 125299350 125299350 single base substitution G A synonymous_variant C186C 558C>T LIRI-JP X 125302014 125302014 single base substitution A C upstream_gene_variant LIRI-JP X 125303396 125303396 single base substitution A G upstream_gene_variant LIRI-JP X 125303981 125303981 single base substitution A T upstream_gene_variant LIRI-JP X 125304292 125304292 single base substitution C T upstream_gene_variant LUSC-KR X 125295597 125295597 single base substitution G T downstream_gene_variant LUSC-KR X 125297149 125297149 single base substitution C G downstream_gene_variant LUSC-KR X 125303024 125303024 single base substitution G T upstream_gene_variant LUSC-US X 125298566 125298566 single base substitution C G missense_variant G448R 1342G>C LUSC-US X 125298856 125298856 single base substitution G T missense_variant T351K 1052C>A LUSC-US X 125298951 125298951 single base substitution G T synonymous_variant S319S 957C>A LUSC-US X 125298952 125298952 single base substitution G T missense_variant S319Y 956C>A LUSC-US X 125299017 125299017 single base substitution C A missense_variant R297S 891G>T LUSC-US X 125299305 125299305 single base substitution G C synonymous_variant A201A 603C>G LUSC-US X 125299528 125299528 single base substitution G A missense_variant S127L 380C>T LUSC-US X 125299535 125299535 single base substitution C G missense_variant V125L 373G>C MALY-DE X 125293913 125293913 single base substitution G T downstream_gene_variant MALY-DE X 125295066 125295066 single base substitution C A downstream_gene_variant MALY-DE X 125295260 125295260 single base substitution C T downstream_gene_variant MALY-DE X 125295509 125295509 single base substitution C T downstream_gene_variant MALY-DE X 125296567 125296567 single base substitution T G downstream_gene_variant MALY-DE X 125297418 125297418 deletion of <=200bp C - downstream_gene_variant MALY-DE X 125297928 125297928 single base substitution A T downstream_gene_variant MALY-DE X 125302746 125302746 single base substitution A T upstream_gene_variant MALY-DE X 125302991 125302991 single base substitution T G upstream_gene_variant MALY-DE X 125303974 125303974 single base substitution T C upstream_gene_variant MALY-DE X 125304844 125304844 single base substitution C G upstream_gene_variant MALY-DE X 125304869 125304869 single base substitution C T upstream_gene_variant MALY-DE X 125304999 125304999 single base substitution G A upstream_gene_variant MELA-AU X 125293702 125293702 single base substitution G A downstream_gene_variant MELA-AU X 125293813 125293813 single base substitution C T downstream_gene_variant MELA-AU X 125293832 125293832 single base substitution C T downstream_gene_variant MELA-AU X 125293980 125293980 single base substitution G A downstream_gene_variant MELA-AU X 125293993 125293993 single base substitution T C downstream_gene_variant MELA-AU X 125294133 125294133 single base substitution C T downstream_gene_variant MELA-AU X 125294287 125294287 single base substitution G A downstream_gene_variant MELA-AU X 125294317 125294317 single base substitution G A downstream_gene_variant MELA-AU X 125294513 125294513 single base substitution G A downstream_gene_variant MELA-AU X 125294542 125294542 single base substitution C T downstream_gene_variant MELA-AU X 125294853 125294853 single base substitution A G downstream_gene_variant MELA-AU X 125294857 125294857 single base substitution T C downstream_gene_variant MELA-AU X 125295121 125295121 single base substitution G A downstream_gene_variant MELA-AU X 125295124 125295124 single base substitution C T downstream_gene_variant MELA-AU X 125295196 125295196 single base substitution C T downstream_gene_variant MELA-AU X 125295298 125295298 single base substitution C T downstream_gene_variant MELA-AU X 125295344 125295344 single base substitution C T downstream_gene_variant MELA-AU X 125295453 125295453 single base substitution C T downstream_gene_variant MELA-AU X 125295568 125295568 single base substitution C T downstream_gene_variant MELA-AU X 125295583 125295583 single base substitution G A downstream_gene_variant MELA-AU X 125295714 125295714 single base substitution T G downstream_gene_variant MELA-AU X 125295807 125295807 single base substitution T C downstream_gene_variant MELA-AU X 125295937 125295937 single base substitution C T downstream_gene_variant MELA-AU X 125296036 125296036 single base substitution A C downstream_gene_variant MELA-AU X 125296082 125296082 single base substitution C T downstream_gene_variant MELA-AU X 125296296 125296296 single base substitution C T downstream_gene_variant MELA-AU X 125296412 125296412 single base substitution G C downstream_gene_variant MELA-AU X 125296509 125296509 single base substitution A T downstream_gene_variant MELA-AU X 125296570 125296570 single base substitution C T downstream_gene_variant MELA-AU X 125296732 125296732 single base substitution A T downstream_gene_variant MELA-AU X 125296738 125296738 single base substitution A G downstream_gene_variant MELA-AU X 125296761 125296761 single base substitution C T downstream_gene_variant MELA-AU X 125296931 125296931 single base substitution G A downstream_gene_variant MELA-AU X 125297017 125297017 single base substitution C T downstream_gene_variant MELA-AU X 125297389 125297389 single base substitution G A downstream_gene_variant MELA-AU X 125297492 125297492 single base substitution G A downstream_gene_variant MELA-AU X 125297717 125297717 single base substitution G A downstream_gene_variant MELA-AU X 125297936 125297936 single base substitution C T downstream_gene_variant MELA-AU X 125298191 125298191 single base substitution G T downstream_gene_variant MELA-AU X 125298627 125298627 single base substitution G A synonymous_variant F427F 1281C>T MELA-AU X 125298742 125298742 single base substitution G A missense_variant S389F 1166C>T MELA-AU X 125298773 125298773 single base substitution C T missense_variant A379T 1135G>A MELA-AU X 125298805 125298805 single base substitution C G missense_variant G368A 1103G>C MELA-AU X 125299020 125299020 single base substitution G A synonymous_variant S296S 888C>T MELA-AU X 125299046 125299046 single base substitution G A synonymous_variant L288L 862C>T MELA-AU X 125299072 125299072 single base substitution G A missense_variant A279V 836C>T MELA-AU X 125299082 125299083 multiple base substitution (>=2bp and <=200bp) CC TT missense_variant QE275QK MELA-AU X 125299290 125299290 single base substitution G A synonymous_variant T206T 618C>T MELA-AU X 125299313 125299313 single base substitution C T missense_variant A199T 595G>A MELA-AU X 125299403 125299403 single base substitution C T missense_variant E169K 505G>A MELA-AU X 125299432 125299432 single base substitution G A missense_variant P159L 476C>T MELA-AU X 125300313 125300313 single base substitution G A upstream_gene_variant MELA-AU X 125300391 125300391 single base substitution G A upstream_gene_variant MELA-AU X 125300564 125300564 single base substitution G A upstream_gene_variant MELA-AU X 125300690 125300691 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU X 125300747 125300747 single base substitution C T upstream_gene_variant MELA-AU X 125301094 125301094 single base substitution G A upstream_gene_variant MELA-AU X 125301147 125301147 single base substitution C T upstream_gene_variant MELA-AU X 125301312 125301312 single base substitution C T upstream_gene_variant MELA-AU X 125301503 125301503 single base substitution C T upstream_gene_variant MELA-AU X 125301527 125301527 single base substitution C T upstream_gene_variant MELA-AU X 125301690 125301690 single base substitution G A upstream_gene_variant MELA-AU X 125301804 125301804 single base substitution C T upstream_gene_variant MELA-AU X 125302082 125302082 single base substitution G A upstream_gene_variant MELA-AU X 125302194 125302194 single base substitution C T upstream_gene_variant MELA-AU X 125302549 125302549 single base substitution T C upstream_gene_variant MELA-AU X 125302902 125302902 single base substitution G A upstream_gene_variant MELA-AU X 125302951 125302951 single base substitution G A upstream_gene_variant MELA-AU X 125302972 125302972 single base substitution C T upstream_gene_variant MELA-AU X 125303001 125303001 single base substitution C T upstream_gene_variant MELA-AU X 125303482 125303482 single base substitution G A upstream_gene_variant MELA-AU X 125303611 125303611 single base substitution C T upstream_gene_variant MELA-AU X 125303721 125303721 single base substitution C T upstream_gene_variant MELA-AU X 125304087 125304087 single base substitution C T upstream_gene_variant MELA-AU X 125304145 125304145 single base substitution G A upstream_gene_variant MELA-AU X 125304203 125304203 single base substitution G A upstream_gene_variant MELA-AU X 125304216 125304216 single base substitution T C upstream_gene_variant MELA-AU X 125304444 125304444 single base substitution C T upstream_gene_variant MELA-AU X 125304535 125304535 single base substitution G A upstream_gene_variant MELA-AU X 125304751 125304751 single base substitution C T upstream_gene_variant MELA-AU X 125304905 125304905 single base substitution C T upstream_gene_variant MELA-AU X 125304913 125304913 single base substitution G A upstream_gene_variant MELA-AU X 125304961 125304961 single base substitution G A upstream_gene_variant ORCA-IN X 125298315 125298315 single base substitution C T downstream_gene_variant ORCA-IN X 125298682 125298682 single base substitution C A missense_variant G409V 1226G>T ORCA-IN X 125299037 125299037 single base substitution C A missense_variant A291S 871G>T ORCA-IN X 125299490 125299490 single base substitution C G missense_variant E140Q 418G>C OV-AU X 125293749 125293749 single base substitution A C downstream_gene_variant OV-AU X 125298203 125298203 single base substitution C G downstream_gene_variant OV-AU X 125301053 125301053 single base substitution G T upstream_gene_variant PACA-AU X 125293496 125293496 single base substitution C T downstream_gene_variant PACA-AU X 125296159 125296159 single base substitution G T downstream_gene_variant PACA-AU X 125296547 125296547 single base substitution G A downstream_gene_variant PACA-AU X 125296576 125296576 single base substitution G T downstream_gene_variant PACA-AU X 125297039 125297039 single base substitution G T downstream_gene_variant PACA-AU X 125297963 125297963 single base substitution T C downstream_gene_variant PACA-AU X 125300990 125300990 single base substitution G A upstream_gene_variant PACA-AU X 125301678 125301678 single base substitution G A upstream_gene_variant PACA-AU X 125302464 125302464 single base substitution A G upstream_gene_variant PACA-CA X 125293446 125293446 single base substitution C T downstream_gene_variant PACA-CA X 125294599 125294599 single base substitution T A downstream_gene_variant PACA-CA X 125295261 125295261 single base substitution G A downstream_gene_variant PACA-CA X 125296123 125296123 single base substitution G T downstream_gene_variant PACA-CA X 125297321 125297321 single base substitution C A downstream_gene_variant PACA-CA X 125298115 125298115 single base substitution C T downstream_gene_variant PACA-CA X 125298905 125298905 single base substitution G A missense_variant R335C 1003C>T PACA-CA X 125298906 125298906 single base substitution C T synonymous_variant P334P 1002G>A PACA-CA X 125300612 125300612 single base substitution C T upstream_gene_variant PACA-CA X 125302089 125302089 single base substitution A T upstream_gene_variant PACA-CA X 125303053 125303053 single base substitution T A upstream_gene_variant PACA-CA X 125303397 125303397 single base substitution T C upstream_gene_variant PACA-CA X 125303825 125303825 single base substitution G T upstream_gene_variant PACA-CA X 125304004 125304004 single base substitution T C upstream_gene_variant PACA-CA X 125304906 125304906 single base substitution G T upstream_gene_variant PACA-CA X 125305060 125305060 single base substitution C A upstream_gene_variant PBCA-DE X 125295329 125295329 insertion of <=200bp - T downstream_gene_variant PBCA-DE X 125298315 125298315 single base substitution C T downstream_gene_variant PBCA-DE X 125298904 125298904 single base substitution C T missense_variant R335H 1004G>A PBCA-DE X 125299691 125299691 single base substitution C A missense_variant G73C 217G>T PRAD-CA X 125298898 125298898 single base substitution C T missense_variant R337H 1010G>A PRAD-UK X 125296262 125296262 single base substitution C A downstream_gene_variant PRAD-US X 125298898 125298898 single base substitution C T missense_variant R337H 1010G>A PRAD-US X 125299264 125299264 single base substitution C T missense_variant G215D 644G>A READ-US X 125299499 125299499 single base substitution G A missense_variant R137W 409C>T READ-US X 125299513 125299513 single base substitution C T missense_variant R132H 395G>A READ-US X 125299567 125299567 single base substitution C T missense_variant G114D 341G>A RECA-EU X 125297500 125297500 single base substitution C T downstream_gene_variant SKCA-BR X 125293484 125293484 single base substitution C T downstream_gene_variant SKCA-BR X 125294000 125294000 single base substitution G A downstream_gene_variant SKCA-BR X 125294068 125294068 single base substitution G A downstream_gene_variant SKCA-BR X 125294196 125294196 single base substitution G A downstream_gene_variant SKCA-BR X 125294300 125294300 single base substitution G A downstream_gene_variant SKCA-BR X 125295597 125295597 single base substitution G A downstream_gene_variant SKCA-BR X 125295921 125295921 single base substitution A C downstream_gene_variant SKCA-BR X 125296148 125296148 single base substitution A G downstream_gene_variant SKCA-BR X 125296563 125296563 single base substitution G A downstream_gene_variant SKCA-BR X 125298402 125298402 single base substitution C T 3_prime_UTR_variant SKCA-BR X 125298402 125298402 single base substitution C T downstream_gene_variant SKCA-BR X 125299110 125299110 single base substitution C T synonymous_variant R266R 798G>A SKCA-BR X 125299644 125299644 single base substitution C T synonymous_variant T88T 264G>A SKCA-BR X 125299926 125299926 single base substitution T C 5_prime_UTR_variant SKCA-BR X 125299926 125299926 single base substitution T C intron_variant SKCA-BR X 125299932 125299932 insertion of <=200bp - AGCG 5_prime_UTR_variant SKCA-BR X 125299932 125299932 insertion of <=200bp - AGCG intron_variant SKCA-BR X 125300668 125300668 single base substitution G A upstream_gene_variant SKCA-BR X 125301426 125301426 single base substitution C T upstream_gene_variant SKCA-BR X 125301617 125301617 single base substitution C T upstream_gene_variant SKCA-BR X 125301858 125301858 single base substitution T G upstream_gene_variant SKCA-BR X 125303760 125303760 single base substitution T A upstream_gene_variant SKCA-BR X 125304087 125304087 single base substitution C T upstream_gene_variant SKCA-BR X 125304375 125304375 single base substitution G A upstream_gene_variant SKCM-US X 125298562 125298562 single base substitution G A missense_variant P449L 1346C>T SKCM-US X 125298602 125298602 single base substitution A G missense_variant Y436H 1306T>C SKCM-US X 125298627 125298627 single base substitution G A synonymous_variant F427F 1281C>T SKCM-US X 125298683 125298683 single base substitution C T missense_variant G409S 1225G>A SKCM-US X 125298729 125298729 single base substitution G A synonymous_variant S393S 1179C>T SKCM-US X 125298807 125298807 single base substitution G T synonymous_variant T367T 1101C>A SKCM-US X 125298919 125298919 single base substitution G A missense_variant S330F 989C>T SKCM-US X 125299027 125299027 single base substitution G T missense_variant T294K 881C>A SKCM-US X 125299075 125299075 single base substitution C T missense_variant G278E 833G>A SKCM-US X 125299163 125299163 single base substitution C T missense_variant D249N 745G>A SKCM-US X 125299167 125299167 single base substitution C T synonymous_variant P247P 741G>A SKCM-US X 125299173 125299173 single base substitution G A synonymous_variant I245I 735C>T SKCM-US X 125299239 125299239 single base substitution G A synonymous_variant D223D 669C>T SKCM-US X 125299290 125299290 single base substitution G A synonymous_variant T206T 618C>T SKCM-US X 125299291 125299291 single base substitution G A missense_variant T206I 617C>T SKCM-US X 125299403 125299403 single base substitution C T missense_variant E169K 505G>A SKCM-US X 125299437 125299437 single base substitution C T synonymous_variant L157L 471G>A SKCM-US X 125299509 125299509 single base substitution G A synonymous_variant I133I 399C>T SKCM-US X 125299644 125299644 single base substitution C T synonymous_variant T88T 264G>A SKCM-US X 125299816 125299816 single base substitution G C missense_variant A31G 92C>G SKCM-US X 125299827 125299827 single base substitution A G synonymous_variant G27G 81T>C SKCM-US X 125299834 125299834 single base substitution G A missense_variant S25L 74C>T STAD-US X 125298575 125298575 single base substitution C G missense_variant V445L 1333G>C STAD-US X 125298618 125298618 single base substitution C T synonymous_variant A430A 1290G>A STAD-US X 125298619 125298619 single base substitution G A missense_variant A430V 1289C>T STAD-US X 125298659 125298659 single base substitution A G missense_variant W417R 1249T>C STAD-US X 125298766 125298766 single base substitution T G missense_variant K381T 1142A>C STAD-US X 125298773 125298773 single base substitution C T missense_variant A379T 1135G>A STAD-US X 125298874 125298874 single base substitution C A missense_variant C345F 1034G>T STAD-US X 125298898 125298898 single base substitution C T missense_variant R337H 1010G>A STAD-US X 125298904 125298904 single base substitution C T missense_variant R335H 1004G>A STAD-US X 125298907 125298907 single base substitution G A missense_variant P334L 1001C>T STAD-US X 125299117 125299117 single base substitution T C missense_variant K264R 791A>G STAD-US X 125299138 125299138 single base substitution C T missense_variant S257N 770G>A STAD-US X 125299259 125299259 single base substitution C T missense_variant V217M 649G>A STAD-US X 125299270 125299270 single base substitution C T missense_variant R213H 638G>A STAD-US X 125299308 125299308 single base substitution G A synonymous_variant V200V 600C>T STAD-US X 125299369 125299369 single base substitution G T missense_variant P180H 539C>A STAD-US X 125299494 125299494 single base substitution G A synonymous_variant D138D 414C>T STAD-US X 125299536 125299536 single base substitution G A synonymous_variant D124D 372C>T STAD-US X 125299569 125299569 single base substitution G A synonymous_variant C113C 339C>T STAD-US X 125299634 125299634 single base substitution G T missense_variant L92M 274C>A STAD-US X 125299671 125299671 single base substitution G C synonymous_variant A79A 237C>G STAD-US X 125299723 125299723 single base substitution G A missense_variant A62V 185C>T STAD-US X 125299770 125299770 single base substitution C T synonymous_variant A46A 138G>A STAD-US X 125299778 125299778 single base substitution G A missense_variant R44W 130C>T STAD-US X 125299809 125299809 single base substitution T G synonymous_variant G33G 99A>C STAD-US X 125299816 125299816 single base substitution G A missense_variant A31V 92C>T THCA-US X 125298907 125298907 single base substitution G A missense_variant P334L 1001C>T THCA-US X 125299510 125299510 single base substitution A T missense_variant I133N 398T>A UCEC-US X 125298551 125298551 single base substitution C A missense_variant G453C 1357G>T UCEC-US X 125298579 125298579 single base substitution G T synonymous_variant L443L 1329C>A UCEC-US X 125298631 125298631 single base substitution T G missense_variant E426A 1277A>C UCEC-US X 125298775 125298775 single base substitution C T missense_variant R378H 1133G>A UCEC-US X 125298811 125298811 single base substitution C T missense_variant G366D 1097G>A UCEC-US X 125298868 125298868 single base substitution C T missense_variant R347Q 1040G>A UCEC-US X 125298869 125298869 single base substitution G A stop_gained R347* 1039C>T UCEC-US X 125298905 125298905 single base substitution G A missense_variant R335C 1003C>T UCEC-US X 125298970 125298970 single base substitution G T missense_variant T313N 938C>A UCEC-US X 125298988 125298988 single base substitution C T missense_variant R307Q 920G>A UCEC-US X 125299013 125299013 single base substitution G A synonymous_variant L299L 895C>T UCEC-US X 125299059 125299059 single base substitution G A synonymous_variant D283D 849C>T UCEC-US X 125299114 125299114 single base substitution A G missense_variant V265A 794T>C UCEC-US X 125299121 125299121 single base substitution G A missense_variant R263C 787C>T UCEC-US X 125299241 125299241 single base substitution C T missense_variant D223N 667G>A UCEC-US X 125299369 125299369 single base substitution G C missense_variant P180R 539C>G UCEC-US X 125299551 125299551 single base substitution C T synonymous_variant T119T 357G>A UCEC-US X 125299580 125299580 single base substitution G A stop_gained Q110* 328C>T UCEC-US X 125299766 125299766 single base substitution G A missense_variant R48C 142C>T

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand EGC20 COSM1114639 c.1133G>A p.R378H Substitution - Missense 23:126164792-126164792 - 2000120 COSM1331275 c.1010G>A p.R337H Substitution - Missense 23:126164915-126164915 - 12586 COSM5616215 c.632G>T p.G211V Substitution - Missense 23:126165293-126165293 - TCGA-ET-A39O-01 COSM3983942 c.398T>A p.I133N Substitution - Missense 23:126165527-126165527 - SW48 COSM1315187 c.737G>A p.R246H Substitution - Missense 23:126165188-126165188 - 1N03-VS-1T03 COSM4106462 c.414C>T p.D138D Substitution - coding silent 23:126165511-126165511 - Pat_41_B COSM5877025 c.1028C>T p.P343L Substitution - Missense 23:126164897-126164897 - TCGA-DB-A4XH-01 COSM1249723 c.788G>A p.R263H Substitution - Missense 23:126165137-126165137 - PD7188a COSM3769820 c.1176C>G p.D392E Substitution - Missense 23:126164749-126164749 - TCGA-06-0141-01 COSM1114647 c.1003C>T p.R335C Substitution - Missense 23:126164922-126164922 - 587316 COSM1203052 c.409C>T p.R137W Substitution - Missense 23:126165516-126165516 - T3724 COSM4676335 c.699G>A p.W233* Substitution - Nonsense 23:126165226-126165226 - TCGA-BR-4188-01 COSM4106452 c.791A>G p.K264R Substitution - Missense 23:126165134-126165134 - T55 COSM4676332 c.1163C>T p.S388F Substitution - Missense 23:126164762-126164762 - TCGA-EB-A44Q-06 COSM3913329 c.92C>G p.A31G Substitution - Missense 23:126165833-126165833 - TCGA-20-1687-01 COSM1331278 c.1169G>A p.S390N Substitution - Missense 23:126164756-126164756 - STC297 COSM5064353 c.140C>T p.T47M Substitution - Missense 23:126165785-126165785 - TCGA-AM-5820-01 COSM1556089 c.807C>A p.A269A Substitution - coding silent 23:126165118-126165118 - TCGA-EE-A20H-06 COSM3557589 c.1225G>A p.G409S Substitution - Missense 23:126164700-126164700 - TCGA-60-2711-01 COSM755473 c.603C>G p.A201A Substitution - coding silent 23:126165322-126165322 - TCGA-EE-A182-06 COSM3557585 c.1306T>C p.Y436H Substitution - Missense 23:126164619-126164619 - LUAD-E01014 COSM403509 c.726T>G p.Y242* Substitution - Nonsense 23:126165199-126165199 - 1604875 COSM141648 c.1006C>T p.Q336* Substitution - Nonsense 23:126164919-126164919 - SW948 COSM4656744 c.624T>C p.A208A Substitution - coding silent 23:126165301-126165301 - TCGA-BT-A3PH-01 COSM1315187 c.737G>A p.R246H Substitution - Missense 23:126165188-126165188 - TCGA-EB-A3Y7-01 COSM2724989 c.735C>T p.I245I Substitution - coding silent 23:126165190-126165190 - 435 COSM4433944 c.721G>A p.V241I Substitution - Missense 23:126165204-126165204 - ICGC_MB127 COSM3764959 c.217G>T p.G73C Substitution - Missense 23:126165708-126165708 - 587316 COSM1203053 c.409C>T p.R137W Substitution - Missense 23:126165516-126165516 - ESCC_158 COSM2724989 c.735C>T p.I245I Substitution - coding silent 23:126165190-126165190 - HCT15 COSM4633082 c.523G>A p.A175T Substitution - Missense 23:126165402-126165402 - TCGA-F4-6460-01 COSM3694326 c.500G>T p.G167V Substitution - Missense 23:126165425-126165425 - PT49 COSM5529579 c.1196G>A p.G399E Substitution - Missense 23:126164729-126164729 - CPCG0251-F1 COSM1331276 c.1010G>A p.R337H Substitution - Missense 23:126164915-126164915 - TCGA-AM-5821-01 COSM3759350 c.441C>A p.H147Q Substitution - Missense 23:126165484-126165484 - OSCC-GB_01100111 COSM4888344 c.418G>C p.E140Q Substitution - Missense 23:126165507-126165507 - TCGA-OL-A66I-01 COSM1331275 c.1010G>A p.R337H Substitution - Missense 23:126164915-126164915 - TCGA-DU-A5TU-01 COSM3973213 c.1004G>C p.R335P Substitution - Missense 23:126164921-126164921 - I2L-P19Ta-Tumor-Organoid COSM5366965 c.1191C>T p.P397P Substitution - coding silent 23:126164734-126164734 - 587222 COSM1203056 c.1240G>T p.D414Y Substitution - Missense 23:126164685-126164685 - Au1 COSM3424441 c.395G>A p.R132H Substitution - Missense 23:126165530-126165530 - TCGA-B2-3923-01 COSM1497174 c.595G>A p.A199T Substitution - Missense 23:126165330-126165330 - TCGA-60-2722-01 COSM755486 c.1342G>C p.G448R Substitution - Missense 23:126164583-126164583 - TCGA-06-0155-01 COSM1315186 c.737G>A p.R246H Substitution - Missense 23:126165188-126165188 - COLO205 COSM2725001 c.601G>A p.A201T Substitution - Missense 23:126165324-126165324 - C086 COSM5529578 c.1196G>A p.G399E Substitution - Missense 23:126164729-126164729 - TCGA-BR-4184-01 COSM4106472 c.130C>T p.R44W Substitution - Missense 23:126165795-126165795 - TCGA-AP-A0LM-01 COSM1114641 c.1097G>A p.G366D Substitution - Missense 23:126164828-126164828 - TCGA-AX-A05Z-01 COSM1114635 c.1329C>A p.L443L Substitution - coding silent 23:126164596-126164596 - LUAD-S01346 COSM404360 c.821A>C p.N274T Substitution - Missense 23:126165104-126165104 - 2492723 COSM5723354 c.997G>A p.D333N Substitution - Missense 23:126164928-126164928 - TCGA-C5-A1MH-01 COSM4820865 c.56G>A p.G19E Substitution - Missense 23:126165869-126165869 - TCGA-EE-A2GO-06 COSM3557597 c.833G>A p.G278E Substitution - Missense 23:126165092-126165092 - sysucc-1317T COSM5450620 c.90G>A p.A30A Substitution - coding silent 23:126165835-126165835 - BD49T COSM5498480 c.306G>A p.A102A Substitution - coding silent 23:126165619-126165619 - TCGA-AO-A12H-01 COSM456698 c.498C>T p.T166T Substitution - coding silent 23:126165427-126165427 - TCGA-HW-A5KL-01 COSM3973214 c.236C>T p.A79V Substitution - Missense 23:126165689-126165689 - TCGA-AX-A0J1-01 COSM1114663 c.357G>A p.T119T Substitution - coding silent 23:126165568-126165568 - TCGA-A5-A0GP-01 COSM1114636 c.1277A>C p.E426A Substitution - Missense 23:126164648-126164648 - 016-0040-02TD COSM146101 c.587G>T p.W196L Substitution - Missense 23:126165338-126165338 - PT49 COSM5529578 c.1196G>A p.G399E Substitution - Missense 23:126164729-126164729 - TCGA-F4-6460-01 COSM3694325 c.500G>T p.G167V Substitution - Missense 23:126165425-126165425 - pfg025T COSM1643940 c.873C>A p.A291A Substitution - coding silent 23:126165052-126165052 - TCGA-43-6647-01 COSM755469 c.373G>C p.V125L Substitution - Missense 23:126165552-126165552 - TCGA-A5-A0G9-01 COSM1114662 c.539C>G p.P180R Substitution - Missense 23:126165386-126165386 - TCGA-ER-A194-01 COSM3557607 c.617C>T p.T206I Substitution - Missense 23:126165308-126165308 - CSCC-29-T COSM4513469 c.939C>T p.T313T Substitution - coding silent 23:126164986-126164986 - sysucc-834T COSM5486769 c.774C>T p.T258T Substitution - coding silent 23:126165151-126165151 - TCGA-BG-A0VZ-01 COSM1114646 c.1003C>T p.R335C Substitution - Missense 23:126164922-126164922 - T3049 COSM259038 c.238G>A p.V80I Substitution - Missense 23:126165687-126165687 - TCGA-F1-A448-01 COSM4106446 c.1249T>C p.W417R Substitution - Missense 23:126164676-126164676 - T3724 COSM4676330 c.1214C>T p.A405V Substitution - Missense 23:126164711-126164711 - TCGA-D3-A2JH-06 COSM3557602 c.741G>A p.P247P Substitution - coding silent 23:126165184-126165184 - 2492723 COSM5723353 c.997G>A p.D333N Substitution - Missense 23:126164928-126164928 - CSCC-30-T COSM4550439 c.500G>A p.G167D Substitution - Missense 23:126165425-126165425 - TCGA-ER-A19D-06 COSM3557594 c.989C>T p.S330F Substitution - Missense 23:126164936-126164936 - LUAD-RT-S01831 COSM384563 c.63G>T p.G21G Substitution - coding silent 23:126165862-126165862 - S00941 COSM5663903 c.1244A>T p.D415V Substitution - Missense 23:126164681-126164681 - TCGA-BR-8384-01 COSM4106471 c.138G>A p.A46A Substitution - coding silent 23:126165787-126165787 - TCGA-29-1696-01 COSM1331275 c.1010G>A p.R337H Substitution - Missense 23:126164915-126164915 - TCGA-D3-A3ML-06 COSM3557609 c.264G>A p.T88T Substitution - coding silent 23:126165661-126165661 - TCGA-CC-A7IH-01 COSM4924280 c.971G>T p.G324V Substitution - Missense 23:126164954-126164954 - T2269 COSM4676342 c.303C>T p.F101F Substitution - coding silent 23:126165622-126165622 - S02384 COSM610576 c.1290G>T p.A430A Substitution - coding silent 23:126164635-126164635 - TCGA-B5-A11E-01 COSM1114653 c.794T>C p.V265A Substitution - Missense 23:126165131-126165131 - 2492721 COSM5723353 c.997G>A p.D333N Substitution - Missense 23:126164928-126164928 - BN49T COSM1625479 c.541_542insA p.T181fs*25 Insertion - Frameshift 23:126165383-126165384 - TCGA-FE-A235-01 COSM385381 c.1001C>T p.P334L Substitution - Missense 23:126164924-126164924 - XHDG35 COSM4769627 c.235G>A p.A79T Substitution - Missense 23:126165690-126165690 - CSCC-29-T COSM4560631 c.850G>A p.G284S Substitution - Missense 23:126165075-126165075 - KPOPBR-03-T COSM5965170 c.1223G>A p.R408K Substitution - Missense 23:126164702-126164702 - HCC2998 COSM2724953 c.1282C>T p.P428S Substitution - Missense 23:126164643-126164643 - TCGA-BG-A0VZ-01 COSM1114647 c.1003C>T p.R335C Substitution - Missense 23:126164922-126164922 - GB19 COSM216851 c.1002G>A p.P334P Substitution - coding silent 23:126164923-126164923 - sysucc-1317T COSM5450621 c.90G>A p.A30A Substitution - coding silent 23:126165835-126165835 - TCGA-AX-A0J1-01 COSM289152 c.849C>T p.D283D Substitution - coding silent 23:126165076-126165076 - TCGA-D3-A2JF-06 COSM3557600 c.745G>A p.D249N Substitution - Missense 23:126165180-126165180 - T2269 COSM4676341 c.303C>T p.F101F Substitution - coding silent 23:126165622-126165622 - TCGA-KK-A6E7-01 COSM4876529 c.644G>A p.G215D Substitution - Missense 23:126165281-126165281 - T3724 COSM4676329 c.1214C>T p.A405V Substitution - Missense 23:126164711-126164711 - PT33 COSM5909966 c.1343G>A p.G448E Substitution - Missense 23:126164582-126164582 - 016 COSM146101 c.587G>T p.W196L Substitution - Missense 23:126165338-126165338 - LUAD-F00089 COSM365565 c.421G>T p.A141S Substitution - Missense 23:126165504-126165504 - TCGA-HU-A4GU-01 COSM4106457 c.638G>A p.R213H Substitution - Missense 23:126165287-126165287 - 1N56-VS-1T56 COSM4977294 c.340G>A p.G114S Substitution - Missense 23:126165585-126165585 - 016-0040-02TD COSM1317237 c.587G>T p.W196L Substitution - Missense 23:126165338-126165338 - ESO-1130 COSM1249717 c.783C>A p.S261R Substitution - Missense 23:126165142-126165142 - TCGA-EI-6882-01 COSM3424440 c.395G>A p.R132H Substitution - Missense 23:126165530-126165530 - CHC1556T COSM4787718 c.844T>G p.L282V Substitution - Missense 23:126165081-126165081 - LUAD-E00443 COSM364161 c.761C>A p.P254H Substitution - Missense 23:126165164-126165164 - TCGA-BR-A4J8-01 COSM4106459 c.600C>T p.V200V Substitution - coding silent 23:126165325-126165325 - TCGA-CD-8535-01 COSM4106441 c.1333G>C p.V445L Substitution - Missense 23:126164592-126164592 - LUAD-CHTN-Z4716A COSM362719 c.648C>T p.T216T Substitution - coding silent 23:126165277-126165277 - 2492724 COSM5725228 c.1200G>A p.R400R Substitution - coding silent 23:126164725-126164725 - T3202 COSM1465448 c.146G>A p.R49H Substitution - Missense 23:126165779-126165779 - TCGA-14-0862-01 COSM3405930 c.631G>A p.G211S Substitution - Missense 23:126165294-126165294 - MT-439-T2 COSM385381 c.1001C>T p.P334L Substitution - Missense 23:126164924-126164924 - TCGA-F4-6570-01 COSM1465440 c.625G>A p.V209M Substitution - Missense 23:126165300-126165300 - TCGA-BR-4188-01 COSM4106453 c.791A>G p.K264R Substitution - Missense 23:126165134-126165134 - C058 COSM2725009 c.505G>A p.E169K Substitution - Missense 23:126165420-126165420 - TCGA-AP-A059-01 COSM1114651 c.895C>T p.L299L Substitution - coding silent 23:126165030-126165030 - TCGA-AP-A0LM-01 COSM1114640 c.1097G>A p.G366D Substitution - Missense 23:126164828-126164828 - TCGA-FW-A5DX-01 COSM3557596 c.881C>A p.T294K Substitution - Missense 23:126165044-126165044 - C086 COSM5529581 c.216G>A p.E72E Substitution - coding silent 23:126165709-126165709 - TCGA-66-2770-01 COSM755482 c.957C>A p.S319S Substitution - coding silent 23:126164968-126164968 - ESO-913 COSM1249728 c.1142A>C p.K381T Substitution - Missense 23:126164783-126164783 - ESO-118 COSM1249719 c.1142A>G p.K381R Substitution - Missense 23:126164783-126164783 - HX13T COSM1625481 c.6C>A p.A2A Substitution - coding silent 23:126165919-126165919 - T3724 COSM4676336 c.699G>A p.W233* Substitution - Nonsense 23:126165226-126165226 - TCGA-AP-A051-01 COSM1114658 c.667G>A p.D223N Substitution - Missense 23:126165258-126165258 - LUAD-S00499 COSM385380 c.1001C>T p.P334L Substitution - Missense 23:126164924-126164924 - TCGA-06-6694-01 COSM1315187 c.737G>A p.R246H Substitution - Missense 23:126165188-126165188 - TCGA-BR-A4J8-01 COSM4106458 c.600C>T p.V200V Substitution - coding silent 23:126165325-126165325 - pfg038T COSM4761043 c.652G>A p.A218T Substitution - Missense 23:126165273-126165273 - BN49T COSM1625478 c.541_542insA p.T181fs*25 Insertion - Frameshift 23:126165383-126165384 - HCC5T COSM1497174 c.595G>A p.A199T Substitution - Missense 23:126165330-126165330 - OSCC-GB_00690111 COSM4886926 c.871G>T p.A291S Substitution - Missense 23:126165054-126165054 - ESO-017 COSM1249716 c.1190C>A p.P397H Substitution - Missense 23:126164735-126164735 - NCI-H2126 COSM25535 c.1173G>T p.L391L Substitution - coding silent 23:126164752-126164752 - TCGA-AP-A0LM-01 COSM1114667 c.142C>T p.R48C Substitution - Missense 23:126165783-126165783 - TCGA-BG-A0M0-01 COSM1114638 c.1133G>A p.R378H Substitution - Missense 23:126164792-126164792 - TCGA-06-0132-01 COSM1203052 c.409C>T p.R137W Substitution - Missense 23:126165516-126165516 - T578 COSM2724952 c.1317G>A p.P439P Substitution - coding silent 23:126164608-126164608 - EGC15 COSM5064350 c.461C>T p.A154V Substitution - Missense 23:126165464-126165464 - LUAD-NYU1021 COSM368263 c.401C>T p.P134L Substitution - Missense 23:126165524-126165524 - B10-Tumor COSM4004992 c.1274G>A p.G425E Substitution - Missense 23:126164651-126164651 - TCGA-BR-6452-01 COSM4106445 c.1289C>T p.A430V Substitution - Missense 23:126164636-126164636 - TCGA-BR-8078-01 COSM122506 c.1004G>A p.R335H Substitution - Missense 23:126164921-126164921 - TCGA-GN-A262-06 COSM3557612 c.81T>C p.G27G Substitution - coding silent 23:126165844-126165844 - TCGA-AG-3909-01 COSM289152 c.849C>T p.D283D Substitution - coding silent 23:126165076-126165076 - TCGA-IR-A3LK-01 COSM1114639 c.1133G>A p.R378H Substitution - Missense 23:126164792-126164792 - 587306 COSM1203048 c.919C>T p.R307* Substitution - Nonsense 23:126165006-126165006 - CHC1028T COSM4790854 c.564C>T p.G188G Substitution - coding silent 23:126165361-126165361 - T407 COSM1249722 c.856T>G p.F286V Substitution - Missense 23:126165069-126165069 - ESCC_84 COSM5636498 c.5C>T p.A2V Substitution - Missense 23:126165920-126165920 - S0051 COSM1497174 c.595G>A p.A199T Substitution - Missense 23:126165330-126165330 - TCGA-GN-A262-06 COSM3557611 c.81T>C p.G27G Substitution - coding silent 23:126165844-126165844 - T2664 COSM4106468 c.185C>T p.A62V Substitution - Missense 23:126165740-126165740 - SE1 COSM1165667 c.372C>T p.D124D Substitution - coding silent 23:126165553-126165553 - HCC4 COSM1625480 c.6C>A p.A2A Substitution - coding silent 23:126165919-126165919 - TCGA-66-2777-01 COSM755475 c.891G>T p.R297S Substitution - Missense 23:126165034-126165034 - TCGA-A6-5665-01 COSM1465450 c.126G>T p.Q42H Substitution - Missense 23:126165799-126165799 - TCGA-06-0155 COSM1315187 c.737G>A p.R246H Substitution - Missense 23:126165188-126165188 - TCGA-D3-A2JF-06 COSM3557599 c.745G>A p.D249N Substitution - Missense 23:126165180-126165180 - Pat_02_B COSM4676345 c.137C>T p.A46V Substitution - Missense 23:126165788-126165788 - TCGA-FU-A3HZ-01 COSM4106444 c.1289C>T p.A430V Substitution - Missense 23:126164636-126164636 - TCGA-AG-4007-01 COSM259038 c.238G>A p.V80I Substitution - Missense 23:126165687-126165687 - TCGA-D1-A17Q-01 COSM1114642 c.1040G>A p.R347Q Substitution - Missense 23:126164885-126164885 - BCM399T COSM4950036 c.671C>A p.P224Q Substitution - Missense 23:126165254-126165254 - S0051 COSM1497173 c.595G>A p.A199T Substitution - Missense 23:126165330-126165330 - TCGA-A5-A0GP-01 COSM1114637 c.1277A>C p.E426A Substitution - Missense 23:126164648-126164648 - TCGA-F5-6814-01 COSM3424442 c.341G>A p.G114D Substitution - Missense 23:126165584-126165584 - TCGA-A5-A0GI-01 COSM1114665 c.328C>T p.Q110* Substitution - Nonsense 23:126165597-126165597 - TCGA-OL-A66I-01 COSM1331276 c.1010G>A p.R337H Substitution - Missense 23:126164915-126164915 - TCGA-HI-7169-01 COSM1331275 c.1010G>A p.R337H Substitution - Missense 23:126164915-126164915 - PD7188a COSM3769821 c.1176C>G p.D392E Substitution - Missense 23:126164749-126164749 - sysucc-657T COSM3759349 c.441C>A p.H147Q Substitution - Missense 23:126165484-126165484 - LUAD-NYU847 COSM376980 c.523G>T p.A175S Substitution - Missense 23:126165402-126165402 - TCGA-D7-A4YU-01 COSM1249728 c.1142A>C p.K381T Substitution - Missense 23:126164783-126164783 - T613 COSM4676340 c.494C>T p.A165V Substitution - Missense 23:126165431-126165431 - TCGA-ER-A19D-06 COSM3557593 c.989C>T p.S330F Substitution - Missense 23:126164936-126164936 - 49M COSM5590463 c.1037C>T p.S346F Substitution - Missense 23:126164888-126164888 - PCSI_0099_Pa_P COSM216851 c.1002G>A p.P334P Substitution - coding silent 23:126164923-126164923 - ESCC_56 COSM5632231 c.1127A>G p.D376G Substitution - Missense 23:126164798-126164798 - HCC4 COSM1625481 c.6C>A p.A2A Substitution - coding silent 23:126165919-126165919 - ICGC_MB102 COSM122506 c.1004G>A p.R335H Substitution - Missense 23:126164921-126164921 - T613 COSM4676339 c.494C>T p.A165V Substitution - Missense 23:126165431-126165431 - TCGA-EE-A3JD-06 COSM4394461 c.399C>T p.I133I Substitution - coding silent 23:126165526-126165526 - TCGA-AP-A056-01 COSM1114645 c.1039C>T p.R347* Substitution - Nonsense 23:126164886-126164886 - 1115202 COSM385381 c.1001C>T p.P334L Substitution - Missense 23:126164924-126164924 - TCGA-02-2485-01 COSM3405935 c.17C>A p.T6K Substitution - Missense 23:126165908-126165908 - CSCC-29-T COSM4513468 c.939C>T p.T313T Substitution - coding silent 23:126164986-126164986 - I2L-P19Ta-Tumor-Biopsy COSM5366965 c.1191C>T p.P397P Substitution - coding silent 23:126164734-126164734 - PCSI_0311_Pa_P_526 COSM1114647 c.1003C>T p.R335C Substitution - Missense 23:126164922-126164922 - TCGA-EI-6506-01 COSM1203052 c.409C>T p.R137W Substitution - Missense 23:126165516-126165516 - Pat_41_B COSM5877024 c.1028C>T p.P343L Substitution - Missense 23:126164897-126164897 - TCGA-EE-A3JD-06 COSM4396684 c.471G>A p.L157L Substitution - coding silent 23:126165454-126165454 - T3049 COSM4619636 c.238G>A p.V80I Substitution - Missense 23:126165687-126165687 - TCGA-F5-6814-01 COSM3424443 c.341G>A p.G114D Substitution - Missense 23:126165584-126165584 - S00472 COSM316533 c.732C>A p.H244Q Substitution - Missense 23:126165193-126165193 - T2664 COSM4106469 c.185C>T p.A62V Substitution - Missense 23:126165740-126165740 - TCGA-BR-6452-01 COSM4106444 c.1289C>T p.A430V Substitution - Missense 23:126164636-126164636 - SNU-175 COSM2725047 c.42C>T p.P14P Substitution - coding silent 23:126165883-126165883 - TCGA-A8-A08R-01 COSM456697 c.1252G>C p.V418L Substitution - Missense 23:126164673-126164673 - CSCC-29-T COSM4560632 c.850G>A p.G284S Substitution - Missense 23:126165075-126165075 - TCGA-IR-A3LK-01 COSM4817078 c.903C>T p.I301I Substitution - coding silent 23:126165022-126165022 - LUAD-NYU284 COSM373458 c.1005C>A p.R335R Substitution - coding silent 23:126164920-126164920 - TCGA-AA-3660-01 COSM385380 c.1001C>T p.P334L Substitution - Missense 23:126164924-126164924 - TCGA-AP-A056-01 COSM1114644 c.1039C>T p.R347* Substitution - Nonsense 23:126164886-126164886 - QC2-40-T2 COSM5656152 c.559C>T p.L187L Substitution - coding silent 23:126165366-126165366 - ICGC_MB102 COSM2724981 c.1004G>A p.R335H Substitution - Missense 23:126164921-126164921 - CSCC-41-T COSM2724966 c.1146C>T p.F382F Substitution - coding silent 23:126164779-126164779 - LUAD-NYU696 COSM376147 c.640G>T p.D214Y Substitution - Missense 23:126165285-126165285 - Gp5D COSM2724998 c.614A>G p.D205G Substitution - Missense 23:126165311-126165311 - LIM2405 COSM4643388 c.226C>T p.R76W Substitution - Missense 23:126165699-126165699 - TCGA-ET-A39O-01 COSM3983941 c.398T>A p.I133N Substitution - Missense 23:126165527-126165527 - TCGA-A6-6654-01 COSM1465447 c.146G>A p.R49H Substitution - Missense 23:126165779-126165779 - LUAD-E01014 COSM403510 c.726T>G p.Y242* Substitution - Nonsense 23:126165199-126165199 - TCGA-A6-5665-01 COSM1114639 c.1133G>A p.R378H Substitution - Missense 23:126164792-126164792 - TCGA-AA-3713-01 COSM1315184 c.1009C>T p.R337C Substitution - Missense 23:126164916-126164916 - TCGA-06-0141-01 COSM1114646 c.1003C>T p.R335C Substitution - Missense 23:126164922-126164922 - TCGA-A6-5665-01 COSM1114638 c.1133G>A p.R378H Substitution - Missense 23:126164792-126164792 - 587304 COSM1203046 c.1211T>C p.L404P Substitution - Missense 23:126164714-126164714 - TCGA-34-5929-01 COSM755483 c.1052C>A p.T351K Substitution - Missense 23:126164873-126164873 - TCGA-CD-A4MG-01 COSM4106455 c.770G>A p.S257N Substitution - Missense 23:126165155-126165155 - TCGA-CC-A7IH-01 COSM4924281 c.971G>T p.G324V Substitution - Missense 23:126164954-126164954 - 1N56-VS-1T56 COSM4977293 c.340G>A p.G114S Substitution - Missense 23:126165585-126165585 - 1N03-VS-1T03 COSM4106463 c.414C>T p.D138D Substitution - coding silent 23:126165511-126165511 - TCGA-02-2485-01 COSM3405936 c.17C>A p.T6K Substitution - Missense 23:126165908-126165908 - TCGA-29-1691-01 COSM1331273 c.321C>T p.N107N Substitution - coding silent 23:126165604-126165604 - 2492721 COSM5723354 c.997G>A p.D333N Substitution - Missense 23:126164928-126164928 - TCGA-06-0174-01 COSM3405933 c.143G>A p.R48H Substitution - Missense 23:126165782-126165782 - TCGA-Q1-A6DT-01 COSM4850891 c.1245C>T p.D415D Substitution - coding silent 23:126164680-126164680 - T3498 COSM1331276 c.1010G>A p.R337H Substitution - Missense 23:126164915-126164915 - C058 COSM2725008 c.505G>A p.E169K Substitution - Missense 23:126165420-126165420 - 2492725 COSM5725228 c.1200G>A p.R400R Substitution - coding silent 23:126164725-126164725 - TCGA-GF-A6C9-06 COSM4903258 c.1179C>T p.S393S Substitution - coding silent 23:126164746-126164746 - TCGA-DB-A4XH-01 COSM1249724 c.788G>A p.R263H Substitution - Missense 23:126165137-126165137 - TCGA-BT-A20X-01 COSM1315184 c.1009C>T p.R337C Substitution - Missense 23:126164916-126164916 - ESO-017 COSM1249715 c.1190C>A p.P397H Substitution - Missense 23:126164735-126164735 - S00472 COSM316532 c.732C>A p.H244Q Substitution - Missense 23:126165193-126165193 - TCGA-CD-A4MG-01 COSM4106449 c.1135G>A p.A379T Substitution - Missense 23:126164790-126164790 - NPC29F COSM4997109 c.1336G>C p.A446P Substitution - Missense 23:126164589-126164589 - C086 COSM5529583 c.1197G>A p.G399G Substitution - coding silent 23:126164728-126164728 - I2L-P19Ta-Tumor-Organoid COSM5366964 c.1191C>T p.P397P Substitution - coding silent 23:126164734-126164734 - MT-439-T2 COSM385380 c.1001C>T p.P334L Substitution - Missense 23:126164924-126164924 - TCGA-B5-A11G-01 COSM1114649 c.938C>A p.T313N Substitution - Missense 23:126164987-126164987 - TCGA-CD-A4MG-01 COSM4106454 c.770G>A p.S257N Substitution - Missense 23:126165155-126165155 - LS174T COSM122506 c.1004G>A p.R335H Substitution - Missense 23:126164921-126164921 - sysucc-657T COSM3759350 c.441C>A p.H147Q Substitution - Missense 23:126165484-126165484 - PCSI_0099_Pa_P_526 COSM1743145 c.1002G>A p.P334P Substitution - coding silent 23:126164923-126164923 - T3024 COSM1203054 c.394C>T p.R132C Substitution - Missense 23:126165531-126165531 - TCGA-66-2770-01 COSM755477 c.956C>A p.S319Y Substitution - Missense 23:126164969-126164969 - CSCC-19-T COSM3557587 c.1281C>T p.F427F Substitution - coding silent 23:126164644-126164644 - TCGA-CG-5723-01 COSM4106463 c.414C>T p.D138D Substitution - coding silent 23:126165511-126165511 - TCGA-AA-A010-01 COSM280303 c.49G>A p.E17K Substitution - Missense 23:126165876-126165876 - SJOS005_D COSM5024244 c.478T>C p.S160P Substitution - Missense 23:126165447-126165447 - PT16_1 COSM3557607 c.617C>T p.T206I Substitution - Missense 23:126165308-126165308 - TCGA-CG-4441-01 COSM385380 c.1001C>T p.P334L Substitution - Missense 23:126164924-126164924 - TCGA-EB-A3Y7-01 COSM2724988 c.735C>T p.I245I Substitution - coding silent 23:126165190-126165190 - 587316 COSM1203054 c.394C>T p.R132C Substitution - Missense 23:126165531-126165531 - TCGA-HT-7689-01 COSM1249723 c.788G>A p.R263H Substitution - Missense 23:126165137-126165137 - T3024 COSM1203055 c.394C>T p.R132C Substitution - Missense 23:126165531-126165531 - TCGA-EE-A3JD-06 COSM4394460 c.399C>T p.I133I Substitution - coding silent 23:126165526-126165526 - T3255 COSM4676346 c.137C>T p.A46V Substitution - Missense 23:126165788-126165788 - ME037T COSM227964 c.1386G>A p.W462* Substitution - Nonsense 23:126164539-126164539 - TCGA-AM-5820-01 COSM1556088 c.807C>A p.A269A Substitution - coding silent 23:126165118-126165118 - Au1 COSM3424440 c.395G>A p.R132H Substitution - Missense 23:126165530-126165530 - PCSI_0099_Pa_P_526 COSM216851 c.1002G>A p.P334P Substitution - coding silent 23:126164923-126164923 - 3498_T COSM3964674 c.450C>A p.C150* Substitution - Nonsense 23:126165475-126165475 - CHC1556T COSM4787719 c.844T>G p.L282V Substitution - Missense 23:126165081-126165081 - TCGA-CG-5723-01 COSM4106462 c.414C>T p.D138D Substitution - coding silent 23:126165511-126165511 - TCGA-AP-A059-01 COSM1114650 c.895C>T p.L299L Substitution - coding silent 23:126165030-126165030 - TCGA-K4-A3WS-01 COSM3800389 c.1060C>G p.R354G Substitution - Missense 23:126164865-126164865 - 51T COSM107315 c.1144T>C p.F382L Substitution - Missense 23:126164781-126164781 - ESO-640 COSM1249723 c.788G>A p.R263H Substitution - Missense 23:126165137-126165137 - OSCC-GB_00500111 COSM3713853 c.1226G>T p.G409V Substitution - Missense 23:126164699-126164699 - TCGA-BS-A0TG-01 COSM1114660 c.647C>T p.T216I Substitution - Missense 23:126165278-126165278 - Gp2D COSM4628966 c.902T>A p.I301N Substitution - Missense 23:126165023-126165023 - TCGA-AD-6901-01 COSM1465436 c.1319A>G p.E440G Substitution - Missense 23:126164606-126164606 - TCGA-A6-5665-01 COSM1465449 c.126G>T p.Q42H Substitution - Missense 23:126165799-126165799 - TCGA-CD-A4MG-01 COSM4106448 c.1135G>A p.A379T Substitution - Missense 23:126164790-126164790 - ESCC_84 COSM5636497 c.5C>T p.A2V Substitution - Missense 23:126165920-126165920 - TCGA-BR-8686-01 COSM4106450 c.1034G>T p.C345F Substitution - Missense 23:126164891-126164891 - TCGA-06-6697-01 COSM3405932 c.466G>A p.E156K Substitution - Missense 23:126165459-126165459 - TCGA-BS-A0TG-01 COSM1114659 c.647C>T p.T216I Substitution - Missense 23:126165278-126165278 - 587228 COSM1203051 c.391A>C p.T131P Substitution - Missense 23:126165534-126165534 - TCGA-06-6697-01 COSM25471 c.466G>A p.E156K Substitution - Missense 23:126165459-126165459 - 2492726 COSM5725229 c.1200G>A p.R400R Substitution - coding silent 23:126164725-126164725 - TCGA-GD-A3OP-01 COSM1315189 c.647C>A p.T216N Substitution - Missense 23:126165278-126165278 - TCGA-FE-A235-01 COSM385380 c.1001C>T p.P334L Substitution - Missense 23:126164924-126164924 - STC297 COSM5064352 c.140C>T p.T47M Substitution - Missense 23:126165785-126165785 - LUAD-NYU847 COSM376981 c.523G>T p.A175S Substitution - Missense 23:126165402-126165402 - CHC1556T COSM4787719 c.844T>G p.L282V Substitution - Missense 23:126165081-126165081 - 19M COSM5578374 c.666G>A p.M222I Substitution - Missense 23:126165259-126165259 - C086 COSM5529582 c.1197G>A p.G399G Substitution - coding silent 23:126164728-126164728 - 2492726 COSM5725228 c.1200G>A p.R400R Substitution - coding silent 23:126164725-126164725 - LUAD-YINHD COSM388629 c.1062G>T p.R354R Substitution - coding silent 23:126164863-126164863 - TCGA-BR-4368-01 COSM1331275 c.1010G>A p.R337H Substitution - Missense 23:126164915-126164915 - TCGA-EB-A44Q-06 COSM3913328 c.92C>G p.A31G Substitution - Missense 23:126165833-126165833 - KPOPBR-03-T COSM5965171 c.1223G>A p.R408K Substitution - Missense 23:126164702-126164702 - LUAD-F00089 COSM365566 c.421G>T p.A141S Substitution - Missense 23:126165504-126165504 - T2420 COSM1114655 c.787C>T p.R263C Substitution - Missense 23:126165138-126165138 - SJACT019_D COSM4968524 c.1382T>A p.L461H Substitution - Missense 23:126164543-126164543 - TCGA-FS-A1ZZ-06 COSM3557613 c.74C>T p.S25L Substitution - Missense 23:126165851-126165851 - TCGA-EE-A2GO-06 COSM3557603 c.669C>T p.D223D Substitution - coding silent 23:126165256-126165256 - 435 COSM4433945 c.721G>A p.V241I Substitution - Missense 23:126165204-126165204 - TCGA-BC-A3KG-01 COSM4942586 c.615C>A p.D205E Substitution - Missense 23:126165310-126165310 - RK121_C01 COSM3747299 c.1299C>G p.T433T Substitution - coding silent 23:126164626-126164626 - TCGA-CD-8535-01 COSM4106442 c.1333G>C p.V445L Substitution - Missense 23:126164592-126164592 - ICGC_MB127 COSM302028 c.217G>T p.G73C Substitution - Missense 23:126165708-126165708 - T407 COSM4676333 c.854A>G p.Y285C Substitution - Missense 23:126165071-126165071 - TCGA-KK-A6E7-01 COSM4876530 c.644G>A p.G215D Substitution - Missense 23:126165281-126165281 - S01297 COSM5667842 c.627G>T p.V209V Substitution - coding silent 23:126165298-126165298 - TCGA-EE-A2GO-06 COSM3557598 c.833G>A p.G278E Substitution - Missense 23:126165092-126165092 - TCGA-BR-7707-01 COSM4106465 c.274C>A p.L92M Substitution - Missense 23:126165651-126165651 - C70 COSM259038 c.238G>A p.V80I Substitution - Missense 23:126165687-126165687 - TCGA-AA-3715-01 COSM268981 c.888C>T p.S296S Substitution - coding silent 23:126165037-126165037 - TCGA-60-2722-01 COSM755485 c.1342G>C p.G448R Substitution - Missense 23:126164583-126164583 - BCM399T COSM4950036 c.671C>A p.P224Q Substitution - Missense 23:126165254-126165254 - T3498 COSM1331275 c.1010G>A p.R337H Substitution - Missense 23:126164915-126164915 - 1115202 COSM385380 c.1001C>T p.P334L Substitution - Missense 23:126164924-126164924 - Gp5D COSM2724999 c.614A>G p.D205G Substitution - Missense 23:126165311-126165311 - TCGA-FS-A1ZZ-06 COSM3557614 c.74C>T p.S25L Substitution - Missense 23:126165851-126165851 - COLO205 COSM2725000 c.601G>A p.A201T Substitution - Missense 23:126165324-126165324 - S02277 COSM5683360 c.846G>T p.L282F Substitution - Missense 23:126165079-126165079 - TCGA-A5-A0G9-01 COSM1114661 c.539C>G p.P180R Substitution - Missense 23:126165386-126165386 - sysucc-783T COSM5485124 c.736C>T p.R246C Substitution - Missense 23:126165189-126165189 - LUAD-S01346 COSM404359 c.821A>C p.N274T Substitution - Missense 23:126165104-126165104 - TCGA-AX-A05Z-01 COSM610564 c.920G>A p.R307Q Substitution - Missense 23:126165005-126165005 - TCGA-FU-A3HZ-01 COSM4106445 c.1289C>T p.A430V Substitution - Missense 23:126164636-126164636 - QC2-40-T2 COSM5656151 c.559C>T p.L187L Substitution - coding silent 23:126165366-126165366 - SW48 COSM1315186 c.737G>A p.R246H Substitution - Missense 23:126165188-126165188 - TCGA-BG-A0M0-01 COSM1114639 c.1133G>A p.R378H Substitution - Missense 23:126164792-126164792 - TCGA-D1-A17Q-01 COSM1114643 c.1040G>A p.R347Q Substitution - Missense 23:126164885-126164885 - SW948 COSM4656742 c.672A>G p.P224P Substitution - coding silent 23:126165253-126165253 - ESO-1130 COSM1249718 c.783C>A p.S261R Substitution - Missense 23:126165142-126165142 - EGC15 COSM5064351 c.461C>T p.A154V Substitution - Missense 23:126165464-126165464 - SC_9054 COSM5564987 c.638G>T p.R213L Substitution - Missense 23:126165287-126165287 - TCGA-A5-A0GI-01 COSM1114666 c.328C>T p.Q110* Substitution - Nonsense 23:126165597-126165597 - LS180 COSM122506 c.1004G>A p.R335H Substitution - Missense 23:126164921-126164921 - TCGA-DK-A3X1-01 COSM3800390 c.318G>T p.L106L Substitution - coding silent 23:126165607-126165607 - 262LT COSM2724981 c.1004G>A p.R335H Substitution - Missense 23:126164921-126164921 - S01297 COSM5667841 c.627G>T p.V209V Substitution - coding silent 23:126165298-126165298 - CHOL12 COSM1465441 c.594C>T p.F198F Substitution - coding silent 23:126165331-126165331 - TCGA-HU-8243-01 COSM4106467 c.237C>G p.A79A Substitution - coding silent 23:126165688-126165688 - TCGA-E2-A1IN-01 COSM1490460 c.1038T>A p.S346S Substitution - coding silent 23:126164887-126164887 - TCGA-AP-A051-01 COSM1114656 c.787C>T p.R263C Substitution - Missense 23:126165138-126165138 - SJOS005_D COSM5024243 c.478T>C p.S160P Substitution - Missense 23:126165447-126165447 - TCGA-FD-A3B4-01 COSM1315191 c.244A>T p.R82W Substitution - Missense 23:126165681-126165681 - TCGA-HU-8602-01 COSM4106468 c.185C>T p.A62V Substitution - Missense 23:126165740-126165740 - ESO-708 COSM1249725 c.813C>T p.S271S Substitution - coding silent 23:126165112-126165112 - TCGA-D7-8579-01 COSM256735 c.1290G>A p.A430A Substitution - coding silent 23:126164635-126164635 - COLO201 COSM2725001 c.601G>A p.A201T Substitution - Missense 23:126165324-126165324 - TCGA-EE-A20H-06 COSM3557590 c.1225G>A p.G409S Substitution - Missense 23:126164700-126164700 - 3N02-VS-3T02 COSM4978560 c.143G>T p.R48L Substitution - Missense 23:126165782-126165782 - 2492720 COSM5723353 c.997G>A p.D333N Substitution - Missense 23:126164928-126164928 - ACINAR29 COSM1733051 c.220G>A p.E74K Substitution - Missense 23:126165705-126165705 - TCGA-20-1687-01 COSM1331277 c.1169G>A p.S390N Substitution - Missense 23:126164756-126164756 - TCGA-D7-A4YU-01 COSM1249727 c.1142A>C p.K381T Substitution - Missense 23:126164783-126164783 - ESO-732 COSM1249714 c.1300delC p.H434fs*8 Deletion - Frameshift 23:126164625-126164625 - TCGA-B5-A11E-01 COSM1114654 c.794T>C p.V265A Substitution - Missense 23:126165131-126165131 - TCGA-AP-A051-01 COSM1114655 c.787C>T p.R263C Substitution - Missense 23:126165138-126165138 - TCGA-29-1691-01 COSM1331274 c.321C>T p.N107N Substitution - coding silent 23:126165604-126165604 - TCGA-AX-A05Z-01 COSM1114634 c.1329C>A p.L443L Substitution - coding silent 23:126164596-126164596 - 12586 COSM5616214 c.632G>T p.G211V Substitution - Missense 23:126165293-126165293 - CHC1556T COSM4787718 c.844T>G p.L282V Substitution - Missense 23:126165081-126165081 - TCGA-HT-7689-01 COSM1249724 c.788G>A p.R263H Substitution - Missense 23:126165137-126165137 - ESO-640 COSM1249724 c.788G>A p.R263H Substitution - Missense 23:126165137-126165137 - ESO-137 COSM1249721 c.856T>G p.F286V Substitution - Missense 23:126165069-126165069 - 12586 COSM5616211 c.1001C>A p.P334Q Substitution - Missense 23:126164924-126164924 - TCGA-06-6694-01 COSM1315186 c.737G>A p.R246H Substitution - Missense 23:126165188-126165188 - TCGA-AU-6004-01 COSM1249723 c.788G>A p.R263H Substitution - Missense 23:126165137-126165137 - TCGA-A6-6654-01 COSM1465448 c.146G>A p.R49H Substitution - Missense 23:126165779-126165779 - CHC1028T COSM4790853 c.564C>T p.G188G Substitution - coding silent 23:126165361-126165361 - TCGA-A8-A08R-01 COSM456696 c.1252G>C p.V418L Substitution - Missense 23:126164673-126164673 - C086 COSM5529579 c.1196G>A p.G399E Substitution - Missense 23:126164729-126164729 - LUAD-NYU1021 COSM368264 c.401C>T p.P134L Substitution - Missense 23:126165524-126165524 - LUAD-RT-S01831 COSM384564 c.63G>T p.G21G Substitution - coding silent 23:126165862-126165862 - TCGA-BR-8687-01 COSM385380 c.1001C>T p.P334L Substitution - Missense 23:126164924-126164924 - sysucc-783T COSM5485125 c.736C>T p.R246C Substitution - Missense 23:126165189-126165189 - PD13298a COSM1114647 c.1003C>T p.R335C Substitution - Missense 23:126164922-126164922 - PT16_1 COSM3557608 c.617C>T p.T206I Substitution - Missense 23:126165308-126165308 - LS180 COSM2724981 c.1004G>A p.R335H Substitution - Missense 23:126164921-126164921 - ESO-732 COSM1249713 c.1300delC p.H434fs*8 Deletion - Frameshift 23:126164625-126164625 - 35M COSM5580775 c.418G>A p.E140K Substitution - Missense 23:126165507-126165507 - 3498_T COSM3964673 c.450C>A p.C150* Substitution - Nonsense 23:126165475-126165475 - sysucc-1397T COSM5475319 c.450C>T p.C150C Substitution - coding silent 23:126165475-126165475 - TCGA-DS-A0VK-01 COSM368264 c.401C>T p.P134L Substitution - Missense 23:126165524-126165524 - TCGA-AM-5821-01 COSM3759348 c.1218C>T p.C406C Substitution - coding silent 23:126164707-126164707 - TCGA-D7-6817-01 COSM1165668 c.372C>T p.D124D Substitution - coding silent 23:126165553-126165553 - 262LT COSM122506 c.1004G>A p.R335H Substitution - Missense 23:126164921-126164921 - ESCC_158 COSM2724988 c.735C>T p.I245I Substitution - coding silent 23:126165190-126165190 - S01297 COSM5667840 c.1123T>G p.Y375D Substitution - Missense 23:126164802-126164802 - TCGA-EE-A185-06 COSM3557605 c.618C>T p.T206T Substitution - coding silent 23:126165307-126165307 - OSCC-GB_01100111 COSM4888343 c.418G>C p.E140Q Substitution - Missense 23:126165507-126165507 - HN_63048 COSM122506 c.1004G>A p.R335H Substitution - Missense 23:126164921-126164921 - BCM399T COSM4950035 c.671C>A p.P224Q Substitution - Missense 23:126165254-126165254 - TCGA-F1-A448-01 COSM2725031 c.339C>T p.C113C Substitution - coding silent 23:126165586-126165586 - TCGA-BR-8687-01 COSM385381 c.1001C>T p.P334L Substitution - Missense 23:126164924-126164924 - TCGA-D3-A3C8-06 COSM3557588 c.1281C>T p.F427F Substitution - coding silent 23:126164644-126164644 - TCGA-IR-A3LK-01 COSM4817077 c.903C>T p.I301I Substitution - coding silent 23:126165022-126165022 - RK308_C01 COSM3747300 c.558C>T p.C186C Substitution - coding silent 23:126165367-126165367 - TCGA-G4-6295-01 COSM3694328 c.485C>T p.T162M Substitution - Missense 23:126165440-126165440 - TCGA-BR-6452-01 COSM4106461 c.539C>A p.P180H Substitution - Missense 23:126165386-126165386 - TCGA-BR-4184-01 COSM4106473 c.130C>T p.R44W Substitution - Missense 23:126165795-126165795 - EGC15 COSM5064349 c.1243G>A p.D415N Substitution - Missense 23:126164682-126164682 - TCGA-A8-A083-01 COSM456695 c.1259A>T p.Y420F Substitution - Missense 23:126164666-126164666 - S02277 COSM5683359 c.846G>T p.L282F Substitution - Missense 23:126165079-126165079 - C086 COSM5529580 c.216G>A p.E72E Substitution - coding silent 23:126165709-126165709 - 202_T COSM3964676 c.364G>A p.V122M Substitution - Missense 23:126165561-126165561 - 2000120 COSM1331276 c.1010G>A p.R337H Substitution - Missense 23:126164915-126164915 - GB19 COSM1743145 c.1002G>A p.P334P Substitution - coding silent 23:126164923-126164923 - S01020 COSM365566 c.421G>T p.A141S Substitution - Missense 23:126165504-126165504 - TCGA-AM-5821-01 COSM3759347 c.1218C>T p.C406C Substitution - coding silent 23:126164707-126164707 - TCGA-IR-A3LK-01 COSM1114638 c.1133G>A p.R378H Substitution - Missense 23:126164792-126164792 - SNU-175 COSM2725046 c.42C>T p.P14P Substitution - coding silent 23:126165883-126165883 - S01297 COSM5667839 c.1123T>G p.Y375D Substitution - Missense 23:126164802-126164802 - RK308_C01 COSM3747301 c.558C>T p.C186C Substitution - coding silent 23:126165367-126165367 - TCGA-K7-A5RF-01 COSM1203048 c.919C>T p.R307* Substitution - Nonsense 23:126165006-126165006 - TCGA-A8-A083-01 COSM456694 c.1259A>T p.Y420F Substitution - Missense 23:126164666-126164666 - LS174T COSM2724981 c.1004G>A p.R335H Substitution - Missense 23:126164921-126164921 - TCGA-CA-6717-01 COSM1465442 c.594C>T p.F198F Substitution - coding silent 23:126165331-126165331 - OSCC-GB_00690111 COSM4886927 c.871G>T p.A291S Substitution - Missense 23:126165054-126165054 - TCGA-BR-7707-01 COSM4106464 c.274C>A p.L92M Substitution - Missense 23:126165651-126165651 - LUAD-LIP77 COSM367949 c.574G>T p.G192C Substitution - Missense 23:126165351-126165351 - SC_9054 COSM5564986 c.638G>T p.R213L Substitution - Missense 23:126165287-126165287 - PT52 COSM5941126 c.1323G>A p.M441I Substitution - Missense 23:126164602-126164602 - TCGA-66-2770-01 COSM755478 c.956C>A p.S319Y Substitution - Missense 23:126164969-126164969 - I2L-P9-Tumor-Organoid COSM1315184 c.1009C>T p.R337C Substitution - Missense 23:126164916-126164916 - TCGA-AM-5821-01 COSM3759349 c.441C>A p.H147Q Substitution - Missense 23:126165484-126165484 - pfg025T COSM1643939 c.873C>A p.A291A Substitution - coding silent 23:126165052-126165052 - OSCC-GB_00500111 COSM3713852 c.1226G>T p.G409V Substitution - Missense 23:126164699-126164699 - TCGA-GF-A6C9-06 COSM4903259 c.1179C>T p.S393S Substitution - coding silent 23:126164746-126164746 - PD6418a COSM385380 c.1001C>T p.P334L Substitution - Missense 23:126164924-126164924 - TCGA-HU-8243-01 COSM4106466 c.237C>G p.A79A Substitution - coding silent 23:126165688-126165688 - ESO-118 COSM1249720 c.1142A>G p.K381R Substitution - Missense 23:126164783-126164783 - S00472 COSM5658048 c.217G>C p.G73R Substitution - Missense 23:126165708-126165708 - TCGA-AX-A0J1-01 COSM1114664 c.357G>A p.T119T Substitution - coding silent 23:126165568-126165568 - ESCC_56 COSM5632230 c.1127A>G p.D376G Substitution - Missense 23:126164798-126164798 - TCGA-29-1696-01 COSM1331276 c.1010G>A p.R337H Substitution - Missense 23:126164915-126164915 - TCGA-HU-A4H2-01 COSM4106477 c.92C>T p.A31V Substitution - Missense 23:126165833-126165833 - TCGA-D7-8579-01 COSM4106443 c.1290G>A p.A430A Substitution - coding silent 23:126164635-126164635 - T2420 COSM1114656 c.787C>T p.R263C Substitution - Missense 23:126165138-126165138 - TCGA-AO-A12H-01 COSM456699 c.498C>T p.T166T Substitution - coding silent 23:126165427-126165427 - LIM2405 COSM4643387 c.226C>T p.R76W Substitution - Missense 23:126165699-126165699 - TCGA-EE-A2GO-06 COSM2725008 c.505G>A p.E169K Substitution - Missense 23:126165420-126165420 - S02384 COSM610577 c.1290G>T p.A430A Substitution - coding silent 23:126164635-126164635 - CHC1028T COSM4790853 c.564C>T p.G188G Substitution - coding silent 23:126165361-126165361 - T407 COSM1249721 c.856T>G p.F286V Substitution - Missense 23:126165069-126165069 - BCM399T COSM4950035 c.671C>A p.P224Q Substitution - Missense 23:126165254-126165254 - TCGA-BR-8686-01 COSM4106451 c.1034G>T p.C345F Substitution - Missense 23:126164891-126164891 - 587304 COSM1203047 c.1211T>C p.L404P Substitution - Missense 23:126164714-126164714 - 35M COSM5580776 c.418G>A p.E140K Substitution - Missense 23:126165507-126165507 - QC2-20-T2 COSM5652880 c.379T>C p.S127P Substitution - Missense 23:126165546-126165546 - 13681 COSM5616212 c.878G>T p.S293I Substitution - Missense 23:126165047-126165047 - TCGA-AA-3660-01 COSM385381 c.1001C>T p.P334L Substitution - Missense 23:126164924-126164924 - sysucc-1397T COSM5475320 c.450C>T p.C150C Substitution - coding silent 23:126165475-126165475 - TCGA-D3-A51T-06 COSM3557591 c.1101C>A p.T367T Substitution - coding silent 23:126164824-126164824 - TCGA-EE-A182-06 COSM3557586 c.1306T>C p.Y436H Substitution - Missense 23:126164619-126164619 - QC2-20-T2 COSM5652879 c.379T>C p.S127P Substitution - Missense 23:126165546-126165546 - TCGA-HU-A4H2-01 COSM4106476 c.92C>T p.A31V Substitution - Missense 23:126165833-126165833 - TCGA-AA-3713-01 COSM1315185 c.1009C>T p.R337C Substitution - Missense 23:126164916-126164916 - TCGA-34-5929-01 COSM755484 c.1052C>A p.T351K Substitution - Missense 23:126164873-126164873 - TCGA-B5-A11E-01 COSM1114633 c.1357G>T p.G453C Substitution - Missense 23:126164568-126164568 - TCGA-AP-A051-01 COSM1114657 c.667G>A p.D223N Substitution - Missense 23:126165258-126165258 - 50T COSM3713852 c.1226G>T p.G409V Substitution - Missense 23:126164699-126164699 - 50T COSM3713853 c.1226G>T p.G409V Substitution - Missense 23:126164699-126164699 - SW948 COSM4656743 c.624T>C p.A208A Substitution - coding silent 23:126165301-126165301 - S01020 COSM365565 c.421G>T p.A141S Substitution - Missense 23:126165504-126165504 - TCGA-DS-A0VK-01 COSM368263 c.401C>T p.P134L Substitution - Missense 23:126165524-126165524 - TCGA-BT-A20X-01 COSM1315185 c.1009C>T p.R337C Substitution - Missense 23:126164916-126164916 - TCGA-FD-A3B4-01 COSM1315190 c.244A>T p.R82W Substitution - Missense 23:126165681-126165681 - SW948 COSM4656741 c.672A>G p.P224P Substitution - coding silent 23:126165253-126165253 - NPC29F COSM4997110 c.1336G>C p.A446P Substitution - Missense 23:126164589-126164589 - TCGA-GD-A3OP-01 COSM1315188 c.647C>A p.T216N Substitution - Missense 23:126165278-126165278 - 202_T COSM3964675 c.364G>A p.V122M Substitution - Missense 23:126165561-126165561 - TCGA-HU-A4GT-01 COSM4106474 c.99A>C p.G33G Substitution - coding silent 23:126165826-126165826 - TCGA-66-2777-01 COSM755476 c.891G>T p.R297S Substitution - Missense 23:126165034-126165034 - TCGA-EE-A185-06 COSM3557606 c.618C>T p.T206T Substitution - coding silent 23:126165307-126165307 - TCGA-D3-A3ML-06 COSM3557610 c.264G>A p.T88T Substitution - coding silent 23:126165661-126165661 - T55 COSM4676331 c.1163C>T p.S388F Substitution - Missense 23:126164762-126164762 - 9 COSM5732559 c.791A>C p.K264T Substitution - Missense 23:126165134-126165134 - TCGA-B5-A11G-01 COSM1114648 c.938C>A p.T313N Substitution - Missense 23:126164987-126164987 - TCGA-DU-A5TU-01 COSM3973212 c.1004G>C p.R335P Substitution - Missense 23:126164921-126164921 - TCGA-DK-A3X1-01 COSM3800391 c.318G>T p.L106L Substitution - coding silent 23:126165607-126165607 - sysucc-834T COSM5486768 c.774C>T p.T258T Substitution - coding silent 23:126165151-126165151 - HCC5 COSM1497173 c.595G>A p.A199T Substitution - Missense 23:126165330-126165330 - PD13298a COSM1114646 c.1003C>T p.R335C Substitution - Missense 23:126164922-126164922 - TCGA-AU-6004-01 COSM1249724 c.788G>A p.R263H Substitution - Missense 23:126165137-126165137 - CSCC-19-T COSM3557588 c.1281C>T p.F427F Substitution - coding silent 23:126164644-126164644 - TCGA-ER-A194-01 COSM3557608 c.617C>T p.T206I Substitution - Missense 23:126165308-126165308 - TCGA-BC-A3KG-01 COSM4942585 c.615C>A p.D205E Substitution - Missense 23:126165310-126165310 - TCGA-66-2786-01 COSM755472 c.380C>T p.S127L Substitution - Missense 23:126165545-126165545 - 442 COSM4434713 c.796C>T p.R266W Substitution - Missense 23:126165129-126165129 - CSCC-41-T COSM2724967 c.1146C>T p.F382F Substitution - coding silent 23:126164779-126164779 - TCGA-DA-A1HV-06 COSM3557583 c.1346C>T p.P449L Substitution - Missense 23:126164579-126164579 - 1T COSM106447 c.662G>A p.R221Q Substitution - Missense 23:126165263-126165263 - TCGA-06-0155-01 COSM1315187 c.737G>A p.R246H Substitution - Missense 23:126165188-126165188 - 587316 COSM1203055 c.394C>T p.R132C Substitution - Missense 23:126165531-126165531 - PT33 COSM5909965 c.1343G>A p.G448E Substitution - Missense 23:126164582-126164582 - XHDG35 COSM4769626 c.235G>A p.A79T Substitution - Missense 23:126165690-126165690 - TCGA-AP-A0LM-01 COSM1114668 c.142C>T p.R48C Substitution - Missense 23:126165783-126165783 - TCGA-06-0174-01 COSM3405934 c.143G>A p.R48H Substitution - Missense 23:126165782-126165782 - TCGA-Q1-A6DT-01 COSM4850890 c.1245C>T p.D415D Substitution - coding silent 23:126164680-126164680 - Patient5 COSM610564 c.920G>A p.R307Q Substitution - Missense 23:126165005-126165005 - TCGA-BT-A3PH-01 COSM1315186 c.737G>A p.R246H Substitution - Missense 23:126165188-126165188 - MD-326 COSM302028 c.217G>T p.G73C Substitution - Missense 23:126165708-126165708 - TCGA-BR-8077-01 COSM610555 c.649G>A p.V217M Substitution - Missense 23:126165276-126165276 - TCGA-E2-A1IN-01 COSM1490461 c.1038T>A p.S346S Substitution - coding silent 23:126164887-126164887 - TCGA-CA-6717-01 COSM1465441 c.594C>T p.F198F Substitution - coding silent 23:126165331-126165331 - ATL011 COSM5711475 c.1315C>A p.P439T Substitution - Missense 23:126164610-126164610 - Pa29C COSM85246 c.637C>T p.R213C Substitution - Missense 23:126165288-126165288 - TCGA-K4-A3WS-01 COSM3800388 c.1060C>G p.R354G Substitution - Missense 23:126164865-126164865 - HCC5T COSM1497173 c.595G>A p.A199T Substitution - Missense 23:126165330-126165330 - TCGA-CG-4441-01 COSM385381 c.1001C>T p.P334L Substitution - Missense 23:126164924-126164924 - TCGA-K7-A5RF-01 COSM1203049 c.919C>T p.R307* Substitution - Nonsense 23:126165006-126165006 - LUAD-YINHD COSM388628 c.1062G>T p.R354R Substitution - coding silent 23:126164863-126164863 - TCGA-BR-6452-01 COSM4106460 c.539C>A p.P180H Substitution - Missense 23:126165386-126165386 - T41 COSM5345889 c.141G>A p.T47T Substitution - coding silent 23:126165784-126165784 - TCGA-30-1891-01 COSM118454 c.186G>T p.A62A Substitution - coding silent 23:126165739-126165739 - PCSI_0099_Pa_P COSM1743145 c.1002G>A p.P334P Substitution - coding silent 23:126164923-126164923 - HCC5 COSM1497174 c.595G>A p.A199T Substitution - Missense 23:126165330-126165330 - TCGA-BR-8077-01 COSM610554 c.649G>A p.V217M Substitution - Missense 23:126165276-126165276 - TCGA-F4-6570-01 COSM1465439 c.625G>A p.V209M Substitution - Missense 23:126165300-126165300 - TCGA-EE-A2GO-06 COSM2725009 c.505G>A p.E169K Substitution - Missense 23:126165420-126165420 - PCSI_0311_Pa_P_526 COSM1114646 c.1003C>T p.R335C Substitution - Missense 23:126164922-126164922 - TCGA-HU-8602-01 COSM4106469 c.185C>T p.A62V Substitution - Missense 23:126165740-126165740 - LUAD-CHTN-Z4716A COSM362720 c.648C>T p.T216T Substitution - coding silent 23:126165277-126165277 - EGC15 COSM5064348 c.1243G>A p.D415N Substitution - Missense 23:126164682-126164682 - TCGA-D3-A51T-06 COSM3557592 c.1101C>A p.T367T Substitution - coding silent 23:126164824-126164824 - TCGA-EE-A2GO-06 COSM3557604 c.669C>T p.D223D Substitution - coding silent 23:126165256-126165256 - ESO-137 COSM1249722 c.856T>G p.F286V Substitution - Missense 23:126165069-126165069 - LUAD-E00443 COSM364162 c.761C>A p.P254H Substitution - Missense 23:126165164-126165164 - TCGA-AX-A05Z-01 COSM610565 c.920G>A p.R307Q Substitution - Missense 23:126165005-126165005 - 49M COSM5590462 c.1037C>T p.S346F Substitution - Missense 23:126164888-126164888 - EGC20 COSM1114638 c.1133G>A p.R378H Substitution - Missense 23:126164792-126164792 - TCGA-06-0155 COSM1315186 c.737G>A p.R246H Substitution - Missense 23:126165188-126165188 - I2L-P19Ta-Tumor-Biopsy COSM5366964 c.1191C>T p.P397P Substitution - coding silent 23:126164734-126164734 - pfg116T COSM4560632 c.850G>A p.G284S Substitution - Missense 23:126165075-126165075 - TCGA-D3-A2JH-06 COSM3557601 c.741G>A p.P247P Substitution - coding silent 23:126165184-126165184 - LUAD-NYU696 COSM376146 c.640G>T p.D214Y Substitution - Missense 23:126165285-126165285 - pfg038T COSM4761044 c.652G>A p.A218T Substitution - Missense 23:126165273-126165273 - T578 COSM2724951 c.1317G>A p.P439P Substitution - coding silent 23:126164608-126164608 - SE1 COSM1165668 c.372C>T p.D124D Substitution - coding silent 23:126165553-126165553 - PDA_062 COSM2725004 c.595G>T p.A199S Substitution - Missense 23:126165330-126165330 - ACINAR29 COSM1733050 c.220G>A p.E74K Substitution - Missense 23:126165705-126165705 - COLO201 COSM2725000 c.601G>A p.A201T Substitution - Missense 23:126165324-126165324 - T1232 COSM4676344 c.187C>T p.R63W Substitution - Missense 23:126165738-126165738 - 587222 COSM1203057 c.1240G>T p.D414Y Substitution - Missense 23:126164685-126164685 - Pat_02_B COSM4676346 c.137C>T p.A46V Substitution - Missense 23:126165788-126165788 - ESO-708 COSM1249726 c.813C>T p.S271S Substitution - coding silent 23:126165112-126165112 - 587306 COSM1203049 c.919C>T p.R307* Substitution - Nonsense 23:126165006-126165006 - TCGA-66-2770-01 COSM755481 c.957C>A p.S319S Substitution - coding silent 23:126164968-126164968 - Gp2D COSM4628965 c.902T>A p.I301N Substitution - Missense 23:126165023-126165023 - T41 COSM5345890 c.141G>A p.T47T Substitution - coding silent 23:126165784-126165784 - 3N02-VS-3T02 COSM4978561 c.143G>T p.R48L Substitution - Missense 23:126165782-126165782 - ESCC_35 COSM5628724 c.170G>A p.G57D Substitution - Missense 23:126165755-126165755 - CSCC-30-T COSM203162 c.500G>A p.G167D Substitution - Missense 23:126165425-126165425 - RK121_C01 COSM3747298 c.1299C>G p.T433T Substitution - coding silent 23:126164626-126164626 - HCC2998 COSM2724954 c.1282C>T p.P428S Substitution - Missense 23:126164643-126164643 - TCGA-AX-A0J1-01 COSM1114652 c.849C>T p.D283D Substitution - coding silent 23:126165076-126165076 - ATL011 COSM5711476 c.1315C>A p.P439T Substitution - Missense 23:126164610-126164610 - SJACT019_D COSM4968525 c.1382T>A p.L461H Substitution - Missense 23:126164543-126164543 - 587228 COSM1203050 c.391A>C p.T131P Substitution - Missense 23:126165534-126165534 - TCGA-43-6647-01 COSM755470 c.373G>C p.V125L Substitution - Missense 23:126165552-126165552 - T3262 COSM4676338 c.642C>T p.D214D Substitution - coding silent 23:126165283-126165283 - 2492720 COSM5723354 c.997G>A p.D333N Substitution - Missense 23:126164928-126164928 - TCGA-C5-A1MH-01 COSM4820864 c.56G>A p.G19E Substitution - Missense 23:126165869-126165869 - TCGA-AA-3821-01 COSM294294 c.304G>A p.A102T Substitution - Missense 23:126165621-126165621 - 13681 COSM5616213 c.878G>T p.S293I Substitution - Missense 23:126165047-126165047 - TCGA-D7-6817-01 COSM1165667 c.372C>T p.D124D Substitution - coding silent 23:126165553-126165553 - CPCG0251-F1 COSM1331275 c.1010G>A p.R337H Substitution - Missense 23:126164915-126164915 - TCGA-B5-A11E-01 COSM1114632 c.1357G>T p.G453C Substitution - Missense 23:126164568-126164568 - TCGA-EI-6882-01 COSM3424441 c.395G>A p.R132H Substitution - Missense 23:126165530-126165530 - ESCC_93 COSM5637322 c.460G>A p.A154T Substitution - Missense 23:126165465-126165465 - LS-1034 COSM25471 c.466G>A p.E156K Substitution - Missense 23:126165459-126165459 - TCGA-60-2711-01 COSM755474 c.603C>G p.A201A Substitution - coding silent 23:126165322-126165322 - T3262 COSM4676337 c.642C>T p.D214D Substitution - coding silent 23:126165283-126165283 - TCGA-HU-A4GT-01 COSM4106475 c.99A>C p.G33G Substitution - coding silent 23:126165826-126165826 - TCGA-66-2786-01 COSM755471 c.380C>T p.S127L Substitution - Missense 23:126165545-126165545 - PT37 COSM5921905 c.565G>A p.D189N Substitution - Missense 23:126165360-126165360 - S00941 COSM5663902 c.1244A>T p.D415V Substitution - Missense 23:126164681-126164681 - 2492722 COSM5723354 c.997G>A p.D333N Substitution - Missense 23:126164928-126164928 - LUAD-LIP77 COSM367948 c.574G>T p.G192C Substitution - Missense 23:126165351-126165351 - TCGA-D3-A3C8-06 COSM3557587 c.1281C>T p.F427F Substitution - coding silent 23:126164644-126164644 - LUAD-S00499 COSM385381 c.1001C>T p.P334L Substitution - Missense 23:126164924-126164924 - TCGA-FW-A5DX-01 COSM3557595 c.881C>A p.T294K Substitution - Missense 23:126165044-126165044 - 442 COSM4434712 c.796C>T p.R266W Substitution - Missense 23:126165129-126165129 - TCGA-BR-4368-01 COSM1331276 c.1010G>A p.R337H Substitution - Missense 23:126164915-126164915 - pfg116T COSM4560631 c.850G>A p.G284S Substitution - Missense 23:126165075-126165075 - PDA_062 COSM2725005 c.595G>T p.A199S Substitution - Missense 23:126165330-126165330 - ESCC_35 COSM5628725 c.170G>A p.G57D Substitution - Missense 23:126165755-126165755 - Patient5 COSM610565 c.920G>A p.R307Q Substitution - Missense 23:126165005-126165005 - TCGA-HU-A4GU-01 COSM4106456 c.638G>A p.R213H Substitution - Missense 23:126165287-126165287 - TCGA-EI-6506-01 COSM1203053 c.409C>T p.R137W Substitution - Missense 23:126165516-126165516 - BD49T COSM5498481 c.306G>A p.A102A Substitution - coding silent 23:126165619-126165619 - T3202 COSM1465447 c.146G>A p.R49H Substitution - Missense 23:126165779-126165779 - 12586 COSM5616210 c.1001C>A p.P334Q Substitution - Missense 23:126164924-126164924 - 2492724 COSM5725229 c.1200G>A p.R400R Substitution - coding silent 23:126164725-126164725 - PT52 COSM5941127 c.1323G>A p.M441I Substitution - Missense 23:126164602-126164602 - B10-Tumor COSM4004993 c.1274G>A p.G425E Substitution - Missense 23:126164651-126164651 - TCGA-F1-A448-01 COSM2725030 c.339C>T p.C113C Substitution - coding silent 23:126165586-126165586 - TCGA-BR-8078-01 COSM2724981 c.1004G>A p.R335H Substitution - Missense 23:126164921-126164921 - S00472 COSM5658047 c.217G>C p.G73R Substitution - Missense 23:126165708-126165708 - 2492725 COSM5725229 c.1200G>A p.R400R Substitution - coding silent 23:126164725-126164725 - TCGA-DA-A1HV-06 COSM3557584 c.1346C>T p.P449L Substitution - Missense 23:126164579-126164579 - TCGA-06-0132-01 COSM1203053 c.409C>T p.R137W Substitution - Missense 23:126165516-126165516 - LUAD-NYU284 COSM373457 c.1005C>A p.R335R Substitution - coding silent 23:126164920-126164920 - CHC1028T COSM4790854 c.564C>T p.G188G Substitution - coding silent 23:126165361-126165361 - TCGA-F1-A448-01 COSM4106447 c.1249T>C p.W417R Substitution - Missense 23:126164676-126164676 - TCGA-EE-A3JD-06 COSM4396685 c.471G>A p.L157L Substitution - coding silent 23:126165454-126165454 - TCGA-AD-6901-01 COSM1465435 c.1319A>G p.E440G Substitution - Missense 23:126164606-126164606 - TCGA-HW-A5KL-01 COSM3973215 c.236C>T p.A79V Substitution - Missense 23:126165689-126165689 - T407 COSM4676334 c.854A>G p.Y285C Substitution - Missense 23:126165071-126165071 - HCC4T COSM1625480 c.6C>A p.A2A Substitution - coding silent 23:126165919-126165919 - C70 COSM4619636 c.238G>A p.V80I Substitution - Missense 23:126165687-126165687 - HN_62741 COSM122507 c.34A>G p.K12E Substitution - Missense 23:126165891-126165891 - TCGA-AG-A002-01 COSM260364 c.252C>T p.P84P Substitution - coding silent 23:126165673-126165673 - I2L-P9-Tumor-Organoid COSM1315185 c.1009C>T p.R337C Substitution - Missense 23:126164916-126164916 - 19M COSM5578373 c.666G>A p.M222I Substitution - Missense 23:126165259-126165259 - TCGA-13-1510-01 COSM70398 c.1252G>T p.V418L Substitution - Missense 23:126164673-126164673 - TCGA-G4-6295-01 COSM3694327 c.485C>T p.T162M Substitution - Missense 23:126165440-126165440 - CHOL12 COSM1465442 c.594C>T p.F198F Substitution - coding silent 23:126165331-126165331 - TCGA-AG-3892-01 COSM256735 c.1290G>A p.A430A Substitution - coding silent 23:126164635-126164635 - T1232 COSM4676343 c.187C>T p.R63W Substitution - Missense 23:126165738-126165738 - 9 COSM5732558 c.791A>C p.K264T Substitution - Missense 23:126165134-126165134 - PT37 COSM5921906 c.565G>A p.D189N Substitution - Missense 23:126165360-126165360 - TCGA-14-0862-01 COSM3405931 c.631G>A p.G211S Substitution - Missense 23:126165294-126165294 - PD6418a COSM385381 c.1001C>T p.P334L Substitution - Missense 23:126164924-126164924 - TCGA-B2-3923-01 COSM1497173 c.595G>A p.A199T Substitution - Missense 23:126165330-126165330 - TCGA-BR-8384-01 COSM4106470 c.138G>A p.A46A Substitution - coding silent 23:126165787-126165787 - T3255 COSM4676345 c.137C>T p.A46V Substitution - Missense 23:126165788-126165788 - ESO-913 COSM1249727 c.1142A>C p.K381T Substitution - Missense 23:126164783-126164783 - HCC4T COSM1625481 c.6C>A p.A2A Substitution - coding silent 23:126165919-126165919 - TCGA-HI-7169-01 COSM1331276 c.1010G>A p.R337H Substitution - Missense 23:126164915-126164915 - 2492722 COSM5723353 c.997G>A p.D333N Substitution - Missense 23:126164928-126164928 - HCT15 COSM4633083 c.523G>A p.A175T Substitution - Missense 23:126165402-126165402 - HX13T COSM1625480 c.6C>A p.A2A Substitution - coding silent 23:126165919-126165919 - ESCC_93 COSM5637323 c.460G>A p.A154T Substitution - Missense 23:126165465-126165465 - NCI-H2126 COSM25616 c.1068G>A p.L356L Substitution - coding silent 23:126164857-126164857 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.181867 Xq25

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C Missense p.F286V c.856T>G X 125299052 ESCA A G Missense p.Y436H c.1306T>C X 125298602 CM A G Synonymous p.G27G c.81T>C X 125299827 CM A T 3-UTRSNV . c.1389+16T>A X 125298503 CM A T Missense p.I133N c.398T>A X 125299510 THCA A T Missense p.L187Q c.560T>A X 125299348 LUAD A T Synonymous p.S346S c.1038T>A X 125298870 BRCA C A Missense p.A15S c.43G>T X 125299865 LUAD C A Missense p.C306F c.917G>T X 125298991 COREAD C A Missense p.E72D c.216G>T X 125299692 LUAD C A Missense p.G211V c.632G>T X 125299276 NSCLC C A Missense p.G447V c.1340G>T X 125298568 LUAD C A Missense p.G460C c.1378G>T X 125298530 LUAD C A Missense p.G73C c.217G>T X 125299691 MB C A Missense p.R109S c.327G>T X 125299581 LUAD C A Missense p.R132L c.395G>T X 125299513 LUAD C A Missense p.R297S c.891G>T X 125299017 LUSC C A Missense p.R354L c.1061G>T X 125298847 LUAD C A Missense p.R50M c.149G>T X 125299759 LUAD C A Missense p.R63L c.188G>T X 125299720 LUAD C A Missense p.S293I c.878G>T X 125299030 NSCLC C A Missense p.V418L c.1252G>T X 125298656 OV C A Nonsense p.E440* c.1318G>T X 125298590 LUAD C A Synonymous p.A430A c.1290G>T X 125298618 LUAD C A Synonymous p.A62A c.186G>T X 125299722 OV CC TT Missense p.G399E c.1196_1197delinsAA X 125298711 CM C G Missense p.G447A c.1340G>C X 125298568 BRCA C G Missense p.G448R c.1342G>C X 125298566 LUSC C G Missense p.V125L c.373G>C X 125299535 LUSC C G Missense p.V418L c.1252G>C X 125298656 BRCA C T 3-UTRSNV . c.1389+5G>A X 125298514 CM C T 3-UTRSNV . c.1389+74G>A X 125298445 HC C T Missense p.D249N c.745G>A X 125299163 CM C T Missense p.E156K c.466G>A X 125299442 GBM C T Missense p.E169K c.505G>A X 125299403 CM C T Missense p.G211S c.631G>A X 125299277 GBM C T Missense p.G215D c.644G>A X 125299264 PRAD C T Missense p.G278E c.833G>A X 125299075 CM C T Missense p.G368D c.1103G>A X 125298805 HNSC C T Missense p.G409S c.1225G>A X 125298683 CM C T Missense p.R190H c.569G>A X 125299339 STAD C T Missense p.R246H c.737G>A X 125299171 BLCA C T Missense p.R246H c.737G>A X 125299171 GBM C T Missense p.R263H c.788G>A X 125299120 ESCA C T Missense p.R263H c.788G>A X 125299120 LGG C T Missense p.R307Q c.920G>A X 125298988 LUAD C T Missense p.R335H c.1004G>A X 125298904 HNSC C T Missense p.R335H c.1004G>A X 125298904 MB C T Missense p.R337H c.1010G>A X 125298898 PRAD C T Missense p.R337H c.1010G>A X 125298898 STAD C T Missense p.R378H c.1133G>A X 125298775 UCEC C T Missense p.R48H c.143G>A X 125299765 GBM C T Missense p.V217M c.649G>A X 125299259 LUAD C T Missense p.V80I c.238G>A X 125299670 COREAD C T Nonsense p.W438* c.1314G>A X 125298594 LUAD C T Nonsense p.W462* c.1386G>A X 125298522 CM C T Synonymous p.L157L c.471G>A X 125299437 CM C T Synonymous p.P247P c.741G>A X 125299167 CM C T Synonymous p.P334P c.1002G>A X 125298906 PAAD C T Synonymous p.Q126Q c.378G>A X 125299530 CM C T Synonymous p.R44R c.132G>A X 125299776 HNSC C T Synonymous p.R58R c.174G>A X 125299734 CM C T Synonymous p.T88T c.264G>A X 125299644 CM G A Missense p.H147Y c.439C>T X 125299469 CM G A Missense p.P134S c.400C>T X 125299508 CM G A Missense p.P334L c.1001C>T X 125298907 STAD G A Missense p.P334L c.1001C>T X 125298907 THCA G A Missense p.P343L c.1028C>T X 125298880 CM G A Missense p.P449L c.1346C>T X 125298562 CM G A Missense p.R137W c.409C>T X 125299499 GBM G A Missense p.R335C c.1003C>T X 125298905 GBM G A Missense p.R335C c.1003C>T X 125298905 UCEC G A Missense p.R337C c.1009C>T X 125298899 BLCA G A Missense p.R378C c.1132C>T X 125298776 LUAD G A Missense p.S127L c.380C>T X 125299528 LUSC G A Missense p.S25L c.74C>T X 125299834 CM G A Missense p.S330F c.989C>T X 125298919 CM G A Missense p.T181I c.542C>T X 125299366 CM G A Missense p.T206I c.617C>T X 125299291 CM G A Nonsense p.Q110* c.328C>T X 125299580 UCEC G A Synonymous p.D124D c.372C>T X 125299536 HNSC G A Synonymous p.D124D c.372C>T X 125299536 STAD G A Synonymous p.D223D c.669C>T X 125299239 CM G A Synonymous p.D283D c.849C>T X 125299059 COREAD G A Synonymous p.F382F c.1146C>T X 125298762 CM G A Synonymous p.F427F c.1281C>T X 125298627 CM G A Synonymous p.I133I c.399C>T X 125299509 CM G A Synonymous p.I155I c.465C>T X 125299443 CM G A Synonymous p.L219L c.655C>T X 125299253 CM G A Synonymous p.P159P c.477C>T X 125299431 THCA G A Synonymous p.R49R c.147C>T X 125299761 LUAD G A Synonymous p.S330S c.990C>T X 125298918 CM G A Synonymous p.T166T c.498C>T X 125299410 BRCA G A Synonymous p.T206T c.618C>T X 125299290 CM G C Missense p.A430G c.1289C>G X 125298619 LUAD G C Missense p.P180R c.539C>G X 125299369 UCEC G C Missense p.S325C c.974C>G X 125298934 LUAD G C Synonymous p.A201A c.603C>G X 125299305 LUSC G C Synonymous p.T206T c.618C>G X 125299290 LUAD G - Frameshift p.H434Tfs*8 c.1300delC X 125298608 ESCA G T Missense p.A430E c.1289C>A X 125298619 LUAD G T Missense p.H244Q c.732C>A X 125299176 SCLC G T Missense p.H287Q c.861C>A X 125299047 LUAD G T Missense p.P334Q c.1001C>A X 125298907 NSCLC G T Missense p.P397H c.1190C>A X 125298718 ESCA G T Missense p.R335S c.1003C>A X 125298905 LUAD G T Missense p.S261R c.783C>A X 125299125 ESCA G T Missense p.S296Y c.887C>A X 125299021 LUAD G T Missense p.S319Y c.956C>A X 125298952 LUSC G T Missense p.T216N c.647C>A X 125299261 BLCA G T Missense p.T313N c.938C>A X 125298970 UCEC G T Missense p.T351K c.1052C>A X 125298856 LUSC G T Missense p.T6K c.17C>A X 125299891 GBM G T Synonymous p.A291A c.873C>A X 125299035 STAD G T Synonymous p.R307R c.919C>A X 125298989 LUAD G T Synonymous p.S296S c.888C>A X 125299020 LUAD G T Synonymous p.S319S c.957C>A X 125298951 LUSC T A Missense p.R82W c.244A>T X 125299664 BLCA T A Missense p.Y420F c.1259A>T X 125298649 BRCA TC GT MultiAAMissense p.W196_I197delins* c.588_589delinsAC X 125299319 CM T C Missense p.K12E c.34A>G X 125299874 HNSC T C Missense p.K264R c.791A>G X 125299117 STAD T C Missense p.K381R c.1142A>G X 125298766 ESCA TG AT Missense p.Q360M c.1078_1079delinsAT X 125298829 HNSC T G Missense p.E426A c.1277A>C X 125298631 UCEC T G Missense p.K381T c.1142A>C X 125298766 ESCA T G Missense p.K41T c.122A>C X 125299786 STAD