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 7 7612191 7612191 + Missense_Mutation SNP C C G TCGA-G2-A2EC-01A-11D-A17V-08 TCGA-G2-A2EC-10A-01D-A17V-08 g.chr7:7612191C>G c.85C>G c.(85-87)Cat>Gat p.H29D BLCA 7 7612385 7612385 + Silent SNP T T C TCGA-XF-AAMH-01A-11D-A42E-08 TCGA-XF-AAMH-10A-01D-A42H-08 g.chr7:7612385T>C c.279T>C c.(277-279)ggT>ggC p.G93G BLCA 7 7612527 7612527 + Missense_Mutation SNP T T C TCGA-XF-A9T0-01A-11D-A391-08 TCGA-XF-A9T0-10A-01D-A394-08 g.chr7:7612527T>C c.421T>C c.(421-423)Tca>Cca p.S141P BLCA 7 7612889 7612889 + Missense_Mutation SNP G G C TCGA-DK-AA6U-01A-11D-A391-08 TCGA-DK-AA6U-10A-01D-A394-08 g.chr7:7612889G>C c.783G>C c.(781-783)ttG>ttC p.L261F BLCA 7 7612950 7612950 + Missense_Mutation SNP C C G TCGA-FD-A5BV-01A-11D-A26M-08 TCGA-FD-A5BV-10A-01D-A26K-08 g.chr7:7612950C>G c.844C>G c.(844-846)Cta>Gta p.L282V BLCA 7 7613733 7613733 + Missense_Mutation SNP G G C TCGA-K4-A4AC-01A-21D-A26M-08 TCGA-K4-A4AC-10A-01D-A26K-08 g.chr7:7613733G>C c.1299G>C c.(1297-1299)atG>atC p.M433I BLCA 7 7622975 7622975 + Missense_Mutation SNP C C G TCGA-G2-A2EO-01A-11D-A17V-08 TCGA-G2-A2EO-11A-21D-A17V-08 g.chr7:7622975C>G c.1620C>G c.(1618-1620)atC>atG p.I540M BLCA 7 7625272 7625272 + Silent SNP C C T TCGA-ZF-AA4V-01A-11D-A38G-08 TCGA-ZF-AA4V-10A-01D-A38J-08 g.chr7:7625272C>T c.1654C>T c.(1654-1656)Ctg>Ttg p.L552L BLCA 7 7625319 7625319 + Missense_Mutation SNP G G C TCGA-XF-A9SJ-01A-11D-A391-08 TCGA-XF-A9SJ-10A-01D-A394-08 g.chr7:7625319G>C c.1701G>C c.(1699-1701)gaG>gaC p.E567D BLCA 7 7625322 7625322 + Silent SNP G G A TCGA-ZF-A9RC-01A-11D-A38G-08 TCGA-ZF-A9RC-10A-01D-A38J-08 g.chr7:7625322G>A c.1704G>A c.(1702-1704)aaG>aaA p.K568K BLCA 7 7625397 7625397 + Silent SNP A A G TCGA-4Z-AA84-01A-11D-A391-08 TCGA-4Z-AA84-10A-01D-A394-08 g.chr7:7625397A>G c.1779A>G c.(1777-1779)gcA>gcG p.A593A BLCA 7 7625410 7625410 + Missense_Mutation SNP G G A TCGA-ZF-A9R7-01A-11D-A38G-08 TCGA-ZF-A9R7-10A-01D-A38J-08 g.chr7:7625410G>A c.1792G>A c.(1792-1794)Gaa>Aaa p.E598K BLCA 7 7628157 7628157 + Missense_Mutation SNP G G C TCGA-BT-A20J-01A-11D-A14W-08 TCGA-BT-A20J-11A-11D-A14W-08 g.chr7:7628157G>C c.1847G>C c.(1846-1848)aGa>aCa p.R616T BLCA 7 7628184 7628184 + Missense_Mutation SNP G G T TCGA-UY-A78K-01A-11D-A339-08 TCGA-UY-A78K-10A-01D-A339-08 g.chr7:7628184G>T c.1874G>T c.(1873-1875)aGt>aTt p.S625I BLCA 7 7628192 7628192 + Missense_Mutation SNP C C G TCGA-ZF-AA4V-01A-11D-A38G-08 TCGA-ZF-AA4V-10A-01D-A38J-08 g.chr7:7628192C>G c.1882C>G c.(1882-1884)Cag>Gag p.Q628E BLCA 7 7635958 7635958 + Missense_Mutation SNP G G C TCGA-FD-A6TC-01A-21D-A339-08 TCGA-FD-A6TC-10A-21D-A339-08 g.chr7:7635958G>C c.2267G>C c.(2266-2268)aGa>aCa p.R756T BLCA 7 7635969 7635969 + Nonsense_Mutation SNP C C T TCGA-MV-A51V-01A-11D-A26M-08 TCGA-MV-A51V-10A-01D-A26K-08 g.chr7:7635969C>T c.2278C>T c.(2278-2280)Cag>Tag p.Q760* BLCA 7 7636000 7636000 + Missense_Mutation SNP C C A TCGA-FJ-A3ZE-01A-11D-A23M-08 TCGA-FJ-A3ZE-10A-01D-A23K-08 g.chr7:7636000C>A c.2309C>A c.(2308-2310)tCt>tAt p.S770Y BRCA 7 7612672 7612672 + Missense_Mutation SNP C C G TCGA-D8-A1JA-01A-11D-A13L-09 TCGA-D8-A1JA-10A-01W-A14R-09 g.chr7:7612672C>G c.566C>G c.(565-567)tCt>tGt p.S189C BRCA 7 7636043 7636043 + Silent SNP A A T TCGA-BH-A0H7-01A-13W-A071-09 TCGA-BH-A0H7-11A-13W-A100-09 g.chr7:7636043A>T c.2352A>T c.(2350-2352)cgA>cgT p.R784R CESC 7 7622951 7622951 + Missense_Mutation SNP G G C TCGA-EK-A3GJ-01A-21D-A20U-09 TCGA-EK-A3GJ-11A-11D-A20U-09 g.chr7:7622951G>C c.1596G>C c.(1594-1596)ttG>ttC p.L532F CESC 7 7634623 7634623 + Missense_Mutation SNP G G A TCGA-FU-A3TQ-01A-11D-A22X-09 TCGA-FU-A3TQ-10A-01D-A22X-09 g.chr7:7634623G>A c.2056G>A c.(2056-2058)Gat>Aat p.D686N CHOL 7 7625410 7625410 + Nonsense_Mutation SNP G G T TCGA-ZU-A8S4-01A-11D-A417-09 TCGA-ZU-A8S4-10A-01D-A41A-09 g.chr7:7625410G>T c.1792G>T c.(1792-1794)Gaa>Taa p.E598* COAD 7 7612410 7612410 + Missense_Mutation SNP G G T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr7:7612410G>T c.304G>T c.(304-306)Gat>Tat p.D102Y COAD 7 7612803 7612803 + Missense_Mutation SNP G G T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr7:7612803G>T c.697G>T c.(697-699)Gac>Tac p.D233Y COAD 7 7613140 7613140 + Missense_Mutation SNP G G A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr7:7613140G>A c.1034G>A c.(1033-1035)cGa>cAa p.R345Q COAD 7 7634642 7634642 + Missense_Mutation SNP G G A TCGA-AD-6895-01A-11D-1924-10 TCGA-AD-6895-10A-01D-1924-10 g.chr7:7634642G>A c.2075G>A c.(2074-2076)aGg>aAg p.R692K COAD 7 7634699 7634699 + Missense_Mutation SNP A A G TCGA-AA-A01R-01A-21W-A096-10 TCGA-AA-A01R-11A-12W-A096-10 g.chr7:7634699A>G c.2132A>G c.(2131-2133)cAt>cGt p.H711R COAD 7 7635908 7635908 + Missense_Mutation SNP C C A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr7:7635908C>A c.2217C>A c.(2215-2217)ttC>ttA p.F739L COAD 7 7636027 7636027 + Missense_Mutation SNP G G A TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr7:7636027G>A c.2336G>A c.(2335-2337)cGa>cAa p.R779Q COAD 7 7645613 7645614 + Frame_Shift_Ins INS - - A TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr7:7645613_7645614insA c.2442_2443insA c.(2443-2445)aaafs p.K815fs COAD 7 7646669 7646669 + Missense_Mutation SNP T T G TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr7:7646669T>G c.2574T>G c.(2572-2574)tgT>tgG p.C858W COADREAD 7 7612410 7612410 + Missense_Mutation SNP G G T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr7:7612410G>T c.304G>T c.(304-306)Gat>Tat p.D102Y COADREAD 7 7612803 7612803 + Missense_Mutation SNP G G T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr7:7612803G>T c.697G>T c.(697-699)Gac>Tac p.D233Y COADREAD 7 7613140 7613140 + Missense_Mutation SNP G G A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr7:7613140G>A c.1034G>A c.(1033-1035)cGa>cAa p.R345Q COADREAD 7 7613247 7613247 + Nonsense_Mutation SNP G G T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr7:7613247G>T c.1141G>T c.(1141-1143)Gaa>Taa p.E381* COADREAD 7 7613282 7613282 + Silent SNP G G A TCGA-AG-A025-01A-01W-A00E-09 TCGA-AG-A025-10A-01W-A00E-09 g.chr7:7613282G>A c.1176G>A c.(1174-1176)acG>acA p.T392T COADREAD 7 7622772 7622772 + Missense_Mutation SNP A A C TCGA-CL-5918-01A-11D-1657-10 TCGA-CL-5918-10A-01D-1657-10 g.chr7:7622772A>C c.1417A>C c.(1417-1419)Aat>Cat p.N473H COADREAD 7 7634642 7634642 + Missense_Mutation SNP G G A TCGA-AD-6895-01A-11D-1924-10 TCGA-AD-6895-10A-01D-1924-10 g.chr7:7634642G>A c.2075G>A c.(2074-2076)aGg>aAg p.R692K COADREAD 7 7634699 7634699 + Missense_Mutation SNP A A G TCGA-AA-A01R-01A-21W-A096-10 TCGA-AA-A01R-11A-12W-A096-10 g.chr7:7634699A>G c.2132A>G c.(2131-2133)cAt>cGt p.H711R COADREAD 7 7635908 7635908 + Missense_Mutation SNP C C A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr7:7635908C>A c.2217C>A c.(2215-2217)ttC>ttA p.F739L COADREAD 7 7636027 7636027 + Missense_Mutation SNP G G A TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr7:7636027G>A c.2336G>A c.(2335-2337)cGa>cAa p.R779Q COADREAD 7 7645613 7645614 + Frame_Shift_Ins INS - - A TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr7:7645613_7645614insA c.2442_2443insA c.(2443-2445)aaafs p.K815fs COADREAD 7 7646629 7646629 + Missense_Mutation SNP A A T TCGA-F5-6811-01A-11D-1826-10 TCGA-F5-6811-10A-01D-1826-10 g.chr7:7646629A>T c.2534A>T c.(2533-2535)gAc>gTc p.D845V COADREAD 7 7646669 7646669 + Missense_Mutation SNP T T G TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr7:7646669T>G c.2574T>G c.(2572-2574)tgT>tgG p.C858W ESCA 7 7612169 7612169 + Silent SNP T T C TCGA-L5-A4OI-01A-11D-A27G-09 TCGA-L5-A4OI-11A-11D-A27G-09 g.chr7:7612169T>C c.63T>C c.(61-63)tgT>tgC p.C21C ESCA 7 7628156 7628156 + Missense_Mutation SNP A A G TCGA-LN-A7HY-01A-12D-A351-09 TCGA-LN-A7HY-10A-01D-A351-09 g.chr7:7628156A>G c.1846A>G c.(1846-1848)Aga>Gga p.R616G ESCA 7 7634722 7634722 + Missense_Mutation SNP C C T TCGA-LN-A4A4-01A-11D-A27G-09 TCGA-LN-A4A4-10A-01D-A27G-09 g.chr7:7634722C>T c.2155C>T c.(2155-2157)Cac>Tac p.H719Y GBM 7 7612689 7612689 + Nonsense_Mutation SNP C C T TCGA-87-5896-01A-01D-1696-08 TCGA-87-5896-10A-01D-1696-08 g.chr7:7612689C>T c.583C>T c.(583-585)Cga>Tga p.R195* GBMLGG 7 7612689 7612689 + Nonsense_Mutation SNP C C T TCGA-87-5896-01A-01D-1696-08 TCGA-87-5896-10A-01D-1696-08 g.chr7:7612689C>T c.583C>T c.(583-585)Cga>Tga p.R195* GBMLGG 7 7612975 7612975 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr7:7612975G>T c.869G>T c.(868-870)aGt>aTt p.S290I GBMLGG 7 7625343 7625343 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr7:7625343G>A c.1725G>A c.(1723-1725)atG>atA p.M575I GBMLGG 7 7625428 7625428 + Frame_Shift_Del DEL G G - TCGA-DB-A64V-01A-11D-A29Q-08 TCGA-DB-A64V-10A-01D-A29Q-08 g.chr7:7625428delG c.1810delG c.(1810-1812)ggafs p.G604fs GBMLGG 7 7646672 7646672 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr7:7646672G>A c.2577G>A c.(2575-2577)atG>atA p.M859I HNSC 7 7612474 7612474 + Missense_Mutation SNP C C T TCGA-CV-A468-01A-11D-A25Y-08 TCGA-CV-A468-10A-01D-A25Y-08 g.chr7:7612474C>T c.368C>T c.(367-369)cCa>cTa p.P123L HNSC 7 7612634 7612634 + Silent SNP A A G TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr7:7612634A>G c.528A>G c.(526-528)aaA>aaG p.K176K HNSC 7 7613368 7613368 + Missense_Mutation SNP C C T TCGA-CV-7177-01A-11D-2012-08 TCGA-CV-7177-10A-01D-2013-08 g.chr7:7613368C>T c.1262C>T c.(1261-1263)cCa>cTa p.P421L HNSC 7 7622858 7622858 + Silent SNP G G A TCGA-CV-7254-01A-11D-2012-08 TCGA-CV-7254-10A-01D-2013-08 g.chr7:7622858G>A c.1503G>A c.(1501-1503)aaG>aaA p.K501K HNSC 7 7628164 7628164 + Silent SNP A A G TCGA-CN-6024-01A-11D-1683-08 TCGA-CN-6024-10A-01D-1683-08 g.chr7:7628164A>G c.1854A>G c.(1852-1854)gcA>gcG p.A618A HNSC 7 7635887 7635887 + Splice_Site SNP G G C TCGA-P3-A6T6-01A-11D-A34J-08 TCGA-P3-A6T6-10A-01D-A34M-08 g.chr7:7635887G>C c.e11-1 HNSC 7 7636027 7636027 + Missense_Mutation SNP G G A TCGA-CV-7435-01A-11D-2129-08 TCGA-CV-7435-10A-01D-2129-08 g.chr7:7636027G>A c.2336G>A c.(2335-2337)cGa>cAa p.R779Q HNSC 7 7636045 7636045 + Missense_Mutation SNP G G A TCGA-DQ-5629-01A-01D-1870-08 TCGA-DQ-5629-10A-01D-1870-08 g.chr7:7636045G>A c.2354G>A c.(2353-2355)tGt>tAt p.C785Y KIPAN 7 7612146 7612146 + Missense_Mutation SNP C C G TCGA-CJ-4875-01A-01D-1373-10 TCGA-CJ-4875-11A-01D-1373-10 g.chr7:7612146C>G c.40C>G c.(40-42)Cat>Gat p.H14D KIPAN 7 7612994 7612994 + Frame_Shift_Del DEL T T - TCGA-SX-A7SL-01A-11D-A34Z-10 TCGA-SX-A7SL-10A-01D-A34Z-10 g.chr7:7612994delT c.888delT c.(886-888)tatfs p.Y296fs KIPAN 7 7635995 7635995 + Silent SNP G G T TCGA-B0-5109-01A-02D-1421-08 TCGA-B0-5109-11A-01D-1421-08 g.chr7:7635995G>T c.2304G>T c.(2302-2304)acG>acT p.T768T KIRC 7 7612146 7612146 + Missense_Mutation SNP C C G TCGA-CJ-4875-01A-01D-1373-10 TCGA-CJ-4875-11A-01D-1373-10 g.chr7:7612146C>G c.40C>G c.(40-42)Cat>Gat p.H14D KIRC 7 7635995 7635995 + Silent SNP G G T TCGA-B0-5109-01A-02D-1421-08 TCGA-B0-5109-11A-01D-1421-08 g.chr7:7635995G>T c.2304G>T c.(2302-2304)acG>acT p.T768T KIRP 7 7612994 7612994 + Frame_Shift_Del DEL T T - TCGA-SX-A7SL-01A-11D-A34Z-10 TCGA-SX-A7SL-10A-01D-A34Z-10 g.chr7:7612994delT c.888delT c.(886-888)tatfs p.Y296fs LGG 7 7612975 7612975 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr7:7612975G>T c.869G>T c.(868-870)aGt>aTt p.S290I LGG 7 7625343 7625343 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr7:7625343G>A c.1725G>A c.(1723-1725)atG>atA p.M575I LGG 7 7625428 7625428 + Frame_Shift_Del DEL G G - TCGA-DB-A64V-01A-11D-A29Q-08 TCGA-DB-A64V-10A-01D-A29Q-08 g.chr7:7625428delG c.1810delG c.(1810-1812)ggafs p.G604fs LGG 7 7646672 7646672 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr7:7646672G>A c.2577G>A c.(2575-2577)atG>atA p.M859I LIHC 7 7612424 7612424 + Silent SNP A A G TCGA-UB-A7MB-01A-11D-A33Q-10 TCGA-UB-A7MB-10A-01D-A33Q-10 g.chr7:7612424A>G c.318A>G c.(316-318)aaA>aaG p.K106K LUAD 7 7612140 7612140 + Missense_Mutation SNP C C A TCGA-86-8073-01A-11D-2238-08 TCGA-86-8073-10A-01D-2238-08 g.chr7:7612140C>A c.34C>A c.(34-36)Cca>Aca p.P12T LUAD 7 7612383 7612383 + Missense_Mutation SNP G G T TCGA-NJ-A4YQ-01A-11D-A25L-08 TCGA-NJ-A4YQ-10A-01D-A25L-08 g.chr7:7612383G>T c.277G>T c.(277-279)Ggt>Tgt p.G93C LUAD 7 7612605 7612605 + Missense_Mutation SNP G G A TCGA-50-5936-01A-11D-1625-08 TCGA-50-5936-11A-01D-1625-08 g.chr7:7612605G>A c.499G>A c.(499-501)Gaa>Aaa p.E167K LUAD 7 7612605 7612605 + Missense_Mutation SNP G G C TCGA-62-A46O-01A-11D-A24D-08 TCGA-62-A46O-10A-01D-A24F-08 g.chr7:7612605G>C c.499G>C c.(499-501)Gaa>Caa p.E167Q LUAD 7 7612758 7612758 + Nonsense_Mutation SNP C C T TCGA-55-8620-01A-11D-2393-08 TCGA-55-8620-10A-01D-2393-08 g.chr7:7612758C>T c.652C>T c.(652-654)Caa>Taa p.Q218* LUAD 7 7612858 7612858 + Frame_Shift_Del DEL G G - TCGA-35-4122-01A-01D-1105-08 TCGA-35-4122-10A-01D-1105-08 g.chr7:7612858delG c.752delG c.(751-753)tggfs p.W251fs LUAD 7 7613214 7613214 + Missense_Mutation SNP T T C TCGA-95-7562-01A-11D-2238-08 TCGA-95-7562-10B-01D-2238-08 g.chr7:7613214T>C c.1108T>C c.(1108-1110)Tgt>Cgt p.C370R LUAD 7 7613232 7613232 + Missense_Mutation SNP G G C TCGA-44-2657-01A-01D-1105-08 TCGA-44-2657-10A-01D-1105-08 g.chr7:7613232G>C c.1126G>C c.(1126-1128)Gaa>Caa p.E376Q LUAD 7 7613240 7613240 + Silent SNP G G T TCGA-NJ-A4YI-01A-11D-A25L-08 TCGA-NJ-A4YI-10A-01D-A25L-08 g.chr7:7613240G>T c.1134G>T c.(1132-1134)acG>acT p.T378T LUAD 7 7613241 7613241 + Missense_Mutation SNP G G C TCGA-NJ-A4YI-01A-11D-A25L-08 TCGA-NJ-A4YI-10A-01D-A25L-08 g.chr7:7613241G>C c.1135G>C c.(1135-1137)Gaa>Caa p.E379Q LUAD 7 7622753 7622753 + Missense_Mutation SNP G G C TCGA-05-4415-01A-22D-1855-08 TCGA-05-4415-10A-01D-1855-08 g.chr7:7622753G>C c.1398G>C c.(1396-1398)atG>atC p.M466I LUAD 7 7622761 7622761 + Missense_Mutation SNP G G T TCGA-78-7220-01A-11D-2036-08 TCGA-78-7220-10A-01D-2036-08 g.chr7:7622761G>T c.1406G>T c.(1405-1407)aGc>aTc p.S469I LUAD 7 7622959 7622959 + Missense_Mutation SNP G G T TCGA-44-8119-01A-11D-2238-08 TCGA-44-8119-10A-01D-2238-08 g.chr7:7622959G>T c.1604G>T c.(1603-1605)cGc>cTc p.R535L LUAD 7 7629038 7629038 + Missense_Mutation SNP A A T TCGA-44-6147-01A-11D-1753-08 TCGA-44-6147-10A-01D-1753-08 g.chr7:7629038A>T c.1887A>T c.(1885-1887)ttA>ttT p.L629F LUAD 7 7636007 7636007 + Silent SNP C C T TCGA-44-6777-01A-11D-1855-08 TCGA-44-6777-10A-01D-1855-08 g.chr7:7636007C>T c.2316C>T c.(2314-2316)gtC>gtT p.V772V LUSC 7 7612493 7612493 + Silent SNP A A T TCGA-56-6546-01A-11D-1817-08 TCGA-56-6546-10A-01D-1817-08 g.chr7:7612493A>T c.387A>T c.(385-387)ctA>ctT p.L129L LUSC 7 7612875 7612875 + Missense_Mutation SNP G G C TCGA-18-5595-01A-01D-1632-08 TCGA-18-5595-11A-01D-1632-08 g.chr7:7612875G>C c.769G>C c.(769-771)Gag>Cag p.E257Q LUSC 7 7612910 7612910 + Missense_Mutation SNP A A T TCGA-18-5592-01A-01D-1632-08 TCGA-18-5592-11A-11D-1632-08 g.chr7:7612910A>T c.804A>T c.(802-804)aaA>aaT p.K268N LUSC 7 7612969 7612969 + Missense_Mutation SNP G G T TCGA-66-2770-01A-01D-1522-08 TCGA-66-2770-11A-01D-1522-08 g.chr7:7612969G>T c.863G>T c.(862-864)aGg>aTg p.R288M LUSC 7 7628158 7628158 + Silent SNP A A G TCGA-85-6561-01A-11D-1817-08 TCGA-85-6561-10A-01D-1817-08 g.chr7:7628158A>G c.1848A>G c.(1846-1848)agA>agG p.R616R LUSC 7 7635937 7635937 + Missense_Mutation SNP C C T TCGA-37-3783-01A-01D-1267-08 TCGA-37-3783-10A-01D-1267-08 g.chr7:7635937C>T c.2246C>T c.(2245-2247)tCa>tTa p.S749L LUSC 7 7636041 7636041 + Silent SNP C C A TCGA-18-3419-01A-01D-0983-08 TCGA-18-3419-11A-01D-0983-08 g.chr7:7636041C>A c.2350C>A c.(2350-2352)Cga>Aga p.R784R LUSC 7 7645637 7645637 + Silent SNP C C T TCGA-37-5819-01A-01D-1632-08 TCGA-37-5819-10A-01D-1632-08 g.chr7:7645637C>T c.2466C>T c.(2464-2466)aaC>aaT p.N822N PAAD 7 7625382 7625382 + Missense_Mutation SNP G G C TCGA-IB-A5SO-01A-11D-A32N-08 TCGA-IB-A5SO-10A-01D-A32N-08 g.chr7:7625382G>C c.1764G>C c.(1762-1764)ttG>ttC p.L588F PRAD 7 7613322 7613322 + Missense_Mutation SNP A A G TCGA-KK-A6E2-01A-11D-A30X-08 TCGA-KK-A6E2-11A-21D-A30X-08 g.chr7:7613322A>G c.1216A>G c.(1216-1218)Aca>Gca p.T406A PRAD 7 7635987 7635987 + Missense_Mutation SNP T T A TCGA-V1-A9OQ-01A-11D-A41K-08 TCGA-V1-A9OQ-10A-01D-A41N-08 g.chr7:7635987T>A c.2296T>A c.(2296-2298)Tca>Aca p.S766T PRAD 7 7645694 7645694 + Silent SNP T T C TCGA-EJ-7782-01A-11D-2114-08 TCGA-EJ-7782-10A-01D-2114-08 g.chr7:7645694T>C c.2523T>C c.(2521-2523)agT>agC p.S841S READ 7 7613247 7613247 + Nonsense_Mutation SNP G G T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr7:7613247G>T c.1141G>T c.(1141-1143)Gaa>Taa p.E381* READ 7 7613282 7613282 + Silent SNP G G A TCGA-AG-A025-01A-01W-A00E-09 TCGA-AG-A025-10A-01W-A00E-09 g.chr7:7613282G>A c.1176G>A c.(1174-1176)acG>acA p.T392T READ 7 7622772 7622772 + Missense_Mutation SNP A A C TCGA-CL-5918-01A-11D-1657-10 TCGA-CL-5918-10A-01D-1657-10 g.chr7:7622772A>C c.1417A>C c.(1417-1419)Aat>Cat p.N473H READ 7 7646629 7646629 + Missense_Mutation SNP A A T TCGA-F5-6811-01A-11D-1826-10 TCGA-F5-6811-10A-01D-1826-10 g.chr7:7646629A>T c.2534A>T c.(2533-2535)gAc>gTc p.D845V SKCM 7 7612814 7612814 + Silent SNP C C T TCGA-EE-A2GO-06A-11D-A196-08 TCGA-EE-A2GO-10A-01D-A198-08 g.chr7:7612814C>T c.708C>T c.(706-708)ttC>ttT p.F236F SKCM 7 7612821 7612821 + Missense_Mutation SNP C C T TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr7:7612821C>T c.715C>T c.(715-717)Cgt>Tgt p.R239C SKCM 7 7628141 7628141 + Missense_Mutation SNP G G A TCGA-D3-A3ML-06A-11D-A21A-08 TCGA-D3-A3ML-10A-01D-A21A-08 g.chr7:7628141G>A c.1831G>A c.(1831-1833)Gtt>Att p.V611I SKCM 7 7628142 7628142 + Missense_Mutation SNP T T A TCGA-D3-A3ML-06A-11D-A21A-08 TCGA-D3-A3ML-10A-01D-A21A-08 g.chr7:7628142T>A c.1832T>A c.(1831-1833)gTt>gAt p.V611D SKCM 7 7628179 7628179 + Silent SNP C C T TCGA-D3-A2JD-06A-11D-A19A-08 TCGA-D3-A2JD-10A-01D-A19A-08 g.chr7:7628179C>T c.1869C>T c.(1867-1869)ttC>ttT p.F623F SKCM 7 7645580 7645580 + Silent SNP C C T TCGA-EE-A29L-06A-12D-A196-08 TCGA-EE-A29L-10A-01D-A198-08 g.chr7:7645580C>T c.2409C>T c.(2407-2409)acC>acT p.T803T SKCM 7 7645637 7645637 + Silent SNP C C T TCGA-EE-A3JA-06A-11D-A20D-08 TCGA-EE-A3JA-10A-01D-A20D-08 g.chr7:7645637C>T c.2466C>T c.(2464-2466)aaC>aaT p.N822N SKCM 7 7646670 7646670 + Missense_Mutation SNP A A G TCGA-DA-A1I1-06A-12D-A196-08 TCGA-DA-A1I1-10A-01D-A198-08 g.chr7:7646670A>G c.2575A>G c.(2575-2577)Atg>Gtg p.M859V

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BLCA-CN 7 7612156 7612156 single base substitution G A missense_variant R17K 50G>A BLCA-CN 7 7625355 7625355 single base substitution G A downstream_gene_variant BLCA-CN 7 7625355 7625355 single base substitution G A exon_variant BLCA-CN 7 7625355 7625355 single base substitution G A synonymous_variant L579L 1737G>A BLCA-US 7 7612191 7612191 single base substitution C G missense_variant H29D 85C>G BLCA-US 7 7622975 7622975 single base substitution C G exon_variant BLCA-US 7 7622975 7622975 single base substitution C G missense_variant I540M 1620C>G BLCA-US 7 7628157 7628157 single base substitution G C exon_variant BLCA-US 7 7628157 7628157 single base substitution G C missense_variant R616T 1847G>C BLCA-US 7 7636000 7636000 single base substitution C A exon_variant BLCA-US 7 7636000 7636000 single base substitution C A missense_variant S770Y 2309C>A BOCA-FR 7 7623009 7623009 single base substitution A C downstream_gene_variant BOCA-FR 7 7623009 7623009 single base substitution A C intron_variant BOCA-FR 7 7623009 7623009 single base substitution A C splice_region_variant BRCA-EU 7 7603052 7603052 single base substitution G T upstream_gene_variant BRCA-EU 7 7603118 7603118 single base substitution G C upstream_gene_variant BRCA-EU 7 7603185 7603185 single base substitution A G upstream_gene_variant BRCA-EU 7 7605138 7605138 insertion of <=200bp - T upstream_gene_variant BRCA-EU 7 7605197 7605197 single base substitution C A upstream_gene_variant BRCA-EU 7 7605614 7605614 single base substitution C G upstream_gene_variant BRCA-EU 7 7605689 7605689 insertion of <=200bp - A upstream_gene_variant BRCA-EU 7 7605936 7605936 single base substitution C A upstream_gene_variant BRCA-EU 7 7606074 7606074 insertion of <=200bp - C upstream_gene_variant BRCA-EU 7 7606540 7606540 single base substitution C A 5_prime_UTR_variant BRCA-EU 7 7606540 7606540 single base substitution C A upstream_gene_variant BRCA-EU 7 7609713 7609713 single base substitution C G intron_variant BRCA-EU 7 7610101 7610101 single base substitution G A intron_variant BRCA-EU 7 7611893 7611893 deletion of <=200bp T - intron_variant BRCA-EU 7 7612342 7612342 single base substitution C G downstream_gene_variant BRCA-EU 7 7612342 7612342 single base substitution C G missense_variant A79G 236C>G BRCA-EU 7 7613290 7613290 single base substitution G A downstream_gene_variant BRCA-EU 7 7613290 7613290 single base substitution G A missense_variant R395H 1184G>A BRCA-EU 7 7613920 7613920 single base substitution T A downstream_gene_variant BRCA-EU 7 7613920 7613920 single base substitution T A intron_variant BRCA-EU 7 7613939 7613939 insertion of <=200bp - T downstream_gene_variant BRCA-EU 7 7613939 7613939 insertion of <=200bp - T intron_variant BRCA-EU 7 7614538 7614538 single base substitution T C downstream_gene_variant BRCA-EU 7 7614538 7614538 single base substitution T C intron_variant BRCA-EU 7 7618548 7618548 single base substitution G A intron_variant BRCA-EU 7 7618548 7618548 single base substitution G A upstream_gene_variant BRCA-EU 7 7618594 7618594 single base substitution G C intron_variant BRCA-EU 7 7618594 7618594 single base substitution G C upstream_gene_variant BRCA-EU 7 7619502 7619502 single base substitution G A intron_variant BRCA-EU 7 7619502 7619502 single base substitution G A upstream_gene_variant BRCA-EU 7 7619622 7619622 single base substitution T A intron_variant BRCA-EU 7 7619622 7619622 single base substitution T A upstream_gene_variant BRCA-EU 7 7621281 7621281 single base substitution T A intron_variant BRCA-EU 7 7621281 7621281 single base substitution T A upstream_gene_variant BRCA-EU 7 7622713 7622713 single base substitution G C exon_variant BRCA-EU 7 7622713 7622713 single base substitution G C intron_variant BRCA-EU 7 7623110 7623110 single base substitution A T downstream_gene_variant BRCA-EU 7 7623110 7623110 single base substitution A T intron_variant BRCA-EU 7 7624727 7624727 single base substitution G C downstream_gene_variant BRCA-EU 7 7624727 7624727 single base substitution G C intron_variant BRCA-EU 7 7625604 7625604 single base substitution T C downstream_gene_variant BRCA-EU 7 7625604 7625604 single base substitution T C intron_variant BRCA-EU 7 7625937 7625937 single base substitution T G downstream_gene_variant BRCA-EU 7 7625937 7625937 single base substitution T G intron_variant BRCA-EU 7 7625974 7625974 single base substitution T A downstream_gene_variant BRCA-EU 7 7625974 7625974 single base substitution T A intron_variant BRCA-EU 7 7628027 7628027 single base substitution A G intron_variant BRCA-EU 7 7630676 7630676 single base substitution T A intron_variant BRCA-EU 7 7630857 7630857 single base substitution C G intron_variant BRCA-EU 7 7632859 7632859 single base substitution T A intron_variant BRCA-EU 7 7633838 7633838 single base substitution G C intron_variant BRCA-EU 7 7635263 7635263 single base substitution C G intron_variant BRCA-EU 7 7637911 7637911 single base substitution C G intron_variant BRCA-EU 7 7638470 7638470 single base substitution G C intron_variant BRCA-EU 7 7639037 7639037 single base substitution G A intron_variant BRCA-EU 7 7639099 7639099 single base substitution G A intron_variant BRCA-EU 7 7639250 7639250 single base substitution G C intron_variant BRCA-EU 7 7639826 7639826 single base substitution A C intron_variant BRCA-EU 7 7639826 7639826 single base substitution A C upstream_gene_variant BRCA-EU 7 7640359 7640359 single base substitution C A intron_variant BRCA-EU 7 7640359 7640359 single base substitution C A upstream_gene_variant BRCA-EU 7 7640366 7640366 single base substitution A T intron_variant BRCA-EU 7 7640366 7640366 single base substitution A T upstream_gene_variant BRCA-EU 7 7640808 7640808 single base substitution C G intron_variant BRCA-EU 7 7640808 7640808 single base substitution C G upstream_gene_variant BRCA-EU 7 7642010 7642010 single base substitution C G intron_variant BRCA-EU 7 7642010 7642010 single base substitution C G upstream_gene_variant BRCA-EU 7 7642121 7642121 single base substitution T A intron_variant BRCA-EU 7 7642121 7642121 single base substitution T A upstream_gene_variant BRCA-EU 7 7642132 7642132 single base substitution G C intron_variant BRCA-EU 7 7642132 7642132 single base substitution G C upstream_gene_variant BRCA-EU 7 7642173 7642173 single base substitution G A intron_variant BRCA-EU 7 7642173 7642173 single base substitution G A upstream_gene_variant BRCA-EU 7 7643394 7643394 single base substitution G A intron_variant BRCA-EU 7 7643394 7643394 single base substitution G A upstream_gene_variant BRCA-EU 7 7644121 7644121 single base substitution G A intron_variant BRCA-EU 7 7644121 7644121 single base substitution G A upstream_gene_variant BRCA-EU 7 7644518 7644518 single base substitution C T intron_variant BRCA-EU 7 7644518 7644518 single base substitution C T upstream_gene_variant BRCA-EU 7 7644525 7644525 single base substitution A G intron_variant BRCA-EU 7 7644525 7644525 single base substitution A G upstream_gene_variant BRCA-EU 7 7646618 7646618 deletion of <=200bp T - intron_variant BRCA-EU 7 7646879 7646879 single base substitution T A 3_prime_UTR_variant BRCA-EU 7 7646879 7646879 single base substitution T A downstream_gene_variant BRCA-EU 7 7646879 7646879 single base substitution T A exon_variant BRCA-EU 7 7649301 7649301 single base substitution A T downstream_gene_variant BRCA-EU 7 7650324 7650324 single base substitution G A downstream_gene_variant BRCA-EU 7 7650730 7650730 single base substitution C G downstream_gene_variant BRCA-EU 7 7651159 7651159 single base substitution C T downstream_gene_variant BRCA-EU 7 7651424 7651424 single base substitution A G downstream_gene_variant BRCA-EU 7 7651469 7651469 single base substitution G T downstream_gene_variant BRCA-EU 7 7652730 7652730 single base substitution C T downstream_gene_variant BRCA-FR 7 7605609 7605609 single base substitution G A upstream_gene_variant BRCA-FR 7 7605936 7605936 single base substitution C A upstream_gene_variant BRCA-FR 7 7610101 7610101 single base substitution G A intron_variant BRCA-FR 7 7614538 7614538 single base substitution T C downstream_gene_variant BRCA-FR 7 7614538 7614538 single base substitution T C intron_variant BRCA-FR 7 7618594 7618594 single base substitution G C intron_variant BRCA-FR 7 7618594 7618594 single base substitution G C upstream_gene_variant BRCA-FR 7 7619622 7619622 single base substitution T A intron_variant BRCA-FR 7 7619622 7619622 single base substitution T A upstream_gene_variant BRCA-FR 7 7640950 7640950 single base substitution T C intron_variant BRCA-FR 7 7640950 7640950 single base substitution T C upstream_gene_variant BRCA-FR 7 7644887 7644887 single base substitution G A exon_variant BRCA-FR 7 7644887 7644887 single base substitution G A intron_variant BRCA-FR 7 7648950 7648950 single base substitution G C downstream_gene_variant BRCA-KR 7 7612899 7612899 single base substitution G A downstream_gene_variant BRCA-KR 7 7612899 7612899 single base substitution G A missense_variant E265K 793G>A BRCA-US 7 7612672 7612672 single base substitution C G downstream_gene_variant BRCA-US 7 7612672 7612672 single base substitution C G missense_variant S189C 566C>G BRCA-US 7 7636043 7636043 single base substitution A T exon_variant BRCA-US 7 7636043 7636043 single base substitution A T synonymous_variant R784R 2352A>T BTCA-JP 7 7629060 7629060 single base substitution A T exon_variant BTCA-JP 7 7629060 7629060 single base substitution A T missense_variant T637S 1909A>T CESC-US 7 7622951 7622951 single base substitution G C exon_variant CESC-US 7 7622951 7622951 single base substitution G C missense_variant L532F 1596G>C CESC-US 7 7634623 7634623 single base substitution G A exon_variant CESC-US 7 7634623 7634623 single base substitution G A missense_variant D686N 2056G>A CLLE-ES 7 7611631 7611631 single base substitution A G intron_variant CLLE-ES 7 7615079 7615079 single base substitution A G downstream_gene_variant CLLE-ES 7 7615079 7615079 single base substitution A G intron_variant CLLE-ES 7 7635991 7635991 single base substitution C G exon_variant CLLE-ES 7 7635991 7635991 single base substitution C G missense_variant P767R 2300C>G CLLE-ES 7 7645013 7645013 single base substitution A G exon_variant CLLE-ES 7 7645013 7645013 single base substitution A G intron_variant COAD-US 7 7612803 7612803 single base substitution G T downstream_gene_variant COAD-US 7 7612803 7612803 single base substitution G T missense_variant D233Y 697G>T COAD-US 7 7613140 7613140 single base substitution G A downstream_gene_variant COAD-US 7 7613140 7613140 single base substitution G A missense_variant R345Q 1034G>A COAD-US 7 7634642 7634642 single base substitution G A exon_variant COAD-US 7 7634642 7634642 single base substitution G A missense_variant R692K 2075G>A COAD-US 7 7636027 7636027 single base substitution G A exon_variant COAD-US 7 7636027 7636027 single base substitution G A missense_variant R779Q 2336G>A COAD-US 7 7645613 7645613 insertion of <=200bp - A exon_variant COAD-US 7 7645613 7645613 insertion of <=200bp - A frameshift_variant D814E? COAD-US 7 7646669 7646669 single base substitution T G exon_variant COAD-US 7 7646669 7646669 single base substitution T G missense_variant C858W 2574T>G COCA-CN 7 7605992 7605992 single base substitution T C upstream_gene_variant COCA-CN 7 7622807 7622807 single base substitution A C exon_variant COCA-CN 7 7622807 7622807 single base substitution A C missense_variant Q484H 1452A>C COCA-CN 7 7622866 7622866 single base substitution C T exon_variant COCA-CN 7 7622866 7622866 single base substitution C T missense_variant T504M 1511C>T COCA-CN 7 7625391 7625391 single base substitution G C downstream_gene_variant COCA-CN 7 7625391 7625391 single base substitution G C exon_variant COCA-CN 7 7625391 7625391 single base substitution G C missense_variant M591I 1773G>C COCA-CN 7 7636059 7636059 single base substitution A C exon_variant COCA-CN 7 7636059 7636059 single base substitution A C missense_variant I790L 2368A>C COCA-CN 7 7643286 7643286 single base substitution G A intron_variant COCA-CN 7 7643286 7643286 single base substitution G A upstream_gene_variant EOPC-DE 7 7608059 7608059 single base substitution C G intron_variant ESAD-UK 7 7601962 7601962 single base substitution C T upstream_gene_variant ESAD-UK 7 7602953 7602953 insertion of <=200bp - A upstream_gene_variant ESAD-UK 7 7603174 7603174 single base substitution A C upstream_gene_variant ESAD-UK 7 7604230 7604230 single base substitution G A upstream_gene_variant ESAD-UK 7 7606172 7606172 single base substitution A C upstream_gene_variant ESAD-UK 7 7607887 7607887 single base substitution C T intron_variant ESAD-UK 7 7608195 7608195 single base substitution G A intron_variant ESAD-UK 7 7611456 7611456 single base substitution G A intron_variant ESAD-UK 7 7612684 7612684 single base substitution T C downstream_gene_variant ESAD-UK 7 7612684 7612684 single base substitution T C missense_variant L193P 578T>C ESAD-UK 7 7613244 7613244 single base substitution G T downstream_gene_variant ESAD-UK 7 7613244 7613244 single base substitution G T stop_gained E380* 1138G>T ESAD-UK 7 7615174 7615174 single base substitution G T downstream_gene_variant ESAD-UK 7 7615174 7615174 single base substitution G T intron_variant ESAD-UK 7 7616065 7616065 single base substitution G A downstream_gene_variant ESAD-UK 7 7616065 7616065 single base substitution G A intron_variant ESAD-UK 7 7616841 7616841 single base substitution T C downstream_gene_variant ESAD-UK 7 7616841 7616841 single base substitution T C intron_variant ESAD-UK 7 7616841 7616841 single base substitution T C upstream_gene_variant ESAD-UK 7 7617088 7617088 single base substitution G A downstream_gene_variant ESAD-UK 7 7617088 7617088 single base substitution G A intron_variant ESAD-UK 7 7617088 7617088 single base substitution G A upstream_gene_variant ESAD-UK 7 7617237 7617237 single base substitution C T downstream_gene_variant ESAD-UK 7 7617237 7617237 single base substitution C T intron_variant ESAD-UK 7 7617237 7617237 single base substitution C T upstream_gene_variant ESAD-UK 7 7618487 7618487 single base substitution G A intron_variant ESAD-UK 7 7618487 7618487 single base substitution G A upstream_gene_variant ESAD-UK 7 7618683 7618683 single base substitution G A intron_variant ESAD-UK 7 7618683 7618683 single base substitution G A upstream_gene_variant ESAD-UK 7 7619501 7619501 single base substitution C T intron_variant ESAD-UK 7 7619501 7619501 single base substitution C T upstream_gene_variant ESAD-UK 7 7620750 7620750 single base substitution C T intron_variant ESAD-UK 7 7620750 7620750 single base substitution C T upstream_gene_variant ESAD-UK 7 7623379 7623379 single base substitution T C downstream_gene_variant ESAD-UK 7 7623379 7623379 single base substitution T C intron_variant ESAD-UK 7 7623593 7623593 single base substitution G A downstream_gene_variant ESAD-UK 7 7623593 7623593 single base substitution G A intron_variant ESAD-UK 7 7624749 7624749 single base substitution A G downstream_gene_variant ESAD-UK 7 7624749 7624749 single base substitution A G intron_variant ESAD-UK 7 7624920 7624920 single base substitution G A downstream_gene_variant ESAD-UK 7 7624920 7624920 single base substitution G A intron_variant ESAD-UK 7 7629595 7629595 single base substitution C G intron_variant ESAD-UK 7 7632438 7632439 deletion of <=200bp AT - intron_variant ESAD-UK 7 7632441 7632447 deletion of <=200bp AAGCTTT - intron_variant ESAD-UK 7 7632543 7632543 single base substitution C A intron_variant ESAD-UK 7 7634303 7634303 single base substitution T C intron_variant ESAD-UK 7 7635398 7635398 single base substitution G T intron_variant ESAD-UK 7 7637673 7637673 single base substitution T A intron_variant ESAD-UK 7 7640158 7640158 single base substitution T C intron_variant ESAD-UK 7 7640158 7640158 single base substitution T C upstream_gene_variant ESAD-UK 7 7641798 7641798 single base substitution A G intron_variant ESAD-UK 7 7641798 7641798 single base substitution A G upstream_gene_variant ESAD-UK 7 7641800 7641800 single base substitution A C intron_variant ESAD-UK 7 7641800 7641800 single base substitution A C upstream_gene_variant ESAD-UK 7 7641804 7641804 single base substitution A G intron_variant ESAD-UK 7 7641804 7641804 single base substitution A G upstream_gene_variant ESAD-UK 7 7645114 7645114 single base substitution C T exon_variant ESAD-UK 7 7645114 7645114 single base substitution C T intron_variant ESAD-UK 7 7645229 7645229 single base substitution C T exon_variant ESAD-UK 7 7645229 7645229 single base substitution C T intron_variant ESAD-UK 7 7646364 7646364 single base substitution C G intron_variant ESAD-UK 7 7646556 7646556 insertion of <=200bp - AAAT intron_variant ESAD-UK 7 7646605 7646605 single base substitution G T intron_variant ESAD-UK 7 7646852 7646852 single base substitution A G 3_prime_UTR_variant ESAD-UK 7 7646852 7646852 single base substitution A G exon_variant ESAD-UK 7 7647149 7647149 single base substitution C T downstream_gene_variant ESAD-UK 7 7647149 7647149 single base substitution C T exon_variant ESAD-UK 7 7647483 7647483 deletion of <=200bp T - downstream_gene_variant ESAD-UK 7 7647483 7647483 deletion of <=200bp T - exon_variant ESAD-UK 7 7647874 7647874 single base substitution C T downstream_gene_variant ESAD-UK 7 7647874 7647874 single base substitution C T exon_variant ESAD-UK 7 7649304 7649304 single base substitution T G downstream_gene_variant ESAD-UK 7 7651700 7651700 single base substitution C A downstream_gene_variant ESAD-UK 7 7652299 7652299 single base substitution C T downstream_gene_variant ESCA-CN 7 7613223 7613223 single base substitution C T downstream_gene_variant ESCA-CN 7 7613223 7613223 single base substitution C T missense_variant H373Y 1117C>T ESCA-CN 7 7613271 7613271 single base substitution G C downstream_gene_variant ESCA-CN 7 7613271 7613271 single base substitution G C missense_variant D389H 1165G>C ESCA-CN 7 7622813 7622813 single base substitution A T exon_variant ESCA-CN 7 7622813 7622813 single base substitution A T missense_variant L486F 1458A>T GACA-CN 7 7612506 7612506 single base substitution G A downstream_gene_variant GACA-CN 7 7612506 7612506 single base substitution G A missense_variant D134N 400G>A GBM-US 7 7612689 7612689 single base substitution C T downstream_gene_variant GBM-US 7 7612689 7612689 single base substitution C T stop_gained R195* 583C>T KIRC-US 7 7612146 7612146 single base substitution C G missense_variant H14D 40C>G KIRC-US 7 7635995 7635995 single base substitution G T exon_variant KIRC-US 7 7635995 7635995 single base substitution G T synonymous_variant T768T 2304G>T KIRC-US 7 7636022 7636022 single base substitution C T exon_variant KIRC-US 7 7636022 7636022 single base substitution C T synonymous_variant G777G 2331C>T LAML-KR 7 7630945 7630945 single base substitution G T intron_variant LGG-US 7 7625428 7625428 deletion of <=200bp G - downstream_gene_variant LGG-US 7 7625428 7625428 deletion of <=200bp G - exon_variant LGG-US 7 7625428 7625428 deletion of <=200bp G - frameshift_variant G604 LICA-CN 7 7625282 7625282 single base substitution A G downstream_gene_variant LICA-CN 7 7625282 7625282 single base substitution A G exon_variant LICA-CN 7 7625282 7625282 single base substitution A G missense_variant N555S 1664A>G LICA-FR 7 7613754 7613754 single base substitution G A downstream_gene_variant LICA-FR 7 7613754 7613754 single base substitution G A missense_variant M440I 1320G>A LICA-FR 7 7614684 7614684 single base substitution A G downstream_gene_variant LICA-FR 7 7614684 7614684 single base substitution A G intron_variant LICA-FR 7 7615677 7615677 single base substitution C A downstream_gene_variant LICA-FR 7 7615677 7615677 single base substitution C A intron_variant LICA-FR 7 7618368 7618368 single base substitution C G intron_variant LICA-FR 7 7618368 7618368 single base substitution C G upstream_gene_variant LICA-FR 7 7630227 7630227 single base substitution G A intron_variant LICA-FR 7 7634494 7634494 insertion of <=200bp - AA intron_variant LICA-FR 7 7644672 7644672 single base substitution A C intron_variant LICA-FR 7 7644672 7644672 single base substitution A C upstream_gene_variant LICA-FR 7 7645613 7645613 single base substitution C A exon_variant LICA-FR 7 7645613 7645613 single base substitution C A missense_variant D814E 2442C>A LICA-FR 7 7647757 7647757 single base substitution A T downstream_gene_variant LICA-FR 7 7647757 7647757 single base substitution A T exon_variant LIHC-US 7 7612424 7612424 single base substitution A G downstream_gene_variant LIHC-US 7 7612424 7612424 single base substitution A G synonymous_variant K106K 318A>G LINC-JP 7 7607162 7607162 single base substitution G T 5_prime_UTR_variant LINC-JP 7 7607162 7607162 single base substitution G T intron_variant LINC-JP 7 7612362 7612362 single base substitution C G downstream_gene_variant LINC-JP 7 7612362 7612362 single base substitution C G missense_variant R86G 256C>G LINC-JP 7 7613015 7613015 single base substitution T G downstream_gene_variant LINC-JP 7 7613015 7613015 single base substitution T G synonymous_variant T303T 909T>G LINC-JP 7 7613668 7613668 single base substitution A G downstream_gene_variant LINC-JP 7 7613668 7613668 single base substitution A G intron_variant LINC-JP 7 7615523 7615523 single base substitution G T downstream_gene_variant LINC-JP 7 7615523 7615523 single base substitution G T intron_variant LINC-JP 7 7625548 7625548 single base substitution A G downstream_gene_variant LINC-JP 7 7625548 7625548 single base substitution A G intron_variant LINC-JP 7 7629242 7629242 single base substitution A G intron_variant LINC-JP 7 7634786 7634786 single base substitution A C intron_variant LINC-JP 7 7636975 7636975 single base substitution T G intron_variant LINC-JP 7 7642210 7642210 single base substitution A T intron_variant LINC-JP 7 7642210 7642210 single base substitution A T upstream_gene_variant LINC-JP 7 7644141 7644141 single base substitution A T intron_variant LINC-JP 7 7644141 7644141 single base substitution A T upstream_gene_variant LINC-JP 7 7645488 7645488 single base substitution A G exon_variant LINC-JP 7 7645488 7645488 single base substitution A G intron_variant LINC-JP 7 7645775 7645775 single base substitution G C intron_variant LIRI-JP 7 7602319 7602319 single base substitution A G upstream_gene_variant LIRI-JP 7 7606070 7606070 single base substitution T C upstream_gene_variant LIRI-JP 7 7607792 7607792 single base substitution G A intron_variant LIRI-JP 7 7608197 7608197 single base substitution A G intron_variant LIRI-JP 7 7608646 7608646 single base substitution G A intron_variant LIRI-JP 7 7608743 7608743 single base substitution A G intron_variant LIRI-JP 7 7608884 7608884 single base substitution A C intron_variant LIRI-JP 7 7609458 7609458 single base substitution G A intron_variant LIRI-JP 7 7610747 7610747 single base substitution G T intron_variant LIRI-JP 7 7612060 7612060 deletion of <=200bp T - intron_variant LIRI-JP 7 7612060 7612060 deletion of <=200bp T - splice_region_variant LIRI-JP 7 7612722 7612722 single base substitution C A downstream_gene_variant LIRI-JP 7 7612722 7612722 single base substitution C A missense_variant R206S 616C>A LIRI-JP 7 7615766 7615766 single base substitution A G downstream_gene_variant LIRI-JP 7 7615766 7615766 single base substitution A G intron_variant LIRI-JP 7 7616114 7616114 single base substitution G T downstream_gene_variant LIRI-JP 7 7616114 7616114 single base substitution G T intron_variant LIRI-JP 7 7618465 7618465 single base substitution C G intron_variant LIRI-JP 7 7618465 7618465 single base substitution C G upstream_gene_variant LIRI-JP 7 7618510 7618510 single base substitution T G intron_variant LIRI-JP 7 7618510 7618510 single base substitution T G upstream_gene_variant LIRI-JP 7 7623451 7623451 single base substitution T G downstream_gene_variant LIRI-JP 7 7623451 7623451 single base substitution T G intron_variant LIRI-JP 7 7623551 7623551 single base substitution A T downstream_gene_variant LIRI-JP 7 7623551 7623551 single base substitution A T intron_variant LIRI-JP 7 7624967 7624967 single base substitution A G downstream_gene_variant LIRI-JP 7 7624967 7624967 single base substitution A G intron_variant LIRI-JP 7 7625566 7625566 single base substitution C T downstream_gene_variant LIRI-JP 7 7625566 7625566 single base substitution C T intron_variant LIRI-JP 7 7630588 7630588 single base substitution A G intron_variant LIRI-JP 7 7630598 7630598 single base substitution T A intron_variant LIRI-JP 7 7630787 7630787 single base substitution G A intron_variant LIRI-JP 7 7631044 7631044 single base substitution G A intron_variant LIRI-JP 7 7631163 7631163 single base substitution G A intron_variant LIRI-JP 7 7631833 7631833 single base substitution T C intron_variant LIRI-JP 7 7636756 7636756 single base substitution G A intron_variant LIRI-JP 7 7637222 7637222 single base substitution A G intron_variant LIRI-JP 7 7637393 7637393 single base substitution G C intron_variant LIRI-JP 7 7638003 7638003 single base substitution T C intron_variant LIRI-JP 7 7640377 7640377 single base substitution C A intron_variant LIRI-JP 7 7640377 7640377 single base substitution C A upstream_gene_variant LIRI-JP 7 7643028 7643028 single base substitution C T intron_variant LIRI-JP 7 7643028 7643028 single base substitution C T upstream_gene_variant LIRI-JP 7 7644290 7644290 single base substitution A G intron_variant LIRI-JP 7 7644290 7644290 single base substitution A G upstream_gene_variant LIRI-JP 7 7644435 7644435 single base substitution A G intron_variant LIRI-JP 7 7644435 7644435 single base substitution A G upstream_gene_variant LIRI-JP 7 7645126 7645126 single base substitution A G exon_variant LIRI-JP 7 7645126 7645126 single base substitution A G intron_variant LIRI-JP 7 7647595 7647595 single base substitution A T downstream_gene_variant LIRI-JP 7 7647595 7647595 single base substitution A T exon_variant LIRI-JP 7 7649358 7649358 single base substitution A G downstream_gene_variant LIRI-JP 7 7649362 7649362 single base substitution A T downstream_gene_variant LIRI-JP 7 7650712 7650712 insertion of <=200bp - A downstream_gene_variant LIRI-JP 7 7651682 7651682 single base substitution C G downstream_gene_variant LIRI-JP 7 7651683 7651683 single base substitution A T downstream_gene_variant LIRI-JP 7 7651718 7651725 deletion of <=200bp ATATATGT - downstream_gene_variant LIRI-JP 7 7651806 7651806 single base substitution A G downstream_gene_variant LIRI-JP 7 7652477 7652477 single base substitution T C downstream_gene_variant LUSC-KR 7 7604192 7604192 single base substitution C A upstream_gene_variant LUSC-KR 7 7604193 7604193 single base substitution C A upstream_gene_variant LUSC-KR 7 7611367 7611367 single base substitution G A intron_variant LUSC-KR 7 7611618 7611618 single base substitution A G intron_variant LUSC-KR 7 7616465 7616465 single base substitution A G downstream_gene_variant LUSC-KR 7 7616465 7616465 single base substitution A G intron_variant LUSC-KR 7 7616465 7616465 single base substitution A G upstream_gene_variant LUSC-KR 7 7617068 7617068 single base substitution A G downstream_gene_variant LUSC-KR 7 7617068 7617068 single base substitution A G intron_variant LUSC-KR 7 7617068 7617068 single base substitution A G upstream_gene_variant LUSC-KR 7 7621954 7621954 single base substitution C A intron_variant LUSC-KR 7 7621954 7621954 single base substitution C A upstream_gene_variant LUSC-KR 7 7623347 7623347 single base substitution A G downstream_gene_variant LUSC-KR 7 7623347 7623347 single base substitution A G intron_variant LUSC-KR 7 7625029 7625029 single base substitution C G downstream_gene_variant LUSC-KR 7 7625029 7625029 single base substitution C G intron_variant LUSC-KR 7 7627714 7627714 single base substitution C A downstream_gene_variant LUSC-KR 7 7627714 7627714 single base substitution C A intron_variant LUSC-KR 7 7631795 7631795 single base substitution A G intron_variant LUSC-KR 7 7633136 7633136 single base substitution A G intron_variant LUSC-KR 7 7633619 7633619 single base substitution A G intron_variant LUSC-KR 7 7640903 7640903 single base substitution T A intron_variant LUSC-KR 7 7640903 7640903 single base substitution T A upstream_gene_variant LUSC-KR 7 7642801 7642801 single base substitution C G intron_variant LUSC-KR 7 7642801 7642801 single base substitution C G upstream_gene_variant LUSC-US 7 7612493 7612493 single base substitution A T downstream_gene_variant LUSC-US 7 7612493 7612493 single base substitution A T synonymous_variant L129L 387A>T LUSC-US 7 7612875 7612875 single base substitution G C downstream_gene_variant LUSC-US 7 7612875 7612875 single base substitution G C missense_variant E257Q 769G>C LUSC-US 7 7612910 7612910 single base substitution A T downstream_gene_variant LUSC-US 7 7612910 7612910 single base substitution A T missense_variant K268N 804A>T LUSC-US 7 7612969 7612969 single base substitution G T downstream_gene_variant LUSC-US 7 7612969 7612969 single base substitution G T missense_variant R288M 863G>T LUSC-US 7 7628158 7628158 single base substitution A G exon_variant LUSC-US 7 7628158 7628158 single base substitution A G synonymous_variant R616R 1848A>G LUSC-US 7 7635937 7635937 single base substitution C T exon_variant LUSC-US 7 7635937 7635937 single base substitution C T missense_variant S749L 2246C>T LUSC-US 7 7636041 7636041 single base substitution C A exon_variant LUSC-US 7 7636041 7636041 single base substitution C A synonymous_variant R784R 2350C>A LUSC-US 7 7645637 7645637 single base substitution C T exon_variant LUSC-US 7 7645637 7645637 single base substitution C T synonymous_variant N822N 2466C>T MALY-DE 7 7602474 7602474 single base substitution A G upstream_gene_variant MALY-DE 7 7603096 7603096 single base substitution A C upstream_gene_variant MALY-DE 7 7605282 7605282 single base substitution C T upstream_gene_variant MALY-DE 7 7606632 7606632 single base substitution C T 5_prime_UTR_variant MALY-DE 7 7606632 7606632 single base substitution C T upstream_gene_variant MALY-DE 7 7607127 7607127 single base substitution T A 5_prime_UTR_variant MALY-DE 7 7607127 7607127 single base substitution T A intron_variant MALY-DE 7 7607961 7607961 single base substitution G A intron_variant MALY-DE 7 7608404 7608404 single base substitution C T intron_variant MALY-DE 7 7609084 7609084 single base substitution G A intron_variant MALY-DE 7 7622163 7622163 single base substitution A G intron_variant MALY-DE 7 7622163 7622163 single base substitution A G upstream_gene_variant MALY-DE 7 7623770 7623770 single base substitution G A downstream_gene_variant MALY-DE 7 7623770 7623770 single base substitution G A intron_variant MALY-DE 7 7628159 7628159 single base substitution G T exon_variant MALY-DE 7 7628159 7628159 single base substitution G T missense_variant V617L 1849G>T MALY-DE 7 7629751 7629751 single base substitution T G intron_variant MALY-DE 7 7637319 7637319 insertion of <=200bp - T intron_variant MALY-DE 7 7651843 7651843 single base substitution G C downstream_gene_variant MELA-AU 7 7601625 7601625 single base substitution A C upstream_gene_variant MELA-AU 7 7602341 7602341 single base substitution A G upstream_gene_variant MELA-AU 7 7602384 7602384 single base substitution G A upstream_gene_variant MELA-AU 7 7602639 7602639 single base substitution A G upstream_gene_variant MELA-AU 7 7602647 7602647 single base substitution G C upstream_gene_variant MELA-AU 7 7602970 7602970 single base substitution A C upstream_gene_variant MELA-AU 7 7603431 7603431 single base substitution G A upstream_gene_variant MELA-AU 7 7603810 7603810 single base substitution G A upstream_gene_variant MELA-AU 7 7604820 7604820 single base substitution G A upstream_gene_variant MELA-AU 7 7605668 7605668 single base substitution G A upstream_gene_variant MELA-AU 7 7605682 7605682 single base substitution C T upstream_gene_variant MELA-AU 7 7605841 7605841 single base substitution C T upstream_gene_variant MELA-AU 7 7605875 7605876 multiple base substitution (>=2bp and <=200bp) AC CA upstream_gene_variant MELA-AU 7 7606903 7606903 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant MELA-AU 7 7606903 7606903 single base substitution C T intron_variant MELA-AU 7 7606903 7606903 single base substitution C T upstream_gene_variant MELA-AU 7 7607154 7607154 single base substitution A T 5_prime_UTR_variant MELA-AU 7 7607154 7607154 single base substitution A T intron_variant MELA-AU 7 7607477 7607477 single base substitution A C intron_variant MELA-AU 7 7609216 7609216 single base substitution C T intron_variant MELA-AU 7 7612102 7612102 single base substitution T C 5_prime_UTR_variant MELA-AU 7 7612850 7612850 single base substitution T G downstream_gene_variant MELA-AU 7 7612850 7612850 single base substitution T G synonymous_variant V248V 744T>G MELA-AU 7 7613405 7613405 single base substitution C T downstream_gene_variant MELA-AU 7 7613405 7613405 single base substitution C T splice_region_variant MELA-AU 7 7614035 7614035 single base substitution C T downstream_gene_variant MELA-AU 7 7614035 7614035 single base substitution C T intron_variant MELA-AU 7 7614257 7614257 single base substitution C T downstream_gene_variant MELA-AU 7 7614257 7614257 single base substitution C T intron_variant MELA-AU 7 7617072 7617072 single base substitution G A downstream_gene_variant MELA-AU 7 7617072 7617072 single base substitution G A intron_variant MELA-AU 7 7617072 7617072 single base substitution G A upstream_gene_variant MELA-AU 7 7617237 7617237 single base substitution C T downstream_gene_variant MELA-AU 7 7617237 7617237 single base substitution C T intron_variant MELA-AU 7 7617237 7617237 single base substitution C T upstream_gene_variant MELA-AU 7 7617392 7617392 single base substitution A G downstream_gene_variant MELA-AU 7 7617392 7617392 single base substitution A G intron_variant MELA-AU 7 7617392 7617392 single base substitution A G upstream_gene_variant MELA-AU 7 7618451 7618451 single base substitution C T intron_variant MELA-AU 7 7618451 7618451 single base substitution C T upstream_gene_variant MELA-AU 7 7618656 7618656 single base substitution T A intron_variant MELA-AU 7 7618656 7618656 single base substitution T A upstream_gene_variant MELA-AU 7 7618794 7618794 single base substitution C T intron_variant MELA-AU 7 7618794 7618794 single base substitution C T upstream_gene_variant MELA-AU 7 7619291 7619291 single base substitution G C intron_variant MELA-AU 7 7619291 7619291 single base substitution G C upstream_gene_variant MELA-AU 7 7619304 7619304 single base substitution C T intron_variant MELA-AU 7 7619304 7619304 single base substitution C T upstream_gene_variant MELA-AU 7 7620569 7620569 single base substitution C T intron_variant MELA-AU 7 7620569 7620569 single base substitution C T upstream_gene_variant MELA-AU 7 7620573 7620573 single base substitution C T intron_variant MELA-AU 7 7620573 7620573 single base substitution C T upstream_gene_variant MELA-AU 7 7620846 7620846 single base substitution C T intron_variant MELA-AU 7 7620846 7620846 single base substitution C T upstream_gene_variant MELA-AU 7 7620869 7620869 single base substitution T C intron_variant MELA-AU 7 7620869 7620869 single base substitution T C upstream_gene_variant MELA-AU 7 7622270 7622270 single base substitution G A exon_variant MELA-AU 7 7622270 7622270 single base substitution G A intron_variant MELA-AU 7 7622270 7622270 single base substitution G A upstream_gene_variant MELA-AU 7 7622916 7622916 single base substitution T C exon_variant MELA-AU 7 7622916 7622916 single base substitution T C missense_variant W521R 1561T>C MELA-AU 7 7623605 7623605 single base substitution C T downstream_gene_variant MELA-AU 7 7623605 7623605 single base substitution C T intron_variant MELA-AU 7 7623649 7623649 single base substitution C T downstream_gene_variant MELA-AU 7 7623649 7623649 single base substitution C T intron_variant MELA-AU 7 7624016 7624016 single base substitution G A downstream_gene_variant MELA-AU 7 7624016 7624016 single base substitution G A intron_variant MELA-AU 7 7625505 7625505 single base substitution A G downstream_gene_variant MELA-AU 7 7625505 7625505 single base substitution A G intron_variant MELA-AU 7 7626837 7626837 single base substitution C T downstream_gene_variant MELA-AU 7 7626837 7626837 single base substitution C T intron_variant MELA-AU 7 7626915 7626915 single base substitution T C downstream_gene_variant MELA-AU 7 7626915 7626915 single base substitution T C intron_variant MELA-AU 7 7627157 7627157 single base substitution C T downstream_gene_variant MELA-AU 7 7627157 7627157 single base substitution C T intron_variant MELA-AU 7 7627229 7627229 single base substitution G C downstream_gene_variant MELA-AU 7 7627229 7627229 single base substitution G C intron_variant MELA-AU 7 7627338 7627338 single base substitution C T downstream_gene_variant MELA-AU 7 7627338 7627338 single base substitution C T intron_variant MELA-AU 7 7627949 7627949 single base substitution C T downstream_gene_variant MELA-AU 7 7627949 7627949 single base substitution C T intron_variant MELA-AU 7 7628659 7628660 multiple base substitution (>=2bp and <=200bp) GG AT intron_variant MELA-AU 7 7628849 7628849 single base substitution A T intron_variant MELA-AU 7 7629238 7629238 single base substitution C T intron_variant MELA-AU 7 7629637 7629637 single base substitution C T intron_variant MELA-AU 7 7630303 7630303 single base substitution C T intron_variant MELA-AU 7 7631034 7631034 single base substitution C T intron_variant MELA-AU 7 7631248 7631248 single base substitution C T intron_variant MELA-AU 7 7631282 7631282 single base substitution T G intron_variant MELA-AU 7 7632561 7632561 single base substitution C T intron_variant MELA-AU 7 7632737 7632738 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 7 7633131 7633131 single base substitution G A intron_variant MELA-AU 7 7633178 7633179 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 7 7633577 7633577 single base substitution G A intron_variant MELA-AU 7 7633761 7633761 single base substitution T A intron_variant MELA-AU 7 7633849 7633849 single base substitution G A intron_variant MELA-AU 7 7634376 7634376 single base substitution C T intron_variant MELA-AU 7 7634687 7634687 single base substitution G A exon_variant MELA-AU 7 7634687 7634687 single base substitution G A stop_gained W707* 2120G>A MELA-AU 7 7635597 7635597 single base substitution G T intron_variant MELA-AU 7 7636579 7636580 multiple base substitution (>=2bp and <=200bp) TC CT intron_variant MELA-AU 7 7636652 7636652 single base substitution C T intron_variant MELA-AU 7 7636753 7636753 single base substitution C T intron_variant MELA-AU 7 7636774 7636774 single base substitution C T intron_variant MELA-AU 7 7637178 7637178 single base substitution A T intron_variant MELA-AU 7 7637398 7637398 single base substitution C T intron_variant MELA-AU 7 7637613 7637613 single base substitution A T intron_variant MELA-AU 7 7637907 7637907 single base substitution C T intron_variant MELA-AU 7 7637944 7637944 single base substitution C T intron_variant MELA-AU 7 7637971 7637971 single base substitution C T intron_variant MELA-AU 7 7637989 7637989 single base substitution G A intron_variant MELA-AU 7 7638402 7638402 single base substitution G A intron_variant MELA-AU 7 7639142 7639142 single base substitution C T intron_variant MELA-AU 7 7639950 7639950 single base substitution G A intron_variant MELA-AU 7 7639950 7639950 single base substitution G A upstream_gene_variant MELA-AU 7 7640425 7640425 single base substitution C T intron_variant MELA-AU 7 7640425 7640425 single base substitution C T upstream_gene_variant MELA-AU 7 7641034 7641034 single base substitution C T intron_variant MELA-AU 7 7641034 7641034 single base substitution C T upstream_gene_variant MELA-AU 7 7641222 7641222 single base substitution A T intron_variant MELA-AU 7 7641222 7641222 single base substitution A T upstream_gene_variant MELA-AU 7 7642332 7642332 single base substitution C T intron_variant MELA-AU 7 7642332 7642332 single base substitution C T upstream_gene_variant MELA-AU 7 7645580 7645580 single base substitution C T exon_variant MELA-AU 7 7645580 7645580 single base substitution C T synonymous_variant T803T 2409C>T MELA-AU 7 7646137 7646137 single base substitution C T intron_variant MELA-AU 7 7646362 7646362 single base substitution C T intron_variant MELA-AU 7 7646593 7646594 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 7 7647305 7647305 single base substitution A G downstream_gene_variant MELA-AU 7 7647305 7647305 single base substitution A G exon_variant MELA-AU 7 7647604 7647604 single base substitution T C downstream_gene_variant MELA-AU 7 7647604 7647604 single base substitution T C exon_variant MELA-AU 7 7647650 7647650 single base substitution C T downstream_gene_variant MELA-AU 7 7647650 7647650 single base substitution C T exon_variant MELA-AU 7 7647750 7647750 single base substitution T C downstream_gene_variant MELA-AU 7 7647750 7647750 single base substitution T C exon_variant MELA-AU 7 7649095 7649095 single base substitution G A downstream_gene_variant MELA-AU 7 7649410 7649410 single base substitution C T downstream_gene_variant MELA-AU 7 7649720 7649720 single base substitution C T downstream_gene_variant MELA-AU 7 7649745 7649745 single base substitution A T downstream_gene_variant MELA-AU 7 7650068 7650068 single base substitution C T downstream_gene_variant MELA-AU 7 7650212 7650212 single base substitution C T downstream_gene_variant MELA-AU 7 7650375 7650375 single base substitution C T downstream_gene_variant MELA-AU 7 7651891 7651891 single base substitution C T downstream_gene_variant MELA-AU 7 7652022 7652022 single base substitution C T downstream_gene_variant MELA-AU 7 7652211 7652211 single base substitution C T downstream_gene_variant MELA-AU 7 7652394 7652394 single base substitution C T downstream_gene_variant MELA-AU 7 7652726 7652726 single base substitution C T downstream_gene_variant MELA-AU 7 7653105 7653105 single base substitution A T downstream_gene_variant MELA-AU 7 7653507 7653507 single base substitution G C downstream_gene_variant ORCA-IN 7 7614603 7614603 single base substitution G T downstream_gene_variant ORCA-IN 7 7614603 7614603 single base substitution G T intron_variant ORCA-IN 7 7622071 7622071 single base substitution C A intron_variant ORCA-IN 7 7622071 7622071 single base substitution C A upstream_gene_variant ORCA-IN 7 7625037 7625037 deletion of <=200bp A - downstream_gene_variant ORCA-IN 7 7625037 7625037 deletion of <=200bp A - intron_variant OV-AU 7 7609411 7609411 single base substitution G C intron_variant OV-AU 7 7615915 7615915 single base substitution C G downstream_gene_variant OV-AU 7 7615915 7615915 single base substitution C G intron_variant OV-AU 7 7622288 7622288 single base substitution T G exon_variant OV-AU 7 7622288 7622288 single base substitution T G intron_variant OV-AU 7 7622288 7622288 single base substitution T G upstream_gene_variant OV-AU 7 7632683 7632683 single base substitution G T intron_variant OV-AU 7 7636275 7636275 single base substitution A G intron_variant OV-AU 7 7644041 7644041 single base substitution C T intron_variant OV-AU 7 7644041 7644041 single base substitution C T upstream_gene_variant OV-AU 7 7648896 7648896 single base substitution C G downstream_gene_variant PACA-AU 7 7613113 7613113 single base substitution A G downstream_gene_variant PACA-AU 7 7613113 7613113 single base substitution A G missense_variant N336S 1007A>G PACA-AU 7 7614239 7614239 single base substitution T G downstream_gene_variant PACA-AU 7 7614239 7614239 single base substitution T G intron_variant PACA-AU 7 7622027 7622027 single base substitution A G intron_variant PACA-AU 7 7622027 7622027 single base substitution A G upstream_gene_variant PACA-AU 7 7623650 7623650 single base substitution G A downstream_gene_variant PACA-AU 7 7623650 7623650 single base substitution G A intron_variant PACA-AU 7 7626211 7626211 single base substitution A C downstream_gene_variant PACA-AU 7 7626211 7626211 single base substitution A C intron_variant PACA-AU 7 7627166 7627166 insertion of <=200bp - C downstream_gene_variant PACA-AU 7 7627166 7627166 insertion of <=200bp - C intron_variant PACA-AU 7 7631392 7631392 single base substitution G C intron_variant PACA-AU 7 7633047 7633047 single base substitution T A intron_variant PACA-AU 7 7636465 7636465 single base substitution G A intron_variant PACA-AU 7 7643118 7643118 deletion of <=200bp A - intron_variant PACA-AU 7 7643118 7643118 deletion of <=200bp A - upstream_gene_variant PACA-AU 7 7645143 7645143 single base substitution C T exon_variant PACA-AU 7 7645143 7645143 single base substitution C T intron_variant PACA-AU 7 7649876 7649876 single base substitution C T downstream_gene_variant PACA-AU 7 7650709 7650709 single base substitution T C downstream_gene_variant PACA-CA 7 7602204 7602204 single base substitution A G upstream_gene_variant PACA-CA 7 7605340 7605340 single base substitution C A upstream_gene_variant PACA-CA 7 7605692 7605692 single base substitution A C upstream_gene_variant PACA-CA 7 7608148 7608148 single base substitution A T intron_variant PACA-CA 7 7608853 7608853 single base substitution C T intron_variant PACA-CA 7 7611368 7611368 single base substitution C T intron_variant PACA-CA 7 7611972 7611972 single base substitution G T intron_variant PACA-CA 7 7613658 7613658 single base substitution C T downstream_gene_variant PACA-CA 7 7613658 7613658 single base substitution C T intron_variant PACA-CA 7 7615844 7615844 single base substitution A C downstream_gene_variant PACA-CA 7 7615844 7615844 single base substitution A C intron_variant PACA-CA 7 7619840 7619840 deletion of <=200bp T - intron_variant PACA-CA 7 7619840 7619840 deletion of <=200bp T - upstream_gene_variant PACA-CA 7 7628150 7628150 single base substitution C T exon_variant PACA-CA 7 7628150 7628150 single base substitution C T missense_variant R614C 1840C>T PACA-CA 7 7634146 7634146 single base substitution G A intron_variant PACA-CA 7 7634509 7634509 single base substitution G A intron_variant PACA-CA 7 7640475 7640475 single base substitution G C intron_variant PACA-CA 7 7640475 7640475 single base substitution G C upstream_gene_variant PACA-CA 7 7640881 7640881 single base substitution G A intron_variant PACA-CA 7 7640881 7640881 single base substitution G A upstream_gene_variant PACA-CA 7 7640892 7640892 single base substitution A G intron_variant PACA-CA 7 7640892 7640892 single base substitution A G upstream_gene_variant PACA-CA 7 7641263 7641263 single base substitution C G intron_variant PACA-CA 7 7641263 7641263 single base substitution C G upstream_gene_variant PACA-CA 7 7643849 7643849 single base substitution A G intron_variant PACA-CA 7 7643849 7643849 single base substitution A G upstream_gene_variant PACA-CA 7 7649492 7649492 single base substitution A G downstream_gene_variant PACA-CA 7 7649554 7649554 single base substitution T A downstream_gene_variant PACA-CA 7 7649564 7649564 single base substitution G C downstream_gene_variant PACA-CA 7 7650674 7650674 single base substitution T G downstream_gene_variant PACA-CA 7 7652768 7652768 deletion of <=200bp A - downstream_gene_variant PBCA-DE 7 7603501 7603501 single base substitution A G upstream_gene_variant PBCA-DE 7 7606131 7606131 single base substitution T C upstream_gene_variant PBCA-DE 7 7613985 7613985 single base substitution A C downstream_gene_variant PBCA-DE 7 7613985 7613985 single base substitution A C intron_variant PBCA-DE 7 7618683 7618683 single base substitution G A intron_variant PBCA-DE 7 7618683 7618683 single base substitution G A upstream_gene_variant PBCA-DE 7 7625050 7625050 single base substitution T C downstream_gene_variant PBCA-DE 7 7625050 7625050 single base substitution T C intron_variant PBCA-DE 7 7627019 7627019 insertion of <=200bp - A downstream_gene_variant PBCA-DE 7 7627019 7627019 insertion of <=200bp - A intron_variant PBCA-DE 7 7629298 7629298 insertion of <=200bp - T intron_variant PBCA-DE 7 7640029 7640029 insertion of <=200bp - A intron_variant PBCA-DE 7 7640029 7640029 insertion of <=200bp - A upstream_gene_variant PRAD-CA 7 7641238 7641238 single base substitution G C intron_variant PRAD-CA 7 7641238 7641238 single base substitution G C upstream_gene_variant PRAD-UK 7 7611067 7611067 single base substitution C T intron_variant PRAD-UK 7 7634858 7634858 single base substitution C T intron_variant PRAD-UK 7 7635321 7635321 single base substitution A C intron_variant PRAD-UK 7 7641828 7641828 single base substitution C T intron_variant PRAD-UK 7 7641828 7641828 single base substitution C T upstream_gene_variant PRAD-UK 7 7643030 7643030 single base substitution A C intron_variant PRAD-UK 7 7643030 7643030 single base substitution A C upstream_gene_variant PRAD-UK 7 7653007 7653007 deletion of <=200bp C - downstream_gene_variant PRAD-US 7 7613322 7613322 single base substitution A G downstream_gene_variant PRAD-US 7 7613322 7613322 single base substitution A G missense_variant T406A 1216A>G PRAD-US 7 7645694 7645694 single base substitution T C exon_variant PRAD-US 7 7645694 7645694 single base substitution T C synonymous_variant S841S 2523T>C READ-US 7 7622772 7622772 single base substitution A C exon_variant READ-US 7 7622772 7622772 single base substitution A C missense_variant N473H 1417A>C READ-US 7 7634705 7634705 single base substitution G A exon_variant READ-US 7 7634705 7634705 single base substitution G A missense_variant R713Q 2138G>A READ-US 7 7636027 7636027 single base substitution G A exon_variant READ-US 7 7636027 7636027 single base substitution G A missense_variant R779Q 2336G>A RECA-EU 7 7616104 7616104 single base substitution A C downstream_gene_variant RECA-EU 7 7616104 7616104 single base substitution A C intron_variant RECA-EU 7 7626386 7626386 single base substitution C T downstream_gene_variant RECA-EU 7 7626386 7626386 single base substitution C T intron_variant RECA-EU 7 7637936 7637936 single base substitution T C intron_variant RECA-EU 7 7638325 7638325 single base substitution T A intron_variant RECA-EU 7 7638331 7638331 single base substitution G T intron_variant SKCA-BR 7 7602936 7602936 single base substitution G A upstream_gene_variant SKCA-BR 7 7605286 7605286 single base substitution G A upstream_gene_variant SKCA-BR 7 7606829 7606829 single base substitution T G 5_prime_UTR_variant SKCA-BR 7 7606829 7606829 single base substitution T G intron_variant SKCA-BR 7 7606829 7606829 single base substitution T G upstream_gene_variant SKCA-BR 7 7607261 7607261 single base substitution A G 5_prime_UTR_variant SKCA-BR 7 7607261 7607261 single base substitution A G intron_variant SKCA-BR 7 7608614 7608614 single base substitution T A intron_variant SKCA-BR 7 7609838 7609838 single base substitution C T intron_variant SKCA-BR 7 7610067 7610067 single base substitution G A intron_variant SKCA-BR 7 7611710 7611710 single base substitution C A intron_variant SKCA-BR 7 7617318 7617318 single base substitution A G downstream_gene_variant SKCA-BR 7 7617318 7617318 single base substitution A G intron_variant SKCA-BR 7 7617318 7617318 single base substitution A G upstream_gene_variant SKCA-BR 7 7623589 7623589 single base substitution C T downstream_gene_variant SKCA-BR 7 7623589 7623589 single base substitution C T intron_variant SKCA-BR 7 7625786 7625802 deletion of <=200bp CGTGTGTGTGTGTGTGT - downstream_gene_variant SKCA-BR 7 7625786 7625802 deletion of <=200bp CGTGTGTGTGTGTGTGT - intron_variant SKCA-BR 7 7626634 7626634 insertion of <=200bp - TG downstream_gene_variant SKCA-BR 7 7626634 7626634 insertion of <=200bp - TG intron_variant SKCA-BR 7 7627597 7627597 single base substitution C A downstream_gene_variant SKCA-BR 7 7627597 7627597 single base substitution C A intron_variant SKCA-BR 7 7627763 7627763 single base substitution C T downstream_gene_variant SKCA-BR 7 7627763 7627763 single base substitution C T intron_variant SKCA-BR 7 7631119 7631119 single base substitution C T intron_variant SKCA-BR 7 7633433 7633433 single base substitution C T intron_variant SKCA-BR 7 7634493 7634493 insertion of <=200bp - CAAA intron_variant SKCA-BR 7 7634603 7634603 single base substitution C T splice_region_variant SKCA-BR 7 7636762 7636762 single base substitution C T intron_variant SKCA-BR 7 7637146 7637146 single base substitution T A intron_variant SKCA-BR 7 7643683 7643683 single base substitution C T intron_variant SKCA-BR 7 7643683 7643683 single base substitution C T upstream_gene_variant SKCA-BR 7 7646131 7646131 single base substitution G A intron_variant SKCA-BR 7 7650668 7650668 single base substitution C T downstream_gene_variant SKCA-BR 7 7653392 7653392 single base substitution T A downstream_gene_variant SKCM-US 7 7612814 7612814 single base substitution C T downstream_gene_variant SKCM-US 7 7612814 7612814 single base substitution C T synonymous_variant F236F 708C>T SKCM-US 7 7612821 7612821 single base substitution C T downstream_gene_variant SKCM-US 7 7612821 7612821 single base substitution C T missense_variant R239C 715C>T SKCM-US 7 7628179 7628179 single base substitution C T exon_variant SKCM-US 7 7628179 7628179 single base substitution C T synonymous_variant F623F 1869C>T SKCM-US 7 7645580 7645580 single base substitution C T exon_variant SKCM-US 7 7645580 7645580 single base substitution C T synonymous_variant T803T 2409C>T SKCM-US 7 7645637 7645637 single base substitution C T exon_variant SKCM-US 7 7645637 7645637 single base substitution C T synonymous_variant N822N 2466C>T SKCM-US 7 7646670 7646670 single base substitution A G exon_variant SKCM-US 7 7646670 7646670 single base substitution A G missense_variant M859V 2575A>G STAD-US 7 7612108 7612108 single base substitution T C start_lost M1T 2T>C STAD-US 7 7612652 7612652 single base substitution A G downstream_gene_variant STAD-US 7 7612652 7612652 single base substitution A G synonymous_variant G182G 546A>G STAD-US 7 7612723 7612723 single base substitution G A downstream_gene_variant STAD-US 7 7612723 7612723 single base substitution G A missense_variant R206H 617G>A STAD-US 7 7612723 7612723 single base substitution G C downstream_gene_variant STAD-US 7 7612723 7612723 single base substitution G C missense_variant R206P 617G>C STAD-US 7 7613797 7613797 single base substitution G A downstream_gene_variant STAD-US 7 7613797 7613797 single base substitution G A missense_variant G455R 1363G>A STAD-US 7 7625282 7625282 single base substitution A G downstream_gene_variant STAD-US 7 7625282 7625282 single base substitution A G exon_variant STAD-US 7 7625282 7625282 single base substitution A G missense_variant N555S 1664A>G STAD-US 7 7636009 7636009 single base substitution C T exon_variant STAD-US 7 7636009 7636009 single base substitution C T missense_variant T773I 2318C>T STAD-US 7 7636049 7636049 single base substitution G A exon_variant STAD-US 7 7636049 7636049 single base substitution G A synonymous_variant A786A 2358G>A UCEC-US 7 7612325 7612325 single base substitution T G downstream_gene_variant UCEC-US 7 7612325 7612325 single base substitution T G missense_variant D73E 219T>G UCEC-US 7 7612370 7612370 single base substitution A G downstream_gene_variant UCEC-US 7 7612370 7612370 single base substitution A G synonymous_variant V88V 264A>G UCEC-US 7 7612447 7612447 single base substitution G A downstream_gene_variant UCEC-US 7 7612447 7612447 single base substitution G A missense_variant R114Q 341G>A UCEC-US 7 7612769 7612769 single base substitution C A downstream_gene_variant UCEC-US 7 7612769 7612769 single base substitution C A missense_variant F221L 663C>A UCEC-US 7 7613140 7613140 single base substitution G A downstream_gene_variant UCEC-US 7 7613140 7613140 single base substitution G A missense_variant R345Q 1034G>A UCEC-US 7 7613271 7613271 single base substitution G T downstream_gene_variant UCEC-US 7 7613271 7613271 single base substitution G T missense_variant D389Y 1165G>T UCEC-US 7 7625357 7625357 single base substitution G A downstream_gene_variant UCEC-US 7 7625357 7625357 single base substitution G A exon_variant UCEC-US 7 7625357 7625357 single base substitution G A missense_variant R580Q 1739G>A UCEC-US 7 7629050 7629050 single base substitution C T exon_variant UCEC-US 7 7629050 7629050 single base substitution C T synonymous_variant I633I 1899C>T

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand E11 COSM1666355 c.1651G>C p.D551H Substitution - Missense 7:7585638-7585638 + T2225 COSM4702219 c.1704G>T p.K568N Substitution - Missense 7:7585691-7585691 + 224 COSM4425701 c.1738C>T p.R580* Substitution - Nonsense 7:7585725-7585725 + BD194T COSM5501283 c.1909A>T p.T637S Substitution - Missense 7:7589429-7589429 + TCGA-HU-8602-01 COSM3882464 c.546A>G p.G182G Substitution - coding silent 7:7573021-7573021 + TCGA-BR-6452-01 COSM3882469 c.1664A>G p.N555S Substitution - Missense 7:7585651-7585651 + SW1417 COSM4655064 c.185A>T p.Y62F Substitution - Missense 7:7572660-7572660 + SNUH_G10_S1 COSM3982270 c.933C>T p.P311P Substitution - coding silent 7:7573408-7573408 + 2250151 COSM5029534 c.1648+6A>C p.? Unknown 7:7583378-7583378 + ESCC-123T COSM3942304 c.1458A>T p.L486F Substitution - Missense 7:7583182-7583182 + TCGA-F5-6814-01 COSM3431759 c.2138G>A p.R713Q Substitution - Missense 7:7595074-7595074 + TCGA-A5-A0VP-01 COSM1091844 c.1034G>A p.R345Q Substitution - Missense 7:7573509-7573509 + TCGA-AA-A010-01 COSM282801 c.2217C>A p.F739L Substitution - Missense 7:7596277-7596277 + B101 COSM1755362 c.1737G>A p.L579L Substitution - coding silent 7:7585724-7585724 + Pat_53_B COSM5873105 c.1807G>A p.D603N Substitution - Missense 7:7585794-7585794 + KPOPBR-03-T COSM5965086 c.793G>A p.E265K Substitution - Missense 7:7573268-7573268 + TCGA-G2-A2EO-01 COSM1313293 c.1620C>G p.I540M Substitution - Missense 7:7583344-7583344 + HCA7 COSM3882479 c.2358G>A p.A786A Substitution - coding silent 7:7596418-7596418 + LUAD-E00934 COSM393798 c.1966A>G p.K656E Substitution - Missense 7:7589486-7589486 + 1_PRE-TREATMENT COSM1719506 c.1542C>T p.S514S Substitution - coding silent 7:7583266-7583266 + TCGA-BR-8295-01 COSM3882466 c.617G>C p.R206P Substitution - Missense 7:7573092-7573092 + TCGA-87-5896-01 COSM3412309 c.583C>T p.R195* Substitution - Nonsense 7:7573058-7573058 + HDC90 COSM4637523 c.22A>G p.I8V Substitution - Missense 7:7572497-7572497 + TCGA-BH-A0H7-01 COSM453407 c.2352A>T p.R784R Substitution - coding silent 7:7596412-7596412 + TP_2010 COSM5568392 c.137C>T p.S46F Substitution - Missense 7:7572612-7572612 + BCM265T COSM4955190 c.1320G>A p.M440I Substitution - Missense 7:7574123-7574123 + SJRHB012_R COSM3737520 c.1159G>T p.E387* Substitution - Nonsense 7:7573634-7573634 + 8068577 COSM4388192 c.1007A>G p.N336S Substitution - Missense 7:7573482-7573482 + TCGA-D1-A103-01 COSM1091852 c.1899C>T p.I633I Substitution - coding silent 7:7589419-7589419 + TCGA-AA-3510-01 COSM1452126 c.2336G>A p.R779Q Substitution - Missense 7:7596396-7596396 + TCGA-CW-6087-01 COSM485568 c.990G>A p.W330* Substitution - Nonsense 7:7573465-7573465 + ESO-717 COSM1242512 c.1374A>G p.S458S Substitution - coding silent 7:7574177-7574177 + WA57 COSM240670 c.309G>C p.L103F Substitution - Missense 7:7572784-7572784 + TCGA-AX-A05Z-01 COSM1091851 c.1739G>A p.R580Q Substitution - Missense 7:7585726-7585726 + CSB13 COSM5026701 c.524C>T p.T175I Substitution - Missense 7:7572999-7572999 + TCGA-56-6546-01 COSM747075 c.387A>T p.L129L Substitution - coding silent 7:7572862-7572862 + TCGA-BR-4184-01 COSM3882479 c.2358G>A p.A786A Substitution - coding silent 7:7596418-7596418 + RK089_C01 COSM1635396 c.616C>A p.R206S Substitution - Missense 7:7573091-7573091 + TCGA-EE-A2GO-06 COSM3640674 c.708C>T p.F236F Substitution - coding silent 7:7573183-7573183 + TCGA-AX-A05Z-01 COSM1091843 c.663C>A p.F221L Substitution - Missense 7:7573138-7573138 + NCI-H522 COSM1197088 c.413C>G p.A138G Substitution - Missense 7:7572888-7572888 + TCGA-KK-A6E2-01 COSM4879379 c.1216A>G p.T406A Substitution - Missense 7:7573691-7573691 + NCI-H747 COSM393798 c.1966A>G p.K656E Substitution - Missense 7:7589486-7589486 + LUAD-E00897 COSM364715 c.1141G>C p.E381Q Substitution - Missense 7:7573616-7573616 + PR-1043 COSM245692 c.2070T>G p.D690E Substitution - Missense 7:7595006-7595006 + Gp5D COSM3029068 c.2271T>C p.G757G Substitution - coding silent 7:7596331-7596331 + TCGA-B5-A0JY-01 COSM1091845 c.1165G>T p.D389Y Substitution - Missense 7:7573640-7573640 + TCGA-AP-A056-01 COSM1091841 c.341G>A p.R114Q Substitution - Missense 7:7572816-7572816 + TCGA-G2-A2EC-01 COSM1313291 c.85C>G p.H29D Substitution - Missense 7:7572560-7572560 + TCGA-BR-6852-01 COSM3882465 c.617G>A p.R206H Substitution - Missense 7:7573092-7573092 + 587376 COSM1215099 c.1457T>G p.L486* Substitution - Nonsense 7:7583181-7583181 + BCM265T COSM4955190 c.1320G>A p.M440I Substitution - Missense 7:7574123-7574123 + SJRHB012_S COSM3737520 c.1159G>T p.E387* Substitution - Nonsense 7:7573634-7573634 + 9227_T COSM5040273 c.1442G>A p.S481N Substitution - Missense 7:7583166-7583166 + ESCC_117 COSM5640094 c.2450T>C p.L817S Substitution - Missense 7:7605990-7605990 + TCGA-AP-A0LG-01 COSM1091840 c.264A>G p.V88V Substitution - coding silent 7:7572739-7572739 + GC7_T COSM150236 c.400G>A p.D134N Substitution - Missense 7:7572875-7572875 + TCGA-BR-6452-01 COSM3882478 c.2318C>T p.T773I Substitution - Missense 7:7596378-7596378 + ICC002T COSM3882469 c.1664A>G p.N555S Substitution - Missense 7:7585651-7585651 + sysucc-274T COSM5476778 c.1511C>T p.T504M Substitution - Missense 7:7583235-7583235 + H522 COSM1197088 c.413C>G p.A138G Substitution - Missense 7:7572888-7572888 + 250LT COSM4383057 c.1807G>T p.D603Y Substitution - Missense 7:7585794-7585794 + TCGA-EE-A29L-06 COSM3640681 c.2409C>T p.T803T Substitution - coding silent 7:7605949-7605949 + HCC111T COSM1623104 c.909T>G p.T303T Substitution - coding silent 7:7573384-7573384 + PCSI_0049_Pa_X COSM3382045 c.1840C>T p.R614C Substitution - Missense 7:7588519-7588519 + B106 COSM1755359 c.50G>A p.R17K Substitution - Missense 7:7572525-7572525 + CSCC-35-T COSM4478382 c.2234C>T p.S745F Substitution - Missense 7:7596294-7596294 + TCGA-18-3419-01 COSM747064 c.2350C>A p.R784R Substitution - coding silent 7:7596410-7596410 + TCGA-CL-5918-01 COSM1568875 c.1417A>C p.N473H Substitution - Missense 7:7583141-7583141 + 2293782 COSM4609343 c.976G>T p.A326S Substitution - Missense 7:7573451-7573451 + TCGA-D8-A1JA-01 COSM3833271 c.566C>G p.S189C Substitution - Missense 7:7573041-7573041 + TCGA-BS-A0UV-01 COSM1091839 c.219T>G p.D73E Substitution - Missense 7:7572694-7572694 + TCGA-66-2770-01 COSM747071 c.863G>T p.R288M Substitution - Missense 7:7573338-7573338 + Pat_41_B COSM5873095 c.958C>T p.P320S Substitution - Missense 7:7573433-7573433 + TCGA-CG-4465-01 COSM3882467 c.1363G>A p.G455R Substitution - Missense 7:7574166-7574166 + YULETA COSM3640682 c.2575A>G p.M859V Substitution - Missense 7:7607039-7607039 + 1_RESISTANT COSM1719506 c.1542C>T p.S514S Substitution - coding silent 7:7583266-7583266 + NB-0982 COSM1286193 c.1987G>T p.E663* Substitution - Nonsense 7:7589507-7589507 + TCGA-18-5595-01 COSM747073 c.769G>C p.E257Q Substitution - Missense 7:7573244-7573244 + ESCC_BICR_036T COSM5432239 c.1117C>T p.H373Y Substitution - Missense 7:7573592-7573592 + TCGA-AG-A002-01 COSM262023 c.1141G>T p.E381* Substitution - Nonsense 7:7573616-7573616 + HCC111 COSM1623104 c.909T>G p.T303T Substitution - coding silent 7:7573384-7573384 + TCGA-FU-A3TQ-01 COSM4854848 c.2056G>A p.D686N Substitution - Missense 7:7594992-7594992 + CSCC-7-T COSM4477755 c.2180C>T p.S727F Substitution - Missense 7:7595116-7595116 + PT35 COSM5912632 c.1085C>T p.P362L Substitution - Missense 7:7573560-7573560 + YUKAT COSM5407910 c.1563G>A p.W521* Substitution - Nonsense 7:7583287-7583287 + 172 COSM145629 c.2300C>G p.P767R Substitution - Missense 7:7596360-7596360 + TCGA-DA-A1I1-06 COSM3640682 c.2575A>G p.M859V Substitution - Missense 7:7607039-7607039 + TCGA-F5-6814-01 COSM1452126 c.2336G>A p.R779Q Substitution - Missense 7:7596396-7596396 + TCGA-CA-6717-01 COSM1452103 c.697G>T p.D233Y Substitution - Missense 7:7573172-7573172 + T276 COSM4702217 c.641G>A p.R214Q Substitution - Missense 7:7573116-7573116 + TCGA-D1-A168-01 COSM1091842 c.538G>T p.E180* Substitution - Nonsense 7:7573013-7573013 + TCGA-AA-3492-01 COSM1452129 c.2442_2443insA p.L817fs*5 Insertion - Frameshift 7:7605982-7605983 + ME009T COSM223145 c.671C>T p.T224I Substitution - Missense 7:7573146-7573146 + TCGA-FJ-A3ZE-01 COSM3778578 c.2309C>A p.S770Y Substitution - Missense 7:7596369-7596369 + TCGA-CJ-4875-01 COSM3367030 c.40C>G p.H14D Substitution - Missense 7:7572515-7572515 + TCGA-CD-A4MI-01 COSM3882462 c.2T>C p.M1T Substitution - Missense 7:7572477-7572477 + TCGA-37-3783-01 COSM747065 c.2246C>T p.S749L Substitution - Missense 7:7596306-7596306 + HCC39 COSM1623103 c.256C>G p.R86G Substitution - Missense 7:7572731-7572731 + B101-Tumor COSM1755362 c.1737G>A p.L579L Substitution - coding silent 7:7585724-7585724 + CHC1592T COSM4791342 c.2442C>A p.D814E Substitution - Missense 7:7605982-7605982 + U343 COSM5712399 c.2565G>T p.T855T Substitution - coding silent 7:7607029-7607029 + TCGA-AZ-4315-01 COSM1091844 c.1034G>A p.R345Q Substitution - Missense 7:7573509-7573509 + LIM1215 COSM4639576 c.487C>T p.L163F Substitution - Missense 7:7572962-7572962 + CHC1592T COSM4791342 c.2442C>A p.D814E Substitution - Missense 7:7605982-7605982 + SNUH_G73_S1 COSM4415526 c.2189T>C p.L730S Substitution - Missense 7:7595125-7595125 + TCGA-AG-A025-01 COSM290376 c.1176G>A p.T392T Substitution - coding silent 7:7573651-7573651 + SJRHB012 COSM3737520 c.1159G>T p.E387* Substitution - Nonsense 7:7573634-7573634 + 250LT COSM4382684 c.964G>A p.D322N Substitution - Missense 7:7573439-7573439 + T3668 COSM4702218 c.1604G>A p.R535H Substitution - Missense 7:7583328-7583328 + 436 COSM4434096 c.1174A>G p.T392A Substitution - Missense 7:7573649-7573649 + TCGA-BT-A20J-01 COSM421878 c.1847G>C p.R616T Substitution - Missense 7:7588526-7588526 + CSCC-57-T COSM3028940 c.142G>A p.D48N Substitution - Missense 7:7572617-7572617 + TCGA-AS-3778-01 COSM485574 c.2331C>T p.G777G Substitution - coding silent 7:7596391-7596391 + TCGA-UB-A7MB-01 COSM4931439 c.318A>G p.K106K Substitution - coding silent 7:7572793-7572793 + Pat_06_B COSM5873094 c.7G>A p.G3S Substitution - Missense 7:7572482-7572482 + TCGA-EK-A3GJ-01 COSM4852373 c.1596G>C p.L532F Substitution - Missense 7:7583320-7583320 + ATL054 COSM5710660 c.1961T>G p.L654R Substitution - Missense 7:7589481-7589481 + PT44 COSM5432239 c.1117C>T p.H373Y Substitution - Missense 7:7573592-7573592 + NB-2074 COSM1286192 c.1773G>A p.M591I Substitution - Missense 7:7585760-7585760 + TCGA-EJ-7782-01 COSM3784086 c.2523T>C p.S841S Substitution - coding silent 7:7606063-7606063 + MedB-1 COSM5621256 c.211A>G p.N71D Substitution - Missense 7:7572686-7572686 + TCGA-D3-A2JD-06 COSM3640680 c.1869C>T p.F623F Substitution - coding silent 7:7588548-7588548 + MOLT-4 COSM1673027 c.1183C>T p.R395C Substitution - Missense 7:7573658-7573658 + TCGA-AD-6895-01 COSM1452125 c.2075G>A p.R692K Substitution - Missense 7:7595011-7595011 + HN_63058 COSM124443 c.630A>G p.I210M Substitution - Missense 7:7573105-7573105 + EGC15 COSM5062582 c.890A>T p.D297V Substitution - Missense 7:7573365-7573365 + 08-P1004 COSM4587563 c.2586T>C p.D862D Substitution - coding silent 7:7607050-7607050 + LUAD-B00523 COSM332141 c.1552G>T p.E518* Substitution - Nonsense 7:7583276-7583276 + HT55 COSM3028970 c.961T>G p.C321G Substitution - Missense 7:7573436-7573436 + EGC3 COSM3882465 c.617G>A p.R206H Substitution - Missense 7:7573092-7573092 + YUVEME COSM5407906 c.1009C>T p.R337* Substitution - Nonsense 7:7573484-7573484 + TCGA-EE-A3JA-06 COSM747063 c.2466C>T p.N822N Substitution - coding silent 7:7606006-7606006 + TCGA-EE-A2MR-06 COSM3640675 c.715C>T p.R239C Substitution - Missense 7:7573190-7573190 + CRC-02T COSM5455601 c.2368A>C p.I790L Substitution - Missense 7:7596428-7596428 + ESCC_BICR_021T COSM5434339 c.1165G>C p.D389H Substitution - Missense 7:7573640-7573640 + HT115 COSM1091844 c.1034G>A p.R345Q Substitution - Missense 7:7573509-7573509 + 172-01-1TD COSM145629 c.2300C>G p.P767R Substitution - Missense 7:7596360-7596360 + SA054 COSM211842 c.1777G>C p.A593P Substitution - Missense 7:7585764-7585764 + tumor_4116738 COSM1161690 c.1849G>T p.V617L Substitution - Missense 7:7588528-7588528 + PTC-14C COSM4162455 c.343C>A p.Q115K Substitution - Missense 7:7572818-7572818 + TCGA-18-5592-01 COSM747072 c.804A>T p.K268N Substitution - Missense 7:7573279-7573279 + TCGA-37-5819-01 COSM747063 c.2466C>T p.N822N Substitution - coding silent 7:7606006-7606006 + TCGA-F5-6811-01 COSM1568871 c.2534A>T p.D845V Substitution - Missense 7:7606998-7606998 + TCGA-B0-5109-01 COSM485573 c.2304G>T p.T768T Substitution - coding silent 7:7596364-7596364 + TCGA-AZ-4315-01 COSM1452130 c.2574T>G p.C858W Substitution - Missense 7:7607038-7607038 + I2L-P26-Tumor-Organoid COSM5358319 c.1148A>G p.D383G Substitution - Missense 7:7573623-7573623 + TCGA-85-6561-01 COSM747066 c.1848A>G p.R616R Substitution - coding silent 7:7588527-7588527 + HCC39T COSM1623103 c.256C>G p.R86G Substitution - Missense 7:7572731-7572731 + PT53 COSM5941287 c.329C>T p.P110L Substitution - Missense 7:7572804-7572804 + B106-Tumor COSM1755359 c.50G>A p.R17K Substitution - Missense 7:7572525-7572525 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.520215 7p21.3

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A G Missense p.I210M c.630A>G 7 7612736 HNSC A G Missense p.M859V c.2575A>G 7 7646670 CM A G Missense p.T406A c.1216A>G 7 7613322 PRAD A G Synonymous p.A618A c.1854A>G 7 7628164 HNSC A G Synonymous p.R616R c.1848A>G 7 7628158 LUSC A G Synonymous p.V88V c.264A>G 7 7612370 UCEC A T Missense p.K268N c.804A>T 7 7612910 LUSC A T Missense p.L629F c.1887A>T 7 7629038 LUAD A T Synonymous p.L129L c.387A>T 7 7612493 LUSC A T Synonymous p.R784R c.2352A>T 7 7636043 BRCA C A Missense p.P586Q c.1757C>A 7 7625375 LUAD C A Nonsense p.S23* c.68C>A 7 7612174 LUAD C A Synonymous p.R784R c.2350C>A 7 7636041 LUSC C G Missense p.H14D c.40C>G 7 7612146 RCCC C G Missense p.H29D c.85C>G 7 7612191 BLCA C G Missense p.I491M c.1473C>G 7 7622828 STAD C G Missense p.I540M c.1620C>G 7 7622975 BLCA C G Missense p.P767R c.2300C>G 7 7635991 CLL C T Missense p.P421L c.1262C>T 7 7613368 HNSC C T Missense p.S749L c.2246C>T 7 7635937 LUSC C T Missense p.T175I c.524C>T 7 7612630 BRCA C T Missense p.T224I c.671C>T 7 7612777 CM C T Nonsense p.R195* c.583C>T 7 7612689 GBM C T Synonymous p.F236F c.708C>T 7 7612814 CM C T Synonymous p.F623F c.1869C>T 7 7628179 CM C T Synonymous p.G777G c.2331C>T 7 7636022 RCCC C T Synonymous p.N822N c.2466C>T 7 7645637 CM C T Synonymous p.N822N c.2466C>T 7 7645637 LUSC C T Synonymous p.T803T c.2409C>T 7 7645580 CM C T Synonymous p.V772V c.2316C>T 7 7636007 LUAD G A Missense p.C785Y c.2354G>A 7 7636045 HNSC G A Missense p.E167K c.499G>A 7 7612605 LUAD G A Missense p.G455R c.1363G>A 7 7613797 STAD G A Missense p.M591I c.1773G>A 7 7625391 NB G A Missense p.R206H c.617G>A 7 7612723 STAD G A Missense p.R345Q c.1034G>A 7 7613140 UCEC G A Missense p.R779Q c.2336G>A 7 7636027 HNSC G A Synonymous p.G498G c.1494G>A 7 7622849 CM G A Synonymous p.K501K c.1503G>A 7 7622858 HNSC G A Synonymous p.T392T c.1176G>A 7 7613282 COREAD G C Missense p.A593P c.1777G>C 7 7625395 BRCA G C Missense p.E257Q c.769G>C 7 7612875 LUSC G C Missense p.E376Q c.1126G>C 7 7613232 LUAD G C Missense p.M466I c.1398G>C 7 7622753 LUAD G C Missense p.R616T c.1847G>C 7 7628157 BLCA G C Missense p.R668T c.2003G>C 7 7629154 MM G - Frameshift p.D252Ifs*10 c.754delG 7 7612858 LUAD GT AA Missense p.V611N c.1831_1832delinsAA 7 7628141 CM G T Missense p.R288M c.863G>T 7 7612969 LUSC G T Missense p.V617L c.1849G>T 7 7628159 DLBCL G T Missense p.W410L c.1229G>T 7 7613335 LUAD G T Nonsense p.E379* c.1135G>T 7 7613241 STAD G T Nonsense p.E663* c.1987G>T 7 7629138 NB G T Synonymous p.T768T c.2304G>T 7 7635995 RCCC T A Missense p.Y28N c.82T>A 7 7612188 CM T C Synonymous p.P6P c.18T>C 7 7612124 STAD T C Synonymous p.R614R c.1842T>C 7 7628152 STAD