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 55515272 55515272 + Missense_Mutation SNP G G A TCGA-OR-A5JF-01A-11D-A29I-10 TCGA-OR-A5JF-10A-01D-A29L-10 g.chrX:55515272G>A c.101C>T c.(100-102)gCg>gTg p.A34V BLCA 23 55514287 55514287 + Silent SNP C C G TCGA-DK-A1AF-01A-11D-A13W-08 TCGA-DK-A1AF-10A-01D-A13W-08 g.chrX:55514287C>G c.1086G>C c.(1084-1086)ctG>ctC p.L362L BLCA 23 55514287 55514287 + Silent SNP C C G TCGA-FD-A3B6-01A-21D-A20D-08 TCGA-FD-A3B6-10A-01D-A20D-08 g.chrX:55514287C>G c.1086G>C c.(1084-1086)ctG>ctC p.L362L BLCA 23 55515340 55515340 + Silent SNP G G A TCGA-GD-A76B-01A-11D-A32B-08 TCGA-GD-A76B-10A-01D-A329-08 g.chrX:55515340G>A c.33C>T c.(31-33)tcC>tcT p.S11S BRCA 23 55513916 55513916 + Missense_Mutation SNP T T C TCGA-AC-A23C-01A-12D-A167-09 TCGA-AC-A23C-10A-01D-A167-09 g.chrX:55513916T>C c.1457A>G c.(1456-1458)cAa>cGa p.Q486R BRCA 23 55513981 55513981 + Missense_Mutation SNP G G C TCGA-A8-A06R-01A-11D-A015-09 TCGA-A8-A06R-10A-01W-A021-09 g.chrX:55513981G>C c.1392C>G c.(1390-1392)caC>caG p.H464Q BRCA 23 55514073 55514073 + Missense_Mutation SNP G G C TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chrX:55514073G>C c.1300C>G c.(1300-1302)Ctg>Gtg p.L434V BRCA 23 55514740 55514740 + Silent SNP C C G TCGA-BH-A0DZ-01A-11W-A019-09 TCGA-BH-A0DZ-10A-01W-A021-09 g.chrX:55514740C>G c.633G>C c.(631-633)ctG>ctC p.L211L CESC 23 55513291 55513291 + Silent SNP G G C TCGA-DG-A2KK-01A-11D-A17W-09 TCGA-DG-A2KK-10A-01D-A17W-09 g.chrX:55513291G>C c.2082C>G c.(2080-2082)ctC>ctG p.L694L CESC 23 55514364 55514364 + Missense_Mutation SNP C C G TCGA-EA-A411-01A-11D-A243-09 TCGA-EA-A411-10A-01D-A243-09 g.chrX:55514364C>G c.1009G>C c.(1009-1011)Gag>Cag p.E337Q CESC 23 55514409 55514409 + Nonsense_Mutation SNP G G A TCGA-UC-A7PF-01A-11D-A351-09 TCGA-UC-A7PF-11A-31D-A351-09 g.chrX:55514409G>A c.964C>T c.(964-966)Caa>Taa p.Q322* CESC 23 55514414 55514414 + Missense_Mutation SNP G G A TCGA-EK-A3GK-01A-11D-A20U-09 TCGA-EK-A3GK-10A-01D-A20U-09 g.chrX:55514414G>A c.959C>T c.(958-960)tCt>tTt p.S320F CESC 23 55514505 55514505 + Missense_Mutation SNP C C T TCGA-EK-A2R7-01A-11D-A18J-09 TCGA-EK-A2R7-10A-01D-A18J-09 g.chrX:55514505C>T c.868G>A c.(868-870)Gat>Aat p.D290N CESC 23 55515182 55515182 + Missense_Mutation SNP C C T TCGA-EK-A2RB-01A-11D-A18J-09 TCGA-EK-A2RB-10A-01D-A18J-09 g.chrX:55515182C>T c.191G>A c.(190-192)cGt>cAt p.R64H CESC 23 55515232 55515232 + Silent SNP C C T TCGA-C5-A7CL-01A-11D-A32I-09 TCGA-C5-A7CL-10A-01D-A32I-09 g.chrX:55515232C>T c.141G>A c.(139-141)gcG>gcA p.A47A COAD 23 55513445 55513445 + Missense_Mutation SNP A A G TCGA-DM-A1D7-01A-11D-A152-10 TCGA-DM-A1D7-10A-01D-A152-10 g.chrX:55513445A>G c.1928T>C c.(1927-1929)gTg>gCg p.V643A COAD 23 55513875 55513875 + Missense_Mutation SNP C C T TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chrX:55513875C>T c.1498G>A c.(1498-1500)Gcc>Acc p.A500T COAD 23 55514326 55514326 + Missense_Mutation SNP C C A TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chrX:55514326C>A c.1047G>T c.(1045-1047)aaG>aaT p.K349N COAD 23 55514507 55514507 + Missense_Mutation SNP T T C TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chrX:55514507T>C c.866A>G c.(865-867)aAg>aGg p.K289R COAD 23 55514578 55514578 + Silent SNP T T C TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chrX:55514578T>C c.795A>G c.(793-795)aaA>aaG p.K265K COAD 23 55515254 55515254 + Missense_Mutation SNP G G T TCGA-AA-3949-01A-01W-0995-10 TCGA-AA-3949-10A-01W-0995-10 g.chrX:55515254G>T c.119C>A c.(118-120)gCg>gAg p.A40E COAD 23 55515257 55515257 + Missense_Mutation SNP T T G TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chrX:55515257T>G c.116A>C c.(115-117)gAg>gCg p.E39A COADREAD 23 55513445 55513445 + Missense_Mutation SNP A A G TCGA-DM-A1D7-01A-11D-A152-10 TCGA-DM-A1D7-10A-01D-A152-10 g.chrX:55513445A>G c.1928T>C c.(1927-1929)gTg>gCg p.V643A COADREAD 23 55513875 55513875 + Missense_Mutation SNP C C T TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chrX:55513875C>T c.1498G>A c.(1498-1500)Gcc>Acc p.A500T COADREAD 23 55513912 55513912 + Silent SNP G G T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chrX:55513912G>T c.1461C>A c.(1459-1461)atC>atA p.I487I COADREAD 23 55513974 55513974 + Missense_Mutation SNP C C A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chrX:55513974C>A c.1399G>T c.(1399-1401)Gat>Tat p.D467Y COADREAD 23 55514071 55514071 + Silent SNP C C G TCGA-DC-6682-01A-11D-1826-10 TCGA-DC-6682-10A-01D-1826-10 g.chrX:55514071C>G c.1302G>C c.(1300-1302)ctG>ctC p.L434L COADREAD 23 55514076 55514076 + Missense_Mutation SNP G G T TCGA-DC-6682-01A-11D-1826-10 TCGA-DC-6682-10A-01D-1826-10 g.chrX:55514076G>T c.1297C>A c.(1297-1299)Cat>Aat p.H433N COADREAD 23 55514326 55514326 + Missense_Mutation SNP C C A TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chrX:55514326C>A c.1047G>T c.(1045-1047)aaG>aaT p.K349N COADREAD 23 55514507 55514507 + Missense_Mutation SNP T T C TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chrX:55514507T>C c.866A>G c.(865-867)aAg>aGg p.K289R COADREAD 23 55514578 55514578 + Silent SNP T T C TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chrX:55514578T>C c.795A>G c.(793-795)aaA>aaG p.K265K COADREAD 23 55515254 55515254 + Missense_Mutation SNP G G T TCGA-AA-3949-01A-01W-0995-10 TCGA-AA-3949-10A-01W-0995-10 g.chrX:55515254G>T c.119C>A c.(118-120)gCg>gAg p.A40E COADREAD 23 55515257 55515257 + Missense_Mutation SNP T T G TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chrX:55515257T>G c.116A>C c.(115-117)gAg>gCg p.E39A ESCA 23 55514608 55514608 + Frame_Shift_Del DEL A A - TCGA-LN-A49V-01A-11D-A247-09 TCGA-LN-A49V-10A-01D-A247-09 g.chrX:55514608delA c.765delT c.(763-765)tttfs p.F255fs ESCA 23 55515146 55515146 + Missense_Mutation SNP C C T TCGA-JY-A93D-01A-11D-A387-09 TCGA-JY-A93D-10A-01D-A38A-09 g.chrX:55515146C>T c.227G>A c.(226-228)aGc>aAc p.S76N ESCA 23 55515327 55515327 + Missense_Mutation SNP G G C TCGA-IC-A6RF-01A-13D-A33E-09 TCGA-IC-A6RF-10A-21D-A33H-09 g.chrX:55515327G>C c.46C>G c.(46-48)Cgc>Ggc p.R16G ESCA 23 55515360 55515360 + Silent SNP G G T TCGA-L5-A43M-01A-11D-A247-09 TCGA-L5-A43M-11A-11D-A247-09 g.chrX:55515360G>T c.13C>A c.(13-15)Cga>Aga p.R5R GBM 23 55513943 55513943 + Missense_Mutation SNP G G A TCGA-19-2631-01A-01D-1353-08 TCGA-19-2631-10B-01D-1353-08 g.chrX:55513943G>A c.1430C>T c.(1429-1431)cCc>cTc p.P477L GBM 23 55514642 55514642 + Missense_Mutation SNP T T C TCGA-76-6285-01A-11D-1696-08 TCGA-76-6285-10A-01D-1696-08 g.chrX:55514642T>C c.731A>G c.(730-732)aAc>aGc p.N244S GBMLGG 23 55513943 55513943 + Missense_Mutation SNP G G A TCGA-19-2631-01A-01D-1353-08 TCGA-19-2631-10B-01D-1353-08 g.chrX:55513943G>A c.1430C>T c.(1429-1431)cCc>cTc p.P477L GBMLGG 23 55514135 55514135 + Missense_Mutation SNP G G A TCGA-CS-6665-01A-11D-1893-08 TCGA-CS-6665-10A-01D-1893-08 g.chrX:55514135G>A c.1238C>T c.(1237-1239)tCg>tTg p.S413L GBMLGG 23 55514642 55514642 + Missense_Mutation SNP T T C TCGA-76-6285-01A-11D-1696-08 TCGA-76-6285-10A-01D-1696-08 g.chrX:55514642T>C c.731A>G c.(730-732)aAc>aGc p.N244S GBMLGG 23 55514658 55514658 + Missense_Mutation SNP A A G TCGA-CS-4942-01A-01D-1468-08 TCGA-CS-4942-10A-01D-1468-08 g.chrX:55514658A>G c.715T>C c.(715-717)Tgt>Cgt p.C239R GBMLGG 23 55514742 55514742 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chrX:55514742G>T c.631C>A c.(631-633)Ctg>Atg p.L211M GBMLGG 23 55515233 55515233 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chrX:55515233G>A c.140C>T c.(139-141)gCg>gTg p.A47V HNSC 23 55513447 55513447 + Nonsense_Mutation SNP A A T TCGA-CV-7248-01A-11D-2012-08 TCGA-CV-7248-10A-01D-2013-08 g.chrX:55513447A>T c.1926T>A c.(1924-1926)tgT>tgA p.C642* HNSC 23 55513554 55513554 + Nonsense_Mutation SNP G G A TCGA-CV-7425-01A-11D-2078-08 TCGA-CV-7425-10A-01D-2078-08 g.chrX:55513554G>A c.1819C>T c.(1819-1821)Cga>Tga p.R607* HNSC 23 55513641 55513641 + Missense_Mutation SNP C C T TCGA-IQ-A61E-01A-22D-A30E-08 TCGA-IQ-A61E-10A-01D-A30H-08 g.chrX:55513641C>T c.1732G>A c.(1732-1734)Gag>Aag p.E578K HNSC 23 55513685 55513685 + Missense_Mutation SNP C C T TCGA-CV-7568-01A-11D-2229-08 TCGA-CV-7568-10A-01D-2229-08 g.chrX:55513685C>T c.1688G>A c.(1687-1689)gGa>gAa p.G563E HNSC 23 55514102 55514102 + Missense_Mutation SNP G G T TCGA-CQ-7063-01A-11D-2394-08 TCGA-CQ-7063-10A-01D-2394-08 g.chrX:55514102G>T c.1271C>A c.(1270-1272)aCt>aAt p.T424N HNSC 23 55515083 55515083 + Missense_Mutation SNP G G A TCGA-CV-7568-01A-11D-2229-08 TCGA-CV-7568-10A-01D-2229-08 g.chrX:55515083G>A c.290C>T c.(289-291)cCc>cTc p.P97L KIPAN 23 55513238 55513238 + Nonstop_Mutation SNP T T A TCGA-BP-5186-01A-01D-1429-08 TCGA-BP-5186-11A-01D-1429-08 g.chrX:55513238T>A c.2135A>T c.(2134-2136)tAg>tTg p.*712L KIPAN 23 55513337 55513337 + Missense_Mutation SNP C C T TCGA-BP-4158-01A-02D-1366-10 TCGA-BP-4158-11A-01D-1366-10 g.chrX:55513337C>T c.2036G>A c.(2035-2037)aGc>aAc p.S679N KIPAN 23 55513642 55513642 + Missense_Mutation SNP C C A TCGA-CJ-4643-01A-02D-1386-10 TCGA-CJ-4643-11A-01D-1251-10 g.chrX:55513642C>A c.1731G>T c.(1729-1731)caG>caT p.Q577H KIPAN 23 55514285 55514285 + Missense_Mutation SNP C C G TCGA-CJ-5677-01A-11D-1534-10 TCGA-CJ-5677-11A-01D-1534-10 g.chrX:55514285C>G c.1088G>C c.(1087-1089)aGa>aCa p.R363T KIPAN 23 55514571 55514571 + Missense_Mutation SNP C C T TCGA-CJ-4638-01A-02D-1386-10 TCGA-CJ-4638-11A-01D-1251-10 g.chrX:55514571C>T c.802G>A c.(802-804)Gaa>Aaa p.E268K KIRC 23 55513238 55513238 + Nonstop_Mutation SNP T T A TCGA-BP-5186-01A-01D-1429-08 TCGA-BP-5186-11A-01D-1429-08 g.chrX:55513238T>A c.2135A>T c.(2134-2136)tAg>tTg p.*712L KIRC 23 55513337 55513337 + Missense_Mutation SNP C C T TCGA-BP-4158-01A-02D-1366-10 TCGA-BP-4158-11A-01D-1366-10 g.chrX:55513337C>T c.2036G>A c.(2035-2037)aGc>aAc p.S679N KIRC 23 55513642 55513642 + Missense_Mutation SNP C C A TCGA-CJ-4643-01A-02D-1386-10 TCGA-CJ-4643-11A-01D-1251-10 g.chrX:55513642C>A c.1731G>T c.(1729-1731)caG>caT p.Q577H KIRC 23 55514285 55514285 + Missense_Mutation SNP C C G TCGA-CJ-5677-01A-11D-1534-10 TCGA-CJ-5677-11A-01D-1534-10 g.chrX:55514285C>G c.1088G>C c.(1087-1089)aGa>aCa p.R363T KIRC 23 55514571 55514571 + Missense_Mutation SNP C C T TCGA-CJ-4638-01A-02D-1386-10 TCGA-CJ-4638-11A-01D-1251-10 g.chrX:55514571C>T c.802G>A c.(802-804)Gaa>Aaa p.E268K LGG 23 55514135 55514135 + Missense_Mutation SNP G G A TCGA-CS-6665-01A-11D-1893-08 TCGA-CS-6665-10A-01D-1893-08 g.chrX:55514135G>A c.1238C>T c.(1237-1239)tCg>tTg p.S413L LGG 23 55514658 55514658 + Missense_Mutation SNP A A G TCGA-CS-4942-01A-01D-1468-08 TCGA-CS-4942-10A-01D-1468-08 g.chrX:55514658A>G c.715T>C c.(715-717)Tgt>Cgt p.C239R LGG 23 55514742 55514742 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chrX:55514742G>T c.631C>A c.(631-633)Ctg>Atg p.L211M LGG 23 55515233 55515233 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chrX:55515233G>A c.140C>T c.(139-141)gCg>gTg p.A47V LIHC 23 55514365 55514365 + Silent SNP A A G TCGA-DD-A3A0-01A-11D-A20W-10 TCGA-DD-A3A0-11A-11D-A20W-10 g.chrX:55514365A>G c.1008T>C c.(1006-1008)tgT>tgC p.C336C LIHC 23 55514722 55514722 + Silent SNP A A G TCGA-2Y-A9GU-01A-11D-A382-10 TCGA-2Y-A9GU-10A-01D-A385-10 g.chrX:55514722A>G c.651T>C c.(649-651)cgT>cgC p.R217R LUAD 23 55513306 55513306 + Silent SNP G G A TCGA-44-6774-01A-21D-1855-08 TCGA-44-6774-10A-01D-1855-08 g.chrX:55513306G>A c.2067C>T c.(2065-2067)acC>acT p.T689T LUAD 23 55513497 55513497 + Missense_Mutation SNP C C A TCGA-50-5933-01A-11D-1753-08 TCGA-50-5933-11A-01D-1753-08 g.chrX:55513497C>A c.1876G>T c.(1876-1878)Gcc>Tcc p.A626S LUAD 23 55513511 55513511 + Missense_Mutation SNP A A G TCGA-55-7727-01A-11D-2167-08 TCGA-55-7727-10A-01D-2167-08 g.chrX:55513511A>G c.1862T>C c.(1861-1863)aTg>aCg p.M621T LUAD 23 55513730 55513730 + Nonsense_Mutation SNP G G C TCGA-75-7031-01A-11D-1945-08 TCGA-75-7031-10A-01D-1946-08 g.chrX:55513730G>C c.1643C>G c.(1642-1644)tCa>tGa p.S548* LUAD 23 55513741 55513741 + Silent SNP T T A TCGA-55-8616-01A-11D-2393-08 TCGA-55-8616-10A-01D-2393-08 g.chrX:55513741T>A c.1632A>T c.(1630-1632)ccA>ccT p.P544P LUAD 23 55513782 55513782 + Missense_Mutation SNP C C G TCGA-17-Z050-01A-01W-0747-08 TCGA-17-Z050-11A-01W-0747-08 g.chrX:55513782C>G c.1591G>C c.(1591-1593)Gag>Cag p.E531Q LUAD 23 55513782 55513782 + Nonsense_Mutation SNP C C A TCGA-95-7043-01A-11D-1945-08 TCGA-95-7043-10A-01D-1946-08 g.chrX:55513782C>A c.1591G>T c.(1591-1593)Gag>Tag p.E531* LUAD 23 55513806 55513806 + Missense_Mutation SNP C C T TCGA-50-6591-01A-11D-1753-08 TCGA-50-6591-11A-01D-1753-08 g.chrX:55513806C>T c.1567G>A c.(1567-1569)Gcc>Acc p.A523T LUAD 23 55513961 55513961 + Missense_Mutation SNP C C A TCGA-78-7155-01A-11D-2036-08 TCGA-78-7155-10A-01D-2036-08 g.chrX:55513961C>A c.1412G>T c.(1411-1413)gGg>gTg p.G471V LUAD 23 55513962 55513962 + Missense_Mutation SNP C C A TCGA-62-A46O-01A-11D-A24D-08 TCGA-62-A46O-10A-01D-A24F-08 g.chrX:55513962C>A c.1411G>T c.(1411-1413)Ggg>Tgg p.G471W LUAD 23 55513992 55513992 + Missense_Mutation SNP G G T TCGA-05-4427-01A-21D-1855-08 TCGA-05-4427-10A-01D-1855-08 g.chrX:55513992G>T c.1381C>A c.(1381-1383)Cta>Ata p.L461I LUAD 23 55514404 55514404 + Missense_Mutation SNP C C G TCGA-86-8668-01A-11D-2393-08 TCGA-86-8668-10A-01D-2393-08 g.chrX:55514404C>G c.969G>C c.(967-969)caG>caC p.Q323H LUAD 23 55514457 55514457 + Nonsense_Mutation SNP C C A TCGA-64-1679-01A-21D-2063-08 TCGA-64-1679-10A-01D-2063-08 g.chrX:55514457C>A c.916G>T c.(916-918)Gaa>Taa p.E306* LUAD 23 55514652 55514652 + Missense_Mutation SNP T T A TCGA-44-8117-01A-11D-2238-08 TCGA-44-8117-10A-01D-2238-08 g.chrX:55514652T>A c.721A>T c.(721-723)Acc>Tcc p.T241S LUAD 23 55514840 55514840 + Missense_Mutation SNP C C A TCGA-J2-8194-01A-11D-2238-08 TCGA-J2-8194-10A-01D-2238-08 g.chrX:55514840C>A c.533G>T c.(532-534)gGc>gTc p.G178V LUAD 23 55514858 55514858 + Missense_Mutation SNP C C A TCGA-05-4398-01A-01D-1265-08 TCGA-05-4398-10A-01D-1265-08 g.chrX:55514858C>A c.515G>T c.(514-516)gGg>gTg p.G172V LUAD 23 55514884 55514884 + Silent SNP C C A TCGA-38-7271-01A-11D-2036-08 TCGA-38-7271-11A-01D-2036-08 g.chrX:55514884C>A c.489G>T c.(487-489)cgG>cgT p.R163R LUAD 23 55514938 55514938 + Missense_Mutation SNP C C A TCGA-55-8507-01A-11D-2393-08 TCGA-55-8507-10A-01D-2393-08 g.chrX:55514938C>A c.435G>T c.(433-435)agG>agT p.R145S LUAD 23 55515098 55515098 + Missense_Mutation SNP T T C TCGA-L9-A444-01A-21D-A24D-08 TCGA-L9-A444-10A-01D-A24F-08 g.chrX:55515098T>C c.275A>G c.(274-276)cAc>cGc p.H92R LUAD 23 55515108 55515108 + Missense_Mutation SNP G G C TCGA-55-7995-01A-11D-2184-08 TCGA-55-7995-10A-01D-2184-08 g.chrX:55515108G>C c.265C>G c.(265-267)Ctt>Gtt p.L89V LUAD 23 55515250 55515250 + Silent SNP C C A TCGA-55-1595-01A-01D-0969-08 TCGA-55-1595-11A-01D-0969-08 g.chrX:55515250C>A c.123G>T c.(121-123)gcG>gcT p.A41A LUSC 23 55513249 55513249 + Silent SNP T T C TCGA-33-4533-01A-01D-1267-08 TCGA-33-4533-11A-01D-1267-08 g.chrX:55513249T>C c.2124A>G c.(2122-2124)ctA>ctG p.L708L LUSC 23 55513251 55513251 + Missense_Mutation SNP G G T TCGA-43-2578-01A-01D-1522-08 TCGA-43-2578-11A-01D-1522-08 g.chrX:55513251G>T c.2122C>A c.(2122-2124)Cta>Ata p.L708I LUSC 23 55514393 55514393 + Missense_Mutation SNP G G A TCGA-66-2757-01A-01D-1522-08 TCGA-66-2757-11A-01D-1522-08 g.chrX:55514393G>A c.980C>T c.(979-981)tCa>tTa p.S327L LUSC 23 55514731 55514731 + Silent SNP G G T TCGA-60-2698-01A-01D-1522-08 TCGA-60-2698-11A-01D-1522-08 g.chrX:55514731G>T c.642C>A c.(640-642)atC>atA p.I214I OV 23 55513444 55513444 + Silent SNP C C T TCGA-04-1347-01A-01W-0488-09 TCGA-04-1347-11A-01W-0489-09 g.chrX:55513444C>T c.1929G>A c.(1927-1929)gtG>gtA p.V643V OV 23 55514319 55514319 + Missense_Mutation SNP T T C TCGA-31-1959-01A-01W-0699-08 TCGA-31-1959-10A-01W-0700-08 g.chrX:55514319T>C c.1054A>G c.(1054-1056)Aga>Gga p.R352G PAAD 23 55515068 55515068 + Missense_Mutation SNP C C T TCGA-US-A779-01A-11D-A32N-08 TCGA-US-A779-11A-11D-A32N-08 g.chrX:55515068C>T c.305G>A c.(304-306)cGc>cAc p.R102H READ 23 55513912 55513912 + Silent SNP G G T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chrX:55513912G>T c.1461C>A c.(1459-1461)atC>atA p.I487I READ 23 55513974 55513974 + Missense_Mutation SNP C C A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chrX:55513974C>A c.1399G>T c.(1399-1401)Gat>Tat p.D467Y READ 23 55514071 55514071 + Silent SNP C C G TCGA-DC-6682-01A-11D-1826-10 TCGA-DC-6682-10A-01D-1826-10 g.chrX:55514071C>G c.1302G>C c.(1300-1302)ctG>ctC p.L434L READ 23 55514076 55514076 + Missense_Mutation SNP G G T TCGA-DC-6682-01A-11D-1826-10 TCGA-DC-6682-10A-01D-1826-10 g.chrX:55514076G>T c.1297C>A c.(1297-1299)Cat>Aat p.H433N SKCM 23 55513531 55513531 + Silent SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chrX:55513531G>A c.1842C>T c.(1840-1842)tcC>tcT p.S614S SKCM 23 55513532 55513532 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chrX:55513532G>A c.1841C>T c.(1840-1842)tCc>tTc p.S614F

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BLCA-US X 55514287 55514287 single base substitution C G exon_variant BLCA-US X 55514287 55514287 single base substitution C G synonymous_variant L362L 1086G>C BRCA-EU X 55508271 55508271 single base substitution G C downstream_gene_variant BRCA-EU X 55508572 55508574 deletion of <=200bp AGA - downstream_gene_variant BRCA-EU X 55508911 55508911 single base substitution G C downstream_gene_variant BRCA-EU X 55510945 55510945 single base substitution G T downstream_gene_variant BRCA-EU X 55511181 55511181 single base substitution G T 3_prime_UTR_variant BRCA-EU X 55511181 55511181 single base substitution G T downstream_gene_variant BRCA-EU X 55511428 55511428 deletion of <=200bp A - 3_prime_UTR_variant BRCA-EU X 55511428 55511428 deletion of <=200bp A - downstream_gene_variant BRCA-EU X 55511808 55511808 single base substitution G A 3_prime_UTR_variant BRCA-EU X 55511808 55511808 single base substitution G A downstream_gene_variant BRCA-EU X 55512611 55512611 single base substitution C G 3_prime_UTR_variant BRCA-EU X 55512611 55512611 single base substitution C G downstream_gene_variant BRCA-EU X 55513459 55513459 single base substitution T A exon_variant BRCA-EU X 55513459 55513459 single base substitution T A synonymous_variant P638P 1914A>T BRCA-EU X 55513744 55513744 single base substitution T A exon_variant BRCA-EU X 55513744 55513744 single base substitution T A synonymous_variant I543I 1629A>T BRCA-EU X 55513937 55513937 single base substitution C G exon_variant BRCA-EU X 55513937 55513937 single base substitution C G missense_variant C479S 1436G>C BRCA-EU X 55514847 55514847 single base substitution G T intron_variant BRCA-EU X 55514847 55514847 single base substitution G T missense_variant P176T 526C>A BRCA-EU X 55514999 55514999 single base substitution G A intron_variant BRCA-EU X 55514999 55514999 single base substitution G A missense_variant P125L 374C>T BRCA-EU X 55515340 55515340 single base substitution G A synonymous_variant S11S 33C>T BRCA-EU X 55515340 55515340 single base substitution G A upstream_gene_variant BRCA-EU X 55515573 55515573 single base substitution G A intron_variant BRCA-EU X 55515573 55515573 single base substitution G A upstream_gene_variant BRCA-EU X 55516162 55516162 single base substitution C T upstream_gene_variant BRCA-EU X 55516597 55516597 single base substitution C G upstream_gene_variant BRCA-EU X 55519565 55519565 single base substitution C T upstream_gene_variant BRCA-FR X 55507916 55507916 single base substitution C T downstream_gene_variant BRCA-FR X 55512381 55512381 single base substitution C G 3_prime_UTR_variant BRCA-FR X 55512381 55512381 single base substitution C G downstream_gene_variant BRCA-KR X 55514742 55514742 single base substitution G A intron_variant BRCA-KR X 55514742 55514742 single base substitution G A synonymous_variant L211L 631C>T BRCA-UK X 55514251 55514251 single base substitution C T exon_variant BRCA-UK X 55514251 55514251 single base substitution C T missense_variant M374I 1122G>A BRCA-US X 55513916 55513916 single base substitution T C exon_variant BRCA-US X 55513916 55513916 single base substitution T C missense_variant Q486R 1457A>G BRCA-US X 55513981 55513981 single base substitution G C exon_variant BRCA-US X 55513981 55513981 single base substitution G C missense_variant H464Q 1392C>G BRCA-US X 55514073 55514073 single base substitution G C exon_variant BRCA-US X 55514073 55514073 single base substitution G C missense_variant L434V 1300C>G BRCA-US X 55514740 55514740 single base substitution C G intron_variant BRCA-US X 55514740 55514740 single base substitution C G synonymous_variant L211L 633G>C CESC-US X 55513291 55513291 single base substitution G C exon_variant CESC-US X 55513291 55513291 single base substitution G C synonymous_variant L694L 2082C>G CESC-US X 55514364 55514364 single base substitution C G exon_variant CESC-US X 55514364 55514364 single base substitution C G missense_variant E337Q 1009G>C CESC-US X 55514409 55514409 single base substitution G A intron_variant CESC-US X 55514409 55514409 single base substitution G A stop_gained Q322* 964C>T CESC-US X 55514414 55514414 single base substitution G A intron_variant CESC-US X 55514414 55514414 single base substitution G A missense_variant S320F 959C>T CESC-US X 55514505 55514505 single base substitution C T intron_variant CESC-US X 55514505 55514505 single base substitution C T missense_variant D290N 868G>A CESC-US X 55515182 55515182 single base substitution C T exon_variant CESC-US X 55515182 55515182 single base substitution C T missense_variant R64H 191G>A CESC-US X 55515232 55515232 single base substitution C T exon_variant CESC-US X 55515232 55515232 single base substitution C T synonymous_variant A47A 141G>A CLLE-ES X 55514707 55514707 single base substitution C A intron_variant CLLE-ES X 55514707 55514707 single base substitution C A synonymous_variant G222G 666G>T COAD-US X 55514326 55514326 single base substitution C A exon_variant COAD-US X 55514326 55514326 single base substitution C A missense_variant K349N 1047G>T COAD-US X 55514507 55514507 single base substitution T C intron_variant COAD-US X 55514507 55514507 single base substitution T C missense_variant K289R 866A>G COCA-CN X 55513292 55513292 single base substitution A C exon_variant COCA-CN X 55513292 55513292 single base substitution A C missense_variant L694R 2081T>G COCA-CN X 55513351 55513351 single base substitution C A exon_variant COCA-CN X 55513351 55513351 single base substitution C A missense_variant K674N 2022G>T COCA-CN X 55514719 55514719 single base substitution G A intron_variant COCA-CN X 55514719 55514719 single base substitution G A synonymous_variant F218F 654C>T GBM-US X 55513943 55513943 single base substitution G A exon_variant GBM-US X 55513943 55513943 single base substitution G A missense_variant P477L 1430C>T GBM-US X 55514642 55514642 single base substitution T C intron_variant GBM-US X 55514642 55514642 single base substitution T C missense_variant N244S 731A>G KIRC-US X 55513238 55513238 single base substitution T A exon_variant KIRC-US X 55513238 55513238 single base substitution T A stop_lost *712L 2135A>T KIRC-US X 55513337 55513337 single base substitution C T exon_variant KIRC-US X 55513337 55513337 single base substitution C T missense_variant S679N 2036G>A KIRC-US X 55513642 55513642 single base substitution C A exon_variant KIRC-US X 55513642 55513642 single base substitution C A missense_variant Q577H 1731G>T KIRC-US X 55514285 55514285 single base substitution C G exon_variant KIRC-US X 55514285 55514285 single base substitution C G missense_variant R363T 1088G>C KIRC-US X 55514571 55514571 single base substitution C T intron_variant KIRC-US X 55514571 55514571 single base substitution C T missense_variant E268K 802G>A LGG-US X 55514135 55514135 single base substitution G A exon_variant LGG-US X 55514135 55514135 single base substitution G A missense_variant S413L 1238C>T LGG-US X 55514658 55514658 single base substitution A G intron_variant LGG-US X 55514658 55514658 single base substitution A G missense_variant C239R 715T>C LICA-CN X 55513601 55513601 single base substitution A G exon_variant LICA-CN X 55513601 55513601 single base substitution A G missense_variant V591A 1772T>C LICA-CN X 55514301 55514301 single base substitution A C exon_variant LICA-CN X 55514301 55514301 single base substitution A C missense_variant Y358D 1072T>G LICA-FR X 55514045 55514045 single base substitution G T exon_variant LICA-FR X 55514045 55514045 single base substitution G T missense_variant A443E 1328C>A LICA-FR X 55518504 55518504 single base substitution G A upstream_gene_variant LIRI-JP X 55507832 55507832 single base substitution C A downstream_gene_variant LIRI-JP X 55509047 55509047 single base substitution A G downstream_gene_variant LIRI-JP X 55513731 55513731 single base substitution A C exon_variant LIRI-JP X 55513731 55513731 single base substitution A C missense_variant S548A 1642T>G LIRI-JP X 55513813 55513823 deletion of <=200bp GCCAGGCAAGT - exon_variant LIRI-JP X 55513813 55513823 deletion of <=200bp GCCAGGCAAGT - frameshift_variant DLPG517 LUSC-KR X 55515283 55515283 single base substitution C T synonymous_variant A30A 90G>A LUSC-KR X 55515283 55515283 single base substitution C T upstream_gene_variant LUSC-US X 55513249 55513249 single base substitution T C exon_variant LUSC-US X 55513249 55513249 single base substitution T C synonymous_variant L708L 2124A>G LUSC-US X 55513251 55513251 single base substitution G T exon_variant LUSC-US X 55513251 55513251 single base substitution G T missense_variant L708I 2122C>A LUSC-US X 55514393 55514393 single base substitution G A exon_variant LUSC-US X 55514393 55514393 single base substitution G A missense_variant S327L 980C>T LUSC-US X 55514731 55514731 single base substitution G T intron_variant LUSC-US X 55514731 55514731 single base substitution G T synonymous_variant I214I 642C>A MELA-AU X 55506657 55506657 single base substitution C T downstream_gene_variant MELA-AU X 55506748 55506748 single base substitution G A downstream_gene_variant MELA-AU X 55506798 55506798 single base substitution C T downstream_gene_variant MELA-AU X 55506818 55506819 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU X 55506831 55506831 single base substitution G A downstream_gene_variant MELA-AU X 55506837 55506837 single base substitution G A downstream_gene_variant MELA-AU X 55507432 55507432 single base substitution C T downstream_gene_variant MELA-AU X 55507515 55507515 single base substitution C T downstream_gene_variant MELA-AU X 55508104 55508104 single base substitution G A downstream_gene_variant MELA-AU X 55508105 55508105 single base substitution G A downstream_gene_variant MELA-AU X 55509018 55509018 single base substitution G A downstream_gene_variant MELA-AU X 55510014 55510014 single base substitution C T downstream_gene_variant MELA-AU X 55510045 55510045 single base substitution G A downstream_gene_variant MELA-AU X 55510068 55510068 single base substitution G A downstream_gene_variant MELA-AU X 55510175 55510175 single base substitution G A downstream_gene_variant MELA-AU X 55510379 55510379 single base substitution G A downstream_gene_variant MELA-AU X 55510476 55510476 single base substitution C T downstream_gene_variant MELA-AU X 55511584 55511584 single base substitution C T 3_prime_UTR_variant MELA-AU X 55511584 55511584 single base substitution C T downstream_gene_variant MELA-AU X 55511635 55511635 single base substitution G A 3_prime_UTR_variant MELA-AU X 55511635 55511635 single base substitution G A downstream_gene_variant MELA-AU X 55512750 55512750 single base substitution G A 3_prime_UTR_variant MELA-AU X 55512750 55512750 single base substitution G A downstream_gene_variant MELA-AU X 55513242 55513242 single base substitution C T exon_variant MELA-AU X 55513242 55513242 single base substitution C T missense_variant D711N 2131G>A MELA-AU X 55514315 55514315 single base substitution C A exon_variant MELA-AU X 55514315 55514315 single base substitution C A missense_variant R353I 1058G>T MELA-AU X 55515496 55515496 single base substitution C T intron_variant MELA-AU X 55515496 55515496 single base substitution C T upstream_gene_variant MELA-AU X 55515929 55515929 single base substitution C T upstream_gene_variant MELA-AU X 55516066 55516066 single base substitution G A upstream_gene_variant MELA-AU X 55516422 55516422 single base substitution C T upstream_gene_variant MELA-AU X 55516583 55516583 single base substitution G A upstream_gene_variant MELA-AU X 55516821 55516821 deletion of <=200bp A - upstream_gene_variant MELA-AU X 55517493 55517493 single base substitution A G upstream_gene_variant MELA-AU X 55518060 55518060 single base substitution C T upstream_gene_variant MELA-AU X 55518371 55518371 single base substitution G A upstream_gene_variant MELA-AU X 55518790 55518790 single base substitution C T upstream_gene_variant MELA-AU X 55518986 55518986 single base substitution C T upstream_gene_variant MELA-AU X 55519535 55519535 single base substitution C T upstream_gene_variant MELA-AU X 55520321 55520321 single base substitution C T upstream_gene_variant ORCA-IN X 55513272 55513272 single base substitution G T exon_variant ORCA-IN X 55513272 55513272 single base substitution G T missense_variant L701M 2101C>A ORCA-IN X 55514627 55514627 single base substitution C T intron_variant ORCA-IN X 55514627 55514627 single base substitution C T missense_variant C249Y 746G>A ORCA-IN X 55519358 55519358 single base substitution G A upstream_gene_variant OV-AU X 55507745 55507745 single base substitution A G downstream_gene_variant OV-AU X 55507817 55507817 single base substitution A G downstream_gene_variant OV-AU X 55508629 55508629 single base substitution G C downstream_gene_variant OV-AU X 55510812 55510812 single base substitution C T downstream_gene_variant OV-AU X 55518138 55518138 single base substitution C G upstream_gene_variant OV-AU X 55518179 55518179 single base substitution G T upstream_gene_variant OV-US X 55513444 55513444 single base substitution C T exon_variant OV-US X 55513444 55513444 single base substitution C T synonymous_variant V643V 1929G>A PACA-AU X 55507173 55507173 single base substitution C G downstream_gene_variant PACA-AU X 55509506 55509506 single base substitution T C downstream_gene_variant PACA-AU X 55511428 55511428 deletion of <=200bp A - 3_prime_UTR_variant PACA-AU X 55511428 55511428 deletion of <=200bp A - downstream_gene_variant PACA-AU X 55514798 55514798 single base substitution G T intron_variant PACA-AU X 55514798 55514798 single base substitution G T missense_variant P192H 575C>A PACA-CA X 55506774 55506774 single base substitution G A downstream_gene_variant PACA-CA X 55510191 55510191 single base substitution A T downstream_gene_variant PACA-CA X 55516400 55516400 single base substitution G A upstream_gene_variant PBCA-DE X 55512550 55512553 deletion of <=200bp TTCA - 3_prime_UTR_variant PBCA-DE X 55512550 55512553 deletion of <=200bp TTCA - downstream_gene_variant PRAD-CA X 55507486 55507486 single base substitution G A downstream_gene_variant PRAD-CA X 55518239 55518239 single base substitution T C upstream_gene_variant PRAD-UK X 55510447 55510447 single base substitution G C downstream_gene_variant READ-US X 55514071 55514071 single base substitution C G exon_variant READ-US X 55514071 55514071 single base substitution C G synonymous_variant L434L 1302G>C READ-US X 55514076 55514076 single base substitution G T exon_variant READ-US X 55514076 55514076 single base substitution G T missense_variant H433N 1297C>A READ-US X 55514105 55514105 single base substitution C T exon_variant READ-US X 55514105 55514105 single base substitution C T missense_variant R423Q 1268G>A RECA-EU X 55508639 55508639 single base substitution T A downstream_gene_variant SKCA-BR X 55508099 55508099 single base substitution T G downstream_gene_variant SKCA-BR X 55517255 55517255 single base substitution G A upstream_gene_variant SKCA-BR X 55517276 55517276 single base substitution A T upstream_gene_variant SKCA-BR X 55519232 55519232 insertion of <=200bp - TACAC upstream_gene_variant SKCA-BR X 55519725 55519725 single base substitution C T upstream_gene_variant SKCM-US X 55513971 55513971 single base substitution C T exon_variant SKCM-US X 55513971 55513971 single base substitution C T missense_variant D468N 1402G>A STAD-US X 55513295 55513295 single base substitution A T exon_variant STAD-US X 55513295 55513295 single base substitution A T stop_gained L693* 2078T>A STAD-US X 55513296 55513296 single base substitution A G exon_variant STAD-US X 55513296 55513296 single base substitution A G synonymous_variant L693L 2077T>C STAD-US X 55513438 55513438 single base substitution A G exon_variant STAD-US X 55513438 55513438 single base substitution A G synonymous_variant N645N 1935T>C STAD-US X 55513611 55513611 single base substitution A C exon_variant STAD-US X 55513611 55513611 single base substitution A C missense_variant L588V 1762T>G STAD-US X 55513741 55513741 single base substitution T C exon_variant STAD-US X 55513741 55513741 single base substitution T C synonymous_variant P544P 1632A>G STAD-US X 55514297 55514297 single base substitution G A exon_variant STAD-US X 55514297 55514297 single base substitution G A missense_variant T359I 1076C>T STAD-US X 55514444 55514444 single base substitution C G intron_variant STAD-US X 55514444 55514444 single base substitution C G missense_variant R310T 929G>C STAD-US X 55514472 55514472 single base substitution C T intron_variant STAD-US X 55514472 55514472 single base substitution C T missense_variant A301T 901G>A STAD-US X 55514661 55514661 single base substitution C T intron_variant STAD-US X 55514661 55514661 single base substitution C T missense_variant V238I 712G>A STAD-US X 55514918 55514918 single base substitution C T intron_variant STAD-US X 55514918 55514918 single base substitution C T missense_variant R152H 455G>A STAD-US X 55515144 55515144 single base substitution T C exon_variant STAD-US X 55515144 55515144 single base substitution T C missense_variant S77G 229A>G STAD-US X 55515175 55515175 single base substitution G A exon_variant STAD-US X 55515175 55515175 single base substitution G A synonymous_variant P66P 198C>T STAD-US X 55515195 55515195 single base substitution G A exon_variant STAD-US X 55515195 55515195 single base substitution G A missense_variant P60S 178C>T STAD-US X 55515232 55515232 single base substitution C T exon_variant STAD-US X 55515232 55515232 single base substitution C T synonymous_variant A47A 141G>A STAD-US X 55515254 55515254 single base substitution G A missense_variant A40V 119C>T STAD-US X 55515254 55515254 single base substitution G A upstream_gene_variant THCA-US X 55514742 55514742 single base substitution G C intron_variant THCA-US X 55514742 55514742 single base substitution G C missense_variant L211V 631C>G UCEC-US X 55513273 55513273 single base substitution T C exon_variant UCEC-US X 55513273 55513273 single base substitution T C synonymous_variant L700L 2100A>G UCEC-US X 55513394 55513394 single base substitution G A exon_variant UCEC-US X 55513394 55513394 single base substitution G A missense_variant T660I 1979C>T UCEC-US X 55513396 55513396 single base substitution T G exon_variant UCEC-US X 55513396 55513396 single base substitution T G synonymous_variant G659G 1977A>C UCEC-US X 55513478 55513478 single base substitution C A exon_variant UCEC-US X 55513478 55513478 single base substitution C A missense_variant R632I 1895G>T UCEC-US X 55513612 55513612 single base substitution T G exon_variant UCEC-US X 55513612 55513612 single base substitution T G missense_variant K587N 1761A>C UCEC-US X 55513614 55513614 single base substitution T G exon_variant UCEC-US X 55513614 55513614 single base substitution T G missense_variant K587Q 1759A>C UCEC-US X 55514105 55514105 single base substitution C T exon_variant UCEC-US X 55514105 55514105 single base substitution C T missense_variant R423Q 1268G>A UCEC-US X 55514189 55514189 single base substitution T G exon_variant UCEC-US X 55514189 55514189 single base substitution T G missense_variant K395T 1184A>C UCEC-US X 55514203 55514203 single base substitution G A exon_variant UCEC-US X 55514203 55514203 single base substitution G A synonymous_variant F390F 1170C>T UCEC-US X 55514676 55514676 single base substitution A G intron_variant UCEC-US X 55514676 55514676 single base substitution A G missense_variant S233P 697T>C UCEC-US X 55514688 55514688 single base substitution G A intron_variant UCEC-US X 55514688 55514688 single base substitution G A missense_variant R229C 685C>T UCEC-US X 55514786 55514786 single base substitution G T intron_variant UCEC-US X 55514786 55514786 single base substitution G T missense_variant S196Y 587C>A UCEC-US X 55514860 55514860 single base substitution G A intron_variant UCEC-US X 55514860 55514860 single base substitution G A synonymous_variant D171D 513C>T UCEC-US X 55515340 55515340 single base substitution G A synonymous_variant S11S 33C>T UCEC-US X 55515340 55515340 single base substitution G A upstream_gene_variant

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand TCGA-AX-A0J0-01 COSM1123653 c.1977A>C p.G659G Substitution - coding silent 23:55486963-55486963 - YUGURT COSM5412901 c.1071C>T p.V357V Substitution - coding silent 23:55487869-55487869 - TCGA-BS-A0UF-01 COSM1123652 c.1979C>T p.T660I Substitution - Missense 23:55486961-55486961 - LU-2349 COSM5616350 c.508C>A p.L170I Substitution - Missense 23:55488432-55488432 - 3206A7_019_T COSM5041512 c.1031A>C p.K344T Substitution - Missense 23:55487909-55487909 - TCGA-D1-A17Q-01 COSM1123658 c.1184A>C p.K395T Substitution - Missense 23:55487756-55487756 - 13280 COSM1123652 c.1979C>T p.T660I Substitution - Missense 23:55486961-55486961 - TCGA-BS-A0UL-01 COSM1123664 c.229A>G p.S77G Substitution - Missense 23:55488711-55488711 - pfg182T COSM4755643 c.1975G>A p.G659R Substitution - Missense 23:55486965-55486965 - TCGA-BR-7707-01 COSM4110412 c.141G>A p.A47A Substitution - coding silent 23:55488799-55488799 - TCGA-AP-A0LN-01 COSM1123665 c.33C>T p.S11S Substitution - coding silent 23:55488907-55488907 - HN_62825 COSM128453 c.1866T>A p.T622T Substitution - coding silent 23:55487074-55487074 - EV001-M2a COSM1161959 c.659G>C p.W220S Substitution - Missense 23:55488281-55488281 - I2L-P14b-Tumor-Biopsy COSM5366942 c.1221G>T p.L407L Substitution - coding silent 23:55487719-55487719 - DLD1 COSM1682664 c.1558G>T p.G520C Substitution - Missense 23:55487382-55487382 - LAU149 COSM235553 c.1581C>T p.S527S Substitution - coding silent 23:55487359-55487359 - HN_62825 COSM130128 c.1872T>A p.F624L Substitution - Missense 23:55487068-55487068 - TCGA-HF-7133-01 COSM4110400 c.2078T>A p.L693* Substitution - Nonsense 23:55486862-55486862 - TCGA-FD-A3B6-01 COSM1315618 c.1086G>C p.L362L Substitution - coding silent 23:55487854-55487854 - TCGA-BR-4292-01 COSM4110406 c.929G>C p.R310T Substitution - Missense 23:55488011-55488011 - TCGA-D5-6928-01 COSM1468777 c.1047G>T p.K349N Substitution - Missense 23:55487893-55487893 - EV001-M2b COSM1161959 c.659G>C p.W220S Substitution - Missense 23:55488281-55488281 - TCGA-BR-8487-01 COSM1123664 c.229A>G p.S77G Substitution - Missense 23:55488711-55488711 - TCGA-60-2698-01 COSM757964 c.642C>A p.I214I Substitution - coding silent 23:55488298-55488298 - S01563 COSM5670135 c.1537G>T p.D513Y Substitution - Missense 23:55487403-55487403 - TCGA-DK-A1AF-01 COSM1315618 c.1086G>C p.L362L Substitution - coding silent 23:55487854-55487854 - TCGA-BR-8296-01 COSM4110413 c.119C>T p.A40V Substitution - Missense 23:55488821-55488821 - TCGA-CS-6665-01 COSM3973759 c.1238C>T p.S413L Substitution - Missense 23:55487702-55487702 - ESO-037 COSM1270106 c.1250C>T p.A417V Substitution - Missense 23:55487690-55487690 - TCGA-CS-4942-01 COSM3973760 c.715T>C p.C239R Substitution - Missense 23:55488225-55488225 - KPOPBR-07-T COSM5964038 c.631C>T p.L211L Substitution - coding silent 23:55488309-55488309 - SNU-175 COSM3093331 c.190C>T p.R64C Substitution - Missense 23:55488750-55488750 - TCGA-EB-A3XD-01 COSM3562577 c.1402G>A p.D468N Substitution - Missense 23:55487538-55487538 - TCGA-BH-A0DZ-01 COSM457811 c.633G>C p.L211L Substitution - coding silent 23:55488307-55488307 - 2492726 COSM5725266 c.1437C>T p.C479C Substitution - coding silent 23:55487503-55487503 - PD4602a COSM165455 c.1122G>A p.M374I Substitution - Missense 23:55487818-55487818 - ESO-161 COSM1270108 c.1405A>C p.S469R Substitution - Missense 23:55487535-55487535 - LUAD-LIP77 COSM367922 c.1009G>A p.E337K Substitution - Missense 23:55487931-55487931 - TCGA-UC-A7PF-01 COSM4830011 c.964C>T p.Q322* Substitution - Nonsense 23:55487976-55487976 - TCGA-04-1347-01 COSM81900 c.1929G>A p.V643V Substitution - coding silent 23:55487011-55487011 - OSCC-GB_00180111 COSM3713922 c.2101C>A p.L701M Substitution - Missense 23:55486839-55486839 - 06-P036 COSM4589493 c.1069G>A p.V357I Substitution - Missense 23:55487871-55487871 - YUAVEY COSM1715046 c.907G>A p.E303K Substitution - Missense 23:55488033-55488033 - YUDIVI COSM5412900 c.1276C>T p.H426Y Substitution - Missense 23:55487664-55487664 - TCGA-CG-5721-01 COSM4110402 c.1935T>C p.N645N Substitution - coding silent 23:55487005-55487005 - T3658 COSM4739923 c.232G>A p.G78S Substitution - Missense 23:55488708-55488708 - TCGA-DC-6682-01 COSM1570107 c.1302G>C p.L434L Substitution - coding silent 23:55487638-55487638 - TCGA-43-2578-01 COSM757966 c.2122C>A p.L708I Substitution - Missense 23:55486818-55486818 - ESO-874 COSM1270109 c.744T>C p.S248S Substitution - coding silent 23:55488196-55488196 - TCGA-AC-A23C-01 COSM1491141 c.1457A>G p.Q486R Substitution - Missense 23:55487483-55487483 - HCC072T COSM5821718 c.1072T>G p.Y358D Substitution - Missense 23:55487868-55487868 - TCGA-EK-A3GK-01 COSM4853833 c.959C>T p.S320F Substitution - Missense 23:55487981-55487981 - 107546 COSM95490 c.137A>G p.K46R Substitution - Missense 23:55488803-55488803 - TCGA-HU-A4GY-01 COSM4110404 c.1632A>G p.P544P Substitution - coding silent 23:55487308-55487308 - T3024 COSM4739922 c.488G>A p.R163Q Substitution - Missense 23:55488452-55488452 - WM3211 COSM3727456 c.1360C>A p.L454I Substitution - Missense 23:55487580-55487580 - PD5935a COSM5772031 c.1436G>C p.C479S Substitution - Missense 23:55487504-55487504 - Gp5D COSM4629239 c.423A>G p.A141A Substitution - coding silent 23:55488517-55488517 - TCGA-BR-8081-01 COSM4110410 c.198C>T p.P66P Substitution - coding silent 23:55488742-55488742 - TCGA-AP-A051-01 COSM1123661 c.685C>T p.R229C Substitution - Missense 23:55488255-55488255 - HCT15 COSM1682664 c.1558G>T p.G520C Substitution - Missense 23:55487382-55487382 - TCGA-19-2631-01 COSM3406499 c.1430C>T p.P477L Substitution - Missense 23:55487510-55487510 - PA285 COSM1163568 c.882C>A p.D294E Substitution - Missense 23:55488058-55488058 - TCGA-BP-4158-01 COSM3364073 c.2036G>A p.S679N Substitution - Missense 23:55486904-55486904 - TCGA-BR-6565-01 COSM4110411 c.178C>T p.P60S Substitution - Missense 23:55488762-55488762 - TCGA-D1-A17A-01 COSM1123655 c.1761A>C p.K587N Substitution - Missense 23:55487179-55487179 - TCGA-G4-6628-01 COSM1468778 c.866A>G p.K289R Substitution - Missense 23:55488074-55488074 - PD13165a COSM1123665 c.33C>T p.S11S Substitution - coding silent 23:55488907-55488907 - LUAD-NYU284 COSM373426 c.1196T>C p.I399T Substitution - Missense 23:55487744-55487744 - Pat_49_B COSM5878095 c.1675C>T p.P559S Substitution - Missense 23:55487265-55487265 - SNU-175 COSM4650896 c.301C>T p.R101C Substitution - Missense 23:55488639-55488639 - 001 COSM1161959 c.659G>C p.W220S Substitution - Missense 23:55488281-55488281 - TCGA-HU-8602-01 COSM4110405 c.1076C>T p.T359I Substitution - Missense 23:55487864-55487864 - TCGA-EK-A2RB-01 COSM4820029 c.191G>A p.R64H Substitution - Missense 23:55488749-55488749 - I2L-P19Ta-Tumor-Biopsy COSM5368019 c.1761_1762insA p.L588fs*13 Insertion - Frameshift 23:55487178-55487179 - LUAD-B00859 COSM355693 c.429G>T p.R143R Substitution - coding silent 23:55488511-55488511 - I2L-P14b-Tumor-Organoid COSM5366942 c.1221G>T p.L407L Substitution - coding silent 23:55487719-55487719 - TCGA-C5-A7CL-01 COSM4110412 c.141G>A p.A47A Substitution - coding silent 23:55488799-55488799 - 105225 COSM95489 c.724C>T p.H242Y Substitution - Missense 23:55488216-55488216 - OSCC-GB_00550111 COSM4884787 c.746G>A p.C249Y Substitution - Missense 23:55488194-55488194 - TCGA-BR-A4J6-01 COSM4110401 c.2077T>C p.L693L Substitution - coding silent 23:55486863-55486863 - CHC1531T COSM4804905 c.1328C>A p.A443E Substitution - Missense 23:55487612-55487612 - U343 COSM5070609 c.1743A>G p.K581K Substitution - coding silent 23:55487197-55487197 - TCGA-AA-3949-01 COSM296966 c.119C>A p.A40E Substitution - Missense 23:55488821-55488821 - 254891 COSM3724867 c.122C>A p.A41E Substitution - Missense 23:55488818-55488818 - TCGA-BS-A0UF-01 COSM1123660 c.697T>C p.S233P Substitution - Missense 23:55488243-55488243 - HCT-15 COSM1682664 c.1558G>T p.G520C Substitution - Missense 23:55487382-55487382 - TCGA-BR-4361-01 COSM4110409 c.455G>A p.R152H Substitution - Missense 23:55488485-55488485 - TCGA-CJ-4643-01 COSM3364074 c.1731G>T p.Q577H Substitution - Missense 23:55487209-55487209 - ESO-120 COSM1270107 c.752C>T p.S251F Substitution - Missense 23:55488188-55488188 - TCGA-CD-8535-01 COSM4110403 c.1762T>G p.L588V Substitution - Missense 23:55487178-55487178 - 8034061 COSM3390730 c.575C>A p.P192H Substitution - Missense 23:55488365-55488365 - TCGA-AP-A0LM-01 COSM1123656 c.1759A>C p.K587Q Substitution - Missense 23:55487181-55487181 - TCGA-AP-A059-01 COSM1123651 c.2100A>G p.L700L Substitution - coding silent 23:55486840-55486840 - TCGA-CJ-5677-01 COSM488507 c.1088G>C p.R363T Substitution - Missense 23:55487852-55487852 - ESCC_107 COSM5638585 c.175delG p.E59fs*14 Deletion - Frameshift 23:55488765-55488765 - 2492724 COSM5725266 c.1437C>T p.C479C Substitution - coding silent 23:55487503-55487503 - TCGA-BS-A0UF-01 COSM1123654 c.1895G>T p.R632I Substitution - Missense 23:55487045-55487045 - TCGA-AP-A059-01 COSM1123663 c.513C>T p.D171D Substitution - coding silent 23:55488427-55488427 - TCGA-AP-A0LM-01 COSM1123662 c.587C>A p.S196Y Substitution - Missense 23:55488353-55488353 - TCGA-BR-6566-01 COSM4110408 c.712G>A p.V238I Substitution - Missense 23:55488228-55488228 - TCGA-66-2757-01 COSM757965 c.980C>T p.S327L Substitution - Missense 23:55487960-55487960 - TCGA-AP-A056-01 COSM1123659 c.1170C>T p.F390F Substitution - coding silent 23:55487770-55487770 - 083-01-2TD COSM5418539 c.666G>T p.G222G Substitution - coding silent 23:55488274-55488274 - TCGA-BR-4184-01 COSM4110407 c.901G>A p.A301T Substitution - Missense 23:55488039-55488039 - PT23_2 COSM5904090 c.1868C>T p.P623L Substitution - Missense 23:55487072-55487072 - TCGA-AP-A0LM-01 COSM1123657 c.1268G>A p.R423Q Substitution - Missense 23:55487672-55487672 - EV001-M1 COSM1161959 c.659G>C p.W220S Substitution - Missense 23:55488281-55488281 - PD8609a COSM5799001 c.526C>A p.P176T Substitution - Missense 23:55488414-55488414 - I2L-P19Ta-Tumor-Organoid COSM5368019 c.1761_1762insA p.L588fs*13 Insertion - Frameshift 23:55487178-55487179 - TCGA-76-6285-01 COSM3406500 c.731A>G p.N244S Substitution - Missense 23:55488209-55488209 - LUAD-S01315 COSM385742 c.929G>A p.R310K Substitution - Missense 23:55488011-55488011 - TCGA-31-1959-01 COSM116277 c.1054A>G p.R352G Substitution - Missense 23:55487886-55487886 - TCGA-DJ-A1QE-01 COSM3372307 c.631C>G p.L211V Substitution - Missense 23:55488309-55488309 - TCGA-EI-6917-01 COSM1123657 c.1268G>A p.R423Q Substitution - Missense 23:55487672-55487672 - SNU-175 COSM3093317 c.902C>T p.A301V Substitution - Missense 23:55488038-55488038 - 169 COSM3729788 c.200C>T p.A67V Substitution - Missense 23:55488740-55488740 - TCGA-A8-A06R-01 COSM457810 c.1392C>G p.H464Q Substitution - Missense 23:55487548-55487548 - HCC074T COSM5810072 c.1772T>C p.V591A Substitution - Missense 23:55487168-55487168 - L21 COSM5369423 c.1572_1573AT>CCTT p.F525fs*14 Complex - frameshift 23:55487367-55487368 - T2 COSM5346026 c.1944G>T p.K648N Substitution - Missense 23:55486996-55486996 - TCGA-EK-A2R7-01 COSM4852158 c.868G>A p.D290N Substitution - Missense 23:55488072-55488072 - TCGA-BP-5186-01 COSM488506 c.2135A>T p.*712L Nonstop extension 23:55486805-55486805 - CHC1531T COSM4804905 c.1328C>A p.A443E Substitution - Missense 23:55487612-55487612 - HCC2998 COSM3093309 c.1461C>T p.I487I Substitution - coding silent 23:55487479-55487479 - SJHYPO039 COSM4775667 c.147G>A p.S49S Substitution - coding silent 23:55488793-55488793 - Gp2D COSM4629048 c.2095T>C p.Y699H Substitution - Missense 23:55486845-55486845 - cSCCP5 COSM138158 c.950C>A p.T317K Substitution - Missense 23:55487990-55487990 - TCGA-CJ-4638-01 COSM488508 c.802G>A p.E268K Substitution - Missense 23:55488138-55488138 - LS411 COSM3093307 c.1536G>T p.W512C Substitution - Missense 23:55487404-55487404 - TCGA-DC-6682-01 COSM1570106 c.1297C>A p.H433N Substitution - Missense 23:55487643-55487643 - TCGA-DG-A2KK-01 COSM4828536 c.2082C>G p.L694L Substitution - coding silent 23:55486858-55486858 - TCGA-AC-A23H-01 COSM3845136 c.1300C>G p.L434V Substitution - Missense 23:55487640-55487640 - I2L-P19Ta-Tumor-Biopsy COSM5367016 c.451C>T p.R151W Substitution - Missense 23:55488489-55488489 - I2L-P19Ta-Tumor-Organoid COSM5367016 c.451C>T p.R151W Substitution - Missense 23:55488489-55488489 - TCGA-33-4533-01 COSM757967 c.2124A>G p.L708L Substitution - coding silent 23:55486816-55486816 - TCGA-EA-A411-01 COSM4838062 c.1009G>C p.E337Q Substitution - Missense 23:55487931-55487931 - PD9004a COSM5785915 c.1629A>T p.I543I Substitution - coding silent 23:55487311-55487311 - 18T COSM3713922 c.2101C>A p.L701M Substitution - Missense 23:55486839-55486839 - 234 COSM3731303 c.442C>T p.R148C Substitution - Missense 23:55488498-55488498 - T578 COSM1558553 c.916G>T p.E306* Substitution - Nonsense 23:55488024-55488024 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.40024;Hs.40061 Xp11.21

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A G Missense p.C239R c.715T>C X 55514658 LGG A G Synonymous p.H451H c.1353T>C X 55514020 STAD A G Synonymous p.S248S c.744T>C X 55514629 ESCA A T Missense p.F624L c.1872T>A X 55513501 HNSC A T Nonsense p.C642* c.1926T>A X 55513447 HNSC A T Synonymous p.T622T c.1866T>A X 55513507 HNSC C A Missense p.A626S c.1876G>T X 55513497 LUAD C A Missense p.G172V c.515G>T X 55514858 LUAD C A Missense p.Q577H c.1731G>T X 55513642 RCCC C A Synonymous p.A41A c.123G>T X 55515250 LUAD C A Synonymous p.G222G c.666G>T X 55514707 CLL C G Missense p.E531Q c.1591G>C X 55513782 LUAD C G Missense p.R310T c.929G>C X 55514444 STAD C G Missense p.R363T c.1088G>C X 55514285 RCCC C G Synonymous p.L362L c.1086G>C X 55514287 BLCA C T Missense p.A523T c.1567G>A X 55513806 LUAD C T Missense p.E268K c.802G>A X 55514571 RCCC C T Missense p.M374I c.1122G>A X 55514251 BRCA C T Missense p.R353K c.1058G>A X 55514315 BRCA C T Missense p.S679N c.2036G>A X 55513337 RCCC C T Synonymous p.V643V c.1929G>A X 55513444 OV G A Missense p.A417V c.1250C>T X 55514123 ESCA G A Missense p.P477L c.1430C>T X 55513943 GBM G A Missense p.P60S c.178C>T X 55515195 STAD G A Missense p.S251F c.752C>T X 55514621 ESCA G A Missense p.S327L c.980C>T X 55514393 LUSC G A Missense p.S413L c.1238C>T X 55514135 LGG G A Missense p.T660I c.1979C>T X 55513394 NSCLC G A Nonsense p.R607* c.1819C>T X 55513554 HNSC G A Synonymous p.S11S c.33C>T X 55515340 UCEC G A Synonymous p.T689T c.2067C>T X 55513306 LUAD G C Missense p.H464Q c.1392C>G X 55513981 BRCA G C Missense p.L211V c.631C>G X 55514742 THCA G T Missense p.L170I c.508C>A X 55514865 NSCLC G T Missense p.L461I c.1381C>A X 55513992 LUAD G T Missense p.L708I c.2122C>A X 55513251 LUSC T - 3-UTRDeletion . c.2133+31delA X 55513209 STAD T A 3-UTRSNV . c.2133+2A>T X 55513238 RCCC T C Missense p.N244S c.731A>G X 55514642 GBM T C Missense p.Q486R c.1457A>G X 55513916 BRCA T C Missense p.R352G c.1054A>G X 55514319 OV T C Synonymous p.L708L c.2124A>G X 55513249 LUSC T G Missense p.K587N c.1761A>C X 55513612 UCEC T G Missense p.S469R c.1405A>C X 55513968 ESCA