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 BLCA 17 7365433 7365433 + Missense_Mutation SNP C C A TCGA-2F-A9KO-01A-11D-A38G-08 TCGA-2F-A9KO-11A-12D-A38J-08 g.chr17:7365433C>A c.2868G>T c.(2866-2868)aaG>aaT p.K956N BLCA 17 7365511 7365511 + Silent SNP G G T TCGA-DK-A3X1-01A-12D-A22Z-08 TCGA-DK-A3X1-10A-01D-A22Z-08 g.chr17:7365511G>T c.2790C>A c.(2788-2790)ctC>ctA p.L930L BLCA 17 7365908 7365908 + Missense_Mutation SNP G G C TCGA-DK-A6B1-01A-12D-A30E-08 TCGA-DK-A6B1-10A-01D-A30H-08 g.chr17:7365908G>C c.2393C>G c.(2392-2394)cCt>cGt p.P798R BLCA 17 7366260 7366260 + Missense_Mutation SNP C C T TCGA-GC-A3WC-01A-31D-A22Z-08 TCGA-GC-A3WC-10A-01D-A22Z-08 g.chr17:7366260C>T c.2041G>A c.(2041-2043)Ggt>Agt p.G681S BLCA 17 7366392 7366392 + Missense_Mutation SNP C C G TCGA-ZF-AA51-01A-21D-A391-08 TCGA-ZF-AA51-10A-01D-A394-08 g.chr17:7366392C>G c.1909G>C c.(1909-1911)Gag>Cag p.E637Q BLCA 17 7366829 7366829 + Missense_Mutation SNP C C G TCGA-K4-A54R-01A-11D-A26M-08 TCGA-K4-A54R-10A-01D-A26K-08 g.chr17:7366829C>G c.1472G>C c.(1471-1473)gGa>gCa p.G491A BLCA 17 7367107 7367107 + Silent SNP C C T TCGA-2F-A9KO-01A-11D-A38G-08 TCGA-2F-A9KO-11A-12D-A38J-08 g.chr17:7367107C>T c.1194G>A c.(1192-1194)gaG>gaA p.E398E BLCA 17 7369149 7369149 + Silent SNP C C G TCGA-FD-A3SO-01A-11D-A22Z-08 TCGA-FD-A3SO-10A-01D-A22Z-08 g.chr17:7369149C>G c.972G>C c.(970-972)ctG>ctC p.L324L BLCA 17 7369927 7369927 + Missense_Mutation SNP A A G TCGA-DK-A6AW-01A-11D-A30E-08 TCGA-DK-A6AW-10A-01D-A30H-08 g.chr17:7369927A>G c.194T>C c.(193-195)cTa>cCa p.L65P BRCA 17 7366057 7366057 + Silent SNP G G A TCGA-A8-A09Z-01A-11W-A019-09 TCGA-A8-A09Z-10A-01W-A021-09 g.chr17:7366057G>A c.2244C>T c.(2242-2244)caC>caT p.H748H BRCA 17 7366443 7366443 + Nonsense_Mutation SNP C C A TCGA-AR-A24Q-01A-12D-A167-09 TCGA-AR-A24Q-10A-01D-A167-09 g.chr17:7366443C>A c.1858G>T c.(1858-1860)Gag>Tag p.E620* BRCA 17 7366623 7366623 + Missense_Mutation SNP G G A TCGA-AR-A24V-01A-21D-A167-09 TCGA-AR-A24V-10A-01D-A167-09 g.chr17:7366623G>A c.1678C>T c.(1678-1680)Cgg>Tgg p.R560W BRCA 17 7369111 7369111 + Missense_Mutation SNP T T A TCGA-D8-A1XQ-01A-11D-A14K-09 TCGA-D8-A1XQ-10A-01D-A14K-09 g.chr17:7369111T>A c.1010A>T c.(1009-1011)tAc>tTc p.Y337F BRCA 17 7370012 7370012 + Missense_Mutation SNP C C T TCGA-D8-A1XM-01A-21D-A14K-09 TCGA-D8-A1XM-10A-01D-A14K-09 g.chr17:7370012C>T c.109G>A c.(109-111)Gga>Aga p.G37R CESC 17 7365529 7365529 + Silent SNP G G A TCGA-FU-A3HZ-01A-11D-A20U-09 TCGA-FU-A3HZ-10A-01D-A20U-09 g.chr17:7365529G>A c.2772C>T c.(2770-2772)ctC>ctT p.L924L CESC 17 7365772 7365772 + Missense_Mutation SNP C C A TCGA-EK-A2R9-01A-11D-A18J-09 TCGA-EK-A2R9-10A-01D-A18J-09 g.chr17:7365772C>A c.2529G>T c.(2527-2529)gaG>gaT p.E843D CESC 17 7365840 7365840 + Missense_Mutation SNP C C G TCGA-JW-A5VL-01A-11D-A28B-09 TCGA-JW-A5VL-10A-01D-A28E-09 g.chr17:7365840C>G c.2461G>C c.(2461-2463)Gag>Cag p.E821Q CESC 17 7366072 7366072 + Silent SNP C C T TCGA-IR-A3LK-01A-12D-A20U-09 TCGA-IR-A3LK-10A-01D-A20U-09 g.chr17:7366072C>T c.2229G>A c.(2227-2229)aaG>aaA p.K743K CESC 17 7366075 7366075 + Silent SNP C C A TCGA-IR-A3LK-01A-12D-A20U-09 TCGA-IR-A3LK-10A-01D-A20U-09 g.chr17:7366075C>A c.2226G>T c.(2224-2226)cgG>cgT p.R742R CESC 17 7369795 7369795 + Missense_Mutation SNP G G C TCGA-DR-A0ZM-01A-12D-A10S-08 TCGA-DR-A0ZM-10A-01D-A10S-08 g.chr17:7369795G>C c.326C>G c.(325-327)tCt>tGt p.S109C CHOL 17 7369566 7369566 + Nonsense_Mutation SNP C C T TCGA-WD-A7RX-01A-12D-A417-09 TCGA-WD-A7RX-10A-01D-A41A-09 g.chr17:7369566C>T c.555G>A c.(553-555)tgG>tgA p.W185* COAD 17 7365390 7365390 + Missense_Mutation SNP C C T TCGA-AA-3811-01A-01W-0995-10 TCGA-AA-3811-10A-01W-0995-10 g.chr17:7365390C>T c.2911G>A c.(2911-2913)Gca>Aca p.A971T COAD 17 7365474 7365474 + Missense_Mutation SNP C C T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr17:7365474C>T c.2827G>A c.(2827-2829)Gct>Act p.A943T COAD 17 7366281 7366281 + Missense_Mutation SNP G G A TCGA-AA-3697-01A-01D-1719-10 TCGA-AA-3697-11A-01D-1719-10 g.chr17:7366281G>A c.2020C>T c.(2020-2022)Cgc>Tgc p.R674C COAD 17 7366385 7366385 + Missense_Mutation SNP T T C TCGA-AY-6386-01A-21D-1719-10 TCGA-AY-6386-10A-01D-1719-10 g.chr17:7366385T>C c.1916A>G c.(1915-1917)gAc>gGc p.D639G COAD 17 7366387 7366387 + Missense_Mutation SNP C C A TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chr17:7366387C>A c.1914G>T c.(1912-1914)gaG>gaT p.E638D COAD 17 7366908 7366908 + Missense_Mutation SNP G G A TCGA-D5-6540-01A-11D-1719-10 TCGA-D5-6540-10A-01D-1719-10 g.chr17:7366908G>A c.1393C>T c.(1393-1395)Cct>Tct p.P465S COAD 17 7366996 7366996 + Silent SNP C C T TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chr17:7366996C>T c.1305G>A c.(1303-1305)ccG>ccA p.P435P COAD 17 7367039 7367039 + Missense_Mutation SNP C C T TCGA-AA-3815-01A-01W-0995-10 TCGA-AA-3815-10A-01W-0995-10 g.chr17:7367039C>T c.1262G>A c.(1261-1263)cGg>cAg p.R421Q COAD 17 7367081 7367081 + Missense_Mutation SNP G G T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr17:7367081G>T c.1220C>A c.(1219-1221)cCc>cAc p.P407H COAD 17 7367147 7367147 + Missense_Mutation SNP C C T TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chr17:7367147C>T c.1154G>A c.(1153-1155)cGa>cAa p.R385Q COAD 17 7369209 7369209 + Silent SNP G G A TCGA-G4-6304-01A-11D-1924-10 TCGA-G4-6304-10A-01D-1924-10 g.chr17:7369209G>A c.912C>T c.(910-912)ggC>ggT p.G304G COAD 17 7369601 7369601 + Missense_Mutation SNP G G A TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr17:7369601G>A c.520C>T c.(520-522)Cgc>Tgc p.R174C COAD 17 7369827 7369827 + Silent SNP G G T TCGA-A6-6780-01A-11D-1835-10 TCGA-A6-6780-10A-01D-1835-10 g.chr17:7369827G>T c.294C>A c.(292-294)tcC>tcA p.S98S COADREAD 17 7365390 7365390 + Missense_Mutation SNP C C T TCGA-AA-3811-01A-01W-0995-10 TCGA-AA-3811-10A-01W-0995-10 g.chr17:7365390C>T c.2911G>A c.(2911-2913)Gca>Aca p.A971T COADREAD 17 7365474 7365474 + Missense_Mutation SNP C C T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr17:7365474C>T c.2827G>A c.(2827-2829)Gct>Act p.A943T COADREAD 17 7366281 7366281 + Missense_Mutation SNP G G A TCGA-AA-3697-01A-01D-1719-10 TCGA-AA-3697-11A-01D-1719-10 g.chr17:7366281G>A c.2020C>T c.(2020-2022)Cgc>Tgc p.R674C COADREAD 17 7366385 7366385 + Missense_Mutation SNP T T C TCGA-AY-6386-01A-21D-1719-10 TCGA-AY-6386-10A-01D-1719-10 g.chr17:7366385T>C c.1916A>G c.(1915-1917)gAc>gGc p.D639G COADREAD 17 7366387 7366387 + Missense_Mutation SNP C C A TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chr17:7366387C>A c.1914G>T c.(1912-1914)gaG>gaT p.E638D COADREAD 17 7366544 7366544 + Missense_Mutation SNP G G C TCGA-AG-4005-01A-01W-1073-09 TCGA-AG-4005-10A-01W-1073-09 g.chr17:7366544G>C c.1757C>G c.(1756-1758)aCa>aGa p.T586R COADREAD 17 7366908 7366908 + Missense_Mutation SNP G G A TCGA-D5-6540-01A-11D-1719-10 TCGA-D5-6540-10A-01D-1719-10 g.chr17:7366908G>A c.1393C>T c.(1393-1395)Cct>Tct p.P465S COADREAD 17 7366996 7366996 + Silent SNP C C T TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chr17:7366996C>T c.1305G>A c.(1303-1305)ccG>ccA p.P435P COADREAD 17 7367039 7367039 + Missense_Mutation SNP C C T TCGA-AA-3815-01A-01W-0995-10 TCGA-AA-3815-10A-01W-0995-10 g.chr17:7367039C>T c.1262G>A c.(1261-1263)cGg>cAg p.R421Q COADREAD 17 7367081 7367081 + Missense_Mutation SNP G G T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr17:7367081G>T c.1220C>A c.(1219-1221)cCc>cAc p.P407H COADREAD 17 7367147 7367147 + Missense_Mutation SNP C C T TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chr17:7367147C>T c.1154G>A c.(1153-1155)cGa>cAa p.R385Q COADREAD 17 7369209 7369209 + Silent SNP G G A TCGA-G4-6304-01A-11D-1924-10 TCGA-G4-6304-10A-01D-1924-10 g.chr17:7369209G>A c.912C>T c.(910-912)ggC>ggT p.G304G COADREAD 17 7369601 7369601 + Missense_Mutation SNP G G A TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr17:7369601G>A c.520C>T c.(520-522)Cgc>Tgc p.R174C COADREAD 17 7369827 7369827 + Silent SNP G G T TCGA-A6-6780-01A-11D-1835-10 TCGA-A6-6780-10A-01D-1835-10 g.chr17:7369827G>T c.294C>A c.(292-294)tcC>tcA p.S98S DLBC 17 7365289 7365289 + Silent SNP A A T TCGA-G8-6324-01A-11D-2210-10 TCGA-G8-6324-10A-01D-2210-10 g.chr17:7365289A>T c.3012T>A c.(3010-3012)gtT>gtA p.V1004V ESCA 17 7365493 7365493 + Nonsense_Mutation SNP G G T TCGA-X8-AAAR-01A-11D-A403-09 TCGA-X8-AAAR-10A-01D-A403-09 g.chr17:7365493G>T c.2808C>A c.(2806-2808)taC>taA p.Y936* ESCA 17 7366573 7366573 + Silent SNP G G A TCGA-VR-A8EQ-01A-11D-A36J-09 TCGA-VR-A8EQ-10A-01D-A36M-09 g.chr17:7366573G>A c.1728C>T c.(1726-1728)ggC>ggT p.G576G ESCA 17 7369066 7369066 + Missense_Mutation SNP C C T TCGA-Q9-A6FW-01A-31D-A31U-09 TCGA-Q9-A6FW-10A-01D-A31U-09 g.chr17:7369066C>T c.1055G>A c.(1054-1056)cGc>cAc p.R352H ESCA 17 7369187 7369187 + Missense_Mutation SNP C C T TCGA-L5-A43J-01A-12D-A247-09 TCGA-L5-A43J-11A-11D-A247-09 g.chr17:7369187C>T c.934G>A c.(934-936)Gcg>Acg p.A312T ESCA 17 7369677 7369677 + Silent SNP G G A TCGA-IC-A6RE-01A-11D-A33E-09 TCGA-IC-A6RE-10A-01D-A33H-09 g.chr17:7369677G>A c.444C>T c.(442-444)ctC>ctT p.L148L HNSC 17 7365712 7365712 + Silent SNP G G A TCGA-CV-A45P-01A-11D-A24D-08 TCGA-CV-A45P-10A-01D-A24F-08 g.chr17:7365712G>A c.2589C>T c.(2587-2589)agC>agT p.S863S HNSC 17 7366417 7366417 + Silent SNP C C A TCGA-CR-7370-01A-11D-2129-08 TCGA-CR-7370-10A-01D-2129-08 g.chr17:7366417C>A c.1884G>T c.(1882-1884)ctG>ctT p.L628L HNSC 17 7366892 7366892 + Missense_Mutation SNP G G C TCGA-UF-A7J9-01A-12D-A34J-08 TCGA-UF-A7J9-10A-01D-A34M-08 g.chr17:7366892G>C c.1409C>G c.(1408-1410)tCt>tGt p.S470C HNSC 17 7370046 7370046 + Silent SNP G G T TCGA-CN-A63W-01A-11D-A30E-08 TCGA-CN-A63W-10A-01D-A30H-08 g.chr17:7370046G>T c.75C>A c.(73-75)ctC>ctA p.L25L HNSC 17 7370078 7370078 + Missense_Mutation SNP C C T TCGA-DQ-5631-01A-01D-1870-08 TCGA-DQ-5631-10A-01D-1870-08 g.chr17:7370078C>T c.43G>A c.(43-45)Gcc>Acc p.A15T HNSC 17 7370091 7370091 + Silent SNP C C T TCGA-CV-5441-01A-01D-1512-08 TCGA-CV-5441-11A-01D-1512-08 g.chr17:7370091C>T c.30G>A c.(28-30)ccG>ccA p.P10P KIPAN 17 7365705 7365705 + Missense_Mutation SNP T T C TCGA-B0-5098-01A-01D-1421-08 TCGA-B0-5098-11A-01D-1421-08 g.chr17:7365705T>C c.2596A>G c.(2596-2598)Agc>Ggc p.S866G KIRC 17 7365705 7365705 + Missense_Mutation SNP T T C TCGA-B0-5098-01A-01D-1421-08 TCGA-B0-5098-11A-01D-1421-08 g.chr17:7365705T>C c.2596A>G c.(2596-2598)Agc>Ggc p.S866G LIHC 17 7366504 7366504 + Silent SNP A A C TCGA-DD-AAE9-01A-11D-A40R-10 TCGA-DD-AAE9-10A-01D-A40U-10 g.chr17:7366504A>C c.1797T>G c.(1795-1797)ccT>ccG p.P599P LIHC 17 7370026 7370026 + Missense_Mutation SNP A A G TCGA-EP-A2KA-01A-11D-A183-10 TCGA-EP-A2KA-10A-01D-A183-10 g.chr17:7370026A>G c.95T>C c.(94-96)gTc>gCc p.V32A LIHC 17 7370078 7370078 + Missense_Mutation SNP C C T TCGA-DD-A4NI-01A-11D-A27I-10 TCGA-DD-A4NI-10A-01D-A27I-10 g.chr17:7370078C>T c.43G>A c.(43-45)Gcc>Acc p.A15T LUAD 17 7365284 7365284 + Missense_Mutation SNP C C G TCGA-91-6830-01A-11D-1945-08 TCGA-91-6830-11A-01D-1945-08 g.chr17:7365284C>G c.3017G>C c.(3016-3018)aGa>aCa p.R1006T LUAD 17 7365426 7365426 + Missense_Mutation SNP C C T TCGA-86-A4JF-01A-11D-A24P-08 TCGA-86-A4JF-10A-01D-A24P-08 g.chr17:7365426C>T c.2875G>A c.(2875-2877)Ggg>Agg p.G959R LUAD 17 7365687 7365687 + Missense_Mutation SNP C C A TCGA-55-6983-01A-11D-1945-08 TCGA-55-6983-11A-01D-1945-08 g.chr17:7365687C>A c.2614G>T c.(2614-2616)Gtg>Ttg p.V872L LUAD 17 7366052 7366052 + Missense_Mutation SNP C C T TCGA-17-Z014-01A-01W-0746-08 TCGA-17-Z014-11A-01W-0746-08 g.chr17:7366052C>T c.2249G>A c.(2248-2250)gGg>gAg p.G750E LUAD 17 7366134 7366134 + Missense_Mutation SNP C C T TCGA-55-8205-01A-11D-2238-08 TCGA-55-8205-10A-01D-2238-08 g.chr17:7366134C>T c.2167G>A c.(2167-2169)Gag>Aag p.E723K LUAD 17 7366181 7366181 + Nonsense_Mutation SNP C C T TCGA-50-5946-01A-11D-1753-08 TCGA-50-5946-10A-01D-1753-08 g.chr17:7366181C>T c.2120G>A c.(2119-2121)tGg>tAg p.W707* LUAD 17 7369062 7369062 + Silent SNP C C T TCGA-55-8205-01A-11D-2238-08 TCGA-55-8205-10A-01D-2238-08 g.chr17:7369062C>T c.1059G>A c.(1057-1059)acG>acA p.T353T LUAD 17 7369684 7369684 + Missense_Mutation SNP G G T TCGA-55-A490-01A-11D-A24D-08 TCGA-55-A490-10A-01D-A24F-08 g.chr17:7369684G>T c.437C>A c.(436-438)gCc>gAc p.A146D LUAD 17 7369753 7369753 + Missense_Mutation SNP G G A TCGA-75-5147-01A-01D-1625-08 TCGA-75-5147-10A-01D-1625-08 g.chr17:7369753G>A c.368C>T c.(367-369)cCc>cTc p.P123L LUSC 17 7365286 7365286 + Silent SNP C C T TCGA-66-2794-01A-01D-1267-08 TCGA-66-2794-11A-01D-1267-08 g.chr17:7365286C>T c.3015G>A c.(3013-3015)gaG>gaA p.E1005E LUSC 17 7365586 7365586 + Missense_Mutation SNP G G T TCGA-22-4613-01A-01D-1441-08 TCGA-22-4613-11A-01D-1441-08 g.chr17:7365586G>T c.2715C>A c.(2713-2715)gaC>gaA p.D905E LUSC 17 7365801 7365801 + Missense_Mutation SNP C C A TCGA-43-3920-01A-01D-0983-08 TCGA-43-3920-10A-01D-0983-08 g.chr17:7365801C>A c.2500G>T c.(2500-2502)Ggg>Tgg p.G834W LUSC 17 7367112 7367112 + Missense_Mutation SNP T T A TCGA-22-4601-01A-01D-1441-08 TCGA-22-4601-11A-01D-1441-08 g.chr17:7367112T>A c.1189A>T c.(1189-1191)Agt>Tgt p.S397C LUSC 17 7367123 7367123 + Missense_Mutation SNP C C A TCGA-22-4601-01A-01D-1441-08 TCGA-22-4601-11A-01D-1441-08 g.chr17:7367123C>A c.1178G>T c.(1177-1179)gGc>gTc p.G393V OV 17 7366384 7366384 + Silent SNP G G A TCGA-09-2050-01A-01W-0799-08 TCGA-09-2050-10A-01W-0799-08 g.chr17:7366384G>A c.1917C>T c.(1915-1917)gaC>gaT p.D639D PAAD 17 7366349 7366351 + In_Frame_Del DEL TCC TCC - TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr17:7366349_7366351delTCC c.1950_1952delGGA c.(1948-1953)gaggat>gat p.E650del PAAD 17 7366455 7366455 + Missense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr17:7366455G>A c.1846C>T c.(1846-1848)Cgc>Tgc p.R616C PAAD 17 7367040 7367040 + Missense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr17:7367040G>A c.1261C>T c.(1261-1263)Cgg>Tgg p.R421W PAAD 17 7369754 7369754 + Missense_Mutation SNP G G A TCGA-US-A77E-01A-11D-A32N-08 TCGA-US-A77E-11A-11D-A32N-08 g.chr17:7369754G>A c.367C>T c.(367-369)Ccc>Tcc p.P123S PRAD 17 7366047 7366047 + Missense_Mutation SNP A A C TCGA-HC-7818-01A-11D-2114-08 TCGA-HC-7818-10A-01D-2115-08 g.chr17:7366047A>C c.2254T>G c.(2254-2256)Tcc>Gcc p.S752A PRAD 17 7366351 7366351 + Missense_Mutation SNP C C A TCGA-KK-A6E7-01A-11D-A31L-08 TCGA-KK-A6E7-11A-11D-A31J-08 g.chr17:7366351C>A c.1950G>T c.(1948-1950)gaG>gaT p.E650D PRAD 17 7367125 7367125 + Silent SNP C C T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr17:7367125C>T c.1176G>A c.(1174-1176)ccG>ccA p.P392P READ 17 7366544 7366544 + Missense_Mutation SNP G G C TCGA-AG-4005-01A-01W-1073-09 TCGA-AG-4005-10A-01W-1073-09 g.chr17:7366544G>C c.1757C>G c.(1756-1758)aCa>aGa p.T586R SARC 17 7366451 7366451 + Missense_Mutation SNP C C T TCGA-MB-A8JL-01A-11D-A36J-09 TCGA-MB-A8JL-10A-01D-A36M-09 g.chr17:7366451C>T c.1850G>A c.(1849-1851)cGc>cAc p.R617H SKCM 17 7365299 7365299 + Missense_Mutation SNP C C T TCGA-ER-A3PL-06A-11D-A23B-08 TCGA-ER-A3PL-10A-01D-A23B-08 g.chr17:7365299C>T c.3002G>A c.(3001-3003)aGg>aAg p.R1001K SKCM 17 7365321 7365321 + Missense_Mutation SNP G G A TCGA-EE-A2MS-06A-11D-A197-08 TCGA-EE-A2MS-10A-01D-A199-08 g.chr17:7365321G>A c.2980C>T c.(2980-2982)Ccc>Tcc p.P994S SKCM 17 7365360 7365360 + Missense_Mutation SNP G G A TCGA-EE-A2GP-06A-11D-A197-08 TCGA-EE-A2GP-10A-01D-A199-08 g.chr17:7365360G>A c.2941C>T c.(2941-2943)Cca>Tca p.P981S SKCM 17 7365457 7365457 + Silent SNP G G A TCGA-D3-A3MU-06A-11D-A21A-08 TCGA-D3-A3MU-10A-01D-A21A-08 g.chr17:7365457G>A c.2844C>T c.(2842-2844)ctC>ctT p.L948L SKCM 17 7365775 7365775 + Silent SNP G G A TCGA-EE-A2GR-06A-11D-A197-08 TCGA-EE-A2GR-10A-01D-A199-08 g.chr17:7365775G>A c.2526C>T c.(2524-2526)tcC>tcT p.S842S SKCM 17 7365776 7365776 + Missense_Mutation SNP G G A TCGA-EE-A2GR-06A-11D-A197-08 TCGA-EE-A2GR-10A-01D-A199-08 g.chr17:7365776G>A c.2525C>T c.(2524-2526)tCc>tTc p.S842F SKCM 17 7365821 7365821 + Missense_Mutation SNP G G A TCGA-FS-A1ZZ-06A-11D-A197-08 TCGA-FS-A1ZZ-10A-01D-A199-08 g.chr17:7365821G>A c.2480C>T c.(2479-2481)tCc>tTc p.S827F SKCM 17 7365848 7365848 + Missense_Mutation SNP G G T TCGA-D3-A3MR-06A-11D-A21A-08 TCGA-D3-A3MR-10A-01D-A21A-08 g.chr17:7365848G>T c.2453C>A c.(2452-2454)gCc>gAc p.A818D SKCM 17 7365869 7365869 + Missense_Mutation SNP G G A TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr17:7365869G>A c.2432C>T c.(2431-2433)cCc>cTc p.P811L SKCM 17 7366011 7366011 + Missense_Mutation SNP G G A TCGA-EE-A2GD-06A-11D-A196-08 TCGA-EE-A2GD-10A-01D-A198-08 g.chr17:7366011G>A c.2290C>T c.(2290-2292)Cgc>Tgc p.R764C SKCM 17 7366122 7366122 + Nonsense_Mutation SNP G G A TCGA-EE-A3AD-06A-11D-A196-08 TCGA-EE-A3AD-10A-01D-A198-08 g.chr17:7366122G>A c.2179C>T c.(2179-2181)Cga>Tga p.R727* SKCM 17 7366123 7366123 + Silent SNP G G A TCGA-EE-A3AD-06A-11D-A196-08 TCGA-EE-A3AD-10A-01D-A198-08 g.chr17:7366123G>A c.2178C>T c.(2176-2178)caC>caT p.H726H SKCM 17 7366262 7366262 + Missense_Mutation SNP C C T TCGA-FS-A4F9-06A-11D-A24R-08 TCGA-FS-A4F9-10A-01D-A24R-08 g.chr17:7366262C>T c.2039G>A c.(2038-2040)gGa>gAa p.G680E SKCM 17 7366368 7366368 + Missense_Mutation SNP C C T TCGA-EE-A20F-06A-21D-A196-08 TCGA-EE-A20F-10A-01D-A198-08 g.chr17:7366368C>T c.1933G>A c.(1933-1935)Gaa>Aaa p.E645K SKCM 17 7366608 7366608 + Missense_Mutation SNP C C T TCGA-D3-A2J8-06A-11D-A196-08 TCGA-D3-A2J8-10A-01D-A198-08 g.chr17:7366608C>T c.1693G>A c.(1693-1695)Gga>Aga p.G565R SKCM 17 7366631 7366631 + Missense_Mutation SNP G G A TCGA-EE-A29E-06A-11D-A197-08 TCGA-EE-A29E-10A-01D-A199-08 g.chr17:7366631G>A c.1670C>T c.(1669-1671)gCc>gTc p.A557V SKCM 17 7366747 7366747 + Silent SNP C C T TCGA-D3-A2JP-06A-11D-A19A-08 TCGA-D3-A2JP-10A-01D-A19A-08 g.chr17:7366747C>T c.1554G>A c.(1552-1554)aaG>aaA p.K518K SKCM 17 7369559 7369559 + Missense_Mutation SNP G G A TCGA-D3-A2J7-06A-11D-A196-08 TCGA-D3-A2J7-10A-01D-A198-08 g.chr17:7369559G>A c.562C>T c.(562-564)Cct>Tct p.P188S SKCM 17 7369619 7369619 + Missense_Mutation SNP G G A TCGA-EE-A2GI-06A-11D-A196-08 TCGA-EE-A2GI-10A-01D-A198-08 g.chr17:7369619G>A c.502C>T c.(502-504)Cgc>Tgc p.R168C SKCM 17 7369840 7369840 + Missense_Mutation SNP G G A TCGA-EE-A29B-06A-11D-A197-08 TCGA-EE-A29B-10A-01D-A199-08 g.chr17:7369840G>A c.281C>T c.(280-282)tCt>tTt p.S94F

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation ALL-US 17 7370028 7370028 single base substitution G A synonymous_variant D31D 93C>T BLCA-CN 17 7358654 7358654 single base substitution G A downstream_gene_variant BLCA-CN 17 7369112 7369112 single base substitution A C missense_variant Y337D 1009T>G BLCA-CN 17 7369360 7369360 single base substitution G A missense_variant A254V 761C>T BLCA-CN 17 7385848 7385848 single base substitution A T intron_variant BLCA-CN 17 7385848 7385848 single base substitution A T upstream_gene_variant BLCA-US 17 7365511 7365511 single base substitution G T synonymous_variant L930L 2790C>A BLCA-US 17 7369149 7369149 single base substitution C G synonymous_variant L324L 972G>C BOCA-FR 17 7386217 7386217 single base substitution T C intron_variant BOCA-FR 17 7386217 7386217 single base substitution T C upstream_gene_variant BRCA-EU 17 7359976 7359976 single base substitution C T downstream_gene_variant BRCA-EU 17 7360744 7360744 deletion of <=200bp A - downstream_gene_variant BRCA-EU 17 7360927 7360927 single base substitution T C downstream_gene_variant BRCA-EU 17 7361214 7361214 single base substitution C T downstream_gene_variant BRCA-EU 17 7361274 7361274 single base substitution G C downstream_gene_variant BRCA-EU 17 7361829 7361829 insertion of <=200bp - G downstream_gene_variant BRCA-EU 17 7363081 7363081 single base substitution G C 3_prime_UTR_variant BRCA-EU 17 7363911 7363911 single base substitution C T 3_prime_UTR_variant BRCA-EU 17 7364438 7364438 single base substitution G T 3_prime_UTR_variant BRCA-EU 17 7364774 7364774 single base substitution C T 3_prime_UTR_variant BRCA-EU 17 7364941 7364941 single base substitution G T 3_prime_UTR_variant BRCA-EU 17 7365318 7365318 single base substitution G T missense_variant P995T 2983C>A BRCA-EU 17 7365664 7365664 single base substitution C G missense_variant L879F 2637G>C BRCA-EU 17 7365849 7365849 single base substitution C A missense_variant A818S 2452G>T BRCA-EU 17 7366044 7366044 single base substitution G T missense_variant H753N 2257C>A BRCA-EU 17 7368307 7368307 single base substitution C G intron_variant BRCA-EU 17 7368443 7368443 single base substitution C G intron_variant BRCA-EU 17 7368751 7368751 single base substitution C G intron_variant BRCA-EU 17 7368884 7368884 single base substitution C T intron_variant BRCA-EU 17 7369466 7369466 single base substitution C T missense_variant E219K 655G>A BRCA-EU 17 7369523 7369523 single base substitution C G missense_variant E200Q 598G>C BRCA-EU 17 7369891 7369891 single base substitution T C missense_variant N77S 230A>G BRCA-EU 17 7371058 7371058 single base substitution C T intron_variant BRCA-EU 17 7371318 7371318 single base substitution T G intron_variant BRCA-EU 17 7371510 7371510 single base substitution T A intron_variant BRCA-EU 17 7371879 7371879 single base substitution A G intron_variant BRCA-EU 17 7373444 7373444 single base substitution C T intron_variant BRCA-EU 17 7373609 7373609 single base substitution C T intron_variant BRCA-EU 17 7374946 7374946 single base substitution A G intron_variant BRCA-EU 17 7375633 7375633 single base substitution C A intron_variant BRCA-EU 17 7378661 7378661 insertion of <=200bp - A intron_variant BRCA-EU 17 7380122 7380122 single base substitution G C intron_variant BRCA-EU 17 7381986 7381986 single base substitution T A intron_variant BRCA-EU 17 7383687 7383687 single base substitution G A intron_variant BRCA-EU 17 7383687 7383687 single base substitution G A upstream_gene_variant BRCA-EU 17 7384929 7384942 deletion of <=200bp AGATACCCACAAAT - intron_variant BRCA-EU 17 7384929 7384942 deletion of <=200bp AGATACCCACAAAT - upstream_gene_variant BRCA-EU 17 7384985 7384985 single base substitution C T intron_variant BRCA-EU 17 7384985 7384985 single base substitution C T upstream_gene_variant BRCA-EU 17 7385201 7385201 single base substitution C A intron_variant BRCA-EU 17 7385201 7385201 single base substitution C A upstream_gene_variant BRCA-EU 17 7386758 7386758 deletion of <=200bp C - intron_variant BRCA-EU 17 7386758 7386758 deletion of <=200bp C - upstream_gene_variant BRCA-EU 17 7386895 7386895 single base substitution C A intron_variant BRCA-EU 17 7386895 7386895 single base substitution C A upstream_gene_variant BRCA-EU 17 7387455 7387455 single base substitution C A 5_prime_UTR_variant BRCA-EU 17 7387455 7387455 single base substitution C A upstream_gene_variant BRCA-EU 17 7387645 7387645 single base substitution G C upstream_gene_variant BRCA-EU 17 7388263 7388263 single base substitution G A upstream_gene_variant BRCA-EU 17 7391326 7391326 single base substitution A G upstream_gene_variant BRCA-EU 17 7391526 7391526 single base substitution A T upstream_gene_variant BRCA-EU 17 7392416 7392416 single base substitution C G upstream_gene_variant BRCA-EU 17 7392468 7392489 deletion of <=200bp AGTTGAATAAACAAGTGAATGA - upstream_gene_variant BRCA-FR 17 7363081 7363081 single base substitution G C 3_prime_UTR_variant BRCA-FR 17 7364941 7364941 single base substitution G T 3_prime_UTR_variant BRCA-FR 17 7365849 7365849 single base substitution C A missense_variant A818S 2452G>T BRCA-FR 17 7369466 7369466 single base substitution C T missense_variant E219K 655G>A BRCA-FR 17 7369523 7369523 single base substitution C G missense_variant E200Q 598G>C BRCA-FR 17 7369891 7369891 single base substitution T C missense_variant N77S 230A>G BRCA-FR 17 7384985 7384985 single base substitution C T intron_variant BRCA-FR 17 7384985 7384985 single base substitution C T upstream_gene_variant BRCA-FR 17 7388072 7388072 single base substitution C G upstream_gene_variant BRCA-UK 17 7365664 7365664 single base substitution C G missense_variant L879F 2637G>C BRCA-UK 17 7369270 7369270 single base substitution G A missense_variant S284L 851C>T BRCA-UK 17 7371593 7371593 single base substitution G A intron_variant BRCA-UK 17 7387849 7387849 single base substitution C T upstream_gene_variant BRCA-US 17 7358701 7358701 single base substitution T G downstream_gene_variant BRCA-US 17 7359155 7359155 single base substitution C A downstream_gene_variant BRCA-US 17 7366057 7366057 single base substitution G A synonymous_variant H748H 2244C>T BRCA-US 17 7366443 7366443 single base substitution C A stop_gained E620* 1858G>T BRCA-US 17 7366623 7366623 single base substitution G A missense_variant R560W 1678C>T BRCA-US 17 7369111 7369111 single base substitution T A missense_variant Y337F 1010A>T BRCA-US 17 7370012 7370012 single base substitution C T missense_variant G37R 109G>A BRCA-US 17 7370109 7370109 insertion of <=200bp - G frameshift_variant P4P? BRCA-US 17 7370110 7370110 deletion of <=200bp G - frameshift_variant P4 BRCA-US 17 7385307 7385307 single base substitution G A intron_variant BRCA-US 17 7385307 7385307 single base substitution G A upstream_gene_variant BRCA-US 17 7386136 7386136 single base substitution A C intron_variant BRCA-US 17 7386136 7386136 single base substitution A C upstream_gene_variant BRCA-US 17 7386279 7386279 single base substitution T C intron_variant BRCA-US 17 7386279 7386279 single base substitution T C upstream_gene_variant BRCA-US 17 7388097 7388097 insertion of <=200bp - C upstream_gene_variant BTCA-JP 17 7359265 7359265 single base substitution G A downstream_gene_variant BTCA-JP 17 7359930 7359930 single base substitution T C downstream_gene_variant BTCA-JP 17 7360004 7360004 single base substitution G A downstream_gene_variant BTCA-JP 17 7365942 7365942 single base substitution G C missense_variant H787D 2359C>G BTCA-JP 17 7370110 7370110 deletion of <=200bp G - frameshift_variant P4 BTCA-JP 17 7370110 7370110 insertion of <=200bp - G frameshift_variant P4P? BTCA-JP 17 7384843 7384843 single base substitution G A intron_variant BTCA-JP 17 7384843 7384843 single base substitution G A upstream_gene_variant CESC-US 17 7357837 7357837 single base substitution C T downstream_gene_variant CESC-US 17 7365529 7365529 single base substitution G A synonymous_variant L924L 2772C>T CESC-US 17 7365772 7365772 single base substitution C A missense_variant E843D 2529G>T CESC-US 17 7365840 7365840 single base substitution C G missense_variant E821Q 2461G>C CESC-US 17 7366072 7366072 single base substitution C T synonymous_variant K743K 2229G>A CESC-US 17 7366075 7366075 single base substitution C A synonymous_variant R742R 2226G>T CESC-US 17 7369795 7369795 single base substitution G C missense_variant S109C 326C>G CESC-US 17 7386113 7386113 single base substitution G A intron_variant CESC-US 17 7386113 7386113 single base substitution G A upstream_gene_variant CESC-US 17 7388154 7388154 single base substitution G C upstream_gene_variant CLLE-ES 17 7363470 7363470 single base substitution C A 3_prime_UTR_variant CLLE-ES 17 7371701 7371701 single base substitution A C intron_variant COAD-US 17 7357816 7357816 insertion of <=200bp - T downstream_gene_variant COAD-US 17 7359178 7359178 single base substitution C T downstream_gene_variant COAD-US 17 7365474 7365474 single base substitution C T missense_variant A943T 2827G>A COAD-US 17 7366116 7366116 single base substitution C T missense_variant G729R 2185G>A COAD-US 17 7366281 7366281 single base substitution G A missense_variant R674C 2020C>T COAD-US 17 7366619 7366619 single base substitution T C missense_variant N561S 1682A>G COAD-US 17 7366908 7366908 single base substitution G A missense_variant P465S 1393C>T COAD-US 17 7366996 7366996 single base substitution C T synonymous_variant P435P 1305G>A COAD-US 17 7367081 7367081 single base substitution G T missense_variant P407H 1220C>A COAD-US 17 7369494 7369494 single base substitution T G synonymous_variant P209P 627A>C COAD-US 17 7369601 7369601 single base substitution G A missense_variant R174C 520C>T COAD-US 17 7369827 7369827 single base substitution G T synonymous_variant S98S 294C>A COAD-US 17 7370110 7370110 deletion of <=200bp G - frameshift_variant P4 COAD-US 17 7385571 7385571 single base substitution C T intron_variant COAD-US 17 7385571 7385571 single base substitution C T upstream_gene_variant COAD-US 17 7386090 7386090 single base substitution G A intron_variant COAD-US 17 7386090 7386090 single base substitution G A upstream_gene_variant COAD-US 17 7386167 7386167 single base substitution C T intron_variant COAD-US 17 7386167 7386167 single base substitution C T upstream_gene_variant COAD-US 17 7386237 7386237 single base substitution G T intron_variant COAD-US 17 7386237 7386237 single base substitution G T upstream_gene_variant COCA-CN 17 7357750 7357750 single base substitution G A downstream_gene_variant COCA-CN 17 7359342 7359342 single base substitution G T downstream_gene_variant COCA-CN 17 7359368 7359368 single base substitution C T downstream_gene_variant COCA-CN 17 7365428 7365428 single base substitution G A missense_variant A958V 2873C>T COCA-CN 17 7365925 7365925 single base substitution G A synonymous_variant P792P 2376C>T COCA-CN 17 7366117 7366117 single base substitution G A synonymous_variant C728C 2184C>T COCA-CN 17 7366369 7366369 single base substitution G C missense_variant D644E 1932C>G COCA-CN 17 7366540 7366540 single base substitution C A synonymous_variant G587G 1761G>T COCA-CN 17 7369600 7369600 single base substitution C T missense_variant R174H 521G>A COCA-CN 17 7370027 7370027 single base substitution C T missense_variant V32I 94G>A COCA-CN 17 7385255 7385255 single base substitution G A intron_variant COCA-CN 17 7385255 7385255 single base substitution G A upstream_gene_variant COCA-CN 17 7385774 7385774 single base substitution C T intron_variant COCA-CN 17 7385774 7385774 single base substitution C T upstream_gene_variant ESAD-UK 17 7358306 7358306 single base substitution G C downstream_gene_variant ESAD-UK 17 7358602 7358602 single base substitution G C downstream_gene_variant ESAD-UK 17 7358658 7358658 single base substitution G A downstream_gene_variant ESAD-UK 17 7358974 7358974 single base substitution G C downstream_gene_variant ESAD-UK 17 7359200 7359200 single base substitution G C downstream_gene_variant ESAD-UK 17 7359279 7359279 single base substitution G C downstream_gene_variant ESAD-UK 17 7359511 7359511 single base substitution G T downstream_gene_variant ESAD-UK 17 7359687 7359687 single base substitution G C downstream_gene_variant ESAD-UK 17 7361536 7361536 single base substitution C T downstream_gene_variant ESAD-UK 17 7362485 7362485 single base substitution A T downstream_gene_variant ESAD-UK 17 7363104 7363104 deletion of <=200bp T - 3_prime_UTR_variant ESAD-UK 17 7363126 7363126 single base substitution A C 3_prime_UTR_variant ESAD-UK 17 7364226 7364226 single base substitution A C 3_prime_UTR_variant ESAD-UK 17 7370130 7370130 single base substitution C G splice_acceptor_variant ESAD-UK 17 7372571 7372571 single base substitution C T intron_variant ESAD-UK 17 7374510 7374510 single base substitution T A intron_variant ESAD-UK 17 7376359 7376359 single base substitution C A intron_variant ESAD-UK 17 7376394 7376394 single base substitution C T intron_variant ESAD-UK 17 7376877 7376877 single base substitution T C intron_variant ESAD-UK 17 7377784 7377784 single base substitution G A intron_variant ESAD-UK 17 7384043 7384043 single base substitution A C intron_variant ESAD-UK 17 7384043 7384043 single base substitution A C upstream_gene_variant ESAD-UK 17 7384607 7384607 single base substitution C T intron_variant ESAD-UK 17 7384607 7384607 single base substitution C T upstream_gene_variant ESAD-UK 17 7386589 7386589 single base substitution G A intron_variant ESAD-UK 17 7386589 7386589 single base substitution G A upstream_gene_variant ESAD-UK 17 7389274 7389274 single base substitution C G upstream_gene_variant ESAD-UK 17 7389288 7389288 single base substitution C T upstream_gene_variant ESAD-UK 17 7389832 7389832 deletion of <=200bp A - upstream_gene_variant ESAD-UK 17 7390385 7390385 single base substitution G A upstream_gene_variant ESCA-CN 17 7364458 7364458 single base substitution A G 3_prime_UTR_variant ESCA-CN 17 7366420 7366420 single base substitution C T synonymous_variant E627E 1881G>A ESCA-CN 17 7367059 7367059 single base substitution G C synonymous_variant L414L 1242C>G ESCA-CN 17 7388106 7388106 single base substitution C T upstream_gene_variant KIRC-US 17 7369782 7369782 single base substitution A G synonymous_variant P113P 339T>C KIRC-US 17 7385621 7385621 single base substitution C T intron_variant KIRC-US 17 7385621 7385621 single base substitution C T upstream_gene_variant KIRC-US 17 7385682 7385682 single base substitution G A intron_variant KIRC-US 17 7385682 7385682 single base substitution G A upstream_gene_variant KIRP-US 17 7357711 7357711 single base substitution C G downstream_gene_variant KIRP-US 17 7385463 7385463 single base substitution G A intron_variant KIRP-US 17 7385463 7385463 single base substitution G A upstream_gene_variant KIRP-US 17 7386013 7386013 single base substitution G C intron_variant KIRP-US 17 7386013 7386013 single base substitution G C upstream_gene_variant KIRP-US 17 7386125 7386125 single base substitution C T intron_variant KIRP-US 17 7386125 7386125 single base substitution C T upstream_gene_variant LAML-CN 17 7366454 7366454 single base substitution C T missense_variant R616H 1847G>A LAML-KR 17 7385454 7385454 single base substitution G A intron_variant LAML-KR 17 7385454 7385454 single base substitution G A upstream_gene_variant LAML-KR 17 7386114 7386114 single base substitution A G intron_variant LAML-KR 17 7386114 7386114 single base substitution A G upstream_gene_variant LAML-KR 17 7386217 7386217 single base substitution T C intron_variant LAML-KR 17 7386217 7386217 single base substitution T C upstream_gene_variant LAML-KR 17 7386234 7386234 single base substitution G A intron_variant LAML-KR 17 7386234 7386234 single base substitution G A upstream_gene_variant LGG-US 17 7385399 7385399 single base substitution G A intron_variant LGG-US 17 7385399 7385399 single base substitution G A upstream_gene_variant LGG-US 17 7385920 7385920 single base substitution G A intron_variant LGG-US 17 7385920 7385920 single base substitution G A upstream_gene_variant LIAD-FR 17 7366619 7366619 single base substitution T C missense_variant N561S 1682A>G LICA-CN 17 7369934 7369934 single base substitution C T missense_variant A63T 187G>A LICA-FR 17 7365648 7365648 single base substitution C A stop_gained E885* 2653G>T LICA-FR 17 7372817 7372817 single base substitution C T intron_variant LICA-FR 17 7375953 7375953 single base substitution C T intron_variant LICA-FR 17 7377727 7377727 single base substitution A G intron_variant LICA-FR 17 7385571 7385571 single base substitution C T intron_variant LICA-FR 17 7385571 7385571 single base substitution C T upstream_gene_variant LICA-FR 17 7385761 7385761 single base substitution G T intron_variant LICA-FR 17 7385761 7385761 single base substitution G T upstream_gene_variant LICA-FR 17 7386217 7386217 single base substitution T C intron_variant LICA-FR 17 7386217 7386217 single base substitution T C upstream_gene_variant LICA-FR 17 7387299 7387299 insertion of <=200bp - CCCGC intron_variant LICA-FR 17 7387299 7387299 insertion of <=200bp - CCCGC upstream_gene_variant LICA-FR 17 7388135 7388135 single base substitution A G upstream_gene_variant LIHC-US 17 7369945 7369945 single base substitution A G missense_variant L59P 176T>C LIHC-US 17 7370078 7370078 single base substitution C T missense_variant A15T 43G>A LINC-JP 17 7359368 7359368 single base substitution C T downstream_gene_variant LINC-JP 17 7360118 7360118 single base substitution T C downstream_gene_variant LINC-JP 17 7360131 7360131 single base substitution T C downstream_gene_variant LINC-JP 17 7365742 7365742 single base substitution T A synonymous_variant S853S 2559A>T LINC-JP 17 7367084 7367084 single base substitution T A missense_variant K406M 1217A>T LINC-JP 17 7369667 7369667 single base substitution C A missense_variant G152C 454G>T LINC-JP 17 7369902 7369902 single base substitution G A synonymous_variant G73G 219C>T LINC-JP 17 7386234 7386234 single base substitution G A intron_variant LINC-JP 17 7386234 7386234 single base substitution G A upstream_gene_variant LIRI-JP 17 7357916 7357916 single base substitution G T downstream_gene_variant LIRI-JP 17 7360333 7360333 single base substitution A G downstream_gene_variant LIRI-JP 17 7360346 7360346 single base substitution A G downstream_gene_variant LIRI-JP 17 7363422 7363422 single base substitution T G 3_prime_UTR_variant LIRI-JP 17 7369620 7369620 deletion of <=200bp C - frameshift_variant G167 LIRI-JP 17 7371566 7371566 single base substitution C T intron_variant LIRI-JP 17 7372014 7372014 single base substitution C T intron_variant LIRI-JP 17 7374940 7374940 single base substitution C A intron_variant LIRI-JP 17 7378590 7378590 single base substitution G C intron_variant LIRI-JP 17 7379868 7379868 single base substitution G A intron_variant LIRI-JP 17 7386217 7386217 single base substitution T C intron_variant LIRI-JP 17 7386217 7386217 single base substitution T C upstream_gene_variant LIRI-JP 17 7392390 7392390 single base substitution G A upstream_gene_variant LUSC-KR 17 7359351 7359351 single base substitution G T downstream_gene_variant LUSC-KR 17 7361365 7361365 single base substitution C A downstream_gene_variant LUSC-KR 17 7367170 7367170 single base substitution G T stop_gained Y377* 1131C>A LUSC-KR 17 7371696 7371696 single base substitution A G intron_variant LUSC-KR 17 7376267 7376267 single base substitution T A intron_variant LUSC-KR 17 7386217 7386217 single base substitution T C intron_variant LUSC-KR 17 7386217 7386217 single base substitution T C upstream_gene_variant LUSC-US 17 7359243 7359243 single base substitution C A downstream_gene_variant LUSC-US 17 7365286 7365286 single base substitution C T synonymous_variant E1005E 3015G>A LUSC-US 17 7365586 7365586 single base substitution G T missense_variant D905E 2715C>A LUSC-US 17 7365801 7365801 single base substitution C A missense_variant G834W 2500G>T LUSC-US 17 7367112 7367112 single base substitution T A missense_variant S397C 1189A>T LUSC-US 17 7367123 7367123 single base substitution C A missense_variant G393V 1178G>T LUSC-US 17 7385380 7385380 single base substitution G A intron_variant LUSC-US 17 7385380 7385380 single base substitution G A upstream_gene_variant LUSC-US 17 7386172 7386172 single base substitution T C intron_variant LUSC-US 17 7386172 7386172 single base substitution T C upstream_gene_variant LUSC-US 17 7386197 7386197 single base substitution T C intron_variant LUSC-US 17 7386197 7386197 single base substitution T C upstream_gene_variant MALY-DE 17 7361053 7361053 single base substitution A G downstream_gene_variant MALY-DE 17 7366783 7366783 single base substitution C T synonymous_variant S506S 1518G>A MALY-DE 17 7372036 7372036 single base substitution G A intron_variant MALY-DE 17 7381395 7381395 single base substitution C G intron_variant MALY-DE 17 7383431 7383431 single base substitution G A intron_variant MALY-DE 17 7383431 7383431 single base substitution G A upstream_gene_variant MALY-DE 17 7388085 7388085 single base substitution T C upstream_gene_variant MELA-AU 17 7357853 7357854 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 17 7357874 7357874 single base substitution C T downstream_gene_variant MELA-AU 17 7358225 7358225 single base substitution G A downstream_gene_variant MELA-AU 17 7358364 7358364 single base substitution C T downstream_gene_variant MELA-AU 17 7358548 7358548 single base substitution C T downstream_gene_variant MELA-AU 17 7358860 7358860 single base substitution C T downstream_gene_variant MELA-AU 17 7360067 7360067 single base substitution C T downstream_gene_variant MELA-AU 17 7361214 7361214 single base substitution C T downstream_gene_variant MELA-AU 17 7361280 7361280 single base substitution G A downstream_gene_variant MELA-AU 17 7361358 7361358 single base substitution C T downstream_gene_variant MELA-AU 17 7361482 7361482 single base substitution G A downstream_gene_variant MELA-AU 17 7362582 7362582 single base substitution G A downstream_gene_variant MELA-AU 17 7363521 7363521 single base substitution G A 3_prime_UTR_variant MELA-AU 17 7363840 7363840 single base substitution C G 3_prime_UTR_variant MELA-AU 17 7364084 7364084 single base substitution G A 3_prime_UTR_variant MELA-AU 17 7364225 7364225 single base substitution G A 3_prime_UTR_variant MELA-AU 17 7366302 7366302 single base substitution A G missense_variant Y667H 1999T>C MELA-AU 17 7366475 7366475 single base substitution C T missense_variant G609E 1826G>A MELA-AU 17 7366511 7366511 single base substitution G A missense_variant A597V 1790C>T MELA-AU 17 7366923 7366923 single base substitution G A missense_variant P460S 1378C>T MELA-AU 17 7367492 7367492 single base substitution G A intron_variant MELA-AU 17 7368458 7368458 single base substitution G A intron_variant MELA-AU 17 7369837 7369837 single base substitution G A missense_variant S95F 284C>T MELA-AU 17 7370383 7370383 single base substitution G A intron_variant MELA-AU 17 7370660 7370660 single base substitution G A intron_variant MELA-AU 17 7370723 7370723 single base substitution G A intron_variant MELA-AU 17 7370736 7370736 single base substitution G A intron_variant MELA-AU 17 7371600 7371600 single base substitution G A intron_variant MELA-AU 17 7371676 7371676 single base substitution G A intron_variant MELA-AU 17 7371980 7371980 single base substitution C T intron_variant MELA-AU 17 7372201 7372201 single base substitution A G intron_variant MELA-AU 17 7372303 7372303 single base substitution C T intron_variant MELA-AU 17 7372903 7372903 single base substitution G A intron_variant MELA-AU 17 7374959 7374959 single base substitution G A intron_variant MELA-AU 17 7375046 7375046 single base substitution G A intron_variant MELA-AU 17 7375772 7375772 single base substitution G A intron_variant MELA-AU 17 7376655 7376655 single base substitution C A intron_variant MELA-AU 17 7377846 7377846 single base substitution G A intron_variant MELA-AU 17 7379082 7379082 single base substitution G A intron_variant MELA-AU 17 7379356 7379356 single base substitution C A intron_variant MELA-AU 17 7380269 7380269 single base substitution G A intron_variant MELA-AU 17 7385024 7385024 single base substitution C T intron_variant MELA-AU 17 7385024 7385024 single base substitution C T upstream_gene_variant MELA-AU 17 7386182 7386182 single base substitution C T intron_variant MELA-AU 17 7386182 7386182 single base substitution C T upstream_gene_variant MELA-AU 17 7386217 7386217 single base substitution T C intron_variant MELA-AU 17 7386217 7386217 single base substitution T C upstream_gene_variant MELA-AU 17 7386333 7386333 single base substitution G A intron_variant MELA-AU 17 7386333 7386333 single base substitution G A upstream_gene_variant MELA-AU 17 7387066 7387066 single base substitution C A intron_variant MELA-AU 17 7387066 7387066 single base substitution C A upstream_gene_variant MELA-AU 17 7387299 7387299 insertion of <=200bp - CCCGC intron_variant MELA-AU 17 7387299 7387299 insertion of <=200bp - CCCGC upstream_gene_variant MELA-AU 17 7387616 7387616 single base substitution G A upstream_gene_variant MELA-AU 17 7387623 7387623 single base substitution G A upstream_gene_variant MELA-AU 17 7387640 7387640 single base substitution G A upstream_gene_variant MELA-AU 17 7387974 7387974 single base substitution C T upstream_gene_variant MELA-AU 17 7389026 7389026 single base substitution C T upstream_gene_variant MELA-AU 17 7389635 7389635 single base substitution T C upstream_gene_variant MELA-AU 17 7390201 7390201 single base substitution A T upstream_gene_variant MELA-AU 17 7390497 7390497 single base substitution C T upstream_gene_variant MELA-AU 17 7390833 7390833 single base substitution C T upstream_gene_variant MELA-AU 17 7391050 7391050 single base substitution C T upstream_gene_variant MELA-AU 17 7391133 7391133 single base substitution C T upstream_gene_variant MELA-AU 17 7391212 7391212 single base substitution C T upstream_gene_variant MELA-AU 17 7391856 7391856 single base substitution T C upstream_gene_variant MELA-AU 17 7392297 7392297 single base substitution C T upstream_gene_variant MELA-AU 17 7392408 7392408 single base substitution T C upstream_gene_variant ORCA-IN 17 7363442 7363442 single base substitution G C 3_prime_UTR_variant ORCA-IN 17 7369541 7369541 single base substitution C T missense_variant A194T 580G>A ORCA-IN 17 7386217 7386217 single base substitution T C intron_variant ORCA-IN 17 7386217 7386217 single base substitution T C upstream_gene_variant OV-AU 17 7360077 7360077 single base substitution T C downstream_gene_variant OV-AU 17 7360265 7360265 single base substitution C G downstream_gene_variant OV-AU 17 7360439 7360439 single base substitution C T downstream_gene_variant OV-AU 17 7361305 7361305 single base substitution T C downstream_gene_variant OV-AU 17 7369056 7369056 single base substitution A G synonymous_variant H355H 1065T>C OV-AU 17 7369613 7369613 single base substitution G C missense_variant L170V 508C>G OV-AU 17 7369882 7369882 single base substitution G A missense_variant T80I 239C>T OV-AU 17 7374429 7374429 single base substitution C T intron_variant OV-AU 17 7377633 7377633 single base substitution C G intron_variant OV-AU 17 7379656 7379656 single base substitution T A intron_variant OV-AU 17 7380621 7380621 single base substitution T C intron_variant OV-AU 17 7383704 7383704 single base substitution T G intron_variant OV-AU 17 7383704 7383704 single base substitution T G upstream_gene_variant PACA-AU 17 7365074 7365074 single base substitution C T 3_prime_UTR_variant PACA-AU 17 7365532 7365532 single base substitution C T synonymous_variant P923P 2769G>A PACA-AU 17 7369637 7369637 single base substitution C G missense_variant E162Q 484G>C PACA-AU 17 7373615 7373615 single base substitution G A intron_variant PACA-AU 17 7382569 7382569 deletion of <=200bp C - intron_variant PACA-CA 17 7359063 7359063 single base substitution C A downstream_gene_variant PACA-CA 17 7362658 7362658 single base substitution C T downstream_gene_variant PACA-CA 17 7364479 7364479 single base substitution T A 3_prime_UTR_variant PACA-CA 17 7369628 7369628 single base substitution C G missense_variant A165P 493G>C PACA-CA 17 7380329 7380329 single base substitution C A intron_variant PACA-CA 17 7383632 7383632 insertion of <=200bp - A intron_variant PACA-CA 17 7383632 7383632 insertion of <=200bp - A upstream_gene_variant PACA-CA 17 7383996 7383996 single base substitution G A intron_variant PACA-CA 17 7383996 7383996 single base substitution G A upstream_gene_variant PACA-CA 17 7387728 7387728 single base substitution G T upstream_gene_variant PACA-CA 17 7387729 7387729 single base substitution G T upstream_gene_variant PACA-CA 17 7390197 7390197 deletion of <=200bp A - upstream_gene_variant PAEN-AU 17 7370987 7370987 single base substitution G C intron_variant PAEN-AU 17 7377884 7377884 single base substitution G A intron_variant PAEN-AU 17 7384775 7384775 single base substitution C G intron_variant PAEN-AU 17 7384775 7384775 single base substitution C G upstream_gene_variant PAEN-AU 17 7386705 7386705 single base substitution G C intron_variant PAEN-AU 17 7386705 7386705 single base substitution G C upstream_gene_variant PBCA-DE 17 7371853 7371853 single base substitution C A intron_variant PBCA-DE 17 7375104 7375104 single base substitution T A intron_variant PBCA-DE 17 7383475 7383475 deletion of <=200bp G - intron_variant PBCA-DE 17 7383475 7383475 deletion of <=200bp G - upstream_gene_variant PBCA-DE 17 7386934 7386936 deletion of <=200bp GGA - intron_variant PBCA-DE 17 7386934 7386936 deletion of <=200bp GGA - upstream_gene_variant PBCA-DE 17 7387504 7387504 single base substitution T A 5_prime_UTR_variant PBCA-DE 17 7387504 7387504 single base substitution T A upstream_gene_variant PRAD-CA 17 7392233 7392233 single base substitution A G upstream_gene_variant PRAD-UK 17 7358413 7358413 single base substitution C T downstream_gene_variant PRAD-UK 17 7358571 7358571 single base substitution G T downstream_gene_variant PRAD-UK 17 7383883 7383883 insertion of <=200bp - A intron_variant PRAD-UK 17 7383883 7383883 insertion of <=200bp - A upstream_gene_variant PRAD-UK 17 7386759 7386759 single base substitution C A intron_variant PRAD-UK 17 7386759 7386759 single base substitution C A upstream_gene_variant PRAD-UK 17 7387694 7387694 single base substitution C T upstream_gene_variant PRAD-US 17 7366047 7366047 single base substitution A C missense_variant S752A 2254T>G PRAD-US 17 7366351 7366351 single base substitution C A missense_variant E650D 1950G>T READ-US 17 7385827 7385840 deletion of <=200bp CTGGACTCTGGACA - intron_variant READ-US 17 7385827 7385840 deletion of <=200bp CTGGACTCTGGACA - upstream_gene_variant RECA-CN 17 7358628 7358628 single base substitution A G downstream_gene_variant RECA-EU 17 7363076 7363076 single base substitution T A 3_prime_UTR_variant SKCA-BR 17 7357824 7357824 single base substitution C T downstream_gene_variant SKCA-BR 17 7358986 7358986 single base substitution A G downstream_gene_variant SKCA-BR 17 7360110 7360110 single base substitution T C downstream_gene_variant SKCA-BR 17 7363181 7363181 single base substitution C T 3_prime_UTR_variant SKCA-BR 17 7365847 7365847 single base substitution G A synonymous_variant A818A 2454C>T SKCA-BR 17 7369111 7369111 single base substitution T G missense_variant Y337S 1010A>C SKCA-BR 17 7373189 7373189 single base substitution T G intron_variant SKCA-BR 17 7376274 7376274 insertion of <=200bp - CT intron_variant SKCA-BR 17 7376429 7376430 deletion of <=200bp AT - intron_variant SKCA-BR 17 7376521 7376521 single base substitution T C intron_variant SKCA-BR 17 7379213 7379213 single base substitution C A intron_variant SKCA-BR 17 7381256 7381256 single base substitution T G intron_variant SKCA-BR 17 7382344 7382344 single base substitution A C intron_variant SKCA-BR 17 7382349 7382349 single base substitution T C intron_variant SKCA-BR 17 7382379 7382379 single base substitution A C intron_variant SKCA-BR 17 7383828 7383828 single base substitution G A intron_variant SKCA-BR 17 7383828 7383828 single base substitution G A upstream_gene_variant SKCA-BR 17 7384831 7384831 single base substitution G A intron_variant SKCA-BR 17 7384831 7384831 single base substitution G A upstream_gene_variant SKCA-BR 17 7387641 7387641 single base substitution A G upstream_gene_variant SKCA-BR 17 7387670 7387670 single base substitution T C upstream_gene_variant SKCA-BR 17 7390707 7390707 single base substitution C T upstream_gene_variant SKCA-BR 17 7391705 7391705 insertion of <=200bp - CA upstream_gene_variant SKCA-BR 17 7391780 7391780 single base substitution G A upstream_gene_variant SKCA-BR 17 7391919 7391919 single base substitution G A upstream_gene_variant SKCA-BR 17 7391920 7391920 single base substitution C T upstream_gene_variant SKCM-US 17 7358731 7358731 single base substitution C T downstream_gene_variant SKCM-US 17 7358761 7358761 single base substitution C T downstream_gene_variant SKCM-US 17 7359208 7359208 single base substitution C T downstream_gene_variant SKCM-US 17 7360037 7360037 single base substitution C T downstream_gene_variant SKCM-US 17 7365299 7365299 single base substitution C T missense_variant R1001K 3002G>A SKCM-US 17 7365321 7365321 single base substitution G A missense_variant P994S 2980C>T SKCM-US 17 7365360 7365360 single base substitution G A missense_variant P981S 2941C>T SKCM-US 17 7365457 7365457 single base substitution G A synonymous_variant L948L 2844C>T SKCM-US 17 7365689 7365689 single base substitution G A missense_variant P871L 2612C>T SKCM-US 17 7365821 7365821 single base substitution G A missense_variant S827F 2480C>T SKCM-US 17 7365848 7365848 single base substitution G T missense_variant A818D 2453C>A SKCM-US 17 7365869 7365869 single base substitution G A missense_variant P811L 2432C>T SKCM-US 17 7366011 7366011 single base substitution G A missense_variant R764C 2290C>T SKCM-US 17 7366262 7366262 single base substitution C T missense_variant G680E 2039G>A SKCM-US 17 7366368 7366368 single base substitution C T missense_variant E645K 1933G>A SKCM-US 17 7366608 7366608 single base substitution C T missense_variant G565R 1693G>A SKCM-US 17 7366631 7366631 single base substitution G A missense_variant A557V 1670C>T SKCM-US 17 7366747 7366747 single base substitution C T synonymous_variant K518K 1554G>A SKCM-US 17 7367126 7367126 single base substitution G T missense_variant P392Q 1175C>A SKCM-US 17 7369506 7369506 single base substitution G A synonymous_variant P205P 615C>T SKCM-US 17 7369559 7369559 single base substitution G A missense_variant P188S 562C>T SKCM-US 17 7369619 7369619 single base substitution G A missense_variant R168C 502C>T SKCM-US 17 7369840 7369840 single base substitution G A missense_variant S94F 281C>T SKCM-US 17 7386012 7386012 single base substitution G A intron_variant SKCM-US 17 7386012 7386012 single base substitution G A upstream_gene_variant STAD-US 17 7357777 7357777 single base substitution G A downstream_gene_variant STAD-US 17 7357799 7357799 single base substitution G A downstream_gene_variant STAD-US 17 7359206 7359208 deletion of <=200bp CTC - downstream_gene_variant STAD-US 17 7365271 7365271 single base substitution G A synonymous_variant G1010G 3030C>T STAD-US 17 7365532 7365532 single base substitution C T synonymous_variant P923P 2769G>A STAD-US 17 7365565 7365565 single base substitution A G synonymous_variant A912A 2736T>C STAD-US 17 7365936 7365936 single base substitution C T missense_variant A789T 2365G>A STAD-US 17 7366256 7366256 single base substitution G A missense_variant A682V 2045C>T STAD-US 17 7366339 7366339 insertion of <=200bp - TCC inframe_insertion E654EG STAD-US 17 7366340 7366340 insertion of <=200bp - TCC disruptive_inframe_insertion E654EE STAD-US 17 7366640 7366640 single base substitution G A missense_variant T554M 1661C>T STAD-US 17 7366997 7366997 single base substitution G A missense_variant P435L 1304C>T STAD-US 17 7369233 7369233 deletion of <=200bp G - frameshift_variant P296 STAD-US 17 7369348 7369348 single base substitution C T missense_variant R258Q 773G>A STAD-US 17 7369455 7369455 single base substitution G A synonymous_variant A222A 666C>T STAD-US 17 7369702 7369702 single base substitution A G missense_variant L140P 419T>C STAD-US 17 7369845 7369845 single base substitution C T synonymous_variant S92S 276G>A STAD-US 17 7369878 7369878 single base substitution G A synonymous_variant T81T 243C>T STAD-US 17 7385573 7385573 single base substitution T C intron_variant STAD-US 17 7385573 7385573 single base substitution T C upstream_gene_variant STAD-US 17 7385797 7385797 single base substitution G T intron_variant STAD-US 17 7385797 7385797 single base substitution G T upstream_gene_variant STAD-US 17 7386029 7386029 single base substitution G A intron_variant STAD-US 17 7386029 7386029 single base substitution G A upstream_gene_variant STAD-US 17 7386191 7386191 single base substitution G A intron_variant STAD-US 17 7386191 7386191 single base substitution G A upstream_gene_variant THCA-SA 17 7357837 7357837 single base substitution C T downstream_gene_variant THCA-SA 17 7358711 7358711 single base substitution C T downstream_gene_variant THCA-SA 17 7366670 7366670 insertion of <=200bp - C frameshift_variant T544T? THCA-SA 17 7386090 7386090 single base substitution G A intron_variant THCA-SA 17 7386090 7386090 single base substitution G A upstream_gene_variant THCA-SA 17 7386234 7386234 single base substitution G A intron_variant THCA-SA 17 7386234 7386234 single base substitution G A upstream_gene_variant THCA-SA 17 7386279 7386279 single base substitution T C intron_variant THCA-SA 17 7386279 7386279 single base substitution T C upstream_gene_variant THCA-SA 17 7386280 7386280 single base substitution G A intron_variant THCA-SA 17 7386280 7386280 single base substitution G A upstream_gene_variant THCA-SA 17 7387357 7387357 single base substitution G A 5_prime_UTR_variant THCA-SA 17 7387357 7387357 single base substitution G A upstream_gene_variant UCEC-US 17 7357776 7357776 single base substitution C T downstream_gene_variant UCEC-US 17 7358672 7358672 single base substitution G C downstream_gene_variant UCEC-US 17 7365389 7365389 single base substitution G A missense_variant A971V 2912C>T UCEC-US 17 7365612 7365612 single base substitution C A missense_variant G897W 2689G>T UCEC-US 17 7365800 7365800 single base substitution C T missense_variant G834E 2501G>A UCEC-US 17 7366113 7366113 single base substitution C A missense_variant D730Y 2188G>T UCEC-US 17 7366166 7366166 single base substitution G A missense_variant A712V 2135C>T UCEC-US 17 7366368 7366368 single base substitution C T missense_variant E645K 1933G>A UCEC-US 17 7366430 7366430 single base substitution C T missense_variant R624H 1871G>A UCEC-US 17 7366586 7366586 single base substitution G A missense_variant A572V 1715C>T UCEC-US 17 7366743 7366743 single base substitution G A stop_gained R520* 1558C>T UCEC-US 17 7366933 7366933 single base substitution C T synonymous_variant P456P 1368G>A UCEC-US 17 7367081 7367081 single base substitution G A missense_variant P407L 1220C>T UCEC-US 17 7369189 7369189 single base substitution C T missense_variant C311Y 932G>A UCEC-US 17 7369289 7369289 single base substitution G T missense_variant P278T 832C>A UCEC-US 17 7385341 7385341 single base substitution C A intron_variant UCEC-US 17 7385341 7385341 single base substitution C A upstream_gene_variant UCEC-US 17 7385529 7385529 single base substitution C T intron_variant UCEC-US 17 7385529 7385529 single base substitution C T upstream_gene_variant UCEC-US 17 7385733 7385733 single base substitution G A intron_variant UCEC-US 17 7385733 7385733 single base substitution G A upstream_gene_variant UCEC-US 17 7385900 7385900 single base substitution A T intron_variant UCEC-US 17 7385900 7385900 single base substitution A T upstream_gene_variant UCEC-US 17 7386013 7386013 single base substitution G A intron_variant UCEC-US 17 7386013 7386013 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 B59-0-Tumor COSM3932734 c.1009T>G p.Y337D Substitution - Missense 17:7465793-7465793 - TCGA-FU-A3HZ-01 COSM1640803 c.2772C>T p.L924L Substitution - coding silent 17:7462210-7462210 - ACINAR01 COSM1582357 c.877C>T p.R293* Substitution - Nonsense 17:7465925-7465925 - T2940 COSM4742161 c.1260G>A p.M420I Substitution - Missense 17:7463722-7463722 - sysucc-679T COSM5480610 c.2376C>T p.P792P Substitution - coding silent 17:7462606-7462606 - TCGA-AX-A0J1-01 COSM984428 c.932G>A p.C311Y Substitution - Missense 17:7465870-7465870 - 35M COSM5583098 c.1940A>G p.E647G Substitution - Missense 17:7463042-7463042 - TCGA-AM-5820-01 COSM3691810 c.627A>C p.P209P Substitution - coding silent 17:7466175-7466175 - 18T COSM106427 c.2585C>T p.A862V Substitution - Missense 17:7462397-7462397 - TCGA-AA-3713-01 COSM3691808 c.2185G>A p.G729R Substitution - Missense 17:7462797-7462797 - BCM257T COSM4951544 c.2653G>T p.E885* Substitution - Nonsense 17:7462329-7462329 - 49M COSM5594017 c.2889C>T p.F963F Substitution - coding silent 17:7462093-7462093 - LUAD-RT-S01810 COSM382817 c.2820C>G p.N940K Substitution - Missense 17:7462162-7462162 - TCGA-AP-A0LM-01 COSM984414 c.1933G>A p.E645K Substitution - Missense 17:7463049-7463049 - TCGA-G4-6321-01 COSM3755856 c.1682A>G p.N561S Substitution - Missense 17:7463300-7463300 - TCGA-FS-A1ZZ-06 COSM1709709 c.2480C>T p.S827F Substitution - Missense 17:7462502-7462502 - SJBALL020013_D1 COSM4993768 c.30G>A p.P10P Substitution - coding silent 17:7466772-7466772 - TCGA-09-2050-01 COSM80758 c.1917C>T p.D639D Substitution - coding silent 17:7463065-7463065 - 2492708 COSM5589390 c.1932_1946del15 p.D644_E648delDEEEE Deletion - In frame 17:7463036-7463050 - QC2-26-T2 COSM5104116 c.1950_1952delGGA p.E650delE Deletion - In frame 17:7463030-7463032 - AOCS-139-12-5 COSM4139829 c.239C>T p.T80I Substitution - Missense 17:7466563-7466563 - T3090 COSM4742157 c.1961_1962insGGA p.E654_S655insE Insertion - In frame 17:7463020-7463021 - pfg008T COSM1640803 c.2772C>T p.L924L Substitution - coding silent 17:7462210-7462210 - TCGA-AZ-6598-01 COSM1386348 c.11delC p.P4fs*4 Deletion - Frameshift 17:7466791-7466791 - BD124T COSM1386348 c.11delC p.P4fs*4 Deletion - Frameshift 17:7466791-7466791 - TCGA-D5-6540-01 COSM1386334 c.1393C>T p.P465S Substitution - Missense 17:7463589-7463589 - 2492710 COSM5589390 c.1932_1946del15 p.D644_E648delDEEEE Deletion - In frame 17:7463036-7463050 - TCGA-ER-A194-01 COSM3522207 c.2612C>T p.P871L Substitution - Missense 17:7462370-7462370 - I2L-P19Tb-Tumor-Biopsy COSM5364117 c.2170C>T p.R724W Substitution - Missense 17:7462812-7462812 - TCGA-EE-A2GI-06 COSM3522236 c.502C>T p.R168C Substitution - Missense 17:7466300-7466300 - TCGA-02-0047 COSM1289009 c.1010A>C p.Y337S Substitution - Missense 17:7465792-7465792 - TCGA-A5-A0GI-01 COSM984432 c.832C>A p.P278T Substitution - Missense 17:7465970-7465970 - T55 COSM4742165 c.1080G>A p.T360T Substitution - coding silent 17:7465722-7465722 - TCGA-BR-4201-01 COSM4069631 c.773G>A p.R258Q Substitution - Missense 17:7466029-7466029 - HCC115T COSM5807094 c.187G>A p.A63T Substitution - Missense 17:7466615-7466615 - 3N47-VS-3T47 COSM4982611 c.1371T>C p.P457P Substitution - coding silent 17:7463611-7463611 - TCGA-A8-A09Z-01 COSM3820562 c.2244C>T p.H748H Substitution - coding silent 17:7462738-7462738 - 587260 COSM1233146 c.1942G>A p.E648K Substitution - Missense 17:7463040-7463040 - 61 COSM5740849 c.790G>T p.G264W Substitution - Missense 17:7466012-7466012 - CSCC-2-T COSM4508258 c.769C>T p.R257* Substitution - Nonsense 17:7466033-7466033 - TCGA-D8-A1XK-01 COSM1386348 c.11delC p.P4fs*4 Deletion - Frameshift 17:7466791-7466791 - 8066440 COSM3773280 c.484G>C p.E162Q Substitution - Missense 17:7466318-7466318 - TCGA-CA-6717-01 COSM1386340 c.1220C>A p.P407H Substitution - Missense 17:7463762-7463762 - B61 COSM1750352 c.761C>T p.A254V Substitution - Missense 17:7466041-7466041 - YUGATOR COSM5387307 c.1354C>T p.P452S Substitution - Missense 17:7463628-7463628 - C70 COSM4619459 c.1247G>A p.R416H Substitution - Missense 17:7463735-7463735 - PT49 COSM5936374 c.2980C>A p.P994T Substitution - Missense 17:7462002-7462002 - TCGA-D1-A103-01 COSM984424 c.1368G>A p.P456P Substitution - coding silent 17:7463614-7463614 - TCGA-AA-3713-01 COSM1386336 c.1305G>A p.P435P Substitution - coding silent 17:7463677-7463677 - 587342 COSM1233148 c.1921G>T p.E641* Substitution - Nonsense 17:7463061-7463061 - TCGA-KK-A6E7-01 COSM4876513 c.1950G>T p.E650D Substitution - Missense 17:7463032-7463032 - pfg146T COSM4749434 c.2984C>G p.P995R Substitution - Missense 17:7461998-7461998 - S02328 COSM5691922 c.884G>T p.G295V Substitution - Missense 17:7465918-7465918 - T55 COSM4742155 c.2057_2058insG p.S687fs*104 Insertion - Frameshift 17:7462924-7462925 - TCGA-EE-A20F-06 COSM984414 c.1933G>A p.E645K Substitution - Missense 17:7463049-7463049 - 084T COSM1731016 c.2836G>T p.V946F Substitution - Missense 17:7462146-7462146 - 19 COSM984430 c.913G>A p.G305S Substitution - Missense 17:7465889-7465889 - AOCS-139-19-0 COSM4139829 c.239C>T p.T80I Substitution - Missense 17:7466563-7466563 - cSCCP1 COSM142953 c.620_621CC>TT p.P207L Substitution - Missense 17:7466181-7466182 - HCC15T COSM1610766 c.2559A>T p.S853S Substitution - coding silent 17:7462423-7462423 - TCGA-AP-A0LN-01 COSM984407 c.2501G>A p.G834E Substitution - Missense 17:7462481-7462481 - 400 COSM4429414 c.2352G>C p.G784G Substitution - coding silent 17:7462630-7462630 - AOCS-034-1-0 COSM4139827 c.508C>G p.L170V Substitution - Missense 17:7466294-7466294 - Pat_45_B COSM5853491 c.2816G>A p.S939N Substitution - Missense 17:7462166-7462166 - STC263 COSM5055777 c.1272G>A p.K424K Substitution - coding silent 17:7463710-7463710 - TCGA-D3-A2J8-06 COSM3522228 c.1693G>A p.G565R Substitution - Missense 17:7463289-7463289 - ESCC_BICR_051T COSM5444017 c.1881G>A p.E627E Substitution - coding silent 17:7463101-7463101 - TCGA-HC-7818-01 COSM3783105 c.2254T>G p.S752A Substitution - Missense 17:7462728-7462728 - 61 COSM5740847 c.1345G>A p.V449M Substitution - Missense 17:7463637-7463637 - CHC1329T COSM3755856 c.1682A>G p.N561S Substitution - Missense 17:7463300-7463300 - T2979 COSM4742159 c.1903delG p.E635fs*104 Deletion - Frameshift 17:7463079-7463079 - CSCC-44-T COSM4481809 c.2547C>T p.D849D Substitution - coding silent 17:7462435-7462435 - B92-Tumor COSM3932734 c.1009T>G p.Y337D Substitution - Missense 17:7465793-7465793 - HCC97 COSM1610768 c.1217A>T p.K406M Substitution - Missense 17:7463765-7463765 - sysucc-783T COSM5484157 c.521G>A p.R174H Substitution - Missense 17:7466281-7466281 - TCGA-AZ-6601-01 COSM1386344 c.520C>T p.R174C Substitution - Missense 17:7466282-7466282 - PDA_011 COSM2741686 c.94G>A p.V32I Substitution - Missense 17:7466708-7466708 - TCGA-AA-3697-01 COSM1386330 c.2020C>T p.R674C Substitution - Missense 17:7462962-7462962 - TCGA-BR-6566-01 COSM4069627 c.1661C>T p.T554M Substitution - Missense 17:7463321-7463321 - TCGA-22-4601-01 COSM707223 c.1189A>T p.S397C Substitution - Missense 17:7463793-7463793 - LAU50_2 COSM233789 c.2944C>T p.P982S Substitution - Missense 17:7462038-7462038 - LUAD-S01304 COSM385428 c.1027G>C p.E343Q Substitution - Missense 17:7465775-7465775 - TCGA-EE-A2GP-06 COSM3522201 c.2941C>T p.P981S Substitution - Missense 17:7462041-7462041 - TCGA-A5-A0G5-01 COSM984430 c.913G>A p.G305S Substitution - Missense 17:7465889-7465889 - TCGA-EE-A2MS-06 COSM3522199 c.2980C>T p.P994S Substitution - Missense 17:7462002-7462002 - TCGA-D3-A3MU-06 COSM3522205 c.2844C>T p.L948L Substitution - coding silent 17:7462138-7462138 - TCGA-DD-A11D-01 COSM4938108 c.176T>C p.L59P Substitution - Missense 17:7466626-7466626 - BD49T COSM1386348 c.11delC p.P4fs*4 Deletion - Frameshift 17:7466791-7466791 - CSCC-31-T COSM4515037 c.995C>T p.S332L Substitution - Missense 17:7465807-7465807 - SNU-175 COSM2741657 c.816C>T p.G272G Substitution - coding silent 17:7465986-7465986 - C008 COSM5524228 c.484G>A p.E162K Substitution - Missense 17:7466318-7466318 - BD57T COSM5509604 c.10_11insC p.A5fs*18 Insertion - Frameshift 17:7466791-7466792 - 2492709 COSM5589390 c.1932_1946del15 p.D644_E648delDEEEE Deletion - In frame 17:7463036-7463050 - TCGA-AP-A059-01 COSM984418 c.1715C>T p.A572V Substitution - Missense 17:7463267-7463267 - TCGA-22-4601-01 COSM707221 c.1178G>T p.G393V Substitution - Missense 17:7463804-7463804 - HCT-15 COSM1679475 c.766T>C p.C256R Substitution - Missense 17:7466036-7466036 - 53M COSM5595580 c.732C>T p.I244I Substitution - coding silent 17:7466070-7466070 - PT46 COSM5929794 c.1183C>T p.L395F Substitution - Missense 17:7463799-7463799 - C106 COSM4616228 c.1820G>A p.R607Q Substitution - Missense 17:7463162-7463162 - CSCC-27-T COSM4466271 c.1425C>T p.A475A Substitution - coding silent 17:7463557-7463557 - TCGA-AP-A051-01 COSM984426 c.1220C>T p.P407L Substitution - Missense 17:7463762-7463762 - PDA_008 COSM3691808 c.2185G>A p.G729R Substitution - Missense 17:7462797-7462797 - TCGA-AG-A02N-01 COSM1386348 c.11delC p.P4fs*4 Deletion - Frameshift 17:7466791-7466791 - D-08 COSM1289009 c.1010A>C p.Y337S Substitution - Missense 17:7465792-7465792 - OSCC-GB_00160111 COSM3712444 c.580G>A p.A194T Substitution - Missense 17:7466222-7466222 - TCGA-22-4613-01 COSM707228 c.2715C>A p.D905E Substitution - Missense 17:7462267-7462267 - HT115 COSM2741620 c.1861A>C p.T621P Substitution - Missense 17:7463121-7463121 - RKO COSM2741651 c.884delG p.G295fs*6 Deletion - Frameshift 17:7465918-7465918 - TCGA-DD-A4NI-01 COSM4926233 c.43G>A p.A15T Substitution - Missense 17:7466759-7466759 - AOCS-166-1-2 COSM4139825 c.1065T>C p.H355H Substitution - coding silent 17:7465737-7465737 - HCC97T COSM1610768 c.1217A>T p.K406M Substitution - Missense 17:7463765-7463765 - TCGA-EB-A431-01 COSM3522234 c.615C>T p.P205P Substitution - coding silent 17:7466187-7466187 - YUHAMA COSM4069629 c.1304C>T p.P435L Substitution - Missense 17:7463678-7463678 - TCGA-AR-A24Q-01 COSM1480013 c.1858G>T p.E620* Substitution - Nonsense 17:7463124-7463124 - pfg160T COSM4749436 c.119A>G p.K40R Substitution - Missense 17:7466683-7466683 - TCGA-D8-A1XM-01 COSM1480017 c.109G>A p.G37R Substitution - Missense 17:7466693-7466693 - TCGA-A8-A097-01 COSM112021 c.11_12insC p.A5fs*18 Insertion - Frameshift 17:7466790-7466791 - HCC55T COSM1610772 c.219C>T p.G73G Substitution - coding silent 17:7466583-7466583 - 35M COSM5583100 c.1437C>T p.P479P Substitution - coding silent 17:7463545-7463545 - TCGA-24-0968-01 COSM112021 c.11_12insC p.A5fs*18 Insertion - Frameshift 17:7466790-7466791 - CML005T COSM5802780 c.1847G>A p.R616H Substitution - Missense 17:7463135-7463135 - TCGA-IR-A3LK-01 COSM4816584 c.2229G>A p.K743K Substitution - coding silent 17:7462753-7462753 - HCC55 COSM1610772 c.219C>T p.G73G Substitution - coding silent 17:7466583-7466583 - sysucc-1163T COSM5458651 c.2873C>T p.A958V Substitution - Missense 17:7462109-7462109 - TCGA-CH-5771-01 COSM1130163 c.1380A>C p.P460P Substitution - coding silent 17:7463602-7463602 - SJHGG073_A COSM4971429 c.1778C>T p.S593F Substitution - Missense 17:7463204-7463204 - TCGA-D3-A3MR-06 COSM3522211 c.2453C>A p.A818D Substitution - Missense 17:7462529-7462529 - B61-Tumor COSM1750352 c.761C>T p.A254V Substitution - Missense 17:7466041-7466041 - TARGET-30-PARYXW COSM1289009 c.1010A>C p.Y337S Substitution - Missense 17:7465792-7465792 - TCGA-HU-A4H8-01 COSM4069639 c.243C>T p.T81T Substitution - coding silent 17:7466559-7466559 - P03-1906 COSM248412 c.1334C>A p.T445K Substitution - Missense 17:7463648-7463648 - 16T COSM3712444 c.580G>A p.A194T Substitution - Missense 17:7466222-7466222 - 19 COSM5747808 c.2279G>T p.R760M Substitution - Missense 17:7462703-7462703 - SNU-C2B COSM4615268 c.2057delG p.G686fs*53 Deletion - Frameshift 17:7462925-7462925 - Pat_06_A COSM5853495 c.1589C>T p.A530V Substitution - Missense 17:7463393-7463393 - BCM257T COSM4951544 c.2653G>T p.E885* Substitution - Nonsense 17:7462329-7462329 - MO_1012 COSM5565994 c.1261C>T p.R421W Substitution - Missense 17:7463721-7463721 - HCC50 COSM1610770 c.454G>T p.G152C Substitution - Missense 17:7466348-7466348 - sysucc-1370T COSM5470753 c.1932C>G p.D644E Substitution - Missense 17:7463050-7463050 - CSCC-18-T COSM4537050 c.2378G>A p.G793E Substitution - Missense 17:7462604-7462604 - 2492728 COSM5725490 c.181A>C p.T61P Substitution - Missense 17:7466621-7466621 - TCGA-A6-6780-01 COSM1386346 c.294C>A p.S98S Substitution - coding silent 17:7466508-7466508 - TCGA-EK-A2R9-01 COSM4822945 c.2529G>T p.E843D Substitution - Missense 17:7462453-7462453 - ESO-1481 COSM1270718 c.2872G>T p.A958S Substitution - Missense 17:7462110-7462110 - HCT8 COSM1679475 c.766T>C p.C256R Substitution - Missense 17:7466036-7466036 - TCGA-BR-4361-01 COSM4069622 c.2365G>A p.A789T Substitution - Missense 17:7462617-7462617 - HCT15 COSM1679475 c.766T>C p.C256R Substitution - Missense 17:7466036-7466036 - YUGURT COSM5387303 c.2983C>T p.P995S Substitution - Missense 17:7461999-7461999 - TCGA-AR-A24V-01 COSM1480015 c.1678C>T p.R560W Substitution - Missense 17:7463304-7463304 - 2492727 COSM5725490 c.181A>C p.T61P Substitution - Missense 17:7466621-7466621 - sysucc-1370T COSM2741686 c.94G>A p.V32I Substitution - Missense 17:7466708-7466708 - PTC-77C COSM4130636 c.823C>A p.P275T Substitution - Missense 17:7465979-7465979 - 53M COSM5595578 c.2303C>T p.P768L Substitution - Missense 17:7462679-7462679 - HCC50T COSM1610770 c.454G>T p.G152C Substitution - Missense 17:7466348-7466348 - TCGA-AN-A04C-01 COSM112021 c.11_12insC p.A5fs*18 Insertion - Frameshift 17:7466790-7466791 - TCGA-D3-A2JP-06 COSM3890427 c.1554G>A p.K518K Substitution - coding silent 17:7463428-7463428 - YUGURT COSM5387305 c.2920C>T p.P974S Substitution - Missense 17:7462062-7462062 - RW2982 COSM4649587 c.1704G>A p.L568L Substitution - coding silent 17:7463278-7463278 - CSCC-27-T COSM4487872 c.323C>T p.S108F Substitution - Missense 17:7466479-7466479 - SNUH_G17_S1 COSM3680558 c.1032A>G p.K344K Substitution - coding silent 17:7465770-7465770 - PD4844a COSM165661 c.2637G>C p.L879F Substitution - Missense 17:7462345-7462345 - 31231321 COSM1582357 c.877C>T p.R293* Substitution - Nonsense 17:7465925-7465925 - Pat_24_A COSM4069629 c.1304C>T p.P435L Substitution - Missense 17:7463678-7463678 - TCGA-DI-A0WH-01 COSM984401 c.2912C>T p.A971V Substitution - Missense 17:7462070-7462070 - TCGA-BR-A4QL-01 COSM4069618 c.2736T>C p.A912A Substitution - coding silent 17:7462246-7462246 - BHY COSM2741618 c.1953_1955delTGA p.D651delD Deletion - In frame 17:7463027-7463029 - TCGA-B0-5098-01 COSM1493977 c.2596A>G p.S866G Substitution - Missense 17:7462386-7462386 - UPCI:SCC090 COSM2741618 c.1953_1955delTGA p.D651delD Deletion - In frame 17:7463027-7463029 - PD4120a COSM165659 c.851C>T p.S284L Substitution - Missense 17:7465951-7465951 - YUDEDE COSM1709709 c.2480C>T p.S827F Substitution - Missense 17:7462502-7462502 - TCGA-AG-4005-01 COSM289416 c.1757C>G p.T586R Substitution - Missense 17:7463225-7463225 - TCGA-AZ-4315-01 COSM1386328 c.2827G>A p.A943T Substitution - Missense 17:7462155-7462155 - CSCC-47-T COSM4485498 c.293C>T p.S98F Substitution - Missense 17:7466509-7466509 - TCGA-EE-A181-06 COSM3522232 c.1175C>A p.P392Q Substitution - Missense 17:7463807-7463807 - pfg143T COSM4765567 c.12_13insC p.A5fs*18 Insertion - Frameshift 17:7466789-7466790 - TCGA-BR-7707-01 COSM4069612 c.3030C>T p.G1010G Substitution - coding silent 17:7461952-7461952 - 18T COSM107941 c.2586A>T p.A862A Substitution - coding silent 17:7462396-7462396 - TCGA-FS-A4F9-06 COSM3522226 c.2039G>A p.G680E Substitution - Missense 17:7462943-7462943 - B102-Tumor COSM3932734 c.1009T>G p.Y337D Substitution - Missense 17:7465793-7465793 - C391 COSM4441685 c.1501G>T p.G501W Substitution - Missense 17:7463481-7463481 - TCGA-AF-3913-01 COSM112021 c.11_12insC p.A5fs*18 Insertion - Frameshift 17:7466790-7466791 - TCGA-EE-A2MR-06 COSM3522217 c.2432C>T p.P811L Substitution - Missense 17:7462550-7462550 - TCGA-D3-A2J7-06 COSM2741663 c.562C>T p.P188S Substitution - Missense 17:7466240-7466240 - CSCC-49-T COSM4468974 c.1573C>T p.P525S Substitution - Missense 17:7463409-7463409 - PTC_285 COSM5958956 c.1630_1631insG p.T544fs*79 Insertion - Frameshift 17:7463351-7463352 - TCGA-10-0926-01 COSM117177 c.2717G>A p.R906Q Substitution - Missense 17:7462265-7462265 - LUAD-F00121 COSM365695 c.2081G>A p.R694Q Substitution - Missense 17:7462901-7462901 - TCGA-AP-A0LM-01 COSM984410 c.2188G>T p.D730Y Substitution - Missense 17:7462794-7462794 - TCGA-D7-6820-01 COSM4069633 c.666C>T p.A222A Substitution - coding silent 17:7466136-7466136 - TCGA-EE-A29B-06 COSM3522238 c.281C>T p.S94F Substitution - Missense 17:7466521-7466521 - TCGA-EE-A29E-06 COSM3522230 c.1670C>T p.A557V Substitution - Missense 17:7463312-7463312 - TCGA-DR-A0ZM-01 COSM460220 c.326C>G p.S109C Substitution - Missense 17:7466476-7466476 - PTC-28C COSM4130632 c.3012T>A p.V1004V Substitution - coding silent 17:7461970-7461970 - TCGA-D1-A174-01 COSM984422 c.1534G>A p.A512T Substitution - Missense 17:7463448-7463448 - 2492730 COSM5725490 c.181A>C p.T61P Substitution - Missense 17:7466621-7466621 - TCGA-43-3920-01 COSM707226 c.2500G>T p.G834W Substitution - Missense 17:7462482-7462482 - TCGA-IR-A3LK-01 COSM4817207 c.2226G>T p.R742R Substitution - coding silent 17:7462756-7462756 - TCGA-AP-A059-01 COSM984416 c.1871G>A p.R624H Substitution - Missense 17:7463111-7463111 - PCSI_0079_Pa_P COSM3378318 c.493G>C p.A165P Substitution - Missense 17:7466309-7466309 - TCGA-BS-A0U8-01 COSM984404 c.2689G>T p.G897W Substitution - Missense 17:7462293-7462293 - S00945 COSM5664436 c.1993A>G p.R665G Substitution - Missense 17:7462989-7462989 - TCGA-ER-A3PL-06 COSM3522197 c.3002G>A p.R1001K Substitution - Missense 17:7461980-7461980 - CRC-34T COSM5460787 c.1761G>T p.G587G Substitution - coding silent 17:7463221-7463221 - TCGA-EJ-5497-01 COSM1130163 c.1380A>C p.P460P Substitution - coding silent 17:7463602-7463602 - 46M COSM5589390 c.1932_1946del15 p.D644_E648delDEEEE Deletion - In frame 17:7463036-7463050 - PT55 COSM5942756 c.2743G>A p.V915I Substitution - Missense 17:7462239-7462239 - PD13760a COSM5786844 c.2983C>A p.P995T Substitution - Missense 17:7461999-7461999 - DLD1 COSM1679475 c.766T>C p.C256R Substitution - Missense 17:7466036-7466036 - TCGA-G4-6586-01 COSM1386348 c.11delC p.P4fs*4 Deletion - Frameshift 17:7466791-7466791 - LUAD-NYU1051S COSM368633 c.930G>C p.V310V Substitution - coding silent 17:7465872-7465872 - TCGA-D7-A4YY-01 COSM3388141 c.2769G>A p.P923P Substitution - coding silent 17:7462213-7462213 - ME050T COSM230755 c.1436C>T p.P479L Substitution - Missense 17:7463546-7463546 - HCC15 COSM1610766 c.2559A>T p.S853S Substitution - coding silent 17:7462423-7462423 - ESO-717 COSM1243011 c.2156G>A p.R719H Substitution - Missense 17:7462826-7462826 - TCGA-EE-A2GD-06 COSM3522224 c.2290C>T p.R764C Substitution - Missense 17:7462692-7462692 - TCGA-AX-A05S-01 COSM984412 c.2135C>T p.A712V Substitution - Missense 17:7462847-7462847 - T3021 COSM4742163 c.1119C>A p.T373T Substitution - coding silent 17:7463863-7463863 - LAU50_1 COSM233789 c.2944C>T p.P982S Substitution - Missense 17:7462038-7462038 - pfg122T COSM1386348 c.11delC p.P4fs*4 Deletion - Frameshift 17:7466791-7466791 - PD4844a COSM165661 c.2637G>C p.L879F Substitution - Missense 17:7462345-7462345 - TCGA-66-2794-01 COSM707230 c.3015G>A p.E1005E Substitution - coding silent 17:7461967-7461967 - AOCS-139-1-5 COSM4139829 c.239C>T p.T80I Substitution - Missense 17:7466563-7466563 - TCGA-BG-A0M9-01 COSM984420 c.1558C>T p.R520* Substitution - Nonsense 17:7463424-7463424 - TCGA-D8-A1XQ-01 COSM3820565 c.1010A>T p.Y337F Substitution - Missense 17:7465792-7465792 - TCGA-FD-A3SO-01 COSM3796092 c.972G>C p.L324L Substitution - coding silent 17:7465830-7465830 - Br27P COSM40778 c.2842C>T p.L948F Substitution - Missense 17:7462140-7462140 - CHC433T COSM3766181 c.1953T>G p.D651E Substitution - Missense 17:7463029-7463029 - Pat_26_A COSM5853493 c.1597C>T p.P533S Substitution - Missense 17:7463385-7463385 - 2492729 COSM5725490 c.181A>C p.T61P Substitution - Missense 17:7466621-7466621 - TCGA-BR-6566-01 COSM4069637 c.276G>A p.S92S Substitution - coding silent 17:7466526-7466526 - TCGA-B0-4710-01 COSM473370 c.339T>C p.P113P Substitution - coding silent 17:7466463-7466463 - 8061185 COSM3388141 c.2769G>A p.P923P Substitution - coding silent 17:7462213-7462213 - TCGA-AF-3914-01 COSM2741653 c.878G>A p.R293Q Substitution - Missense 17:7465924-7465924 - sysucc-1315T COSM5480110 c.2184C>T p.C728C Substitution - coding silent 17:7462798-7462798 - AOCS-139-6-3 COSM4139829 c.239C>T p.T80I Substitution - Missense 17:7466563-7466563 - ESCC_BICR_024T COSM5440884 c.1242C>G p.L414L Substitution - coding silent 17:7463740-7463740 - pfg129T COSM1386348 c.11delC p.P4fs*4 Deletion - Frameshift 17:7466791-7466791 - TCGA-BR-8361-01 COSM4069624 c.2045C>T p.A682V Substitution - Missense 17:7462937-7462937 - CAL27 COSM2741618 c.1953_1955delTGA p.D651delD Deletion - In frame 17:7463027-7463029 - 587376 COSM1233150 c.2311G>A p.A771T Substitution - Missense 17:7462671-7462671 - TCGA-BR-4363-01 COSM4069629 c.1304C>T p.P435L Substitution - Missense 17:7463678-7463678 - Pat_41_B COSM5853497 c.698C>T p.P233L Substitution - Missense 17:7466104-7466104 - TCGA-HF-7132-01 COSM4069635 c.419T>C p.L140P Substitution - Missense 17:7466383-7466383 - 255 COSM3731808 c.2049T>C p.S683S Substitution - coding silent 17:7462933-7462933 - TCGA-DK-A3X1-01 COSM3796089 c.2790C>A p.L930L Substitution - coding silent 17:7462192-7462192 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.35090;Hs.35096 17p13.1 612308

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C IntronicSNV . c.1-1581T>G 17 7371701 CLL A C Missense p.S752A c.2254T>G 17 7366047 PRAD A G Synonymous p.P113P c.339T>C 17 7369782 RCCC A G Synonymous p.S97S c.291T>C 17 7369830 STAD C A Missense p.A958S c.2872G>T 17 7365429 ESCA C A Missense p.E650D c.1950G>T 17 7366351 PRAD C A Missense p.G393V c.1178G>T 17 7367123 LUSC C A Missense p.G834W c.2500G>T 17 7365801 LUSC C A Missense p.G897W c.2689G>T 17 7365612 UCEC C A Nonsense p.E620* c.1858G>T 17 7366443 BRCA C A Nonsense p.E830* c.2488G>T 17 7365813 CM C A Synonymous p.L628L c.1884G>T 17 7366417 HNSC C G Missense p.L879F c.2637G>C 17 7365664 BRCA C T Missense p.A15T c.43G>A 17 7370078 HNSC C T Missense p.E645K c.1933G>A 17 7366368 CM C T Missense p.G37R c.109G>A 17 7370012 BRCA C T Missense p.G565R c.1693G>A 17 7366608 CM C T Missense p.G750E c.2249G>A 17 7366052 LUAD C T Missense p.G834E c.2501G>A 17 7365800 UCEC C T Missense p.L948F c.2842C>T 17 7365459 GBM C T Missense p.R258Q c.773G>A 17 7369348 STAD C T Synonymous p.E1005E c.3015G>A 17 7365286 LUSC C T Synonymous p.K518K c.1554G>A 17 7366747 CM C T Synonymous p.P10P c.30G>A 17 7370091 HNSC G A Missense p.A712V c.2135C>T 17 7366166 UCEC G A Missense p.A971V c.2912C>T 17 7365389 UCEC G A Missense p.P123L c.368C>T 17 7369753 LUAD G A Missense p.P188S c.562C>T 17 7369559 CM G A Missense p.P435L c.1304C>T 17 7366997 STAD G A Missense p.P479L c.1436C>T 17 7366865 CM G A Missense p.P599L c.1796C>T 17 7366505 CM G A Missense p.P871L c.2612C>T 17 7365689 CM G A Missense p.P876S c.2626C>T 17 7365675 BRCA G A Missense p.P981S c.2941C>T 17 7365360 CM G A Missense p.P994S c.2980C>T 17 7365321 CM G A Missense p.P995L c.2984C>T 17 7365317 CM G A Missense p.R168C c.502C>T 17 7369619 CM G A Missense p.R560W c.1678C>T 17 7366623 BRCA G A Missense p.R764C c.2290C>T 17 7366011 CM G A Missense p.S228F c.683C>T 17 7369438 CM G A Missense p.S284L c.851C>T 17 7369270 BRCA G A Missense p.S827F c.2480C>T 17 7365821 CM G A Missense p.S94F c.281C>T 17 7369840 CM G A Nonsense p.Q662* c.1984C>T 17 7366317 CM G A Nonsense p.R520* c.1558C>T 17 7366743 UCEC G A Synonymous p.A222A c.666C>T 17 7369455 STAD G A Synonymous p.D639D c.1917C>T 17 7366384 OV G A Synonymous p.L924L c.2772C>T 17 7365529 STAD G A Synonymous p.L948L c.2844C>T 17 7365457 CM G A Synonymous p.S317S c.951C>T 17 7369170 CM G C Missense p.H298D c.892C>G 17 7369229 CM G C Missense p.T586R c.1757C>G 17 7366544 COREAD - G Frameshift p.A5Cfs*18 c.11dupC 17 7370110 OV GG AA Missense p.R727* c.2178_2179delinsTT 17 7366122 CM GG AA Missense p.S842F c.2525_2526delinsTT 17 7365775 CM G T Missense p.A818D c.2453C>A 17 7365848 CM G T Missense p.D905E c.2715C>A 17 7365586 LUSC G T Missense p.P278T c.832C>A 17 7369289 UCEC G T Missense p.P392Q c.1175C>A 17 7367126 CM T A Missense p.S397C c.1189A>T 17 7367112 LUSC T G 3-UTRSNV . c.3039+1840A>C 17 7363422 HC