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 27998833 27998833 + Missense_Mutation SNP G G T TCGA-OR-A5KB-01A-11D-A30A-10 TCGA-OR-A5KB-11A-11D-A30A-10 g.chrX:27998833G>T c.619C>A c.(619-621)Cgt>Agt p.R207S BLCA 23 27997802 27997802 + Missense_Mutation SNP G G T TCGA-DK-A6AW-01A-11D-A30E-08 TCGA-DK-A6AW-10A-01D-A30H-08 g.chrX:27997802G>T c.1650C>A c.(1648-1650)ttC>ttA p.F550L BLCA 23 27997889 27997889 + Missense_Mutation SNP T T A TCGA-2F-A9KP-01A-11D-A38G-08 TCGA-2F-A9KP-10A-01D-A38J-08 g.chrX:27997889T>A c.1563A>T c.(1561-1563)ttA>ttT p.L521F BLCA 23 27998068 27998068 + Missense_Mutation SNP C C T TCGA-E7-A7DU-01A-11D-A32B-08 TCGA-E7-A7DU-10A-01D-A329-08 g.chrX:27998068C>T c.1384G>A c.(1384-1386)Gtc>Atc p.V462I BLCA 23 27998165 27998165 + Silent SNP C C T TCGA-XF-A9ST-01A-11D-A42E-08 TCGA-XF-A9ST-10A-01D-A42H-08 g.chrX:27998165C>T c.1287G>A c.(1285-1287)aaG>aaA p.K429K BLCA 23 27998204 27998204 + Silent SNP G G A TCGA-LT-A5Z6-01A-11D-A289-08 TCGA-LT-A5Z6-10A-01D-A289-08 g.chrX:27998204G>A c.1248C>T c.(1246-1248)ctC>ctT p.L416L BLCA 23 27998290 27998290 + Missense_Mutation SNP C C T TCGA-ZF-A9RD-01A-11D-A42E-08 TCGA-ZF-A9RD-10A-01D-A42H-08 g.chrX:27998290C>T c.1162G>A c.(1162-1164)Gat>Aat p.D388N BLCA 23 27998745 27998745 + Missense_Mutation SNP C C A TCGA-FD-A3B3-01A-12D-A202-08 TCGA-FD-A3B3-10A-01D-A202-08 g.chrX:27998745C>A c.707G>T c.(706-708)aGt>aTt p.S236I BLCA 23 27999090 27999090 + Missense_Mutation SNP G G T TCGA-E5-A4U1-01A-11D-A31L-08 TCGA-E5-A4U1-10B-01D-A31J-08 g.chrX:27999090G>T c.362C>A c.(361-363)cCa>cAa p.P121Q BLCA 23 27999131 27999131 + Missense_Mutation SNP C C T TCGA-BL-A0C8-01A-11D-A10S-08 TCGA-BL-A0C8-10A-01D-A10S-08 g.chrX:27999131C>T c.321G>A c.(319-321)atG>atA p.M107I BLCA 23 27999223 27999223 + Missense_Mutation SNP C C T TCGA-GU-AATO-01A-11D-A391-08 TCGA-GU-AATO-10A-01D-A394-08 g.chrX:27999223C>T c.229G>A c.(229-231)Gaa>Aaa p.E77K BLCA 23 27999385 27999385 + Missense_Mutation SNP G G T TCGA-UY-A9PB-01A-11D-A38G-08 TCGA-UY-A9PB-10A-01D-A38J-08 g.chrX:27999385G>T c.67C>A c.(67-69)Cca>Aca p.P23T BRCA 23 27997690 27997690 + Missense_Mutation SNP C C T TCGA-A8-A09X-01A-11W-A019-09 TCGA-A8-A09X-10A-01W-A021-09 g.chrX:27997690C>T c.1762G>A c.(1762-1764)Gag>Aag p.E588K BRCA 23 27998516 27998516 + Missense_Mutation SNP G G C TCGA-A1-A0SQ-01A-21D-A142-09 TCGA-A1-A0SQ-10B-01W-A187-09 g.chrX:27998516G>C c.936C>G c.(934-936)ttC>ttG p.F312L BRCA 23 27998944 27998944 + Missense_Mutation SNP C C A TCGA-A2-A0EY-01A-11W-A050-09 TCGA-A2-A0EY-10A-01W-A055-09 g.chrX:27998944C>A c.508G>T c.(508-510)Gcc>Tcc p.A170S BRCA 23 27999024 27999024 + Missense_Mutation SNP A A T TCGA-AR-A1AJ-01A-21D-A12Q-09 TCGA-AR-A1AJ-10A-01D-A12Q-09 g.chrX:27999024A>T c.428T>A c.(427-429)aTt>aAt p.I143N BRCA 23 27999081 27999081 + Missense_Mutation SNP C C A TCGA-E9-A1N4-01A-11D-A14K-09 TCGA-E9-A1N4-10A-01D-A14K-09 g.chrX:27999081C>A c.371G>T c.(370-372)gGt>gTt p.G124V BRCA 23 27999139 27999139 + Nonsense_Mutation SNP C C A TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chrX:27999139C>A c.313G>T c.(313-315)Gaa>Taa p.E105* BRCA 23 27999269 27999269 + Missense_Mutation SNP G G T TCGA-B6-A2IU-01A-32D-A19T-09 TCGA-B6-A2IU-10A-01D-A18P-09 g.chrX:27999269G>T c.183C>A c.(181-183)aaC>aaA p.N61K CESC 23 27997787 27997787 + Silent SNP C C G TCGA-JW-A5VL-01A-11D-A28B-09 TCGA-JW-A5VL-10A-01D-A28E-09 g.chrX:27997787C>G c.1665G>C c.(1663-1665)ctG>ctC p.L555L CESC 23 27998107 27998107 + Missense_Mutation SNP G G A TCGA-C5-A3HE-01A-21D-A22X-09 TCGA-C5-A3HE-10A-01D-A22X-09 g.chrX:27998107G>A c.1345C>T c.(1345-1347)Cgg>Tgg p.R449W CESC 23 27998204 27998204 + Silent SNP G G A TCGA-UC-A7PF-01A-11D-A351-09 TCGA-UC-A7PF-11A-31D-A351-09 g.chrX:27998204G>A c.1248C>T c.(1246-1248)ctC>ctT p.L416L COAD 23 27997672 27997672 + Nonsense_Mutation SNP G G A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chrX:27997672G>A c.1780C>T c.(1780-1782)Cga>Tga p.R594* COAD 23 27997802 27997802 + Missense_Mutation SNP G G T TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chrX:27997802G>T c.1650C>A c.(1648-1650)ttC>ttA p.F550L COAD 23 27997865 27997865 + Silent SNP C C T TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chrX:27997865C>T c.1587G>A c.(1585-1587)aaG>aaA p.K529K COAD 23 27997962 27997962 + Missense_Mutation SNP G G A TCGA-AA-3558-01A-01W-0831-10 TCGA-AA-3558-10A-01W-0831-10 g.chrX:27997962G>A c.1490C>T c.(1489-1491)gCg>gTg p.A497V COAD 23 27998054 27998054 + Silent SNP C C T TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chrX:27998054C>T c.1398G>A c.(1396-1398)gaG>gaA p.E466E COAD 23 27998107 27998107 + Frame_Shift_Del DEL G G - TCGA-CK-5916-01A-11D-1650-10 TCGA-CK-5916-10A-01D-1650-10 g.chrX:27998107delG c.1345delC c.(1345-1347)cggfs p.R449fs COAD 23 27998125 27998125 + Missense_Mutation SNP C C G TCGA-AA-A00K-01A-02W-A005-10 TCGA-AA-A00K-10A-01W-A005-10 g.chrX:27998125C>G c.1327G>C c.(1327-1329)Gtt>Ctt p.V443L COAD 23 27998150 27998150 + Silent SNP G G A TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chrX:27998150G>A c.1302C>T c.(1300-1302)caC>caT p.H434H COAD 23 27998166 27998166 + Missense_Mutation SNP T T C TCGA-AA-3660-01A-01D-1719-10 TCGA-AA-3660-11A-01D-1719-10 g.chrX:27998166T>C c.1286A>G c.(1285-1287)aAg>aGg p.K429R COAD 23 27998166 27998166 + Missense_Mutation SNP T T C TCGA-CM-5860-01A-01D-1650-10 TCGA-CM-5860-10A-01D-1650-10 g.chrX:27998166T>C c.1286A>G c.(1285-1287)aAg>aGg p.K429R COAD 23 27998167 27998167 + Missense_Mutation SNP T T C TCGA-A6-6652-01A-11D-1771-10 TCGA-A6-6652-10A-01D-1771-10 g.chrX:27998167T>C c.1285A>G c.(1285-1287)Aag>Gag p.K429E COAD 23 27998264 27998264 + Silent SNP A A G TCGA-A6-6654-01A-21D-1835-10 TCGA-A6-6654-10A-01D-1835-10 g.chrX:27998264A>G c.1188T>C c.(1186-1188)gtT>gtC p.V396V COAD 23 27998264 27998264 + Silent SNP A A G TCGA-DM-A1D9-01A-11D-A152-10 TCGA-DM-A1D9-10A-01D-A152-10 g.chrX:27998264A>G c.1188T>C c.(1186-1188)gtT>gtC p.V396V COAD 23 27998265 27998265 + Missense_Mutation SNP A A G TCGA-CM-5344-01A-21D-1719-10 TCGA-CM-5344-10A-01D-1719-10 g.chrX:27998265A>G c.1187T>C c.(1186-1188)gTt>gCt p.V396A COAD 23 27998265 27998265 + Missense_Mutation SNP A A G TCGA-F4-6806-01A-11D-1835-10 TCGA-F4-6806-10A-01D-1835-10 g.chrX:27998265A>G c.1187T>C c.(1186-1188)gTt>gCt p.V396A COAD 23 27998387 27998387 + Silent SNP A A G TCGA-AD-5900-01A-11D-1650-10 TCGA-AD-5900-10A-01D-1650-10 g.chrX:27998387A>G c.1065T>C c.(1063-1065)caT>caC p.H355H COAD 23 27998446 27998446 + Missense_Mutation SNP C C T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chrX:27998446C>T c.1006G>A c.(1006-1008)Gga>Aga p.G336R COAD 23 27998574 27998574 + Missense_Mutation SNP G G A TCGA-AA-3949-01A-01W-0995-10 TCGA-AA-3949-10A-01W-0995-10 g.chrX:27998574G>A c.878C>T c.(877-879)gCt>gTt p.A293V COAD 23 27998645 27998645 + Missense_Mutation SNP T T A TCGA-AA-3854-01A-01W-0900-09 TCGA-AA-3854-10A-01W-0900-09 g.chrX:27998645T>A c.807A>T c.(805-807)gaA>gaT p.E269D COAD 23 27998668 27998668 + Missense_Mutation SNP C C G TCGA-DM-A0X9-01A-11D-A152-10 TCGA-DM-A0X9-10A-01D-A152-10 g.chrX:27998668C>G c.784G>C c.(784-786)Gat>Cat p.D262H COAD 23 27998681 27998681 + Frame_Shift_Del DEL G G - TCGA-CM-5861-01A-01D-1650-10 TCGA-CM-5861-10A-01D-1650-10 g.chrX:27998681delG c.771delC c.(769-771)gccfs p.A257fs COAD 23 27998990 27998990 + Silent SNP G G T TCGA-AA-3672-01A-01W-0900-09 TCGA-AA-3672-10A-01W-0900-09 g.chrX:27998990G>T c.462C>A c.(460-462)cgC>cgA p.R154R COAD 23 27999100 27999100 + Missense_Mutation SNP G G A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chrX:27999100G>A c.352C>T c.(352-354)Cgg>Tgg p.R118W COAD 23 27999214 27999214 + Missense_Mutation SNP C C T TCGA-AA-3555-01A-01W-0831-10 TCGA-AA-3555-10A-01W-0831-10 g.chrX:27999214C>T c.238G>A c.(238-240)Gaa>Aaa p.E80K COADREAD 23 27997672 27997672 + Nonsense_Mutation SNP G G A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chrX:27997672G>A c.1780C>T c.(1780-1782)Cga>Tga p.R594* COADREAD 23 27997802 27997802 + Missense_Mutation SNP G G T TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chrX:27997802G>T c.1650C>A c.(1648-1650)ttC>ttA p.F550L COADREAD 23 27997865 27997865 + Silent SNP C C T TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chrX:27997865C>T c.1587G>A c.(1585-1587)aaG>aaA p.K529K COADREAD 23 27997962 27997962 + Missense_Mutation SNP G G A TCGA-AA-3558-01A-01W-0831-10 TCGA-AA-3558-10A-01W-0831-10 g.chrX:27997962G>A c.1490C>T c.(1489-1491)gCg>gTg p.A497V COADREAD 23 27998054 27998054 + Silent SNP C C T TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chrX:27998054C>T c.1398G>A c.(1396-1398)gaG>gaA p.E466E COADREAD 23 27998107 27998107 + Frame_Shift_Del DEL G G - TCGA-CK-5916-01A-11D-1650-10 TCGA-CK-5916-10A-01D-1650-10 g.chrX:27998107delG c.1345delC c.(1345-1347)cggfs p.R449fs COADREAD 23 27998125 27998125 + Missense_Mutation SNP C C G TCGA-AA-A00K-01A-02W-A005-10 TCGA-AA-A00K-10A-01W-A005-10 g.chrX:27998125C>G c.1327G>C c.(1327-1329)Gtt>Ctt p.V443L COADREAD 23 27998150 27998150 + Silent SNP G G A TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chrX:27998150G>A c.1302C>T c.(1300-1302)caC>caT p.H434H COADREAD 23 27998166 27998166 + Missense_Mutation SNP T T C TCGA-AA-3660-01A-01D-1719-10 TCGA-AA-3660-11A-01D-1719-10 g.chrX:27998166T>C c.1286A>G c.(1285-1287)aAg>aGg p.K429R COADREAD 23 27998166 27998166 + Missense_Mutation SNP T T C TCGA-CM-5860-01A-01D-1650-10 TCGA-CM-5860-10A-01D-1650-10 g.chrX:27998166T>C c.1286A>G c.(1285-1287)aAg>aGg p.K429R COADREAD 23 27998167 27998167 + Missense_Mutation SNP T T C TCGA-A6-6652-01A-11D-1771-10 TCGA-A6-6652-10A-01D-1771-10 g.chrX:27998167T>C c.1285A>G c.(1285-1287)Aag>Gag p.K429E COADREAD 23 27998264 27998264 + Silent SNP A A G TCGA-A6-6654-01A-21D-1835-10 TCGA-A6-6654-10A-01D-1835-10 g.chrX:27998264A>G c.1188T>C c.(1186-1188)gtT>gtC p.V396V COADREAD 23 27998264 27998264 + Silent SNP A A G TCGA-DM-A1D9-01A-11D-A152-10 TCGA-DM-A1D9-10A-01D-A152-10 g.chrX:27998264A>G c.1188T>C c.(1186-1188)gtT>gtC p.V396V COADREAD 23 27998265 27998265 + Missense_Mutation SNP A A G TCGA-CM-5344-01A-21D-1719-10 TCGA-CM-5344-10A-01D-1719-10 g.chrX:27998265A>G c.1187T>C c.(1186-1188)gTt>gCt p.V396A COADREAD 23 27998265 27998265 + Missense_Mutation SNP A A G TCGA-EI-6507-01A-11D-1733-10 TCGA-EI-6507-10A-01D-1733-10 g.chrX:27998265A>G c.1187T>C c.(1186-1188)gTt>gCt p.V396A COADREAD 23 27998265 27998265 + Missense_Mutation SNP A A G TCGA-F4-6806-01A-11D-1835-10 TCGA-F4-6806-10A-01D-1835-10 g.chrX:27998265A>G c.1187T>C c.(1186-1188)gTt>gCt p.V396A COADREAD 23 27998387 27998387 + Silent SNP A A G TCGA-AD-5900-01A-11D-1650-10 TCGA-AD-5900-10A-01D-1650-10 g.chrX:27998387A>G c.1065T>C c.(1063-1065)caT>caC p.H355H COADREAD 23 27998446 27998446 + Missense_Mutation SNP C C T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chrX:27998446C>T c.1006G>A c.(1006-1008)Gga>Aga p.G336R COADREAD 23 27998574 27998574 + Missense_Mutation SNP G G A TCGA-AA-3949-01A-01W-0995-10 TCGA-AA-3949-10A-01W-0995-10 g.chrX:27998574G>A c.878C>T c.(877-879)gCt>gTt p.A293V COADREAD 23 27998645 27998645 + Missense_Mutation SNP T T A TCGA-AA-3854-01A-01W-0900-09 TCGA-AA-3854-10A-01W-0900-09 g.chrX:27998645T>A c.807A>T c.(805-807)gaA>gaT p.E269D COADREAD 23 27998668 27998668 + Missense_Mutation SNP C C G TCGA-DM-A0X9-01A-11D-A152-10 TCGA-DM-A0X9-10A-01D-A152-10 g.chrX:27998668C>G c.784G>C c.(784-786)Gat>Cat p.D262H COADREAD 23 27998681 27998681 + Frame_Shift_Del DEL G G - TCGA-CM-5861-01A-01D-1650-10 TCGA-CM-5861-10A-01D-1650-10 g.chrX:27998681delG c.771delC c.(769-771)gccfs p.A257fs COADREAD 23 27998990 27998990 + Silent SNP G G T TCGA-AA-3672-01A-01W-0900-09 TCGA-AA-3672-10A-01W-0900-09 g.chrX:27998990G>T c.462C>A c.(460-462)cgC>cgA p.R154R COADREAD 23 27999100 27999100 + Missense_Mutation SNP G G A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chrX:27999100G>A c.352C>T c.(352-354)Cgg>Tgg p.R118W COADREAD 23 27999204 27999204 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chrX:27999204C>T c.248G>A c.(247-249)aGc>aAc p.S83N COADREAD 23 27999214 27999214 + Missense_Mutation SNP C C T TCGA-AA-3555-01A-01W-0831-10 TCGA-AA-3555-10A-01W-0831-10 g.chrX:27999214C>T c.238G>A c.(238-240)Gaa>Aaa p.E80K ESCA 23 27998247 27998247 + Missense_Mutation SNP C C T TCGA-LN-A8I0-01A-11D-A36J-09 TCGA-LN-A8I0-10A-01D-A36M-09 g.chrX:27998247C>T c.1205G>A c.(1204-1206)gGc>gAc p.G402D ESCA 23 27998866 27998866 + Missense_Mutation SNP C C A TCGA-LN-A9FP-01A-31D-A387-09 TCGA-LN-A9FP-10A-01D-A38A-09 g.chrX:27998866C>A c.586G>T c.(586-588)Gcc>Tcc p.A196S GBM 23 27998447 27998447 + Silent SNP G G C TCGA-06-6391-01A-11D-1696-08 TCGA-06-6391-10A-01D-1696-08 g.chrX:27998447G>C c.1005C>G c.(1003-1005)gtC>gtG p.V335V GBM 23 27998785 27998785 + Missense_Mutation SNP A A G TCGA-26-5132-01A-01D-1486-08 TCGA-26-5132-10A-01D-1486-08 g.chrX:27998785A>G c.667T>C c.(667-669)Tgg>Cgg p.W223R GBM 23 27999269 27999269 + Silent SNP G G A TCGA-74-6584-01A-11D-1845-08 TCGA-74-6584-10A-01D-1845-08 g.chrX:27999269G>A c.183C>T c.(181-183)aaC>aaT p.N61N GBM 23 27999308 27999308 + Silent SNP G G A TCGA-06-6693-01A-11D-1845-08 TCGA-06-6693-10A-01D-1845-08 g.chrX:27999308G>A c.144C>T c.(142-144)acC>acT p.T48T GBM 23 27999353 27999353 + Silent SNP C C T TCGA-19-5954-01A-11D-1696-08 TCGA-19-5954-11A-01D-1696-08 g.chrX:27999353C>T c.99G>A c.(97-99)acG>acA p.T33T GBMLGG 23 27997794 27997794 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chrX:27997794C>T c.1658G>A c.(1657-1659)cGt>cAt p.R553H GBMLGG 23 27998066 27998066 + Silent SNP G G C TCGA-DU-A7T6-01A-11D-A33T-08 TCGA-DU-A7T6-10A-01D-A33W-08 g.chrX:27998066G>C c.1386C>G c.(1384-1386)gtC>gtG p.V462V GBMLGG 23 27998106 27998106 + Missense_Mutation SNP C C A TCGA-DU-A6S8-01A-12D-A32B-08 TCGA-DU-A6S8-10A-01D-A329-08 g.chrX:27998106C>A c.1346G>T c.(1345-1347)cGg>cTg p.R449L GBMLGG 23 27998163 27998163 + Missense_Mutation SNP C C G TCGA-E1-A7YQ-01A-11D-A34J-08 TCGA-E1-A7YQ-10A-01D-A34M-08 g.chrX:27998163C>G c.1289G>C c.(1288-1290)aGa>aCa p.R430T GBMLGG 23 27998291 27998291 + Silent SNP A A G TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chrX:27998291A>G c.1161T>C c.(1159-1161)tgT>tgC p.C387C GBMLGG 23 27998447 27998447 + Silent SNP G G C TCGA-06-6391-01A-11D-1696-08 TCGA-06-6391-10A-01D-1696-08 g.chrX:27998447G>C c.1005C>G c.(1003-1005)gtC>gtG p.V335V GBMLGG 23 27998474 27998474 + Silent SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chrX:27998474C>T c.978G>A c.(976-978)gtG>gtA p.V326V GBMLGG 23 27998600 27998600 + Missense_Mutation SNP C C A TCGA-DU-6400-01A-12D-1705-08 TCGA-DU-6400-10A-01D-1705-08 g.chrX:27998600C>A c.852G>T c.(850-852)aaG>aaT p.K284N GBMLGG 23 27998604 27998604 + Missense_Mutation SNP G G A TCGA-E1-A7YH-01A-11D-A34A-08 TCGA-E1-A7YH-10A-01D-A34A-08 g.chrX:27998604G>A c.848C>T c.(847-849)gCc>gTc p.A283V GBMLGG 23 27998610 27998610 + Missense_Mutation SNP C C T TCGA-S9-A7QY-01A-11D-A34A-08 TCGA-S9-A7QY-10A-01D-A34A-08 g.chrX:27998610C>T c.842G>A c.(841-843)cGt>cAt p.R281H GBMLGG 23 27998785 27998785 + Missense_Mutation SNP A A G TCGA-26-5132-01A-01D-1486-08 TCGA-26-5132-10A-01D-1486-08 g.chrX:27998785A>G c.667T>C c.(667-669)Tgg>Cgg p.W223R GBMLGG 23 27999088 27999088 + Nonsense_Mutation SNP G G A TCGA-CS-6667-01A-12D-2024-08 TCGA-CS-6667-10A-01D-2024-08 g.chrX:27999088G>A c.364C>T c.(364-366)Cga>Tga p.R122* GBMLGG 23 27999269 27999269 + Silent SNP G G A TCGA-74-6584-01A-11D-1845-08 TCGA-74-6584-10A-01D-1845-08 g.chrX:27999269G>A c.183C>T c.(181-183)aaC>aaT p.N61N GBMLGG 23 27999308 27999308 + Silent SNP G G A TCGA-06-6693-01A-11D-1845-08 TCGA-06-6693-10A-01D-1845-08 g.chrX:27999308G>A c.144C>T c.(142-144)acC>acT p.T48T GBMLGG 23 27999353 27999353 + Silent SNP C C T TCGA-19-5954-01A-11D-1696-08 TCGA-19-5954-11A-01D-1696-08 g.chrX:27999353C>T c.99G>A c.(97-99)acG>acA p.T33T GBMLGG 23 27999353 27999353 + Silent SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chrX:27999353C>T c.99G>A c.(97-99)acG>acA p.T33T HNSC 23 27997958 27997958 + Silent SNP G G T TCGA-UF-A71A-01A-22D-A34J-08 TCGA-UF-A71A-10A-01D-A34M-08 g.chrX:27997958G>T c.1494C>A c.(1492-1494)acC>acA p.T498T HNSC 23 27998027 27998027 + Silent SNP G G A TCGA-CR-7398-01A-11D-2012-08 TCGA-CR-7398-10A-01D-2013-08 g.chrX:27998027G>A c.1425C>T c.(1423-1425)ttC>ttT p.F475F HNSC 23 27998101 27998101 + Missense_Mutation SNP C C T TCGA-CN-A498-01A-11D-A24D-08 TCGA-CN-A498-10A-01D-A24F-08 g.chrX:27998101C>T c.1351G>A c.(1351-1353)Gag>Aag p.E451K HNSC 23 27998267 27998267 + Missense_Mutation SNP G G C TCGA-CV-7422-01A-21D-2078-08 TCGA-CV-7422-10A-01D-2078-08 g.chrX:27998267G>C c.1185C>G c.(1183-1185)tgC>tgG p.C395W HNSC 23 27998283 27998283 + Missense_Mutation SNP G G T TCGA-CV-A461-01A-41D-A25Y-08 TCGA-CV-A461-10A-01D-A25Y-08 g.chrX:27998283G>T c.1169C>A c.(1168-1170)cCa>cAa p.P390Q HNSC 23 27998581 27998581 + Missense_Mutation SNP C C T TCGA-BA-A6DA-01A-31D-A31L-08 TCGA-BA-A6DA-10A-01D-A31J-08 g.chrX:27998581C>T c.871G>A c.(871-873)Gag>Aag p.E291K HNSC 23 27998655 27998655 + Missense_Mutation SNP C C T TCGA-CN-5356-01A-01D-1434-08 TCGA-CN-5356-10A-01D-1434-08 g.chrX:27998655C>T c.797G>A c.(796-798)cGg>cAg p.R266Q HNSC 23 27999220 27999220 + Missense_Mutation SNP C C G TCGA-CN-4723-01A-01D-1434-08 TCGA-CN-4723-10A-01D-1434-08 g.chrX:27999220C>G c.232G>C c.(232-234)Gac>Cac p.D78H HNSC 23 27999311 27999311 + Silent SNP C C G TCGA-CR-7386-01A-11D-2012-08 TCGA-CR-7386-10A-01D-2013-08 g.chrX:27999311C>G c.141G>C c.(139-141)tcG>tcC p.S47S KIPAN 23 27997690 27997690 + Missense_Mutation SNP C C T TCGA-CJ-6028-01A-11D-1669-08 TCGA-CJ-6028-11A-01D-1669-08 g.chrX:27997690C>T c.1762G>A c.(1762-1764)Gag>Aag p.E588K KIPAN 23 27998267 27998267 + Silent SNP G G A TCGA-BP-4964-01A-01D-1462-08 TCGA-BP-4964-11A-01D-1462-08 g.chrX:27998267G>A c.1185C>T c.(1183-1185)tgC>tgT p.C395C KIRC 23 27997690 27997690 + Missense_Mutation SNP C C T TCGA-CJ-6028-01A-11D-1669-08 TCGA-CJ-6028-11A-01D-1669-08 g.chrX:27997690C>T c.1762G>A c.(1762-1764)Gag>Aag p.E588K KIRC 23 27998267 27998267 + Silent SNP G G A TCGA-BP-4964-01A-01D-1462-08 TCGA-BP-4964-11A-01D-1462-08 g.chrX:27998267G>A c.1185C>T c.(1183-1185)tgC>tgT p.C395C LGG 23 27997794 27997794 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chrX:27997794C>T c.1658G>A c.(1657-1659)cGt>cAt p.R553H LGG 23 27998066 27998066 + Silent SNP G G C TCGA-DU-A7T6-01A-11D-A33T-08 TCGA-DU-A7T6-10A-01D-A33W-08 g.chrX:27998066G>C c.1386C>G c.(1384-1386)gtC>gtG p.V462V LGG 23 27998106 27998106 + Missense_Mutation SNP C C A TCGA-DU-A6S8-01A-12D-A32B-08 TCGA-DU-A6S8-10A-01D-A329-08 g.chrX:27998106C>A c.1346G>T c.(1345-1347)cGg>cTg p.R449L LGG 23 27998163 27998163 + Missense_Mutation SNP C C G TCGA-E1-A7YQ-01A-11D-A34J-08 TCGA-E1-A7YQ-10A-01D-A34M-08 g.chrX:27998163C>G c.1289G>C c.(1288-1290)aGa>aCa p.R430T LGG 23 27998291 27998291 + Silent SNP A A G TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chrX:27998291A>G c.1161T>C c.(1159-1161)tgT>tgC p.C387C LGG 23 27998474 27998474 + Silent SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chrX:27998474C>T c.978G>A c.(976-978)gtG>gtA p.V326V LGG 23 27998600 27998600 + Missense_Mutation SNP C C A TCGA-DU-6400-01A-12D-1705-08 TCGA-DU-6400-10A-01D-1705-08 g.chrX:27998600C>A c.852G>T c.(850-852)aaG>aaT p.K284N LGG 23 27998604 27998604 + Missense_Mutation SNP G G A TCGA-E1-A7YH-01A-11D-A34A-08 TCGA-E1-A7YH-10A-01D-A34A-08 g.chrX:27998604G>A c.848C>T c.(847-849)gCc>gTc p.A283V LGG 23 27998610 27998610 + Missense_Mutation SNP C C T TCGA-S9-A7QY-01A-11D-A34A-08 TCGA-S9-A7QY-10A-01D-A34A-08 g.chrX:27998610C>T c.842G>A c.(841-843)cGt>cAt p.R281H LGG 23 27999088 27999088 + Nonsense_Mutation SNP G G A TCGA-CS-6667-01A-12D-2024-08 TCGA-CS-6667-10A-01D-2024-08 g.chrX:27999088G>A c.364C>T c.(364-366)Cga>Tga p.R122* LGG 23 27999353 27999353 + Silent SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chrX:27999353C>T c.99G>A c.(97-99)acG>acA p.T33T LIHC 23 27997984 27997984 + Frame_Shift_Del DEL G G - TCGA-DD-A1EG-01A-11D-A20W-10 TCGA-DD-A1EG-10A-01D-A20W-10 g.chrX:27997984delG c.1468delC c.(1468-1470)cacfs p.H490fs LIHC 23 27998516 27998516 + Silent SNP G G A TCGA-DD-A1EB-01A-11D-A12Z-10 TCGA-DD-A1EB-10A-01D-A12Z-10 g.chrX:27998516G>A c.936C>T c.(934-936)ttC>ttT p.F312F LIHC 23 27999289 27999289 + Missense_Mutation SNP T T A TCGA-G3-A7M5-01A-11D-A33Q-10 TCGA-G3-A7M5-10A-01D-A33Q-10 g.chrX:27999289T>A c.163A>T c.(163-165)Agg>Tgg p.R55W LUAD 23 27997756 27997756 + Missense_Mutation SNP C C T TCGA-50-6590-01A-12D-1855-08 TCGA-50-6590-11A-01D-1855-08 g.chrX:27997756C>T c.1696G>A c.(1696-1698)Gat>Aat p.D566N LUAD 23 27997759 27997759 + Nonsense_Mutation SNP T T A TCGA-05-4427-01A-21D-1855-08 TCGA-05-4427-10A-01D-1855-08 g.chrX:27997759T>A c.1693A>T c.(1693-1695)Aga>Tga p.R565* LUAD 23 27997831 27997831 + Missense_Mutation SNP C C A TCGA-05-4424-01A-22D-1855-08 TCGA-05-4424-10A-01D-1855-08 g.chrX:27997831C>A c.1621G>T c.(1621-1623)Gac>Tac p.D541Y LUAD 23 27997945 27997945 + Missense_Mutation SNP G G T TCGA-69-7978-01A-11D-2184-08 TCGA-69-7978-10A-01D-2184-08 g.chrX:27997945G>T c.1507C>A c.(1507-1509)Cag>Aag p.Q503K LUAD 23 27997961 27997962 + Frame_Shift_Del DEL CG CG - TCGA-67-3771-01A-01D-1040-01 TCGA-67-3771-10A-01D-1040-01 g.chrX:27997961_27997962delCG c.1490_1491delCG c.(1489-1491)gcgfs p.A497fs LUAD 23 27998021 27998021 + Missense_Mutation SNP C C A TCGA-17-Z022-01A-01W-0746-08 TCGA-17-Z022-11A-01W-0746-08 g.chrX:27998021C>A c.1431G>T c.(1429-1431)gaG>gaT p.E477D LUAD 23 27998033 27998033 + Silent SNP G G T TCGA-17-Z045-01A-01W-0746-08 TCGA-17-Z045-11A-01W-0747-08 g.chrX:27998033G>T c.1419C>A c.(1417-1419)atC>atA p.I473I LUAD 23 27998043 27998043 + Missense_Mutation SNP G G A TCGA-17-Z016-01A-01W-0746-08 TCGA-17-Z016-11A-01W-0746-08 g.chrX:27998043G>A c.1409C>T c.(1408-1410)tCc>tTc p.S470F LUAD 23 27998072 27998072 + Silent SNP C C A TCGA-05-5425-01A-02D-1625-08 TCGA-05-5425-10A-01D-1625-08 g.chrX:27998072C>A c.1380G>T c.(1378-1380)ggG>ggT p.G460G LUAD 23 27998107 27998107 + Silent SNP G G T TCGA-17-Z018-01A-01W-0746-08 TCGA-17-Z018-11A-01W-0746-08 g.chrX:27998107G>T c.1345C>A c.(1345-1347)Cgg>Agg p.R449R LUAD 23 27998161 27998161 + Missense_Mutation SNP A A T TCGA-62-A46R-01A-11D-A24D-08 TCGA-62-A46R-10A-01D-A24F-08 g.chrX:27998161A>T c.1291T>A c.(1291-1293)Tat>Aat p.Y431N LUAD 23 27998408 27998408 + Nonsense_Mutation SNP G G T TCGA-86-8279-01A-11D-2284-08 TCGA-86-8279-10A-01D-2284-08 g.chrX:27998408G>T c.1044C>A c.(1042-1044)taC>taA p.Y348* LUAD 23 27998429 27998429 + Silent SNP A A G TCGA-78-7155-01A-11D-2036-08 TCGA-78-7155-10A-01D-2036-08 g.chrX:27998429A>G c.1023T>C c.(1021-1023)tcT>tcC p.S341S LUAD 23 27998441 27998441 + Silent SNP C C A TCGA-17-Z013-01A-01W-0746-08 TCGA-17-Z013-11A-01W-0746-08 g.chrX:27998441C>A c.1011G>T c.(1009-1011)ctG>ctT p.L337L LUAD 23 27998524 27998524 + Missense_Mutation SNP C C A TCGA-44-7670-01A-11D-2063-08 TCGA-44-7670-10A-01D-2063-08 g.chrX:27998524C>A c.928G>T c.(928-930)Gtt>Ttt p.V310F LUAD 23 27998545 27998545 + Missense_Mutation SNP G G T TCGA-17-Z022-01A-01W-0746-08 TCGA-17-Z022-11A-01W-0746-08 g.chrX:27998545G>T c.907C>A c.(907-909)Ctc>Atc p.L303I LUAD 23 27998546 27998546 + Missense_Mutation SNP G G T TCGA-17-Z022-01A-01W-0746-08 TCGA-17-Z022-11A-01W-0746-08 g.chrX:27998546G>T c.906C>A c.(904-906)ttC>ttA p.F302L LUAD 23 27998579 27998579 + Missense_Mutation SNP C C A TCGA-49-4507-01A-01D-1265-08 TCGA-49-4507-11A-01D-1265-08 g.chrX:27998579C>A c.873G>T c.(871-873)gaG>gaT p.E291D LUAD 23 27998776 27998776 + Missense_Mutation SNP C C A TCGA-MN-A4N5-01A-11D-A24P-08 TCGA-MN-A4N5-10A-01D-A24P-08 g.chrX:27998776C>A c.676G>T c.(676-678)Gtg>Ttg p.V226L LUAD 23 27998808 27998808 + Missense_Mutation SNP C C T TCGA-05-4396-01A-21D-1855-08 TCGA-05-4396-10A-01D-1855-08 g.chrX:27998808C>T c.644G>A c.(643-645)gGt>gAt p.G215D LUAD 23 27998829 27998829 + Missense_Mutation SNP C C G TCGA-55-7910-01A-11D-2167-08 TCGA-55-7910-11A-01D-2167-08 g.chrX:27998829C>G c.623G>C c.(622-624)gGc>gCc p.G208A LUAD 23 27998837 27998837 + Missense_Mutation SNP G G T TCGA-64-1679-01A-21D-2063-08 TCGA-64-1679-10A-01D-2063-08 g.chrX:27998837G>T c.615C>A c.(613-615)aaC>aaA p.N205K LUAD 23 27998992 27998992 + Missense_Mutation SNP G G T TCGA-55-8205-01A-11D-2238-08 TCGA-55-8205-10A-01D-2238-08 g.chrX:27998992G>T c.460C>A c.(460-462)Cgc>Agc p.R154S LUAD 23 27999004 27999004 + Missense_Mutation SNP G G T TCGA-17-Z030-01A-01W-0746-08 TCGA-17-Z030-11A-01W-0746-08 g.chrX:27999004G>T c.448C>A c.(448-450)Ctg>Atg p.L150M LUAD 23 27999035 27999035 + Silent SNP C C T TCGA-78-7148-01A-11D-2036-08 TCGA-78-7148-10A-01D-2036-08 g.chrX:27999035C>T c.417G>A c.(415-417)ttG>ttA p.L139L LUAD 23 27999046 27999046 + Missense_Mutation SNP C C A TCGA-64-5781-01A-01D-1625-08 TCGA-64-5781-10A-01D-1625-08 g.chrX:27999046C>A c.406G>T c.(406-408)Gat>Tat p.D136Y LUAD 23 27999166 27999166 + Nonsense_Mutation SNP C C A TCGA-91-6829-01A-21D-1855-08 TCGA-91-6829-11A-01D-1855-08 g.chrX:27999166C>A c.286G>T c.(286-288)Gag>Tag p.E96* LUAD 23 27999258 27999258 + Missense_Mutation SNP G G C TCGA-MP-A4TC-01A-11D-A24P-08 TCGA-MP-A4TC-10A-01D-A24P-08 g.chrX:27999258G>C c.194C>G c.(193-195)aCa>aGa p.T65R LUAD 23 27999351 27999351 + Missense_Mutation SNP G G T TCGA-44-2656-01A-02D-0969-08 TCGA-44-2656-10A-01D-0969-08 g.chrX:27999351G>T c.101C>A c.(100-102)gCg>gAg p.A34E LUAD 23 27999365 27999365 + Silent SNP T T A TCGA-44-A4SU-01A-11D-A24P-08 TCGA-44-A4SU-10A-01D-A24P-08 g.chrX:27999365T>A c.87A>T c.(85-87)gtA>gtT p.V29V LUAD 23 27999372 27999372 + Missense_Mutation SNP G G C TCGA-93-7347-01A-11D-2184-08 TCGA-93-7347-10A-01D-2184-08 g.chrX:27999372G>C c.80C>G c.(79-81)tCt>tGt p.S27C LUAD 23 27999395 27999395 + Silent SNP C C A TCGA-73-7498-01A-12D-2184-08 TCGA-73-7498-10A-01D-2184-08 g.chrX:27999395C>A c.57G>T c.(55-57)ctG>ctT p.L19L LUAD 23 27999418 27999418 + Missense_Mutation SNP G G C TCGA-44-8117-01A-11D-2238-08 TCGA-44-8117-10A-01D-2238-08 g.chrX:27999418G>C c.34C>G c.(34-36)Cca>Gca p.P12A LUSC 23 27997796 27997796 + Silent SNP C C A TCGA-22-1016-01A-01D-1521-08 TCGA-22-1016-11A-01D-1521-08 g.chrX:27997796C>A c.1656G>T c.(1654-1656)gtG>gtT p.V552V LUSC 23 27997798 27997798 + Missense_Mutation SNP C C A TCGA-66-2727-01A-01D-0983-08 TCGA-66-2727-11A-01D-0983-08 g.chrX:27997798C>A c.1654G>T c.(1654-1656)Gtg>Ttg p.V552L LUSC 23 27998327 27998327 + Silent SNP T T A TCGA-39-5028-01A-01D-1441-08 TCGA-39-5028-11A-01D-1441-08 g.chrX:27998327T>A c.1125A>T c.(1123-1125)gtA>gtT p.V375V LUSC 23 27998340 27998340 + Missense_Mutation SNP T T C TCGA-39-5028-01A-01D-1441-08 TCGA-39-5028-11A-01D-1441-08 g.chrX:27998340T>C c.1112A>G c.(1111-1113)gAa>gGa p.E371G LUSC 23 27998447 27998447 + Silent SNP G G T TCGA-21-1070-01A-01D-1521-08 TCGA-21-1070-11A-01D-1521-08 g.chrX:27998447G>T c.1005C>A c.(1003-1005)gtC>gtA p.V335V LUSC 23 27998521 27998521 + Missense_Mutation SNP C C A TCGA-18-3416-01A-01D-0983-08 TCGA-18-3416-11A-01D-0983-08 g.chrX:27998521C>A c.931G>T c.(931-933)Gtg>Ttg p.V311L LUSC 23 27998586 27998586 + Missense_Mutation SNP G G A TCGA-39-5030-01A-01D-1441-08 TCGA-39-5030-11A-01D-1441-08 g.chrX:27998586G>A c.866C>T c.(865-867)gCc>gTc p.A289V LUSC 23 27998849 27998849 + Silent SNP G G T TCGA-21-1070-01A-01D-1521-08 TCGA-21-1070-11A-01D-1521-08 g.chrX:27998849G>T c.603C>A c.(601-603)acC>acA p.T201T LUSC 23 27999094 27999094 + Missense_Mutation SNP A A T TCGA-85-6560-01A-11D-1817-08 TCGA-85-6560-10A-01D-1817-08 g.chrX:27999094A>T c.358T>A c.(358-360)Tgt>Agt p.C120S LUSC 23 27999274 27999274 + Missense_Mutation SNP G G T TCGA-43-6647-01A-11D-1817-08 TCGA-43-6647-11A-01D-1817-08 g.chrX:27999274G>T c.178C>A c.(178-180)Ctg>Atg p.L60M OV 23 27998165 27998165 + Silent SNP C C T TCGA-13-0791-01A-01W-0372-09 TCGA-13-0791-10A-01W-0372-09 g.chrX:27998165C>T c.1287G>A c.(1285-1287)aaG>aaA p.K429K OV 23 27998266 27998266 + Missense_Mutation SNP C C T TCGA-13-0920-01A-01W-0421-09 TCGA-13-0920-10A-01W-0421-09 g.chrX:27998266C>T c.1186G>A c.(1186-1188)Gtt>Att p.V396I OV 23 27998772 27998772 + Missense_Mutation SNP C C G TCGA-61-2097-01A-02W-0722-08 TCGA-61-2097-11A-01W-0723-08 g.chrX:27998772C>G c.680G>C c.(679-681)cGg>cCg p.R227P PAAD 23 27998523 27998523 + Missense_Mutation SNP A A C TCGA-IB-AAUR-01A-21D-A38G-08 TCGA-IB-AAUR-10A-01D-A38J-08 g.chrX:27998523A>C c.929T>G c.(928-930)gTt>gGt p.V310G PAAD 23 27998727 27998727 + Missense_Mutation SNP A A G TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chrX:27998727A>G c.725T>C c.(724-726)gTc>gCc p.V242A PRAD 23 27997690 27997690 + Missense_Mutation SNP C C T TCGA-EJ-A65G-01A-21D-A29Q-08 TCGA-EJ-A65G-10A-01D-A29Q-08 g.chrX:27997690C>T c.1762G>A c.(1762-1764)Gag>Aag p.E588K PRAD 23 27997700 27997700 + Silent SNP T T C TCGA-V1-A9O5-01A-11D-A41K-08 TCGA-V1-A9O5-10A-01D-A41N-08 g.chrX:27997700T>C c.1752A>G c.(1750-1752)tcA>tcG p.S584S READ 23 27998265 27998265 + Missense_Mutation SNP A A G TCGA-EI-6507-01A-11D-1733-10 TCGA-EI-6507-10A-01D-1733-10 g.chrX:27998265A>G c.1187T>C c.(1186-1188)gTt>gCt p.V396A READ 23 27999204 27999204 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chrX:27999204C>T c.248G>A c.(247-249)aGc>aAc p.S83N SARC 23 27997691 27997691 + Silent SNP G G A TCGA-DX-A8BL-01A-11D-A417-09 TCGA-DX-A8BL-10A-01D-A41A-09 g.chrX:27997691G>A c.1761C>T c.(1759-1761)tcC>tcT p.S587S SARC 23 27998918 27998918 + Silent SNP C C T TCGA-QQ-A5VD-01A-21D-A32I-09 TCGA-QQ-A5VD-10A-01D-A32I-09 g.chrX:27998918C>T c.534G>A c.(532-534)ggG>ggA p.G178G SARC 23 27998919 27998919 + Missense_Mutation SNP C C T TCGA-QQ-A5VD-01A-21D-A32I-09 TCGA-QQ-A5VD-10A-01D-A32I-09 g.chrX:27998919C>T c.533G>A c.(532-534)gGg>gAg p.G178E SKCM 23 27997672 27997672 + Nonsense_Mutation SNP G G A TCGA-EE-A29D-06A-11D-A197-08 TCGA-EE-A29D-10A-01D-A199-08 g.chrX:27997672G>A c.1780C>T c.(1780-1782)Cga>Tga p.R594* SKCM 23 27997684 27997684 + Missense_Mutation SNP C C T TCGA-EE-A181-06A-11D-A196-08 TCGA-EE-A181-10A-01D-A198-08 g.chrX:27997684C>T c.1768G>A c.(1768-1770)Gag>Aag p.E590K SKCM 23 27997756 27997756 + Missense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chrX:27997756C>T c.1696G>A c.(1696-1698)Gat>Aat p.D566N SKCM 23 27997849 27997849 + Missense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chrX:27997849C>T c.1603G>A c.(1603-1605)Gac>Aac p.D535N SKCM 23 27998033 27998033 + Silent SNP G G A TCGA-EE-A180-06A-11D-A21A-08 TCGA-EE-A180-10B-01D-A21A-08 g.chrX:27998033G>A c.1419C>T c.(1417-1419)atC>atT p.I473I SKCM 23 27998043 27998043 + Missense_Mutation SNP G G A TCGA-GN-A266-06A-11D-A197-08 TCGA-GN-A266-10A-01D-A199-08 g.chrX:27998043G>A c.1409C>T c.(1408-1410)tCc>tTc p.S470F SKCM 23 27998063 27998063 + Missense_Mutation SNP G G C TCGA-D9-A6E9-06A-12D-A30X-08 TCGA-D9-A6E9-10A-01D-A30X-08 g.chrX:27998063G>C c.1389C>G c.(1387-1389)ttC>ttG p.F463L SKCM 23 27998066 27998066 + Silent SNP G G T TCGA-EE-A2A2-06A-11D-A196-08 TCGA-EE-A2A2-10A-01D-A198-08 g.chrX:27998066G>T c.1386C>A c.(1384-1386)gtC>gtA p.V462V SKCM 23 27998305 27998305 + Missense_Mutation SNP G G A TCGA-GN-A4U8-06A-11D-A32N-08 TCGA-GN-A4U8-10B-01D-A32N-08 g.chrX:27998305G>A c.1147C>T c.(1147-1149)Cat>Tat p.H383Y SKCM 23 27998321 27998321 + Silent SNP C C T TCGA-EE-A182-06A-11D-A196-08 TCGA-EE-A182-10A-01D-A198-08 g.chrX:27998321C>T c.1131G>A c.(1129-1131)aaG>aaA p.K377K SKCM 23 27998538 27998538 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chrX:27998538G>A c.914C>T c.(913-915)tCa>tTa p.S305L SKCM 23 27998711 27998711 + Silent SNP G G A TCGA-FS-A1ZK-06A-11D-A197-08 TCGA-FS-A1ZK-10A-01D-A199-08 g.chrX:27998711G>A c.741C>T c.(739-741)ttC>ttT p.F247F SKCM 23 27998737 27998737 + Missense_Mutation SNP C C T TCGA-DA-A1IC-06A-11D-A197-08 TCGA-DA-A1IC-10A-01D-A199-08 g.chrX:27998737C>T c.715G>A c.(715-717)Gat>Aat p.D239N SKCM 23 27998893 27998893 + Missense_Mutation SNP G G A TCGA-FS-A1ZA-06A-11D-A197-08 TCGA-FS-A1ZA-10A-01D-A199-08 g.chrX:27998893G>A c.559C>T c.(559-561)Cgc>Tgc p.R187C SKCM 23 27998981 27998981 + Silent SNP G G A TCGA-EE-A2MS-06A-11D-A197-08 TCGA-EE-A2MS-10A-01D-A199-08 g.chrX:27998981G>A c.471C>T c.(469-471)gtC>gtT p.V157V SKCM 23 27999004 27999004 + Silent SNP G G A TCGA-EE-A29D-06A-11D-A197-08 TCGA-EE-A29D-10A-01D-A199-08 g.chrX:27999004G>A c.448C>T c.(448-450)Ctg>Ttg p.L150L SKCM 23 27999038 27999038 + Silent SNP C C T TCGA-EE-A2M6-06A-12D-A197-08 TCGA-EE-A2M6-10A-01D-A199-08 g.chrX:27999038C>T c.414G>A c.(412-414)gcG>gcA p.A138A SKCM 23 27999112 27999112 + Missense_Mutation SNP C C T TCGA-ER-A19Q-06A-11D-A197-08 TCGA-ER-A19Q-10A-01D-A199-08 g.chrX:27999112C>T c.340G>A c.(340-342)Gaa>Aaa p.E114K SKCM 23 27999123 27999123 + Missense_Mutation SNP T T A TCGA-FS-A1ZK-06A-11D-A197-08 TCGA-FS-A1ZK-10A-01D-A199-08 g.chrX:27999123T>A c.329A>T c.(328-330)gAa>gTa p.E110V SKCM 23 27999147 27999147 + Missense_Mutation SNP T T C TCGA-ER-A2NC-06A-11D-A197-08 TCGA-ER-A2NC-10A-01D-A199-08 g.chrX:27999147T>C c.305A>G c.(304-306)gAg>gGg p.E102G SKCM 23 27999149 27999149 + Silent SNP C C T TCGA-ER-A2NC-06A-11D-A197-08 TCGA-ER-A2NC-10A-01D-A199-08 g.chrX:27999149C>T c.303G>A c.(301-303)gaG>gaA p.E101E SKCM 23 27999153 27999153 + Missense_Mutation SNP C C A TCGA-ER-A3ET-06A-11D-A20D-08 TCGA-ER-A3ET-10A-01D-A20D-08 g.chrX:27999153C>A c.299G>T c.(298-300)aGg>aTg p.R100M SKCM 23 27999214 27999214 + Missense_Mutation SNP C C T TCGA-EE-A20B-06A-11D-A196-08 TCGA-EE-A20B-10A-01D-A198-08 g.chrX:27999214C>T c.238G>A c.(238-240)Gaa>Aaa p.E80K SKCM 23 27999214 27999214 + Missense_Mutation SNP C C T TCGA-EE-A2ME-06A-11D-A197-08 TCGA-EE-A2ME-10A-01D-A199-08 g.chrX:27999214C>T c.238G>A c.(238-240)Gaa>Aaa p.E80K SKCM 23 27999214 27999214 + Missense_Mutation SNP C C T TCGA-EE-A3J7-06A-11D-A20D-08 TCGA-EE-A3J7-10A-01D-A20D-08 g.chrX:27999214C>T c.238G>A c.(238-240)Gaa>Aaa p.E80K SKCM 23 27999223 27999223 + Missense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chrX:27999223C>T c.229G>A c.(229-231)Gaa>Aaa p.E77K SKCM 23 27999268 27999268 + Missense_Mutation SNP C C T TCGA-DA-A1HV-06A-21D-A196-08 TCGA-DA-A1HV-10A-01D-A198-08 g.chrX:27999268C>T c.184G>A c.(184-186)Gat>Aat p.D62N SKCM 23 27999275 27999275 + Silent SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chrX:27999275G>A c.177C>T c.(175-177)ttC>ttT p.F59F SKCM 23 27999286 27999286 + Missense_Mutation SNP C C T TCGA-GN-A266-06A-11D-A197-08 TCGA-GN-A266-10A-01D-A199-08 g.chrX:27999286C>T c.166G>A c.(166-168)Gat>Aat p.D56N SKCM 23 27999379 27999379 + Missense_Mutation SNP C C G TCGA-D9-A6EA-06A-11D-A30X-08 TCGA-D9-A6EA-10A-01D-A30X-08 g.chrX:27999379C>G c.73G>C c.(73-75)Gag>Cag p.E25Q SKCM 23 27999379 27999379 + Missense_Mutation SNP C C T TCGA-FR-A3YN-06A-11D-A23B-08 TCGA-FR-A3YN-10A-01D-A23B-08 g.chrX:27999379C>T c.73G>A c.(73-75)Gag>Aag p.E25K

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 27997990 27997990 single base substitution C T missense_variant E488K 1462G>A BLCA-CN X 27998639 27998639 single base substitution A G synonymous_variant I271I 813T>C BLCA-CN X 27999327 27999327 single base substitution G T missense_variant A42E 125C>A BLCA-US X 27998745 27998745 single base substitution C A missense_variant S236I 707G>T BLCA-US X 27999131 27999131 single base substitution C T missense_variant M107I 321G>A BRCA-EU X 27991428 27991428 insertion of <=200bp - A downstream_gene_variant BRCA-EU X 27991941 27991941 single base substitution C T downstream_gene_variant BRCA-EU X 27992523 27992523 single base substitution G T downstream_gene_variant BRCA-EU X 27992577 27992577 single base substitution G A downstream_gene_variant BRCA-EU X 27992974 27992974 single base substitution G C downstream_gene_variant BRCA-EU X 27993465 27993465 single base substitution G A downstream_gene_variant BRCA-EU X 27993516 27993516 single base substitution G A downstream_gene_variant BRCA-EU X 27994116 27994116 deletion of <=200bp A - downstream_gene_variant BRCA-EU X 27994649 27994649 single base substitution C T downstream_gene_variant BRCA-EU X 27995123 27995123 single base substitution C A downstream_gene_variant BRCA-EU X 27996626 27996626 single base substitution G A 3_prime_UTR_variant BRCA-EU X 27996677 27996677 single base substitution C T 3_prime_UTR_variant BRCA-EU X 27997307 27997307 single base substitution G T 3_prime_UTR_variant BRCA-EU X 27997642 27997642 single base substitution G A 3_prime_UTR_variant BRCA-EU X 27997777 27997777 single base substitution C A missense_variant A559S 1675G>T BRCA-EU X 27998362 27998362 single base substitution G T missense_variant Q364K 1090C>A BRCA-EU X 27998492 27998492 single base substitution C T synonymous_variant R320R 960G>A BRCA-EU X 27998694 27998694 single base substitution T A missense_variant D253V 758A>T BRCA-EU X 27999269 27999269 single base substitution G T missense_variant N61K 183C>A BRCA-EU X 27999959 27999959 single base substitution C A upstream_gene_variant BRCA-EU X 27999978 27999978 single base substitution G A upstream_gene_variant BRCA-EU X 28000078 28000078 single base substitution T C upstream_gene_variant BRCA-EU X 28000282 28000282 single base substitution G A upstream_gene_variant BRCA-EU X 28000371 28000371 single base substitution C G upstream_gene_variant BRCA-EU X 28001295 28001295 single base substitution C G upstream_gene_variant BRCA-EU X 28001760 28001760 single base substitution G C upstream_gene_variant BRCA-EU X 28001948 28001948 single base substitution C G upstream_gene_variant BRCA-EU X 28002169 28002169 insertion of <=200bp - A upstream_gene_variant BRCA-EU X 28002501 28002501 single base substitution C T upstream_gene_variant BRCA-EU X 28002744 28002744 single base substitution G C upstream_gene_variant BRCA-EU X 28002902 28002902 single base substitution C T upstream_gene_variant BRCA-EU X 28003109 28003109 single base substitution A T upstream_gene_variant BRCA-EU X 28003494 28003494 single base substitution C T upstream_gene_variant BRCA-EU X 28003999 28003999 single base substitution T C upstream_gene_variant BRCA-EU X 28004216 28004216 single base substitution A C upstream_gene_variant BRCA-EU X 28004266 28004266 single base substitution G A upstream_gene_variant BRCA-FR X 27991941 27991941 single base substitution C T downstream_gene_variant BRCA-FR X 27995465 27995465 single base substitution A T downstream_gene_variant BRCA-FR X 27998362 27998362 single base substitution G T missense_variant Q364K 1090C>A BRCA-FR X 27998492 27998492 single base substitution C T synonymous_variant R320R 960G>A BRCA-FR X 28002501 28002501 single base substitution C T upstream_gene_variant BRCA-FR X 28003775 28003775 single base substitution A G upstream_gene_variant BRCA-KR X 27999269 27999269 single base substitution G A synonymous_variant N61N 183C>T BRCA-UK X 27993516 27993516 single base substitution G A downstream_gene_variant BRCA-UK X 27999112 27999112 single base substitution C T missense_variant E114K 340G>A BRCA-US X 27997690 27997690 single base substitution C T missense_variant E588K 1762G>A BRCA-US X 27998516 27998516 single base substitution G C missense_variant F312L 936C>G BRCA-US X 27998944 27998944 single base substitution C A missense_variant A170S 508G>T BRCA-US X 27999024 27999024 single base substitution A T missense_variant I143N 428T>A BRCA-US X 27999081 27999081 single base substitution C A missense_variant G124V 371G>T BRCA-US X 27999139 27999139 single base substitution C A stop_gained E105* 313G>T BRCA-US X 27999269 27999269 single base substitution G T missense_variant N61K 183C>A BTCA-JP X 27998314 27998314 single base substitution T G missense_variant T380P 1138A>C BTCA-JP X 27998758 27998758 single base substitution G A synonymous_variant L232L 694C>T CESC-US X 27997787 27997787 single base substitution C G synonymous_variant L555L 1665G>C CESC-US X 27998107 27998107 single base substitution G A missense_variant R449W 1345C>T CESC-US X 27998204 27998204 single base substitution G A synonymous_variant L416L 1248C>T CLLE-ES X 27994773 27994773 single base substitution T A downstream_gene_variant CLLE-ES X 27997009 27997009 single base substitution T A 3_prime_UTR_variant CLLE-ES X 27998637 27998637 single base substitution T A missense_variant N272I 815A>T CLLE-ES X 28001938 28001938 single base substitution G T upstream_gene_variant CLLE-ES X 28003381 28003381 single base substitution T A upstream_gene_variant COAD-US X 27997672 27997672 single base substitution G A stop_gained R594* 1780C>T COAD-US X 27998150 27998150 single base substitution G A synonymous_variant H434H 1302C>T COAD-US X 27998387 27998387 single base substitution A G synonymous_variant H355H 1065T>C COAD-US X 27998446 27998446 single base substitution C T missense_variant G336R 1006G>A COAD-US X 27998668 27998668 single base substitution C G missense_variant D262H 784G>C COAD-US X 27998681 27998681 deletion of <=200bp G - frameshift_variant A257 COAD-US X 27998926 27998926 single base substitution C T missense_variant A176T 526G>A COAD-US X 27999100 27999100 single base substitution G A missense_variant R118W 352C>T COAD-US X 27999146 27999146 single base substitution C T synonymous_variant E102E 306G>A COCA-CN X 27997832 27997832 single base substitution C T synonymous_variant T540T 1620G>A COCA-CN X 27998278 27998278 single base substitution T C missense_variant N392D 1174A>G COCA-CN X 27999214 27999214 single base substitution C T missense_variant E80K 238G>A COCA-CN X 27999350 27999350 single base substitution C T synonymous_variant A34A 102G>A COCA-CN X 27999455 27999455 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant ESCA-CN X 27997719 27997719 single base substitution T C missense_variant D578G 1733A>G ESCA-CN X 27997990 27997990 single base substitution C A stop_gained E488* 1462G>T ESCA-CN X 27998610 27998610 single base substitution C T missense_variant R281H 842G>A GACA-CN X 27999010 27999010 single base substitution A G missense_variant S148P 442T>C GBM-US X 27998785 27998785 single base substitution A G missense_variant W223R 667T>C GBM-US X 27999269 27999269 single base substitution G A synonymous_variant N61N 183C>T GBM-US X 27999308 27999308 single base substitution G A synonymous_variant T48T 144C>T KIRC-US X 27997690 27997690 single base substitution C T missense_variant E588K 1762G>A KIRC-US X 27998267 27998267 single base substitution G A synonymous_variant C395C 1185C>T LGG-US X 27998600 27998600 single base substitution C A missense_variant K284N 852G>T LGG-US X 27999088 27999088 single base substitution G A stop_gained R122* 364C>T LICA-FR X 27994388 27994388 single base substitution T C downstream_gene_variant LICA-FR X 27995722 27995722 single base substitution C A downstream_gene_variant LICA-FR X 27999532 27999532 single base substitution C T 5_prime_UTR_variant LIHC-US X 27998516 27998516 single base substitution G A synonymous_variant F312F 936C>T LIHC-US X 27999289 27999289 single base substitution T A missense_variant R55W 163A>T LINC-JP X 27996308 27996308 single base substitution A T 3_prime_UTR_variant LINC-JP X 27997818 27997818 single base substitution T C missense_variant N545S 1634A>G LINC-JP X 27998638 27998638 single base substitution T C missense_variant N272D 814A>G LIRI-JP X 27992015 27992015 single base substitution C A downstream_gene_variant LIRI-JP X 27992077 27992077 single base substitution T C downstream_gene_variant LIRI-JP X 27992803 27992803 single base substitution G T downstream_gene_variant LIRI-JP X 27993029 27993029 single base substitution G A downstream_gene_variant LIRI-JP X 27994617 27994617 single base substitution T G downstream_gene_variant LIRI-JP X 27996201 27996201 single base substitution A G 3_prime_UTR_variant LIRI-JP X 27996757 27996757 single base substitution A G 3_prime_UTR_variant LIRI-JP X 27997803 27997803 single base substitution A G missense_variant F550S 1649T>C LIRI-JP X 27998383 27998383 single base substitution G A stop_gained Q357* 1069C>T LIRI-JP X 27998652 27998652 single base substitution A G missense_variant V267A 800T>C LIRI-JP X 27998968 27998968 single base substitution G A missense_variant R162C 484C>T LIRI-JP X 27999932 27999932 single base substitution T C upstream_gene_variant LIRI-JP X 28000022 28000022 single base substitution G A upstream_gene_variant LIRI-JP X 28000264 28000264 single base substitution G C upstream_gene_variant LIRI-JP X 28000504 28000504 single base substitution G T upstream_gene_variant LIRI-JP X 28000599 28000599 single base substitution A T upstream_gene_variant LIRI-JP X 28002428 28002428 single base substitution A G upstream_gene_variant LIRI-JP X 28003168 28003168 single base substitution C G upstream_gene_variant LIRI-JP X 28003877 28003877 single base substitution A G upstream_gene_variant LIRI-JP X 28004006 28004006 single base substitution C T upstream_gene_variant LUSC-KR X 27991331 27991331 single base substitution T C downstream_gene_variant LUSC-KR X 27993893 27993893 single base substitution C T downstream_gene_variant LUSC-KR X 27995473 27995473 single base substitution C A downstream_gene_variant LUSC-KR X 27996301 27996301 single base substitution C T 3_prime_UTR_variant LUSC-KR X 28000969 28000969 single base substitution C A upstream_gene_variant LUSC-US X 27997796 27997796 single base substitution C A synonymous_variant V552V 1656G>T LUSC-US X 27997798 27997798 single base substitution C A missense_variant V552L 1654G>T LUSC-US X 27998327 27998327 single base substitution T A synonymous_variant V375V 1125A>T LUSC-US X 27998340 27998340 single base substitution T C missense_variant E371G 1112A>G LUSC-US X 27998447 27998447 single base substitution G T synonymous_variant V335V 1005C>A LUSC-US X 27998521 27998521 single base substitution C A missense_variant V311L 931G>T LUSC-US X 27998586 27998586 single base substitution G A missense_variant A289V 866C>T LUSC-US X 27998849 27998849 single base substitution G T synonymous_variant T201T 603C>A LUSC-US X 27999094 27999094 single base substitution A T missense_variant C120S 358T>A LUSC-US X 27999274 27999274 single base substitution G T missense_variant L60M 178C>A MALY-DE X 27991184 27991184 single base substitution A G downstream_gene_variant MALY-DE X 27992016 27992016 single base substitution T G downstream_gene_variant MALY-DE X 27992153 27992153 single base substitution C A downstream_gene_variant MALY-DE X 27993911 27993912 deletion of <=200bp CA - downstream_gene_variant MALY-DE X 27994432 27994432 single base substitution T A downstream_gene_variant MALY-DE X 27996432 27996432 single base substitution A T 3_prime_UTR_variant MALY-DE X 27998867 27998867 single base substitution A T missense_variant H195Q 585T>A MALY-DE X 28001961 28001961 single base substitution T A upstream_gene_variant MALY-DE X 28004552 28004552 single base substitution C T upstream_gene_variant MELA-AU X 27991345 27991345 single base substitution C T downstream_gene_variant MELA-AU X 27991432 27991432 single base substitution A T downstream_gene_variant MELA-AU X 27991439 27991439 single base substitution G A downstream_gene_variant MELA-AU X 27991448 27991448 single base substitution C T downstream_gene_variant MELA-AU X 27991933 27991934 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU X 27992419 27992419 single base substitution G C downstream_gene_variant MELA-AU X 27992493 27992493 single base substitution G A downstream_gene_variant MELA-AU X 27992874 27992874 single base substitution C T downstream_gene_variant MELA-AU X 27993101 27993101 single base substitution C T downstream_gene_variant MELA-AU X 27993246 27993246 single base substitution T C downstream_gene_variant MELA-AU X 27993274 27993274 single base substitution C T downstream_gene_variant MELA-AU X 27993286 27993286 single base substitution T C downstream_gene_variant MELA-AU X 27993324 27993324 single base substitution T A downstream_gene_variant MELA-AU X 27993724 27993724 single base substitution G A downstream_gene_variant MELA-AU X 27993798 27993798 single base substitution G T downstream_gene_variant MELA-AU X 27993850 27993850 single base substitution G T downstream_gene_variant MELA-AU X 27993925 27993925 single base substitution C T downstream_gene_variant MELA-AU X 27993937 27993937 single base substitution C T downstream_gene_variant MELA-AU X 27994444 27994444 single base substitution G A downstream_gene_variant MELA-AU X 27994472 27994472 deletion of <=200bp A - downstream_gene_variant MELA-AU X 27994535 27994535 single base substitution G A downstream_gene_variant MELA-AU X 27994840 27994840 single base substitution G A downstream_gene_variant MELA-AU X 27994900 27994900 single base substitution A G downstream_gene_variant MELA-AU X 27995265 27995265 single base substitution G A downstream_gene_variant MELA-AU X 27995405 27995405 single base substitution G A downstream_gene_variant MELA-AU X 27995453 27995453 single base substitution G A downstream_gene_variant MELA-AU X 27995733 27995733 single base substitution G A downstream_gene_variant MELA-AU X 27995823 27995823 single base substitution C T downstream_gene_variant MELA-AU X 27995847 27995847 single base substitution G A downstream_gene_variant MELA-AU X 27995985 27995985 single base substitution C T downstream_gene_variant MELA-AU X 27996023 27996023 single base substitution C T downstream_gene_variant MELA-AU X 27996368 27996368 single base substitution G A 3_prime_UTR_variant MELA-AU X 27996765 27996765 single base substitution C T 3_prime_UTR_variant MELA-AU X 27996874 27996874 single base substitution C T 3_prime_UTR_variant MELA-AU X 27997055 27997055 single base substitution C T 3_prime_UTR_variant MELA-AU X 27997064 27997064 single base substitution C T 3_prime_UTR_variant MELA-AU X 27997068 27997068 single base substitution C T 3_prime_UTR_variant MELA-AU X 27997197 27997197 single base substitution G A 3_prime_UTR_variant MELA-AU X 27997321 27997321 single base substitution C T 3_prime_UTR_variant MELA-AU X 27997370 27997370 single base substitution A T 3_prime_UTR_variant MELA-AU X 27997425 27997425 single base substitution A G 3_prime_UTR_variant MELA-AU X 27997486 27997486 single base substitution G A 3_prime_UTR_variant MELA-AU X 27997672 27997672 single base substitution G A stop_gained R594* 1780C>T MELA-AU X 27997803 27997803 single base substitution A T missense_variant F550Y 1649T>A MELA-AU X 27998185 27998185 single base substitution C T missense_variant D423N 1267G>A MELA-AU X 27998290 27998290 single base substitution C T missense_variant D388N 1162G>A MELA-AU X 27998372 27998372 single base substitution C T synonymous_variant R360R 1080G>A MELA-AU X 27998992 27998992 single base substitution G A missense_variant R154C 460C>T MELA-AU X 27998998 27998998 single base substitution G A stop_gained R152* 454C>T MELA-AU X 27999021 27999021 single base substitution G A missense_variant S144F 431C>T MELA-AU X 27999145 27999145 single base substitution C T missense_variant E103K 307G>A MELA-AU X 27999178 27999178 single base substitution G A missense_variant P92S 274C>T MELA-AU X 27999214 27999214 single base substitution C T missense_variant E80K 238G>A MELA-AU X 27999459 27999459 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant MELA-AU X 27999487 27999487 single base substitution G A 5_prime_UTR_variant MELA-AU X 27999771 27999771 single base substitution G A upstream_gene_variant MELA-AU X 27999815 27999815 single base substitution G A upstream_gene_variant MELA-AU X 27999953 27999953 single base substitution A T upstream_gene_variant MELA-AU X 27999956 27999956 single base substitution G A upstream_gene_variant MELA-AU X 28000018 28000018 single base substitution G A upstream_gene_variant MELA-AU X 28000104 28000104 single base substitution C T upstream_gene_variant MELA-AU X 28000515 28000515 single base substitution G A upstream_gene_variant MELA-AU X 28000523 28000523 single base substitution C T upstream_gene_variant MELA-AU X 28000550 28000550 single base substitution C G upstream_gene_variant MELA-AU X 28000758 28000758 single base substitution G A upstream_gene_variant MELA-AU X 28000765 28000765 single base substitution C T upstream_gene_variant MELA-AU X 28001001 28001001 single base substitution C A upstream_gene_variant MELA-AU X 28001135 28001135 single base substitution C T upstream_gene_variant MELA-AU X 28001362 28001362 single base substitution G A upstream_gene_variant MELA-AU X 28001468 28001468 single base substitution C T upstream_gene_variant MELA-AU X 28001481 28001481 single base substitution G A upstream_gene_variant MELA-AU X 28001530 28001530 deletion of <=200bp T - upstream_gene_variant MELA-AU X 28001542 28001542 single base substitution C T upstream_gene_variant MELA-AU X 28001652 28001652 single base substitution C T upstream_gene_variant MELA-AU X 28001931 28001931 single base substitution A T upstream_gene_variant MELA-AU X 28002025 28002025 single base substitution C T upstream_gene_variant MELA-AU X 28002184 28002184 single base substitution G A upstream_gene_variant MELA-AU X 28003099 28003099 single base substitution G A upstream_gene_variant MELA-AU X 28003136 28003136 single base substitution G A upstream_gene_variant MELA-AU X 28003259 28003259 single base substitution C T upstream_gene_variant MELA-AU X 28003348 28003348 single base substitution T A upstream_gene_variant MELA-AU X 28003488 28003488 single base substitution T A upstream_gene_variant MELA-AU X 28003872 28003872 single base substitution A T upstream_gene_variant MELA-AU X 28003880 28003880 single base substitution T G upstream_gene_variant MELA-AU X 28004045 28004045 single base substitution C T upstream_gene_variant MELA-AU X 28004083 28004083 single base substitution G A upstream_gene_variant MELA-AU X 28004201 28004201 single base substitution T A upstream_gene_variant MELA-AU X 28004493 28004493 single base substitution G A upstream_gene_variant MELA-AU X 28004563 28004563 single base substitution G A upstream_gene_variant ORCA-IN X 27992563 27992563 single base substitution G A downstream_gene_variant OV-US X 27998165 27998165 single base substitution C T synonymous_variant K429K 1287G>A OV-US X 27998266 27998266 single base substitution C T missense_variant V396I 1186G>A PACA-AU X 27991170 27991170 single base substitution C G downstream_gene_variant PACA-AU X 27993471 27993471 single base substitution C G downstream_gene_variant PACA-AU X 27994434 27994434 single base substitution A G downstream_gene_variant PACA-AU X 27998249 27998249 single base substitution A T missense_variant D401E 1203T>A PACA-AU X 28000618 28000618 single base substitution C T upstream_gene_variant PACA-AU X 28001453 28001453 single base substitution C A upstream_gene_variant PACA-CA X 27997494 27997494 single base substitution G T 3_prime_UTR_variant PACA-CA X 27999543 27999543 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant PACA-CA X 27999711 27999711 single base substitution C A upstream_gene_variant PACA-CA X 28001275 28001275 single base substitution A T upstream_gene_variant PACA-CA X 28002922 28002922 single base substitution C T upstream_gene_variant PAEN-AU X 28002180 28002180 single base substitution T A upstream_gene_variant PBCA-DE X 27993670 27993670 single base substitution C T downstream_gene_variant PBCA-DE X 27993911 27993912 deletion of <=200bp CA - downstream_gene_variant PBCA-DE X 27994480 27994481 deletion of <=200bp TG - downstream_gene_variant PBCA-DE X 27998192 27998192 single base substitution A G synonymous_variant S420S 1260T>C PBCA-DE X 27999404 27999404 single base substitution A G synonymous_variant T16T 48T>C PBCA-DE X 28000484 28000484 single base substitution C A upstream_gene_variant PBCA-DE X 28001481 28001481 single base substitution G A upstream_gene_variant PBCA-DE X 28002576 28002576 single base substitution C T upstream_gene_variant PRAD-CA X 27991198 27991198 single base substitution C G downstream_gene_variant PRAD-CA X 27991224 27991224 single base substitution C A downstream_gene_variant PRAD-CA X 27997765 27997765 single base substitution C T missense_variant G563S 1687G>A PRAD-CA X 28002245 28002245 single base substitution A T upstream_gene_variant PRAD-UK X 27998997 27998997 single base substitution C T missense_variant R152Q 455G>A PRAD-US X 27997690 27997690 single base substitution C T missense_variant E588K 1762G>A RECA-EU X 27995510 27995510 single base substitution C T downstream_gene_variant RECA-EU X 27999042 27999042 single base substitution T A missense_variant Q137L 410A>T SKCA-BR X 27992159 27992159 single base substitution G A downstream_gene_variant SKCA-BR X 27994031 27994031 single base substitution G A downstream_gene_variant SKCA-BR X 27994871 27994871 single base substitution G A downstream_gene_variant SKCA-BR X 27996025 27996025 single base substitution C T downstream_gene_variant SKCA-BR X 27996127 27996127 single base substitution T A 3_prime_UTR_variant SKCA-BR X 27996457 27996457 single base substitution A G 3_prime_UTR_variant SKCA-BR X 27997226 27997226 single base substitution C T 3_prime_UTR_variant SKCA-BR X 27997435 27997435 single base substitution T A 3_prime_UTR_variant SKCA-BR X 27999885 27999887 deletion of <=200bp TAC - upstream_gene_variant SKCA-BR X 28001368 28001368 single base substitution T C upstream_gene_variant SKCA-BR X 28004564 28004564 single base substitution C T upstream_gene_variant SKCM-US X 27997672 27997672 single base substitution G A stop_gained R594* 1780C>T SKCM-US X 27997684 27997684 single base substitution C T missense_variant E590K 1768G>A SKCM-US X 27997756 27997756 single base substitution C T missense_variant D566N 1696G>A SKCM-US X 27997849 27997849 single base substitution C T missense_variant D535N 1603G>A SKCM-US X 27998033 27998033 single base substitution G A synonymous_variant I473I 1419C>T SKCM-US X 27998043 27998043 single base substitution G A missense_variant S470F 1409C>T SKCM-US X 27998063 27998063 single base substitution G C missense_variant F463L 1389C>G SKCM-US X 27998066 27998066 single base substitution G T synonymous_variant V462V 1386C>A SKCM-US X 27998105 27998105 single base substitution C T synonymous_variant R449R 1347G>A SKCM-US X 27998321 27998321 single base substitution C T synonymous_variant K377K 1131G>A SKCM-US X 27998538 27998538 single base substitution G A missense_variant S305L 914C>T SKCM-US X 27998691 27998691 single base substitution G A missense_variant S254F 761C>T SKCM-US X 27998711 27998711 single base substitution G A synonymous_variant F247F 741C>T SKCM-US X 27998737 27998737 single base substitution C T missense_variant D239N 715G>A SKCM-US X 27998893 27998893 single base substitution G A missense_variant R187C 559C>T SKCM-US X 27998981 27998981 single base substitution G A synonymous_variant V157V 471C>T SKCM-US X 27999004 27999004 single base substitution G A synonymous_variant L150L 448C>T SKCM-US X 27999038 27999038 single base substitution C T synonymous_variant A138A 414G>A SKCM-US X 27999112 27999112 single base substitution C T missense_variant E114K 340G>A SKCM-US X 27999123 27999123 single base substitution T A missense_variant E110V 329A>T SKCM-US X 27999147 27999147 single base substitution T C missense_variant E102G 305A>G SKCM-US X 27999149 27999149 single base substitution C T synonymous_variant E101E 303G>A SKCM-US X 27999153 27999153 single base substitution C A missense_variant R100M 299G>T SKCM-US X 27999214 27999214 single base substitution C T missense_variant E80K 238G>A SKCM-US X 27999223 27999223 single base substitution C T missense_variant E77K 229G>A SKCM-US X 27999268 27999268 single base substitution C T missense_variant D62N 184G>A SKCM-US X 27999275 27999275 single base substitution G A synonymous_variant F59F 177C>T SKCM-US X 27999286 27999286 single base substitution C T missense_variant D56N 166G>A SKCM-US X 27999379 27999379 single base substitution C G missense_variant E25Q 73G>C SKCM-US X 27999379 27999379 single base substitution C T missense_variant E25K 73G>A SKCM-US X 27999382 27999382 single base substitution C T missense_variant E24K 70G>A STAD-US X 27997798 27997798 single base substitution C T missense_variant V552M 1654G>A STAD-US X 27997832 27997832 single base substitution C T synonymous_variant T540T 1620G>A STAD-US X 27998016 27998016 single base substitution T C missense_variant D479G 1436A>G STAD-US X 27998107 27998107 single base substitution G A missense_variant R449W 1345C>T STAD-US X 27998138 27998138 single base substitution G A synonymous_variant D438D 1314C>T STAD-US X 27998141 27998141 single base substitution A G synonymous_variant N437N 1311T>C STAD-US X 27998625 27998625 single base substitution C T missense_variant C276Y 827G>A STAD-US X 27998645 27998645 single base substitution T C synonymous_variant E269E 807A>G STAD-US X 27998685 27998685 single base substitution A G missense_variant L256P 767T>C STAD-US X 27998761 27998761 single base substitution C T missense_variant V231I 691G>A STAD-US X 27998805 27998805 single base substitution T C missense_variant D216G 647A>G STAD-US X 27999203 27999203 single base substitution G A synonymous_variant S83S 249C>T STAD-US X 27999217 27999217 single base substitution C T missense_variant V79I 235G>A STAD-US X 27999324 27999324 single base substitution G A missense_variant A43V 128C>T THCA-SA X 27999146 27999146 single base substitution C T synonymous_variant E102E 306G>A THCA-US X 27998790 27998790 single base substitution A G missense_variant I221T 662T>C UCEC-US X 27997716 27997716 single base substitution T C missense_variant E579G 1736A>G UCEC-US X 27997795 27997795 single base substitution G A missense_variant R553C 1657C>T UCEC-US X 27997858 27997858 single base substitution G A stop_gained R532* 1594C>T UCEC-US X 27997948 27997948 single base substitution C A missense_variant D502Y 1504G>T UCEC-US X 27998032 27998032 single base substitution G A stop_gained Q474* 1420C>T UCEC-US X 27998088 27998088 single base substitution C T missense_variant S455N 1364G>A UCEC-US X 27998092 27998092 single base substitution C T missense_variant V454M 1360G>A UCEC-US X 27998293 27998293 single base substitution A G missense_variant C387R 1159T>C UCEC-US X 27998341 27998341 single base substitution C A stop_gained E371* 1111G>T UCEC-US X 27998497 27998497 insertion of <=200bp - T frameshift_variant D319E? UCEC-US X 27998711 27998711 single base substitution G T missense_variant F247L 741C>A UCEC-US X 27998726 27998726 single base substitution G A synonymous_variant V242V 726C>T UCEC-US X 27998727 27998727 single base substitution A C missense_variant V242G 725T>G UCEC-US X 27998801 27998801 single base substitution G A synonymous_variant D217D 651C>T UCEC-US X 27998823 27998823 single base substitution C T missense_variant R210Q 629G>A UCEC-US X 27998898 27998898 single base substitution C T missense_variant R185H 554G>A UCEC-US X 27998992 27998992 single base substitution G A missense_variant R154C 460C>T UCEC-US X 27999214 27999214 single base substitution C T missense_variant E80K 238G>A

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand TCGA-EE-A2ME-06 COSM184529 c.238G>A p.E80K Substitution - Missense 23:27981097-27981097 - HCC130 COSM1625808 c.1634A>G p.N545S Substitution - Missense 23:27979701-27979701 - TCGA-AP-A0LM-01 COSM1119706 c.629G>A p.R210Q Substitution - Missense 23:27980706-27980706 - TCGA-CM-5861-01 COSM1467370 c.771delC p.M258fs*10 Deletion - Frameshift 23:27980564-27980564 - TCGA-D9-A6E9-06 COSM4399454 c.1389C>G p.F463L Substitution - Missense 23:27979946-27979946 - TCGA-CS-6667-01 COSM3973578 c.364C>T p.R122* Substitution - Nonsense 23:27980971-27980971 - TCGA-39-5028-01 COSM756407 c.1112A>G p.E371G Substitution - Missense 23:27980223-27980223 - TCGA-BR-4368-01 COSM4108820 c.1311T>C p.N437N Substitution - coding silent 23:27980024-27980024 - TCGA-AP-A056-01 COSM1119699 c.1159T>C p.C387R Substitution - Missense 23:27980176-27980176 - TCGA-EE-A20B-06 COSM184529 c.238G>A p.E80K Substitution - Missense 23:27981097-27981097 - 3N52-VS-3T52 COSM4983525 c.530G>T p.C177F Substitution - Missense 23:27980805-27980805 - TCGA-FW-A3R5-06 COSM3913826 c.914C>T p.S305L Substitution - Missense 23:27980421-27980421 - TCGA-AX-A0J0-01 COSM1119707 c.554G>A p.R185H Substitution - Missense 23:27980781-27980781 - sysucc-1397T COSM4108816 c.1620G>A p.T540T Substitution - coding silent 23:27979715-27979715 - 2334201 COSM319812 c.7C>A p.H3N Substitution - Missense 23:27981328-27981328 - Pat_44_B COSM5877707 c.841C>T p.R281C Substitution - Missense 23:27980494-27980494 - CPCG0232-F1 COSM4966579 c.1687G>A p.G563S Substitution - Missense 23:27979648-27979648 - QC2-40-T2 COSM4108827 c.235G>A p.V79I Substitution - Missense 23:27981100-27981100 - TCGA-AZ-4315-01 COSM1467360 c.1780C>T p.R594* Substitution - Nonsense 23:27979555-27979555 - YUAKER COSM1714772 c.198A>T p.E66D Substitution - Missense 23:27981137-27981137 - RK034_C01 COSM1636492 c.1649T>C p.F550S Substitution - Missense 23:27979686-27979686 - tumor_4124542 COSM5947207 c.585T>A p.H195Q Substitution - Missense 23:27980750-27980750 - TCGA-FW-A3R5-06 COSM3913828 c.177C>T p.F59F Substitution - coding silent 23:27981158-27981158 - TCGA-ER-A3ET-06 COSM3560672 c.299G>T p.R100M Substitution - Missense 23:27981036-27981036 - ESCC-015T COSM3939930 c.842G>A p.R281H Substitution - Missense 23:27980493-27980493 - TCGA-26-5132 COSM2156947 c.667T>C p.W223R Substitution - Missense 23:27980668-27980668 - PT52 COSM5941128 c.39C>A p.D13E Substitution - Missense 23:27981296-27981296 - ccRCC-4 COSM1661378 c.187G>T p.A63S Substitution - Missense 23:27981148-27981148 - TCGA-FS-A1ZA-06 COSM3560665 c.559C>T p.R187C Substitution - Missense 23:27980776-27980776 - 49M COSM5590465 c.328G>A p.E110K Substitution - Missense 23:27981007-27981007 - YUDUTY COSM1467368 c.1006G>A p.G336R Substitution - Missense 23:27980329-27980329 - SNUH_G45_S1 COSM3681754 c.1194C>T p.Y398Y Substitution - coding silent 23:27980141-27980141 - 49M COSM5590466 c.1653C>T p.F551F Substitution - coding silent 23:27979682-27979682 - S01023 COSM5666881 c.627C>A p.T209T Substitution - coding silent 23:27980708-27980708 - TCGA-FR-A3YN-06 COSM3560674 c.73G>A p.E25K Substitution - Missense 23:27981262-27981262 - TCGA-B5-A0JY-01 COSM1119702 c.741C>A p.F247L Substitution - Missense 23:27980594-27980594 - 2492722 COSM5724414 c.5C>T p.S2F Substitution - Missense 23:27981330-27981330 - S00944 COSM316536 c.1490C>G p.A497G Substitution - Missense 23:27979845-27979845 - B65 COSM1756513 c.813T>C p.I271I Substitution - coding silent 23:27980522-27980522 - TCGA-CJ-6028-01 COSM457314 c.1762G>A p.E588K Substitution - Missense 23:27979573-27979573 - cSCCP6 COSM137259 c.184G>A p.D62N Substitution - Missense 23:27981151-27981151 - TCGA-DU-6400-01 COSM3973577 c.852G>T p.K284N Substitution - Missense 23:27980483-27980483 - 2492723 COSM5723294 c.1359C>T p.V453V Substitution - coding silent 23:27979976-27979976 - PT34 COSM5911107 c.184G>T p.D62Y Substitution - Missense 23:27981151-27981151 - TCGA-AD-5900-01 COSM1467367 c.1065T>C p.H355H Substitution - coding silent 23:27980270-27980270 - TCGA-BS-A0UV-01 COSM1119708 c.460C>T p.R154C Substitution - Missense 23:27980875-27980875 - T3658 COSM4676394 c.65G>A p.S22N Substitution - Missense 23:27981270-27981270 - TCGA-AA-3558-01 COSM292482 c.1490C>T p.A497V Substitution - Missense 23:27979845-27979845 - Pat_26_A COSM5877709 c.289G>A p.E97K Substitution - Missense 23:27981046-27981046 - HCC6T COSM1625809 c.814A>G p.N272D Substitution - Missense 23:27980521-27980521 - Pat_06_B COSM5877708 c.679C>T p.R227W Substitution - Missense 23:27980656-27980656 - TCGA-A8-A09X-01 COSM457314 c.1762G>A p.E588K Substitution - Missense 23:27979573-27979573 - 2951_CLM COSM5757522 c.200A>C p.N67T Substitution - Missense 23:27981135-27981135 - TCGA-D9-A6EA-06 COSM4398343 c.73G>C p.E25Q Substitution - Missense 23:27981262-27981262 - TCGA-EE-A2A2-06 COSM3560660 c.1386C>A p.V462V Substitution - coding silent 23:27979949-27979949 - 16461 COSM5616294 c.1002A>T p.K334N Substitution - Missense 23:27980333-27980333 - TCGA-13-0791-01 COSM81077 c.1287G>A p.K429K Substitution - coding silent 23:27980048-27980048 - C086 COSM1756512 c.1462G>A p.E488K Substitution - Missense 23:27979873-27979873 - 180 COSM3721417 c.1749C>T p.T583T Substitution - coding silent 23:27979586-27979586 - 2492720 COSM5723294 c.1359C>T p.V453V Substitution - coding silent 23:27979976-27979976 - YUMOOK COSM1714768 c.1660C>T p.H554Y Substitution - Missense 23:27979675-27979675 - TCGA-19-5954-01 COSM2156771 c.99G>A p.T33T Substitution - coding silent 23:27981236-27981236 - TCGA-BR-4184-01 COSM4108816 c.1620G>A p.T540T Substitution - coding silent 23:27979715-27979715 - VCB-PH-14T COSM4770725 c.514T>A p.F172I Substitution - Missense 23:27980821-27980821 - TCGA-AZ-4615-01 COSM3694524 c.526G>A p.A176T Substitution - Missense 23:27980809-27980809 - TCGA-EE-A2M6-06 COSM3560668 c.414G>A p.A138A Substitution - coding silent 23:27980921-27980921 - CLL144 COSM1292985 c.112G>T p.D38Y Substitution - Missense 23:27981223-27981223 - TCGA-FW-A3R5-06 COSM3913827 c.229G>A p.E77K Substitution - Missense 23:27981106-27981106 - TCGA-DD-A1EB-01 COSM4928867 c.936C>T p.F312F Substitution - coding silent 23:27980399-27980399 - GC1_T COSM150774 c.442T>C p.S148P Substitution - Missense 23:27980893-27980893 - PD4127a COSM160340 c.340G>A p.E114K Substitution - Missense 23:27980995-27980995 - 6115219 COSM1119707 c.554G>A p.R185H Substitution - Missense 23:27980781-27980781 - TCGA-AM-5821-01 COSM3759458 c.306G>A p.E102E Substitution - coding silent 23:27981029-27981029 - LUAD-E01317 COSM403886 c.927C>T p.A309A Substitution - coding silent 23:27980408-27980408 - QC2-22-T2 COSM5653119 c.767T>A p.L256Q Substitution - Missense 23:27980568-27980568 - ESO-874 COSM1249754 c.454C>T p.R152* Substitution - Nonsense 23:27980881-27980881 - YUDEXA COSM1714769 c.1030C>T p.P344S Substitution - Missense 23:27980305-27980305 - Pat_41_B COSM5877706 c.995A>G p.D332G Substitution - Missense 23:27980340-27980340 - TCGA-EE-A182-06 COSM3560662 c.1131G>A p.K377K Substitution - coding silent 23:27980204-27980204 - T473 COSM4676390 c.910_911delAC p.T304fs*3 Deletion - Frameshift 23:27980424-27980425 - S02244 COSM5678337 c.841C>A p.R281S Substitution - Missense 23:27980494-27980494 - TCGA-FP-A4BE-01 COSM4108823 c.767T>C p.L256P Substitution - Missense 23:27980568-27980568 - ESCC-069T COSM3939929 c.1462G>T p.E488* Substitution - Nonsense 23:27979873-27979873 - LAU165 COSM233760 c.295G>A p.E99K Substitution - Missense 23:27981040-27981040 - 8067800 COSM4388754 c.1203T>A p.D401E Substitution - Missense 23:27980132-27980132 - MO_1084 COSM5559520 c.1213C>T p.L405F Substitution - Missense 23:27980122-27980122 - YUTEPA COSM1714773 c.80C>T p.S27F Substitution - Missense 23:27981255-27981255 - BD72T COSM5513771 c.694C>T p.L232L Substitution - coding silent 23:27980641-27980641 - T207 COSM4676391 c.750C>T p.N250N Substitution - coding silent 23:27980585-27980585 - TCGA-26-5132-01 COSM2156947 c.667T>C p.W223R Substitution - Missense 23:27980668-27980668 - TCGA-06-6693-01 COSM3406257 c.144C>T p.T48T Substitution - coding silent 23:27981191-27981191 - TCGA-D1-A101-01 COSM1119709 c.78G>A p.Q26Q Substitution - coding silent 23:27981257-27981257 - 93T COSM109974 c.316G>A p.E106K Substitution - Missense 23:27981019-27981019 - C086 COSM227959 c.715G>A p.D239N Substitution - Missense 23:27980620-27980620 - WA16 COSM239524 c.952_953insA p.D319fs*14 Insertion - Frameshift 23:27980382-27980383 - B89-12-Tumor COSM4005068 c.125C>A p.A42E Substitution - Missense 23:27981210-27981210 - TCGA-CD-A4MG-01 COSM4108818 c.1345C>T p.R449W Substitution - Missense 23:27979990-27979990 - 2492720 COSM5724414 c.5C>T p.S2F Substitution - Missense 23:27981330-27981330 - PT23_1 COSM5903279 c.1022C>T p.S341F Substitution - Missense 23:27980313-27980313 - TCGA-AZ-4315-01 COSM1467368 c.1006G>A p.G336R Substitution - Missense 23:27980329-27980329 - TCGA-AA-3854-01 COSM295709 c.807A>T p.E269D Substitution - Missense 23:27980528-27980528 - 396 COSM4428895 c.1619C>G p.T540R Substitution - Missense 23:27979716-27979716 - Pat_26_B COSM5877709 c.289G>A p.E97K Substitution - Missense 23:27981046-27981046 - TCGA-61-2097-01 COSM70401 c.680G>C p.R227P Substitution - Missense 23:27980655-27980655 - DN11120 COSM5780057 c.1090C>A p.Q364K Substitution - Missense 23:27980245-27980245 - 12M COSM5577395 c.681G>A p.R227R Substitution - coding silent 23:27980654-27980654 - B105-0-Tumor COSM1756512 c.1462G>A p.E488K Substitution - Missense 23:27979873-27979873 - HCC6 COSM1625809 c.814A>G p.N272D Substitution - Missense 23:27980521-27980521 - TCGA-C5-A3HE-01 COSM4108818 c.1345C>T p.R449W Substitution - Missense 23:27979990-27979990 - 509LT COSM74329 c.1186G>A p.V396I Substitution - Missense 23:27980149-27980149 - TCGA-B6-A2IU-01 COSM3844421 c.183C>A p.N61K Substitution - Missense 23:27981152-27981152 - PD4958a COSM3844421 c.183C>A p.N61K Substitution - Missense 23:27981152-27981152 - TCGA-EJ-A65G-01 COSM457314 c.1762G>A p.E588K Substitution - Missense 23:27979573-27979573 - S00944 COSM316536 c.1490C>G p.A497G Substitution - Missense 23:27979845-27979845 - 0006_CRUK_PC_0006_T3_DNA COSM3849618 c.455G>A p.R152Q Substitution - Missense 23:27980880-27980880 - TCGA-D7-8573-01 COSM4108819 c.1314C>T p.D438D Substitution - coding silent 23:27980021-27980021 - TCGA-19-5954 COSM2156771 c.99G>A p.T33T Substitution - coding silent 23:27981236-27981236 - TCGA-BP-4964-01 COSM488282 c.1185C>T p.C395C Substitution - coding silent 23:27980150-27980150 - TCGA-GN-A266-06 COSM3560673 c.166G>A p.D56N Substitution - Missense 23:27981169-27981169 - 417 COSM4431790 c.1241T>C p.I414T Substitution - Missense 23:27980094-27980094 - LN229 COSM3037563 c.155G>A p.G52D Substitution - Missense 23:27981180-27981180 - TCGA-FW-A3R5-06 COSM3913825 c.1603G>A p.D535N Substitution - Missense 23:27979732-27979732 - S02255 COSM5681108 c.568T>C p.Y190H Substitution - Missense 23:27980767-27980767 - ESCC_135 COSM5642955 c.643G>A p.G215S Substitution - Missense 23:27980692-27980692 - 2492723 COSM5724414 c.5C>T p.S2F Substitution - Missense 23:27981330-27981330 - pfg016T COSM1644007 c.93G>A p.A31A Substitution - coding silent 23:27981242-27981242 - TCGA-EE-A181-06 COSM3560657 c.1768G>A p.E590K Substitution - Missense 23:27979567-27979567 - TCGA-22-1016-01 COSM756410 c.1656G>T p.V552V Substitution - coding silent 23:27979679-27979679 - ESCC_91 COSM5636986 c.1063C>T p.H355Y Substitution - Missense 23:27980272-27980272 - TCGA-HU-8604-01 COSM4108822 c.807A>G p.E269E Substitution - coding silent 23:27980528-27980528 - YURUS COSM184529 c.238G>A p.E80K Substitution - Missense 23:27981097-27981097 - TCGA-DA-A1IC-06 COSM227959 c.715G>A p.D239N Substitution - Missense 23:27980620-27980620 - B105-0 COSM1756512 c.1462G>A p.E488K Substitution - Missense 23:27979873-27979873 - TCGA-EB-A41A-01 COSM3560663 c.761C>T p.S254F Substitution - Missense 23:27980574-27980574 - 280-01-4TD COSM146102 c.815A>T p.N272I Substitution - Missense 23:27980520-27980520 - ME044T COSM184529 c.238G>A p.E80K Substitution - Missense 23:27981097-27981097 - RK073_C01 COSM1636493 c.484C>T p.R162C Substitution - Missense 23:27980851-27980851 - TCGA-66-2727-01 COSM756409 c.1654G>T p.V552L Substitution - Missense 23:27979681-27979681 - TCGA-AP-A0LN-01 COSM1119698 c.1360G>A p.V454M Substitution - Missense 23:27979975-27979975 - 041T COSM1729591 c.1589A>T p.Q530L Substitution - Missense 23:27979746-27979746 - TCGA-EE-A3J7-06 COSM184529 c.238G>A p.E80K Substitution - Missense 23:27981097-27981097 - TCGA-BR-8361-01 COSM4108825 c.647A>G p.D216G Substitution - Missense 23:27980688-27980688 - TCGA-FD-A3B3-01 COSM1315440 c.707G>T p.S236I Substitution - Missense 23:27980628-27980628 - CSCC-5-T COSM4542804 c.325G>A p.E109K Substitution - Missense 23:27981010-27981010 - TCGA-ER-A19Q-06 COSM160340 c.340G>A p.E114K Substitution - Missense 23:27980995-27980995 - TCGA-EB-A41A-01 COSM3913828 c.177C>T p.F59F Substitution - coding silent 23:27981158-27981158 - 2492721 COSM5723294 c.1359C>T p.V453V Substitution - coding silent 23:27979976-27979976 - TCGA-CG-4442-01 COSM4108826 c.249C>T p.S83S Substitution - coding silent 23:27981086-27981086 - 3844_T COSM3965094 c.1468C>A p.H490N Substitution - Missense 23:27979867-27979867 - C086 COSM5529586 c.1095G>A p.R365R Substitution - coding silent 23:27980240-27980240 - RK308_C01 COSM3747425 c.800T>C p.V267A Substitution - Missense 23:27980535-27980535 - TCGA-A2-A0EY-01 COSM457315 c.508G>T p.A170S Substitution - Missense 23:27980827-27980827 - KPOPBR-48-T COSM3406256 c.183C>T p.N61N Substitution - coding silent 23:27981152-27981152 - TCGA-FW-A3R5-06 COSM612161 c.1696G>A p.D566N Substitution - Missense 23:27979639-27979639 - TCGA-EB-A44P-01 COSM3560675 c.70G>A p.E24K Substitution - Missense 23:27981265-27981265 - 2293782 COSM4609521 c.1144C>A p.H382N Substitution - Missense 23:27980191-27980191 - TCGA-85-6560-01 COSM756402 c.358T>A p.C120S Substitution - Missense 23:27980977-27980977 - TCGA-AD-6889-01 COSM1467362 c.1302C>T p.H434H Substitution - coding silent 23:27980033-27980033 - TCGA-21-1070-01 COSM756406 c.1005C>A p.V335V Substitution - coding silent 23:27980330-27980330 - TCGA-B5-A0JR-01 COSM1119693 c.1657C>T p.R553C Substitution - Missense 23:27979678-27979678 - PT38 COSM137259 c.184G>A p.D62N Substitution - Missense 23:27981151-27981151 - TCGA-AR-A1AJ-01 COSM457316 c.428T>A p.I143N Substitution - Missense 23:27980907-27980907 - TCGA-39-5028-01 COSM756408 c.1125A>T p.V375V Substitution - coding silent 23:27980210-27980210 - 61 COSM5742226 c.490C>T p.R164W Substitution - Missense 23:27980845-27980845 - QC2-22-T2 COSM5653118 c.1376G>A p.C459Y Substitution - Missense 23:27979959-27979959 - TCGA-13-0920-01 COSM74329 c.1186G>A p.V396I Substitution - Missense 23:27980149-27980149 - TCGA-AP-A059-01 COSM1119694 c.1594C>T p.R532* Substitution - Nonsense 23:27979741-27979741 - TCGA-B5-A0JY-01 COSM1119695 c.1504G>T p.D502Y Substitution - Missense 23:27979831-27979831 - TCGA-ER-A2NC-06 COSM3560671 c.303G>A p.E101E Substitution - coding silent 23:27981032-27981032 - TCGA-AX-A05Z-01 COSM184529 c.238G>A p.E80K Substitution - Missense 23:27981097-27981097 - TCGA-AP-A0LM-01 COSM1119692 c.1736A>G p.E579G Substitution - Missense 23:27979599-27979599 - ME037T COSM227959 c.715G>A p.D239N Substitution - Missense 23:27980620-27980620 - REC-1 COSM1740815 c.92C>T p.A31V Substitution - Missense 23:27981243-27981243 - UM-SCC-17B COSM4598585 c.34C>A p.P12T Substitution - Missense 23:27981301-27981301 - TCGA-BS-A0UV-01 COSM1119700 c.1111G>T p.E371* Substitution - Nonsense 23:27980224-27980224 - TCGA-FS-A1ZK-06 COSM3560669 c.329A>T p.E110V Substitution - Missense 23:27981006-27981006 - D28 COSM5544802 c.1304G>A p.R435K Substitution - Missense 23:27980031-27980031 - LUAD-B02594 COSM356533 c.751T>A p.C251S Substitution - Missense 23:27980584-27980584 - TCGA-AP-A0LE-01 COSM1119704 c.725T>G p.V242G Substitution - Missense 23:27980610-27980610 - TCGA-BS-A0UL-01 COSM1119701 c.954_955insA p.D319fs*14 Insertion - Frameshift 23:27980380-27980381 - TCGA-EM-A4FM-01 COSM3372233 c.662T>C p.I221T Substitution - Missense 23:27980673-27980673 - TCGA-BL-A0C8-01 COSM422599 c.321G>A p.M107I Substitution - Missense 23:27981014-27981014 - pfg212T COSM4751727 c.100G>A p.A34T Substitution - Missense 23:27981235-27981235 - U343 COSM5712987 c.418G>A p.E140K Substitution - Missense 23:27980917-27980917 - TCGA-21-1070-01 COSM756403 c.603C>A p.T201T Substitution - coding silent 23:27980732-27980732 - In-6 COSM144806 c.877G>A p.A293T Substitution - Missense 23:27980458-27980458 - RK034_C COSM1636492 c.1649T>C p.F550S Substitution - Missense 23:27979686-27979686 - PT29 COSM184529 c.238G>A p.E80K Substitution - Missense 23:27981097-27981097 - TCGA-AA-A00K-01 COSM298539 c.1327G>C p.V443L Substitution - Missense 23:27980008-27980008 - S00035 COSM5656955 c.735T>A p.A245A Substitution - coding silent 23:27980600-27980600 - TCGA-B5-A11X-01 COSM1119696 c.1420C>T p.Q474* Substitution - Nonsense 23:27979915-27979915 - TCGA-FS-A1ZK-06 COSM3560664 c.741C>T p.F247F Substitution - coding silent 23:27980594-27980594 - TCGA-D1-A15X-01 COSM1119703 c.726C>T p.V242V Substitution - coding silent 23:27980609-27980609 - PT50 COSM1467360 c.1780C>T p.R594* Substitution - Nonsense 23:27979555-27979555 - TCGA-74-6584-01 COSM3406256 c.183C>T p.N61N Substitution - coding silent 23:27981152-27981152 - YUZEST COSM184529 c.238G>A p.E80K Substitution - Missense 23:27981097-27981097 - 1N05-VS-1T05 COSM4972932 c.1658G>A p.R553H Substitution - Missense 23:27979677-27979677 - TCGA-GN-A266-06 COSM3560659 c.1409C>T p.S470F Substitution - Missense 23:27979926-27979926 - ESCC_BICR_025T COSM5434488 c.1733A>G p.D578G Substitution - Missense 23:27979602-27979602 - 2492722 COSM5723294 c.1359C>T p.V453V Substitution - coding silent 23:27979976-27979976 - TCGA-E9-A1N4-01 COSM1490820 c.371G>T p.G124V Substitution - Missense 23:27980964-27980964 - LUAD-F00162 COSM366752 c.1384G>T p.V462F Substitution - Missense 23:27979951-27979951 - T2939 COSM4676392 c.166G>C p.D56H Substitution - Missense 23:27981169-27981169 - 1517_CLM COSM5757521 c.1528C>T p.P510S Substitution - Missense 23:27979807-27979807 - TCGA-EE-A180-06 COSM3560658 c.1419C>T p.I473I Substitution - coding silent 23:27979916-27979916 - CRC-02T COSM5455873 c.102G>A p.A34A Substitution - coding silent 23:27981233-27981233 - TCGA-IH-A3EA-01 COSM3560661 c.1347G>A p.R449R Substitution - coding silent 23:27979988-27979988 - SJHGG011_D COSM4969123 c.221G>T p.S74I Substitution - Missense 23:27981114-27981114 - B65-Tumor COSM1756513 c.813T>C p.I271I Substitution - coding silent 23:27980522-27980522 - 2492721 COSM5724414 c.5C>T p.S2F Substitution - Missense 23:27981330-27981330 - CSCC-5-T COSM4499513 c.543C>T p.T181T Substitution - coding silent 23:27980792-27980792 - 509T COSM74329 c.1186G>A p.V396I Substitution - Missense 23:27980149-27980149 - PD14465a COSM5786998 c.1675G>T p.A559S Substitution - Missense 23:27979660-27979660 - TCGA-B5-A0JY-01 COSM184529 c.238G>A p.E80K Substitution - Missense 23:27981097-27981097 - SA212 COSM213910 c.862C>G p.P288A Substitution - Missense 23:27980473-27980473 - TCGA-AN-A046-01 COSM3844420 c.313G>T p.E105* Substitution - Nonsense 23:27981022-27981022 - 331 COSM3721416 c.45G>T p.V15V Substitution - coding silent 23:27981290-27981290 - TCGA-DA-A1HV-06 COSM137259 c.184G>A p.D62N Substitution - Missense 23:27981151-27981151 - YUSPO COSM5412509 c.1394G>T p.W465L Substitution - Missense 23:27979941-27979941 - TCGA-UC-A7PF-01 COSM4829932 c.1248C>T p.L416L Substitution - coding silent 23:27980087-27980087 - C0055T COSM4154931 c.410A>T p.Q137L Substitution - Missense 23:27980925-27980925 - TCGA-DM-A0X9-01 COSM1467369 c.784G>C p.D262H Substitution - Missense 23:27980551-27980551 - TCGA-BR-4368-01 COSM4108824 c.691G>A p.V231I Substitution - Missense 23:27980644-27980644 - TCGA-BR-6566-01 COSM4108817 c.1436A>G p.D479G Substitution - Missense 23:27979899-27979899 - 280 COSM146102 c.815A>T p.N272I Substitution - Missense 23:27980520-27980520 - TCGA-CA-6717-01 COSM1467371 c.352C>T p.R118W Substitution - Missense 23:27980983-27980983 - TCGA-G3-A7M5-01 COSM4941910 c.163A>T p.R55W Substitution - Missense 23:27981172-27981172 - TCGA-BR-8081-01 COSM4108827 c.235G>A p.V79I Substitution - Missense 23:27981100-27981100 - YUAKER COSM1714771 c.503C>T p.S168L Substitution - Missense 23:27980832-27980832 - TCGA-ER-A2NC-06 COSM3560670 c.305A>G p.E102G Substitution - Missense 23:27981030-27981030 - TCGA-AA-3672-01 COSM266345 c.462C>A p.R154R Substitution - coding silent 23:27980873-27980873 - TCGA-AX-A0J1-01 COSM1119705 c.651C>T p.D217D Substitution - coding silent 23:27980684-27980684 - TCGA-EE-A29D-06 COSM3560667 c.448C>T p.L150L Substitution - coding silent 23:27980887-27980887 - HCC130T COSM1625808 c.1634A>G p.N545S Substitution - Missense 23:27979701-27979701 - TCGA-EE-A2MS-06 COSM3560666 c.471C>T p.V157V Substitution - coding silent 23:27980864-27980864 - TCGA-BS-A0UV-01 COSM1119697 c.1364G>A p.S455N Substitution - Missense 23:27979971-27979971 - YUOTHO COSM5412510 c.533_534GG>AA p.G178E Substitution - Missense 23:27980801-27980802 - TCGA-39-5030-01 COSM756404 c.866C>T p.A289V Substitution - Missense 23:27980469-27980469 - sysucc-834T COSM184529 c.238G>A p.E80K Substitution - Missense 23:27981097-27981097 - RK267_C01 COSM4946379 c.1069C>T p.Q357* Substitution - Nonsense 23:27980266-27980266 - TCGA-EE-A29D-06 COSM1467360 c.1780C>T p.R594* Substitution - Nonsense 23:27979555-27979555 - YULAN COSM1714770 c.985A>T p.R329* Substitution - Nonsense 23:27980350-27980350 - TCGA-BR-4201-01 COSM4108815 c.1654G>A p.V552M Substitution - Missense 23:27979681-27979681 - PT25 COSM184529 c.238G>A p.E80K Substitution - Missense 23:27981097-27981097 - S01297 COSM5667865 c.985A>G p.R329G Substitution - Missense 23:27980350-27980350 - TCGA-BR-4368-01 COSM4108821 c.827G>A p.C276Y Substitution - Missense 23:27980508-27980508 - CSCC-62-T COSM4559261 c.798G>A p.R266R Substitution - coding silent 23:27980537-27980537 - TCGA-BR-8078-01 COSM4108828 c.128C>T p.A43V Substitution - Missense 23:27981207-27981207 - PT23_1 COSM5903280 c.674G>T p.W225L Substitution - Missense 23:27980661-27980661 - T2458 COSM4676393 c.80C>A p.S27Y Substitution - Missense 23:27981255-27981255 - TCGA-A1-A0SQ-01 COSM1490819 c.936C>G p.F312L Substitution - Missense 23:27980399-27980399 - PTC-14C COSM4156785 c.1092G>T p.Q364H Substitution - Missense 23:27980243-27980243 - TCGA-43-6647-01 COSM756401 c.178C>A p.L60M Substitution - Missense 23:27981157-27981157 - D28 COSM137259 c.184G>A p.D62N Substitution - Missense 23:27981151-27981151 - 2951_PT COSM5757522 c.200A>C p.N67T Substitution - Missense 23:27981135-27981135 - TCGA-18-3416-01 COSM756405 c.931G>T p.V311L Substitution - Missense 23:27980404-27980404 - PD13602a COSM5780057 c.1090C>A p.Q364K Substitution - Missense 23:27980245-27980245 - LUAD-S01409 COSM388223 c.633G>A p.L211L Substitution - coding silent 23:27980702-27980702 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.447365 Xp21.3

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C Missense p.V242G c.725T>G X 27998727 UCEC A G Missense p.F550S c.1649T>C X 27997803 HC A G Missense p.W223R c.667T>C X 27998785 GBM A G Synonymous p.N437N c.1311T>C X 27998141 STAD A G Synonymous p.S420S c.1260T>C X 27998192 MB A T Missense p.C120S c.358T>A X 27999094 LUSC A T Missense p.I143N c.428T>A X 27999024 BRCA C A Missense p.A170S c.508G>T X 27998944 BRCA C A Missense p.D136Y c.406G>T X 27999046 LUAD C A Missense p.D38Y c.112G>T X 27999340 CLL C A Missense p.D541Y c.1621G>T X 27997831 LUAD C A Missense p.E291D c.873G>T X 27998579 LUAD C A Missense p.E477D c.1431G>T X 27998021 LUAD C A Missense p.G124V c.371G>T X 27999081 BRCA C A Missense p.K284N c.852G>T X 27998600 LGG C A Missense p.R100M c.299G>T X 27999153 CM C A Missense p.S236I c.707G>T X 27998745 BLCA C A Missense p.V311L c.931G>T X 27998521 LUSC C A Missense p.V552L c.1654G>T X 27997798 LUSC C A Nonsense p.E96* c.286G>T X 27999166 LUAD C A Synonymous p.L337L c.1011G>T X 27998441 LUAD C A Synonymous p.V552V c.1656G>T X 27997796 LUSC CG - Frameshift p.A497Dfs*16 c.1490_1491delCG X 27997961 LUAD C G Missense p.R227P c.680G>C X 27998772 OV C G Missense p.V443L c.1327G>C X 27998125 COREAD C G Synonymous p.S47S c.141G>C X 27999311 HNSC C T 3-UTRSNV . c.1800+779G>A X 27996873 CM C T Missense p.C276Y c.827G>A X 27998625 STAD C T Missense p.D239N c.715G>A X 27998737 CM C T Missense p.D566N c.1696G>A X 27997756 LUAD C T Missense p.D62N c.184G>A X 27999268 CM C T Missense p.E114K c.340G>A X 27999112 BRCA C T Missense p.E114K c.340G>A X 27999112 CM C T Missense p.E466K c.1396G>A X 27998056 CM C T Missense p.E588K c.1762G>A X 27997690 BRCA C T Missense p.E588K c.1762G>A X 27997690 PRAD C T Missense p.E588K c.1762G>A X 27997690 RCCC C T Missense p.E590K c.1768G>A X 27997684 CM C T Missense p.E80K c.238G>A X 27999214 CM C T Missense p.R266Q c.797G>A X 27998655 HNSC C T Missense p.V231I c.691G>A X 27998761 STAD C T Missense p.V396I c.1186G>A X 27998266 OV C T Missense p.V454M c.1360G>A X 27998092 UCEC C T Missense p.V552M c.1654G>A X 27997798 STAD C T Synonymous p.A138A c.414G>A X 27999038 CM C T Synonymous p.A31A c.93G>A X 27999359 STAD C T Synonymous p.E101E c.303G>A X 27999149 CM C T Synonymous p.K377K c.1131G>A X 27998321 CM C T Synonymous p.K429K c.1287G>A X 27998165 OV C T Synonymous p.R365R c.1095G>A X 27998357 CM C T Synonymous p.R449R c.1347G>A X 27998105 CM C T Synonymous p.T33T c.99G>A X 27999353 GBM G A 3-UTRSNV . c.1800+563C>T X 27997089 ESCA G A 5-UTRSNV . c.1-36C>T X 27999487 CM G A Missense p.A289V c.866C>T X 27998586 LUSC G A Missense p.A497V c.1490C>T X 27997962 COREAD G A Missense p.R154C c.460C>T X 27998992 STAD G A Missense p.R162C c.484C>T X 27998968 CM G A Missense p.R187C c.559C>T X 27998893 CM G A Missense p.R553C c.1657C>T X 27997795 UCEC G A Missense p.S323L c.968C>T X 27998484 STAD G A Missense p.S470F c.1409C>T X 27998043 LUAD G A Nonsense p.Q426* c.1276C>T X 27998176 CM G A Nonsense p.Q474* c.1420C>T X 27998032 UCEC G A Nonsense p.R122* c.364C>T X 27999088 LGG G A Nonsense p.R152* c.454C>T X 27998998 ESCA G A Synonymous p.C395C c.1185C>T X 27998267 RCCC G A Synonymous p.F247F c.741C>T X 27998711 CM G A Synonymous p.G125G c.375C>T X 27999077 BRCA G A Synonymous p.I473I c.1419C>T X 27998033 CM G A Synonymous p.N61N c.183C>T X 27999269 GBM G A Synonymous p.S2S c.6C>T X 27999446 CM G A Synonymous p.S587S c.1761C>T X 27997691 CM G A Synonymous p.T48T c.144C>T X 27999308 GBM G A Synonymous p.V157V c.471C>T X 27998981 CM G A Synonymous p.V505V c.1515C>T X 27997937 CM G C Missense p.A497G c.1490C>G X 27997962 SCLC G C Missense p.C395W c.1185C>G X 27998267 HNSC G C Missense p.F312L c.936C>G X 27998516 BRCA G C Missense p.P288A c.862C>G X 27998590 BRCA G C Missense p.R152G c.454C>G X 27998998 HNSC G C Synonymous p.V335V c.1005C>G X 27998447 GBM GG TT MultiAAMissense p.F302_L303delinsLI c.906_907delinsAA X 27998545 LUAD G T 5-UTRSNV . c.1-106C>A X 27999557 NB G T Missense p.A34E c.101C>A X 27999351 LUAD G T Missense p.H3N c.7C>A X 27999445 SCLC G T Missense p.L150M c.448C>A X 27999004 LUAD G T Missense p.L60M c.178C>A X 27999274 LUSC G T Missense p.T583N c.1748C>A X 27997704 BRCA G T Synonymous p.I473I c.1419C>A X 27998033 LUAD G T Synonymous p.R449R c.1345C>A X 27998107 LUAD G T Synonymous p.R594R c.1780C>A X 27997672 LUAD G T Synonymous p.T201T c.603C>A X 27998849 LUSC G T Synonymous p.V335V c.1005C>A X 27998447 LUSC G T Synonymous p.V462V c.1386C>A X 27998066 CM T A 3-UTRSNV . c.1800+643A>T X 27997009 CLL T A Missense p.E110V c.329A>T X 27999123 CM T A Missense p.E269D c.807A>T X 27998645 COREAD T A Missense p.K334N c.1002A>T X 27998450 NSCLC T A Missense p.K432M c.1295A>T X 27998157 COREAD T A Missense p.N272I c.815A>T X 27998637 CLL T A Nonsense p.R565* c.1693A>T X 27997759 LUAD T A Synonymous p.V375V c.1125A>T X 27998327 LUSC T C Missense p.E102G c.305A>G X 27999147 CM T C Missense p.E371G c.1112A>G X 27998340 LUSC - T Frameshift p.D319Rfs*14 c.954dupA X 27998498 UCEC