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 9 96398772 96398772 + Silent SNP C C G TCGA-FD-A43X-01A-11D-A23U-08 TCGA-FD-A43X-10A-01D-A23U-08 g.chr9:96398772C>G c.264C>G c.(262-264)ctC>ctG p.L88L BLCA 9 96415473 96415473 + Silent SNP C C T TCGA-CF-A1HR-01A-11D-A13W-08 TCGA-CF-A1HR-10A-01D-A13W-08 g.chr9:96415473C>T c.615C>T c.(613-615)ttC>ttT p.F205F BLCA 9 96415636 96415636 + Missense_Mutation SNP C C T TCGA-4Z-AA87-01A-11D-A391-08 TCGA-4Z-AA87-10A-01D-A394-08 g.chr9:96415636C>T c.778C>T c.(778-780)Cac>Tac p.H260Y BLCA 9 96425260 96425260 + Missense_Mutation SNP A A C TCGA-HQ-A5NE-01A-12D-A289-08 TCGA-HQ-A5NE-10A-01D-A289-08 g.chr9:96425260A>C c.1770A>C c.(1768-1770)gaA>gaC p.E590D BLCA 9 96436024 96436024 + Missense_Mutation SNP G G T TCGA-ZF-A9RN-01A-11D-A42E-08 TCGA-ZF-A9RN-10A-01D-A42H-08 g.chr9:96436024G>T c.2506G>T c.(2506-2508)Ggc>Tgc p.G836C BRCA 9 96339128 96339128 + Missense_Mutation SNP G G A TCGA-AO-A128-01A-11D-A10M-09 TCGA-AO-A128-10A-01D-A10M-09 g.chr9:96339128G>A c.73G>A c.(73-75)Gcc>Acc p.A25T BRCA 9 96425264 96425264 + Nonsense_Mutation SNP C C T TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr9:96425264C>T c.1774C>T c.(1774-1776)Cga>Tga p.R592* BRCA 9 96439907 96439907 + Missense_Mutation SNP G G C TCGA-AC-A62Y-01A-11D-A29N-09 TCGA-AC-A62Y-10A-01D-A29N-09 g.chr9:96439907G>C c.3240G>C c.(3238-3240)caG>caC p.Q1080H BRCA 9 96439925 96439925 + Silent SNP G G A TCGA-D8-A1J8-01A-11D-A13L-09 TCGA-D8-A1J8-10A-01D-A13O-09 g.chr9:96439925G>A c.3258G>A c.(3256-3258)ttG>ttA p.L1086L CESC 9 96339125 96339125 + Missense_Mutation SNP G G C TCGA-C5-A1BL-01A-11D-A13W-08 TCGA-C5-A1BL-10A-01D-A13W-08 g.chr9:96339125G>C c.70G>C c.(70-72)Gac>Cac p.D24H CESC 9 96398778 96398778 + Silent SNP C C T TCGA-WL-A834-01A-11D-A351-09 TCGA-WL-A834-10A-01D-A351-09 g.chr9:96398778C>T c.270C>T c.(268-270)atC>atT p.I90I CESC 9 96421802 96421802 + Missense_Mutation SNP G G C TCGA-UC-A7PF-01A-11D-A351-09 TCGA-UC-A7PF-11A-31D-A351-09 g.chr9:96421802G>C c.1249G>C c.(1249-1251)Gag>Cag p.E417Q COAD 9 96398693 96398693 + Splice_Site SNP T T C TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr9:96398693T>C c.185T>C c.(184-186)tTa>tCa p.L62S COAD 9 96398789 96398789 + Missense_Mutation SNP G G A TCGA-AA-A00J-01A-02W-A005-10 TCGA-AA-A00J-10A-01W-A005-10 g.chr9:96398789G>A c.281G>A c.(280-282)cGg>cAg p.R94Q COAD 9 96411440 96411440 + Missense_Mutation SNP G G A TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr9:96411440G>A c.548G>A c.(547-549)aGc>aAc p.S183N COAD 9 96411465 96411465 + Silent SNP C C T TCGA-A6-5662-01A-01D-1650-10 TCGA-A6-5662-10A-01D-1650-10 g.chr9:96411465C>T c.573C>T c.(571-573)aaC>aaT p.N191N COAD 9 96415578 96415578 + Silent SNP C C T TCGA-AA-3837-01A-01W-0900-09 TCGA-AA-3837-10A-01W-0900-09 g.chr9:96415578C>T c.720C>T c.(718-720)tgC>tgT p.C240C COAD 9 96416729 96416729 + Missense_Mutation SNP C C T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr9:96416729C>T c.824C>T c.(823-825)tCg>tTg p.S275L COAD 9 96418259 96418259 + Silent SNP C C T TCGA-AD-6895-01A-11D-1924-10 TCGA-AD-6895-10A-01D-1924-10 g.chr9:96418259C>T c.996C>T c.(994-996)ttC>ttT p.F332F COAD 9 96418817 96418817 + Missense_Mutation SNP T T C TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chr9:96418817T>C c.1087T>C c.(1087-1089)Ttt>Ctt p.F363L COAD 9 96422489 96422489 + Missense_Mutation SNP G G A TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr9:96422489G>A c.1345G>A c.(1345-1347)Gtc>Atc p.V449I COAD 9 96422497 96422497 + Silent SNP G G A TCGA-A6-6780-01A-11D-1835-10 TCGA-A6-6780-10A-01D-1835-10 g.chr9:96422497G>A c.1353G>A c.(1351-1353)ccG>ccA p.P451P COAD 9 96422563 96422563 + Silent SNP G G A TCGA-G4-6309-01A-21D-1835-10 TCGA-G4-6309-10A-01D-1835-10 g.chr9:96422563G>A c.1419G>A c.(1417-1419)ccG>ccA p.P473P COAD 9 96422668 96422668 + Silent SNP C C A TCGA-AA-A022-01A-21W-A096-10 TCGA-AA-A022-11A-11W-A096-10 g.chr9:96422668C>A c.1524C>A c.(1522-1524)ccC>ccA p.P508P COAD 9 96422703 96422703 + Missense_Mutation SNP C C T TCGA-D5-6930-01A-11D-1924-10 TCGA-D5-6930-10A-01D-1924-10 g.chr9:96422703C>T c.1559C>T c.(1558-1560)aCg>aTg p.T520M COAD 9 96425189 96425189 + Splice_Site SNP G G A TCGA-AA-A01R-01A-21W-A096-10 TCGA-AA-A01R-11A-12W-A096-10 g.chr9:96425189G>A c.1699G>A c.(1699-1701)Gcc>Acc p.A567T COAD 9 96425264 96425264 + Nonsense_Mutation SNP C C T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr9:96425264C>T c.1774C>T c.(1774-1776)Cga>Tga p.R592* COAD 9 96425863 96425863 + Missense_Mutation SNP C C T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr9:96425863C>T c.1883C>T c.(1882-1884)gCt>gTt p.A628V COAD 9 96425881 96425881 + Missense_Mutation SNP A A C TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr9:96425881A>C c.1901A>C c.(1900-1902)aAg>aCg p.K634T COAD 9 96429455 96429455 + Missense_Mutation SNP G G A TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr9:96429455G>A c.2281G>A c.(2281-2283)Gca>Aca p.A761T COAD 9 96435977 96435977 + Missense_Mutation SNP C C T TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr9:96435977C>T c.2459C>T c.(2458-2460)gCc>gTc p.A820V COAD 9 96438003 96438003 + Missense_Mutation SNP C C T TCGA-AA-3516-01A-02W-0833-10 TCGA-AA-3516-10A-01W-0833-10 g.chr9:96438003C>T c.2764C>T c.(2764-2766)Cgt>Tgt p.R922C COAD 9 96438893 96438894 + Frame_Shift_Ins INS - - A TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr9:96438893_96438894insA c.2850_2851insA c.(2851-2853)aaafs p.K951fs COAD 9 96438992 96438992 + Silent SNP A A T TCGA-AY-6386-01A-21D-1719-10 TCGA-AY-6386-10A-01D-1719-10 g.chr9:96438992A>T c.2949A>T c.(2947-2949)ccA>ccT p.P983P COAD 9 96439161 96439161 + Missense_Mutation SNP A A G TCGA-AD-6964-01A-11D-1924-10 TCGA-AD-6964-10A-01D-1924-10 g.chr9:96439161A>G c.3118A>G c.(3118-3120)Acc>Gcc p.T1040A COADREAD 9 96398693 96398693 + Splice_Site SNP T T C TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr9:96398693T>C c.185T>C c.(184-186)tTa>tCa p.L62S COADREAD 9 96398789 96398789 + Missense_Mutation SNP G G A TCGA-AA-A00J-01A-02W-A005-10 TCGA-AA-A00J-10A-01W-A005-10 g.chr9:96398789G>A c.281G>A c.(280-282)cGg>cAg p.R94Q COADREAD 9 96411440 96411440 + Missense_Mutation SNP G G A TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr9:96411440G>A c.548G>A c.(547-549)aGc>aAc p.S183N COADREAD 9 96411465 96411465 + Silent SNP C C T TCGA-A6-5662-01A-01D-1650-10 TCGA-A6-5662-10A-01D-1650-10 g.chr9:96411465C>T c.573C>T c.(571-573)aaC>aaT p.N191N COADREAD 9 96415578 96415578 + Silent SNP C C T TCGA-AA-3837-01A-01W-0900-09 TCGA-AA-3837-10A-01W-0900-09 g.chr9:96415578C>T c.720C>T c.(718-720)tgC>tgT p.C240C COADREAD 9 96416729 96416729 + Missense_Mutation SNP C C T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr9:96416729C>T c.824C>T c.(823-825)tCg>tTg p.S275L COADREAD 9 96418259 96418259 + Silent SNP C C T TCGA-AD-6895-01A-11D-1924-10 TCGA-AD-6895-10A-01D-1924-10 g.chr9:96418259C>T c.996C>T c.(994-996)ttC>ttT p.F332F COADREAD 9 96418817 96418817 + Missense_Mutation SNP T T C TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chr9:96418817T>C c.1087T>C c.(1087-1089)Ttt>Ctt p.F363L COADREAD 9 96422489 96422489 + Missense_Mutation SNP G G A TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr9:96422489G>A c.1345G>A c.(1345-1347)Gtc>Atc p.V449I COADREAD 9 96422497 96422497 + Silent SNP G G A TCGA-A6-6780-01A-11D-1835-10 TCGA-A6-6780-10A-01D-1835-10 g.chr9:96422497G>A c.1353G>A c.(1351-1353)ccG>ccA p.P451P COADREAD 9 96422563 96422563 + Silent SNP G G A TCGA-G4-6309-01A-21D-1835-10 TCGA-G4-6309-10A-01D-1835-10 g.chr9:96422563G>A c.1419G>A c.(1417-1419)ccG>ccA p.P473P COADREAD 9 96422668 96422668 + Silent SNP C C A TCGA-AA-A022-01A-21W-A096-10 TCGA-AA-A022-11A-11W-A096-10 g.chr9:96422668C>A c.1524C>A c.(1522-1524)ccC>ccA p.P508P COADREAD 9 96422703 96422703 + Missense_Mutation SNP C C T TCGA-D5-6930-01A-11D-1924-10 TCGA-D5-6930-10A-01D-1924-10 g.chr9:96422703C>T c.1559C>T c.(1558-1560)aCg>aTg p.T520M COADREAD 9 96425189 96425189 + Splice_Site SNP G G A TCGA-AA-A01R-01A-21W-A096-10 TCGA-AA-A01R-11A-12W-A096-10 g.chr9:96425189G>A c.1699G>A c.(1699-1701)Gcc>Acc p.A567T COADREAD 9 96425264 96425264 + Nonsense_Mutation SNP C C T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr9:96425264C>T c.1774C>T c.(1774-1776)Cga>Tga p.R592* COADREAD 9 96425863 96425863 + Missense_Mutation SNP C C T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr9:96425863C>T c.1883C>T c.(1882-1884)gCt>gTt p.A628V COADREAD 9 96425881 96425881 + Missense_Mutation SNP A A C TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr9:96425881A>C c.1901A>C c.(1900-1902)aAg>aCg p.K634T COADREAD 9 96429455 96429455 + Missense_Mutation SNP G G A TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr9:96429455G>A c.2281G>A c.(2281-2283)Gca>Aca p.A761T COADREAD 9 96435977 96435977 + Missense_Mutation SNP C C T TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr9:96435977C>T c.2459C>T c.(2458-2460)gCc>gTc p.A820V COADREAD 9 96436063 96436063 + Missense_Mutation SNP G G A TCGA-EI-6507-01A-11D-1733-10 TCGA-EI-6507-10A-01D-1733-10 g.chr9:96436063G>A c.2545G>A c.(2545-2547)Gct>Act p.A849T COADREAD 9 96436080 96436080 + Silent SNP C C T TCGA-EI-6507-01A-11D-1733-10 TCGA-EI-6507-10A-01D-1733-10 g.chr9:96436080C>T c.2562C>T c.(2560-2562)gtC>gtT p.V854V COADREAD 9 96438003 96438003 + Missense_Mutation SNP C C T TCGA-AA-3516-01A-02W-0833-10 TCGA-AA-3516-10A-01W-0833-10 g.chr9:96438003C>T c.2764C>T c.(2764-2766)Cgt>Tgt p.R922C COADREAD 9 96438893 96438894 + Frame_Shift_Ins INS - - A TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr9:96438893_96438894insA c.2850_2851insA c.(2851-2853)aaafs p.K951fs COADREAD 9 96438992 96438992 + Silent SNP A A T TCGA-AY-6386-01A-21D-1719-10 TCGA-AY-6386-10A-01D-1719-10 g.chr9:96438992A>T c.2949A>T c.(2947-2949)ccA>ccT p.P983P COADREAD 9 96439161 96439161 + Missense_Mutation SNP A A G TCGA-AD-6964-01A-11D-1924-10 TCGA-AD-6964-10A-01D-1924-10 g.chr9:96439161A>G c.3118A>G c.(3118-3120)Acc>Gcc p.T1040A DLBC 9 96407953 96407953 + Silent SNP G G A TCGA-G8-6326-01A-11D-2210-10 TCGA-G8-6326-10A-01D-2210-10 g.chr9:96407953G>A c.342G>A c.(340-342)acG>acA p.T114T DLBC 9 96411414 96411414 + Silent SNP G G A TCGA-G8-6326-01A-11D-2210-10 TCGA-G8-6326-10A-01D-2210-10 g.chr9:96411414G>A c.522G>A c.(520-522)ctG>ctA p.L174L DLBC 9 96416812 96416812 + Missense_Mutation SNP T T A TCGA-GS-A9TT-01A-11D-A382-10 TCGA-GS-A9TT-10A-01D-A385-10 g.chr9:96416812T>A c.907T>A c.(907-909)Tac>Aac p.Y303N DLBC 9 96436037 96436037 + Missense_Mutation SNP G G A TCGA-G8-6326-01A-11D-2210-10 TCGA-G8-6326-10A-01D-2210-10 g.chr9:96436037G>A c.2519G>A c.(2518-2520)aGt>aAt p.S840N ESCA 9 96420441 96420441 + Missense_Mutation SNP G G T TCGA-L5-A88Z-01A-11D-A36J-09 TCGA-L5-A88Z-11A-11D-A36M-09 g.chr9:96420441G>T c.1162G>T c.(1162-1164)Ggg>Tgg p.G388W ESCA 9 96420446 96420446 + Missense_Mutation SNP G G T TCGA-L5-A88W-01A-11D-A351-09 TCGA-L5-A88W-11A-11D-A351-09 g.chr9:96420446G>T c.1167G>T c.(1165-1167)aaG>aaT p.K389N ESCA 9 96422621 96422621 + Missense_Mutation SNP A A G TCGA-L5-A4OI-01A-11D-A27G-09 TCGA-L5-A4OI-11A-11D-A27G-09 g.chr9:96422621A>G c.1477A>G c.(1477-1479)Act>Gct p.T493A ESCA 9 96422642 96422642 + Missense_Mutation SNP C C A TCGA-L5-A4OI-01A-11D-A27G-09 TCGA-L5-A4OI-11A-11D-A27G-09 g.chr9:96422642C>A c.1498C>A c.(1498-1500)Ccc>Acc p.P500T ESCA 9 96422679 96422679 + Missense_Mutation SNP C C A TCGA-L5-A4OI-01A-11D-A27G-09 TCGA-L5-A4OI-11A-11D-A27G-09 g.chr9:96422679C>A c.1535C>A c.(1534-1536)cCt>cAt p.P512H ESCA 9 96428105 96428105 + Missense_Mutation SNP C C T TCGA-L5-A88T-01A-11D-A351-09 TCGA-L5-A88T-11A-11D-A351-09 g.chr9:96428105C>T c.2075C>T c.(2074-2076)cCc>cTc p.P692L ESCA 9 96428130 96428130 + Silent SNP G G A TCGA-R6-A8W8-01B-11D-A37C-09 TCGA-R6-A8W8-10A-01D-A37F-09 g.chr9:96428130G>A c.2100G>A c.(2098-2100)ccG>ccA p.P700P ESCA 9 96428302 96428302 + Missense_Mutation SNP C C T TCGA-LN-A9FQ-01A-31D-A387-09 TCGA-LN-A9FQ-10A-01D-A38A-09 g.chr9:96428302C>T c.2147C>T c.(2146-2148)aCg>aTg p.T716M ESCA 9 96429413 96429413 + Missense_Mutation SNP C C T TCGA-R6-A6DQ-01B-11D-A31U-09 TCGA-R6-A6DQ-10A-01D-A31U-09 g.chr9:96429413C>T c.2239C>T c.(2239-2241)Ccc>Tcc p.P747S ESCA 9 96438978 96438979 + Frame_Shift_Ins INS - - G TCGA-LN-A49Y-01A-11D-A27G-09 TCGA-LN-A49Y-10A-01D-A27G-09 g.chr9:96438978_96438979insG c.2935_2936insG c.(2935-2937)accfs p.T979fs ESCA 9 96439033 96439033 + Missense_Mutation SNP G G C TCGA-L5-A893-01A-11D-A36J-09 TCGA-L5-A893-11A-21D-A36M-09 g.chr9:96439033G>C c.2990G>C c.(2989-2991)aGc>aCc p.S997T GBM 9 96408031 96408031 + Silent SNP G G A TCGA-76-6663-01A-11D-1845-08 TCGA-76-6663-10A-01D-1845-08 g.chr9:96408031G>A c.420G>A c.(418-420)ccG>ccA p.P140P GBM 9 96421820 96421820 + Missense_Mutation SNP C C T TCGA-74-6584-01A-11D-1845-08 TCGA-74-6584-10A-01D-1845-08 g.chr9:96421820C>T c.1267C>T c.(1267-1269)Ccg>Tcg p.P423S GBMLGG 9 96339133 96339133 + Silent SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr9:96339133C>T c.78C>T c.(76-78)tgC>tgT p.C26C GBMLGG 9 96408031 96408031 + Silent SNP G G A TCGA-76-6663-01A-11D-1845-08 TCGA-76-6663-10A-01D-1845-08 g.chr9:96408031G>A c.420G>A c.(418-420)ccG>ccA p.P140P GBMLGG 9 96421820 96421820 + Missense_Mutation SNP C C T TCGA-74-6584-01A-11D-1845-08 TCGA-74-6584-10A-01D-1845-08 g.chr9:96421820C>T c.1267C>T c.(1267-1269)Ccg>Tcg p.P423S HNSC 9 96339120 96339120 + Missense_Mutation SNP A A G TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr9:96339120A>G c.65A>G c.(64-66)gAg>gGg p.E22G HNSC 9 96408047 96408047 + Missense_Mutation SNP G G A TCGA-MT-A51W-01A-21D-A25Y-08 TCGA-MT-A51W-10A-01D-A25Y-08 g.chr9:96408047G>A c.436G>A c.(436-438)Gtc>Atc p.V146I HNSC 9 96418259 96418259 + Silent SNP C C T TCGA-CV-7180-01A-11D-2012-08 TCGA-CV-7180-10A-01D-2013-08 g.chr9:96418259C>T c.996C>T c.(994-996)ttC>ttT p.F332F HNSC 9 96418829 96418829 + Missense_Mutation SNP G G A TCGA-F7-A50J-01A-21D-A28R-08 TCGA-F7-A50J-10A-01D-A28U-08 g.chr9:96418829G>A c.1099G>A c.(1099-1101)Gaa>Aaa p.E367K HNSC 9 96418870 96418870 + Silent SNP A A C TCGA-D6-A6EP-01A-11D-A31L-08 TCGA-D6-A6EP-10A-01D-A31J-08 g.chr9:96418870A>C c.1140A>C c.(1138-1140)gcA>gcC p.A380A HNSC 9 96435940 96435940 + Missense_Mutation SNP G G A TCGA-CV-5970-01A-11D-1683-08 TCGA-CV-5970-10A-01D-1870-08 g.chr9:96435940G>A c.2422G>A c.(2422-2424)Gac>Aac p.D808N HNSC 9 96437210 96437210 + Splice_Site SNP T T C TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr9:96437210T>C c.2628T>C c.(2626-2628)gtT>gtC p.V876V HNSC 9 96437264 96437264 + Missense_Mutation SNP G G C TCGA-CV-5436-01A-01D-1512-08 TCGA-CV-5436-10A-01D-1870-08 g.chr9:96437264G>C c.2682G>C c.(2680-2682)aaG>aaC p.K894N KIPAN 9 96416716 96416716 + Missense_Mutation SNP A A C TCGA-EV-5903-01A-11D-1589-08 TCGA-EV-5903-10A-01D-1589-08 g.chr9:96416716A>C c.811A>C c.(811-813)Atc>Ctc p.I271L KIPAN 9 96421819 96421819 + Silent SNP C C T TCGA-2Z-A9J2-01A-11D-A382-10 TCGA-2Z-A9J2-10A-01D-A385-10 g.chr9:96421819C>T c.1266C>T c.(1264-1266)ctC>ctT p.L422L KIPAN 9 96435951 96435951 + Silent SNP G G C TCGA-UZ-A9PZ-01A-11D-A42J-10 TCGA-UZ-A9PZ-10A-01D-A42M-10 g.chr9:96435951G>C c.2433G>C c.(2431-2433)ctG>ctC p.L811L KIRP 9 96416716 96416716 + Missense_Mutation SNP A A C TCGA-EV-5903-01A-11D-1589-08 TCGA-EV-5903-10A-01D-1589-08 g.chr9:96416716A>C c.811A>C c.(811-813)Atc>Ctc p.I271L KIRP 9 96421819 96421819 + Silent SNP C C T TCGA-2Z-A9J2-01A-11D-A382-10 TCGA-2Z-A9J2-10A-01D-A385-10 g.chr9:96421819C>T c.1266C>T c.(1264-1266)ctC>ctT p.L422L KIRP 9 96435951 96435951 + Silent SNP G G C TCGA-UZ-A9PZ-01A-11D-A42J-10 TCGA-UZ-A9PZ-10A-01D-A42M-10 g.chr9:96435951G>C c.2433G>C c.(2431-2433)ctG>ctC p.L811L LGG 9 96339133 96339133 + Silent SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr9:96339133C>T c.78C>T c.(76-78)tgC>tgT p.C26C LIHC 9 96416768 96416768 + Missense_Mutation SNP C C G TCGA-UB-A7MC-01A-11D-A33Q-10 TCGA-UB-A7MC-10A-01D-A33Q-10 g.chr9:96416768C>G c.863C>G c.(862-864)tCt>tGt p.S288C LIHC 9 96428080 96428080 + Missense_Mutation SNP G G T TCGA-EP-A2KB-01A-11D-A183-10 TCGA-EP-A2KB-10A-01D-A183-10 g.chr9:96428080G>T c.2050G>T c.(2050-2052)Ggt>Tgt p.G684C LIHC 9 96429513 96429513 + Missense_Mutation SNP A A G TCGA-DD-A1ED-01A-11D-A152-10 TCGA-DD-A1ED-10A-01D-A152-10 g.chr9:96429513A>G c.2339A>G c.(2338-2340)aAc>aGc p.N780S LIHC 9 96435949 96435949 + Silent SNP C C T TCGA-DD-A4NJ-01A-11D-A27I-10 TCGA-DD-A4NJ-10A-01D-A27I-10 g.chr9:96435949C>T c.2431C>T c.(2431-2433)Ctg>Ttg p.L811L LIHC 9 96438992 96438992 + Silent SNP A A T TCGA-BC-A3KF-01A-11D-A20W-10 TCGA-BC-A3KF-10A-01D-A20W-10 g.chr9:96438992A>T c.2949A>T c.(2947-2949)ccA>ccT p.P983P LUAD 9 96392312 96392312 + Missense_Mutation SNP T T G TCGA-NJ-A4YF-01A-12D-A25L-08 TCGA-NJ-A4YF-10A-01D-A25L-08 g.chr9:96392312T>G c.159T>G c.(157-159)tgT>tgG p.C53W LUAD 9 96392313 96392313 + Nonsense_Mutation SNP G G T TCGA-NJ-A4YF-01A-12D-A25L-08 TCGA-NJ-A4YF-10A-01D-A25L-08 g.chr9:96392313G>T c.160G>T c.(160-162)Gag>Tag p.E54* LUAD 9 96408012 96408012 + Missense_Mutation SNP G G T TCGA-86-8073-01A-11D-2238-08 TCGA-86-8073-10A-01D-2238-08 g.chr9:96408012G>T c.401G>T c.(400-402)gGg>gTg p.G134V LUAD 9 96408013 96408013 + Silent SNP G G T TCGA-86-8073-01A-11D-2238-08 TCGA-86-8073-10A-01D-2238-08 g.chr9:96408013G>T c.402G>T c.(400-402)ggG>ggT p.G134G LUAD 9 96421880 96421880 + Nonsense_Mutation SNP G G T TCGA-55-7283-01A-11D-2036-08 TCGA-55-7283-10A-01D-2036-08 g.chr9:96421880G>T c.1327G>T c.(1327-1329)Gag>Tag p.E443* LUAD 9 96427980 96427980 + Silent SNP C C G TCGA-49-4514-01A-21D-1855-08 TCGA-49-4514-11A-01D-1855-08 g.chr9:96427980C>G c.1950C>G c.(1948-1950)ctC>ctG p.L650L LUAD 9 96428051 96428051 + Missense_Mutation SNP G G A TCGA-17-Z048-01A-01W-0746-08 TCGA-17-Z048-11A-01W-0746-08 g.chr9:96428051G>A c.2021G>A c.(2020-2022)cGg>cAg p.R674Q LUAD 9 96428055 96428055 + Missense_Mutation SNP T T A TCGA-55-A492-01A-11D-A24D-08 TCGA-55-A492-10A-01D-A24F-08 g.chr9:96428055T>A c.2025T>A c.(2023-2025)gaT>gaA p.D675E LUAD 9 96428303 96428303 + Silent SNP G G C TCGA-86-8073-01A-11D-2238-08 TCGA-86-8073-10A-01D-2238-08 g.chr9:96428303G>C c.2148G>C c.(2146-2148)acG>acC p.T716T LUAD 9 96429477 96429477 + Missense_Mutation SNP T T G TCGA-95-7043-01A-11D-1945-08 TCGA-95-7043-10A-01D-1946-08 g.chr9:96429477T>G c.2303T>G c.(2302-2304)cTg>cGg p.L768R LUAD 9 96435944 96435944 + Missense_Mutation SNP C C A TCGA-NJ-A4YI-01A-11D-A25L-08 TCGA-NJ-A4YI-10A-01D-A25L-08 g.chr9:96435944C>A c.2426C>A c.(2425-2427)tCc>tAc p.S809Y LUAD 9 96436116 96436116 + Silent SNP G G T TCGA-50-5930-01A-11D-1753-08 TCGA-50-5930-11A-01D-1753-08 g.chr9:96436116G>T c.2598G>T c.(2596-2598)ctG>ctT p.L866L LUAD 9 96438008 96438008 + Missense_Mutation SNP G G C TCGA-55-8511-01A-11D-2393-08 TCGA-55-8511-10A-01D-2393-08 g.chr9:96438008G>C c.2769G>C c.(2767-2769)gaG>gaC p.E923D LUAD 9 96438932 96438932 + Silent SNP C C T TCGA-55-8507-01A-11D-2393-08 TCGA-55-8507-10A-01D-2393-08 g.chr9:96438932C>T c.2889C>T c.(2887-2889)acC>acT p.T963T LUAD 9 96439152 96439152 + Missense_Mutation SNP G G T TCGA-55-8616-01A-11D-2393-08 TCGA-55-8616-10A-01D-2393-08 g.chr9:96439152G>T c.3109G>T c.(3109-3111)Gct>Tct p.A1037S LUAD 9 96439907 96439907 + Silent SNP G G A TCGA-78-7539-01A-11D-2063-08 TCGA-78-7539-10A-01D-2063-08 g.chr9:96439907G>A c.3240G>A c.(3238-3240)caG>caA p.Q1080Q LUSC 9 96407915 96407915 + Missense_Mutation SNP G G A TCGA-22-1011-01A-01D-1521-08 TCGA-22-1011-11A-01D-1521-08 g.chr9:96407915G>A c.304G>A c.(304-306)Gaa>Aaa p.E102K LUSC 9 96407921 96407921 + Missense_Mutation SNP G G C TCGA-37-5819-01A-01D-1632-08 TCGA-37-5819-10A-01D-1632-08 g.chr9:96407921G>C c.310G>C c.(310-312)Gtg>Ctg p.V104L LUSC 9 96416756 96416756 + Missense_Mutation SNP G G T TCGA-66-2727-01A-01D-0983-08 TCGA-66-2727-11A-01D-0983-08 g.chr9:96416756G>T c.851G>T c.(850-852)tGg>tTg p.W284L LUSC 9 96418814 96418814 + Missense_Mutation SNP C C G TCGA-66-2787-01A-01D-0983-08 TCGA-66-2787-11A-01D-0983-08 g.chr9:96418814C>G c.1084C>G c.(1084-1086)Cag>Gag p.Q362E LUSC 9 96437969 96437969 + Silent SNP C C T TCGA-66-2727-01A-01D-0983-08 TCGA-66-2727-11A-01D-0983-08 g.chr9:96437969C>T c.2730C>T c.(2728-2730)gtC>gtT p.V910V OV 9 96416841 96416841 + Silent SNP C C T TCGA-24-0979-01A-01W-0486-08 TCGA-24-0979-10B-01W-0486-08 g.chr9:96416841C>T c.936C>T c.(934-936)acC>acT p.T312T OV 9 96439081 96439081 + Missense_Mutation SNP C C T TCGA-13-2057-01A-02D-1526-09 TCGA-13-2057-10A-01D-1526-09 g.chr9:96439081C>T c.3038C>T c.(3037-3039)cCg>cTg p.P1013L PAAD 9 96392276 96392276 + Silent SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr9:96392276G>A c.123G>A c.(121-123)gaG>gaA p.E41E PAAD 9 96418827 96418827 + Missense_Mutation SNP T T A TCGA-XN-A8T5-01A-12D-A36O-08 TCGA-XN-A8T5-10A-01D-A367-08 g.chr9:96418827T>A c.1097T>A c.(1096-1098)tTt>tAt p.F366Y PAAD 9 96425295 96425295 + Missense_Mutation SNP A A G TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr9:96425295A>G c.1805A>G c.(1804-1806)aAg>aGg p.K602R PAAD 9 96435918 96435918 + Silent SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr9:96435918C>T c.2400C>T c.(2398-2400)tcC>tcT p.S800S PRAD 9 96418836 96418836 + Missense_Mutation SNP C C T TCGA-VP-A87D-01A-11D-A34U-08 TCGA-VP-A87D-10A-01D-A34X-08 g.chr9:96418836C>T c.1106C>T c.(1105-1107)gCg>gTg p.A369V PRAD 9 96420442 96420442 + Missense_Mutation SNP G G C TCGA-KK-A8IK-01A-11D-A364-08 TCGA-KK-A8IK-11A-11D-A362-08 g.chr9:96420442G>C c.1163G>C c.(1162-1164)gGg>gCg p.G388A PRAD 9 96439899 96439899 + Missense_Mutation SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr9:96439899G>A c.3232G>A c.(3232-3234)Gcc>Acc p.A1078T READ 9 96436063 96436063 + Missense_Mutation SNP G G A TCGA-EI-6507-01A-11D-1733-10 TCGA-EI-6507-10A-01D-1733-10 g.chr9:96436063G>A c.2545G>A c.(2545-2547)Gct>Act p.A849T READ 9 96436080 96436080 + Silent SNP C C T TCGA-EI-6507-01A-11D-1733-10 TCGA-EI-6507-10A-01D-1733-10 g.chr9:96436080C>T c.2562C>T c.(2560-2562)gtC>gtT p.V854V SKCM 9 96407930 96407930 + Missense_Mutation SNP C C A TCGA-ER-A2NE-06A-21D-A196-08 TCGA-ER-A2NE-10A-01D-A198-08 g.chr9:96407930C>A c.319C>A c.(319-321)Cgt>Agt p.R107S SKCM 9 96407999 96407999 + Missense_Mutation SNP C C T TCGA-EE-A2GO-06A-11D-A196-08 TCGA-EE-A2GO-10A-01D-A198-08 g.chr9:96407999C>T c.388C>T c.(388-390)Cct>Tct p.P130S SKCM 9 96416852 96416852 + Missense_Mutation SNP C C T TCGA-EE-A29M-06A-11D-A196-08 TCGA-EE-A29M-10A-01D-A198-08 g.chr9:96416852C>T c.947C>T c.(946-948)cCc>cTc p.P316L SKCM 9 96418822 96418822 + Silent SNP C C T TCGA-D3-A2JG-06A-11D-A196-08 TCGA-D3-A2JG-10A-01D-A198-08 g.chr9:96418822C>T c.1092C>T c.(1090-1092)ccC>ccT p.P364P SKCM 9 96420455 96420455 + Silent SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr9:96420455C>T c.1176C>T c.(1174-1176)ccC>ccT p.P392P SKCM 9 96422565 96422565 + Missense_Mutation SNP C C T TCGA-ER-A19W-06A-41D-A23B-08 TCGA-ER-A19W-10A-01D-A23B-08 g.chr9:96422565C>T c.1421C>T c.(1420-1422)tCt>tTt p.S474F SKCM 9 96425206 96425206 + Silent SNP G G T TCGA-FW-A3TU-06A-11D-A23B-08 TCGA-FW-A3TU-10A-01D-A23B-08 g.chr9:96425206G>T c.1716G>T c.(1714-1716)ctG>ctT p.L572L SKCM 9 96425208 96425208 + Missense_Mutation SNP G G A TCGA-FW-A3TU-06A-11D-A23B-08 TCGA-FW-A3TU-10A-01D-A23B-08 g.chr9:96425208G>A c.1718G>A c.(1717-1719)aGt>aAt p.S573N SKCM 9 96425891 96425891 + Missense_Mutation SNP T T A TCGA-GF-A6C8-06A-12D-A30X-08 TCGA-GF-A6C8-10A-01D-A30X-08 g.chr9:96425891T>A c.1911T>A c.(1909-1911)ttT>ttA p.F637L SKCM 9 96428031 96428031 + Silent SNP G G A TCGA-EE-A3AA-06A-11D-A196-08 TCGA-EE-A3AA-10A-01D-A198-08 g.chr9:96428031G>A c.2001G>A c.(1999-2001)gaG>gaA p.E667E SKCM 9 96428317 96428317 + Missense_Mutation SNP C C T TCGA-FS-A1ZW-06A-12D-A197-08 TCGA-FS-A1ZW-10A-01D-A199-08 g.chr9:96428317C>T c.2162C>T c.(2161-2163)cCa>cTa p.P721L SKCM 9 96429433 96429433 + Silent SNP C C T TCGA-EE-A2MS-06A-11D-A197-08 TCGA-EE-A2MS-10A-01D-A199-08 g.chr9:96429433C>T c.2259C>T c.(2257-2259)gtC>gtT p.V753V SKCM 9 96429453 96429453 + Missense_Mutation SNP C C T TCGA-GN-A262-06A-11D-A196-08 TCGA-GN-A262-10A-01D-A198-08 g.chr9:96429453C>T c.2279C>T c.(2278-2280)tCg>tTg p.S760L SKCM 9 96435917 96435917 + Missense_Mutation SNP C C T TCGA-EE-A29B-06A-11D-A197-08 TCGA-EE-A29B-10A-01D-A199-08 g.chr9:96435917C>T c.2399C>T c.(2398-2400)tCc>tTc p.S800F SKCM 9 96437255 96437255 + Silent SNP C C T TCGA-EE-A29G-06A-12D-A196-08 TCGA-EE-A29G-10A-01D-A198-08 g.chr9:96437255C>T c.2673C>T c.(2671-2673)tcC>tcT p.S891S SKCM 9 96437289 96437289 + Missense_Mutation SNP C C T TCGA-EE-A20C-06A-11D-A196-08 TCGA-EE-A20C-10A-01D-A198-08 g.chr9:96437289C>T c.2707C>T c.(2707-2709)Ccc>Tcc p.P903S SKCM 9 96437290 96437290 + Missense_Mutation SNP C C T TCGA-EE-A20C-06A-11D-A196-08 TCGA-EE-A20C-10A-01D-A198-08 g.chr9:96437290C>T c.2708C>T c.(2707-2709)cCc>cTc p.P903L

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 9 96416759 96416759 single base substitution G A intron_variant ALL-US 9 96416759 96416759 single base substitution G A missense_variant R285Q 854G>A BLCA-CN 9 96407920 96407920 single base substitution C T intron_variant BLCA-CN 9 96407920 96407920 single base substitution C T synonymous_variant D103D 309C>T BLCA-US 9 96415473 96415473 single base substitution C T intron_variant BLCA-US 9 96415473 96415473 single base substitution C T synonymous_variant F205F 615C>T BRCA-EU 9 96337879 96337879 single base substitution C T upstream_gene_variant BRCA-EU 9 96339120 96339120 single base substitution A T missense_variant E22V 65A>T BRCA-EU 9 96339222 96339222 single base substitution C T intron_variant BRCA-EU 9 96339470 96339470 single base substitution C T intron_variant BRCA-EU 9 96339867 96339867 deletion of <=200bp G - intron_variant BRCA-EU 9 96339872 96339872 single base substitution G T intron_variant BRCA-EU 9 96340147 96340147 single base substitution T A intron_variant BRCA-EU 9 96341899 96341899 single base substitution T G intron_variant BRCA-EU 9 96345522 96345522 single base substitution C T intron_variant BRCA-EU 9 96347610 96347610 single base substitution C T intron_variant BRCA-EU 9 96349517 96349517 single base substitution C T intron_variant BRCA-EU 9 96351141 96351141 single base substitution C G intron_variant BRCA-EU 9 96352787 96352787 single base substitution C T intron_variant BRCA-EU 9 96355627 96355627 single base substitution T C intron_variant BRCA-EU 9 96356200 96356200 single base substitution C T intron_variant BRCA-EU 9 96356236 96356236 single base substitution C G intron_variant BRCA-EU 9 96356799 96356799 single base substitution C T intron_variant BRCA-EU 9 96360077 96360077 single base substitution C G intron_variant BRCA-EU 9 96361163 96361163 single base substitution A C intron_variant BRCA-EU 9 96362042 96362042 single base substitution G A intron_variant BRCA-EU 9 96366136 96366136 single base substitution C T intron_variant BRCA-EU 9 96367210 96367210 single base substitution C T intron_variant BRCA-EU 9 96368511 96368511 single base substitution C G intron_variant BRCA-EU 9 96368736 96368736 single base substitution G A intron_variant BRCA-EU 9 96368826 96368826 single base substitution A G intron_variant BRCA-EU 9 96369622 96369622 single base substitution C T intron_variant BRCA-EU 9 96371365 96371365 single base substitution A C intron_variant BRCA-EU 9 96372990 96372990 single base substitution C T intron_variant BRCA-EU 9 96373510 96373510 single base substitution C T intron_variant BRCA-EU 9 96373732 96373732 single base substitution T C intron_variant BRCA-EU 9 96374102 96374102 single base substitution T G intron_variant BRCA-EU 9 96375372 96375372 single base substitution G T intron_variant BRCA-EU 9 96379207 96379207 single base substitution G A intron_variant BRCA-EU 9 96379414 96379457 deletion of <=200bp CAGGGCCAGGTGTCGGTCATTCCTGGCTGGGCTTCTGTGCTGGA - intron_variant BRCA-EU 9 96381412 96381412 single base substitution G A intron_variant BRCA-EU 9 96382570 96382570 single base substitution T C intron_variant BRCA-EU 9 96383312 96383312 single base substitution G A intron_variant BRCA-EU 9 96384317 96384317 single base substitution G T intron_variant BRCA-EU 9 96384704 96384704 single base substitution C T intron_variant BRCA-EU 9 96386121 96386121 single base substitution G T intron_variant BRCA-EU 9 96387214 96387214 single base substitution A G intron_variant BRCA-EU 9 96388535 96388535 deletion of <=200bp A - intron_variant BRCA-EU 9 96391099 96391099 single base substitution A T intron_variant BRCA-EU 9 96391184 96391184 deletion of <=200bp T - intron_variant BRCA-EU 9 96391184 96391184 single base substitution T A intron_variant BRCA-EU 9 96392456 96392456 single base substitution C T intron_variant BRCA-EU 9 96394219 96394219 single base substitution C T intron_variant BRCA-EU 9 96397798 96397798 single base substitution G A intron_variant BRCA-EU 9 96400456 96400456 single base substitution C G intron_variant BRCA-EU 9 96401011 96401011 deletion of <=200bp T - intron_variant BRCA-EU 9 96401644 96401644 single base substitution C G intron_variant BRCA-EU 9 96401741 96401741 deletion of <=200bp T - intron_variant BRCA-EU 9 96404448 96404448 single base substitution G A intron_variant BRCA-EU 9 96405498 96405498 single base substitution C A intron_variant BRCA-EU 9 96405985 96405985 single base substitution C T intron_variant BRCA-EU 9 96407095 96407095 single base substitution C T intron_variant BRCA-EU 9 96407449 96407449 single base substitution G T intron_variant BRCA-EU 9 96408226 96408226 single base substitution T G intron_variant BRCA-EU 9 96408819 96408819 single base substitution G A intron_variant BRCA-EU 9 96409708 96409708 single base substitution C T intron_variant BRCA-EU 9 96409981 96409981 single base substitution G T intron_variant BRCA-EU 9 96410000 96410000 single base substitution C T intron_variant BRCA-EU 9 96410731 96410731 single base substitution C A intron_variant BRCA-EU 9 96412153 96412153 single base substitution C T intron_variant BRCA-EU 9 96412961 96412961 single base substitution C T intron_variant BRCA-EU 9 96415624 96415624 single base substitution T G intron_variant BRCA-EU 9 96415624 96415624 single base substitution T G missense_variant S256A 766T>G BRCA-EU 9 96416128 96416128 single base substitution C A intron_variant BRCA-EU 9 96416798 96416798 single base substitution A G intron_variant BRCA-EU 9 96416798 96416798 single base substitution A G missense_variant Q298R 893A>G BRCA-EU 9 96416899 96416899 single base substitution C T intron_variant BRCA-EU 9 96418193 96418193 single base substitution A G intron_variant BRCA-EU 9 96419725 96419725 single base substitution C T intron_variant BRCA-EU 9 96419866 96419866 single base substitution C A intron_variant BRCA-EU 9 96421172 96421172 single base substitution T G intron_variant BRCA-EU 9 96421844 96421844 single base substitution C G intron_variant BRCA-EU 9 96421844 96421844 single base substitution C G missense_variant L431V 1291C>G BRCA-EU 9 96426818 96426818 single base substitution C A intron_variant BRCA-EU 9 96428622 96428622 single base substitution A T intron_variant BRCA-EU 9 96432037 96432037 single base substitution C G intron_variant BRCA-EU 9 96433881 96433881 single base substitution G C intron_variant BRCA-EU 9 96433898 96433898 single base substitution G A intron_variant BRCA-EU 9 96434019 96434019 single base substitution T A intron_variant BRCA-EU 9 96434716 96434716 single base substitution G A intron_variant BRCA-EU 9 96435368 96435368 single base substitution G A intron_variant BRCA-EU 9 96437756 96437756 single base substitution A C intron_variant BRCA-EU 9 96440482 96440482 single base substitution C G 3_prime_UTR_variant BRCA-EU 9 96444352 96444352 single base substitution G A downstream_gene_variant BRCA-EU 9 96446531 96446531 deletion of <=200bp C - downstream_gene_variant BRCA-FR 9 96361083 96361083 single base substitution C T intron_variant BRCA-FR 9 96391184 96391184 single base substitution T A intron_variant BRCA-FR 9 96400456 96400456 single base substitution C G intron_variant BRCA-FR 9 96410731 96410731 single base substitution C A intron_variant BRCA-FR 9 96416128 96416128 single base substitution C A intron_variant BRCA-FR 9 96422137 96422137 single base substitution C T intron_variant BRCA-FR 9 96444352 96444352 single base substitution G A downstream_gene_variant BRCA-UK 9 96368826 96368826 single base substitution A G intron_variant BRCA-UK 9 96374102 96374102 single base substitution T G intron_variant BRCA-UK 9 96377860 96377860 single base substitution G A intron_variant BRCA-UK 9 96390806 96390806 single base substitution C G intron_variant BRCA-UK 9 96407095 96407095 single base substitution C T intron_variant BRCA-UK 9 96429205 96429205 single base substitution C G intron_variant BRCA-UK 9 96435633 96435633 single base substitution C G intron_variant BRCA-US 9 96339128 96339128 single base substitution G A missense_variant A25T 73G>A BRCA-US 9 96422612 96422612 deletion of <=200bp A - frameshift_variant K490 BRCA-US 9 96422612 96422612 deletion of <=200bp A - splice_region_variant BRCA-US 9 96425264 96425264 single base substitution C T intron_variant BRCA-US 9 96425264 96425264 single base substitution C T stop_gained R592* 1774C>T BRCA-US 9 96439907 96439907 single base substitution G C missense_variant Q1080H 3240G>C BRCA-US 9 96439907 96439907 single base substitution G C missense_variant Q311H 933G>C BRCA-US 9 96439925 96439925 single base substitution G A synonymous_variant L1086L 3258G>A BRCA-US 9 96439925 96439925 single base substitution G A synonymous_variant L317L 951G>A BTCA-JP 9 96398831 96398831 single base substitution C G intron_variant BTCA-JP 9 96411500 96411500 single base substitution T C intron_variant BTCA-JP 9 96411500 96411500 single base substitution T C splice_region_variant BTCA-JP 9 96420348 96420348 single base substitution G A intron_variant BTCA-JP 9 96422612 96422612 deletion of <=200bp A - frameshift_variant K490 BTCA-JP 9 96422612 96422612 deletion of <=200bp A - splice_region_variant BTCA-JP 9 96425125 96425125 single base substitution G A intron_variant BTCA-JP 9 96428243 96428243 single base substitution C T intron_variant BTCA-JP 9 96437285 96437285 single base substitution C T synonymous_variant D132D 396C>T BTCA-JP 9 96437285 96437285 single base substitution C T synonymous_variant D901D 2703C>T BTCA-JP 9 96439019 96439019 single base substitution C A synonymous_variant T223T 669C>A BTCA-JP 9 96439019 96439019 single base substitution C A synonymous_variant T992T 2976C>A CESC-US 9 96339125 96339125 single base substitution G C missense_variant D24H 70G>C CESC-US 9 96398778 96398778 single base substitution C T intron_variant CESC-US 9 96398778 96398778 single base substitution C T synonymous_variant I90I 270C>T CESC-US 9 96421802 96421802 single base substitution G C intron_variant CESC-US 9 96421802 96421802 single base substitution G C missense_variant E417Q 1249G>C CLLE-ES 9 96378844 96378844 single base substitution G A intron_variant CLLE-ES 9 96423838 96423838 single base substitution C T intron_variant COAD-US 9 96398693 96398693 single base substitution T C missense_variant L62S 185T>C COAD-US 9 96411440 96411440 single base substitution G A intron_variant COAD-US 9 96411440 96411440 single base substitution G A missense_variant S183N 548G>A COAD-US 9 96411465 96411465 single base substitution C T intron_variant COAD-US 9 96411465 96411465 single base substitution C T synonymous_variant N191N 573C>T COAD-US 9 96416729 96416729 single base substitution C T intron_variant COAD-US 9 96416729 96416729 single base substitution C T missense_variant S275L 824C>T COAD-US 9 96416778 96416778 single base substitution C T intron_variant COAD-US 9 96416778 96416778 single base substitution C T synonymous_variant S291S 873C>T COAD-US 9 96418259 96418259 single base substitution C T intron_variant COAD-US 9 96418259 96418259 single base substitution C T synonymous_variant F332F 996C>T COAD-US 9 96422489 96422489 single base substitution G A intron_variant COAD-US 9 96422489 96422489 single base substitution G A missense_variant V449I 1345G>A COAD-US 9 96422497 96422497 single base substitution G A intron_variant COAD-US 9 96422497 96422497 single base substitution G A synonymous_variant P451P 1353G>A COAD-US 9 96422563 96422563 single base substitution G A intron_variant COAD-US 9 96422563 96422563 single base substitution G A synonymous_variant P473P 1419G>A COAD-US 9 96422612 96422612 deletion of <=200bp A - frameshift_variant K490 COAD-US 9 96422612 96422612 deletion of <=200bp A - splice_region_variant COAD-US 9 96422703 96422703 single base substitution C T intron_variant COAD-US 9 96422703 96422703 single base substitution C T missense_variant T520M 1559C>T COAD-US 9 96425264 96425264 single base substitution C T intron_variant COAD-US 9 96425264 96425264 single base substitution C T stop_gained R592* 1774C>T COAD-US 9 96425863 96425863 single base substitution C T intron_variant COAD-US 9 96425863 96425863 single base substitution C T missense_variant A628V 1883C>T COAD-US 9 96428124 96428124 single base substitution C T intron_variant COAD-US 9 96428124 96428124 single base substitution C T synonymous_variant N698N 2094C>T COAD-US 9 96435977 96435977 single base substitution C T intron_variant COAD-US 9 96435977 96435977 single base substitution C T missense_variant A820V 2459C>T COAD-US 9 96438893 96438893 insertion of <=200bp - AA frameshift_variant K181K? COAD-US 9 96438893 96438893 insertion of <=200bp - AA frameshift_variant K950K? COAD-US 9 96438893 96438893 insertion of <=200bp - A frameshift_variant K181K? COAD-US 9 96438893 96438893 insertion of <=200bp - A frameshift_variant K950K? COAD-US 9 96438894 96438894 deletion of <=200bp A - frameshift_variant K182 COAD-US 9 96438894 96438894 deletion of <=200bp A - frameshift_variant K951 COAD-US 9 96438998 96438998 insertion of <=200bp - ACCACCCCTGCCTCC disruptive_inframe_insertion S216SPPLPP COAD-US 9 96438998 96438998 insertion of <=200bp - ACCACCCCTGCCTCC disruptive_inframe_insertion S985SPPLPP COAD-US 9 96439004 96439004 insertion of <=200bp - CCTGCCTCCACCACA inframe_insertion T218TLPPPH COAD-US 9 96439004 96439004 insertion of <=200bp - CCTGCCTCCACCACA inframe_insertion T987TLPPPH COAD-US 9 96439004 96439004 single base substitution C A synonymous_variant T218T 654C>A COAD-US 9 96439004 96439004 single base substitution C A synonymous_variant T987T 2961C>A COAD-US 9 96439006 96439006 insertion of <=200bp - TGCCTCCACCACACC disruptive_inframe_insertion P219LPPPHP COAD-US 9 96439006 96439006 insertion of <=200bp - TGCCTCCACCACACC disruptive_inframe_insertion P988LPPPHP COAD-US 9 96439007 96439007 single base substitution G T synonymous_variant P219P 657G>T COAD-US 9 96439007 96439007 single base substitution G T synonymous_variant P988P 2964G>T COCA-CN 9 96347890 96347890 single base substitution G A intron_variant COCA-CN 9 96349538 96349538 single base substitution A C intron_variant COCA-CN 9 96357313 96357313 single base substitution A C intron_variant COCA-CN 9 96374252 96374252 single base substitution C G intron_variant COCA-CN 9 96377470 96377470 single base substitution C T intron_variant COCA-CN 9 96381916 96381916 single base substitution T G intron_variant COCA-CN 9 96382164 96382164 single base substitution C T intron_variant COCA-CN 9 96384999 96384999 single base substitution T C intron_variant COCA-CN 9 96385063 96385063 single base substitution G C intron_variant COCA-CN 9 96385078 96385078 single base substitution C A intron_variant COCA-CN 9 96385093 96385093 single base substitution C T intron_variant COCA-CN 9 96385211 96385211 single base substitution A G intron_variant COCA-CN 9 96386212 96386212 single base substitution C T intron_variant COCA-CN 9 96386245 96386245 single base substitution G A intron_variant COCA-CN 9 96386447 96386447 single base substitution G T intron_variant COCA-CN 9 96386731 96386731 single base substitution T G intron_variant COCA-CN 9 96387312 96387312 single base substitution G A intron_variant COCA-CN 9 96387317 96387317 single base substitution T G intron_variant COCA-CN 9 96387385 96387385 single base substitution C T intron_variant COCA-CN 9 96387397 96387397 single base substitution A T intron_variant COCA-CN 9 96387574 96387574 single base substitution T C intron_variant COCA-CN 9 96398508 96398508 single base substitution A G intron_variant COCA-CN 9 96408053 96408053 single base substitution G A intron_variant COCA-CN 9 96408053 96408053 single base substitution G A missense_variant D148N 442G>A COCA-CN 9 96411466 96411466 single base substitution G A intron_variant COCA-CN 9 96411466 96411466 single base substitution G A missense_variant V192I 574G>A COCA-CN 9 96416759 96416759 single base substitution G A intron_variant COCA-CN 9 96416759 96416759 single base substitution G A missense_variant R285Q 854G>A COCA-CN 9 96422420 96422420 single base substitution T C intron_variant COCA-CN 9 96425335 96425335 single base substitution C T intron_variant COCA-CN 9 96433349 96433349 single base substitution G C intron_variant COCA-CN 9 96433910 96433910 single base substitution A G intron_variant COCA-CN 9 96434411 96434411 single base substitution C T intron_variant COCA-CN 9 96434654 96434654 single base substitution G A intron_variant COCA-CN 9 96434992 96434992 single base substitution A G intron_variant COCA-CN 9 96435968 96435968 single base substitution C A intron_variant COCA-CN 9 96435968 96435968 single base substitution C A missense_variant A817D 2450C>A COCA-CN 9 96437959 96437959 single base substitution C T splice_region_variant COCA-CN 9 96439019 96439019 single base substitution C A synonymous_variant T223T 669C>A COCA-CN 9 96439019 96439019 single base substitution C A synonymous_variant T992T 2976C>A COCA-CN 9 96445204 96445204 single base substitution C T downstream_gene_variant EOPC-DE 9 96381190 96381190 single base substitution C T intron_variant EOPC-DE 9 96384908 96384908 single base substitution C T intron_variant EOPC-DE 9 96434717 96434717 single base substitution C T intron_variant EOPC-DE 9 96438998 96438998 single base substitution T C synonymous_variant S216S 648T>C EOPC-DE 9 96438998 96438998 single base substitution T C synonymous_variant S985S 2955T>C ESAD-UK 9 96333725 96333725 single base substitution A C upstream_gene_variant ESAD-UK 9 96334704 96334704 single base substitution G A upstream_gene_variant ESAD-UK 9 96334838 96334838 single base substitution T G upstream_gene_variant ESAD-UK 9 96335752 96335752 single base substitution G A upstream_gene_variant ESAD-UK 9 96336208 96336239 deletion of <=200bp CGGGAGGCTGAGGCAGGAGAATCACTTGAACC - upstream_gene_variant ESAD-UK 9 96338220 96338220 single base substitution G A upstream_gene_variant ESAD-UK 9 96338550 96338550 single base substitution C T upstream_gene_variant ESAD-UK 9 96339341 96339341 single base substitution C T intron_variant ESAD-UK 9 96339452 96339452 single base substitution T C intron_variant ESAD-UK 9 96344590 96344590 single base substitution C G intron_variant ESAD-UK 9 96349336 96349336 single base substitution G A intron_variant ESAD-UK 9 96350792 96350792 single base substitution C G intron_variant ESAD-UK 9 96357134 96357134 single base substitution C T intron_variant ESAD-UK 9 96358531 96358531 single base substitution G C intron_variant ESAD-UK 9 96359401 96359401 single base substitution C T intron_variant ESAD-UK 9 96362565 96362565 single base substitution G C intron_variant ESAD-UK 9 96364214 96364214 single base substitution G A intron_variant ESAD-UK 9 96364252 96364252 single base substitution T C intron_variant ESAD-UK 9 96364442 96364442 single base substitution C T intron_variant ESAD-UK 9 96365161 96365161 single base substitution T C intron_variant ESAD-UK 9 96365621 96365621 single base substitution G A intron_variant ESAD-UK 9 96368140 96368140 single base substitution T C intron_variant ESAD-UK 9 96370882 96370882 single base substitution A C intron_variant ESAD-UK 9 96371136 96371136 single base substitution C T intron_variant ESAD-UK 9 96371402 96371402 single base substitution C T intron_variant ESAD-UK 9 96374099 96374099 single base substitution G C intron_variant ESAD-UK 9 96375089 96375089 single base substitution G A intron_variant ESAD-UK 9 96378610 96378610 single base substitution C T intron_variant ESAD-UK 9 96386744 96386744 single base substitution A G intron_variant ESAD-UK 9 96392334 96392334 single base substitution A G missense_variant T61A 181A>G ESAD-UK 9 96392795 96392795 single base substitution C T intron_variant ESAD-UK 9 96393643 96393643 single base substitution G A intron_variant ESAD-UK 9 96395512 96395512 single base substitution G A intron_variant ESAD-UK 9 96400231 96400231 single base substitution T C intron_variant ESAD-UK 9 96404318 96404318 single base substitution T G intron_variant ESAD-UK 9 96405574 96405574 single base substitution T C intron_variant ESAD-UK 9 96405775 96405775 single base substitution G A intron_variant ESAD-UK 9 96407616 96407616 single base substitution C T intron_variant ESAD-UK 9 96408973 96408973 single base substitution G C intron_variant ESAD-UK 9 96413360 96413360 single base substitution C T intron_variant ESAD-UK 9 96415002 96415002 single base substitution C T intron_variant ESAD-UK 9 96416723 96416723 single base substitution C T intron_variant ESAD-UK 9 96416723 96416723 single base substitution C T missense_variant P273L 818C>T ESAD-UK 9 96424930 96424930 single base substitution C T intron_variant ESAD-UK 9 96427350 96427350 single base substitution G C intron_variant ESAD-UK 9 96427477 96427477 insertion of <=200bp - A intron_variant ESAD-UK 9 96427493 96427493 single base substitution T G intron_variant ESAD-UK 9 96429625 96429625 single base substitution G A intron_variant ESAD-UK 9 96429691 96429691 single base substitution C T intron_variant ESAD-UK 9 96429996 96429996 single base substitution C G intron_variant ESAD-UK 9 96431180 96431180 single base substitution T G intron_variant ESAD-UK 9 96433048 96433048 single base substitution T A intron_variant ESAD-UK 9 96433049 96433049 single base substitution C T intron_variant ESAD-UK 9 96434695 96434695 single base substitution G A intron_variant ESAD-UK 9 96435271 96435271 single base substitution G A intron_variant ESAD-UK 9 96436087 96436087 single base substitution G C missense_variant D857H 2569G>C ESAD-UK 9 96436087 96436087 single base substitution G C missense_variant D88H 262G>C ESAD-UK 9 96436520 96436520 single base substitution A C intron_variant ESAD-UK 9 96438704 96438704 single base substitution G A intron_variant ESAD-UK 9 96439875 96439875 single base substitution C T missense_variant R1070C 3208C>T ESAD-UK 9 96439875 96439875 single base substitution C T missense_variant R301C 901C>T ESAD-UK 9 96440628 96440628 single base substitution C T 3_prime_UTR_variant ESAD-UK 9 96442074 96442074 single base substitution C T downstream_gene_variant ESAD-UK 9 96446043 96446043 single base substitution G A downstream_gene_variant ESAD-UK 9 96446727 96446727 single base substitution G A downstream_gene_variant ESCA-CN 9 96415412 96415412 single base substitution A G intron_variant ESCA-CN 9 96415653 96415653 single base substitution C T intron_variant ESCA-CN 9 96415653 96415653 single base substitution C T splice_region_variant ESCA-CN 9 96428231 96428231 single base substitution C T intron_variant ESCA-CN 9 96439941 96439941 single base substitution G A missense_variant G1092R 3274G>A ESCA-CN 9 96439941 96439941 single base substitution G A missense_variant G323R 967G>A GBM-US 9 96408031 96408031 single base substitution G A intron_variant GBM-US 9 96408031 96408031 single base substitution G A synonymous_variant P140P 420G>A GBM-US 9 96421820 96421820 single base substitution C T intron_variant GBM-US 9 96421820 96421820 single base substitution C T missense_variant P423S 1267C>T KIRC-US 9 96439004 96439004 single base substitution C A synonymous_variant T218T 654C>A KIRC-US 9 96439004 96439004 single base substitution C A synonymous_variant T987T 2961C>A KIRP-US 9 96416716 96416716 single base substitution A C intron_variant KIRP-US 9 96416716 96416716 single base substitution A C missense_variant I271L 811A>C LAML-KR 9 96377470 96377470 single base substitution C T intron_variant LAML-KR 9 96377492 96377492 single base substitution G A intron_variant LAML-KR 9 96387146 96387146 single base substitution A G intron_variant LAML-KR 9 96387147 96387147 single base substitution G A intron_variant LAML-KR 9 96392371 96392371 single base substitution G A intron_variant LAML-KR 9 96433882 96433882 single base substitution T A intron_variant LAML-KR 9 96434006 96434006 single base substitution G A intron_variant LAML-KR 9 96434018 96434018 single base substitution A G intron_variant LAML-KR 9 96434019 96434019 single base substitution T A intron_variant LAML-KR 9 96434042 96434042 single base substitution A G intron_variant LAML-KR 9 96434078 96434078 single base substitution G A intron_variant LAML-KR 9 96434659 96434659 single base substitution A G intron_variant LAML-KR 9 96444397 96444397 single base substitution G A downstream_gene_variant LICA-CN 9 96428283 96428283 single base substitution A T intron_variant LICA-CN 9 96428283 96428283 single base substitution A T stop_gained K710* 2128A>T LICA-CN 9 96438992 96438992 single base substitution A T synonymous_variant P214P 642A>T LICA-CN 9 96438992 96438992 single base substitution A T synonymous_variant P983P 2949A>T LICA-FR 9 96340617 96340617 single base substitution C A intron_variant LICA-FR 9 96374943 96374943 single base substitution T C intron_variant LICA-FR 9 96384852 96384852 single base substitution G A intron_variant LICA-FR 9 96386541 96386541 single base substitution G T intron_variant LICA-FR 9 96411395 96411395 single base substitution A C intron_variant LICA-FR 9 96411395 96411395 single base substitution A C missense_variant K168T 503A>C LICA-FR 9 96419110 96419110 single base substitution A G intron_variant LICA-FR 9 96429508 96429508 single base substitution G T intron_variant LICA-FR 9 96429508 96429508 single base substitution G T missense_variant E778D 2334G>T LICA-FR 9 96435033 96435033 single base substitution A G intron_variant LIHC-US 9 96411461 96411461 single base substitution T A intron_variant LIHC-US 9 96411461 96411461 single base substitution T A missense_variant L190H 569T>A LIHC-US 9 96415567 96415567 single base substitution T G intron_variant LIHC-US 9 96415567 96415567 single base substitution T G missense_variant C237G 709T>G LIHC-US 9 96416768 96416768 single base substitution C G intron_variant LIHC-US 9 96416768 96416768 single base substitution C G missense_variant S288C 863C>G LIHC-US 9 96435949 96435949 single base substitution C T intron_variant LIHC-US 9 96435949 96435949 single base substitution C T synonymous_variant L811L 2431C>T LINC-JP 9 96334397 96334397 single base substitution G A upstream_gene_variant LINC-JP 9 96348679 96348679 single base substitution C G intron_variant LINC-JP 9 96362965 96362965 single base substitution C A intron_variant LINC-JP 9 96374045 96374045 single base substitution C T intron_variant LINC-JP 9 96375071 96375071 single base substitution G C intron_variant LINC-JP 9 96375608 96375608 single base substitution T G intron_variant LINC-JP 9 96375611 96375611 single base substitution C T intron_variant LINC-JP 9 96379731 96379731 insertion of <=200bp - G intron_variant LINC-JP 9 96379818 96379818 single base substitution C T intron_variant LINC-JP 9 96379819 96379819 single base substitution A G intron_variant LINC-JP 9 96386191 96386191 deletion of <=200bp T - intron_variant LINC-JP 9 96386236 96386236 insertion of <=200bp - CG intron_variant LINC-JP 9 96392323 96392323 single base substitution A G missense_variant H57R 170A>G LINC-JP 9 96394386 96394386 single base substitution G A intron_variant LINC-JP 9 96398868 96398868 single base substitution C T intron_variant LINC-JP 9 96403336 96403336 single base substitution A C intron_variant LINC-JP 9 96417573 96417573 single base substitution C T intron_variant LINC-JP 9 96426060 96426060 single base substitution A C intron_variant LINC-JP 9 96435919 96435919 single base substitution A G intron_variant LINC-JP 9 96435919 96435919 single base substitution A G missense_variant M801V 2401A>G LINC-JP 9 96437140 96437140 insertion of <=200bp - C intron_variant LINC-JP 9 96437331 96437331 single base substitution C G intron_variant LINC-JP 9 96438942 96438942 single base substitution T G missense_variant S198A 592T>G LINC-JP 9 96438942 96438942 single base substitution T G missense_variant S967A 2899T>G LINC-JP 9 96439019 96439019 single base substitution C A synonymous_variant T223T 669C>A LINC-JP 9 96439019 96439019 single base substitution C A synonymous_variant T992T 2976C>A LINC-JP 9 96439033 96439033 single base substitution G C missense_variant S228T 683G>C LINC-JP 9 96439033 96439033 single base substitution G C missense_variant S997T 2990G>C LINC-JP 9 96439035 96439035 single base substitution A C missense_variant T229P 685A>C LINC-JP 9 96439035 96439035 single base substitution A C missense_variant T998P 2992A>C LINC-JP 9 96445201 96445201 insertion of <=200bp - CGAGCTGCAAAGTGGC downstream_gene_variant LIRI-JP 9 96338070 96338070 single base substitution T C upstream_gene_variant LIRI-JP 9 96339892 96339892 single base substitution C A intron_variant LIRI-JP 9 96341682 96341682 single base substitution C T intron_variant LIRI-JP 9 96341708 96341708 single base substitution G T intron_variant LIRI-JP 9 96343661 96343661 single base substitution A T intron_variant LIRI-JP 9 96345343 96345343 single base substitution C A intron_variant LIRI-JP 9 96350016 96350016 single base substitution A G intron_variant LIRI-JP 9 96356483 96356483 single base substitution A G intron_variant LIRI-JP 9 96365380 96365380 single base substitution G T intron_variant LIRI-JP 9 96365842 96365842 single base substitution T G intron_variant LIRI-JP 9 96370156 96370156 single base substitution A G intron_variant LIRI-JP 9 96371920 96371920 single base substitution A T intron_variant LIRI-JP 9 96373185 96373185 single base substitution T G intron_variant LIRI-JP 9 96374882 96374882 single base substitution T A intron_variant LIRI-JP 9 96375017 96375017 single base substitution A G intron_variant LIRI-JP 9 96376290 96376290 single base substitution G A intron_variant LIRI-JP 9 96376362 96376362 single base substitution G A intron_variant LIRI-JP 9 96379473 96379476 deletion of <=200bp GAAG - intron_variant LIRI-JP 9 96380528 96380528 single base substitution G T intron_variant LIRI-JP 9 96385946 96385946 single base substitution A G intron_variant LIRI-JP 9 96386622 96386622 single base substitution A G intron_variant LIRI-JP 9 96389425 96389425 single base substitution A G intron_variant LIRI-JP 9 96390716 96390716 single base substitution T C intron_variant LIRI-JP 9 96391994 96391994 single base substitution A G intron_variant LIRI-JP 9 96393851 96393851 single base substitution C T intron_variant LIRI-JP 9 96395749 96395749 single base substitution G T intron_variant LIRI-JP 9 96398877 96398877 single base substitution C T intron_variant LIRI-JP 9 96398909 96398909 single base substitution C A intron_variant LIRI-JP 9 96400941 96400941 single base substitution T C intron_variant LIRI-JP 9 96404322 96404322 single base substitution C T intron_variant LIRI-JP 9 96404688 96404688 single base substitution T A intron_variant LIRI-JP 9 96405087 96405087 single base substitution A G intron_variant LIRI-JP 9 96405767 96405767 single base substitution T C intron_variant LIRI-JP 9 96407428 96407428 single base substitution C T intron_variant LIRI-JP 9 96411810 96411810 single base substitution T G intron_variant LIRI-JP 9 96413093 96413093 single base substitution G T intron_variant LIRI-JP 9 96413782 96413782 single base substitution A C intron_variant LIRI-JP 9 96414350 96414350 single base substitution G T intron_variant LIRI-JP 9 96415286 96415286 single base substitution G A intron_variant LIRI-JP 9 96416221 96416221 single base substitution A T intron_variant LIRI-JP 9 96416867 96416867 single base substitution G T intron_variant LIRI-JP 9 96417239 96417239 single base substitution G A intron_variant LIRI-JP 9 96419069 96419069 single base substitution C G intron_variant LIRI-JP 9 96419106 96419106 single base substitution G A intron_variant LIRI-JP 9 96430173 96430173 single base substitution T A intron_variant LIRI-JP 9 96430256 96430256 single base substitution T A intron_variant LIRI-JP 9 96430359 96430359 single base substitution A G intron_variant LIRI-JP 9 96431861 96431861 single base substitution G A intron_variant LIRI-JP 9 96438597 96438597 single base substitution A G intron_variant LIRI-JP 9 96438873 96438873 single base substitution A G splice_region_variant LIRI-JP 9 96438881 96438881 single base substitution G A synonymous_variant E177E 531G>A LIRI-JP 9 96438881 96438881 single base substitution G A synonymous_variant E946E 2838G>A LIRI-JP 9 96440523 96440523 single base substitution G T 3_prime_UTR_variant LIRI-JP 9 96442497 96442497 single base substitution G A downstream_gene_variant LIRI-JP 9 96446046 96446046 single base substitution G C downstream_gene_variant LIRI-JP 9 96446505 96446505 single base substitution T C downstream_gene_variant LUSC-KR 9 96341939 96341939 single base substitution T C intron_variant LUSC-KR 9 96343296 96343296 single base substitution A G intron_variant LUSC-KR 9 96344926 96344926 single base substitution G A intron_variant LUSC-KR 9 96351728 96351728 single base substitution C T intron_variant LUSC-KR 9 96370012 96370012 single base substitution C G intron_variant LUSC-KR 9 96377492 96377492 single base substitution G A intron_variant LUSC-KR 9 96379262 96379262 single base substitution T C intron_variant LUSC-KR 9 96379292 96379292 single base substitution G C intron_variant LUSC-KR 9 96382150 96382150 single base substitution G T intron_variant LUSC-KR 9 96386976 96386976 single base substitution C T intron_variant LUSC-KR 9 96390024 96390024 single base substitution A G intron_variant LUSC-KR 9 96395491 96395491 single base substitution G T intron_variant LUSC-KR 9 96398014 96398014 single base substitution C T intron_variant LUSC-KR 9 96401318 96401318 single base substitution C G intron_variant LUSC-KR 9 96405579 96405579 single base substitution C T intron_variant LUSC-KR 9 96408704 96408704 single base substitution G T intron_variant LUSC-KR 9 96410237 96410237 single base substitution G T intron_variant LUSC-KR 9 96413566 96413566 single base substitution C T intron_variant LUSC-KR 9 96413569 96413569 single base substitution A T intron_variant LUSC-KR 9 96413672 96413672 single base substitution G A intron_variant LUSC-KR 9 96424141 96424141 single base substitution G C intron_variant LUSC-KR 9 96426533 96426533 single base substitution C A intron_variant LUSC-KR 9 96432546 96432546 single base substitution C T intron_variant LUSC-KR 9 96433910 96433910 single base substitution A G intron_variant LUSC-KR 9 96433946 96433946 single base substitution A G intron_variant LUSC-KR 9 96434018 96434018 single base substitution A G intron_variant LUSC-KR 9 96434019 96434019 single base substitution T A intron_variant LUSC-KR 9 96434042 96434042 single base substitution A G intron_variant LUSC-KR 9 96434134 96434134 single base substitution A T intron_variant LUSC-KR 9 96434206 96434206 single base substitution T A intron_variant LUSC-KR 9 96434277 96434277 single base substitution G C intron_variant LUSC-KR 9 96434278 96434278 single base substitution T A intron_variant LUSC-KR 9 96434546 96434546 single base substitution G A intron_variant LUSC-KR 9 96434731 96434731 single base substitution G A intron_variant LUSC-KR 9 96435132 96435132 single base substitution A G intron_variant LUSC-KR 9 96443802 96443802 single base substitution G A downstream_gene_variant LUSC-US 9 96407915 96407915 single base substitution G A intron_variant LUSC-US 9 96407915 96407915 single base substitution G A missense_variant E102K 304G>A LUSC-US 9 96407921 96407921 single base substitution G C intron_variant LUSC-US 9 96407921 96407921 single base substitution G C missense_variant V104L 310G>C LUSC-US 9 96416756 96416756 single base substitution G T intron_variant LUSC-US 9 96416756 96416756 single base substitution G T missense_variant W284L 851G>T LUSC-US 9 96418814 96418814 single base substitution C G intron_variant LUSC-US 9 96418814 96418814 single base substitution C G missense_variant Q362E 1084C>G LUSC-US 9 96437969 96437969 single base substitution C T synonymous_variant V141V 423C>T LUSC-US 9 96437969 96437969 single base substitution C T synonymous_variant V910V 2730C>T MALY-DE 9 96337386 96337386 single base substitution G A upstream_gene_variant MALY-DE 9 96343686 96343686 single base substitution C T intron_variant MALY-DE 9 96346598 96346598 single base substitution C T intron_variant MALY-DE 9 96352392 96352392 single base substitution C T intron_variant MALY-DE 9 96362532 96362533 deletion of <=200bp TG - intron_variant MALY-DE 9 96377144 96377144 single base substitution G A intron_variant MALY-DE 9 96377506 96377506 single base substitution T G intron_variant MALY-DE 9 96391426 96391426 single base substitution G A intron_variant MALY-DE 9 96391834 96391834 single base substitution C A intron_variant MALY-DE 9 96391857 96391857 single base substitution T C intron_variant MALY-DE 9 96396463 96396463 single base substitution C T intron_variant MALY-DE 9 96399683 96399683 single base substitution T C intron_variant MALY-DE 9 96400404 96400404 single base substitution T G intron_variant MALY-DE 9 96400763 96400763 insertion of <=200bp - T intron_variant MALY-DE 9 96405414 96405414 single base substitution G T intron_variant MALY-DE 9 96407989 96407989 single base substitution C T intron_variant MALY-DE 9 96407989 96407989 single base substitution C T synonymous_variant P126P 378C>T MALY-DE 9 96431235 96431235 single base substitution A T intron_variant MALY-DE 9 96432160 96432160 single base substitution C T intron_variant MALY-DE 9 96435619 96435619 single base substitution C G intron_variant MALY-DE 9 96439007 96439007 single base substitution G T synonymous_variant P219P 657G>T MALY-DE 9 96439007 96439007 single base substitution G T synonymous_variant P988P 2964G>T MALY-DE 9 96439019 96439019 single base substitution C A synonymous_variant T223T 669C>A MALY-DE 9 96439019 96439019 single base substitution C A synonymous_variant T992T 2976C>A MELA-AU 9 96334242 96334242 single base substitution G A upstream_gene_variant MELA-AU 9 96337952 96337952 single base substitution G A upstream_gene_variant MELA-AU 9 96338121 96338121 single base substitution G A upstream_gene_variant MELA-AU 9 96338152 96338152 single base substitution G A upstream_gene_variant MELA-AU 9 96339430 96339430 single base substitution C T intron_variant MELA-AU 9 96341553 96341553 single base substitution C T intron_variant MELA-AU 9 96341674 96341674 single base substitution C T intron_variant MELA-AU 9 96341681 96341681 single base substitution C T intron_variant MELA-AU 9 96341828 96341828 single base substitution C T intron_variant MELA-AU 9 96342165 96342165 single base substitution C G intron_variant MELA-AU 9 96343013 96343013 single base substitution A T intron_variant MELA-AU 9 96343277 96343277 single base substitution C T intron_variant MELA-AU 9 96344128 96344128 single base substitution C T intron_variant MELA-AU 9 96344734 96344734 single base substitution C T intron_variant MELA-AU 9 96345266 96345266 single base substitution A G intron_variant MELA-AU 9 96347150 96347150 single base substitution G A intron_variant MELA-AU 9 96348013 96348013 single base substitution C T intron_variant MELA-AU 9 96348070 96348070 single base substitution C T intron_variant MELA-AU 9 96348520 96348520 single base substitution C T intron_variant MELA-AU 9 96348546 96348546 single base substitution G A intron_variant MELA-AU 9 96348644 96348644 single base substitution A G intron_variant MELA-AU 9 96349566 96349566 single base substitution G A intron_variant MELA-AU 9 96350525 96350525 single base substitution C T intron_variant MELA-AU 9 96350670 96350670 single base substitution G A intron_variant MELA-AU 9 96350844 96350844 single base substitution C T intron_variant MELA-AU 9 96350865 96350865 single base substitution C T intron_variant MELA-AU 9 96352082 96352083 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 9 96352685 96352685 single base substitution C T intron_variant MELA-AU 9 96353965 96353965 single base substitution G A intron_variant MELA-AU 9 96354788 96354788 single base substitution C T intron_variant MELA-AU 9 96355515 96355515 single base substitution C T intron_variant MELA-AU 9 96355862 96355862 single base substitution C T intron_variant MELA-AU 9 96356178 96356178 single base substitution C T intron_variant MELA-AU 9 96357851 96357851 single base substitution C T intron_variant MELA-AU 9 96357868 96357868 single base substitution C T intron_variant MELA-AU 9 96358035 96358035 single base substitution C T intron_variant MELA-AU 9 96358138 96358138 single base substitution C T intron_variant MELA-AU 9 96358644 96358644 single base substitution C T intron_variant MELA-AU 9 96358859 96358859 single base substitution C T intron_variant MELA-AU 9 96359005 96359005 single base substitution C T intron_variant MELA-AU 9 96359702 96359702 single base substitution G A intron_variant MELA-AU 9 96359988 96359988 single base substitution C T intron_variant MELA-AU 9 96360401 96360401 single base substitution C T intron_variant MELA-AU 9 96360886 96360886 single base substitution C T intron_variant MELA-AU 9 96361171 96361171 single base substitution C T intron_variant MELA-AU 9 96361545 96361545 single base substitution C A intron_variant MELA-AU 9 96361996 96361996 single base substitution C T intron_variant MELA-AU 9 96363400 96363400 single base substitution C T intron_variant MELA-AU 9 96364326 96364326 single base substitution C T intron_variant MELA-AU 9 96364381 96364381 single base substitution C T intron_variant MELA-AU 9 96364400 96364400 single base substitution C T intron_variant MELA-AU 9 96364792 96364793 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 9 96364897 96364897 single base substitution C T intron_variant MELA-AU 9 96365222 96365223 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 9 96365354 96365354 single base substitution C T intron_variant MELA-AU 9 96365359 96365359 single base substitution C T intron_variant MELA-AU 9 96366087 96366087 single base substitution C T intron_variant MELA-AU 9 96366556 96366556 single base substitution C T intron_variant MELA-AU 9 96366856 96366857 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 9 96367017 96367018 multiple base substitution (>=2bp and <=200bp) CC TA intron_variant MELA-AU 9 96368229 96368229 single base substitution C T intron_variant MELA-AU 9 96368298 96368298 single base substitution C T intron_variant MELA-AU 9 96368346 96368346 single base substitution C T intron_variant MELA-AU 9 96368739 96368739 single base substitution G A intron_variant MELA-AU 9 96370351 96370351 single base substitution C T intron_variant MELA-AU 9 96370360 96370360 single base substitution C T intron_variant MELA-AU 9 96370616 96370616 single base substitution A T intron_variant MELA-AU 9 96370619 96370619 single base substitution T A intron_variant MELA-AU 9 96370752 96370752 single base substitution G A intron_variant MELA-AU 9 96371481 96371481 single base substitution C T intron_variant MELA-AU 9 96371639 96371639 single base substitution C T intron_variant MELA-AU 9 96372380 96372380 single base substitution C T intron_variant MELA-AU 9 96372909 96372909 single base substitution T A intron_variant MELA-AU 9 96373052 96373052 single base substitution C T intron_variant MELA-AU 9 96373286 96373286 single base substitution C T intron_variant MELA-AU 9 96375138 96375138 single base substitution C T intron_variant MELA-AU 9 96375172 96375172 single base substitution C T intron_variant MELA-AU 9 96375328 96375328 single base substitution T A intron_variant MELA-AU 9 96375373 96375373 single base substitution T C intron_variant MELA-AU 9 96375876 96375876 single base substitution C T intron_variant MELA-AU 9 96376533 96376533 single base substitution C T intron_variant MELA-AU 9 96376842 96376842 single base substitution T G intron_variant MELA-AU 9 96376891 96376891 single base substitution C T intron_variant MELA-AU 9 96377186 96377186 single base substitution G A intron_variant MELA-AU 9 96377212 96377212 single base substitution T C intron_variant MELA-AU 9 96377434 96377434 single base substitution T C intron_variant MELA-AU 9 96377779 96377779 single base substitution C T intron_variant MELA-AU 9 96378301 96378302 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 9 96379266 96379266 single base substitution T C intron_variant MELA-AU 9 96379835 96379835 single base substitution C T intron_variant MELA-AU 9 96380283 96380283 single base substitution C A intron_variant MELA-AU 9 96381508 96381508 single base substitution C T intron_variant MELA-AU 9 96381654 96381654 single base substitution C T intron_variant MELA-AU 9 96381688 96381688 single base substitution T C intron_variant MELA-AU 9 96381840 96381840 single base substitution C T intron_variant MELA-AU 9 96382225 96382225 single base substitution C T intron_variant MELA-AU 9 96382571 96382571 single base substitution C T intron_variant MELA-AU 9 96382585 96382585 single base substitution C T intron_variant MELA-AU 9 96385524 96385524 single base substitution C T intron_variant MELA-AU 9 96385805 96385805 single base substitution A G intron_variant MELA-AU 9 96385884 96385884 single base substitution C T intron_variant MELA-AU 9 96387262 96387262 single base substitution C T intron_variant MELA-AU 9 96388311 96388311 single base substitution G A intron_variant MELA-AU 9 96388891 96388891 single base substitution C T intron_variant MELA-AU 9 96389150 96389150 single base substitution T G intron_variant MELA-AU 9 96389815 96389815 single base substitution C T intron_variant MELA-AU 9 96389982 96389982 single base substitution G A intron_variant MELA-AU 9 96390268 96390268 single base substitution C T intron_variant MELA-AU 9 96390644 96390644 single base substitution T A intron_variant MELA-AU 9 96391030 96391030 single base substitution C T intron_variant MELA-AU 9 96391153 96391153 single base substitution T C intron_variant MELA-AU 9 96391379 96391379 single base substitution C T intron_variant MELA-AU 9 96391659 96391659 single base substitution C T intron_variant MELA-AU 9 96391728 96391728 single base substitution A T intron_variant MELA-AU 9 96391765 96391765 single base substitution G C intron_variant MELA-AU 9 96391970 96391970 single base substitution C T intron_variant MELA-AU 9 96392397 96392397 single base substitution G A intron_variant MELA-AU 9 96392420 96392420 single base substitution C T intron_variant MELA-AU 9 96392484 96392485 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 9 96392561 96392561 single base substitution G A intron_variant MELA-AU 9 96393187 96393187 single base substitution C T intron_variant MELA-AU 9 96393303 96393303 single base substitution C T intron_variant MELA-AU 9 96393337 96393337 single base substitution C T intron_variant MELA-AU 9 96394278 96394278 single base substitution G T intron_variant MELA-AU 9 96394591 96394591 single base substitution C T intron_variant MELA-AU 9 96395292 96395292 single base substitution G A intron_variant MELA-AU 9 96395353 96395353 single base substitution G A intron_variant MELA-AU 9 96395611 96395611 single base substitution C T intron_variant MELA-AU 9 96396170 96396170 single base substitution T A intron_variant MELA-AU 9 96396243 96396243 single base substitution G A intron_variant MELA-AU 9 96396527 96396527 single base substitution C T intron_variant MELA-AU 9 96396851 96396851 single base substitution C T intron_variant MELA-AU 9 96397174 96397174 single base substitution G A intron_variant MELA-AU 9 96397341 96397342 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 9 96397419 96397419 single base substitution A T intron_variant MELA-AU 9 96397642 96397642 single base substitution C T intron_variant MELA-AU 9 96397667 96397667 single base substitution C T intron_variant MELA-AU 9 96398057 96398057 single base substitution C T intron_variant MELA-AU 9 96398677 96398677 single base substitution C T intron_variant MELA-AU 9 96398750 96398750 single base substitution C T missense_variant P81L 242C>T MELA-AU 9 96398974 96398974 single base substitution C T intron_variant MELA-AU 9 96399432 96399432 single base substitution C T intron_variant MELA-AU 9 96400366 96400366 single base substitution G A intron_variant MELA-AU 9 96400900 96400900 single base substitution C T intron_variant MELA-AU 9 96401751 96401751 single base substitution G T intron_variant MELA-AU 9 96401869 96401869 single base substitution C T intron_variant MELA-AU 9 96402170 96402170 single base substitution A G intron_variant MELA-AU 9 96402290 96402290 single base substitution G T intron_variant MELA-AU 9 96402299 96402299 single base substitution C T intron_variant MELA-AU 9 96402652 96402652 single base substitution C T intron_variant MELA-AU 9 96402948 96402948 single base substitution C T intron_variant MELA-AU 9 96403088 96403088 single base substitution G A intron_variant MELA-AU 9 96403744 96403744 single base substitution T C intron_variant MELA-AU 9 96404187 96404187 single base substitution A G intron_variant MELA-AU 9 96404484 96404484 single base substitution T C intron_variant MELA-AU 9 96405207 96405207 single base substitution C T intron_variant MELA-AU 9 96405707 96405707 single base substitution C T intron_variant MELA-AU 9 96405782 96405782 single base substitution C T intron_variant MELA-AU 9 96405866 96405866 single base substitution C T intron_variant MELA-AU 9 96406065 96406065 single base substitution C T intron_variant MELA-AU 9 96406252 96406252 single base substitution C T intron_variant MELA-AU 9 96406893 96406893 single base substitution C T intron_variant MELA-AU 9 96407268 96407268 single base substitution C T intron_variant MELA-AU 9 96407367 96407367 single base substitution G A intron_variant MELA-AU 9 96407473 96407473 single base substitution C T intron_variant MELA-AU 9 96407751 96407751 single base substitution C T intron_variant MELA-AU 9 96408559 96408559 single base substitution T A intron_variant MELA-AU 9 96408778 96408778 single base substitution C T intron_variant MELA-AU 9 96408784 96408784 single base substitution C T intron_variant MELA-AU 9 96409306 96409306 single base substitution C T intron_variant MELA-AU 9 96409841 96409841 single base substitution C T intron_variant MELA-AU 9 96410817 96410817 single base substitution C T intron_variant MELA-AU 9 96410854 96410854 single base substitution C T intron_variant MELA-AU 9 96411759 96411759 single base substitution G A intron_variant MELA-AU 9 96411803 96411803 single base substitution C T intron_variant MELA-AU 9 96412821 96412821 single base substitution C T intron_variant MELA-AU 9 96412994 96412994 single base substitution C T intron_variant MELA-AU 9 96413009 96413009 single base substitution C T intron_variant MELA-AU 9 96413381 96413381 single base substitution A T intron_variant MELA-AU 9 96413666 96413666 single base substitution C T intron_variant MELA-AU 9 96413949 96413949 single base substitution C T intron_variant MELA-AU 9 96415677 96415677 single base substitution C T intron_variant MELA-AU 9 96416128 96416128 single base substitution C T intron_variant MELA-AU 9 96416329 96416329 single base substitution C G intron_variant MELA-AU 9 96416533 96416533 single base substitution C T intron_variant MELA-AU 9 96416741 96416741 single base substitution C T intron_variant MELA-AU 9 96416741 96416741 single base substitution C T missense_variant S279F 836C>T MELA-AU 9 96416882 96416882 single base substitution C T intron_variant MELA-AU 9 96417252 96417252 single base substitution C T intron_variant MELA-AU 9 96417788 96417788 single base substitution T C intron_variant MELA-AU 9 96417851 96417851 single base substitution C T intron_variant MELA-AU 9 96418281 96418281 single base substitution C T intron_variant MELA-AU 9 96418281 96418281 single base substitution C T synonymous_variant L340L 1018C>T MELA-AU 9 96418448 96418448 single base substitution C T intron_variant MELA-AU 9 96418488 96418488 single base substitution C T intron_variant MELA-AU 9 96418567 96418567 single base substitution C T intron_variant MELA-AU 9 96419030 96419030 single base substitution C T intron_variant MELA-AU 9 96419991 96419991 single base substitution C T intron_variant MELA-AU 9 96420169 96420169 single base substitution C T intron_variant MELA-AU 9 96420261 96420261 single base substitution C T intron_variant MELA-AU 9 96420933 96420934 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 9 96421099 96421099 single base substitution C T intron_variant MELA-AU 9 96421439 96421439 single base substitution C T intron_variant MELA-AU 9 96421645 96421645 single base substitution C T intron_variant MELA-AU 9 96421915 96421915 single base substitution C T intron_variant MELA-AU 9 96422642 96422643 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 9 96422642 96422643 multiple base substitution (>=2bp and <=200bp) CC TT missense_variant P500F 1498CC>TT MELA-AU 9 96422855 96422855 single base substitution C T intron_variant MELA-AU 9 96423210 96423210 single base substitution C T intron_variant MELA-AU 9 96423414 96423415 multiple base substitution (>=2bp and <=200bp) GA AT intron_variant MELA-AU 9 96423558 96423558 single base substitution C T intron_variant MELA-AU 9 96425036 96425036 single base substitution C T intron_variant MELA-AU 9 96425140 96425140 single base substitution C T intron_variant MELA-AU 9 96426151 96426151 single base substitution C T intron_variant MELA-AU 9 96426255 96426255 single base substitution C T intron_variant MELA-AU 9 96426347 96426348 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 9 96427258 96427259 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 9 96427460 96427460 single base substitution C T intron_variant MELA-AU 9 96427781 96427781 single base substitution C T intron_variant MELA-AU 9 96428031 96428031 single base substitution G A intron_variant MELA-AU 9 96428031 96428031 single base substitution G A synonymous_variant E667E 2001G>A MELA-AU 9 96428046 96428046 single base substitution C G intron_variant MELA-AU 9 96428046 96428046 single base substitution C G synonymous_variant P672P 2016C>G MELA-AU 9 96428190 96428190 single base substitution C T intron_variant MELA-AU 9 96429042 96429042 single base substitution C T intron_variant MELA-AU 9 96429289 96429289 single base substitution C T intron_variant MELA-AU 9 96429741 96429741 single base substitution C T intron_variant MELA-AU 9 96430240 96430240 single base substitution C T intron_variant MELA-AU 9 96430634 96430634 single base substitution G A intron_variant MELA-AU 9 96434587 96434587 single base substitution G T intron_variant MELA-AU 9 96434647 96434647 single base substitution G A intron_variant MELA-AU 9 96434737 96434737 single base substitution G A intron_variant MELA-AU 9 96435350 96435350 single base substitution T C intron_variant MELA-AU 9 96436361 96436361 single base substitution C T intron_variant MELA-AU 9 96436808 96436808 single base substitution C T intron_variant MELA-AU 9 96437023 96437023 single base substitution C T intron_variant MELA-AU 9 96437168 96437168 single base substitution C T intron_variant MELA-AU 9 96437192 96437192 single base substitution C T intron_variant MELA-AU 9 96437201 96437202 multiple base substitution (>=2bp and <=200bp) CC TT splice_region_variant MELA-AU 9 96437289 96437289 single base substitution C T missense_variant P134S 400C>T MELA-AU 9 96437289 96437289 single base substitution C T missense_variant P903S 2707C>T MELA-AU 9 96437289 96437290 multiple base substitution (>=2bp and <=200bp) CC TT missense_variant P134F 400CC>TT MELA-AU 9 96437289 96437290 multiple base substitution (>=2bp and <=200bp) CC TT missense_variant P903F 2707CC>TT MELA-AU 9 96437717 96437717 single base substitution C T intron_variant MELA-AU 9 96437783 96437783 single base substitution C T intron_variant MELA-AU 9 96438108 96438108 single base substitution C T intron_variant MELA-AU 9 96438140 96438140 single base substitution C T intron_variant MELA-AU 9 96438158 96438158 single base substitution C T intron_variant MELA-AU 9 96438250 96438250 single base substitution C T intron_variant MELA-AU 9 96438251 96438251 single base substitution C T intron_variant MELA-AU 9 96438334 96438334 single base substitution C T intron_variant MELA-AU 9 96438460 96438460 single base substitution C T intron_variant MELA-AU 9 96438626 96438626 single base substitution G A intron_variant MELA-AU 9 96439678 96439678 single base substitution G A intron_variant MELA-AU 9 96439856 96439857 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 9 96439892 96439892 single base substitution G T missense_variant M1075I 3225G>T MELA-AU 9 96439892 96439892 single base substitution G T missense_variant M306I 918G>T MELA-AU 9 96439935 96439935 single base substitution C T missense_variant R1090W 3268C>T MELA-AU 9 96439935 96439935 single base substitution C T missense_variant R321W 961C>T MELA-AU 9 96440275 96440275 single base substitution C T 3_prime_UTR_variant MELA-AU 9 96441958 96441959 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 9 96442108 96442108 single base substitution T A downstream_gene_variant MELA-AU 9 96442359 96442360 multiple base substitution (>=2bp and <=200bp) AC TT downstream_gene_variant MELA-AU 9 96442881 96442881 single base substitution C T downstream_gene_variant MELA-AU 9 96443189 96443189 single base substitution C T downstream_gene_variant MELA-AU 9 96443580 96443580 single base substitution C T downstream_gene_variant MELA-AU 9 96444123 96444123 single base substitution G A downstream_gene_variant MELA-AU 9 96444335 96444335 single base substitution T A downstream_gene_variant MELA-AU 9 96444867 96444867 single base substitution G A downstream_gene_variant MELA-AU 9 96444975 96444975 single base substitution G A downstream_gene_variant MELA-AU 9 96445998 96445998 single base substitution G A downstream_gene_variant MELA-AU 9 96446079 96446079 single base substitution C T downstream_gene_variant MELA-AU 9 96446098 96446098 single base substitution C T downstream_gene_variant MELA-AU 9 96446190 96446190 single base substitution C T downstream_gene_variant MELA-AU 9 96446214 96446214 single base substitution C T downstream_gene_variant MELA-AU 9 96446248 96446249 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 9 96446259 96446259 single base substitution G A downstream_gene_variant MELA-AU 9 96446484 96446484 single base substitution G A downstream_gene_variant MELA-AU 9 96446710 96446710 single base substitution C T downstream_gene_variant MELA-AU 9 96446869 96446869 single base substitution C T downstream_gene_variant ORCA-IN 9 96359069 96359069 single base substitution C A intron_variant ORCA-IN 9 96360830 96360830 single base substitution C G intron_variant ORCA-IN 9 96372095 96372095 single base substitution C G intron_variant ORCA-IN 9 96378069 96378069 single base substitution C T intron_variant ORCA-IN 9 96410375 96410375 single base substitution C A intron_variant ORCA-IN 9 96414368 96414368 single base substitution G A intron_variant ORCA-IN 9 96416056 96416056 single base substitution G A intron_variant ORCA-IN 9 96416722 96416722 single base substitution C A intron_variant ORCA-IN 9 96416722 96416722 single base substitution C A missense_variant P273T 817C>A ORCA-IN 9 96416723 96416723 single base substitution C A intron_variant ORCA-IN 9 96416723 96416723 single base substitution C A missense_variant P273Q 818C>A ORCA-IN 9 96427999 96427999 single base substitution G T intron_variant ORCA-IN 9 96427999 96427999 single base substitution G T missense_variant G657C 1969G>T ORCA-IN 9 96429383 96429383 single base substitution G T intron_variant ORCA-IN 9 96429383 96429383 single base substitution G T missense_variant G737C 2209G>T ORCA-IN 9 96435971 96435971 single base substitution G T intron_variant ORCA-IN 9 96435971 96435971 single base substitution G T missense_variant G818V 2453G>T ORCA-IN 9 96437966 96437966 single base substitution G T missense_variant R140S 420G>T ORCA-IN 9 96437966 96437966 single base substitution G T missense_variant R909S 2727G>T ORCA-IN 9 96443622 96443622 deletion of <=200bp C - downstream_gene_variant OV-AU 9 96337212 96337212 single base substitution A T upstream_gene_variant OV-AU 9 96337589 96337589 single base substitution A G upstream_gene_variant OV-AU 9 96342843 96342843 single base substitution C A intron_variant OV-AU 9 96349052 96349052 single base substitution G T intron_variant OV-AU 9 96355569 96355569 single base substitution C G intron_variant OV-AU 9 96372093 96372093 single base substitution C T intron_variant OV-AU 9 96382892 96382892 single base substitution T G intron_variant OV-AU 9 96384777 96384777 single base substitution G C intron_variant OV-AU 9 96397400 96397400 single base substitution G A intron_variant OV-AU 9 96404665 96404665 single base substitution C G intron_variant OV-AU 9 96405686 96405686 single base substitution G A intron_variant OV-AU 9 96414279 96414279 single base substitution G C intron_variant OV-AU 9 96417193 96417193 single base substitution G A intron_variant OV-AU 9 96424099 96424099 single base substitution T A intron_variant OV-AU 9 96424590 96424590 single base substitution T A intron_variant OV-AU 9 96425199 96425224 deletion of <=200bp GTGTCCTGAGTGTGCCCAACAAAGAT - frameshift_variant SVLSVPNKD570 OV-AU 9 96425199 96425224 deletion of <=200bp GTGTCCTGAGTGTGCCCAACAAAGAT - intron_variant OV-AU 9 96425478 96425478 single base substitution C T intron_variant OV-AU 9 96428052 96428052 single base substitution G A intron_variant OV-AU 9 96428052 96428052 single base substitution G A synonymous_variant R674R 2022G>A OV-AU 9 96439058 96439058 single base substitution G T missense_variant Q1005H 3015G>T OV-AU 9 96439058 96439058 single base substitution G T missense_variant Q236H 708G>T OV-AU 9 96441713 96441713 single base substitution T C 3_prime_UTR_variant OV-AU 9 96443208 96443208 single base substitution C T downstream_gene_variant PACA-AU 9 96346610 96346610 single base substitution A C intron_variant PACA-AU 9 96352762 96352762 single base substitution C G intron_variant PACA-AU 9 96367136 96367136 single base substitution C T intron_variant PACA-AU 9 96369510 96369510 insertion of <=200bp - AAT intron_variant PACA-AU 9 96370213 96370213 single base substitution G A intron_variant PACA-AU 9 96370458 96370458 single base substitution A G intron_variant PACA-AU 9 96370497 96370497 single base substitution C T intron_variant PACA-AU 9 96370662 96370662 single base substitution G A intron_variant PACA-AU 9 96375482 96375482 single base substitution G A intron_variant PACA-AU 9 96375484 96375484 single base substitution G T intron_variant PACA-AU 9 96396995 96396995 single base substitution G A intron_variant PACA-AU 9 96412973 96412973 single base substitution C G intron_variant PACA-AU 9 96421431 96421431 single base substitution G A intron_variant PACA-AU 9 96431827 96431827 single base substitution C T intron_variant PACA-AU 9 96442687 96442687 single base substitution A C downstream_gene_variant PACA-AU 9 96446141 96446141 single base substitution C T downstream_gene_variant PACA-AU 9 96446616 96446616 single base substitution C A downstream_gene_variant PACA-AU 9 96446799 96446799 single base substitution C A downstream_gene_variant PACA-CA 9 96336265 96336265 single base substitution G A upstream_gene_variant PACA-CA 9 96337589 96337589 single base substitution A C upstream_gene_variant PACA-CA 9 96342301 96342301 single base substitution G A intron_variant PACA-CA 9 96347521 96347521 single base substitution C T intron_variant PACA-CA 9 96353331 96353331 single base substitution C T intron_variant PACA-CA 9 96360331 96360331 single base substitution C T intron_variant PACA-CA 9 96361151 96361151 deletion of <=200bp C - intron_variant PACA-CA 9 96363528 96363528 single base substitution C T intron_variant PACA-CA 9 96365304 96365304 single base substitution G A intron_variant PACA-CA 9 96366322 96366322 single base substitution C T intron_variant PACA-CA 9 96367120 96367120 insertion of <=200bp - T intron_variant PACA-CA 9 96374556 96374556 deletion of <=200bp T - intron_variant PACA-CA 9 96380871 96380871 single base substitution G A intron_variant PACA-CA 9 96386792 96386792 single base substitution C T intron_variant PACA-CA 9 96410070 96410070 single base substitution C T intron_variant PACA-CA 9 96410534 96410534 single base substitution G A intron_variant PACA-CA 9 96410795 96410795 single base substitution C T intron_variant PACA-CA 9 96411665 96411665 single base substitution T C intron_variant PACA-CA 9 96411666 96411666 single base substitution T C intron_variant PACA-CA 9 96412444 96412444 single base substitution C T intron_variant PACA-CA 9 96413286 96413286 single base substitution G C intron_variant PACA-CA 9 96417091 96417091 single base substitution T G intron_variant PACA-CA 9 96421944 96421947 deletion of <=200bp TCTC - intron_variant PACA-CA 9 96422612 96422612 deletion of <=200bp A - frameshift_variant K490 PACA-CA 9 96422612 96422612 deletion of <=200bp A - splice_region_variant PACA-CA 9 96426920 96426920 single base substitution G A intron_variant PACA-CA 9 96427898 96427898 single base substitution C T intron_variant PACA-CA 9 96428666 96428666 single base substitution C A intron_variant PACA-CA 9 96431553 96431553 single base substitution G A intron_variant PACA-CA 9 96440046 96440046 single base substitution C A 3_prime_UTR_variant PACA-CA 9 96440477 96440477 single base substitution C T 3_prime_UTR_variant PAEN-AU 9 96354442 96354442 single base substitution C A intron_variant PAEN-AU 9 96361618 96361618 single base substitution T G intron_variant PAEN-AU 9 96380950 96380950 single base substitution T G intron_variant PAEN-AU 9 96428163 96428163 single base substitution T G intron_variant PAEN-IT 9 96436191 96436191 single base substitution A C intron_variant PAEN-IT 9 96445582 96445582 single base substitution C A downstream_gene_variant PBCA-DE 9 96349768 96349769 deletion of <=200bp AT - intron_variant PBCA-DE 9 96360609 96360609 single base substitution C T intron_variant PBCA-DE 9 96376747 96376747 insertion of <=200bp - G intron_variant PBCA-DE 9 96377144 96377144 single base substitution G A intron_variant PBCA-DE 9 96377492 96377492 single base substitution G A intron_variant PBCA-DE 9 96392800 96392800 single base substitution C T intron_variant PBCA-DE 9 96392841 96392841 single base substitution C T intron_variant PBCA-DE 9 96422164 96422164 single base substitution C A intron_variant PBCA-DE 9 96424842 96424842 single base substitution A G intron_variant PBCA-DE 9 96426050 96426058 deletion of <=200bp CACACACAC - intron_variant PBCA-DE 9 96428545 96428545 single base substitution C T intron_variant PBCA-DE 9 96433720 96433720 insertion of <=200bp - GT intron_variant PBCA-DE 9 96434695 96434695 single base substitution G A intron_variant PBCA-DE 9 96436896 96436896 single base substitution G A intron_variant PBCA-DE 9 96438992 96438992 single base substitution A T synonymous_variant P214P 642A>T PBCA-DE 9 96438992 96438992 single base substitution A T synonymous_variant P983P 2949A>T PBCA-DE 9 96439019 96439019 single base substitution C A synonymous_variant T223T 669C>A PBCA-DE 9 96439019 96439019 single base substitution C A synonymous_variant T992T 2976C>A PBCA-DE 9 96442675 96442675 deletion of <=200bp T - downstream_gene_variant PBCA-DE 9 96443206 96443206 single base substitution A C downstream_gene_variant PBCA-DE 9 96445202 96445202 single base substitution C G downstream_gene_variant PBCA-DE 9 96446623 96446623 single base substitution G T downstream_gene_variant PRAD-CA 9 96341710 96341710 single base substitution G C intron_variant PRAD-CA 9 96349534 96349534 single base substitution T C intron_variant PRAD-CA 9 96349803 96349803 single base substitution A C intron_variant PRAD-CA 9 96361176 96361176 single base substitution C A intron_variant PRAD-CA 9 96370695 96370695 single base substitution C T intron_variant PRAD-CA 9 96377139 96377139 single base substitution A G intron_variant PRAD-CA 9 96381626 96381626 single base substitution G A intron_variant PRAD-CA 9 96425363 96425363 single base substitution G A intron_variant PRAD-CA 9 96434695 96434695 single base substitution G A intron_variant PRAD-UK 9 96334229 96334229 single base substitution A T upstream_gene_variant PRAD-UK 9 96339940 96339940 single base substitution G A intron_variant PRAD-UK 9 96340838 96340838 single base substitution C A intron_variant PRAD-UK 9 96376030 96376030 insertion of <=200bp - T intron_variant PRAD-UK 9 96390042 96390042 single base substitution G A intron_variant PRAD-UK 9 96391005 96391005 single base substitution G C intron_variant PRAD-UK 9 96396034 96396034 single base substitution C T intron_variant PRAD-UK 9 96434675 96434716 deletion of <=200bp CAGGTGCAGGTGCAGGTGTGGGTGTGGGAGTAGGCACAGGTG - intron_variant PRAD-UK 9 96434687 96434687 single base substitution C T intron_variant PRAD-UK 9 96436105 96436105 single base substitution C A missense_variant Q863K 2587C>A PRAD-UK 9 96436105 96436105 single base substitution C A missense_variant Q94K 280C>A PRAD-UK 9 96439488 96439488 single base substitution C G intron_variant READ-US 9 96436080 96436080 single base substitution C T synonymous_variant V854V 2562C>T READ-US 9 96436080 96436080 single base substitution C T synonymous_variant V85V 255C>T READ-US 9 96438998 96438998 insertion of <=200bp - ACCACCCCTGCCTCC disruptive_inframe_insertion S216SPPLPP READ-US 9 96438998 96438998 insertion of <=200bp - ACCACCCCTGCCTCC disruptive_inframe_insertion S985SPPLPP READ-US 9 96439004 96439004 insertion of <=200bp - CCTGCCTCCACCACA inframe_insertion T218TLPPPH READ-US 9 96439004 96439004 insertion of <=200bp - CCTGCCTCCACCACA inframe_insertion T987TLPPPH READ-US 9 96439007 96439007 single base substitution G T synonymous_variant P219P 657G>T READ-US 9 96439007 96439007 single base substitution G T synonymous_variant P988P 2964G>T READ-US 9 96439019 96439019 single base substitution C A synonymous_variant T223T 669C>A READ-US 9 96439019 96439019 single base substitution C A synonymous_variant T992T 2976C>A READ-US 9 96439936 96439936 single base substitution G A missense_variant R1090Q 3269G>A READ-US 9 96439936 96439936 single base substitution G A missense_variant R321Q 962G>A RECA-EU 9 96333710 96333710 single base substitution C T upstream_gene_variant RECA-EU 9 96346491 96346491 single base substitution T A intron_variant RECA-EU 9 96348698 96348698 single base substitution G T intron_variant RECA-EU 9 96349310 96349310 single base substitution G A intron_variant RECA-EU 9 96349376 96349376 single base substitution A T intron_variant RECA-EU 9 96364933 96364933 single base substitution G T intron_variant RECA-EU 9 96366636 96366636 single base substitution A G intron_variant RECA-EU 9 96374764 96374764 single base substitution A G intron_variant RECA-EU 9 96377476 96377476 single base substitution T C intron_variant RECA-EU 9 96377481 96377481 single base substitution A G intron_variant RECA-EU 9 96387385 96387385 single base substitution C T intron_variant RECA-EU 9 96390646 96390646 single base substitution C G intron_variant RECA-EU 9 96400615 96400615 single base substitution T G intron_variant RECA-EU 9 96405795 96405795 single base substitution G A intron_variant RECA-EU 9 96408154 96408154 single base substitution C T intron_variant RECA-EU 9 96410191 96410191 single base substitution A C intron_variant RECA-EU 9 96415621 96415621 single base substitution G A intron_variant RECA-EU 9 96415621 96415621 single base substitution G A missense_variant A255T 763G>A RECA-EU 9 96421073 96421073 single base substitution G T intron_variant RECA-EU 9 96427263 96427263 single base substitution C G intron_variant RECA-EU 9 96431762 96431762 single base substitution G C intron_variant RECA-EU 9 96433708 96433708 single base substitution G A intron_variant RECA-EU 9 96434681 96434681 single base substitution C T intron_variant RECA-EU 9 96434684 96434684 single base substitution G A intron_variant RECA-EU 9 96434772 96434772 single base substitution A T intron_variant RECA-EU 9 96436608 96436608 single base substitution T C intron_variant RECA-EU 9 96438577 96438577 single base substitution C G intron_variant RECA-EU 9 96438989 96438989 single base substitution G C synonymous_variant T213T 639G>C RECA-EU 9 96438989 96438989 single base substitution G C synonymous_variant T982T 2946G>C RECA-EU 9 96438992 96438992 single base substitution A T synonymous_variant P214P 642A>T RECA-EU 9 96438992 96438992 single base substitution A T synonymous_variant P983P 2949A>T RECA-EU 9 96438998 96438998 single base substitution T C synonymous_variant S216S 648T>C RECA-EU 9 96438998 96438998 single base substitution T C synonymous_variant S985S 2955T>C RECA-EU 9 96439019 96439019 single base substitution C A synonymous_variant T223T 669C>A RECA-EU 9 96439019 96439019 single base substitution C A synonymous_variant T992T 2976C>A RECA-EU 9 96442745 96442745 single base substitution C T downstream_gene_variant RECA-EU 9 96444330 96444330 single base substitution G A downstream_gene_variant SKCA-BR 9 96341511 96341511 single base substitution G C intron_variant SKCA-BR 9 96342566 96342566 single base substitution A G intron_variant SKCA-BR 9 96342606 96342606 single base substitution T G intron_variant SKCA-BR 9 96343088 96343088 single base substitution G T intron_variant SKCA-BR 9 96346108 96346112 deletion of <=200bp CTTTT - intron_variant SKCA-BR 9 96349784 96349784 single base substitution G C intron_variant SKCA-BR 9 96349787 96349787 single base substitution T G intron_variant SKCA-BR 9 96351362 96351362 single base substitution C A intron_variant SKCA-BR 9 96351363 96351363 single base substitution A G intron_variant SKCA-BR 9 96352969 96352969 single base substitution C T intron_variant SKCA-BR 9 96354730 96354730 single base substitution C T intron_variant SKCA-BR 9 96360647 96360647 single base substitution T C intron_variant SKCA-BR 9 96363714 96363714 single base substitution T G intron_variant SKCA-BR 9 96365753 96365753 single base substitution G A intron_variant SKCA-BR 9 96367539 96367539 single base substitution G A intron_variant SKCA-BR 9 96369266 96369266 single base substitution C T intron_variant SKCA-BR 9 96369721 96369723 deletion of <=200bp ATT - intron_variant SKCA-BR 9 96369835 96369835 single base substitution G A intron_variant SKCA-BR 9 96369994 96369994 single base substitution A T intron_variant SKCA-BR 9 96370680 96370680 insertion of <=200bp - GT intron_variant SKCA-BR 9 96371319 96371319 single base substitution C T intron_variant SKCA-BR 9 96377136 96377136 single base substitution A G intron_variant SKCA-BR 9 96377463 96377463 insertion of <=200bp - GTGATGA intron_variant SKCA-BR 9 96377470 96377470 single base substitution C T intron_variant SKCA-BR 9 96380132 96380132 single base substitution C T intron_variant SKCA-BR 9 96381190 96381190 single base substitution C T intron_variant SKCA-BR 9 96384471 96384471 single base substitution C T intron_variant SKCA-BR 9 96387972 96387972 single base substitution C T intron_variant SKCA-BR 9 96389382 96389382 single base substitution C T intron_variant SKCA-BR 9 96391870 96391870 single base substitution C T intron_variant SKCA-BR 9 96392779 96392779 single base substitution C T intron_variant SKCA-BR 9 96393233 96393233 single base substitution T G intron_variant SKCA-BR 9 96393360 96393360 single base substitution C T intron_variant SKCA-BR 9 96393610 96393610 single base substitution C T intron_variant SKCA-BR 9 96397124 96397124 single base substitution C T intron_variant SKCA-BR 9 96397426 96397426 single base substitution C T intron_variant SKCA-BR 9 96405918 96405918 single base substitution C T intron_variant SKCA-BR 9 96407173 96407173 single base substitution G A intron_variant SKCA-BR 9 96409288 96409288 single base substitution C T intron_variant SKCA-BR 9 96410782 96410782 single base substitution C T intron_variant SKCA-BR 9 96412617 96412617 single base substitution C T intron_variant SKCA-BR 9 96413380 96413380 insertion of <=200bp - TA intron_variant SKCA-BR 9 96413381 96413381 single base substitution A T intron_variant SKCA-BR 9 96415445 96415445 single base substitution C T intron_variant SKCA-BR 9 96416610 96416610 single base substitution T G intron_variant SKCA-BR 9 96418184 96418184 single base substitution T G intron_variant SKCA-BR 9 96418190 96418190 single base substitution A C intron_variant SKCA-BR 9 96421737 96421737 single base substitution T G intron_variant SKCA-BR 9 96422482 96422482 single base substitution C T intron_variant SKCA-BR 9 96422482 96422482 single base substitution C T synonymous_variant S446S 1338C>T SKCA-BR 9 96424815 96424823 deletion of <=200bp CGGATGGAT - intron_variant SKCA-BR 9 96424933 96424933 single base substitution G A intron_variant SKCA-BR 9 96425454 96425455 deletion of <=200bp TA - intron_variant SKCA-BR 9 96425457 96425457 single base substitution G C intron_variant SKCA-BR 9 96429866 96429866 single base substitution C T intron_variant SKCA-BR 9 96430597 96430597 single base substitution T G intron_variant SKCA-BR 9 96432383 96432383 single base substitution G A intron_variant SKCA-BR 9 96433862 96433862 single base substitution A G intron_variant SKCA-BR 9 96434018 96434018 single base substitution A G intron_variant SKCA-BR 9 96434960 96434960 single base substitution T G intron_variant SKCA-BR 9 96441950 96441950 single base substitution T C downstream_gene_variant SKCA-BR 9 96445200 96445200 insertion of <=200bp - ACGAGCTGCAAAGTGGC downstream_gene_variant SKCA-BR 9 96446129 96446129 single base substitution C T downstream_gene_variant SKCM-US 9 96407999 96407999 single base substitution C T intron_variant SKCM-US 9 96407999 96407999 single base substitution C T missense_variant P130S 388C>T SKCM-US 9 96408008 96408008 single base substitution G A intron_variant SKCM-US 9 96408008 96408008 single base substitution G A missense_variant D133N 397G>A SKCM-US 9 96416852 96416852 single base substitution C T intron_variant SKCM-US 9 96416852 96416852 single base substitution C T missense_variant P316L 947C>T SKCM-US 9 96418822 96418822 single base substitution C T intron_variant SKCM-US 9 96418822 96418822 single base substitution C T synonymous_variant P364P 1092C>T SKCM-US 9 96420455 96420455 single base substitution C T intron_variant SKCM-US 9 96420455 96420455 single base substitution C T synonymous_variant P392P 1176C>T SKCM-US 9 96422565 96422565 single base substitution C T intron_variant SKCM-US 9 96422565 96422565 single base substitution C T missense_variant S474F 1421C>T SKCM-US 9 96425206 96425206 single base substitution G T intron_variant SKCM-US 9 96425206 96425206 single base substitution G T synonymous_variant L572L 1716G>T SKCM-US 9 96425208 96425208 single base substitution G A intron_variant SKCM-US 9 96425208 96425208 single base substitution G A missense_variant S573N 1718G>A SKCM-US 9 96425891 96425891 single base substitution T A intron_variant SKCM-US 9 96425891 96425891 single base substitution T A missense_variant F637L 1911T>A SKCM-US 9 96428031 96428031 single base substitution G A intron_variant SKCM-US 9 96428031 96428031 single base substitution G A synonymous_variant E667E 2001G>A SKCM-US 9 96428317 96428317 single base substitution C T intron_variant SKCM-US 9 96428317 96428317 single base substitution C T missense_variant P721L 2162C>T SKCM-US 9 96429433 96429433 single base substitution C T intron_variant SKCM-US 9 96429433 96429433 single base substitution C T synonymous_variant V753V 2259C>T SKCM-US 9 96429453 96429453 single base substitution C T intron_variant SKCM-US 9 96429453 96429453 single base substitution C T missense_variant S760L 2279C>T SKCM-US 9 96435917 96435917 single base substitution C T intron_variant SKCM-US 9 96435917 96435917 single base substitution C T missense_variant S800F 2399C>T SKCM-US 9 96437255 96437255 single base substitution C T synonymous_variant S122S 366C>T SKCM-US 9 96437255 96437255 single base substitution C T synonymous_variant S891S 2673C>T STAD-US 9 96415473 96415473 single base substitution C T intron_variant STAD-US 9 96415473 96415473 single base substitution C T synonymous_variant F205F 615C>T STAD-US 9 96415507 96415507 single base substitution T C intron_variant STAD-US 9 96415507 96415507 single base substitution T C missense_variant W217R 649T>C STAD-US 9 96422584 96422584 single base substitution G A intron_variant STAD-US 9 96422584 96422584 single base substitution G A synonymous_variant P480P 1440G>A STAD-US 9 96422621 96422621 single base substitution A G intron_variant STAD-US 9 96422621 96422621 single base substitution A G missense_variant T493A 1477A>G STAD-US 9 96422642 96422642 single base substitution C A intron_variant STAD-US 9 96422642 96422642 single base substitution C A missense_variant P500T 1498C>A STAD-US 9 96425855 96425855 single base substitution G A intron_variant STAD-US 9 96425855 96425855 single base substitution G A synonymous_variant S625S 1875G>A STAD-US 9 96428047 96428047 single base substitution G A intron_variant STAD-US 9 96428047 96428047 single base substitution G A missense_variant V673M 2017G>A STAD-US 9 96428055 96428055 single base substitution T C intron_variant STAD-US 9 96428055 96428055 single base substitution T C synonymous_variant D675D 2025T>C STAD-US 9 96428068 96428068 single base substitution G A intron_variant STAD-US 9 96428068 96428068 single base substitution G A missense_variant V680M 2038G>A STAD-US 9 96428129 96428129 single base substitution C T intron_variant STAD-US 9 96428129 96428129 single base substitution C T missense_variant P700L 2099C>T STAD-US 9 96435920 96435920 single base substitution T C intron_variant STAD-US 9 96435920 96435920 single base substitution T C missense_variant M801T 2402T>C STAD-US 9 96437269 96437269 single base substitution G T missense_variant R127M 380G>T STAD-US 9 96437269 96437269 single base substitution G T missense_variant R896M 2687G>T STAD-US 9 96437282 96437282 single base substitution C T synonymous_variant D131D 393C>T STAD-US 9 96437282 96437282 single base substitution C T synonymous_variant D900D 2700C>T STAD-US 9 96438029 96438029 single base substitution C T synonymous_variant I161I 483C>T STAD-US 9 96438029 96438029 single base substitution C T synonymous_variant I930I 2790C>T STAD-US 9 96438043 96438043 single base substitution C T missense_variant A166V 497C>T STAD-US 9 96438043 96438043 single base substitution C T missense_variant A935V 2804C>T STAD-US 9 96439875 96439875 single base substitution C T missense_variant R1070C 3208C>T STAD-US 9 96439875 96439875 single base substitution C T missense_variant R301C 901C>T UCEC-US 9 96408059 96408059 single base substitution G A intron_variant UCEC-US 9 96408059 96408059 single base substitution G A missense_variant E150K 448G>A UCEC-US 9 96411441 96411441 single base substitution C T intron_variant UCEC-US 9 96411441 96411441 single base substitution C T synonymous_variant S183S 549C>T UCEC-US 9 96415497 96415497 single base substitution G T intron_variant UCEC-US 9 96415497 96415497 single base substitution G T missense_variant K213N 639G>T UCEC-US 9 96415578 96415578 single base substitution C T intron_variant UCEC-US 9 96415578 96415578 single base substitution C T synonymous_variant C240C 720C>T UCEC-US 9 96416753 96416753 single base substitution G A intron_variant UCEC-US 9 96416753 96416753 single base substitution G A missense_variant R283H 848G>A UCEC-US 9 96422512 96422512 single base substitution C T intron_variant UCEC-US 9 96422512 96422512 single base substitution C T synonymous_variant V456V 1368C>T UCEC-US 9 96422789 96422789 single base substitution G A intron_variant UCEC-US 9 96422789 96422789 single base substitution G A missense_variant E549K 1645G>A UCEC-US 9 96428007 96428007 single base substitution C T intron_variant UCEC-US 9 96428007 96428007 single base substitution C T synonymous_variant F659F 1977C>T UCEC-US 9 96428011 96428011 single base substitution G A intron_variant UCEC-US 9 96428011 96428011 single base substitution G A missense_variant A661T 1981G>A UCEC-US 9 96428110 96428110 single base substitution A T intron_variant UCEC-US 9 96428110 96428110 single base substitution A T missense_variant R694W 2080A>T UCEC-US 9 96436081 96436081 single base substitution G A missense_variant D855N 2563G>A UCEC-US 9 96436081 96436081 single base substitution G A missense_variant D86N 256G>A UCEC-US 9 96436132 96436132 single base substitution G A missense_variant D103N 307G>A UCEC-US 9 96436132 96436132 single base substitution G A missense_variant D872N 2614G>A UCEC-US 9 96437249 96437249 single base substitution T C synonymous_variant F120F 360T>C UCEC-US 9 96437249 96437249 single base substitution T C synonymous_variant F889F 2667T>C UCEC-US 9 96437264 96437264 single base substitution G T missense_variant K125N 375G>T UCEC-US 9 96437264 96437264 single base substitution G T missense_variant K894N 2682G>T UCEC-US 9 96438039 96438039 single base substitution C T synonymous_variant L165L 493C>T UCEC-US 9 96438039 96438039 single base substitution C T synonymous_variant L934L 2800C>T

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand HCC143 COSM1625263 c.2401A>G p.M801V Substitution - Missense 9:93673637-93673637 + TCGA-D5-6927-01 COSM305500 c.2961_2962ins15 p.T987_P988insPASTT Insertion - In frame 9:93676722-93676723 + LUAD-S01302 COSM396351 c.2676G>T p.R892R Substitution - coding silent 9:93674976-93674976 + 258 COSM3723034 c.2976C>A p.T992T Substitution - coding silent 9:93676737-93676737 + TCGA-AO-A128-01 COSM3849111 c.73G>A p.A25T Substitution - Missense 9:93576846-93576846 + TCGA-CD-A4MG-01 COSM1220356 c.1498C>A p.P500T Substitution - Missense 9:93660360-93660360 + I2L-P19Ta-Tumor-Organoid COSM198796 c.1468delA p.K492fs*6 Deletion - Frameshift 9:93660330-93660330 + LOVO COSM198796 c.1468delA p.K492fs*6 Deletion - Frameshift 9:93660330-93660330 + PTC-54C COSM4139020 c.2946G>C p.T982T Substitution - coding silent 9:93676707-93676707 + LS174T COSM2732580 c.353T>C p.M118T Substitution - Missense 9:93645682-93645682 + PT51 COSM5938235 c.836C>A p.S279Y Substitution - Missense 9:93654459-93654459 + YUBER COSM1686590 c.1329+1G>A p.? Unknown 9:93659601-93659601 + HCC162T COSM3747771 c.2990G>C p.S997T Substitution - Missense 9:93676751-93676751 + SCC-15 COSM305500 c.2961_2962ins15 p.T987_P988insPASTT Insertion - In frame 9:93676722-93676723 + 587222 COSM1220358 c.1559C>T p.T520M Substitution - Missense 9:93660421-93660421 + TCGA-AD-6890-01 COSM3750192 c.2964G>T p.P988P Substitution - coding silent 9:93676725-93676725 + TCGA-AZ-6598-01 COSM1463724 c.548G>A p.S183N Substitution - Missense 9:93649158-93649158 + TCGA-HU-A4H8-01 COSM1220355 c.1477A>G p.T493A Substitution - Missense 9:93660339-93660339 + TCGA-A6-5662-01 COSM1463725 c.573C>T p.N191N Substitution - coding silent 9:93649183-93649183 + T263 COSM4611878 c.1467_1468insA p.T493fs*21 Insertion - Frameshift 9:93660329-93660330 + YUNEXUS COSM5411507 c.494C>T p.T165I Substitution - Missense 9:93649104-93649104 + YUDIALE COSM1701347 c.1000G>A p.G334R Substitution - Missense 9:93655981-93655981 + TCGA-DM-A285-01 COSM305500 c.2961_2962ins15 p.T987_P988insPASTT Insertion - In frame 9:93676722-93676723 + C0044T COSM1463737 c.2949A>T p.P983P Substitution - coding silent 9:93676710-93676710 + HCC143T COSM1625263 c.2401A>G p.M801V Substitution - Missense 9:93673637-93673637 + 587220 COSM1220352 c.2099C>T p.P700L Substitution - Missense 9:93665847-93665847 + pfg122T COSM198796 c.1468delA p.K492fs*6 Deletion - Frameshift 9:93660330-93660330 + ESO-0013 COSM1262044 c.2488G>A p.A830T Substitution - Missense 9:93673724-93673724 + cSCCP4 COSM138718 c.1415C>T p.P472L Substitution - Missense 9:93660277-93660277 + 4537_T COSM297068 c.2961C>A p.T987T Substitution - coding silent 9:93676722-93676722 + TCGA-D5-6920-01 COSM305500 c.2961_2962ins15 p.T987_P988insPASTT Insertion - In frame 9:93676722-93676723 + TCGA-DM-A28F-01 COSM305500 c.2961_2962ins15 p.T987_P988insPASTT Insertion - In frame 9:93676722-93676723 + PTC-54C COSM4007303 c.309C>T p.D103D Substitution - coding silent 9:93645638-93645638 + pfg143T COSM4747649 c.3241delA p.R1081fs*6 Deletion - Frameshift 9:93677626-93677626 + TCGA-CM-5349-01 COSM305500 c.2961_2962ins15 p.T987_P988insPASTT Insertion - In frame 9:93676722-93676723 + 148632 COSM1644889 c.443A>G p.D148G Substitution - Missense 9:93645772-93645772 + C086 COSM5536977 c.1174C>T p.P392S Substitution - Missense 9:93658171-93658171 + SB_06 COSM5752973 c.2256_2257ins13 p.G758fs*19 Insertion - Frameshift 9:93667148-93667149 + TCGA-CD-8528-01 COSM3909080 c.2038G>A p.V680M Substitution - Missense 9:93665786-93665786 + 587376 COSM1220360 c.1204C>A p.L402I Substitution - Missense 9:93658201-93658201 + CSCC-19-T COSM4466264 c.1424C>T p.P475L Substitution - Missense 9:93660286-93660286 + TCGA-GN-A262-06 COSM3659719 c.2279C>T p.S760L Substitution - Missense 9:93667171-93667171 + PR-09-3566 COSM246564 c.2620G>A p.D874N Substitution - Missense 9:93673856-93673856 + CSCC-29-T COSM4487523 c.319C>T p.R107C Substitution - Missense 9:93645648-93645648 + CCRF-CEM COSM298373 c.281G>A p.R94Q Substitution - Missense 9:93636507-93636507 + TCGA-AZ-5403-01 COSM305500 c.2961_2962ins15 p.T987_P988insPASTT Insertion - In frame 9:93676722-93676723 + TCGA-G5-6572-01 COSM305500 c.2961_2962ins15 p.T987_P988insPASTT Insertion - In frame 9:93676722-93676723 + 6948_PT COSM5757438 c.1831G>A p.D611N Substitution - Missense 9:93663529-93663529 + BD72T COSM198796 c.1468delA p.K492fs*6 Deletion - Frameshift 9:93660330-93660330 + TCGA-ER-A194-01 COSM3659712 c.397G>A p.D133N Substitution - Missense 9:93645726-93645726 + 522_T COSM4139691 c.2194G>A p.D732N Substitution - Missense 9:93667086-93667086 + 587284 COSM1220359 c.1196C>A p.A399D Substitution - Missense 9:93658193-93658193 + TCGA-B5-A11E-01 COSM1111300 c.1981G>A p.A661T Substitution - Missense 9:93665729-93665729 + PTC-1C COSM297068 c.2961C>A p.T987T Substitution - coding silent 9:93676722-93676722 + TCGA-AD-6889-01 COSM297068 c.2961C>A p.T987T Substitution - coding silent 9:93676722-93676722 + 19 COSM5747022 c.1346T>C p.V449A Substitution - Missense 9:93660208-93660208 + P84 COSM1736326 c.2252C>G p.A751G Substitution - Missense 9:93667144-93667144 + TCGA-ED-A459-01 COSM4935546 c.569T>A p.L190H Substitution - Missense 9:93649179-93649179 + CSCC-29-T COSM4468397 c.1541C>T p.P514L Substitution - Missense 9:93660403-93660403 + TCGA-AB-2854-03 COSM1319564 c.324G>A p.V108V Substitution - coding silent 9:93645653-93645653 + TCGA-AA-A00N-01 COSM276727 c.1901A>C p.K634T Substitution - Missense 9:93663599-93663599 + sysucc-1163T COSM5459454 c.574G>A p.V192I Substitution - Missense 9:93649184-93649184 + TCGA-DV-5575-01 COSM297068 c.2961C>A p.T987T Substitution - coding silent 9:93676722-93676722 + 4132_T COSM297068 c.2961C>A p.T987T Substitution - coding silent 9:93676722-93676722 + T3202 COSM4713967 c.421G>T p.A141S Substitution - Missense 9:93645750-93645750 + T3024 COSM198796 c.1468delA p.K492fs*6 Deletion - Frameshift 9:93660330-93660330 + HCC172T COSM3723034 c.2976C>A p.T992T Substitution - coding silent 9:93676737-93676737 + UM-SCC-47 COSM305500 c.2961_2962ins15 p.T987_P988insPASTT Insertion - In frame 9:93676722-93676723 + LUAD-B01811 COSM334955 c.2700C>T p.D900D Substitution - coding silent 9:93675000-93675000 + TCGA-EI-6882-01 COSM3433363 c.3269G>A p.R1090Q Substitution - Missense 9:93677654-93677654 + 428 COSM4433253 c.3085G>A p.A1029T Substitution - Missense 9:93676846-93676846 + 1848_T COSM3750192 c.2964G>T p.P988P Substitution - coding silent 9:93676725-93676725 + TCGA-AD-6895-01 COSM198796 c.1468delA p.K492fs*6 Deletion - Frameshift 9:93660330-93660330 + TCGA-FW-A3TU-06 COSM2732614 c.1716G>T p.L572L Substitution - coding silent 9:93662924-93662924 + TCGA-AD-6888-01 COSM305500 c.2961_2962ins15 p.T987_P988insPASTT Insertion - In frame 9:93676722-93676723 + OSCC-GB_00260111 COSM3716319 c.1969G>T p.G657C Substitution - Missense 9:93665717-93665717 + TCGA-A6-6781-01 COSM3750192 c.2964G>T p.P988P Substitution - coding silent 9:93676725-93676725 + UPCI:SCC090 COSM305500 c.2961_2962ins15 p.T987_P988insPASTT Insertion - In frame 9:93676722-93676723 + SNUH_G01_S1 COSM3685904 c.1239+8T>A p.? Unknown 9:93658244-93658244 + TCGA-HU-A4H4-01 COSM3909077 c.1875G>A p.S625S Substitution - coding silent 9:93663573-93663573 + TCGA-66-2727-01 COSM753852 c.851G>T p.W284L Substitution - Missense 9:93654474-93654474 + 258 COSM3723035 c.2955T>C p.S985S Substitution - coding silent 9:93676716-93676716 + C135 COSM4618887 c.419C>T p.P140L Substitution - Missense 9:93645748-93645748 + HCC38 COSM1625264 c.2899T>G p.S967A Substitution - Missense 9:93676660-93676660 + TCGA-CG-5723-01 COSM3909084 c.2804C>T p.A935V Substitution - Missense 9:93675761-93675761 + TCGA-BR-4363-01 COSM3909082 c.2687G>T p.R896M Substitution - Missense 9:93674987-93674987 + TCGA-G4-6320-01 COSM3699793 c.873C>T p.S291S Substitution - coding silent 9:93654496-93654496 + C0044T COSM3723035 c.2955T>C p.S985S Substitution - coding silent 9:93676716-93676716 + S01020 COSM5701170 c.2962_2963ins15 p.P988_A989insCLHHT Insertion - In frame 9:93676723-93676724 + TCGA-EE-A29B-06 COSM3659720 c.2399C>T p.S800F Substitution - Missense 9:93673635-93673635 + TCGA-EI-7004-01 COSM305500 c.2961_2962ins15 p.T987_P988insPASTT Insertion - In frame 9:93676722-93676723 + PTC-46C COSM3723035 c.2955T>C p.S985S Substitution - coding silent 9:93676716-93676716 + PTC-70C COSM3747771 c.2990G>C p.S997T Substitution - Missense 9:93676751-93676751 + S02284 COSM5684279 c.3096C>T p.F1032F Substitution - coding silent 9:93676857-93676857 + TCGA-CI-6622-01 COSM305500 c.2961_2962ins15 p.T987_P988insPASTT Insertion - In frame 9:93676722-93676723 + TCGA-13-2057-01 COSM1331438 c.3038C>T p.P1013L Substitution - Missense 9:93676799-93676799 + pfg008T COSM1643903 c.833T>C p.I278T Substitution - Missense 9:93654456-93654456 + PTC-70C COSM3723034 c.2976C>A p.T992T Substitution - coding silent 9:93676737-93676737 + C0044T COSM3723034 c.2976C>A p.T992T Substitution - coding silent 9:93676737-93676737 + PTC-7C COSM4164139 c.1795T>G p.S599A Substitution - Missense 9:93663003-93663003 + TCGA-37-5819-01 COSM753853 c.310G>C p.V104L Substitution - Missense 9:93645639-93645639 + TCGA-66-2787-01 COSM753851 c.1084C>G p.Q362E Substitution - Missense 9:93656532-93656532 + pfg008T COSM1643903 c.833T>C p.I278T Substitution - Missense 9:93654456-93654456 + TCGA-D1-A16X-01 COSM1111297 c.1645G>A p.E549K Substitution - Missense 9:93660507-93660507 + 16246 COSM5616167 c.2129A>T p.K710M Substitution - Missense 9:93666002-93666002 + TCGA-AF-6136-01 COSM305500 c.2961_2962ins15 p.T987_P988insPASTT Insertion - In frame 9:93676722-93676723 + WSU-HN30 COSM305500 c.2961_2962ins15 p.T987_P988insPASTT Insertion - In frame 9:93676722-93676723 + NOKSI COSM305500 c.2961_2962ins15 p.T987_P988insPASTT Insertion - In frame 9:93676722-93676723 + TCGA-D5-6930-01 COSM1220358 c.1559C>T p.T520M Substitution - Missense 9:93660421-93660421 + 2293759 COSM4609839 c.3283delC p.L1095fs*>2 Deletion - Frameshift 9:93677668-93677668 + TCGA-DM-A1DA-01 COSM305500 c.2961_2962ins15 p.T987_P988insPASTT Insertion - In frame 9:93676722-93676723 + 587228 COSM1220353 c.854G>A p.R285Q Substitution - Missense 9:93654477-93654477 + PTC-1C COSM4164140 c.2940C>T p.S980S Substitution - coding silent 9:93676701-93676701 + GC_337T-GC_337N COSM4771861 c.3273C>T p.N1091N Substitution - coding silent 9:93677658-93677658 + TCGA-EI-6507-01 COSM1569866 c.2562C>T p.V854V Substitution - coding silent 9:93673798-93673798 + D16 COSM5007144 c.442G>A p.D148N Substitution - Missense 9:93645771-93645771 + TCGA-F5-6812-01 COSM5826522 c.2955_2956ins15 p.T996_S997insTPAST Insertion - In frame 9:93676716-93676717 + tumor_4189200 COSM3358380 c.378C>T p.P126P Substitution - coding silent 9:93645707-93645707 + 09-125 COSM305500 c.2961_2962ins15 p.T987_P988insPASTT Insertion - In frame 9:93676722-93676723 + 4132_T COSM3723035 c.2955T>C p.S985S Substitution - coding silent 9:93676716-93676716 + TCGA-CF-A1HR-01 COSM422311 c.615C>T p.F205F Substitution - coding silent 9:93653191-93653191 + TCGA-AZ-4615-01 COSM3699794 c.2094C>T p.N698N Substitution - coding silent 9:93665842-93665842 + TCGA-F4-6856-01 COSM305500 c.2961_2962ins15 p.T987_P988insPASTT Insertion - In frame 9:93676722-93676723 + TCGA-AZ-6603-01 COSM305500 c.2961_2962ins15 p.T987_P988insPASTT Insertion - In frame 9:93676722-93676723 + YUZEST COSM1701348 c.1616C>T p.S539L Substitution - Missense 9:93660478-93660478 + TCGA-CM-4743-01 COSM1463723 c.185T>C p.L62S Substitution - Missense 9:93636411-93636411 + T2940 COSM198796 c.1468delA p.K492fs*6 Deletion - Frameshift 9:93660330-93660330 + BD179T COSM5499857 c.602+6T>C p.? Unknown 9:93649218-93649218 + YUKIL COSM1701346 c.325C>T p.P109S Substitution - Missense 9:93645654-93645654 + TCGA-G4-6309-01 COSM1463731 c.1419G>A p.P473P Substitution - coding silent 9:93660281-93660281 + HN_63021 COSM121541 c.2736A>G p.P912P Substitution - coding silent 9:93675693-93675693 + 07-P8041 COSM4589051 c.2003A>G p.D668G Substitution - Missense 9:93665751-93665751 + TCGA-AP-A0LT-01 COSM1111302 c.2193T>C p.D731D Substitution - coding silent 9:93667085-93667085 + TCGA-A6-6780-01 COSM1463730 c.1353G>A p.P451P Substitution - coding silent 9:93660215-93660215 + TCGA-BR-4280-01 COSM3909079 c.2025T>C p.D675D Substitution - coding silent 9:93665773-93665773 + LC_S11 COSM1187769 c.2436G>T p.Q812H Substitution - Missense 9:93673672-93673672 + PTC-515C COSM4164137 c.1032G>T p.M344I Substitution - Missense 9:93656013-93656013 + BD49T COSM5497950 c.2703C>T p.D901D Substitution - coding silent 9:93675003-93675003 + sysucc-854T COSM3723034 c.2976C>A p.T992T Substitution - coding silent 9:93676737-93676737 + TCGA-DY-A0XA-01 COSM3723034 c.2976C>A p.T992T Substitution - coding silent 9:93676737-93676737 + TCGA-FW-A3R5-06 COSM3927263 c.1176C>T p.P392P Substitution - coding silent 9:93658173-93658173 + TCGA-AH-6544-01 COSM305500 c.2961_2962ins15 p.T987_P988insPASTT Insertion - In frame 9:93676722-93676723 + TCGA-D1-A103-01 COSM1111307 c.2800C>T p.L934L Substitution - coding silent 9:93675757-93675757 + PTC-54C COSM3723034 c.2976C>A p.T992T Substitution - coding silent 9:93676737-93676737 + TCGA-24-0979-01 COSM80332 c.936C>T p.T312T Substitution - coding silent 9:93654559-93654559 + TCGA-AZ-4315-01 COSM1463733 c.1883C>T p.A628V Substitution - Missense 9:93663581-93663581 + 587222 COSM1220357 c.136G>A p.D46N Substitution - Missense 9:93630007-93630007 + TCGA-EV-5903-01 COSM3996693 c.811A>C p.I271L Substitution - Missense 9:93654434-93654434 + TCGA-HU-A4GX-01 COSM3909081 c.2402T>C p.M801T Substitution - Missense 9:93673638-93673638 + LS411 COSM326139 c.3161G>A p.R1054Q Substitution - Missense 9:93676922-93676922 + TCGA-AA-A00J-01 COSM298373 c.281G>A p.R94Q Substitution - Missense 9:93636507-93636507 + TCGA-AD-6901-01 COSM305500 c.2961_2962ins15 p.T987_P988insPASTT Insertion - In frame 9:93676722-93676723 + 26T COSM3716319 c.1969G>T p.G657C Substitution - Missense 9:93665717-93665717 + 2492710 COSM5718394 c.442G>C p.D148H Substitution - Missense 9:93645771-93645771 + BN05T COSM297068 c.2961C>A p.T987T Substitution - coding silent 9:93676722-93676722 + TCGA-CM-6680-01 COSM305500 c.2961_2962ins15 p.T987_P988insPASTT Insertion - In frame 9:93676722-93676723 + Pat_01_B COSM5876601 c.1343C>T p.A448V Substitution - Missense 9:93660205-93660205 + TCGA-BS-A0TA-01 COSM1111299 c.1977C>T p.F659F Substitution - coding silent 9:93665725-93665725 + WSU-HN6 COSM305500 c.2961_2962ins15 p.T987_P988insPASTT Insertion - In frame 9:93676722-93676723 + YUNEKI COSM753850 c.2730C>T p.V910V Substitution - coding silent 9:93675687-93675687 + TCGA-G4-6588-01 COSM3750192 c.2964G>T p.P988P Substitution - coding silent 9:93676725-93676725 + AOCS-093-3-6 COSM4149566 c.3015G>T p.Q1005H Substitution - Missense 9:93676776-93676776 + BICR_22 COSM305500 c.2961_2962ins15 p.T987_P988insPASTT Insertion - In frame 9:93676722-93676723 + TCGA-F4-6809-01 COSM5826522 c.2955_2956ins15 p.T996_S997insTPAST Insertion - In frame 9:93676716-93676717 + ESCC_62 COSM5633232 c.2037C>T p.Y679Y Substitution - coding silent 9:93665785-93665785 + U373 COSM2732586 c.741C>T p.D247D Substitution - coding silent 9:93653317-93653317 + SNUH_G16_S1 COSM456270 c.372C>T p.T124T Substitution - coding silent 9:93645701-93645701 + TCGA-CM-6161-01 COSM305500 c.2961_2962ins15 p.T987_P988insPASTT Insertion - In frame 9:93676722-93676723 + PARBRK COSM1220353 c.854G>A p.R285Q Substitution - Missense 9:93654477-93654477 + T407 COSM4713971 c.1106C>T p.A369V Substitution - Missense 9:93656554-93656554 + TCGA-BR-4361-01 COSM3909075 c.649T>C p.W217R Substitution - Missense 9:93653225-93653225 + TCGA-CM-5861-01 COSM297068 c.2961C>A p.T987T Substitution - coding silent 9:93676722-93676722 + TCGA-CM-4750-01 COSM305500 c.2961_2962ins15 p.T987_P988insPASTT Insertion - In frame 9:93676722-93676723 + PTC-54C COSM1463737 c.2949A>T p.P983P Substitution - coding silent 9:93676710-93676710 + TCGA-D8-A1J8-01 COSM3849113 c.3258G>A p.L1086L Substitution - coding silent 9:93677643-93677643 + TCGA-DM-A28C-01 COSM5826522 c.2955_2956ins15 p.T996_S997insTPAST Insertion - In frame 9:93676716-93676717 + UM-SCC-4 COSM305500 c.2961_2962ins15 p.T987_P988insPASTT Insertion - In frame 9:93676722-93676723 + BN40 COSM1625262 c.170A>G p.H57R Substitution - Missense 9:93630041-93630041 + CSCC-16-T COSM4477741 c.217C>T p.P73S Substitution - Missense 9:93636443-93636443 + PTC-70C COSM3723035 c.2955T>C p.S985S Substitution - coding silent 9:93676716-93676716 + 926_T COSM3750192 c.2964G>T p.P988P Substitution - coding silent 9:93676725-93676725 + 4095_T COSM3750192 c.2964G>T p.P988P Substitution - coding silent 9:93676725-93676725 + LUAD-RT-S01477 COSM377771 c.2088G>C p.K696N Substitution - Missense 9:93665836-93665836 + T1154 COSM1463735 c.2850_2851insA p.S954fs*9 Insertion - Frameshift 9:93676611-93676612 + TCGA-D5-6534-01 COSM305500 c.2961_2962ins15 p.T987_P988insPASTT Insertion - In frame 9:93676722-93676723 + UD-SCC-2 COSM305500 c.2961_2962ins15 p.T987_P988insPASTT Insertion - In frame 9:93676722-93676723 + ESCC-147T COSM3943115 c.3274G>A p.G1092R Substitution - Missense 9:93677659-93677659 + TCGA-EE-A2GO-06 COSM3659711 c.388C>T p.P130S Substitution - Missense 9:93645717-93645717 + CHC258T COSM3670074 c.2334G>T p.E778D Substitution - Missense 9:93667226-93667226 + TCGA-AA-3955-01 COSM297068 c.2961C>A p.T987T Substitution - coding silent 9:93676722-93676722 + BN40T COSM1625262 c.170A>G p.H57R Substitution - Missense 9:93630041-93630041 + T2664 COSM4713970 c.804C>G p.F268L Substitution - Missense 9:93654427-93654427 + TCGA-AP-A059-01 COSM295171 c.720C>T p.C240C Substitution - coding silent 9:93653296-93653296 + S00501 COSM314120 c.2683delA p.R896fs*64 Deletion - Frameshift 9:93674983-93674983 + TCGA-BG-A2AE-01 COSM1111308 c.3089G>A p.G1030D Substitution - Missense 9:93676850-93676850 + Gp2D COSM4611878 c.1467_1468insA p.T493fs*21 Insertion - Frameshift 9:93660329-93660330 + STC252 COSM1111302 c.2193T>C p.D731D Substitution - coding silent 9:93667085-93667085 + TCGA-AA-3510-01 COSM305500 c.2961_2962ins15 p.T987_P988insPASTT Insertion - In frame 9:93676722-93676723 + TCGA-F4-6704-01 COSM305500 c.2961_2962ins15 p.T987_P988insPASTT Insertion - In frame 9:93676722-93676723 + CHEWS031 COSM4589050 c.1107G>A p.A369A Substitution - coding silent 9:93656555-93656555 + TCGA-D3-A2JG-06 COSM3659714 c.1092C>T p.P364P Substitution - coding silent 9:93656540-93656540 + CHC793T COSM4801375 c.503A>C p.K168T Substitution - Missense 9:93649113-93649113 + TCGA-EI-6507-01 COSM5826522 c.2955_2956ins15 p.T996_S997insTPAST Insertion - In frame 9:93676716-93676717 + 234 COSM198796 c.1468delA p.K492fs*6 Deletion - Frameshift 9:93660330-93660330 + RK165_C01 COSM1636291 c.2833-3A>G p.? Unknown 9:93676591-93676591 + TCGA-GF-A6C8-06 COSM3927264 c.1911T>A p.F637L Substitution - Missense 9:93663609-93663609 + PTC-1C COSM3747772 c.2992A>C p.T998P Substitution - Missense 9:93676753-93676753 + TCGA-CD-8536-01 COSM3909078 c.2017G>A p.V673M Substitution - Missense 9:93665765-93665765 + PTC-28C COSM3723035 c.2955T>C p.S985S Substitution - coding silent 9:93676716-93676716 + SJMB020 COSM255626 c.1261G>C p.E421Q Substitution - Missense 9:93659532-93659532 + SNUH_G10_S1 COSM3982985 c.1122G>A p.G374G Substitution - coding silent 9:93656570-93656570 + C709 COSM4444176 c.692C>A p.P231H Substitution - Missense 9:93653268-93653268 + KM12 COSM2732609 c.1517C>A p.P506H Substitution - Missense 9:93660379-93660379 + TCGA-A6-4105-01 COSM3750192 c.2964G>T p.P988P Substitution - coding silent 9:93676725-93676725 + TCGA-CM-6169-01 COSM305500 c.2961_2962ins15 p.T987_P988insPASTT Insertion - In frame 9:93676722-93676723 + 1946219 COSM1578427 c.2963_2964ins15 p.T996_S997insTPAST Insertion - In frame 9:93676724-93676725 + SCC-9 COSM305500 c.2961_2962ins15 p.T987_P988insPASTT Insertion - In frame 9:93676722-93676723 + TCGA-AY-6386-01 COSM305500 c.2961_2962ins15 p.T987_P988insPASTT Insertion - In frame 9:93676722-93676723 + AOCS-148-1-4 COSM4149565 c.2022G>A p.R674R Substitution - coding silent 9:93665770-93665770 + 2492708 COSM5718394 c.442G>C p.D148H Substitution - Missense 9:93645771-93645771 + SNU-175 COSM2732635 c.3242G>T p.R1081M Substitution - Missense 9:93677627-93677627 + TCGA-AZ-6599-01 COSM3750192 c.2964G>T p.P988P Substitution - coding silent 9:93676725-93676725 + CSCC-31-T COSM233098 c.296C>T p.P99L Substitution - Missense 9:93636522-93636522 + TCGA-D5-6929-01 COSM305500 c.2961_2962ins15 p.T987_P988insPASTT Insertion - In frame 9:93676722-93676723 + TCGA-AZ-4315-01 COSM1463732 c.1774C>T p.R592* Substitution - Nonsense 9:93662982-93662982 + ACINAR28 COSM198796 c.1468delA p.K492fs*6 Deletion - Frameshift 9:93660330-93660330 + 2521259 COSM5890432 c.1196C>T p.A399V Substitution - Missense 9:93658193-93658193 + PTC-1C COSM1463737 c.2949A>T p.P983P Substitution - coding silent 9:93676710-93676710 + 2492709 COSM5718394 c.442G>C p.D148H Substitution - Missense 9:93645771-93645771 + I2L-P19Ta-Tumor-Biopsy COSM198796 c.1468delA p.K492fs*6 Deletion - Frameshift 9:93660330-93660330 + SNU-C2B COSM4611878 c.1467_1468insA p.T493fs*21 Insertion - Frameshift 9:93660329-93660330 + TCGA-G5-6235-01 COSM3750192 c.2964G>T p.P988P Substitution - coding silent 9:93676725-93676725 + TCGA-D1-A16E-01 COSM1111301 c.2080A>T p.R694W Substitution - Missense 9:93665828-93665828 + STC252 COSM5064167 c.2731G>A p.G911S Substitution - Missense 9:93675688-93675688 + 587316 COSM1220355 c.1477A>G p.T493A Substitution - Missense 9:93660339-93660339 + SJHGG099_D COSM4971765 c.534G>A p.V178V Substitution - coding silent 9:93649144-93649144 + PTC-1C COSM3723035 c.2955T>C p.S985S Substitution - coding silent 9:93676716-93676716 + TCGA-CD-A4MG-01 COSM1220355 c.1477A>G p.T493A Substitution - Missense 9:93660339-93660339 + LAU165 COSM233098 c.296C>T p.P99L Substitution - Missense 9:93636522-93636522 + LUAD-F00162 COSM366729 c.141A>T p.I47I Substitution - coding silent 9:93630012-93630012 + 88_T COSM3723035 c.2955T>C p.S985S Substitution - coding silent 9:93676716-93676716 + TCGA-BH-A0HA-01 COSM198796 c.1468delA p.K492fs*6 Deletion - Frameshift 9:93660330-93660330 + Gp5D COSM2732605 c.1433C>T p.A478V Substitution - Missense 9:93660295-93660295 + 587316 COSM1220356 c.1498C>A p.P500T Substitution - Missense 9:93660360-93660360 + TCGA-76-6663-01 COSM3413843 c.420G>A p.P140P Substitution - coding silent 9:93645749-93645749 + PTC-70C COSM3747772 c.2992A>C p.T998P Substitution - Missense 9:93676753-93676753 + tumor_4146289 COSM3750192 c.2964G>T p.P988P Substitution - coding silent 9:93676725-93676725 + RK126_C01 COSM1636290 c.952+10G>T p.? Unknown 9:93654585-93654585 + SNUH_G76_S1 COSM4417122 c.789+6C>T p.? Unknown 9:93653371-93653371 + TCGA-24-2254-01 COSM118603 c.2610C>T p.F870F Substitution - coding silent 9:93673846-93673846 + T3535 COSM1220355 c.1477A>G p.T493A Substitution - Missense 9:93660339-93660339 + BD73T COSM3723034 c.2976C>A p.T992T Substitution - coding silent 9:93676737-93676737 + S00501 COSM314120 c.2683delA p.R896fs*64 Deletion - Frameshift 9:93674983-93674983 + SJMB020 COSM255626 c.1261G>C p.E421Q Substitution - Missense 9:93659532-93659532 + CHC258T COSM3670074 c.2334G>T p.E778D Substitution - Missense 9:93667226-93667226 + RKO COSM198796 c.1468delA p.K492fs*6 Deletion - Frameshift 9:93660330-93660330 + TCGA-A6-5667-01 COSM305500 c.2961_2962ins15 p.T987_P988insPASTT Insertion - In frame 9:93676722-93676723 + TCGA-CG-4304-01 COSM3909083 c.2790C>T p.I930I Substitution - coding silent 9:93675747-93675747 + ME009T COSM223348 c.1330-1G>A p.? Unknown 9:93660191-93660191 + PD5925a COSM5788374 c.1291C>G p.L431V Substitution - Missense 9:93659562-93659562 + SJHGG010_D COSM2732578 c.234C>T p.D78D Substitution - coding silent 9:93636460-93636460 + TCGA-AD-6889-01 COSM1463736 c.2850_2851insAA p.S954fs*7 Insertion - Frameshift 9:93676611-93676612 + TCGA-EE-A29G-06 COSM3659721 c.2673C>T p.S891S Substitution - coding silent 9:93674973-93674973 + OSCC-GB_00350111 COSM3716320 c.2453G>T p.G818V Substitution - Missense 9:93673689-93673689 + TCGA-WL-A834-01 COSM4830585 c.270C>T p.I90I Substitution - coding silent 9:93636496-93636496 + Pat_01_A COSM5876601 c.1343C>T p.A448V Substitution - Missense 9:93660205-93660205 + PD9597a COSM5789553 c.893A>G p.Q298R Substitution - Missense 9:93654516-93654516 + OSCC-GB_00660111 COSM4888808 c.818C>A p.P273Q Substitution - Missense 9:93654441-93654441 + TCGA-EI-6884-01 COSM305500 c.2961_2962ins15 p.T987_P988insPASTT Insertion - In frame 9:93676722-93676723 + sysucc-1370T COSM1220353 c.854G>A p.R285Q Substitution - Missense 9:93654477-93654477 + TCGA-C5-A1BL-01 COSM4837068 c.70G>C p.D24H Substitution - Missense 9:93576843-93576843 + Pat_76_A COSM5876602 c.2074C>T p.P692S Substitution - Missense 9:93665822-93665822 + ESO15T COSM1173530 c.1724C>T p.P575L Substitution - Missense 9:93662932-93662932 + TCGA-BR-4184-01 COSM422311 c.615C>T p.F205F Substitution - coding silent 9:93653191-93653191 + T3225 COSM198796 c.1468delA p.K492fs*6 Deletion - Frameshift 9:93660330-93660330 + HCC38T COSM1625264 c.2899T>G p.S967A Substitution - Missense 9:93676660-93676660 + TCGA-CM-5868-01 COSM305500 c.2961_2962ins15 p.T987_P988insPASTT Insertion - In frame 9:93676722-93676723 + TCGA-G4-6586-01 COSM3750192 c.2964G>T p.P988P Substitution - coding silent 9:93676725-93676725 + TCGA-D1-A103-01 COSM1111296 c.1368C>T p.V456V Substitution - coding silent 9:93660230-93660230 + Pat_76_B COSM5876602 c.2074C>T p.P692S Substitution - Missense 9:93665822-93665822 + YUNEKI COSM5411508 c.702C>T p.T234T Substitution - coding silent 9:93653278-93653278 + TCGA-EE-A3AA-06 COSM3659716 c.2001G>A p.E667E Substitution - coding silent 9:93665749-93665749 + tumor_4157186 COSM3723034 c.2976C>A p.T992T Substitution - coding silent 9:93676737-93676737 + C0044T COSM4139020 c.2946G>C p.T982T Substitution - coding silent 9:93676707-93676707 + 258 COSM297068 c.2961C>A p.T987T Substitution - coding silent 9:93676722-93676722 + CHC793T COSM4801375 c.503A>C p.K168T Substitution - Missense 9:93649113-93649113 + EOPC-135_tumor_01 COSM3723035 c.2955T>C p.S985S Substitution - coding silent 9:93676716-93676716 + G18 COSM1191882 c.1613C>A p.A538D Substitution - Missense 9:93660475-93660475 + TCGA-CM-4746-01 COSM3750192 c.2964G>T p.P988P Substitution - coding silent 9:93676725-93676725 + TCGA-66-2727-01 COSM753850 c.2730C>T p.V910V Substitution - coding silent 9:93675687-93675687 + SNUH_G30_S1 COSM3685903 c.40T>A p.Y14N Substitution - Missense 9:93576813-93576813 + S00841 COSM5662080 c.3070C>A p.H1024N Substitution - Missense 9:93676831-93676831 + T3080 COSM4713968 c.460+2T>C p.? Unknown 9:93645791-93645791 + TCGA-BR-4292-01 COSM1220352 c.2099C>T p.P700L Substitution - Missense 9:93665847-93665847 + TCGA-DM-A1D9-01 COSM5826522 c.2955_2956ins15 p.T996_S997insTPAST Insertion - In frame 9:93676716-93676717 + 88_T COSM297068 c.2961C>A p.T987T Substitution - coding silent 9:93676722-93676722 + PTC-70C COSM4164140 c.2940C>T p.S980S Substitution - coding silent 9:93676701-93676701 + TCGA-CI-6624-01 COSM305500 c.2961_2962ins15 p.T987_P988insPASTT Insertion - In frame 9:93676722-93676723 + TCGA-BS-A0UV-01 COSM1111306 c.2682G>T p.K894N Substitution - Missense 9:93674982-93674982 + TCGA-FS-A1ZW-06 COSM3659717 c.2162C>T p.P721L Substitution - Missense 9:93666035-93666035 + I2L-P8-Tumor-Organoid COSM1111295 c.848G>A p.R283H Substitution - Missense 9:93654471-93654471 + 88_T COSM3750192 c.2964G>T p.P988P Substitution - coding silent 9:93676725-93676725 + TCGA-HU-A4H8-01 COSM1220356 c.1498C>A p.P500T Substitution - Missense 9:93660360-93660360 + TCGA-BS-A0UA-01 COSM1111304 c.2614G>A p.D872N Substitution - Missense 9:93673850-93673850 + T1743 COSM4713972 c.2100G>A p.P700P Substitution - coding silent 9:93665848-93665848 + TCGA-AZ-4315-01 COSM1463726 c.824C>T p.S275L Substitution - Missense 9:93654447-93654447 + TCGA-EE-A2MS-06 COSM3659718 c.2259C>T p.V753V Substitution - coding silent 9:93667151-93667151 + 49M COSM5592501 c.3213G>A p.T1071T Substitution - coding silent 9:93677598-93677598 + T3535 COSM1220356 c.1498C>A p.P500T Substitution - Missense 9:93660360-93660360 + TCGA-BR-8368-01 COSM3909085 c.3208C>T p.R1070C Substitution - Missense 9:93677593-93677593 + SC_9028 COSM5573336 c.2833-1G>T p.? Unknown 9:93676593-93676593 + UM-SCC-11B COSM305500 c.2961_2962ins15 p.T987_P988insPASTT Insertion - In frame 9:93676722-93676723 + ICC012T COSM1463737 c.2949A>T p.P983P Substitution - coding silent 9:93676710-93676710 + LC_S27 COSM1187770 c.2986A>T p.T996S Substitution - Missense 9:93676747-93676747 + TCGA-AD-6899-01 COSM5826522 c.2955_2956ins15 p.T996_S997insTPAST Insertion - In frame 9:93676716-93676717 + T16 COSM3413843 c.420G>A p.P140P Substitution - coding silent 9:93645749-93645749 + TCGA-F1-6177-01 COSM334955 c.2700C>T p.D900D Substitution - coding silent 9:93675000-93675000 + 3006_T COSM3750192 c.2964G>T p.P988P Substitution - coding silent 9:93676725-93676725 + TCGA-DY-A0XA-01 COSM3750192 c.2964G>T p.P988P Substitution - coding silent 9:93676725-93676725 + SNU-175 COSM2732578 c.234C>T p.D78D Substitution - coding silent 9:93636460-93636460 + TCGA-UB-A7MC-01 COSM4915037 c.863C>G p.S288C Substitution - Missense 9:93654486-93654486 + PTC-1C COSM4139020 c.2946G>C p.T982T Substitution - coding silent 9:93676707-93676707 + HX22T COSM3747772 c.2992A>C p.T998P Substitution - Missense 9:93676753-93676753 + SC_9008 COSM198796 c.1468delA p.K492fs*6 Deletion - Frameshift 9:93660330-93660330 + TCGA-BS-A0TA-01 COSM1111295 c.848G>A p.R283H Substitution - Missense 9:93654471-93654471 + LS180 COSM2732580 c.353T>C p.M118T Substitution - Missense 9:93645682-93645682 + TCGA-B5-A11E-01 COSM1111293 c.549C>T p.S183S Substitution - coding silent 9:93649159-93649159 + SNU-175 COSM198796 c.1468delA p.K492fs*6 Deletion - Frameshift 9:93660330-93660330 + TCGA-AZ-4615-01 COSM2732633 c.2851delA p.K953fs*7 Deletion - Frameshift 9:93676612-93676612 + WT052-T1 COSM5352128 c.2242G>A p.G748S Substitution - Missense 9:93667134-93667134 + T3498 COSM198796 c.1468delA p.K492fs*6 Deletion - Frameshift 9:93660330-93660330 + SNU-C4 COSM198796 c.1468delA p.K492fs*6 Deletion - Frameshift 9:93660330-93660330 + PTC-46C COSM297068 c.2961C>A p.T987T Substitution - coding silent 9:93676722-93676722 + SNU-C2B COSM2732625 c.2309C>T p.A770V Substitution - Missense 9:93667201-93667201 + TCGA-G4-6310-01 COSM5826522 c.2955_2956ins15 p.T996_S997insTPAST Insertion - In frame 9:93676716-93676717 + PTC-54C COSM3747771 c.2990G>C p.S997T Substitution - Missense 9:93676751-93676751 + TCGA-CI-6619-01 COSM305500 c.2961_2962ins15 p.T987_P988insPASTT Insertion - In frame 9:93676722-93676723 + TCGA-ER-A19W-06 COSM4398696 c.1421C>T p.S474F Substitution - Missense 9:93660283-93660283 + pfg167T COSM4759064 c.1186G>A p.V396I Substitution - Missense 9:93658183-93658183 + 587224 COSM1220354 c.386T>C p.V129A Substitution - Missense 9:93645715-93645715 + PTC-28C COSM3750192 c.2964G>T p.P988P Substitution - coding silent 9:93676725-93676725 + LUAD-S01346 COSM397914 c.110T>C p.V37A Substitution - Missense 9:93629981-93629981 + PT24_2 COSM5943093 c.2042_2043insG p.D682fs*2 Insertion - Frameshift 9:93665790-93665791 + 871_T COSM3750192 c.2964G>T p.P988P Substitution - coding silent 9:93676725-93676725 + PTC-70C COSM297068 c.2961C>A p.T987T Substitution - coding silent 9:93676722-93676722 + TCGA-AP-A056-01 COSM1111303 c.2563G>A p.D855N Substitution - Missense 9:93673799-93673799 + LIM1215 COSM198796 c.1468delA p.K492fs*6 Deletion - Frameshift 9:93660330-93660330 + T3498 COSM2732633 c.2851delA p.K953fs*7 Deletion - Frameshift 9:93676612-93676612 + TCGA-EE-A29M-06 COSM3659713 c.947C>T p.P316L Substitution - Missense 9:93654570-93654570 + BD236T COSM198796 c.1468delA p.K492fs*6 Deletion - Frameshift 9:93660330-93660330 + 1_RESISTANT COSM1721319 c.1193G>A p.G398E Substitution - Missense 9:93658190-93658190 + TCGA-AN-A046-01 COSM1463732 c.1774C>T p.R592* Substitution - Nonsense 9:93662982-93662982 + TCGA-AZ-4615-01 COSM198796 c.1468delA p.K492fs*6 Deletion - Frameshift 9:93660330-93660330 + T3535 COSM198796 c.1468delA p.K492fs*6 Deletion - Frameshift 9:93660330-93660330 + T3058 COSM4713969 c.738C>T p.T246T Substitution - coding silent 9:93653314-93653314 + TCGA-FW-A3TU-06 COSM3659715 c.1718G>A p.S573N Substitution - Missense 9:93662926-93662926 + HCC002T COSM5819388 c.2128A>T p.K710* Substitution - Nonsense 9:93666001-93666001 + PTC-73C COSM3723034 c.2976C>A p.T992T Substitution - coding silent 9:93676737-93676737 + SJHGG099_D COSM4971766 c.461-1G>A p.? Unknown 9:93649070-93649070 + TCGA-A6-6781-01 COSM1463729 c.1345G>A p.V449I Substitution - Missense 9:93660207-93660207 + OSCC-GB_00860111 COSM4885372 c.2209G>T p.G737C Substitution - Missense 9:93667101-93667101 + 585208 COSM326139 c.3161G>A p.R1054Q Substitution - Missense 9:93676922-93676922 + TCGA-DM-A28E-01 COSM1578427 c.2963_2964ins15 p.T996_S997insTPAST Insertion - In frame 9:93676724-93676725 + TCGA-D1-A17Q-01 COSM1111292 c.448G>A p.E150K Substitution - Missense 9:93645777-93645777 + TCGA-AD-6889-01 COSM3750192 c.2964G>T p.P988P Substitution - coding silent 9:93676725-93676725 + T407 COSM2732633 c.2851delA p.K953fs*7 Deletion - Frameshift 9:93676612-93676612 + TCGA-AA-3837-01 COSM295171 c.720C>T p.C240C Substitution - coding silent 9:93653296-93653296 + Patient_4 COSM3723034 c.2976C>A p.T992T Substitution - coding silent 9:93676737-93676737 + 35T COSM3716320 c.2453G>T p.G818V Substitution - Missense 9:93673689-93673689 + TCGA-AA-3663-01 COSM1463735 c.2850_2851insA p.S954fs*9 Insertion - Frameshift 9:93676611-93676612 + TCGA-AZ-6601-01 COSM1463734 c.2459C>T p.A820V Substitution - Missense 9:93673695-93673695 + LUAD-B01811 COSM334956 c.3162G>T p.R1054R Substitution - coding silent 9:93676923-93676923 + ZZUFHECRKL-G060T COSM4417122 c.789+6C>T p.? Unknown 9:93653371-93653371 + TCGA-CM-4748-01 COSM305500 c.2961_2962ins15 p.T987_P988insPASTT Insertion - In frame 9:93676722-93676723 + TCGA-BS-A0UJ-01 COSM1111305 c.2667T>C p.F889F Substitution - coding silent 9:93674967-93674967 + TCGA-DD-A4NJ-01 COSM4921060 c.2431C>T p.L811L Substitution - coding silent 9:93673667-93673667 + TCGA-CM-5344-01 COSM3750192 c.2964G>T p.P988P Substitution - coding silent 9:93676725-93676725 + OSCC-GB_00580111 COSM4886656 c.817C>A p.P273T Substitution - Missense 9:93654440-93654440 + Pat_11_A COSM5876603 c.2501G>A p.G834E Substitution - Missense 9:93673737-93673737 + C0082T COSM4139019 c.763G>A p.A255T Substitution - Missense 9:93653339-93653339 + 587342 COSM1220352 c.2099C>T p.P700L Substitution - Missense 9:93665847-93665847 + YUKLAB COSM233098 c.296C>T p.P99L Substitution - Missense 9:93636522-93636522 + TCGA-G4-6315-01 COSM5826522 c.2955_2956ins15 p.T996_S997insTPAST Insertion - In frame 9:93676716-93676717 + TCGA-AD-6895-01 COSM1463727 c.996C>T p.F332F Substitution - coding silent 9:93655977-93655977 + Gp2D COSM2732605 c.1433C>T p.A478V Substitution - Missense 9:93660295-93660295 + 18 COSM5352128 c.2242G>A p.G748S Substitution - Missense 9:93667134-93667134 + I2L-P8-Tumor-Biopsy COSM1111295 c.848G>A p.R283H Substitution - Missense 9:93654471-93654471 + TCGA-AH-6903-01 COSM3750192 c.2964G>T p.P988P Substitution - coding silent 9:93676725-93676725 + TCGA-UC-A7PF-01 COSM4830299 c.1249G>C p.E417Q Substitution - Missense 9:93659520-93659520 + PTC-54C COSM4164138 c.1435A>C p.T479P Substitution - Missense 9:93660297-93660297 + TCGA-FV-A3I1-01 COSM4929225 c.709T>G p.C237G Substitution - Missense 9:93653285-93653285 + TCGA-BS-A0UF-01 COSM1111294 c.639G>T p.K213N Substitution - Missense 9:93653215-93653215 + SW48 COSM198796 c.1468delA p.K492fs*6 Deletion - Frameshift 9:93660330-93660330 + TCGA-AD-6964-01 COSM305500 c.2961_2962ins15 p.T987_P988insPASTT Insertion - In frame 9:93676722-93676723 + C0019T COSM3723035 c.2955T>C p.S985S Substitution - coding silent 9:93676716-93676716 + TCGA-HU-A4H8-01 COSM3909076 c.1440G>A p.P480P Substitution - coding silent 9:93660302-93660302 + TCGA-CI-6620-01 COSM305500 c.2961_2962ins15 p.T987_P988insPASTT Insertion - In frame 9:93676722-93676723 + TCGA-22-1011-01 COSM753854 c.304G>A p.E102K Substitution - Missense 9:93645633-93645633 + TCGA-G4-6317-01 COSM3750192 c.2964G>T p.P988P Substitution - coding silent 9:93676725-93676725 + CSCC-7-T COSM3659711 c.388C>T p.P130S Substitution - Missense 9:93645717-93645717 + Region-30 COSM5701170 c.2962_2963ins15 p.P988_A989insCLHHT Insertion - In frame 9:93676723-93676724 + Pat_46_A COSM198796 c.1468delA p.K492fs*6 Deletion - Frameshift 9:93660330-93660330 + VACO10 COSM4657053 c.233A>T p.D78V Substitution - Missense 9:93636459-93636459 + WT052-T2 COSM5352128 c.2242G>A p.G748S Substitution - Missense 9:93667134-93667134 + ESOSCC164T COSM1173529 c.209A>G p.K70R Substitution - Missense 9:93636435-93636435 + sysucc-1925T COSM5450938 c.2723-3C>T p.? Unknown 9:93675677-93675677 + B89-16-Tumor COSM4007303 c.309C>T p.D103D Substitution - coding silent 9:93645638-93645638 + 0110_CRUK_PC_0110_T1_DNA COSM5424012 c.2587C>A p.Q863K Substitution - Missense 9:93673823-93673823 + TCGA-74-6584-01 COSM3413844 c.1267C>T p.P423S Substitution - Missense 9:93659538-93659538 + TCGA-D1-A17U-01 COSM1111298 c.1740T>G p.V580V Substitution - coding silent 9:93662948-93662948 + CSCC-27-T COSM4487286 c.3168C>T p.S1056S Substitution - coding silent 9:93676929-93676929 + RK195_C01 COSM3746109 c.2838G>A p.E946E Substitution - coding silent 9:93676599-93676599 + OSCC-GB_00650111 COSM4890491 c.2727G>T p.R909S Substitution - Missense 9:93675684-93675684 + TCGA-AD-6965-01 COSM5826522 c.2955_2956ins15 p.T996_S997insTPAST Insertion - In frame 9:93676716-93676717 + CSCC-31-T COSM4569639 c.1908T>G p.S636S Substitution - coding silent 9:93663606-93663606 + TCGA-AC-A62Y-01 COSM3849112 c.3240G>C p.Q1080H Substitution - Missense 9:93677625-93677625 + ESO-0292 COSM1241576 c.159T>C p.C53C Substitution - coding silent 9:93630030-93630030 + C008 COSM5523455 c.135C>T p.I45I Substitution - coding silent 9:93630006-93630006 + TCGA-CK-4952-01 COSM3750192 c.2964G>T p.P988P Substitution - coding silent 9:93676725-93676725 + CRC-02T COSM5455810 c.2450C>A p.A817D Substitution - Missense 9:93673686-93673686 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.211441 9q22.31 604351

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A - Frameshift p.K492Rfs*6 c.1475delA 9 96422612 STAD A - Frameshift p.N576Tfs*39 c.1727delA 9 96425216 BRCA A - Frameshift p.R896Gfs*64 c.2686delA 9 96437265 SCLC A G Synonymous p.P912P c.2736A>G 9 96437975 HNSC A T Missense p.R694W c.2080A>T 9 96428110 UCEC - CCTGCCTCCACCACA InFrameInsertion p.P988_A989insCLHHT c.2963_2964insCTGCCTCCACCACAC 9 96439005 HNSC CC TT Missense p.P903F c.2707_2708delinsTT 9 96437289 CM C G Missense p.Q362E c.1084C>G 9 96418814 LUSC C G Synonymous p.L650L c.1950C>G 9 96427980 LUAD C G Synonymous p.S279S c.837C>G 9 96416742 LUAD C T IntronicSNV . c.2833-38C>T 9 96438838 STAD C T Missense p.L313F c.937C>T 9 96416842 CM C T Missense p.P130S c.388C>T 9 96407999 CM C T Missense p.P316L c.947C>T 9 96416852 CM C T Missense p.P364S c.1090C>T 9 96418820 CM C T Missense p.P423S c.1267C>T 9 96421820 GBM C T Missense p.P672L c.2015C>T 9 96428045 CM C T Missense p.P700L c.2099C>T 9 96428129 STAD C T Missense p.P721L c.2162C>T 9 96428317 CM C T Missense p.S760L c.2279C>T 9 96429453 CM C T Missense p.S800F c.2399C>T 9 96435917 CM C T Missense p.T312I c.935C>T 9 96416840 CM C T Synonymous p.C240C c.720C>T 9 96415578 COREAD C T Synonymous p.D900D c.2700C>T 9 96437282 STAD C T Synonymous p.F205F c.615C>T 9 96415473 BLCA C T Synonymous p.F332F c.996C>T 9 96418259 HNSC C T Synonymous p.F659F c.1977C>T 9 96428007 UCEC C T Synonymous p.F870F c.2610C>T 9 96436128 OV C T Synonymous p.H260H c.780C>T 9 96415638 RCCC C T Synonymous p.I930I c.2790C>T 9 96438029 STAD C T Synonymous p.N886N c.2658C>T 9 96437240 CM C T Synonymous p.P126P c.378C>T 9 96407989 DLBCL C T Synonymous p.P364P c.1092C>T 9 96418822 CM C T Synonymous p.S891S c.2673C>T 9 96437255 CM C T Synonymous p.T312T c.936C>T 9 96416841 OV C T Synonymous p.V753V c.2259C>T 9 96429433 CM C T Synonymous p.V910V c.2730C>T 9 96437969 LUSC G A IntronicSNV . c.99-13408G>A 9 96378844 CLL G A Missense p.A830T c.2488G>A 9 96436006 ESCA G A Missense p.D133N c.397G>A 9 96408008 CM G A Missense p.D872N c.2614G>A 9 96436132 UCEC G A Missense p.E102K c.304G>A 9 96407915 LUSC G A Missense p.R1054Q c.3161G>A 9 96439204 SCLC G A Missense p.R283H c.848G>A 9 96416753 UCEC G A Synonymous p.E292E c.876G>A 9 96416781 CM G A Synonymous p.E667E c.2001G>A 9 96428031 CM G A Synonymous p.P140P c.420G>A 9 96408031 GBM G C Missense p.E38Q c.112G>C 9 96392265 STAD G C Missense p.K894N c.2682G>C 9 96437264 HNSC G C Missense p.V104L c.310G>C 9 96407921 LUSC G C Missense p.V307L c.919G>C 9 96416824 CM G T Missense p.K958N c.2874G>T 9 96438917 LUAD G T Missense p.R896M c.2687G>T 9 96437269 STAD G T Missense p.W284L c.851G>T 9 96416756 LUSC T C Missense p.I278T c.833T>C 9 96416738 STAD T C Synonymous p.D675D c.2025T>C 9 96428055 STAD