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 125685583 125685583 + Missense_Mutation SNP C C T TCGA-P6-A5OH-01A-11D-A30A-10 TCGA-P6-A5OH-11A-01D-A30A-10 g.chrX:125685583C>T c.1009G>A c.(1009-1011)Gac>Aac p.D337N ACC 23 125685622 125685622 + Missense_Mutation SNP C C T TCGA-P6-A5OH-01A-11D-A30A-10 TCGA-P6-A5OH-11A-01D-A30A-10 g.chrX:125685622C>T c.970G>A c.(970-972)Ggc>Agc p.G324S ACC 23 125686226 125686226 + Silent SNP C C G TCGA-OR-A5KB-01A-11D-A30A-10 TCGA-OR-A5KB-11A-11D-A30A-10 g.chrX:125686226C>G c.366G>C c.(364-366)gtG>gtC p.V122V BLCA 23 125685222 125685222 + Missense_Mutation SNP T T G TCGA-BT-A20W-01A-21D-A14W-08 TCGA-BT-A20W-11A-11D-A14W-08 g.chrX:125685222T>G c.1370A>C c.(1369-1371)aAc>aCc p.N457T BLCA 23 125685668 125685668 + Missense_Mutation SNP A A T TCGA-YF-AA3L-01A-11D-A38G-08 TCGA-YF-AA3L-10A-01D-A38J-08 g.chrX:125685668A>T c.924T>A c.(922-924)gaT>gaA p.D308E BLCA 23 125685766 125685766 + Nonsense_Mutation SNP C C A TCGA-G2-A2EJ-01A-11D-A17V-08 TCGA-G2-A2EJ-10A-01D-A17V-08 g.chrX:125685766C>A c.826G>T c.(826-828)Gaa>Taa p.E276* BLCA 23 125685907 125685907 + Missense_Mutation SNP C C T TCGA-K4-A3WU-01B-11D-A23M-08 TCGA-K4-A3WU-10A-01D-A23K-08 g.chrX:125685907C>T c.685G>A c.(685-687)Gac>Aac p.D229N BLCA 23 125685911 125685911 + Silent SNP G G A TCGA-FD-A6TI-01A-11D-A32B-08 TCGA-FD-A6TI-10A-01D-A329-08 g.chrX:125685911G>A c.681C>T c.(679-681)ttC>ttT p.F227F BLCA 23 125685954 125685954 + Missense_Mutation SNP C C T TCGA-DK-AA71-01A-31D-A391-08 TCGA-DK-AA71-10A-01D-A394-08 g.chrX:125685954C>T c.638G>A c.(637-639)cGc>cAc p.R213H BLCA 23 125686235 125686235 + Silent SNP C C T TCGA-LT-A5Z6-01A-11D-A289-08 TCGA-LT-A5Z6-10A-01D-A289-08 g.chrX:125686235C>T c.357G>A c.(355-357)acG>acA p.T119T BLCA 23 125686243 125686243 + Missense_Mutation SNP A A G TCGA-YC-A9TC-01A-22D-A391-08 TCGA-YC-A9TC-10A-01D-A394-08 g.chrX:125686243A>G c.349T>C c.(349-351)Tgt>Cgt p.C117R BLCA 23 125686323 125686323 + Missense_Mutation SNP C C T TCGA-DK-A1AD-01A-11D-A13W-08 TCGA-DK-A1AD-10A-01D-A13W-08 g.chrX:125686323C>T c.269G>A c.(268-270)cGc>cAc p.R90H BLCA 23 125686427 125686427 + Silent SNP C C G TCGA-ZF-A9R7-01A-11D-A38G-08 TCGA-ZF-A9R7-10A-01D-A38J-08 g.chrX:125686427C>G c.165G>C c.(163-165)ctG>ctC p.L55L BLCA 23 125686549 125686549 + Missense_Mutation SNP C C T TCGA-BL-A0C8-01A-11D-A10S-08 TCGA-BL-A0C8-10A-01D-A10S-08 g.chrX:125686549C>T c.43G>A c.(43-45)Gcg>Acg p.A15T BLCA 23 125686553 125686553 + Silent SNP C C T TCGA-KQ-A41R-01A-21D-A34U-08 TCGA-KQ-A41R-10G-01D-A34X-08 g.chrX:125686553C>T c.39G>A c.(37-39)gcG>gcA p.A13A BRCA 23 125685470 125685470 + Missense_Mutation SNP G G C TCGA-AR-A0TX-01A-11D-A099-09 TCGA-AR-A0TX-10A-01D-A099-09 g.chrX:125685470G>C c.1122C>G c.(1120-1122)ttC>ttG p.F374L BRCA 23 125685532 125685532 + Missense_Mutation SNP G G A TCGA-A2-A0EU-01A-22W-A071-09 TCGA-A2-A0EU-10A-01W-A071-09 g.chrX:125685532G>A c.1060C>T c.(1060-1062)Cgg>Tgg p.R354W BRCA 23 125685656 125685656 + Silent SNP C C G TCGA-A8-A09W-01A-11W-A019-09 TCGA-A8-A09W-10A-01W-A021-09 g.chrX:125685656C>G c.936G>C c.(934-936)ctG>ctC p.L312L BRCA 23 125685704 125685704 + Silent SNP G G T TCGA-BH-A0B4-01A-11W-A019-09 TCGA-BH-A0B4-10A-01W-A021-09 g.chrX:125685704G>T c.888C>A c.(886-888)tcC>tcA p.S296S BRCA 23 125685742 125685742 + Missense_Mutation SNP C C T TCGA-A8-A06X-01A-21W-A019-09 TCGA-A8-A06X-10A-01W-A021-09 g.chrX:125685742C>T c.850G>A c.(850-852)Ggc>Agc p.G284S BRCA 23 125685957 125685957 + Missense_Mutation SNP G G A TCGA-BH-A0B6-01A-11D-A19Y-09 TCGA-BH-A0B6-10A-01D-A19Y-09 g.chrX:125685957G>A c.635C>T c.(634-636)tCc>tTc p.S212F BRCA 23 125686114 125686114 + Missense_Mutation SNP A A C TCGA-BH-A28Q-01A-11D-A16D-09 TCGA-BH-A28Q-10A-01D-A16D-09 g.chrX:125686114A>C c.478T>G c.(478-480)Tcc>Gcc p.S160A BRCA 23 125686220 125686220 + Silent SNP G G A TCGA-C8-A12K-01A-21D-A10Y-09 TCGA-C8-A12K-10A-01D-A110-09 g.chrX:125686220G>A c.372C>T c.(370-372)gaC>gaT p.D124D CESC 23 125685755 125685755 + Silent SNP C C A TCGA-DS-A0VN-01A-21D-A10S-08 TCGA-DS-A0VN-10A-01D-A10S-08 g.chrX:125685755C>A c.837G>T c.(835-837)gcG>gcT p.A279A CESC 23 125685980 125685980 + Missense_Mutation SNP A A T TCGA-EK-A2H0-01A-11D-A17W-09 TCGA-EK-A2H0-10A-01D-A17W-09 g.chrX:125685980A>T c.612T>A c.(610-612)agT>agA p.S204R CESC 23 125686155 125686155 + Missense_Mutation SNP T T C TCGA-EA-A5ZD-01A-11D-A28B-09 TCGA-EA-A5ZD-10A-01D-A28E-09 g.chrX:125686155T>C c.437A>G c.(436-438)gAc>gGc p.D146G COAD 23 125685313 125685313 + Missense_Mutation SNP A A T TCGA-AA-3514-01A-02W-0831-10 TCGA-AA-3514-10A-01W-0831-10 g.chrX:125685313A>T c.1279T>A c.(1279-1281)Ttt>Att p.F427I COAD 23 125685347 125685347 + Silent SNP A A G TCGA-G4-6310-01A-11D-1719-10 TCGA-G4-6310-10A-01D-1720-10 g.chrX:125685347A>G c.1245T>C c.(1243-1245)gaT>gaC p.D415D COAD 23 125685439 125685439 + Missense_Mutation SNP C C T TCGA-AA-3833-01A-01W-0900-09 TCGA-AA-3833-10A-01W-0900-09 g.chrX:125685439C>T c.1153G>A c.(1153-1155)Gaa>Aaa p.E385K COAD 23 125685532 125685532 + Missense_Mutation SNP G G A TCGA-CK-5913-01A-11D-1650-10 TCGA-CK-5913-10A-01D-1650-10 g.chrX:125685532G>A c.1060C>T c.(1060-1062)Cgg>Tgg p.R354W COAD 23 125685629 125685629 + Silent SNP G G A TCGA-AA-A01D-01A-01W-A00E-09 TCGA-AA-A01D-10A-01W-A00E-09 g.chrX:125685629G>A c.963C>T c.(961-963)taC>taT p.Y321Y COAD 23 125685700 125685700 + Missense_Mutation SNP G G T TCGA-AA-3697-01A-01D-1719-10 TCGA-AA-3697-11A-01D-1719-10 g.chrX:125685700G>T c.892C>A c.(892-894)Ctg>Atg p.L298M COAD 23 125685751 125685751 + Missense_Mutation SNP A A G TCGA-CM-5868-01A-01D-1650-10 TCGA-CM-5868-10A-01D-1650-10 g.chrX:125685751A>G c.841T>C c.(841-843)Tcc>Ccc p.S281P COAD 23 125685785 125685785 + Silent SNP G G T TCGA-AA-3950-01A-02W-0995-10 TCGA-AA-3950-10A-01W-0995-10 g.chrX:125685785G>T c.807C>A c.(805-807)gcC>gcA p.A269A COAD 23 125685911 125685911 + Silent SNP G G A TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chrX:125685911G>A c.681C>T c.(679-681)ttC>ttT p.F227F COAD 23 125685947 125685947 + Silent SNP G G A TCGA-A6-5665-01A-01D-1650-10 TCGA-A6-5665-10A-01D-1650-10 g.chrX:125685947G>A c.645C>T c.(643-645)ggC>ggT p.G215G COAD 23 125685953 125685953 + Silent SNP G G A TCGA-CM-4752-01A-01D-1408-10 TCGA-CM-4752-10A-01D-1408-10 g.chrX:125685953G>A c.639C>T c.(637-639)cgC>cgT p.R213R COAD 23 125686040 125686040 + Silent SNP G G T TCGA-AY-6196-01A-11D-1719-10 TCGA-AY-6196-10A-01D-1719-10 g.chrX:125686040G>T c.552C>A c.(550-552)ccC>ccA p.P184P COAD 23 125686183 125686183 + Missense_Mutation SNP G G A TCGA-A6-2676-01A-01W-0833-10 TCGA-A6-2676-10A-01W-0833-10 g.chrX:125686183G>A c.409C>T c.(409-411)Cgg>Tgg p.R137W COAD 23 125686197 125686197 + Missense_Mutation SNP C C T TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chrX:125686197C>T c.395G>A c.(394-396)cGc>cAc p.R132H COAD 23 125686237 125686237 + Missense_Mutation SNP T T C TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chrX:125686237T>C c.355A>G c.(355-357)Acg>Gcg p.T119A COAD 23 125686354 125686354 + Missense_Mutation SNP C C A TCGA-G4-6309-01A-21D-1835-10 TCGA-G4-6309-10A-01D-1835-10 g.chrX:125686354C>A c.238G>T c.(238-240)Gta>Tta p.V80L COAD 23 125686560 125686560 + Missense_Mutation SNP C C T TCGA-AA-3986-01A-02W-0995-10 TCGA-AA-3986-10A-01W-0999-10 g.chrX:125686560C>T c.32G>A c.(31-33)cGg>cAg p.R11Q COADREAD 23 125685313 125685313 + Missense_Mutation SNP A A T TCGA-AA-3514-01A-02W-0831-10 TCGA-AA-3514-10A-01W-0831-10 g.chrX:125685313A>T c.1279T>A c.(1279-1281)Ttt>Att p.F427I COADREAD 23 125685347 125685347 + Silent SNP A A G TCGA-G4-6310-01A-11D-1719-10 TCGA-G4-6310-10A-01D-1720-10 g.chrX:125685347A>G c.1245T>C c.(1243-1245)gaT>gaC p.D415D COADREAD 23 125685439 125685439 + Missense_Mutation SNP C C T TCGA-AA-3833-01A-01W-0900-09 TCGA-AA-3833-10A-01W-0900-09 g.chrX:125685439C>T c.1153G>A c.(1153-1155)Gaa>Aaa p.E385K COADREAD 23 125685532 125685532 + Missense_Mutation SNP G G A TCGA-CK-5913-01A-11D-1650-10 TCGA-CK-5913-10A-01D-1650-10 g.chrX:125685532G>A c.1060C>T c.(1060-1062)Cgg>Tgg p.R354W COADREAD 23 125685629 125685629 + Silent SNP G G A TCGA-AA-A01D-01A-01W-A00E-09 TCGA-AA-A01D-10A-01W-A00E-09 g.chrX:125685629G>A c.963C>T c.(961-963)taC>taT p.Y321Y COADREAD 23 125685700 125685700 + Missense_Mutation SNP G G T TCGA-AA-3697-01A-01D-1719-10 TCGA-AA-3697-11A-01D-1719-10 g.chrX:125685700G>T c.892C>A c.(892-894)Ctg>Atg p.L298M COADREAD 23 125685751 125685751 + Missense_Mutation SNP A A G TCGA-CM-5868-01A-01D-1650-10 TCGA-CM-5868-10A-01D-1650-10 g.chrX:125685751A>G c.841T>C c.(841-843)Tcc>Ccc p.S281P COADREAD 23 125685785 125685785 + Silent SNP G G T TCGA-AA-3950-01A-02W-0995-10 TCGA-AA-3950-10A-01W-0995-10 g.chrX:125685785G>T c.807C>A c.(805-807)gcC>gcA p.A269A COADREAD 23 125685911 125685911 + Silent SNP G G A TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chrX:125685911G>A c.681C>T c.(679-681)ttC>ttT p.F227F COADREAD 23 125685947 125685947 + Silent SNP G G A TCGA-A6-5665-01A-01D-1650-10 TCGA-A6-5665-10A-01D-1650-10 g.chrX:125685947G>A c.645C>T c.(643-645)ggC>ggT p.G215G COADREAD 23 125685953 125685953 + Silent SNP G G A TCGA-CM-4752-01A-01D-1408-10 TCGA-CM-4752-10A-01D-1408-10 g.chrX:125685953G>A c.639C>T c.(637-639)cgC>cgT p.R213R COADREAD 23 125686040 125686040 + Silent SNP G G T TCGA-AY-6196-01A-11D-1719-10 TCGA-AY-6196-10A-01D-1719-10 g.chrX:125686040G>T c.552C>A c.(550-552)ccC>ccA p.P184P COADREAD 23 125686183 125686183 + Missense_Mutation SNP G G A TCGA-A6-2676-01A-01W-0833-10 TCGA-A6-2676-10A-01W-0833-10 g.chrX:125686183G>A c.409C>T c.(409-411)Cgg>Tgg p.R137W COADREAD 23 125686197 125686197 + Missense_Mutation SNP C C T TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chrX:125686197C>T c.395G>A c.(394-396)cGc>cAc p.R132H COADREAD 23 125686237 125686237 + Missense_Mutation SNP T T C TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chrX:125686237T>C c.355A>G c.(355-357)Acg>Gcg p.T119A COADREAD 23 125686354 125686354 + Missense_Mutation SNP C C A TCGA-G4-6309-01A-21D-1835-10 TCGA-G4-6309-10A-01D-1835-10 g.chrX:125686354C>A c.238G>T c.(238-240)Gta>Tta p.V80L COADREAD 23 125686560 125686560 + Missense_Mutation SNP C C T TCGA-AA-3986-01A-02W-0995-10 TCGA-AA-3986-10A-01W-0999-10 g.chrX:125686560C>T c.32G>A c.(31-33)cGg>cAg p.R11Q ESCA 23 125685222 125685222 + Missense_Mutation SNP T T C TCGA-VR-AA7I-01A-11D-A403-09 TCGA-VR-AA7I-10A-01D-A403-09 g.chrX:125685222T>C c.1370A>G c.(1369-1371)aAc>aGc p.N457S ESCA 23 125685285 125685285 + Missense_Mutation SNP T T G TCGA-X8-AAAR-01A-11D-A403-09 TCGA-X8-AAAR-10A-01D-A403-09 g.chrX:125685285T>G c.1307A>C c.(1306-1308)tAc>tCc p.Y436S ESCA 23 125685531 125685531 + Missense_Mutation SNP C C T TCGA-VR-AA7B-01A-31D-A403-09 TCGA-VR-AA7B-10A-01D-A403-09 g.chrX:125685531C>T c.1061G>A c.(1060-1062)cGg>cAg p.R354Q ESCA 23 125685850 125685850 + Missense_Mutation SNP T T C TCGA-2H-A9GL-01A-12D-A37C-09 TCGA-2H-A9GL-11A-11D-A37F-09 g.chrX:125685850T>C c.742A>G c.(742-744)Agg>Ggg p.R248G ESCA 23 125685869 125685869 + Silent SNP T T C TCGA-VR-A8EP-01A-31D-A403-09 TCGA-VR-A8EP-10B-01D-A403-09 g.chrX:125685869T>C c.723A>G c.(721-723)gtA>gtG p.V241V ESCA 23 125685998 125685998 + Silent SNP G G A TCGA-VR-AA7D-01A-11D-A403-09 TCGA-VR-AA7D-10A-01D-A403-09 g.chrX:125685998G>A c.594C>T c.(592-594)ttC>ttT p.F198F ESCA 23 125686171 125686171 + Missense_Mutation SNP C C A TCGA-R6-A8W8-01B-11D-A37C-09 TCGA-R6-A8W8-10A-01D-A37F-09 g.chrX:125686171C>A c.421G>T c.(421-423)Gcc>Tcc p.A141S ESCA 23 125686220 125686220 + Silent SNP G G A TCGA-L5-A4OI-01A-11D-A27G-09 TCGA-L5-A4OI-11A-11D-A27G-09 g.chrX:125686220G>A c.372C>T c.(370-372)gaC>gaT p.D124D GBM 23 125685359 125685359 + Silent SNP G G A TCGA-32-1979-01A-01D-1696-08 TCGA-32-1979-10A-01D-1696-08 g.chrX:125685359G>A c.1233C>T c.(1231-1233)ctC>ctT p.L411L GBM 23 125685564 125685564 + Missense_Mutation SNP G G A TCGA-76-6283-01A-11D-1845-08 TCGA-76-6283-10A-01D-1845-08 g.chrX:125685564G>A c.1028C>T c.(1027-1029)cCc>cTc p.P343L GBM 23 125685588 125685588 + Missense_Mutation SNP C C T TCGA-14-1825-01A-01W-0643-08 TCGA-14-1825-10A-01W-0644-08 g.chrX:125685588C>T c.1004G>A c.(1003-1005)cGc>cAc p.R335H GBM 23 125685588 125685588 + Missense_Mutation SNP C C T TCGA-76-6193-01A-11D-1696-08 TCGA-76-6193-10A-01D-1696-08 g.chrX:125685588C>T c.1004G>A c.(1003-1005)cGc>cAc p.R335H GBM 23 125686304 125686304 + Silent SNP C C T TCGA-27-1838-01A-01D-1494-08 TCGA-27-1838-10A-01D-1494-08 g.chrX:125686304C>T c.288G>A c.(286-288)acG>acA p.T96T GBM 23 125686329 125686329 + Missense_Mutation SNP G G A TCGA-12-0616-01A-01D-1492-08 TCGA-12-0616-10A-01D-1492-08 g.chrX:125686329G>A c.263C>T c.(262-264)aCg>aTg p.T88M GBMLGG 23 125685359 125685359 + Silent SNP G G A TCGA-32-1979-01A-01D-1696-08 TCGA-32-1979-10A-01D-1696-08 g.chrX:125685359G>A c.1233C>T c.(1231-1233)ctC>ctT p.L411L GBMLGG 23 125685396 125685396 + Missense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chrX:125685396C>A c.1196G>T c.(1195-1197)aGg>aTg p.R399M GBMLGG 23 125685564 125685564 + Missense_Mutation SNP G G A TCGA-76-6283-01A-11D-1845-08 TCGA-76-6283-10A-01D-1845-08 g.chrX:125685564G>A c.1028C>T c.(1027-1029)cCc>cTc p.P343L GBMLGG 23 125685588 125685588 + Missense_Mutation SNP C C T TCGA-14-1825-01A-01W-0643-08 TCGA-14-1825-10A-01W-0644-08 g.chrX:125685588C>T c.1004G>A c.(1003-1005)cGc>cAc p.R335H GBMLGG 23 125685588 125685588 + Missense_Mutation SNP C C T TCGA-76-6193-01A-11D-1696-08 TCGA-76-6193-10A-01D-1696-08 g.chrX:125685588C>T c.1004G>A c.(1003-1005)cGc>cAc p.R335H GBMLGG 23 125685778 125685778 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chrX:125685778C>T c.814G>A c.(814-816)Ggc>Agc p.G272S GBMLGG 23 125685930 125685930 + Missense_Mutation SNP C C T TCGA-DU-5847-01A-11D-1705-08 TCGA-DU-5847-10A-01D-1705-08 g.chrX:125685930C>T c.662G>A c.(661-663)cGg>cAg p.R221Q GBMLGG 23 125686253 125686253 + Silent SNP G G A TCGA-HT-A5RC-01A-11D-A289-08 TCGA-HT-A5RC-10A-01D-A289-08 g.chrX:125686253G>A c.339C>T c.(337-339)tgC>tgT p.C113C GBMLGG 23 125686304 125686304 + Silent SNP C C T TCGA-27-1838-01A-01D-1494-08 TCGA-27-1838-10A-01D-1494-08 g.chrX:125686304C>T c.288G>A c.(286-288)acG>acA p.T96T GBMLGG 23 125686329 125686329 + Missense_Mutation SNP G G A TCGA-12-0616-01A-01D-1492-08 TCGA-12-0616-10A-01D-1492-08 g.chrX:125686329G>A c.263C>T c.(262-264)aCg>aTg p.T88M GBMLGG 23 125686452 125686452 + Missense_Mutation SNP G G A TCGA-DU-8158-01A-11D-2253-08 TCGA-DU-8158-10A-01D-2253-08 g.chrX:125686452G>A c.140C>T c.(139-141)aCg>aTg p.T47M HNSC 23 125685234 125685234 + Missense_Mutation SNP C C A TCGA-CR-7388-01A-11D-2012-08 TCGA-CR-7388-10A-01D-2013-08 g.chrX:125685234C>A c.1358G>T c.(1357-1359)gGc>gTc p.G453V HNSC 23 125685408 125685408 + Missense_Mutation SNP G G A TCGA-CV-A45W-01A-11D-A25D-08 TCGA-CV-A45W-10A-01D-A25E-08 g.chrX:125685408G>A c.1184C>T c.(1183-1185)tCg>tTg p.S395L HNSC 23 125685553 125685553 + Nonsense_Mutation SNP G G A TCGA-CQ-5333-01A-01D-2394-08 TCGA-CQ-5333-10A-01D-2394-08 g.chrX:125685553G>A c.1039C>T c.(1039-1041)Cga>Tga p.R347* HNSC 23 125685629 125685629 + Silent SNP G G A TCGA-CQ-5326-01A-01D-1870-08 TCGA-CQ-5326-10A-01D-1870-08 g.chrX:125685629G>A c.963C>T c.(961-963)taC>taT p.Y321Y HNSC 23 125685719 125685719 + Silent SNP G G A TCGA-BA-7269-01A-11D-2012-08 TCGA-BA-7269-10A-01D-2013-08 g.chrX:125685719G>A c.873C>T c.(871-873)gcC>gcT p.A291A HNSC 23 125685745 125685745 + Missense_Mutation SNP C C T TCGA-RS-A6TO-01A-32D-A34J-08 TCGA-RS-A6TO-10A-01D-A34M-08 g.chrX:125685745C>T c.847G>A c.(847-849)Gac>Aac p.D283N HNSC 23 125685766 125685766 + Missense_Mutation SNP C C T TCGA-CV-7568-01A-11D-2229-08 TCGA-CV-7568-10A-01D-2229-08 g.chrX:125685766C>T c.826G>A c.(826-828)Gaa>Aaa p.E276K HNSC 23 125685920 125685920 + Silent SNP C C T TCGA-CN-4726-01A-01D-1434-08 TCGA-CN-4726-10A-01D-1434-08 g.chrX:125685920C>T c.672G>A c.(670-672)ccG>ccA p.P224P HNSC 23 125686073 125686073 + Missense_Mutation SNP G G C TCGA-CV-A461-01A-41D-A25Y-08 TCGA-CV-A461-10A-01D-A25Y-08 g.chrX:125686073G>C c.519C>G c.(517-519)agC>agG p.S173R HNSC 23 125686094 125686094 + Silent SNP G G T TCGA-CR-7402-01A-11D-2012-08 TCGA-CR-7402-10A-01D-2013-08 g.chrX:125686094G>T c.498C>A c.(496-498)acC>acA p.T166T HNSC 23 125686182 125686182 + Missense_Mutation SNP C C T TCGA-UF-A71E-01A-31D-A34J-08 TCGA-UF-A71E-10B-01D-A34M-08 g.chrX:125686182C>T c.410G>A c.(409-411)cGg>cAg p.R137Q HNSC 23 125686191 125686191 + Missense_Mutation SNP G G C TCGA-CV-7255-01A-11D-2012-08 TCGA-CV-7255-10A-01D-2013-08 g.chrX:125686191G>C c.401C>G c.(400-402)cCc>cGc p.P134R HNSC 23 125686264 125686264 + Missense_Mutation SNP G G T TCGA-CV-6956-01A-21D-2012-08 TCGA-CV-6956-10A-01D-2013-08 g.chrX:125686264G>T c.328C>A c.(328-330)Cag>Aag p.Q110K HNSC 23 125686312 125686312 + Missense_Mutation SNP G G T TCGA-CN-4738-01A-02D-1512-08 TCGA-CN-4738-10A-01D-1512-08 g.chrX:125686312G>T c.280C>A c.(280-282)Ctg>Atg p.L94M KIPAN 23 125685459 125685459 + Missense_Mutation SNP C C T TCGA-B2-4099-01A-02D-1251-10 TCGA-B2-4099-11A-01D-1251-10 g.chrX:125685459C>T c.1133G>A c.(1132-1134)cGg>cAg p.R378Q KIPAN 23 125685498 125685498 + Missense_Mutation SNP A A C TCGA-DW-7840-01A-11D-2136-08 TCGA-DW-7840-10A-01D-2136-08 g.chrX:125685498A>C c.1094T>G c.(1093-1095)gTg>gGg p.V365G KIPAN 23 125686496 125686496 + Silent SNP G G A TCGA-CW-5580-01A-01D-1669-08 TCGA-CW-5580-11A-02D-1669-08 g.chrX:125686496G>A c.96C>T c.(94-96)gaC>gaT p.D32D KIRC 23 125685459 125685459 + Missense_Mutation SNP C C T TCGA-B2-4099-01A-02D-1251-10 TCGA-B2-4099-11A-01D-1251-10 g.chrX:125685459C>T c.1133G>A c.(1132-1134)cGg>cAg p.R378Q KIRC 23 125686496 125686496 + Silent SNP G G A TCGA-CW-5580-01A-01D-1669-08 TCGA-CW-5580-11A-02D-1669-08 g.chrX:125686496G>A c.96C>T c.(94-96)gaC>gaT p.D32D KIRP 23 125685498 125685498 + Missense_Mutation SNP A A C TCGA-DW-7840-01A-11D-2136-08 TCGA-DW-7840-10A-01D-2136-08 g.chrX:125685498A>C c.1094T>G c.(1093-1095)gTg>gGg p.V365G LGG 23 125685396 125685396 + Missense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chrX:125685396C>A c.1196G>T c.(1195-1197)aGg>aTg p.R399M LGG 23 125685778 125685778 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chrX:125685778C>T c.814G>A c.(814-816)Ggc>Agc p.G272S LGG 23 125685930 125685930 + Missense_Mutation SNP C C T TCGA-DU-5847-01A-11D-1705-08 TCGA-DU-5847-10A-01D-1705-08 g.chrX:125685930C>T c.662G>A c.(661-663)cGg>cAg p.R221Q LGG 23 125686253 125686253 + Silent SNP G G A TCGA-HT-A5RC-01A-11D-A289-08 TCGA-HT-A5RC-10A-01D-A289-08 g.chrX:125686253G>A c.339C>T c.(337-339)tgC>tgT p.C113C LGG 23 125686452 125686452 + Missense_Mutation SNP G G A TCGA-DU-8158-01A-11D-2253-08 TCGA-DU-8158-10A-01D-2253-08 g.chrX:125686452G>A c.140C>T c.(139-141)aCg>aTg p.T47M LIHC 23 125685361 125685361 + Missense_Mutation SNP G G A TCGA-DD-A4NF-01A-11D-A27I-10 TCGA-DD-A4NF-10A-01D-A27I-10 g.chrX:125685361G>A c.1231C>T c.(1231-1233)Ctc>Ttc p.L411F LIHC 23 125685427 125685427 + Missense_Mutation SNP C C T TCGA-DD-A4NV-01A-11D-A30V-10 TCGA-DD-A4NV-10A-01D-A30V-10 g.chrX:125685427C>T c.1165G>A c.(1165-1167)Gcc>Acc p.A389T LIHC 23 125686535 125686535 + Silent SNP G G A TCGA-DD-AACZ-01A-11D-A40R-10 TCGA-DD-AACZ-10A-01D-A40U-10 g.chrX:125686535G>A c.57C>T c.(55-57)gaC>gaT p.D19D LUAD 23 125685236 125685236 + Silent SNP T T G TCGA-49-4486-01A-01D-1265-08 TCGA-49-4486-11A-01D-1265-08 g.chrX:125685236T>G c.1356A>C c.(1354-1356)gcA>gcC p.A452A LUAD 23 125685253 125685253 + Missense_Mutation SNP C C A TCGA-44-8120-01A-11D-2238-08 TCGA-44-8120-10A-01D-2238-08 g.chrX:125685253C>A c.1339G>T c.(1339-1341)Ggg>Tgg p.G447W LUAD 23 125685253 125685253 + Missense_Mutation SNP C C A TCGA-50-6590-01A-12D-1855-08 TCGA-50-6590-11A-01D-1855-08 g.chrX:125685253C>A c.1339G>T c.(1339-1341)Ggg>Tgg p.G447W LUAD 23 125685270 125685270 + Missense_Mutation SNP A A T TCGA-97-8179-01A-11D-2284-08 TCGA-97-8179-10A-01D-2284-08 g.chrX:125685270A>T c.1322T>A c.(1321-1323)aTg>aAg p.M441K LUAD 23 125685292 125685292 + Missense_Mutation SNP G G T TCGA-78-7536-01A-11D-2063-08 TCGA-78-7536-10A-01D-2063-08 g.chrX:125685292G>T c.1300C>A c.(1300-1302)Cac>Aac p.H434N LUAD 23 125685302 125685302 + Silent SNP C C G TCGA-99-8028-01A-11D-2238-08 TCGA-99-8028-10A-01D-2238-08 g.chrX:125685302C>G c.1290G>C c.(1288-1290)gcG>gcC p.A430A LUAD 23 125685303 125685303 + Missense_Mutation SNP G G T TCGA-44-8117-01A-11D-2238-08 TCGA-44-8117-10A-01D-2238-08 g.chrX:125685303G>T c.1289C>A c.(1288-1290)gCg>gAg p.A430E LUAD 23 125685331 125685331 + Missense_Mutation SNP A A T TCGA-80-5608-01A-31D-1945-08 TCGA-80-5608-10A-01D-1946-08 g.chrX:125685331A>T c.1261T>A c.(1261-1263)Ttt>Att p.F421I LUAD 23 125685341 125685341 + Missense_Mutation SNP C C A TCGA-97-8179-01A-11D-2284-08 TCGA-97-8179-10A-01D-2284-08 g.chrX:125685341C>A c.1251G>T c.(1249-1251)tgG>tgT p.W417C LUAD 23 125685379 125685379 + Missense_Mutation SNP C C A TCGA-55-7574-01A-11D-2036-08 TCGA-55-7574-10A-01D-2036-08 g.chrX:125685379C>A c.1213G>T c.(1213-1215)Gcc>Tcc p.A405S LUAD 23 125685398 125685398 + Silent SNP T T A TCGA-69-7974-01A-11D-2184-08 TCGA-69-7974-10A-01D-2184-08 g.chrX:125685398T>A c.1194A>T c.(1192-1194)gcA>gcT p.A398A LUAD 23 125685455 125685455 + Silent SNP G G T TCGA-73-4677-01A-01D-1265-08 TCGA-73-4677-11A-01D-1265-08 g.chrX:125685455G>T c.1137C>A c.(1135-1137)gcC>gcA p.A379A LUAD 23 125685464 125685464 + Silent SNP G G A TCGA-55-8203-01A-11D-2238-08 TCGA-55-8203-10A-01D-2238-08 g.chrX:125685464G>A c.1128C>T c.(1126-1128)gaC>gaT p.D376D LUAD 23 125685509 125685509 + Missense_Mutation SNP G G T TCGA-55-A4DG-01A-11D-A24D-08 TCGA-55-A4DG-10A-01D-A24F-08 g.chrX:125685509G>T c.1083C>A c.(1081-1083)caC>caA p.H361Q LUAD 23 125685528 125685528 + Nonsense_Mutation SNP G G T TCGA-MP-A4T4-01A-11D-A25L-08 TCGA-MP-A4T4-10A-01D-A25L-08 g.chrX:125685528G>T c.1064C>A c.(1063-1065)tCg>tAg p.S355* LUAD 23 125685540 125685540 + Missense_Mutation SNP G G T TCGA-78-7146-01A-11D-2036-08 TCGA-78-7146-10A-01D-2036-08 g.chrX:125685540G>T c.1052C>A c.(1051-1053)aCa>aAa p.T351K LUAD 23 125685551 125685551 + Silent SNP T T A TCGA-55-A490-01A-11D-A24D-08 TCGA-55-A490-10A-01D-A24F-08 g.chrX:125685551T>A c.1041A>T c.(1039-1041)cgA>cgT p.R347R LUAD 23 125685608 125685608 + Missense_Mutation SNP G G T TCGA-97-A4M0-01A-11D-A24P-08 TCGA-97-A4M0-10A-01D-A24P-08 g.chrX:125685608G>T c.984C>A c.(982-984)caC>caA p.H328Q LUAD 23 125685650 125685650 + Nonsense_Mutation SNP G G T TCGA-55-8096-01A-11D-2238-08 TCGA-55-8096-10A-01D-2238-08 g.chrX:125685650G>T c.942C>A c.(940-942)taC>taA p.Y314* LUAD 23 125685659 125685659 + Silent SNP G G A TCGA-75-6214-01A-41D-1945-08 TCGA-75-6214-10A-01D-1946-08 g.chrX:125685659G>A c.933C>T c.(931-933)tgC>tgT p.C311C LUAD 23 125685683 125685683 + Silent SNP C C A TCGA-50-6590-01A-12D-1855-08 TCGA-50-6590-11A-01D-1855-08 g.chrX:125685683C>A c.909G>T c.(907-909)ctG>ctT p.L303L LUAD 23 125685683 125685683 + Silent SNP C C G TCGA-44-7670-01A-11D-2063-08 TCGA-44-7670-10A-01D-2063-08 g.chrX:125685683C>G c.909G>C c.(907-909)ctG>ctC p.L303L LUAD 23 125685797 125685797 + Silent SNP C C T TCGA-73-4659-01A-01D-1265-08 TCGA-73-4659-11A-01D-1265-08 g.chrX:125685797C>T c.795G>A c.(793-795)gtG>gtA p.V265V LUAD 23 125685831 125685831 + Missense_Mutation SNP G G T TCGA-05-4389-01A-01D-1265-08 TCGA-05-4389-10A-01D-1265-08 g.chrX:125685831G>T c.761C>A c.(760-762)cCc>cAc p.P254H LUAD 23 125685862 125685862 + Missense_Mutation SNP G G T TCGA-75-6214-01A-41D-1945-08 TCGA-75-6214-10A-01D-1946-08 g.chrX:125685862G>T c.730C>A c.(730-732)Cac>Aac p.H244N LUAD 23 125685886 125685886 + Nonsense_Mutation SNP C C A TCGA-05-4382-01A-01D-1931-08 TCGA-05-4382-10A-01D-1265-08 g.chrX:125685886C>A c.706G>T c.(706-708)Gag>Tag p.E236* LUAD 23 125685889 125685889 + Missense_Mutation SNP T T A TCGA-55-1595-01A-01D-0969-08 TCGA-55-1595-11A-01D-0969-08 g.chrX:125685889T>A c.703A>T c.(703-705)Agc>Tgc p.S235C LUAD 23 125685959 125685959 + Silent SNP G G A TCGA-69-7979-01A-11D-2184-08 TCGA-69-7979-10A-01D-2184-08 g.chrX:125685959G>A c.633C>T c.(631-633)ggC>ggT p.G211G LUAD 23 125685987 125685987 + Missense_Mutation SNP C C A TCGA-49-4488-01A-01D-1753-08 TCGA-49-4488-11A-01D-1753-08 g.chrX:125685987C>A c.605G>T c.(604-606)tGg>tTg p.W202L LUAD 23 125686013 125686013 + Missense_Mutation SNP G G T TCGA-95-A4VN-01A-11D-A25L-08 TCGA-95-A4VN-10A-01D-A25L-08 g.chrX:125686013G>T c.579C>A c.(577-579)caC>caA p.H193Q LUAD 23 125686015 125686015 + Missense_Mutation SNP G G T TCGA-86-8073-01A-11D-2238-08 TCGA-86-8073-10A-01D-2238-08 g.chrX:125686015G>T c.577C>A c.(577-579)Cac>Aac p.H193N LUAD 23 125686024 125686024 + Missense_Mutation SNP G G T TCGA-55-A491-01A-11D-A24D-08 TCGA-55-A491-10A-01D-A24F-08 g.chrX:125686024G>T c.568C>A c.(568-570)Cgc>Agc p.R190S LUAD 23 125686031 125686031 + Silent SNP C C A TCGA-55-7907-01A-11D-2167-08 TCGA-55-7907-10A-01D-2167-08 g.chrX:125686031C>A c.561G>T c.(559-561)ctG>ctT p.L187L LUAD 23 125686109 125686109 + Missense_Mutation SNP C C A TCGA-86-8073-01A-11D-2238-08 TCGA-86-8073-10A-01D-2238-08 g.chrX:125686109C>A c.483G>T c.(481-483)aaG>aaT p.K161N LUAD 23 125686176 125686176 + Missense_Mutation SNP C C A TCGA-49-4488-01A-01D-1753-08 TCGA-49-4488-11A-01D-1753-08 g.chrX:125686176C>A c.416G>T c.(415-417)aGt>aTt p.S139I LUAD 23 125686198 125686198 + Missense_Mutation SNP G G T TCGA-55-8620-01A-11D-2393-08 TCGA-55-8620-10A-01D-2393-08 g.chrX:125686198G>T c.394C>A c.(394-396)Cgc>Agc p.R132S LUAD 23 125686201 125686201 + Missense_Mutation SNP C C T TCGA-17-Z022-01A-01W-0746-08 TCGA-17-Z022-11A-01W-0746-08 g.chrX:125686201C>T c.391G>A c.(391-393)Gcg>Acg p.A131T LUAD 23 125686235 125686235 + Silent SNP C C A TCGA-86-A456-01A-11D-A24D-08 TCGA-86-A456-10A-01D-A24F-08 g.chrX:125686235C>A c.357G>T c.(355-357)acG>acT p.T119T LUAD 23 125686243 125686243 + Missense_Mutation SNP A A G TCGA-55-1592-01A-01D-0969-08 TCGA-55-1592-11A-01D-0969-08 g.chrX:125686243A>G c.349T>C c.(349-351)Tgt>Cgt p.C117R LUAD 23 125686260 125686260 + Missense_Mutation SNP A A G TCGA-86-8358-01A-11D-2323-08 TCGA-86-8358-10A-01D-2323-08 g.chrX:125686260A>G c.332T>C c.(331-333)gTg>gCg p.V111A LUAD 23 125686305 125686305 + Missense_Mutation SNP G G C TCGA-05-4390-01A-02D-1753-08 TCGA-05-4390-10A-01D-1753-08 g.chrX:125686305G>C c.287C>G c.(286-288)aCg>aGg p.T96R LUAD 23 125686318 125686318 + Missense_Mutation SNP G G T TCGA-99-8032-01A-11D-2238-08 TCGA-99-8032-10A-01D-2238-08 g.chrX:125686318G>T c.274C>A c.(274-276)Ctg>Atg p.L92M LUAD 23 125686366 125686366 + Missense_Mutation SNP G G C TCGA-95-A4VN-01A-11D-A25L-08 TCGA-95-A4VN-10A-01D-A25L-08 g.chrX:125686366G>C c.226C>G c.(226-228)Cgg>Ggg p.R76G LUAD 23 125686414 125686414 + Missense_Mutation SNP C C A TCGA-55-8507-01A-11D-2393-08 TCGA-55-8507-10A-01D-2393-08 g.chrX:125686414C>A c.178G>T c.(178-180)Gta>Tta p.V60L LUAD 23 125686417 125686417 + Nonsense_Mutation SNP C C A TCGA-17-Z045-01A-01W-0746-08 TCGA-17-Z045-11A-01W-0747-08 g.chrX:125686417C>A c.175G>T c.(175-177)Gag>Tag p.E59* LUAD 23 125686465 125686465 + Missense_Mutation SNP T T A TCGA-44-7670-01A-11D-2063-08 TCGA-44-7670-10A-01D-2063-08 g.chrX:125686465T>A c.127A>T c.(127-129)Agg>Tgg p.R43W LUAD 23 125686488 125686488 + Missense_Mutation SNP C C T TCGA-55-8620-01A-11D-2393-08 TCGA-55-8620-10A-01D-2393-08 g.chrX:125686488C>T c.104G>A c.(103-105)gGg>gAg p.G35E LUAD 23 125686504 125686504 + Missense_Mutation SNP C C A TCGA-55-8085-01A-11D-2238-08 TCGA-55-8085-10A-01D-2238-08 g.chrX:125686504C>A c.88G>T c.(88-90)Gca>Tca p.A30S LUAD 23 125686524 125686524 + Missense_Mutation SNP G G A TCGA-49-6745-01A-11D-1855-08 TCGA-49-6745-11A-01D-1855-08 g.chrX:125686524G>A c.68C>T c.(67-69)tCg>tTg p.S23L LUAD 23 125686543 125686543 + Nonsense_Mutation SNP C C A TCGA-44-5644-01A-21D-2036-08 TCGA-44-5644-10A-01D-2036-08 g.chrX:125686543C>A c.49G>T c.(49-51)Gag>Tag p.E17* LUAD 23 125686544 125686544 + Silent SNP G G T TCGA-NJ-A4YI-01A-11D-A25L-08 TCGA-NJ-A4YI-10A-01D-A25L-08 g.chrX:125686544G>T c.48C>A c.(46-48)gtC>gtA p.V16V LUAD 23 125686548 125686548 + Missense_Mutation SNP G G A TCGA-17-Z007-01A-01W-0746-08 TCGA-17-Z007-11A-01W-0746-08 g.chrX:125686548G>A c.44C>T c.(43-45)gCg>gTg p.A15V LUAD 23 125686553 125686553 + Silent SNP C C A TCGA-L9-A444-01A-21D-A24D-08 TCGA-L9-A444-10A-01D-A24F-08 g.chrX:125686553C>A c.39G>T c.(37-39)gcG>gcT p.A13A LUAD 23 125686586 125686586 + Silent SNP G G C TCGA-50-5946-01A-11D-1753-08 TCGA-50-5946-10A-01D-1753-08 g.chrX:125686586G>C c.6C>G c.(4-6)gcC>gcG p.A2A LUSC 23 125685298 125685298 + Missense_Mutation SNP A A T TCGA-18-3416-01A-01D-0983-08 TCGA-18-3416-11A-01D-0983-08 g.chrX:125685298A>T c.1294T>A c.(1294-1296)Tac>Aac p.Y432N LUSC 23 125685379 125685379 + Missense_Mutation SNP C C A TCGA-33-4586-01A-01D-1441-08 TCGA-33-4586-11A-01D-1441-08 g.chrX:125685379C>A c.1213G>T c.(1213-1215)Gcc>Tcc p.A405S LUSC 23 125685455 125685455 + Silent SNP G G C TCGA-66-2780-01A-01D-1522-08 TCGA-66-2780-11A-01D-1522-08 g.chrX:125685455G>C c.1137C>G c.(1135-1137)gcC>gcG p.A379A LUSC 23 125685490 125685490 + Missense_Mutation SNP C C A TCGA-22-4613-01A-01D-1441-08 TCGA-22-4613-11A-01D-1441-08 g.chrX:125685490C>A c.1102G>T c.(1102-1104)Ggt>Tgt p.G368C LUSC 23 125685517 125685517 + Missense_Mutation SNP A A G TCGA-60-2698-01A-01D-1522-08 TCGA-60-2698-11A-01D-1522-08 g.chrX:125685517A>G c.1075T>C c.(1075-1077)Tac>Cac p.Y359H LUSC 23 125685530 125685530 + Silent SNP C C T TCGA-43-5668-01A-01D-1632-08 TCGA-43-5668-11A-01D-1632-08 g.chrX:125685530C>T c.1062G>A c.(1060-1062)cgG>cgA p.R354R LUSC 23 125685718 125685718 + Missense_Mutation SNP C C A TCGA-22-4613-01A-01D-1441-08 TCGA-22-4613-11A-01D-1441-08 g.chrX:125685718C>A c.874G>T c.(874-876)Ggg>Tgg p.G292W LUSC 23 125685917 125685917 + Missense_Mutation SNP G G T TCGA-33-4582-01A-01D-1441-08 TCGA-33-4582-11A-01D-1441-08 g.chrX:125685917G>T c.675C>A c.(673-675)gaC>gaA p.D225E LUSC 23 125685932 125685932 + Frame_Shift_Del DEL C C - TCGA-66-2771-01A-01D-0983-08 TCGA-66-2771-11A-01D-0983-08 g.chrX:125685932delC c.660delG c.(658-660)tggfs p.W220fs LUSC 23 125686050 125686050 + Missense_Mutation SNP G G C TCGA-43-2578-01A-01D-1522-08 TCGA-43-2578-11A-01D-1522-08 g.chrX:125686050G>C c.542C>G c.(541-543)tCc>tGc p.S181C LUSC 23 125686112 125686112 + Silent SNP G G A TCGA-66-2742-01A-01D-0983-08 TCGA-66-2742-11A-01D-0983-08 g.chrX:125686112G>A c.480C>T c.(478-480)tcC>tcT p.S160S LUSC 23 125686130 125686131 + Missense_Mutation DNP GG GG AC TCGA-33-4566-01A-01D-1441-08 TCGA-33-4566-11A-01D-1441-08 g.chrX:125686130_125686131GG>AC c.461_462CC>GT c.(460-462)gCC>gGT p.A154G LUSC 23 125686327 125686327 + Nonsense_Mutation SNP C C A TCGA-46-3765-01A-01D-0983-08 TCGA-46-3765-10A-01D-0983-08 g.chrX:125686327C>A c.265G>T c.(265-267)Gag>Tag p.E89* LUSC 23 125686398 125686398 + Missense_Mutation SNP G G A TCGA-66-2777-01A-01D-1267-08 TCGA-66-2777-11A-01D-1267-08 g.chrX:125686398G>A c.194C>T c.(193-195)cCc>cTc p.P65L LUSC 23 125686402 125686402 + Missense_Mutation SNP C C A TCGA-63-5131-01A-01D-1441-08 TCGA-63-5131-10A-01D-1441-08 g.chrX:125686402C>A c.190G>T c.(190-192)Ggc>Tgc p.G64C LUSC 23 125686548 125686548 + Missense_Mutation SNP G G A TCGA-56-5898-01A-11D-1632-08 TCGA-56-5898-10A-01D-1632-08 g.chrX:125686548G>A c.44C>T c.(43-45)gCg>gTg p.A15V OV 23 125685995 125685995 + Silent SNP G G T TCGA-61-1722-01A-01D-1556-09 TCGA-61-1722-11A-01W-0639-09 g.chrX:125685995G>T c.597C>A c.(595-597)gcC>gcA p.A199A PAAD 23 125685629 125685629 + Silent SNP G G A TCGA-FZ-5921-01A-11D-1609-08 TCGA-FZ-5921-11A-01D-1609-08 g.chrX:125685629G>A c.963C>T c.(961-963)taC>taT p.Y321Y PAAD 23 125685938 125685938 + Silent SNP C C T TCGA-FB-A78T-01A-12D-A32N-08 TCGA-FB-A78T-10A-01D-A32N-08 g.chrX:125685938C>T c.654G>A c.(652-654)gcG>gcA p.A218A PAAD 23 125686253 125686253 + Silent SNP G G A TCGA-HV-AA8X-01A-11D-A397-08 TCGA-HV-AA8X-10A-01D-A39A-08 g.chrX:125686253G>A c.339C>T c.(337-339)tgC>tgT p.C113C PAAD 23 125686333 125686333 + Silent SNP G G A TCGA-XD-AAUG-01A-61D-A40W-08 TCGA-XD-AAUG-10A-01D-A40W-08 g.chrX:125686333G>A c.259C>T c.(259-261)Ctg>Ttg p.L87L PAAD 23 125686396 125686397 + Frame_Shift_Ins INS - - G TCGA-IB-AAUP-01A-11D-A377-08 TCGA-IB-AAUP-10A-01D-A37A-08 g.chrX:125686396_125686397insG c.195_196insC c.(193-198)cccgccfs p.A66fs PCPG 23 125685938 125685938 + Silent SNP C C T TCGA-QT-A5XL-01A-11D-A35D-08 TCGA-QT-A5XL-10A-01D-A35B-08 g.chrX:125685938C>T c.654G>A c.(652-654)gcG>gcA p.A218A PRAD 23 125685212 125685212 + Silent SNP G G A TCGA-EJ-7218-01B-11D-A32B-08 TCGA-EJ-7218-10A-01D-A329-08 g.chrX:125685212G>A c.1380C>T c.(1378-1380)ggC>ggT p.G460G PRAD 23 125685734 125685734 + Missense_Mutation SNP G G T TCGA-V1-A9O9-01A-11D-A41K-08 TCGA-V1-A9O9-10A-01D-A41N-08 g.chrX:125685734G>T c.858C>A c.(856-858)ttC>ttA p.F286L PRAD 23 125685748 125685748 + Silent SNP A A G TCGA-4L-AA1F-01A-11D-A41K-08 TCGA-4L-AA1F-10A-01D-A41N-08 g.chrX:125685748A>G c.844T>C c.(844-846)Ttg>Ctg p.L282L PRAD 23 125685777 125685777 + Missense_Mutation SNP C C T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chrX:125685777C>T c.815G>A c.(814-816)gGc>gAc p.G272D PRAD 23 125685920 125685920 + Silent SNP C C T TCGA-HC-7231-01A-11D-2114-08 TCGA-HC-7231-10A-01D-2115-08 g.chrX:125685920C>T c.672G>A c.(670-672)ccG>ccA p.P224P PRAD 23 125685925 125685925 + Missense_Mutation SNP C C G TCGA-J9-A52B-01A-11D-A26M-08 TCGA-J9-A52B-10A-01D-A26K-08 g.chrX:125685925C>G c.667G>C c.(667-669)Gac>Cac p.D223H SARC 23 125686013 125686013 + Missense_Mutation SNP G G T TCGA-DX-AB2J-01A-11D-A387-09 TCGA-DX-AB2J-10A-01D-A38A-09 g.chrX:125686013G>T c.579C>A c.(577-579)caC>caA p.H193Q SKCM 23 125685242 125685242 + Silent SNP G G A TCGA-DA-A1HY-06A-11D-A19A-08 TCGA-DA-A1HY-10A-01D-A19A-08 g.chrX:125685242G>A c.1350C>T c.(1348-1350)ctC>ctT p.L450L SKCM 23 125685274 125685274 + Missense_Mutation SNP C C T TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chrX:125685274C>T c.1318G>A c.(1318-1320)Gag>Aag p.E440K SKCM 23 125685344 125685344 + Silent SNP G G A TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chrX:125685344G>A c.1248C>T c.(1246-1248)ttC>ttT p.F416F SKCM 23 125685446 125685446 + Silent SNP G G A TCGA-D9-A6EA-06A-11D-A30X-08 TCGA-D9-A6EA-10A-01D-A30X-08 g.chrX:125685446G>A c.1146C>T c.(1144-1146)ttC>ttT p.F382F SKCM 23 125685448 125685448 + Missense_Mutation SNP A A G TCGA-FS-A4F8-06A-11D-A25O-08 TCGA-FS-A4F8-10B-01D-A25O-08 g.chrX:125685448A>G c.1144T>C c.(1144-1146)Ttc>Ctc p.F382L SKCM 23 125685552 125685552 + Missense_Mutation SNP C C T TCGA-EE-A29D-06A-11D-A197-08 TCGA-EE-A29D-10A-01D-A199-08 g.chrX:125685552C>T c.1040G>A c.(1039-1041)cGa>cAa p.R347Q SKCM 23 125685552 125685552 + Missense_Mutation SNP C C T TCGA-FS-A1Z3-06A-11D-A197-08 TCGA-FS-A1Z3-10A-01D-A199-08 g.chrX:125685552C>T c.1040G>A c.(1039-1041)cGa>cAa p.R347Q SKCM 23 125685672 125685672 + Missense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chrX:125685672C>T c.920G>A c.(919-921)cGg>cAg p.R307Q SKCM 23 125685746 125685746 + Silent SNP C C T TCGA-EE-A3JD-06A-11D-A20D-08 TCGA-EE-A3JD-10A-01D-A20D-08 g.chrX:125685746C>T c.846G>A c.(844-846)ttG>ttA p.L282L SKCM 23 125685857 125685857 + Silent SNP G G A TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chrX:125685857G>A c.735C>T c.(733-735)atC>atT p.I245I SKCM 23 125685875 125685875 + Silent SNP G G A TCGA-EE-A29L-06A-12D-A196-08 TCGA-EE-A29L-10A-01D-A198-08 g.chrX:125685875G>A c.717C>T c.(715-717)ctC>ctT p.L239L SKCM 23 125685886 125685886 + Missense_Mutation SNP C C T TCGA-D3-A5GN-06A-11D-A27K-08 TCGA-D3-A5GN-10A-01D-A27N-08 g.chrX:125685886C>T c.706G>A c.(706-708)Gag>Aag p.E236K SKCM 23 125685897 125685897 + Missense_Mutation SNP G G A TCGA-EE-A2MS-06A-11D-A197-08 TCGA-EE-A2MS-10A-01D-A199-08 g.chrX:125685897G>A c.695C>T c.(694-696)gCc>gTc p.A232V SKCM 23 125686004 125686004 + Nonsense_Mutation SNP C C T TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chrX:125686004C>T c.588G>A c.(586-588)tgG>tgA p.W196* SKCM 23 125686141 125686141 + Missense_Mutation SNP C C T TCGA-ER-A19N-06A-11D-A197-08 TCGA-ER-A19N-10A-01D-A199-08 g.chrX:125686141C>T c.451G>A c.(451-453)Ggc>Agc p.G151S SKCM 23 125686156 125686156 + Missense_Mutation SNP C C T TCGA-FS-A1Z3-06A-11D-A197-08 TCGA-FS-A1Z3-10A-01D-A199-08 g.chrX:125686156C>T c.436G>A c.(436-438)Gac>Aac p.D146N SKCM 23 125686229 125686229 + Silent SNP G G A TCGA-D3-A1Q6-06A-11D-A196-08 TCGA-D3-A1Q6-10A-01D-A198-08 g.chrX:125686229G>A c.363C>T c.(361-363)ttC>ttT p.F121F SKCM 23 125686405 125686405 + Missense_Mutation SNP A A C TCGA-EE-A2A2-06A-11D-A196-08 TCGA-EE-A2A2-10A-01D-A198-08 g.chrX:125686405A>C c.187T>G c.(187-189)Tgg>Ggg p.W63G SKCM 23 125686526 125686526 + Missense_Mutation SNP G G C TCGA-FR-A3YN-06A-11D-A23B-08 TCGA-FR-A3YN-10A-01D-A23B-08 g.chrX:125686526G>C c.66C>G c.(64-66)agC>agG p.S22R SKCM 23 125686565 125686565 + Missense_Mutation SNP C C G TCGA-EB-A5UL-06A-11D-A30X-08 TCGA-EB-A5UL-10A-01D-A30X-08 g.chrX:125686565C>G c.27G>C c.(25-27)agG>agC p.R9S

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 125685401 125685401 single base substitution A T synonymous_variant P397P 1191T>A BLCA-US X 125685766 125685766 single base substitution C A stop_gained E276* 826G>T BLCA-US X 125685907 125685907 single base substitution C T missense_variant D229N 685G>A BLCA-US X 125686323 125686323 single base substitution C T missense_variant R90H 269G>A BLCA-US X 125686549 125686549 single base substitution C T missense_variant A15T 43G>A BRCA-EU X 125678462 125678462 single base substitution G A downstream_gene_variant BRCA-EU X 125678890 125678890 single base substitution C A downstream_gene_variant BRCA-EU X 125679767 125679767 single base substitution C T downstream_gene_variant BRCA-EU X 125680362 125680362 single base substitution G T downstream_gene_variant BRCA-EU X 125680761 125680761 single base substitution C T downstream_gene_variant BRCA-EU X 125681676 125681676 single base substitution T C downstream_gene_variant BRCA-EU X 125682870 125682870 single base substitution G A downstream_gene_variant BRCA-EU X 125682871 125682871 single base substitution G A downstream_gene_variant BRCA-EU X 125683149 125683149 insertion of <=200bp - A downstream_gene_variant BRCA-EU X 125683753 125683753 single base substitution A G 3_prime_UTR_variant BRCA-EU X 125684372 125684372 single base substitution A T 3_prime_UTR_variant BRCA-EU X 125685029 125685029 single base substitution G A 3_prime_UTR_variant BRCA-EU X 125685303 125685303 single base substitution G A missense_variant A430V 1289C>T BRCA-EU X 125685377 125685377 single base substitution G T synonymous_variant A405A 1215C>A BRCA-EU X 125685941 125685941 single base substitution C T synonymous_variant V217V 651G>A BRCA-EU X 125686779 125686779 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant BRCA-EU X 125686793 125686793 single base substitution C T 5_prime_UTR_variant BRCA-EU X 125687034 125687034 single base substitution A G upstream_gene_variant BRCA-EU X 125687332 125687332 single base substitution C G upstream_gene_variant BRCA-EU X 125687460 125687460 single base substitution G A upstream_gene_variant BRCA-EU X 125687884 125687884 single base substitution C G upstream_gene_variant BRCA-EU X 125688707 125688707 single base substitution G T upstream_gene_variant BRCA-EU X 125688898 125688898 single base substitution C T upstream_gene_variant BRCA-EU X 125688949 125688949 single base substitution C T upstream_gene_variant BRCA-EU X 125688950 125688950 single base substitution G T upstream_gene_variant BRCA-EU X 125689401 125689401 single base substitution A G upstream_gene_variant BRCA-EU X 125689531 125689531 single base substitution G T upstream_gene_variant BRCA-EU X 125690414 125690414 single base substitution C G upstream_gene_variant BRCA-EU X 125691407 125691407 deletion of <=200bp A - upstream_gene_variant BRCA-FR X 125680362 125680362 single base substitution G T downstream_gene_variant BRCA-FR X 125682871 125682871 single base substitution G A downstream_gene_variant BRCA-FR X 125686779 125686779 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant BRCA-FR X 125687034 125687034 single base substitution A G upstream_gene_variant BRCA-FR X 125687332 125687332 single base substitution C G upstream_gene_variant BRCA-FR X 125689531 125689531 single base substitution G T upstream_gene_variant BRCA-FR X 125690414 125690414 single base substitution C G upstream_gene_variant BRCA-UK X 125680288 125680288 single base substitution C T downstream_gene_variant BRCA-UK X 125685029 125685029 single base substitution G A 3_prime_UTR_variant BRCA-UK X 125685975 125685975 single base substitution G T missense_variant T206N 617C>A BRCA-US X 125685470 125685470 single base substitution G C missense_variant F374L 1122C>G BRCA-US X 125685532 125685532 single base substitution G A missense_variant R354W 1060C>T BRCA-US X 125685656 125685656 single base substitution C G synonymous_variant L312L 936G>C BRCA-US X 125685704 125685704 single base substitution G T synonymous_variant S296S 888C>A BRCA-US X 125685742 125685742 single base substitution C T missense_variant G284S 850G>A BRCA-US X 125685957 125685957 single base substitution G A missense_variant S212F 635C>T BRCA-US X 125686114 125686114 single base substitution A C missense_variant S160A 478T>G BRCA-US X 125686220 125686220 single base substitution G A synonymous_variant D124D 372C>T BTCA-JP X 125685535 125685535 single base substitution C T missense_variant V353M 1057G>A BTCA-JP X 125685660 125685660 single base substitution C T missense_variant C311Y 932G>A BTCA-JP X 125686234 125686234 single base substitution G T missense_variant L120I 358C>A BTCA-JP X 125686357 125686357 single base substitution C T missense_variant A79T 235G>A BTCA-JP X 125686535 125686535 single base substitution G A synonymous_variant D19D 57C>T BTCA-JP X 125686673 125686673 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant CESC-US X 125685755 125685755 single base substitution C A synonymous_variant A279A 837G>T CESC-US X 125685980 125685980 single base substitution A T missense_variant S204R 612T>A CESC-US X 125686155 125686155 single base substitution T C missense_variant D146G 437A>G CLLE-ES X 125682565 125682565 single base substitution T A downstream_gene_variant CLLE-ES X 125690371 125690371 single base substitution C A upstream_gene_variant CLLE-ES X 125691327 125691327 single base substitution T C upstream_gene_variant CLLE-ES X 125691760 125691760 single base substitution G C upstream_gene_variant COAD-US X 125685347 125685347 single base substitution A G synonymous_variant D415D 1245T>C COAD-US X 125685532 125685532 single base substitution G A missense_variant R354W 1060C>T COAD-US X 125685700 125685700 single base substitution G T missense_variant L298M 892C>A COAD-US X 125685730 125685730 single base substitution G T missense_variant L288M 862C>A COAD-US X 125685947 125685947 single base substitution G A synonymous_variant G215G 645C>T COAD-US X 125685953 125685953 single base substitution G A synonymous_variant R213R 639C>T COAD-US X 125686197 125686197 single base substitution C T missense_variant R132H 395G>A COAD-US X 125686354 125686354 single base substitution C A missense_variant V80L 238G>T COCA-CN X 125685413 125685413 single base substitution G T synonymous_variant S393S 1179C>A COCA-CN X 125685512 125685512 single base substitution G A synonymous_variant R360R 1080C>T COCA-CN X 125685626 125685626 single base substitution G A synonymous_variant A322A 966C>T COCA-CN X 125685872 125685872 single base substitution G A synonymous_variant P240P 720C>T COCA-CN X 125686024 125686024 single base substitution G A missense_variant R190C 568C>T COCA-CN X 125686141 125686141 single base substitution C T missense_variant G151S 451G>A COCA-CN X 125686235 125686235 single base substitution C T synonymous_variant T119T 357G>A COCA-CN X 125686397 125686397 single base substitution G A synonymous_variant P65P 195C>T COCA-CN X 125686442 125686442 single base substitution C T synonymous_variant S50S 150G>A COCA-CN X 125686490 125686490 single base substitution C A missense_variant E34D 102G>T COCA-CN X 125686547 125686547 single base substitution C T synonymous_variant A15A 45G>A EOPC-DE X 125679763 125679763 single base substitution G A downstream_gene_variant ESCA-CN X 125684813 125684813 single base substitution C G 3_prime_UTR_variant ESCA-CN X 125685280 125685280 single base substitution A T missense_variant W438R 1312T>A ESCA-CN X 125685394 125685394 single base substitution T A missense_variant R400W 1198A>T ESCA-CN X 125685440 125685440 single base substitution C A missense_variant E384D 1152G>T ESCA-CN X 125685589 125685589 single base substitution G A missense_variant R335C 1003C>T ESCA-CN X 125685742 125685742 single base substitution C T missense_variant G284S 850G>A ESCA-CN X 125685796 125685796 single base substitution G A missense_variant R266W 796C>T ESCA-CN X 125685821 125685821 single base substitution G A synonymous_variant I257I 771C>T GACA-CN X 125685210 125685210 single base substitution A C missense_variant L461R 1382T>G GBM-US X 125685359 125685359 single base substitution G A synonymous_variant L411L 1233C>T GBM-US X 125685588 125685588 single base substitution C T missense_variant R335H 1004G>A GBM-US X 125686304 125686304 single base substitution C T synonymous_variant T96T 288G>A GBM-US X 125686329 125686329 single base substitution G A missense_variant T88M 263C>T KIRC-US X 125685459 125685459 single base substitution C T missense_variant R378Q 1133G>A KIRC-US X 125686496 125686496 single base substitution G A synonymous_variant D32D 96C>T KIRP-US X 125685498 125685498 single base substitution A C missense_variant V365G 1094T>G LAML-KR X 125678513 125678513 single base substitution A T downstream_gene_variant LGG-US X 125685930 125685930 single base substitution C T missense_variant R221Q 662G>A LGG-US X 125686452 125686452 single base substitution G A missense_variant T47M 140C>T LICA-CN X 125686146 125686146 single base substitution C T missense_variant G149D 446G>A LICA-CN X 125686407 125686407 single base substitution C A missense_variant G62V 185G>T LICA-FR X 125685588 125685588 single base substitution C T missense_variant R335H 1004G>A LICA-FR X 125685856 125685856 single base substitution G A missense_variant R246C 736C>T LICA-FR X 125686282 125686282 single base substitution G T missense_variant Q104K 310C>A LICA-FR X 125686309 125686309 single base substitution C G missense_variant G95R 283G>C LICA-FR X 125686310 125686310 single base substitution C G synonymous_variant L94L 282G>C LICA-FR X 125686403 125686403 single base substitution C T stop_gained W63* 189G>A LICA-FR X 125686406 125686406 single base substitution C T synonymous_variant G62G 186G>A LICA-FR X 125688938 125688938 single base substitution C G upstream_gene_variant LICA-FR X 125691085 125691085 single base substitution C G upstream_gene_variant LIHC-US X 125685361 125685361 single base substitution G A missense_variant L411F 1231C>T LIHC-US X 125685427 125685427 single base substitution C T missense_variant A389T 1165G>A LINC-JP X 125684070 125684070 deletion of <=200bp A - 3_prime_UTR_variant LINC-JP X 125685244 125685244 single base substitution G A missense_variant L450F 1348C>T LINC-JP X 125686197 125686197 single base substitution C A missense_variant R132L 395G>T LIRI-JP X 125678668 125678668 single base substitution T C downstream_gene_variant LIRI-JP X 125678674 125678674 single base substitution C T downstream_gene_variant LIRI-JP X 125678819 125678819 single base substitution G A downstream_gene_variant LIRI-JP X 125679124 125679124 single base substitution G C downstream_gene_variant LIRI-JP X 125679217 125679217 single base substitution T C downstream_gene_variant LIRI-JP X 125679673 125679673 single base substitution C A downstream_gene_variant LIRI-JP X 125679763 125679763 single base substitution G A downstream_gene_variant LIRI-JP X 125680593 125680593 single base substitution T A downstream_gene_variant LIRI-JP X 125681202 125681202 single base substitution C A downstream_gene_variant LIRI-JP X 125682272 125682272 single base substitution T A downstream_gene_variant LIRI-JP X 125683454 125683454 single base substitution A T 3_prime_UTR_variant LIRI-JP X 125685278 125685278 single base substitution C G missense_variant W438C 1314G>C LIRI-JP X 125685590 125685590 single base substitution C T synonymous_variant L334L 1002G>A LIRI-JP X 125689549 125689549 single base substitution C G upstream_gene_variant LIRI-JP X 125690212 125690212 single base substitution A G upstream_gene_variant LUSC-KR X 125681990 125681990 single base substitution C A downstream_gene_variant LUSC-KR X 125683969 125683969 single base substitution C G 3_prime_UTR_variant LUSC-KR X 125684851 125684851 single base substitution A T 3_prime_UTR_variant LUSC-KR X 125686917 125686917 single base substitution C G upstream_gene_variant LUSC-KR X 125687702 125687702 single base substitution C A upstream_gene_variant LUSC-KR X 125689231 125689231 single base substitution C T upstream_gene_variant LUSC-KR X 125689232 125689232 single base substitution C A upstream_gene_variant LUSC-KR X 125689265 125689265 single base substitution C A upstream_gene_variant LUSC-KR X 125689965 125689965 single base substitution G T upstream_gene_variant LUSC-KR X 125691107 125691107 single base substitution C T upstream_gene_variant LUSC-KR X 125691151 125691151 single base substitution C A upstream_gene_variant LUSC-KR X 125691152 125691152 single base substitution C G upstream_gene_variant LUSC-KR X 125691405 125691405 single base substitution C T upstream_gene_variant LUSC-US X 125685298 125685298 single base substitution A T missense_variant Y432N 1294T>A LUSC-US X 125685379 125685379 single base substitution C A missense_variant A405S 1213G>T LUSC-US X 125685455 125685455 single base substitution G C synonymous_variant A379A 1137C>G LUSC-US X 125685490 125685490 single base substitution C A missense_variant G368C 1102G>T LUSC-US X 125685517 125685517 single base substitution A G missense_variant Y359H 1075T>C LUSC-US X 125685530 125685530 single base substitution C T synonymous_variant R354R 1062G>A LUSC-US X 125685718 125685718 single base substitution C A missense_variant G292W 874G>T LUSC-US X 125685917 125685917 single base substitution G T missense_variant D225E 675C>A LUSC-US X 125685932 125685932 deletion of <=200bp C - frameshift_variant W220 LUSC-US X 125686050 125686050 single base substitution G C missense_variant S181C 542C>G LUSC-US X 125686112 125686112 single base substitution G A synonymous_variant S160S 480C>T LUSC-US X 125686130 125686130 single base substitution G A synonymous_variant A154A 462C>T LUSC-US X 125686131 125686131 single base substitution G C missense_variant A154G 461C>G LUSC-US X 125686327 125686327 single base substitution C A stop_gained E89* 265G>T LUSC-US X 125686398 125686398 single base substitution G A missense_variant P65L 194C>T LUSC-US X 125686402 125686402 single base substitution C A missense_variant G64C 190G>T LUSC-US X 125686548 125686548 single base substitution G A missense_variant A15V 44C>T MALY-DE X 125679416 125679416 single base substitution G T downstream_gene_variant MALY-DE X 125679420 125679420 single base substitution T C downstream_gene_variant MALY-DE X 125680451 125680451 single base substitution T C downstream_gene_variant MALY-DE X 125683012 125683012 deletion of <=200bp A - downstream_gene_variant MALY-DE X 125683032 125683032 single base substitution A C downstream_gene_variant MALY-DE X 125684937 125684937 deletion of <=200bp A - 3_prime_UTR_variant MALY-DE X 125688799 125688799 single base substitution C A upstream_gene_variant MALY-DE X 125689103 125689103 single base substitution C T upstream_gene_variant MALY-DE X 125690390 125690390 single base substitution A T upstream_gene_variant MALY-DE X 125690547 125690547 single base substitution C T upstream_gene_variant MALY-DE X 125691656 125691656 insertion of <=200bp - T upstream_gene_variant MELA-AU X 125678424 125678424 single base substitution C T downstream_gene_variant MELA-AU X 125678440 125678440 single base substitution C T downstream_gene_variant MELA-AU X 125678506 125678506 single base substitution G T downstream_gene_variant MELA-AU X 125678537 125678537 single base substitution T A downstream_gene_variant MELA-AU X 125678595 125678595 single base substitution G A downstream_gene_variant MELA-AU X 125679176 125679176 single base substitution C T downstream_gene_variant MELA-AU X 125679183 125679183 single base substitution G A downstream_gene_variant MELA-AU X 125679319 125679319 single base substitution G A downstream_gene_variant MELA-AU X 125679494 125679494 single base substitution C T downstream_gene_variant MELA-AU X 125679725 125679725 single base substitution G A downstream_gene_variant MELA-AU X 125679807 125679807 single base substitution G A downstream_gene_variant MELA-AU X 125680371 125680371 single base substitution A T downstream_gene_variant MELA-AU X 125680396 125680396 single base substitution C T downstream_gene_variant MELA-AU X 125680400 125680400 single base substitution C T downstream_gene_variant MELA-AU X 125680428 125680428 single base substitution G A downstream_gene_variant MELA-AU X 125680480 125680480 single base substitution G A downstream_gene_variant MELA-AU X 125680609 125680609 single base substitution C T downstream_gene_variant MELA-AU X 125680640 125680640 single base substitution C T downstream_gene_variant MELA-AU X 125680681 125680681 single base substitution C T downstream_gene_variant MELA-AU X 125681143 125681144 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU X 125681273 125681273 single base substitution C T downstream_gene_variant MELA-AU X 125681464 125681464 single base substitution G A downstream_gene_variant MELA-AU X 125681490 125681490 single base substitution C T downstream_gene_variant MELA-AU X 125681511 125681511 single base substitution G A downstream_gene_variant MELA-AU X 125681801 125681801 single base substitution G A downstream_gene_variant MELA-AU X 125681858 125681858 single base substitution G A downstream_gene_variant MELA-AU X 125682259 125682259 single base substitution C T downstream_gene_variant MELA-AU X 125682296 125682296 single base substitution G A downstream_gene_variant MELA-AU X 125682745 125682745 single base substitution C A downstream_gene_variant MELA-AU X 125682850 125682850 single base substitution G A downstream_gene_variant MELA-AU X 125682936 125682936 single base substitution C T downstream_gene_variant MELA-AU X 125682942 125682942 single base substitution C T downstream_gene_variant MELA-AU X 125682988 125682988 single base substitution C G downstream_gene_variant MELA-AU X 125683078 125683078 single base substitution G A downstream_gene_variant MELA-AU X 125683127 125683127 single base substitution G A downstream_gene_variant MELA-AU X 125683209 125683209 single base substitution T A downstream_gene_variant MELA-AU X 125683339 125683339 single base substitution G T downstream_gene_variant MELA-AU X 125683552 125683552 single base substitution C T 3_prime_UTR_variant MELA-AU X 125683966 125683966 single base substitution G A 3_prime_UTR_variant MELA-AU X 125684286 125684286 single base substitution C T 3_prime_UTR_variant MELA-AU X 125684398 125684398 single base substitution C A 3_prime_UTR_variant MELA-AU X 125684452 125684452 single base substitution A G 3_prime_UTR_variant MELA-AU X 125684656 125684657 multiple base substitution (>=2bp and <=200bp) TT AA 3_prime_UTR_variant MELA-AU X 125685071 125685071 single base substitution T C 3_prime_UTR_variant MELA-AU X 125685152 125685152 single base substitution C T intron_variant MELA-AU X 125685429 125685429 single base substitution G C missense_variant S388C 1163C>G MELA-AU X 125685875 125685875 single base substitution G A synonymous_variant L239L 717C>T MELA-AU X 125685922 125685922 single base substitution G A missense_variant P224S 670C>T MELA-AU X 125686004 125686004 single base substitution C T stop_gained W196* 588G>A MELA-AU X 125686087 125686087 single base substitution C T missense_variant E169K 505G>A MELA-AU X 125686115 125686115 single base substitution G A synonymous_variant P159P 477C>T MELA-AU X 125686126 125686126 single base substitution C T missense_variant E156K 466G>A MELA-AU X 125686216 125686216 single base substitution C T missense_variant E126K 376G>A MELA-AU X 125686248 125686248 single base substitution G A missense_variant T115I 344C>T MELA-AU X 125686268 125686268 single base substitution G A synonymous_variant S108S 324C>T MELA-AU X 125686289 125686289 single base substitution G A synonymous_variant F101F 303C>T MELA-AU X 125686316 125686316 single base substitution C T synonymous_variant L92L 276G>A MELA-AU X 125686470 125686470 single base substitution C T missense_variant R41K 122G>A MELA-AU X 125686573 125686573 single base substitution C T missense_variant G7S 19G>A MELA-AU X 125686846 125686846 single base substitution G A upstream_gene_variant MELA-AU X 125686877 125686877 single base substitution G A upstream_gene_variant MELA-AU X 125687011 125687011 single base substitution C T upstream_gene_variant MELA-AU X 125687348 125687348 single base substitution C T upstream_gene_variant MELA-AU X 125687517 125687517 single base substitution G A upstream_gene_variant MELA-AU X 125687627 125687627 single base substitution C T upstream_gene_variant MELA-AU X 125687696 125687696 single base substitution G A upstream_gene_variant MELA-AU X 125687857 125687857 single base substitution G A upstream_gene_variant MELA-AU X 125688058 125688058 single base substitution G A upstream_gene_variant MELA-AU X 125688327 125688327 single base substitution G A upstream_gene_variant MELA-AU X 125688359 125688359 single base substitution G T upstream_gene_variant MELA-AU X 125688517 125688517 single base substitution C T upstream_gene_variant MELA-AU X 125688761 125688761 single base substitution G A upstream_gene_variant MELA-AU X 125688863 125688863 single base substitution G A upstream_gene_variant MELA-AU X 125688934 125688934 single base substitution A G upstream_gene_variant MELA-AU X 125689019 125689019 single base substitution G A upstream_gene_variant MELA-AU X 125689076 125689076 single base substitution G A upstream_gene_variant MELA-AU X 125689107 125689107 single base substitution T G upstream_gene_variant MELA-AU X 125689200 125689200 single base substitution G A upstream_gene_variant MELA-AU X 125689595 125689595 single base substitution C T upstream_gene_variant MELA-AU X 125689612 125689612 single base substitution C T upstream_gene_variant MELA-AU X 125689913 125689913 single base substitution C T upstream_gene_variant MELA-AU X 125689974 125689974 single base substitution G A upstream_gene_variant MELA-AU X 125690045 125690045 single base substitution G A upstream_gene_variant MELA-AU X 125690084 125690084 single base substitution C T upstream_gene_variant MELA-AU X 125690131 125690131 single base substitution G A upstream_gene_variant MELA-AU X 125690244 125690244 single base substitution G A upstream_gene_variant MELA-AU X 125690248 125690248 single base substitution G A upstream_gene_variant MELA-AU X 125690350 125690350 single base substitution G A upstream_gene_variant MELA-AU X 125690435 125690435 single base substitution G T upstream_gene_variant MELA-AU X 125690456 125690456 single base substitution C T upstream_gene_variant MELA-AU X 125690582 125690582 single base substitution C T upstream_gene_variant MELA-AU X 125690664 125690664 single base substitution A T upstream_gene_variant MELA-AU X 125690771 125690771 single base substitution G A upstream_gene_variant MELA-AU X 125691202 125691202 single base substitution C T upstream_gene_variant MELA-AU X 125691379 125691379 single base substitution G T upstream_gene_variant MELA-AU X 125691386 125691386 single base substitution G A upstream_gene_variant MELA-AU X 125691395 125691395 single base substitution G A upstream_gene_variant ORCA-IN X 125680649 125680649 single base substitution G T downstream_gene_variant ORCA-IN X 125683949 125683949 single base substitution C A 3_prime_UTR_variant ORCA-IN X 125688285 125688285 single base substitution C T upstream_gene_variant ORCA-IN X 125691459 125691459 single base substitution A G upstream_gene_variant OV-AU X 125681193 125681193 single base substitution C A downstream_gene_variant OV-AU X 125687564 125687564 single base substitution G A upstream_gene_variant OV-AU X 125690578 125690578 single base substitution G T upstream_gene_variant PACA-AU X 125678460 125678460 single base substitution C T downstream_gene_variant PACA-AU X 125679715 125679715 single base substitution C T downstream_gene_variant PACA-AU X 125681243 125681243 single base substitution G T downstream_gene_variant PACA-AU X 125682941 125682941 single base substitution C T downstream_gene_variant PACA-AU X 125683333 125683333 insertion of <=200bp - A downstream_gene_variant PACA-AU X 125683588 125683588 single base substitution A G 3_prime_UTR_variant PACA-AU X 125683804 125683804 single base substitution C T 3_prime_UTR_variant PACA-AU X 125684005 125684005 single base substitution A G 3_prime_UTR_variant PACA-AU X 125684582 125684582 single base substitution G T 3_prime_UTR_variant PACA-AU X 125684738 125684738 single base substitution T C 3_prime_UTR_variant PACA-AU X 125685589 125685589 single base substitution G A missense_variant R335C 1003C>T PACA-AU X 125685847 125685847 single base substitution C T missense_variant D249N 745G>A PACA-AU X 125686822 125686822 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant PACA-AU X 125687342 125687342 insertion of <=200bp - T upstream_gene_variant PACA-AU X 125688336 125688336 single base substitution A G upstream_gene_variant PACA-AU X 125689678 125689678 single base substitution G A upstream_gene_variant PACA-AU X 125691231 125691231 single base substitution A G upstream_gene_variant PACA-CA X 125678980 125678980 single base substitution C A downstream_gene_variant PACA-CA X 125679302 125679302 single base substitution G A downstream_gene_variant PACA-CA X 125680033 125680033 single base substitution C T downstream_gene_variant PACA-CA X 125681518 125681518 single base substitution T A downstream_gene_variant PACA-CA X 125681687 125681687 deletion of <=200bp T - downstream_gene_variant PACA-CA X 125682320 125682320 single base substitution A C downstream_gene_variant PACA-CA X 125684905 125684905 single base substitution A T 3_prime_UTR_variant PACA-CA X 125687363 125687363 single base substitution G T upstream_gene_variant PACA-CA X 125689028 125689028 single base substitution A C upstream_gene_variant PACA-CA X 125689669 125689669 single base substitution C A upstream_gene_variant PACA-CA X 125689702 125689702 single base substitution G A upstream_gene_variant PACA-CA X 125691086 125691086 single base substitution G A upstream_gene_variant PACA-CA X 125691192 125691192 insertion of <=200bp - A upstream_gene_variant PAEN-AU X 125690686 125690686 single base substitution C A upstream_gene_variant PBCA-DE X 125683149 125683149 insertion of <=200bp - A downstream_gene_variant PBCA-DE X 125684570 125684570 single base substitution C T 3_prime_UTR_variant PBCA-DE X 125685264 125685264 single base substitution A C missense_variant L443R 1328T>G PBCA-DE X 125690883 125690883 single base substitution G A upstream_gene_variant PBCA-DE X 125691241 125691241 single base substitution C A upstream_gene_variant PRAD-UK X 125680204 125680204 single base substitution T G downstream_gene_variant PRAD-UK X 125684616 125684616 single base substitution C T 3_prime_UTR_variant PRAD-UK X 125687964 125687964 single base substitution C T upstream_gene_variant PRAD-US X 125685920 125685920 single base substitution C T synonymous_variant P224P 672G>A PRAD-US X 125685925 125685925 single base substitution C G missense_variant D223H 667G>C READ-US X 125685527 125685527 single base substitution C T synonymous_variant S355S 1065G>A READ-US X 125685756 125685756 single base substitution G A missense_variant A279V 836C>T SKCA-BR X 125679438 125679438 single base substitution T A downstream_gene_variant SKCA-BR X 125681611 125681611 single base substitution A C downstream_gene_variant SKCA-BR X 125681661 125681661 single base substitution C T downstream_gene_variant SKCA-BR X 125684837 125684837 single base substitution G A 3_prime_UTR_variant SKCA-BR X 125685460 125685460 single base substitution G A missense_variant R378W 1132C>T SKCA-BR X 125685461 125685461 single base substitution G A synonymous_variant V377V 1131C>T SKCA-BR X 125686332 125686332 single base substitution A G missense_variant L87P 260T>C SKCA-BR X 125687089 125687089 single base substitution C T upstream_gene_variant SKCA-BR X 125687348 125687348 single base substitution C T upstream_gene_variant SKCA-BR X 125687403 125687403 single base substitution C T upstream_gene_variant SKCA-BR X 125689918 125689918 single base substitution G A upstream_gene_variant SKCA-BR X 125690493 125690493 single base substitution G A upstream_gene_variant SKCA-BR X 125690613 125690613 insertion of <=200bp - AT upstream_gene_variant SKCM-US X 125685224 125685224 single base substitution C T synonymous_variant G456G 1368G>A SKCM-US X 125685242 125685242 single base substitution G A synonymous_variant L450L 1350C>T SKCM-US X 125685274 125685274 single base substitution C T missense_variant E440K 1318G>A SKCM-US X 125685344 125685344 single base substitution G A synonymous_variant F416F 1248C>T SKCM-US X 125685446 125685446 single base substitution G A synonymous_variant F382F 1146C>T SKCM-US X 125685448 125685448 single base substitution A G missense_variant F382L 1144T>C SKCM-US X 125685552 125685552 single base substitution C T missense_variant R347Q 1040G>A SKCM-US X 125685672 125685672 single base substitution C T missense_variant R307Q 920G>A SKCM-US X 125685746 125685746 single base substitution C T synonymous_variant L282L 846G>A SKCM-US X 125685857 125685857 single base substitution G A synonymous_variant I245I 735C>T SKCM-US X 125685875 125685875 single base substitution G A synonymous_variant L239L 717C>T SKCM-US X 125685886 125685886 single base substitution C T missense_variant E236K 706G>A SKCM-US X 125685897 125685897 single base substitution G A missense_variant A232V 695C>T SKCM-US X 125686004 125686004 single base substitution C T stop_gained W196* 588G>A SKCM-US X 125686141 125686141 single base substitution C T missense_variant G151S 451G>A SKCM-US X 125686156 125686156 single base substitution C T missense_variant D146N 436G>A SKCM-US X 125686229 125686229 single base substitution G A synonymous_variant F121F 363C>T SKCM-US X 125686526 125686526 single base substitution G C missense_variant S22R 66C>G SKCM-US X 125686565 125686565 single base substitution C G missense_variant R9S 27G>C STAD-US X 125685267 125685267 single base substitution T G missense_variant K442T 1325A>C STAD-US X 125685294 125685294 single base substitution G A missense_variant T433I 1298C>T STAD-US X 125685428 125685428 single base substitution G A synonymous_variant S388S 1164C>T STAD-US X 125685489 125685489 single base substitution C A missense_variant G368V 1103G>T STAD-US X 125685490 125685490 single base substitution C T missense_variant G368S 1102G>A STAD-US X 125685509 125685509 single base substitution G C missense_variant H361Q 1083C>G STAD-US X 125685584 125685584 single base substitution C A missense_variant Q336H 1008G>T STAD-US X 125685718 125685718 single base substitution C T missense_variant G292R 874G>A STAD-US X 125685736 125685736 single base substitution A C missense_variant F286V 856T>G STAD-US X 125685743 125685743 single base substitution G A synonymous_variant D283D 849C>T STAD-US X 125685809 125685809 single base substitution A G synonymous_variant S261S 783T>C STAD-US X 125685810 125685810 single base substitution C A missense_variant S261I 782G>T STAD-US X 125685821 125685821 single base substitution G A synonymous_variant I257I 771C>T STAD-US X 125685932 125685932 single base substitution C A missense_variant W220C 660G>T STAD-US X 125685932 125685932 single base substitution C T stop_gained W220* 660G>A STAD-US X 125685967 125685967 single base substitution C T missense_variant V209M 625G>A STAD-US X 125686047 125686047 single base substitution A T missense_variant L182Q 545T>A STAD-US X 125686062 125686062 single base substitution T A missense_variant Y177F 530A>T STAD-US X 125686084 125686084 single base substitution T G missense_variant N170H 508A>C STAD-US X 125686201 125686201 single base substitution C T missense_variant A131T 391G>A STAD-US X 125686323 125686323 single base substitution C T missense_variant R90H 269G>A STAD-US X 125686328 125686328 single base substitution C A synonymous_variant T88T 264G>T STAD-US X 125686358 125686358 single base substitution G A synonymous_variant Y78Y 234C>T STAD-US X 125686397 125686397 single base substitution G A synonymous_variant P65P 195C>T STAD-US X 125686436 125686436 single base substitution C T synonymous_variant A52A 156G>A STAD-US X 125686437 125686437 single base substitution G A missense_variant A52V 155C>T UCEC-US X 125685420 125685420 single base substitution A G missense_variant L391P 1172T>C UCEC-US X 125685725 125685725 single base substitution C T stop_gained W289* 867G>A UCEC-US X 125685911 125685911 single base substitution G A synonymous_variant F227F 681C>T UCEC-US X 125685920 125685920 single base substitution C T synonymous_variant P224P 672G>A UCEC-US X 125685930 125685930 single base substitution C T missense_variant R221Q 662G>A UCEC-US X 125685938 125685938 single base substitution C T synonymous_variant A218A 654G>A UCEC-US X 125686010 125686010 single base substitution C A missense_variant K194N 582G>T UCEC-US X 125686023 125686023 single base substitution C T missense_variant R190H 569G>A UCEC-US X 125686027 125686027 single base substitution C T missense_variant D189N 565G>A UCEC-US X 125686089 125686089 single base substitution C T missense_variant G168D 503G>A UCEC-US X 125686189 125686189 single base substitution G A missense_variant L135F 403C>T UCEC-US X 125686197 125686197 single base substitution C T missense_variant R132H 395G>A UCEC-US X 125686340 125686340 single base substitution G A synonymous_variant P84P 252C>T UCEC-US X 125686436 125686436 single base substitution C T synonymous_variant A52A 156G>A UCEC-US X 125686451 125686451 single base substitution C T synonymous_variant T47T 141G>A UCEC-US X 125686554 125686554 single base substitution G A missense_variant A13V 38C>T

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand COLO678 COSM2725063 c.1129G>A p.V377I Substitution - Missense 23:126551480-126551480 - WA10 COSM237274 c.57C>T p.D19D Substitution - coding silent 23:126552552-126552552 - ESCC-191T COSM3939779 c.796C>T p.R266W Substitution - Missense 23:126551813-126551813 - TCGA-AX-A0J1-01 COSM1114680 c.654G>A p.A218A Substitution - coding silent 23:126551955-126551955 - TCGA-33-4582-01 COSM755461 c.675C>A p.D225E Substitution - Missense 23:126551934-126551934 - TCGA-FS-A1Z3-06 COSM3557625 c.436G>A p.D146N Substitution - Missense 23:126552173-126552173 - SC_9038 COSM456701 c.1060C>T p.R354W Substitution - Missense 23:126551549-126551549 - GC6_T COSM150823 c.1382T>G p.L461R Substitution - Missense 23:126551227-126551227 - CSCC-20-T COSM4464785 c.1351C>T p.P451S Substitution - Missense 23:126551258-126551258 - CHC892T COSM4794866 c.189G>A p.W63* Substitution - Nonsense 23:126552420-126552420 - TCGA-AA-3713-01 COSM1114692 c.395G>A p.R132H Substitution - Missense 23:126552214-126552214 - TCGA-DW-7840-01 COSM3992343 c.1094T>G p.V365G Substitution - Missense 23:126551515-126551515 - TCGA-DK-A1AD-01 COSM1315193 c.269G>A p.R90H Substitution - Missense 23:126552340-126552340 - TCGA-C8-A12K-01 COSM456705 c.372C>T p.D124D Substitution - coding silent 23:126552237-126552237 - A673 COSM4589168 c.1137C>T p.A379A Substitution - coding silent 23:126551472-126551472 - TCGA-AX-A0J1-01 COSM1114694 c.252C>T p.P84P Substitution - coding silent 23:126552357-126552357 - TCGA-EI-6884-01 COSM3424444 c.1065G>A p.S355S Substitution - coding silent 23:126551544-126551544 - AD82 COSM5966890 c.373G>T p.V125L Substitution - Missense 23:126552236-126552236 - TCGA-18-3416-01 COSM755468 c.1294T>A p.Y432N Substitution - Missense 23:126551315-126551315 - CSCC-29-T COSM4514444 c.974C>T p.S325F Substitution - Missense 23:126551635-126551635 - BD114T COSM5504795 c.358C>A p.L120I Substitution - Missense 23:126552251-126552251 - 53M COSM3557616 c.1350C>T p.L450L Substitution - coding silent 23:126551259-126551259 - sysucc-679T COSM5480694 c.1080C>T p.R360R Substitution - coding silent 23:126551529-126551529 - 230 COSM203201 c.409C>T p.R137W Substitution - Missense 23:126552200-126552200 - TCGA-DA-A1HY-06 COSM3557616 c.1350C>T p.L450L Substitution - coding silent 23:126551259-126551259 - D01 COSM5543820 c.163C>T p.L55L Substitution - coding silent 23:126552446-126552446 - ESO-0025 COSM1249711 c.618C>T p.T206T Substitution - coding silent 23:126551991-126551991 - TCGA-G4-6310-01 COSM1465451 c.1245T>C p.D415D Substitution - coding silent 23:126551364-126551364 - TCGA-BR-6452-01 COSM4106491 c.660G>T p.W220C Substitution - Missense 23:126551949-126551949 - TCGA-D1-A103-01 COSM1114700 c.38C>T p.A13V Substitution - Missense 23:126552571-126552571 - RKO COSM1465455 c.645C>T p.G215G Substitution - coding silent 23:126551964-126551964 - TCGA-F1-A448-01 COSM4106497 c.391G>A p.A131T Substitution - Missense 23:126552218-126552218 - TCGA-66-2780-01 COSM755466 c.1137C>G p.A379A Substitution - coding silent 23:126551472-126551472 - TCGA-EE-A29D-06 COSM3557619 c.1040G>A p.R347Q Substitution - Missense 23:126551569-126551569 - TCGA-HU-A4G8-01 COSM4106492 c.660G>A p.W220* Substitution - Nonsense 23:126551949-126551949 - TCGA-EE-A2MR-06 COSM3557617 c.1318G>A p.E440K Substitution - Missense 23:126551291-126551291 - TCGA-AA-3514-01 COSM291505 c.1279T>A p.F427I Substitution - Missense 23:126551330-126551330 - LUAD-F00162 COSM366766 c.392C>T p.A131V Substitution - Missense 23:126552217-126552217 - LUAD-CHTN-MAD06-00678 COSM361080 c.97G>T p.G33C Substitution - Missense 23:126552512-126552512 - TCGA-46-3765-01 COSM755455 c.265G>T p.E89* Substitution - Nonsense 23:126552344-126552344 - T16 COSM5345891 c.1209G>T p.R403S Substitution - Missense 23:126551400-126551400 - TCGA-ER-A19N-06 COSM3557624 c.451G>A p.G151S Substitution - Missense 23:126552158-126552158 - HCC018T COSM5820144 c.185G>T p.G62V Substitution - Missense 23:126552424-126552424 - ESCC_136 COSM5643084 c.1367G>T p.G456V Substitution - Missense 23:126551242-126551242 - CSCC-44-T COSM4457293 c.1039C>T p.R347* Substitution - Nonsense 23:126551570-126551570 - TCGA-FS-A4F8-06 COSM3557618 c.1144T>C p.F382L Substitution - Missense 23:126551465-126551465 - CSCC-60-T COSM4505315 c.68C>G p.S23W Substitution - Missense 23:126552541-126552541 - AA1924 COSM4168808 c.1012C>T p.Q338* Substitution - Nonsense 23:126551597-126551597 - COLO-829 COSM36778 c.842C>T p.S281F Substitution - Missense 23:126551767-126551767 - TCGA-43-2578-01 COSM755460 c.542C>G p.S181C Substitution - Missense 23:126552067-126552067 - SNU-C2B COSM2725072 c.967G>A p.V323M Substitution - Missense 23:126551642-126551642 - T3062 COSM4676317 c.1021A>G p.I341V Substitution - Missense 23:126551588-126551588 - YUGURT COSM5411946 c.922G>A p.D308N Substitution - Missense 23:126551687-126551687 - TCGA-22-4613-01 COSM755462 c.874G>T p.G292W Substitution - Missense 23:126551735-126551735 - S02344 COSM5693925 c.1103G>C p.G368A Substitution - Missense 23:126551506-126551506 - TCGA-EE-A2MR-06 COSM3557623 c.588G>A p.W196* Substitution - Nonsense 23:126552021-126552021 - TCGA-D3-A5GN-06 COSM2725083 c.706G>A p.E236K Substitution - Missense 23:126551903-126551903 - T3118 COSM4676324 c.319A>T p.N107Y Substitution - Missense 23:126552290-126552290 - 2334191 COSM319809 c.858C>A p.F286L Substitution - Missense 23:126551751-126551751 - TCGA-D7-6521-01 COSM4106479 c.1298C>T p.T433I Substitution - Missense 23:126551311-126551311 - ESO-1130 COSM1249712 c.624C>T p.A208A Substitution - coding silent 23:126551985-126551985 - 627LT COSM4382848 c.1003C>T p.R335C Substitution - Missense 23:126551606-126551606 - TCGA-BR-A453-01 COSM1114696 c.156G>A p.A52A Substitution - coding silent 23:126552453-126552453 - B57-Tumor COSM1756376 c.1191T>A p.P397P Substitution - coding silent 23:126551418-126551418 - CCK81 COSM2725063 c.1129G>A p.V377I Substitution - Missense 23:126551480-126551480 - LS411 COSM2725067 c.1069A>G p.S357G Substitution - Missense 23:126551540-126551540 - 8068988 COSM4382848 c.1003C>T p.R335C Substitution - Missense 23:126551606-126551606 - LUAD-YINHD COSM388630 c.1137C>A p.A379A Substitution - coding silent 23:126551472-126551472 - DF01 COSM1643941 c.1056C>T p.G352G Substitution - coding silent 23:126551553-126551553 - TCGA-HU-8602-01 COSM4106478 c.1325A>C p.K442T Substitution - Missense 23:126551284-126551284 - YUSIV COSM4676328 c.31C>T p.R11W Substitution - Missense 23:126552578-126552578 - TCGA-AP-A056-01 COSM1114674 c.681C>T p.F227F Substitution - coding silent 23:126551928-126551928 - ESCC-162T COSM3939777 c.1198A>T p.R400W Substitution - Missense 23:126551411-126551411 - TCGA-43-5668-01 COSM755463 c.1062G>A p.R354R Substitution - coding silent 23:126551547-126551547 - TCGA-A5-A0GP-01 COSM1114696 c.156G>A p.A52A Substitution - coding silent 23:126552453-126552453 - HT55 COSM2725055 c.1250G>T p.W417L Substitution - Missense 23:126551359-126551359 - LIM1899 COSM2725081 c.720C>T p.P240P Substitution - coding silent 23:126551889-126551889 - TCGA-EE-A2MR-06 COSM3557620 c.735C>T p.I245I Substitution - coding silent 23:126551874-126551874 - TCGA-BS-A0UA-01 COSM1114692 c.395G>A p.R132H Substitution - Missense 23:126552214-126552214 - sysucc-880T COSM3557624 c.451G>A p.G151S Substitution - Missense 23:126552158-126552158 - TCGA-CG-5718-01 COSM4106485 c.874G>A p.G292R Substitution - Missense 23:126551735-126551735 - 61 COSM5742410 c.40C>T p.P14S Substitution - Missense 23:126552569-126552569 - TCGA-G4-6302-01 COSM3694329 c.862C>A p.L288M Substitution - Missense 23:126551747-126551747 - LUAD-CHTN-4090680 COSM357792 c.243G>C p.Q81H Substitution - Missense 23:126552366-126552366 - COLO-829 COSM36778 c.842C>T p.S281F Substitution - Missense 23:126551767-126551767 - ESCC-148T COSM3939778 c.1152G>T p.E384D Substitution - Missense 23:126551457-126551457 - TCGA-BR-4184-01 COSM4106498 c.264G>T p.T88T Substitution - coding silent 23:126552345-126552345 - T2963 COSM4676323 c.513C>G p.P171P Substitution - coding silent 23:126552096-126552096 - YUKAT COSM5411947 c.858C>T p.F286F Substitution - coding silent 23:126551751-126551751 - HCC100T COSM1625482 c.1348C>T p.L450F Substitution - Missense 23:126551261-126551261 - CSCC-40-T COSM4542871 c.326G>A p.R109K Substitution - Missense 23:126552283-126552283 - PD18775a COSM5777488 c.1289C>T p.A430V Substitution - Missense 23:126551320-126551320 - TCGA-DD-A4NV-01 COSM4916465 c.1165G>A p.A389T Substitution - Missense 23:126551444-126551444 - TCGA-DU-8158-01 COSM302027 c.140C>T p.T47M Substitution - Missense 23:126552469-126552469 - sysucc-1240T COSM4106500 c.195C>T p.P65P Substitution - coding silent 23:126552414-126552414 - TCGA-EE-A2MS-06 COSM3557622 c.695C>T p.A232V Substitution - Missense 23:126551914-126551914 - TCGA-66-2777-01 COSM755454 c.194C>T p.P65L Substitution - Missense 23:126552415-126552415 - CHC1715T COSM4789476 c.310C>A p.Q104K Substitution - Missense 23:126552299-126552299 - 2521252 COSM2725083 c.706G>A p.E236K Substitution - Missense 23:126551903-126551903 - pfg068T COSM4761068 c.1057G>A p.V353M Substitution - Missense 23:126551552-126551552 - TCGA-13-1494-01 COSM117989 c.1318G>T p.E440* Substitution - Nonsense 23:126551291-126551291 - HN_62739 COSM122505 c.1307A>G p.Y436C Substitution - Missense 23:126551302-126551302 - MD-144 COSM302027 c.140C>T p.T47M Substitution - Missense 23:126552469-126552469 - S02384 COSM5698622 c.45G>T p.A15A Substitution - coding silent 23:126552564-126552564 - 2334191 COSM319808 c.859C>A p.H287N Substitution - Missense 23:126551750-126551750 - SW403 COSM4655460 c.662G>T p.R221L Substitution - Missense 23:126551947-126551947 - TCGA-76-6193-01 COSM3405938 c.1004G>A p.R335H Substitution - Missense 23:126551605-126551605 - 587338 COSM1203043 c.226C>T p.R76W Substitution - Missense 23:126552383-126552383 - TCGA-AR-A0TX-01 COSM456700 c.1122C>G p.F374L Substitution - Missense 23:126551487-126551487 - TCGA-EE-A29L-06 COSM3557621 c.717C>T p.L239L Substitution - coding silent 23:126551892-126551892 - TCGA-DU-5847-01 COSM1114678 c.662G>A p.R221Q Substitution - Missense 23:126551947-126551947 - 250LT COSM4382399 c.214G>A p.D72N Substitution - Missense 23:126552395-126552395 - TCGA-BR-4191-01 COSM4106496 c.508A>C p.N170H Substitution - Missense 23:126552101-126552101 - HT55 COSM2725074 c.830T>A p.L277Q Substitution - Missense 23:126551779-126551779 - HF-23896 COSM1197823 c.799G>T p.A267S Substitution - Missense 23:126551810-126551810 - CHC1531T COSM4804862 c.736C>T p.R246C Substitution - Missense 23:126551873-126551873 - ZZUFHECRKL-G019T COSM456704 c.850G>A p.G284S Substitution - Missense 23:126551759-126551759 - TCGA-B5-A0JZ-01 COSM1114670 c.1172T>C p.L391P Substitution - Missense 23:126551437-126551437 - ESCC_BICR_052T COSM4382848 c.1003C>T p.R335C Substitution - Missense 23:126551606-126551606 - CHC891T COSM3405938 c.1004G>A p.R335H Substitution - Missense 23:126551605-126551605 - TCGA-33-4566-01 COSM755456 c.461C>G p.A154G Substitution - Missense 23:126552148-126552148 - CSCC-40-T COSM4398319 c.1146C>T p.F382F Substitution - coding silent 23:126551463-126551463 - TCGA-B5-A0JR-01 COSM1114688 c.503G>A p.G168D Substitution - Missense 23:126552106-126552106 - TCGA-CM-4752-01 COSM1465456 c.639C>T p.R213R Substitution - coding silent 23:126551970-126551970 - T3225 COSM2725063 c.1129G>A p.V377I Substitution - Missense 23:126551480-126551480 - CX-1 COSM4621742 c.55G>A p.D19N Substitution - Missense 23:126552554-126552554 - TCGA-AA-3833-01 COSM271194 c.1153G>A p.E385K Substitution - Missense 23:126551456-126551456 - TCGA-CD-A487-01 COSM4106480 c.1164C>T p.S388S Substitution - coding silent 23:126551445-126551445 - TCGA-EI-6882-01 COSM3424445 c.836C>T p.A279V Substitution - Missense 23:126551773-126551773 - SYN08PT2 COSM1732305 c.188G>T p.W63L Substitution - Missense 23:126552421-126552421 - HCT116 COSM1114698 c.141G>A p.T47T Substitution - coding silent 23:126552468-126552468 - BD72T COSM4761068 c.1057G>A p.V353M Substitution - Missense 23:126551552-126551552 - SNU-175 COSM2725073 c.837G>A p.A279A Substitution - coding silent 23:126551772-126551772 - TCGA-D1-A103-01 COSM1114690 c.403C>T p.L135F Substitution - Missense 23:126552206-126552206 - CSCC-55-T COSM4520050 c.103G>A p.G35R Substitution - Missense 23:126552506-126552506 - sysucc-1067T COSM2725081 c.720C>T p.P240P Substitution - coding silent 23:126551889-126551889 - 401 COSM4429724 c.627G>A p.V209V Substitution - coding silent 23:126551982-126551982 - 16461 COSM5616216 c.1009G>A p.D337N Substitution - Missense 23:126551600-126551600 - TCGA-33-4566-01 COSM755458 c.462C>T p.A154A Substitution - coding silent 23:126552147-126552147 - TCGA-27-1838-01 COSM3405939 c.288G>A p.T96T Substitution - coding silent 23:126552321-126552321 - TCGA-66-2742-01 COSM755459 c.480C>T p.S160S Substitution - coding silent 23:126552129-126552129 - TCGA-AP-A0LM-01 COSM1114682 c.582G>T p.K194N Substitution - Missense 23:126552027-126552027 - CSCC-17-T COSM4559242 c.797G>C p.R266P Substitution - Missense 23:126551812-126551812 - BD236T COSM5519910 c.932G>A p.C311Y Substitution - Missense 23:126551677-126551677 - TCGA-BR-8361-01 COSM4106488 c.783T>C p.S261S Substitution - coding silent 23:126551826-126551826 - TCGA-CD-5798-01 COSM4106486 c.856T>G p.F286V Substitution - Missense 23:126551753-126551753 - 389 COSM4427776 c.465C>A p.I155I Substitution - coding silent 23:126552144-126552144 - PD4125a COSM160336 c.617C>A p.T206N Substitution - Missense 23:126551992-126551992 - CHC891T COSM3405938 c.1004G>A p.R335H Substitution - Missense 23:126551605-126551605 - TCGA-12-0616 COSM2153576 c.263C>T p.T88M Substitution - Missense 23:126552346-126552346 - TCGA-BL-A0C8-01 COSM422241 c.43G>A p.A15T Substitution - Missense 23:126552566-126552566 - HCC137T COSM1625483 c.395G>T p.R132L Substitution - Missense 23:126552214-126552214 - pfg034T COSM1743144 c.304G>A p.A102T Substitution - Missense 23:126552305-126552305 - sysucc-1370T COSM5472814 c.102G>T p.E34D Substitution - Missense 23:126552507-126552507 - TCGA-CW-5580-01 COSM487914 c.96C>T p.D32D Substitution - coding silent 23:126552513-126552513 - CHC892T COSM4960617 c.186G>A p.G62G Substitution - coding silent 23:126552423-126552423 - RKO COSM4649379 c.396C>T p.R132R Substitution - coding silent 23:126552213-126552213 - TCGA-AP-A0LM-01 COSM1114672 c.867G>A p.W289* Substitution - Nonsense 23:126551742-126551742 - LUAD-YINHD COSM388631 c.1095G>T p.V365V Substitution - coding silent 23:126551514-126551514 - D01 COSM5543819 c.826G>A p.E276K Substitution - Missense 23:126551783-126551783 - I2L-P10-Tumor-Organoid COSM5366917 c.898T>C p.S300P Substitution - Missense 23:126551711-126551711 - 600 COSM3721412 c.550C>T p.P184S Substitution - Missense 23:126552059-126552059 - TCGA-CG-4306-01 COSM4106500 c.195C>T p.P65P Substitution - coding silent 23:126552414-126552414 - PT33 COSM5543819 c.826G>A p.E276K Substitution - Missense 23:126551783-126551783 - H1672 COSM316531 c.1122C>T p.F374F Substitution - coding silent 23:126551487-126551487 - LUAD-RT-S01777 COSM382631 c.1134G>T p.R378R Substitution - coding silent 23:126551475-126551475 - TCGA-A8-A09W-01 COSM456702 c.936G>C p.L312L Substitution - coding silent 23:126551673-126551673 - TCGA-DD-A4NF-01 COSM4912703 c.1231C>T p.L411F Substitution - Missense 23:126551378-126551378 - 8053200 COSM3390400 c.745G>A p.D249N Substitution - Missense 23:126551864-126551864 - BD57T COSM4746067 c.235G>A p.A79T Substitution - Missense 23:126552374-126552374 - TCGA-63-5131-01 COSM755453 c.190G>T p.G64C Substitution - Missense 23:126552419-126552419 - MO_1192 COSM203201 c.409C>T p.R137W Substitution - Missense 23:126552200-126552200 - TCGA-BT-A20W-01 COSM422242 c.1370A>C p.N457T Substitution - Missense 23:126551239-126551239 - CHC1597T COSM4787758 c.283G>C p.G95R Substitution - Missense 23:126552326-126552326 - CSCC-54-T COSM4456055 c.1129_1130GT>AA p.V377N Substitution - Missense 23:126551479-126551480 - TCGA-BR-7715-01 COSM4106490 c.771C>T p.I257I Substitution - coding silent 23:126551838-126551838 - TCGA-D9-A6EA-06 COSM4398319 c.1146C>T p.F382F Substitution - coding silent 23:126551463-126551463 - ESCC_11 COSM5624770 c.518G>T p.S173I Substitution - Missense 23:126552091-126552091 - pfg008T COSM1643941 c.1056C>T p.G352G Substitution - coding silent 23:126551553-126551553 - 585258 COSM319807 c.516C>A p.N172K Substitution - Missense 23:126552093-126552093 - HCC137 COSM1625483 c.395G>T p.R132L Substitution - Missense 23:126552214-126552214 - T2944 COSM4676320 c.813C>T p.G271G Substitution - coding silent 23:126551796-126551796 - CSCC-30-T COSM4496459 c.475C>T p.P159S Substitution - Missense 23:126552134-126552134 - TCGA-12-0616-01 COSM2153576 c.263C>T p.T88M Substitution - Missense 23:126552346-126552346 - TCGA-CG-4465-01 COSM4106499 c.234C>T p.Y78Y Substitution - coding silent 23:126552375-126552375 - TCGA-D3-A1Q6-06 COSM3557626 c.363C>T p.F121F Substitution - coding silent 23:126552246-126552246 - TCGA-EE-A3JD-06 COSM4394661 c.846G>A p.L282L Substitution - coding silent 23:126551763-126551763 - S02139 COSM5674695 c.1056C>A p.G352G Substitution - coding silent 23:126551553-126551553 - TCGA-BF-A3DL-01 COSM2725083 c.706G>A p.E236K Substitution - Missense 23:126551903-126551903 - ESO-717 COSM1242175 c.601G>A p.A201T Substitution - Missense 23:126552008-126552008 - T3336 COSM4676328 c.31C>T p.R11W Substitution - Missense 23:126552578-126552578 - TCGA-D1-A17T-01 COSM1114676 c.672G>A p.P224P Substitution - coding silent 23:126551937-126551937 - SNU-175 COSM1114692 c.395G>A p.R132H Substitution - Missense 23:126552214-126552214 - CRC-14T COSM5452178 c.966C>T p.A322A Substitution - coding silent 23:126551643-126551643 - 4-42-T1 COSM4745807 c.540C>T p.P180P Substitution - coding silent 23:126552069-126552069 - TCGA-A2-A0EU-01 COSM456701 c.1060C>T p.R354W Substitution - Missense 23:126551549-126551549 - S02139 COSM5674696 c.595G>A p.A199T Substitution - Missense 23:126552014-126552014 - 587316 COSM1203042 c.373G>A p.V125M Substitution - Missense 23:126552236-126552236 - TCGA-BH-A28Q-01 COSM1490462 c.478T>G p.S160A Substitution - Missense 23:126552131-126552131 - TCGA-BR-7703-01 COSM4106482 c.1102G>A p.G368S Substitution - Missense 23:126551507-126551507 - TCGA-BR-8380-01 COSM4106487 c.849C>T p.D283D Substitution - coding silent 23:126551760-126551760 - TCGA-BS-A0UF-01 COSM1114686 c.565G>A p.D189N Substitution - Missense 23:126552044-126552044 - CSCC-27-T COSM4548337 c.444G>A p.Q148Q Substitution - coding silent 23:126552165-126552165 - TCGA-BR-8372-01 COSM1315193 c.269G>A p.R90H Substitution - Missense 23:126552340-126552340 - TCGA-14-1825-01 COSM3405938 c.1004G>A p.R335H Substitution - Missense 23:126551605-126551605 - TCGA-AA-3986-01 COSM297942 c.32G>A p.R11Q Substitution - Missense 23:126552577-126552577 - TCGA-EE-A2MR-06 COSM3913330 c.1248C>T p.F416F Substitution - coding silent 23:126551361-126551361 - 6115117 COSM5567864 c.74C>T p.S25L Substitution - Missense 23:126552535-126552535 - TCGA-AX-A0J1-01 COSM1114698 c.141G>A p.T47T Substitution - coding silent 23:126552468-126552468 - ESCC_135 COSM2725065 c.1079G>A p.R360H Substitution - Missense 23:126551530-126551530 - CSCC-44-T COSM4506406 c.719C>T p.P240L Substitution - Missense 23:126551890-126551890 - YUKAT COSM5411945 c.1200G>A p.R400R Substitution - coding silent 23:126551409-126551409 - 587256 COSM1203045 c.196G>A p.A66T Substitution - Missense 23:126552413-126552413 - ICC004T COSM5817428 c.446G>A p.G149D Substitution - Missense 23:126552163-126552163 - TCGA-HC-7231-01 COSM1114676 c.672G>A p.P224P Substitution - coding silent 23:126551937-126551937 - CSCC-27-T COSM3557624 c.451G>A p.G151S Substitution - Missense 23:126552158-126552158 - TCGA-J9-A52B-01 COSM4876977 c.667G>C p.D223H Substitution - Missense 23:126551942-126551942 - OCC05PT COSM88479 c.1156A>T p.R386* Substitution - Nonsense 23:126551453-126551453 - TCGA-BH-A0B4-01 COSM456703 c.888C>A p.S296S Substitution - coding silent 23:126551721-126551721 - GB07 COSM1743144 c.304G>A p.A102T Substitution - Missense 23:126552305-126552305 - T3092 COSM4676326 c.188G>C p.W63S Substitution - Missense 23:126552421-126552421 - TCGA-56-5898-01 COSM755452 c.44C>T p.A15V Substitution - Missense 23:126552565-126552565 - ESCC-178T COSM3939776 c.1312T>A p.W438R Substitution - Missense 23:126551297-126551297 - T96 COSM4676319 c.873C>T p.A291A Substitution - coding silent 23:126551736-126551736 - TCGA-FW-A3R5-06 COSM3913331 c.920G>A p.R307Q Substitution - Missense 23:126551689-126551689 - NB-2074 COSM1284415 c.449G>A p.C150Y Substitution - Missense 23:126552160-126552160 - Patient_1 COSM4398319 c.1146C>T p.F382F Substitution - coding silent 23:126551463-126551463 - CHC1597T COSM4787798 c.282G>C p.L94L Substitution - coding silent 23:126552327-126552327 - QC2-09-T2 COSM4106486 c.856T>G p.F286V Substitution - Missense 23:126551753-126551753 - Au4 COSM5603345 c.27G>A p.R9R Substitution - coding silent 23:126552582-126552582 - TCGA-AA-A01D-01 COSM299721 c.963C>T p.Y321Y Substitution - coding silent 23:126551646-126551646 - TCGA-G2-A2EJ-01 COSM1315192 c.826G>T p.E276* Substitution - Nonsense 23:126551783-126551783 - TCGA-AX-A0J1-01 COSM1114692 c.395G>A p.R132H Substitution - Missense 23:126552214-126552214 - TCGA-FR-A3YN-06 COSM3557627 c.66C>G p.S22R Substitution - Missense 23:126552543-126552543 - CSCC-38-T COSM4522894 c.1186G>A p.G396R Substitution - Missense 23:126551423-126551423 - CHC892T COSM4960617 c.186G>A p.G62G Substitution - coding silent 23:126552423-126552423 - CSCC-62-T COSM4559146 c.793G>A p.V265M Substitution - Missense 23:126551816-126551816 - TCGA-EB-A5UL-06 COSM3557628 c.27G>C p.R9S Substitution - Missense 23:126552582-126552582 - T2999 COSM4676321 c.737G>A p.R246H Substitution - Missense 23:126551872-126551872 - TCGA-EK-A2H0-01 COSM4818926 c.612T>A p.S204R Substitution - Missense 23:126551997-126551997 - TCGA-FP-A4BF-01 COSM4106495 c.530A>T p.Y177F Substitution - Missense 23:126552079-126552079 - CSCC-31-T COSM4559621 c.811G>A p.G271S Substitution - Missense 23:126551798-126551798 - TCGA-33-4586-01 COSM755467 c.1213G>T p.A405S Substitution - Missense 23:126551396-126551396 - TCGA-A6-5665-01 COSM1465455 c.645C>T p.G215G Substitution - coding silent 23:126551964-126551964 - CSCC-56-T COSM4514838 c.989C>T p.S330F Substitution - Missense 23:126551620-126551620 - 61 COSM1114692 c.395G>A p.R132H Substitution - Missense 23:126552214-126552214 - TCGA-BH-A0B6-01 COSM3843494 c.635C>T p.S212F Substitution - Missense 23:126551974-126551974 - 4537_T COSM3964677 c.1312T>C p.W438R Substitution - Missense 23:126551297-126551297 - LFS_MB1 COSM216179 c.1328T>G p.L443R Substitution - Missense 23:126551281-126551281 - T263 COSM4676322 c.572A>G p.H191R Substitution - Missense 23:126552037-126552037 - TCGA-EQ-8122-01 COSM4106481 c.1103G>T p.G368V Substitution - Missense 23:126551506-126551506 - 627T COSM4382848 c.1003C>T p.R335C Substitution - Missense 23:126551606-126551606 - CSCC-27-T COSM4501634 c.594C>T p.F198F Substitution - coding silent 23:126552015-126552015 - TCGA-A8-A06X-01 COSM456704 c.850G>A p.G284S Substitution - Missense 23:126551759-126551759 - T2940 COSM4676325 c.293A>G p.N98S Substitution - Missense 23:126552316-126552316 - 587376 COSM1203044 c.517A>C p.S173R Substitution - Missense 23:126552092-126552092 - TCGA-BR-8361-01 COSM4106484 c.1008G>T p.Q336H Substitution - Missense 23:126551601-126551601 - LUAD-F00162 COSM366765 c.577C>A p.H193N Substitution - Missense 23:126552032-126552032 - TCGA-DS-A0VN-01 COSM462323 c.837G>T p.A279A Substitution - coding silent 23:126551772-126551772 - sysucc-1370T COSM5472813 c.568C>T p.R190C Substitution - Missense 23:126552041-126552041 - TCGA-61-1722-01 COSM1331272 c.597C>A p.A199A Substitution - coding silent 23:126552012-126552012 - CHC1715T COSM4789476 c.310C>A p.Q104K Substitution - Missense 23:126552299-126552299 - TCGA-B2-4099-01 COSM487913 c.1133G>A p.R378Q Substitution - Missense 23:126551476-126551476 - KYSE-150 COSM2725092 c.577C>T p.H193Y Substitution - Missense 23:126552032-126552032 - T3094 COSM4676318 c.959T>C p.V320A Substitution - Missense 23:126551650-126551650 - 134427 COSM319806 c.838G>T p.V280L Substitution - Missense 23:126551771-126551771 - TCGA-22-4613-01 COSM755465 c.1102G>T p.G368C Substitution - Missense 23:126551507-126551507 - TCGA-G4-6309-01 COSM1465458 c.238G>T p.V80L Substitution - Missense 23:126552371-126552371 - CX-1 COSM4621743 c.54G>A p.A18A Substitution - coding silent 23:126552555-126552555 - T1204 COSM4676316 c.1024C>T p.R342W Substitution - Missense 23:126551585-126551585 - HSJD_DIPG001 COSM4746067 c.235G>A p.A79T Substitution - Missense 23:126552374-126552374 - TCGA-EA-A5ZD-01 COSM4828674 c.437A>G p.D146G Substitution - Missense 23:126552172-126552172 - I2L-P7-Tumor-Organoid COSM1114700 c.38C>T p.A13V Substitution - Missense 23:126552571-126552571 - CHC892T COSM4794866 c.189G>A p.W63* Substitution - Nonsense 23:126552420-126552420 - 585208 COSM325119 c.1078C>A p.R360S Substitution - Missense 23:126551531-126551531 - CP66-MEL COSM26317 c.551C>T p.P184L Substitution - Missense 23:126552058-126552058 - TCGA-AA-3697-01 COSM1465452 c.892C>A p.L298M Substitution - Missense 23:126551717-126551717 - Patient2 COSM1166837 c.721G>C p.V241L Substitution - Missense 23:126551888-126551888 - TCGA-ER-A194-01 COSM3557615 c.1368G>A p.G456G Substitution - coding silent 23:126551241-126551241 - T1204 COSM4676327 c.108G>A p.P36P Substitution - coding silent 23:126552501-126552501 - T3433 COSM1114680 c.654G>A p.A218A Substitution - coding silent 23:126551955-126551955 - TCGA-BS-A0UL-01 COSM1114692 c.395G>A p.R132H Substitution - Missense 23:126552214-126552214 - TCGA-BR-7707-01 COSM4106501 c.155C>T p.A52V Substitution - Missense 23:126552454-126552454 - 98711 COSM319805 c.1016A>C p.Q339P Substitution - Missense 23:126551593-126551593 - TCGA-CD-A486-01 COSM4106493 c.625G>A p.V209M Substitution - Missense 23:126551984-126551984 - 1N22-VS-1T22 COSM4973163 c.306G>A p.A102A Substitution - coding silent 23:126552303-126552303 - CHC1597T COSM4787798 c.282G>C p.L94L Substitution - coding silent 23:126552327-126552327 - SJHGG009_A COSM4969050 c.741G>A p.P247P Substitution - coding silent 23:126551868-126551868 - 1946219 COSM1197823 c.799G>T p.A267S Substitution - Missense 23:126551810-126551810 - PD18280a COSM3770347 c.107C>T p.P36L Substitution - Missense 23:126552502-126552502 - LUAD-NYU201 COSM371516 c.2T>C p.M1T Substitution - Missense 23:126552607-126552607 - LUAD-RT-S01702 COSM379520 c.1230G>C p.W410C Substitution - Missense 23:126551379-126551379 - TCGA-EQ-8122-01 COSM4106483 c.1083C>G p.H361Q Substitution - Missense 23:126551526-126551526 - KYSE-30 COSM4377387 c.1350C>A p.L450L Substitution - coding silent 23:126551259-126551259 - HN_62741 COSM127782 c.720C>A p.P240P Substitution - coding silent 23:126551889-126551889 - TCGA-60-2698-01 COSM755464 c.1075T>C p.Y359H Substitution - Missense 23:126551534-126551534 - TCGA-HU-A4GU-01 COSM4106494 c.545T>A p.L182Q Substitution - Missense 23:126552064-126552064 - TCGA-FS-A1Z3-06 COSM3557619 c.1040G>A p.R347Q Substitution - Missense 23:126551569-126551569 - CHC1531T COSM4804862 c.736C>T p.R246C Substitution - Missense 23:126551873-126551873 - SNU-175 COSM2725081 c.720C>T p.P240P Substitution - coding silent 23:126551889-126551889 - T3724 COSM1114696 c.156G>A p.A52A Substitution - coding silent 23:126552453-126552453 - SC_9030 COSM5555396 c.1110C>T p.G370G Substitution - coding silent 23:126551499-126551499 - TCGA-K4-A3WU-01 COSM3800392 c.685G>A p.D229N Substitution - Missense 23:126551924-126551924 - HCC100 COSM1625482 c.1348C>T p.L450F Substitution - Missense 23:126551261-126551261 - PT35 COSM4520050 c.103G>A p.G35R Substitution - Missense 23:126552506-126552506 - T2944 COSM3424445 c.836C>T p.A279V Substitution - Missense 23:126551773-126551773 - CHC1597T COSM4787758 c.283G>C p.G95R Substitution - Missense 23:126552326-126552326 - TCGA-AP-A0LM-01 COSM1114678 c.662G>A p.R221Q Substitution - Missense 23:126551947-126551947 - ESCC_BICR_036T COSM4106490 c.771C>T p.I257I Substitution - coding silent 23:126551838-126551838 - LFS_MB1 COSM216179 c.1328T>G p.L443R Substitution - Missense 23:126551281-126551281 - B57 COSM1756376 c.1191T>A p.P397P Substitution - coding silent 23:126551418-126551418 - TCGA-32-1979-01 COSM3405937 c.1233C>T p.L411L Substitution - coding silent 23:126551376-126551376 - TCGA-EQ-5647-01 COSM4106489 c.782G>T p.S261I Substitution - Missense 23:126551827-126551827 - T2999 COSM2725086 c.661C>T p.R221W Substitution - Missense 23:126551948-126551948 - CSCC-29-T COSM4456981 c.1029C>T p.P343P Substitution - coding silent 23:126551580-126551580 - TCGA-CK-5913-01 COSM456701 c.1060C>T p.R354W Substitution - Missense 23:126551549-126551549 - LUAD-LIP77 COSM367950 c.1314G>C p.W438C Substitution - Missense 23:126551295-126551295 - Au4 COSM5603344 c.663G>A p.R221R Substitution - coding silent 23:126551946-126551946 - TCGA-A5-A0GP-01 COSM1114684 c.569G>A p.R190H Substitution - Missense 23:126552040-126552040 - 49M COSM5590461 c.980C>T p.S327F Substitution - Missense 23:126551629-126551629 - T3090 COSM3939779 c.796C>T p.R266W Substitution - Missense 23:126551813-126551813 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.120403 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 125685736 STAD A C Missense p.L443R c.1328T>G X 125685264 MB A C Missense p.S160A c.478T>G X 125686114 BRCA A C Missense p.W63G c.187T>G X 125686405 CM A G Missense p.C117R c.349T>C X 125686243 LUAD A G Missense p.L391P c.1172T>C X 125685420 UCEC A T 3-UTRSNV . c.1389+1749T>A X 125683454 HC A T Missense p.F427I c.1279T>A X 125685313 COREAD A T Missense p.Y432N c.1294T>A X 125685298 LUSC C A Missense p.A405S c.1213G>T X 125685379 LUSC C A Missense p.G292W c.874G>T X 125685718 LUSC C A Missense p.G368C c.1102G>T X 125685490 LUSC C A Missense p.G447W c.1339G>T X 125685253 LUAD C A Missense p.G64C c.190G>T X 125686402 LUSC C A Missense p.S139I c.416G>T X 125686176 LUAD C A Missense p.S261I c.782G>T X 125685810 STAD C A Missense p.V280L c.838G>T X 125685754 SCLC C A Missense p.W202L c.605G>T X 125685987 LUAD C A Nonsense p.E236* c.706G>T X 125685886 LUAD C A Nonsense p.E276* c.826G>T X 125685766 BLCA C A Nonsense p.E440* c.1318G>T X 125685274 OV C A Nonsense p.E59* c.175G>T X 125686417 LUAD C A Nonsense p.E89* c.265G>T X 125686327 LUSC C A Synonymous p.L303L c.909G>T X 125685683 LUAD C A Synonymous p.V209V c.627G>T X 125685965 LUAD CC AA Missense p.G407F c.1219_1220delinsTT X 125685372 HNSC C - Frameshift p.W220Cfs*93 c.660delG X 125685932 LUSC C G Missense p.D223H c.667G>C X 125685925 PRAD C G Synonymous p.L312L c.936G>C X 125685656 BRCA C T Missense p.A131T c.391G>A X 125686201 LUAD C T Missense p.A15T c.43G>A X 125686549 BLCA C T Missense p.C150Y c.449G>A X 125686143 NB C T Missense p.D146N c.436G>A X 125686156 CM C T Missense p.D337N c.1009G>A X 125685583 NSCLC C T Missense p.E236K c.706G>A X 125685886 CM C T Missense p.G149D c.446G>A X 125686146 CM C T Missense p.G151S c.451G>A X 125686141 CM C T Missense p.G168D c.503G>A X 125686089 UCEC C T Missense p.G284S c.850G>A X 125685742 BRCA C T Missense p.G292R c.874G>A X 125685718 STAD C T Missense p.G370D c.1109G>A X 125685483 CM C T Missense p.R11Q c.32G>A X 125686560 COREAD C T Missense p.R132H c.395G>A X 125686197 UCEC C T Missense p.R190H c.569G>A X 125686023 UCEC C T Missense p.R221Q c.662G>A X 125685930 LGG C T Missense p.R335H c.1004G>A X 125685588 GBM C T Missense p.R347Q c.1040G>A X 125685552 CM C T Missense p.R378Q c.1133G>A X 125685459 RCCC C T Missense p.R90H c.269G>A X 125686323 BLCA C T Synonymous p.A31A c.93G>A X 125686499 CM C T Synonymous p.A52A c.156G>A X 125686436 UCEC C T Synonymous p.G456G c.1368G>A X 125685224 CM C T Synonymous p.L282L c.846G>A X 125685746 CM C T Synonymous p.P224P c.672G>A X 125685920 HNSC C T Synonymous p.P224P c.672G>A X 125685920 PRAD C T Synonymous p.P224P c.672G>A X 125685920 UCEC C T Synonymous p.R354R c.1062G>A X 125685530 LUSC C T Synonymous p.R76R c.228G>A X 125686364 CM C T Synonymous p.R9R c.27G>A X 125686565 CM C T Synonymous p.S395S c.1185G>A X 125685407 CM C T Synonymous p.T96T c.288G>A X 125686304 GBM C T Synonymous p.V265V c.795G>A X 125685797 LUAD G A 5-UTRSNV . c.1-1C>T X 125686592 CM G A Missense p.A15V c.44C>T X 125686548 LUAD G A Missense p.A15V c.44C>T X 125686548 LUSC G A Missense p.A232V c.695C>T X 125685897 CM G A Missense p.A387V c.1160C>T X 125685432 CM G A Missense p.P343L c.1028C>T X 125685564 GBM G A Missense p.P65L c.194C>T X 125686398 LUSC G A Missense p.R354W c.1060C>T X 125685532 BRCA G A Missense p.S23L c.68C>T X 125686524 LUAD G A Missense p.T47M c.140C>T X 125686452 LGG G A Missense p.T88M c.263C>T X 125686329 GBM G A Synonymous p.A208A c.624C>T X 125685968 ESCA G A Synonymous p.A291A c.873C>T X 125685719 HNSC G A Synonymous p.D124D c.372C>T X 125686220 BRCA G A Synonymous p.D32D c.96C>T X 125686496 RCCC G A Synonymous p.F121F c.363C>T X 125686229 CM G A Synonymous p.F198F c.594C>T X 125685998 CM G A Synonymous p.G352G c.1056C>T X 125685536 STAD G A Synonymous p.L239L c.717C>T X 125685875 CM G A Synonymous p.L411L c.1233C>T X 125685359 GBM G A Synonymous p.L450L c.1350C>T X 125685242 CM G A Synonymous p.P65P c.195C>T X 125686397 STAD G A Synonymous p.S160S c.480C>T X 125686112 LUSC G A Synonymous p.T206T c.618C>T X 125685974 ESCA G A Synonymous p.Y321Y c.963C>T X 125685629 COREAD G A Synonymous p.Y321Y c.963C>T X 125685629 HNSC G A Synonymous p.Y78Y c.234C>T X 125686358 STAD G C Missense p.P134R c.401C>G X 125686191 HNSC G C Missense p.S181C c.542C>G X 125686050 LUSC G C Missense p.T96R c.287C>G X 125686305 LUAD G C Synonymous p.A379A c.1137C>G X 125685455 LUSC G T 5-UTRSNV . c.1-1C>A X 125686592 ESCA G T Missense p.D225E c.675C>A X 125685917 LUSC G T Missense p.F286L c.858C>A X 125685734 SCLC G T Missense p.H287N c.859C>A X 125685733 SCLC G T Missense p.L94M c.280C>A X 125686312 HNSC G T Missense p.N172K c.516C>A X 125686076 SCLC G T Missense p.P254H c.761C>A X 125685831 LUAD G T Missense p.P254T c.760C>A X 125685832 STAD G T Missense p.Q110K c.328C>A X 125686264 HNSC G T Missense p.R360S c.1078C>A X 125685514 SCLC G T Missense p.T206N c.617C>A X 125685975 BRCA G T Synonymous p.A379A c.1137C>A X 125685455 LUAD G T Synonymous p.P240P c.720C>A X 125685872 HNSC G T Synonymous p.S296S c.888C>A X 125685704 BRCA T A Missense p.S235C c.703A>T X 125685889 LUAD T C Missense p.Y436C c.1307A>G X 125685285 HNSC T G Missense p.N170H c.508A>C X 125686084 STAD T G Missense p.N457T c.1370A>C X 125685222 BLCA T G Missense p.Q339P c.1016A>C X 125685576 SCLC T G Synonymous p.A452A c.1356A>C X 125685236 LUAD