Mutation - TCGA Type Chromosome Start Position End Position Strand Variant Classification Variant Type Reference Allele Tumor_seq Allele 1 Tumor_seq Allele 2 Tumor Sample Barcode Matched Norm Sample Barcode Genome Change cDNA Change Codon Change Protein Change ACC 16 23119496 23119496 + Silent SNP C C T TCGA-P6-A5OF-01A-11D-A29I-10 TCGA-P6-A5OF-10A-01D-A29L-10 g.chr16:23119496C>T c.642G>A c.(640-642)gtG>gtA p.V214V BLCA 16 23080076 23080076 + Missense_Mutation SNP G G A TCGA-DK-A6B6-01A-11D-A30E-08 TCGA-DK-A6B6-10A-01D-A30H-08 g.chr16:23080076G>A c.3350C>T c.(3349-3351)tCa>tTa p.S1117L BLCA 16 23080278 23080278 + Missense_Mutation SNP C C T TCGA-FT-A61P-01A-11D-A30E-08 TCGA-FT-A61P-10A-01D-A30H-08 g.chr16:23080278C>T c.3148G>A c.(3148-3150)Gag>Aag p.E1050K BLCA 16 23080758 23080758 + Missense_Mutation SNP G G T TCGA-XF-A9T5-01A-11D-A42E-08 TCGA-XF-A9T5-10A-01D-A42H-08 g.chr16:23080758G>T c.2668C>A c.(2668-2670)Cac>Aac p.H890N BLCA 16 23083506 23083506 + Missense_Mutation SNP G G A TCGA-E5-A2PC-01A-11D-A202-08 TCGA-E5-A2PC-10B-01D-A202-08 g.chr16:23083506G>A c.2348C>T c.(2347-2349)tCt>tTt p.S783F BLCA 16 23085191 23085191 + Silent SNP C C T TCGA-ZF-AA4V-01A-11D-A38G-08 TCGA-ZF-AA4V-10A-01D-A38J-08 g.chr16:23085191C>T c.2187G>A c.(2185-2187)aaG>aaA p.K729K BLCA 16 23091365 23091365 + Missense_Mutation SNP C C T TCGA-KQ-A41R-01A-21D-A34U-08 TCGA-KQ-A41R-10G-01D-A34X-08 g.chr16:23091365C>T c.2078G>A c.(2077-2079)aGa>aAa p.R693K BLCA 16 23091477 23091478 + Frame_Shift_Ins INS - - GCGCCTGTCTC TCGA-FJ-A3Z9-01A-11D-A26M-08 TCGA-FJ-A3Z9-10A-01D-A26K-08 g.chr16:23091477_23091478insGCGCCTGTCTC c.1965_1966insGAGACAGGCGC c.(1963-1968)cgcatgfs p.M656fs BLCA 16 23091486 23091486 + Missense_Mutation SNP C C G TCGA-G2-AA3B-01A-11D-A391-08 TCGA-G2-AA3B-10A-01D-A394-08 g.chr16:23091486C>G c.1957G>C c.(1957-1959)Gac>Cac p.D653H BLCA 16 23096215 23096215 + Missense_Mutation SNP G G A TCGA-G2-A2EO-01A-11D-A17V-08 TCGA-G2-A2EO-11A-21D-A17V-08 g.chr16:23096215G>A c.1796C>T c.(1795-1797)tCc>tTc p.S599F BLCA 16 23098411 23098411 + Splice_Site SNP A A C TCGA-ZF-AA4U-01A-11D-A38G-08 TCGA-ZF-AA4U-10A-01D-A38J-08 g.chr16:23098411A>C c.e9+1 BLCA 16 23099153 23099153 + Silent SNP A A G TCGA-4Z-AA84-01A-11D-A391-08 TCGA-4Z-AA84-10A-01D-A394-08 g.chr16:23099153A>G c.1419T>C c.(1417-1419)ttT>ttC p.F473F BLCA 16 23116802 23116802 + Missense_Mutation SNP C C G TCGA-DK-A1A7-01A-11D-A13W-08 TCGA-DK-A1A7-10A-01D-A13W-08 g.chr16:23116802C>G c.1049G>C c.(1048-1050)cGg>cCg p.R350P BLCA 16 23119406 23119406 + Silent SNP G G C TCGA-DK-A3X1-01A-12D-A22Z-08 TCGA-DK-A3X1-10A-01D-A22Z-08 g.chr16:23119406G>C c.732C>G c.(730-732)ctC>ctG p.L244L BRCA 16 23080829 23080829 + Missense_Mutation SNP G G A TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr16:23080829G>A c.2597C>T c.(2596-2598)tCa>tTa p.S866L BRCA 16 23080922 23080922 + Missense_Mutation SNP C C T TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr16:23080922C>T c.2504G>A c.(2503-2505)cGa>cAa p.R835Q BRCA 16 23083474 23083474 + Missense_Mutation SNP G G A TCGA-AC-A62Y-01A-11D-A29N-09 TCGA-AC-A62Y-10A-01D-A29N-09 g.chr16:23083474G>A c.2380C>T c.(2380-2382)Ccg>Tcg p.P794S BRCA 16 23085069 23085069 + Missense_Mutation SNP G G A TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr16:23085069G>A c.2309C>T c.(2308-2310)tCa>tTa p.S770L BRCA 16 23085124 23085124 + Missense_Mutation SNP C C A TCGA-A8-A06Y-01A-21W-A019-09 TCGA-A8-A06Y-10A-01W-A021-09 g.chr16:23085124C>A c.2254G>T c.(2254-2256)Gtc>Ttc p.V752F BRCA 16 23096260 23096260 + Missense_Mutation SNP C C T TCGA-E2-A14T-01A-11D-A10Y-09 TCGA-E2-A14T-10A-01D-A110-09 g.chr16:23096260C>T c.1751G>A c.(1750-1752)cGt>cAt p.R584H BRCA 16 23098496 23098496 + Silent SNP G G A TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr16:23098496G>A c.1539C>T c.(1537-1539)ttC>ttT p.F513F BRCA 16 23116870 23116870 + Silent SNP T T C TCGA-E2-A14X-01A-11D-A10Y-09 TCGA-E2-A14X-10A-01D-A110-09 g.chr16:23116870T>C c.981A>G c.(979-981)caA>caG p.Q327Q BRCA 16 23117794 23117794 + Silent SNP A A C TCGA-D8-A1XK-01A-21D-A14K-09 TCGA-D8-A1XK-10A-01D-A14K-09 g.chr16:23117794A>C c.786T>G c.(784-786)acT>acG p.T262T CESC 16 23079813 23079813 + Missense_Mutation SNP G G A TCGA-EA-A44S-01A-12D-A26G-09 TCGA-EA-A44S-10A-01D-A26G-09 g.chr16:23079813G>A c.3613C>T c.(3613-3615)Cgc>Tgc p.R1205C CESC 16 23080124 23080124 + Missense_Mutation SNP G G T TCGA-C5-A7CG-01A-11D-A32I-09 TCGA-C5-A7CG-10A-01D-A32I-09 g.chr16:23080124G>T c.3302C>A c.(3301-3303)cCg>cAg p.P1101Q CESC 16 23098489 23098489 + Missense_Mutation SNP G G A TCGA-C5-A7UC-01A-11D-A351-09 TCGA-C5-A7UC-10A-01D-A351-09 g.chr16:23098489G>A c.1546C>T c.(1546-1548)Cgt>Tgt p.R516C CESC 16 23116857 23116857 + Missense_Mutation SNP G G A TCGA-Q1-A73O-01A-11D-A32I-09 TCGA-Q1-A73O-10B-01D-A32I-09 g.chr16:23116857G>A c.994C>T c.(994-996)Cac>Tac p.H332Y CESC 16 23117742 23117742 + Nonsense_Mutation SNP C C A TCGA-FU-A3HZ-01A-11D-A20U-09 TCGA-FU-A3HZ-10A-01D-A20U-09 g.chr16:23117742C>A c.838G>T c.(838-840)Gaa>Taa p.E280* CESC 16 23119422 23119422 + Missense_Mutation SNP C C A TCGA-JW-A5VL-01A-11D-A28B-09 TCGA-JW-A5VL-10A-01D-A28E-09 g.chr16:23119422C>A c.716G>T c.(715-717)cGa>cTa p.R239L COAD 16 23079392 23079392 + Missense_Mutation SNP G G A TCGA-A6-6653-01A-11D-1771-10 TCGA-A6-6653-10A-01D-1771-10 g.chr16:23079392G>A c.4034C>T c.(4033-4035)gCa>gTa p.A1345V COAD 16 23079554 23079554 + Missense_Mutation SNP T T C TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr16:23079554T>C c.3872A>G c.(3871-3873)gAg>gGg p.E1291G COAD 16 23079554 23079554 + Missense_Mutation SNP T T C TCGA-CK-6751-01A-11D-1835-10 TCGA-CK-6751-10A-01D-1835-10 g.chr16:23079554T>C c.3872A>G c.(3871-3873)gAg>gGg p.E1291G COAD 16 23079576 23079576 + Missense_Mutation SNP T T G TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr16:23079576T>G c.3850A>C c.(3850-3852)Aat>Cat p.N1284H COAD 16 23079650 23079650 + Missense_Mutation SNP A A C TCGA-DM-A1HB-01A-21D-A183-10 TCGA-DM-A1HB-10A-01D-A183-10 g.chr16:23079650A>C c.3776T>G c.(3775-3777)gTt>gGt p.V1259G COAD 16 23080004 23080004 + Missense_Mutation SNP G G T TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chr16:23080004G>T c.3422C>A c.(3421-3423)cCt>cAt p.P1141H COAD 16 23080107 23080107 + Missense_Mutation SNP C C T TCGA-AA-3558-01A-01W-0831-10 TCGA-AA-3558-10A-01W-0831-10 g.chr16:23080107C>T c.3319G>A c.(3319-3321)Gtg>Atg p.V1107M COAD 16 23080123 23080123 + Silent SNP C C T TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr16:23080123C>T c.3303G>A c.(3301-3303)ccG>ccA p.P1101P COAD 16 23080134 23080135 + Nonsense_Mutation DNP CC CC AT TCGA-AA-A01D-01A-01W-A00E-09 TCGA-AA-A01D-10A-01W-A00E-09 g.chr16:23080134_23080135CC>AT c.3291_3292GG>AT c.(3289-3294)aaGGag>aaATag p.E1098* COAD 16 23080649 23080649 + Missense_Mutation SNP C C A TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr16:23080649C>A c.2777G>T c.(2776-2778)aGc>aTc p.S926I COAD 16 23080809 23080809 + Silent SNP G G A TCGA-AA-3511-01A-21D-1835-10 TCGA-AA-3511-11A-01D-1835-10 g.chr16:23080809G>A c.2617C>T c.(2617-2619)Ctg>Ttg p.L873L COAD 16 23085072 23085072 + Missense_Mutation SNP G G T TCGA-AA-3712-01A-21D-1719-10 TCGA-AA-3712-11A-01D-1719-10 g.chr16:23085072G>T c.2306C>A c.(2305-2307)cCg>cAg p.P769Q COAD 16 23096260 23096260 + Missense_Mutation SNP C C T TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr16:23096260C>T c.1751G>A c.(1750-1752)cGt>cAt p.R584H COAD 16 23098489 23098489 + Missense_Mutation SNP G G A TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr16:23098489G>A c.1546C>T c.(1546-1548)Cgt>Tgt p.R516C COAD 16 23102074 23102074 + Missense_Mutation SNP T T C TCGA-AA-3955-01A-02W-0995-10 TCGA-AA-3955-10A-01W-0995-10 g.chr16:23102074T>C c.1286A>G c.(1285-1287)cAt>cGt p.H429R COAD 16 23113703 23113703 + Missense_Mutation SNP C C T TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr16:23113703C>T c.1171G>A c.(1171-1173)Gac>Aac p.D391N COAD 16 23113703 23113703 + Missense_Mutation SNP C C T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr16:23113703C>T c.1171G>A c.(1171-1173)Gac>Aac p.D391N COAD 16 23116808 23116808 + Missense_Mutation SNP C C A TCGA-AA-3949-01A-01W-0995-10 TCGA-AA-3949-10A-01W-0995-10 g.chr16:23116808C>A c.1043G>T c.(1042-1044)aGa>aTa p.R348I COAD 16 23119414 23119414 + Nonsense_Mutation SNP C C A TCGA-A6-6141-01A-11D-1771-10 TCGA-A6-6141-10A-01D-1771-10 g.chr16:23119414C>A c.724G>T c.(724-726)Gaa>Taa p.E242* COADREAD 16 23079392 23079392 + Missense_Mutation SNP G G A TCGA-A6-6653-01A-11D-1771-10 TCGA-A6-6653-10A-01D-1771-10 g.chr16:23079392G>A c.4034C>T c.(4033-4035)gCa>gTa p.A1345V COADREAD 16 23079554 23079554 + Missense_Mutation SNP T T C TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr16:23079554T>C c.3872A>G c.(3871-3873)gAg>gGg p.E1291G COADREAD 16 23079554 23079554 + Missense_Mutation SNP T T C TCGA-CK-6751-01A-11D-1835-10 TCGA-CK-6751-10A-01D-1835-10 g.chr16:23079554T>C c.3872A>G c.(3871-3873)gAg>gGg p.E1291G COADREAD 16 23079576 23079576 + Missense_Mutation SNP T T G TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr16:23079576T>G c.3850A>C c.(3850-3852)Aat>Cat p.N1284H COADREAD 16 23079650 23079650 + Missense_Mutation SNP A A C TCGA-DM-A1HB-01A-21D-A183-10 TCGA-DM-A1HB-10A-01D-A183-10 g.chr16:23079650A>C c.3776T>G c.(3775-3777)gTt>gGt p.V1259G COADREAD 16 23079661 23079661 + Silent SNP A A C TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr16:23079661A>C c.3765T>G c.(3763-3765)ggT>ggG p.G1255G COADREAD 16 23080004 23080004 + Missense_Mutation SNP G G T TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chr16:23080004G>T c.3422C>A c.(3421-3423)cCt>cAt p.P1141H COADREAD 16 23080107 23080107 + Missense_Mutation SNP C C T TCGA-AA-3558-01A-01W-0831-10 TCGA-AA-3558-10A-01W-0831-10 g.chr16:23080107C>T c.3319G>A c.(3319-3321)Gtg>Atg p.V1107M COADREAD 16 23080123 23080123 + Silent SNP C C T TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr16:23080123C>T c.3303G>A c.(3301-3303)ccG>ccA p.P1101P COADREAD 16 23080134 23080135 + Nonsense_Mutation DNP CC CC AT TCGA-AA-A01D-01A-01W-A00E-09 TCGA-AA-A01D-10A-01W-A00E-09 g.chr16:23080134_23080135CC>AT c.3291_3292GG>AT c.(3289-3294)aaGGag>aaATag p.E1098* COADREAD 16 23080649 23080649 + Missense_Mutation SNP C C A TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr16:23080649C>A c.2777G>T c.(2776-2778)aGc>aTc p.S926I COADREAD 16 23080809 23080809 + Silent SNP G G A TCGA-AA-3511-01A-21D-1835-10 TCGA-AA-3511-11A-01D-1835-10 g.chr16:23080809G>A c.2617C>T c.(2617-2619)Ctg>Ttg p.L873L COADREAD 16 23085072 23085072 + Missense_Mutation SNP G G T TCGA-AA-3712-01A-21D-1719-10 TCGA-AA-3712-11A-01D-1719-10 g.chr16:23085072G>T c.2306C>A c.(2305-2307)cCg>cAg p.P769Q COADREAD 16 23085117 23085117 + Missense_Mutation SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr16:23085117G>A c.2261C>T c.(2260-2262)aCg>aTg p.T754M COADREAD 16 23085170 23085170 + Nonsense_Mutation SNP C C T TCGA-AG-A02N-01A-11W-A096-10 TCGA-AG-A02N-11A-11W-A096-10 g.chr16:23085170C>T c.2208G>A c.(2206-2208)tgG>tgA p.W736* COADREAD 16 23096260 23096260 + Missense_Mutation SNP C C T TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr16:23096260C>T c.1751G>A c.(1750-1752)cGt>cAt p.R584H COADREAD 16 23098489 23098489 + Missense_Mutation SNP G G A TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr16:23098489G>A c.1546C>T c.(1546-1548)Cgt>Tgt p.R516C COADREAD 16 23102074 23102074 + Missense_Mutation SNP T T C TCGA-AA-3955-01A-02W-0995-10 TCGA-AA-3955-10A-01W-0995-10 g.chr16:23102074T>C c.1286A>G c.(1285-1287)cAt>cGt p.H429R COADREAD 16 23113703 23113703 + Missense_Mutation SNP C C T TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr16:23113703C>T c.1171G>A c.(1171-1173)Gac>Aac p.D391N COADREAD 16 23113703 23113703 + Missense_Mutation SNP C C T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr16:23113703C>T c.1171G>A c.(1171-1173)Gac>Aac p.D391N COADREAD 16 23116808 23116808 + Missense_Mutation SNP C C A TCGA-AA-3949-01A-01W-0995-10 TCGA-AA-3949-10A-01W-0995-10 g.chr16:23116808C>A c.1043G>T c.(1042-1044)aGa>aTa p.R348I COADREAD 16 23116834 23116834 + Frame_Shift_Del DEL G G - TCGA-AH-6544-01A-11D-1826-10 TCGA-AH-6544-10A-01D-1826-10 g.chr16:23116834delG c.1017delC c.(1015-1017)gccfs p.A339fs COADREAD 16 23119414 23119414 + Nonsense_Mutation SNP C C A TCGA-A6-6141-01A-11D-1771-10 TCGA-A6-6141-10A-01D-1771-10 g.chr16:23119414C>A c.724G>T c.(724-726)Gaa>Taa p.E242* DLBC 16 23079408 23079408 + Missense_Mutation SNP T T C TCGA-G8-6906-01A-11D-2210-10 TCGA-G8-6906-14A-01D-2210-10 g.chr16:23079408T>C c.4018A>G c.(4018-4020)Agc>Ggc p.S1340G DLBC 16 23091371 23091371 + Missense_Mutation SNP G G A TCGA-GR-7353-01A-11D-2210-10 TCGA-GR-7353-10A-01D-2210-10 g.chr16:23091371G>A c.2072C>T c.(2071-2073)cCg>cTg p.P691L DLBC 16 23117736 23117736 + Missense_Mutation SNP A A C TCGA-FA-8693-01A-11D-2397-10 TCGA-FA-8693-10A-01D-2397-10 g.chr16:23117736A>C c.844T>G c.(844-846)Ttt>Gtt p.F282V ESCA 16 23080011 23080011 + Missense_Mutation SNP T T A TCGA-L5-A8NI-01A-11D-A37C-09 TCGA-L5-A8NI-11A-11D-A37F-09 g.chr16:23080011T>A c.3415A>T c.(3415-3417)Agg>Tgg p.R1139W ESCA 16 23080832 23080832 + Missense_Mutation SNP G G T TCGA-L5-A8NQ-01A-11D-A36J-09 TCGA-L5-A8NQ-11A-11D-A36M-09 g.chr16:23080832G>T c.2594C>A c.(2593-2595)cCt>cAt p.P865H ESCA 16 23085053 23085053 + Missense_Mutation SNP G G T TCGA-L5-A4OI-01A-11D-A27G-09 TCGA-L5-A4OI-11A-11D-A27G-09 g.chr16:23085053G>T c.2325C>A c.(2323-2325)agC>agA p.S775R ESCA 16 23091494 23091494 + Splice_Site SNP T T G TCGA-JY-A6FG-01A-11D-A33E-09 TCGA-JY-A6FG-10A-01D-A33H-09 g.chr16:23091494T>G c.e13-2 ESCA 16 23093847 23093847 + Missense_Mutation SNP T T C TCGA-XP-A8T8-01A-11D-A36J-09 TCGA-XP-A8T8-10A-01D-A36M-09 g.chr16:23093847T>C c.1862A>G c.(1861-1863)cAc>cGc p.H621R ESCA 16 23093862 23093862 + Missense_Mutation SNP G G T TCGA-L5-A43I-01A-11D-A247-09 TCGA-L5-A43I-11A-11D-A247-09 g.chr16:23093862G>T c.1847C>A c.(1846-1848)gCc>gAc p.A616D ESCA 16 23102050 23102050 + Missense_Mutation SNP G G T TCGA-LN-A4A9-01A-11D-A28B-09 TCGA-LN-A4A9-10A-01D-A28E-09 g.chr16:23102050G>T c.1310C>A c.(1309-1311)aCa>aAa p.T437K GBMLGG 16 23080469 23080469 + Missense_Mutation SNP T T G TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr16:23080469T>G c.2957A>C c.(2956-2958)aAt>aCt p.N986T GBMLGG 16 23080559 23080559 + Missense_Mutation SNP C C T TCGA-HT-7620-01A-11D-2253-08 TCGA-HT-7620-10A-01D-2253-08 g.chr16:23080559C>T c.2867G>A c.(2866-2868)cGc>cAc p.R956H GBMLGG 16 23085199 23085199 + Missense_Mutation SNP A A G TCGA-DU-8165-01A-11D-2253-08 TCGA-DU-8165-10A-01D-2253-08 g.chr16:23085199A>G c.2179T>C c.(2179-2181)Tac>Cac p.Y727H GBMLGG 16 23113642 23113642 + Missense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr16:23113642C>A c.1232G>T c.(1231-1233)aGa>aTa p.R411I HNSC 16 23079773 23079773 + Missense_Mutation SNP T T C TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr16:23079773T>C c.3653A>G c.(3652-3654)gAc>gGc p.D1218G HNSC 16 23080082 23080082 + Missense_Mutation SNP T T C TCGA-HD-8224-01A-11D-2394-08 TCGA-HD-8224-10A-01D-2394-08 g.chr16:23080082T>C c.3344A>G c.(3343-3345)cAg>cGg p.Q1115R HNSC 16 23091305 23091305 + Missense_Mutation SNP C C A TCGA-CV-A45W-01A-11D-A25D-08 TCGA-CV-A45W-10A-01D-A25E-08 g.chr16:23091305C>A c.2138G>T c.(2137-2139)tGc>tTc p.C713F HNSC 16 23091426 23091426 + Missense_Mutation SNP G G A TCGA-UF-A7JT-01A-11D-A34J-08 TCGA-UF-A7JT-10A-01D-A34M-08 g.chr16:23091426G>A c.2017C>T c.(2017-2019)Cct>Tct p.P673S HNSC 16 23113727 23113727 + Missense_Mutation SNP C C A TCGA-UF-A7JA-01A-12D-A34J-08 TCGA-UF-A7JA-10A-01D-A34M-08 g.chr16:23113727C>A c.1147G>T c.(1147-1149)Gac>Tac p.D383Y HNSC 16 23113736 23113736 + Missense_Mutation SNP C C G TCGA-BA-5152-01A-02D-1870-08 TCGA-BA-5152-10A-01D-1870-08 g.chr16:23113736C>G c.1138G>C c.(1138-1140)Gat>Cat p.D380H HNSC 16 23116857 23116857 + Missense_Mutation SNP G G C TCGA-CV-7414-01A-11D-2078-08 TCGA-CV-7414-10A-01D-2078-08 g.chr16:23116857G>C c.994C>G c.(994-996)Cac>Gac p.H332D HNSC 16 23116891 23116891 + Silent SNP G G A TCGA-CQ-5331-01A-02D-1870-08 TCGA-CQ-5331-10A-01D-1870-08 g.chr16:23116891G>A c.960C>T c.(958-960)ctC>ctT p.L320L HNSC 16 23117549 23117549 + Missense_Mutation SNP G G A TCGA-CV-5966-01A-11D-1683-08 TCGA-CV-5966-10A-01D-1870-08 g.chr16:23117549G>A c.938C>T c.(937-939)cCt>cTt p.P313L HNSC 16 23117561 23117561 + Missense_Mutation SNP G G A TCGA-CN-6989-01A-11D-1912-08 TCGA-CN-6989-10A-01D-1912-08 g.chr16:23117561G>A c.926C>T c.(925-927)tCt>tTt p.S309F KIPAN 16 23079995 23079995 + Missense_Mutation SNP G G T TCGA-BP-5169-01A-01D-1429-08 TCGA-BP-5169-11A-01D-1429-08 g.chr16:23079995G>T c.3431C>A c.(3430-3432)cCt>cAt p.P1144H KIPAN 16 23083424 23083424 + Silent SNP G G T TCGA-BQ-5890-01A-11D-1589-08 TCGA-BQ-5890-11A-01D-1589-08 g.chr16:23083424G>T c.2430C>A c.(2428-2430)acC>acA p.T810T KIRC 16 23079995 23079995 + Missense_Mutation SNP G G T TCGA-BP-5169-01A-01D-1429-08 TCGA-BP-5169-11A-01D-1429-08 g.chr16:23079995G>T c.3431C>A c.(3430-3432)cCt>cAt p.P1144H KIRP 16 23083424 23083424 + Silent SNP G G T TCGA-BQ-5890-01A-11D-1589-08 TCGA-BQ-5890-11A-01D-1589-08 g.chr16:23083424G>T c.2430C>A c.(2428-2430)acC>acA p.T810T LGG 16 23080469 23080469 + Missense_Mutation SNP T T G TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr16:23080469T>G c.2957A>C c.(2956-2958)aAt>aCt p.N986T LGG 16 23080559 23080559 + Missense_Mutation SNP C C T TCGA-HT-7620-01A-11D-2253-08 TCGA-HT-7620-10A-01D-2253-08 g.chr16:23080559C>T c.2867G>A c.(2866-2868)cGc>cAc p.R956H LGG 16 23085199 23085199 + Missense_Mutation SNP A A G TCGA-DU-8165-01A-11D-2253-08 TCGA-DU-8165-10A-01D-2253-08 g.chr16:23085199A>G c.2179T>C c.(2179-2181)Tac>Cac p.Y727H LGG 16 23113642 23113642 + Missense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr16:23113642C>A c.1232G>T c.(1231-1233)aGa>aTa p.R411I LIHC 16 23080459 23080459 + Silent SNP G G T TCGA-EP-A2KA-01A-11D-A183-10 TCGA-EP-A2KA-10A-01D-A183-10 g.chr16:23080459G>T c.2967C>A c.(2965-2967)atC>atA p.I989I LIHC 16 23080584 23080584 + Missense_Mutation SNP C C A TCGA-UB-A7MB-01A-11D-A33Q-10 TCGA-UB-A7MB-10A-01D-A33Q-10 g.chr16:23080584C>A c.2842G>T c.(2842-2844)Gtg>Ttg p.V948L LIHC 16 23080589 23080589 + Missense_Mutation SNP T T C TCGA-EP-A2KA-01A-11D-A183-10 TCGA-EP-A2KA-10A-01D-A183-10 g.chr16:23080589T>C c.2837A>G c.(2836-2838)gAa>gGa p.E946G LIHC 16 23083412 23083412 + Silent SNP C C A TCGA-DD-AACI-01A-11D-A40R-10 TCGA-DD-AACI-10A-01D-A40U-10 g.chr16:23083412C>A c.2442G>T c.(2440-2442)tcG>tcT p.S814S LIHC 16 23091273 23091273 + Missense_Mutation SNP A A G TCGA-EP-A2KA-01A-11D-A183-10 TCGA-EP-A2KA-10A-01D-A183-10 g.chr16:23091273A>G c.2170T>C c.(2170-2172)Tac>Cac p.Y724H LIHC 16 23093795 23093795 + Silent SNP A A G TCGA-DD-A39Z-01A-11D-A20W-10 TCGA-DD-A39Z-11A-21D-A20W-10 g.chr16:23093795A>G c.1914T>C c.(1912-1914)ccT>ccC p.P638P LIHC 16 23093870 23093870 + Frame_Shift_Del DEL G G - TCGA-G3-A3CJ-01A-11D-A20W-10 TCGA-G3-A3CJ-10A-01D-A20W-10 g.chr16:23093870delG c.1839delC c.(1837-1839)cccfs p.P613fs LIHC 16 23093878 23093878 + Splice_Site SNP G G C TCGA-BC-A112-01A-11D-A12Z-10 TCGA-BC-A112-11A-11D-A12Z-10 g.chr16:23093878G>C c.1831C>G c.(1831-1833)Ctt>Gtt p.L611V LIHC 16 23117594 23117594 + Missense_Mutation SNP T T C TCGA-BC-A3KF-01A-11D-A20W-10 TCGA-BC-A3KF-10A-01D-A20W-10 g.chr16:23117594T>C c.893A>G c.(892-894)cAg>cGg p.Q298R LUAD 16 23079370 23079370 + Missense_Mutation SNP C C A TCGA-44-8120-01A-11D-2238-08 TCGA-44-8120-10A-01D-2238-08 g.chr16:23079370C>A c.4056G>T c.(4054-4056)caG>caT p.Q1352H LUAD 16 23079778 23079778 + Silent SNP C C T TCGA-53-7624-01A-11D-2063-08 TCGA-53-7624-10A-01D-2063-08 g.chr16:23079778C>T c.3648G>A c.(3646-3648)aaG>aaA p.K1216K LUAD 16 23079849 23079849 + Missense_Mutation SNP C C A TCGA-69-7974-01A-11D-2184-08 TCGA-69-7974-10A-01D-2184-08 g.chr16:23079849C>A c.3577G>T c.(3577-3579)Ggg>Tgg p.G1193W LUAD 16 23080011 23080011 + Missense_Mutation SNP T T A TCGA-99-8028-01A-11D-2238-08 TCGA-99-8028-10A-01D-2238-08 g.chr16:23080011T>A c.3415A>T c.(3415-3417)Agg>Tgg p.R1139W LUAD 16 23080040 23080040 + Missense_Mutation SNP G G C TCGA-55-A48X-01A-11D-A24D-08 TCGA-55-A48X-10A-01D-A24F-08 g.chr16:23080040G>C c.3386C>G c.(3385-3387)tCt>tGt p.S1129C LUAD 16 23080339 23080339 + Silent SNP G G C TCGA-50-5049-01A-01D-1625-08 TCGA-50-5049-10A-01D-1625-08 g.chr16:23080339G>C c.3087C>G c.(3085-3087)tcC>tcG p.S1029S LUAD 16 23080432 23080432 + Silent SNP T T A TCGA-91-6836-01A-21D-1855-08 TCGA-91-6836-11A-01D-1855-08 g.chr16:23080432T>A c.2994A>T c.(2992-2994)gtA>gtT p.V998V LUAD 16 23080434 23080434 + Missense_Mutation SNP C C A TCGA-44-8117-01A-11D-2238-08 TCGA-44-8117-10A-01D-2238-08 g.chr16:23080434C>A c.2992G>T c.(2992-2994)Gta>Tta p.V998L LUAD 16 23080502 23080502 + Missense_Mutation SNP C C T TCGA-05-4430-01A-02D-1265-08 TCGA-05-4430-10A-01D-1265-08 g.chr16:23080502C>T c.2924G>A c.(2923-2925)cGc>cAc p.R975H LUAD 16 23080722 23080722 + Missense_Mutation SNP C C A TCGA-78-7145-01A-11D-2036-08 TCGA-78-7145-10A-01D-2036-08 g.chr16:23080722C>A c.2704G>T c.(2704-2706)Gca>Tca p.A902S LUAD 16 23080836 23080836 + Nonsense_Mutation SNP T T A TCGA-69-7974-01A-11D-2184-08 TCGA-69-7974-10A-01D-2184-08 g.chr16:23080836T>A c.2590A>T c.(2590-2592)Aga>Tga p.R864* LUAD 16 23085047 23085047 + Silent SNP C C A TCGA-62-A46O-01A-11D-A24D-08 TCGA-62-A46O-10A-01D-A24F-08 g.chr16:23085047C>A c.2331G>T c.(2329-2331)gtG>gtT p.V777V LUAD 16 23085050 23085050 + Silent SNP C C A TCGA-97-7547-01A-11D-2036-08 TCGA-97-7547-10A-01D-2036-08 g.chr16:23085050C>A c.2328G>T c.(2326-2328)tcG>tcT p.S776S LUAD 16 23085137 23085137 + Silent SNP C C G TCGA-50-5049-01A-01D-1625-08 TCGA-50-5049-10A-01D-1625-08 g.chr16:23085137C>G c.2241G>C c.(2239-2241)ctG>ctC p.L747L LUAD 16 23093759 23093759 + Splice_Site SNP C C A TCGA-44-4112-01A-01D-1105-08 TCGA-44-4112-10A-01D-1458-08 g.chr16:23093759C>A c.1950G>T c.(1948-1950)caG>caT p.Q650H LUAD 16 23093767 23093767 + Missense_Mutation SNP A A G TCGA-55-8301-01A-11D-2284-08 TCGA-55-8301-10A-01D-2284-08 g.chr16:23093767A>G c.1942T>C c.(1942-1944)Ttt>Ctt p.F648L LUAD 16 23093869 23093869 + Missense_Mutation SNP C C A TCGA-78-7146-01A-11D-2036-08 TCGA-78-7146-10A-01D-2036-08 g.chr16:23093869C>A c.1840G>T c.(1840-1842)Gat>Tat p.D614Y LUAD 16 23096295 23096295 + Silent SNP A A G TCGA-95-7567-01A-11D-2063-08 TCGA-95-7567-10A-01D-2063-08 g.chr16:23096295A>G c.1716T>C c.(1714-1716)acT>acC p.T572T LUAD 16 23099057 23099057 + Silent SNP C C A TCGA-17-Z031-01A-01W-0746-08 TCGA-17-Z031-11A-01W-0746-08 g.chr16:23099057C>A c.1515G>T c.(1513-1515)acG>acT p.T505T LUAD 16 23101960 23101960 + Missense_Mutation SNP C C A TCGA-50-5946-01A-11D-1753-08 TCGA-50-5946-10A-01D-1753-08 g.chr16:23101960C>A c.1400G>T c.(1399-1401)gGg>gTg p.G467V LUAD 16 23101980 23101980 + Silent SNP C C T TCGA-95-7039-01A-11D-1945-08 TCGA-95-7039-10A-01D-1946-08 g.chr16:23101980C>T c.1380G>A c.(1378-1380)gtG>gtA p.V460V LUAD 16 23119382 23119382 + Silent SNP G G T TCGA-NJ-A4YF-01A-12D-A25L-08 TCGA-NJ-A4YF-10A-01D-A25L-08 g.chr16:23119382G>T c.756C>A c.(754-756)ggC>ggA p.G252G LUAD 16 23119414 23119414 + Missense_Mutation SNP C C T TCGA-44-3918-01A-01D-1105-08 TCGA-44-3918-11A-01D-1105-08 g.chr16:23119414C>T c.724G>A c.(724-726)Gaa>Aaa p.E242K LUAD 16 23160107 23160107 + Missense_Mutation SNP C C A TCGA-50-5051-01A-21D-1855-08 TCGA-50-5051-10A-01D-1855-08 g.chr16:23160107C>A c.485G>T c.(484-486)cGg>cTg p.R162L LUSC 16 23079455 23079455 + Missense_Mutation SNP G G A TCGA-60-2711-01A-01D-1522-08 TCGA-60-2711-11A-01D-1522-08 g.chr16:23079455G>A c.3971C>T c.(3970-3972)cCg>cTg p.P1324L LUSC 16 23079561 23079561 + Nonsense_Mutation SNP C C A TCGA-43-5668-01A-01D-1632-08 TCGA-43-5668-11A-01D-1632-08 g.chr16:23079561C>A c.3865G>T c.(3865-3867)Gga>Tga p.G1289* LUSC 16 23079989 23079989 + Missense_Mutation SNP T T C TCGA-60-2711-01A-01D-1522-08 TCGA-60-2711-11A-01D-1522-08 g.chr16:23079989T>C c.3437A>G c.(3436-3438)aAg>aGg p.K1146R OV 16 23079555 23079555 + Missense_Mutation SNP C C T TCGA-10-0934-01A-02W-0420-08 TCGA-10-0934-11A-01W-0420-08 g.chr16:23079555C>T c.3871G>A c.(3871-3873)Gag>Aag p.E1291K OV 16 23080132 23080132 + Silent SNP C C T TCGA-04-1343-01A-01W-0488-09 TCGA-04-1343-10A-01W-0489-09 g.chr16:23080132C>T c.3294G>A c.(3292-3294)gaG>gaA p.E1098E OV 16 23080857 23080857 + Missense_Mutation SNP C C T TCGA-30-1891-01A-01W-0699-08 TCGA-30-1891-10A-01W-0699-08 g.chr16:23080857C>T c.2569G>A c.(2569-2571)Gcc>Acc p.A857T PAAD 16 23080093 23080093 + Silent SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr16:23080093C>T c.3333G>A c.(3331-3333)tcG>tcA p.S1111S PAAD 16 23093780 23093780 + Missense_Mutation SNP T T C TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr16:23093780T>C c.1929A>G c.(1927-1929)atA>atG p.I643M PAAD 16 23119457 23119457 + Silent SNP A A G TCGA-3A-A9J0-01A-11D-A40W-08 TCGA-3A-A9J0-10A-01D-A40W-08 g.chr16:23119457A>G c.681T>C c.(679-681)caT>caC p.H227H PCPG 16 23117810 23117810 + Splice_Site SNP T T A TCGA-SQ-A6I6-01A-11D-A35I-08 TCGA-SQ-A6I6-10A-01D-A35G-08 g.chr16:23117810T>A c.e3-2 PRAD 16 23079700 23079700 + Silent SNP C C T TCGA-KK-A7AW-01A-11D-A32B-08 TCGA-KK-A7AW-11A-11D-A329-08 g.chr16:23079700C>T c.3726G>A c.(3724-3726)acG>acA p.T1242T PRAD 16 23080009 23080009 + Missense_Mutation SNP C C A TCGA-YL-A8SF-01A-11D-A377-08 TCGA-YL-A8SF-10A-01D-A37A-08 g.chr16:23080009C>A c.3417G>T c.(3415-3417)agG>agT p.R1139S PRAD 16 23080212 23080212 + Missense_Mutation SNP G G A TCGA-KK-A59V-01A-11D-A29Q-08 TCGA-KK-A59V-11A-11D-A29Q-08 g.chr16:23080212G>A c.3214C>T c.(3214-3216)Cgc>Tgc p.R1072C PRAD 16 23080594 23080594 + Silent SNP G G A TCGA-V1-A9O7-01A-21D-A41K-08 TCGA-V1-A9O7-10A-01D-A41N-08 g.chr16:23080594G>A c.2832C>T c.(2830-2832)gtC>gtT p.V944V PRAD 16 23080883 23080883 + Missense_Mutation SNP G G A TCGA-HI-7168-01A-11D-2114-08 TCGA-HI-7168-10A-01D-2115-08 g.chr16:23080883G>A c.2543C>T c.(2542-2544)tCc>tTc p.S848F PRAD 16 23080918 23080918 + Frame_Shift_Del DEL T T - TCGA-EJ-5514-01A-01D-1576-08 TCGA-EJ-5514-10A-01D-1577-08 g.chr16:23080918delT c.2508delA c.(2506-2508)ccafs p.P836fs PRAD 16 23116855 23116855 + Missense_Mutation SNP G G C TCGA-YL-A8SK-01B-21D-A377-08 TCGA-YL-A8SK-10A-01D-A37A-08 g.chr16:23116855G>C c.996C>G c.(994-996)caC>caG p.H332Q READ 16 23079661 23079661 + Silent SNP A A C TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr16:23079661A>C c.3765T>G c.(3763-3765)ggT>ggG p.G1255G READ 16 23085117 23085117 + Missense_Mutation SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr16:23085117G>A c.2261C>T c.(2260-2262)aCg>aTg p.T754M READ 16 23085170 23085170 + Nonsense_Mutation SNP C C T TCGA-AG-A02N-01A-11W-A096-10 TCGA-AG-A02N-11A-11W-A096-10 g.chr16:23085170C>T c.2208G>A c.(2206-2208)tgG>tgA p.W736* READ 16 23116834 23116834 + Frame_Shift_Del DEL G G - TCGA-AH-6544-01A-11D-1826-10 TCGA-AH-6544-10A-01D-1826-10 g.chr16:23116834delG c.1017delC c.(1015-1017)gccfs p.A339fs SARC 16 23119385 23119387 + In_Frame_Del DEL ACT ACT - TCGA-3B-A9HZ-01A-11D-A38Z-09 TCGA-3B-A9HZ-10A-01D-A38Z-09 g.chr16:23119385_23119387delACT c.751_753delAGT c.(751-753)agtdel p.S251del SKCM 16 23079464 23079464 + Missense_Mutation SNP G G A TCGA-EE-A29C-06A-21D-A197-08 TCGA-EE-A29C-10A-01D-A199-08 g.chr16:23079464G>A c.3962C>T c.(3961-3963)cCc>cTc p.P1321L SKCM 16 23079465 23079465 + Missense_Mutation SNP G G A TCGA-FW-A5DY-06A-11D-A30X-08 TCGA-FW-A5DY-11A-12D-A30X-08 g.chr16:23079465G>A c.3961C>T c.(3961-3963)Ccc>Tcc p.P1321S SKCM 16 23079694 23079695 + Frame_Shift_Del DEL AA AA - TCGA-EE-A2A2-06A-11D-A196-08 TCGA-EE-A2A2-10A-01D-A198-08 g.chr16:23079694_23079695delAA c.3731_3732delTT c.(3730-3732)cttfs p.L1244fs SKCM 16 23079830 23079830 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr16:23079830G>A c.3596C>T c.(3595-3597)tCc>tTc p.S1199F SKCM 16 23079890 23079890 + Missense_Mutation SNP G G A TCGA-EE-A20F-06A-21D-A196-08 TCGA-EE-A20F-10A-01D-A198-08 g.chr16:23079890G>A c.3536C>T c.(3535-3537)cCt>cTt p.P1179L SKCM 16 23079959 23079959 + Missense_Mutation SNP C C T TCGA-EE-A3JD-06A-11D-A20D-08 TCGA-EE-A3JD-10A-01D-A20D-08 g.chr16:23079959C>T c.3467G>A c.(3466-3468)aGa>aAa p.R1156K SKCM 16 23080094 23080094 + Missense_Mutation SNP G G A TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr16:23080094G>A c.3332C>T c.(3331-3333)tCg>tTg p.S1111L SKCM 16 23080169 23080169 + Missense_Mutation SNP C C T TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr16:23080169C>T c.3257G>A c.(3256-3258)cGg>cAg p.R1086Q SKCM 16 23080218 23080218 + Missense_Mutation SNP G G A TCGA-D3-A51R-06A-11D-A25O-08 TCGA-D3-A51R-10A-01D-A25O-08 g.chr16:23080218G>A c.3208C>T c.(3208-3210)Ccc>Tcc p.P1070S SKCM 16 23080255 23080255 + Silent SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr16:23080255G>A c.3171C>T c.(3169-3171)tcC>tcT p.S1057S SKCM 16 23080496 23080496 + Missense_Mutation SNP G G A TCGA-EE-A181-06A-11D-A196-08 TCGA-EE-A181-10A-01D-A198-08 g.chr16:23080496G>A c.2930C>T c.(2929-2931)cCc>cTc p.P977L SKCM 16 23080528 23080528 + Missense_Mutation SNP C C G TCGA-FS-A4F0-06A-11D-A24R-08 TCGA-FS-A4F0-10A-01D-A24R-08 g.chr16:23080528C>G c.2898G>C c.(2896-2898)caG>caC p.Q966H SKCM 16 23080546 23080546 + Silent SNP G G A TCGA-EE-A2GI-06A-11D-A196-08 TCGA-EE-A2GI-10A-01D-A198-08 g.chr16:23080546G>A c.2880C>T c.(2878-2880)tcC>tcT p.S960S SKCM 16 23080766 23080766 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr16:23080766G>A c.2660C>T c.(2659-2661)tCg>tTg p.S887L SKCM 16 23080775 23080775 + Missense_Mutation SNP G G A TCGA-DA-A1I0-06A-11D-A20D-08 TCGA-DA-A1I0-10B-01D-A20D-08 g.chr16:23080775G>A c.2651C>T c.(2650-2652)tCa>tTa p.S884L SKCM 16 23080856 23080856 + Missense_Mutation SNP G G A TCGA-DA-A3F8-06A-11D-A20D-08 TCGA-DA-A3F8-10A-01D-A20D-08 g.chr16:23080856G>A c.2570C>T c.(2569-2571)gCc>gTc p.A857V SKCM 16 23083400 23083400 + Silent SNP G G A TCGA-EE-A29D-06A-11D-A197-08 TCGA-EE-A29D-10A-01D-A199-08 g.chr16:23083400G>A c.2454C>T c.(2452-2454)tcC>tcT p.S818S SKCM 16 23083503 23083503 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr16:23083503G>A c.2351C>T c.(2350-2352)tCc>tTc p.S784F SKCM 16 23096193 23096193 + Silent SNP G G A TCGA-EE-A2MJ-06A-11D-A197-08 TCGA-EE-A2MJ-10A-01D-A199-08 g.chr16:23096193G>A c.1818C>T c.(1816-1818)acC>acT p.T606T SKCM 16 23099047 23099047 + Nonsense_Mutation SNP G G A TCGA-D3-A51J-06A-11D-A25O-08 TCGA-D3-A51J-10A-01D-A25O-08 g.chr16:23099047G>A c.1525C>T c.(1525-1527)Cag>Tag p.Q509* SKCM 16 23117550 23117550 + Missense_Mutation SNP G G A TCGA-EE-A3AE-06A-11D-A196-08 TCGA-EE-A3AE-10A-01D-A198-08 g.chr16:23117550G>A c.937C>T c.(937-939)Cct>Tct p.P313S SKCM 16 23117572 23117572 + Silent SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr16:23117572G>A c.915C>T c.(913-915)ttC>ttT p.F305F SKCM 16 23117577 23117577 + Missense_Mutation SNP G G A TCGA-EE-A29H-06A-12D-A197-08 TCGA-EE-A29H-10A-01D-A199-08 g.chr16:23117577G>A c.910C>T c.(910-912)Cct>Tct p.P304S SKCM 16 23117767 23117767 + Silent SNP G G A TCGA-EE-A3AF-06A-11D-A196-08 TCGA-EE-A3AF-10A-01D-A198-08 g.chr16:23117767G>A c.813C>T c.(811-813)ttC>ttT p.F271F

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BLCA-CN 16 23080081 23080081 single base substitution C A intron_variant BLCA-CN 16 23080081 23080081 single base substitution C A missense_variant Q1115H 3345G>T BLCA-CN 16 23080081 23080081 single base substitution C A missense_variant Q408H 1224G>T BLCA-CN 16 23080572 23080572 single base substitution C T exon_variant BLCA-CN 16 23080572 23080572 single base substitution C T missense_variant E245K 733G>A BLCA-CN 16 23080572 23080572 single base substitution C T missense_variant E952K 2854G>A BLCA-US 16 23083506 23083506 single base substitution G A exon_variant BLCA-US 16 23083506 23083506 single base substitution G A missense_variant S76F 227C>T BLCA-US 16 23083506 23083506 single base substitution G A missense_variant S783F 2348C>T BLCA-US 16 23096215 23096215 single base substitution G A exon_variant BLCA-US 16 23096215 23096215 single base substitution G A missense_variant S599F 1796C>T BLCA-US 16 23116802 23116802 single base substitution C G missense_variant R350P 1049G>C BLCA-US 16 23119406 23119406 single base substitution G C synonymous_variant L244L 732C>G BOCA-FR 16 23096820 23096820 single base substitution T A intron_variant BOCA-UK 16 23079676 23079676 single base substitution G A exon_variant BOCA-UK 16 23079676 23079676 single base substitution G A synonymous_variant L1250L 3750C>T BOCA-UK 16 23079676 23079676 single base substitution G A synonymous_variant L543L 1629C>T BRCA-EU 16 23067937 23067937 insertion of <=200bp - CT downstream_gene_variant BRCA-EU 16 23068003 23068004 deletion of <=200bp AA - downstream_gene_variant BRCA-EU 16 23070864 23070864 single base substitution G A downstream_gene_variant BRCA-EU 16 23071464 23071464 single base substitution G A downstream_gene_variant BRCA-EU 16 23071826 23071826 single base substitution G T downstream_gene_variant BRCA-EU 16 23071911 23071911 single base substitution C G downstream_gene_variant BRCA-EU 16 23072248 23072248 single base substitution C A downstream_gene_variant BRCA-EU 16 23073602 23073602 single base substitution G T 3_prime_UTR_variant BRCA-EU 16 23075141 23075141 single base substitution T C 3_prime_UTR_variant BRCA-EU 16 23075141 23075141 single base substitution T C downstream_gene_variant BRCA-EU 16 23075501 23075501 single base substitution C G 3_prime_UTR_variant BRCA-EU 16 23075501 23075501 single base substitution C G downstream_gene_variant BRCA-EU 16 23078880 23078880 single base substitution G A 3_prime_UTR_variant BRCA-EU 16 23078880 23078880 single base substitution G A downstream_gene_variant BRCA-EU 16 23079209 23079209 single base substitution G C 3_prime_UTR_variant BRCA-EU 16 23079209 23079209 single base substitution G C downstream_gene_variant BRCA-EU 16 23079352 23079355 deletion of <=200bp TTGA - 3_prime_UTR_variant BRCA-EU 16 23079352 23079355 deletion of <=200bp TTGA - exon_variant BRCA-EU 16 23079704 23079704 single base substitution G A exon_variant BRCA-EU 16 23079704 23079704 single base substitution G A missense_variant S1241L 3722C>T BRCA-EU 16 23079704 23079704 single base substitution G A missense_variant S534L 1601C>T BRCA-EU 16 23081033 23081033 single base substitution G T intron_variant BRCA-EU 16 23081384 23081384 single base substitution A C intron_variant BRCA-EU 16 23082583 23082583 single base substitution C T intron_variant BRCA-EU 16 23084004 23084004 single base substitution C T intron_variant BRCA-EU 16 23084004 23084004 single base substitution C T upstream_gene_variant BRCA-EU 16 23084544 23084544 single base substitution G C intron_variant BRCA-EU 16 23084544 23084544 single base substitution G C upstream_gene_variant BRCA-EU 16 23085742 23085742 single base substitution G A exon_variant BRCA-EU 16 23085742 23085742 single base substitution G A intron_variant BRCA-EU 16 23085742 23085742 single base substitution G A upstream_gene_variant BRCA-EU 16 23086066 23086066 single base substitution G A exon_variant BRCA-EU 16 23086066 23086066 single base substitution G A intron_variant BRCA-EU 16 23086066 23086066 single base substitution G A upstream_gene_variant BRCA-EU 16 23086659 23086659 single base substitution A G downstream_gene_variant BRCA-EU 16 23086659 23086659 single base substitution A G intron_variant BRCA-EU 16 23086659 23086659 single base substitution A G upstream_gene_variant BRCA-EU 16 23087450 23087450 single base substitution T A downstream_gene_variant BRCA-EU 16 23087450 23087450 single base substitution T A intron_variant BRCA-EU 16 23087450 23087450 single base substitution T A upstream_gene_variant BRCA-EU 16 23089031 23089031 single base substitution C T downstream_gene_variant BRCA-EU 16 23089031 23089031 single base substitution C T intron_variant BRCA-EU 16 23089031 23089031 single base substitution C T upstream_gene_variant BRCA-EU 16 23089295 23089295 single base substitution T C downstream_gene_variant BRCA-EU 16 23089295 23089295 single base substitution T C intron_variant BRCA-EU 16 23089295 23089295 single base substitution T C upstream_gene_variant BRCA-EU 16 23091459 23091459 single base substitution C T exon_variant BRCA-EU 16 23091459 23091459 single base substitution C T missense_variant V662I 1984G>A BRCA-EU 16 23091781 23091901 deletion of <=200bp AAAAAAATGACAGTATCAGGTGGCTCTTCCTGATACCTCTGTCAAAGAGACATGAAAACTAATGATGTGATGGCTCCATGAAGGGCAAACCACAGCGCCTGGTGCAGAAGAGCCTCTTGAT - intron_variant BRCA-EU 16 23092144 23092144 single base substitution G C intron_variant BRCA-EU 16 23092718 23092718 single base substitution G A intron_variant BRCA-EU 16 23092925 23092925 single base substitution A G intron_variant BRCA-EU 16 23093362 23093362 single base substitution T A intron_variant BRCA-EU 16 23093700 23093700 single base substitution A C intron_variant BRCA-EU 16 23093999 23093999 single base substitution G A intron_variant BRCA-EU 16 23094522 23094522 single base substitution A G intron_variant BRCA-EU 16 23095727 23095727 single base substitution G C intron_variant BRCA-EU 16 23096303 23096303 single base substitution C T exon_variant BRCA-EU 16 23096303 23096303 single base substitution C T missense_variant V570I 1708G>A BRCA-EU 16 23096767 23096767 single base substitution A G intron_variant BRCA-EU 16 23098403 23098404 deletion of <=200bp TT - intron_variant BRCA-EU 16 23099218 23099218 deletion of <=200bp T - intron_variant BRCA-EU 16 23099218 23099218 deletion of <=200bp T - upstream_gene_variant BRCA-EU 16 23099372 23099372 single base substitution G T intron_variant BRCA-EU 16 23099372 23099372 single base substitution G T upstream_gene_variant BRCA-EU 16 23101176 23101176 single base substitution T C intron_variant BRCA-EU 16 23101176 23101176 single base substitution T C upstream_gene_variant BRCA-EU 16 23101744 23101744 single base substitution C A intron_variant BRCA-EU 16 23101744 23101744 single base substitution C A upstream_gene_variant BRCA-EU 16 23101751 23101751 single base substitution C A intron_variant BRCA-EU 16 23101751 23101751 single base substitution C A upstream_gene_variant BRCA-EU 16 23101806 23101806 single base substitution G T intron_variant BRCA-EU 16 23101806 23101806 single base substitution G T upstream_gene_variant BRCA-EU 16 23103229 23103229 single base substitution A C intron_variant BRCA-EU 16 23103229 23103229 single base substitution A C upstream_gene_variant BRCA-EU 16 23103762 23103762 single base substitution T C intron_variant BRCA-EU 16 23104013 23104013 single base substitution A G intron_variant BRCA-EU 16 23107491 23107491 deletion of <=200bp A - intron_variant BRCA-EU 16 23108108 23108108 single base substitution G C intron_variant BRCA-EU 16 23108797 23108797 single base substitution G C intron_variant BRCA-EU 16 23108834 23108834 single base substitution A T intron_variant BRCA-EU 16 23109179 23109179 single base substitution C T intron_variant BRCA-EU 16 23110323 23110323 single base substitution C T intron_variant BRCA-EU 16 23111072 23111072 single base substitution G A intron_variant BRCA-EU 16 23111211 23111211 single base substitution A C intron_variant BRCA-EU 16 23112255 23112255 single base substitution G C intron_variant BRCA-EU 16 23112408 23112408 single base substitution A G intron_variant BRCA-EU 16 23112690 23112690 single base substitution G C intron_variant BRCA-EU 16 23113065 23113065 single base substitution G A intron_variant BRCA-EU 16 23113540 23113540 insertion of <=200bp - A intron_variant BRCA-EU 16 23113575 23113575 deletion of <=200bp A - intron_variant BRCA-EU 16 23113976 23113976 single base substitution C T intron_variant BRCA-EU 16 23116802 23116802 single base substitution C G missense_variant R350P 1049G>C BRCA-EU 16 23116929 23116929 single base substitution G T intron_variant BRCA-EU 16 23118522 23118522 single base substitution T C intron_variant BRCA-EU 16 23119640 23119640 single base substitution A C intron_variant BRCA-EU 16 23120166 23120166 single base substitution G A intron_variant BRCA-EU 16 23124176 23124176 single base substitution C A intron_variant BRCA-EU 16 23125370 23125370 single base substitution G A intron_variant BRCA-EU 16 23126037 23126037 single base substitution A T intron_variant BRCA-EU 16 23127479 23127479 single base substitution T G intron_variant BRCA-EU 16 23128556 23128556 single base substitution C T intron_variant BRCA-EU 16 23128758 23128758 single base substitution G A intron_variant BRCA-EU 16 23129051 23129051 single base substitution A G intron_variant BRCA-EU 16 23129763 23129763 insertion of <=200bp - T intron_variant BRCA-EU 16 23130595 23130595 deletion of <=200bp T - intron_variant BRCA-EU 16 23132731 23132731 single base substitution T C intron_variant BRCA-EU 16 23132961 23132961 single base substitution G C intron_variant BRCA-EU 16 23132978 23132978 single base substitution C G intron_variant BRCA-EU 16 23133643 23133643 single base substitution G T intron_variant BRCA-EU 16 23133646 23133646 single base substitution G T intron_variant BRCA-EU 16 23133960 23133960 single base substitution G A intron_variant BRCA-EU 16 23136375 23136375 single base substitution T C intron_variant BRCA-EU 16 23136977 23136977 single base substitution T G intron_variant BRCA-EU 16 23137961 23137961 single base substitution A T intron_variant BRCA-EU 16 23138250 23138250 single base substitution C A intron_variant BRCA-EU 16 23138793 23138793 deletion of <=200bp T - intron_variant BRCA-EU 16 23139743 23139743 single base substitution G C intron_variant BRCA-EU 16 23140790 23140790 single base substitution T C intron_variant BRCA-EU 16 23142068 23142068 single base substitution G T intron_variant BRCA-EU 16 23142556 23142556 single base substitution A C intron_variant BRCA-EU 16 23143525 23143525 single base substitution G C intron_variant BRCA-EU 16 23144772 23144772 deletion of <=200bp G - intron_variant BRCA-EU 16 23144919 23144919 single base substitution G C intron_variant BRCA-EU 16 23145758 23145758 single base substitution G A intron_variant BRCA-EU 16 23147348 23147348 single base substitution G C intron_variant BRCA-EU 16 23147598 23147598 single base substitution C T intron_variant BRCA-EU 16 23149625 23149625 single base substitution A C intron_variant BRCA-EU 16 23154460 23154460 deletion of <=200bp A - intron_variant BRCA-EU 16 23154460 23154460 single base substitution A G intron_variant BRCA-EU 16 23154555 23154556 deletion of <=200bp CT - intron_variant BRCA-EU 16 23156374 23156374 single base substitution T C intron_variant BRCA-EU 16 23158383 23158383 single base substitution G T intron_variant BRCA-EU 16 23158769 23158769 single base substitution G C intron_variant BRCA-EU 16 23159069 23159069 single base substitution C T intron_variant BRCA-EU 16 23160570 23160570 single base substitution C G missense_variant G8R 22G>C BRCA-EU 16 23160587 23160587 single base substitution G C missense_variant S2C 5C>G BRCA-EU 16 23162273 23162273 single base substitution G C upstream_gene_variant BRCA-EU 16 23163869 23163869 single base substitution G T upstream_gene_variant BRCA-FR 16 23072248 23072248 single base substitution C A downstream_gene_variant BRCA-FR 16 23081033 23081033 single base substitution G T intron_variant BRCA-FR 16 23085742 23085742 single base substitution G A exon_variant BRCA-FR 16 23085742 23085742 single base substitution G A intron_variant BRCA-FR 16 23085742 23085742 single base substitution G A upstream_gene_variant BRCA-FR 16 23091587 23091587 single base substitution G A intron_variant BRCA-FR 16 23108108 23108108 single base substitution G C intron_variant BRCA-FR 16 23111072 23111072 single base substitution G A intron_variant BRCA-FR 16 23113065 23113065 single base substitution G A intron_variant BRCA-FR 16 23122473 23122473 single base substitution T A intron_variant BRCA-FR 16 23128758 23128758 single base substitution G A intron_variant BRCA-FR 16 23143525 23143525 single base substitution G C intron_variant BRCA-FR 16 23143907 23143907 single base substitution A G intron_variant BRCA-FR 16 23144919 23144919 single base substitution G C intron_variant BRCA-FR 16 23160254 23160254 single base substitution G C missense_variant S113C 338C>G BRCA-FR 16 23160587 23160587 single base substitution G C missense_variant S2C 5C>G BRCA-FR 16 23161731 23161731 single base substitution G T upstream_gene_variant BRCA-FR 16 23162273 23162273 single base substitution G C upstream_gene_variant BRCA-UK 16 23075501 23075501 single base substitution C G 3_prime_UTR_variant BRCA-UK 16 23075501 23075501 single base substitution C G downstream_gene_variant BRCA-UK 16 23081384 23081384 single base substitution A C intron_variant BRCA-UK 16 23136779 23136779 single base substitution G A intron_variant BRCA-UK 16 23148084 23148084 single base substitution G C intron_variant BRCA-US 16 23080829 23080829 single base substitution G A exon_variant BRCA-US 16 23080829 23080829 single base substitution G A missense_variant S159L 476C>T BRCA-US 16 23080829 23080829 single base substitution G A missense_variant S866L 2597C>T BRCA-US 16 23080922 23080922 single base substitution C T exon_variant BRCA-US 16 23080922 23080922 single base substitution C T missense_variant R128Q 383G>A BRCA-US 16 23080922 23080922 single base substitution C T missense_variant R835Q 2504G>A BRCA-US 16 23083474 23083474 single base substitution G A exon_variant BRCA-US 16 23083474 23083474 single base substitution G A missense_variant P794S 2380C>T BRCA-US 16 23083474 23083474 single base substitution G A missense_variant P87S 259C>T BRCA-US 16 23085069 23085069 single base substitution G A exon_variant BRCA-US 16 23085069 23085069 single base substitution G A missense_variant S770L 2309C>T BRCA-US 16 23085069 23085069 single base substitution G A upstream_gene_variant BRCA-US 16 23085124 23085124 single base substitution C A exon_variant BRCA-US 16 23085124 23085124 single base substitution C A missense_variant V752F 2254G>T BRCA-US 16 23085124 23085124 single base substitution C A upstream_gene_variant BRCA-US 16 23096260 23096260 single base substitution C T exon_variant BRCA-US 16 23096260 23096260 single base substitution C T missense_variant R584H 1751G>A BRCA-US 16 23098496 23098496 single base substitution G A synonymous_variant F513F 1539C>T BRCA-US 16 23098496 23098496 single base substitution G A upstream_gene_variant BRCA-US 16 23116870 23116870 single base substitution T C synonymous_variant Q327Q 981A>G BRCA-US 16 23117794 23117794 single base substitution A C synonymous_variant T262T 786T>G BTCA-JP 16 23080566 23080566 single base substitution C T exon_variant BTCA-JP 16 23080566 23080566 single base substitution C T missense_variant D247N 739G>A BTCA-JP 16 23080566 23080566 single base substitution C T missense_variant D954N 2860G>A BTCA-JP 16 23080764 23080764 single base substitution G A exon_variant BTCA-JP 16 23080764 23080764 single base substitution G A missense_variant P181S 541C>T BTCA-JP 16 23080764 23080764 single base substitution G A missense_variant P888S 2662C>T BTCA-JP 16 23083634 23083634 single base substitution C A intron_variant BTCA-JP 16 23083634 23083634 single base substitution C A synonymous_variant G33G 99G>T BTCA-JP 16 23093590 23093590 single base substitution G C intron_variant BTCA-JP 16 23093860 23093860 single base substitution A G exon_variant BTCA-JP 16 23093860 23093860 single base substitution A G missense_variant W617R 1849T>C BTCA-JP 16 23096413 23096413 deletion of <=200bp A - intron_variant BTCA-JP 16 23113540 23113540 deletion of <=200bp A - intron_variant BTCA-JP 16 23116764 23116764 single base substitution G A stop_gained Q363* 1087C>T CESC-US 16 23079813 23079813 single base substitution G A exon_variant CESC-US 16 23079813 23079813 single base substitution G A missense_variant R1205C 3613C>T CESC-US 16 23079813 23079813 single base substitution G A missense_variant R498C 1492C>T CESC-US 16 23080124 23080124 single base substitution G T intron_variant CESC-US 16 23080124 23080124 single base substitution G T missense_variant P1101Q 3302C>A CESC-US 16 23080124 23080124 single base substitution G T missense_variant P394Q 1181C>A CESC-US 16 23098489 23098489 single base substitution G A missense_variant R516C 1546C>T CESC-US 16 23098489 23098489 single base substitution G A upstream_gene_variant CESC-US 16 23116857 23116857 single base substitution G A missense_variant H332Y 994C>T CESC-US 16 23117742 23117742 single base substitution C A stop_gained E280* 838G>T CESC-US 16 23119422 23119422 single base substitution C A missense_variant R239L 716G>T CLLE-ES 16 23071451 23071451 single base substitution G T downstream_gene_variant CLLE-ES 16 23093973 23093973 single base substitution A G intron_variant CLLE-ES 16 23094354 23094354 single base substitution G A intron_variant CLLE-ES 16 23135714 23135714 single base substitution C T intron_variant CLLE-ES 16 23136678 23136678 single base substitution C T intron_variant CLLE-ES 16 23146153 23146153 single base substitution G A intron_variant COAD-US 16 23079392 23079392 single base substitution G A exon_variant COAD-US 16 23079392 23079392 single base substitution G A missense_variant A1345V 4034C>T COAD-US 16 23079392 23079392 single base substitution G A missense_variant A638V 1913C>T COAD-US 16 23079501 23079501 single base substitution G A exon_variant COAD-US 16 23079501 23079501 single base substitution G A missense_variant R1309C 3925C>T COAD-US 16 23079501 23079501 single base substitution G A missense_variant R602C 1804C>T COAD-US 16 23080004 23080004 single base substitution G T intron_variant COAD-US 16 23080004 23080004 single base substitution G T missense_variant P1141H 3422C>A COAD-US 16 23080004 23080004 single base substitution G T missense_variant P434H 1301C>A COAD-US 16 23080123 23080123 single base substitution C T intron_variant COAD-US 16 23080123 23080123 single base substitution C T synonymous_variant P1101P 3303G>A COAD-US 16 23080123 23080123 single base substitution C T synonymous_variant P394P 1182G>A COAD-US 16 23080634 23080634 single base substitution C A exon_variant COAD-US 16 23080634 23080634 single base substitution C A missense_variant R224L 671G>T COAD-US 16 23080634 23080634 single base substitution C A missense_variant R931L 2792G>T COAD-US 16 23080809 23080809 single base substitution G A exon_variant COAD-US 16 23080809 23080809 single base substitution G A synonymous_variant L166L 496C>T COAD-US 16 23080809 23080809 single base substitution G A synonymous_variant L873L 2617C>T COAD-US 16 23113727 23113727 single base substitution C T missense_variant D383N 1147G>A COAD-US 16 23119414 23119414 single base substitution C A stop_gained E242* 724G>T COAD-US 16 23160061 23160061 single base substitution G A synonymous_variant G177G 531C>T COCA-CN 16 23079188 23079188 single base substitution C T 3_prime_UTR_variant COCA-CN 16 23079188 23079188 single base substitution C T downstream_gene_variant COCA-CN 16 23079353 23079353 single base substitution T C 3_prime_UTR_variant COCA-CN 16 23079353 23079353 single base substitution T C exon_variant COCA-CN 16 23079711 23079711 single base substitution G T exon_variant COCA-CN 16 23079711 23079711 single base substitution G T synonymous_variant R1239R 3715C>A COCA-CN 16 23079711 23079711 single base substitution G T synonymous_variant R532R 1594C>A COCA-CN 16 23080459 23080459 single base substitution G A exon_variant COCA-CN 16 23080459 23080459 single base substitution G A synonymous_variant I282I 846C>T COCA-CN 16 23080459 23080459 single base substitution G A synonymous_variant I989I 2967C>T COCA-CN 16 23080540 23080540 single base substitution G A exon_variant COCA-CN 16 23080540 23080540 single base substitution G A synonymous_variant V255V 765C>T COCA-CN 16 23080540 23080540 single base substitution G A synonymous_variant V962V 2886C>T COCA-CN 16 23080568 23080568 single base substitution G A exon_variant COCA-CN 16 23080568 23080568 single base substitution G A missense_variant S246L 737C>T COCA-CN 16 23080568 23080568 single base substitution G A missense_variant S953L 2858C>T COCA-CN 16 23080800 23080800 single base substitution G A exon_variant COCA-CN 16 23080800 23080800 single base substitution G A missense_variant R169C 505C>T COCA-CN 16 23080800 23080800 single base substitution G A missense_variant R876C 2626C>T COCA-CN 16 23083204 23083204 single base substitution T C intron_variant COCA-CN 16 23093788 23093788 single base substitution G C exon_variant COCA-CN 16 23093788 23093788 single base substitution G C missense_variant L641V 1921C>G COCA-CN 16 23098406 23098406 single base substitution T G intron_variant COCA-CN 16 23098406 23098406 single base substitution T G splice_region_variant COCA-CN 16 23101786 23101786 single base substitution C A intron_variant COCA-CN 16 23101786 23101786 single base substitution C A upstream_gene_variant COCA-CN 16 23113727 23113727 single base substitution C T missense_variant D383N 1147G>A COCA-CN 16 23117475 23117475 single base substitution C T intron_variant EOPC-DE 16 23097721 23097721 single base substitution A T intron_variant EOPC-DE 16 23131469 23131469 single base substitution T A intron_variant ESAD-UK 16 23068331 23068331 single base substitution G T downstream_gene_variant ESAD-UK 16 23068361 23068361 single base substitution A C downstream_gene_variant ESAD-UK 16 23068470 23068470 single base substitution A T downstream_gene_variant ESAD-UK 16 23069352 23069352 deletion of <=200bp A - downstream_gene_variant ESAD-UK 16 23070319 23070319 single base substitution G C downstream_gene_variant ESAD-UK 16 23070558 23070558 single base substitution C T downstream_gene_variant ESAD-UK 16 23071127 23071127 single base substitution C G downstream_gene_variant ESAD-UK 16 23071534 23071534 single base substitution C A downstream_gene_variant ESAD-UK 16 23075001 23075001 single base substitution G T 3_prime_UTR_variant ESAD-UK 16 23075001 23075001 single base substitution G T downstream_gene_variant ESAD-UK 16 23075631 23075631 single base substitution G A 3_prime_UTR_variant ESAD-UK 16 23075631 23075631 single base substitution G A downstream_gene_variant ESAD-UK 16 23075641 23075641 single base substitution A G 3_prime_UTR_variant ESAD-UK 16 23075641 23075641 single base substitution A G downstream_gene_variant ESAD-UK 16 23076272 23076272 single base substitution C T 3_prime_UTR_variant ESAD-UK 16 23076272 23076272 single base substitution C T downstream_gene_variant ESAD-UK 16 23076849 23076849 single base substitution C T 3_prime_UTR_variant ESAD-UK 16 23076849 23076849 single base substitution C T downstream_gene_variant ESAD-UK 16 23078649 23078649 single base substitution C T 3_prime_UTR_variant ESAD-UK 16 23078649 23078649 single base substitution C T downstream_gene_variant ESAD-UK 16 23080475 23080475 single base substitution T A exon_variant ESAD-UK 16 23080475 23080475 single base substitution T A missense_variant D277V 830A>T ESAD-UK 16 23080475 23080475 single base substitution T A missense_variant D984V 2951A>T ESAD-UK 16 23081759 23081759 single base substitution G A intron_variant ESAD-UK 16 23081951 23081951 single base substitution C T intron_variant ESAD-UK 16 23083815 23083815 single base substitution G A 5_prime_UTR_variant ESAD-UK 16 23083815 23083815 single base substitution G A intron_variant ESAD-UK 16 23086079 23086079 single base substitution A C downstream_gene_variant ESAD-UK 16 23086079 23086079 single base substitution A C exon_variant ESAD-UK 16 23086079 23086079 single base substitution A C intron_variant ESAD-UK 16 23086079 23086079 single base substitution A C upstream_gene_variant ESAD-UK 16 23086656 23086658 deletion of <=200bp AGA - downstream_gene_variant ESAD-UK 16 23086656 23086658 deletion of <=200bp AGA - intron_variant ESAD-UK 16 23086656 23086658 deletion of <=200bp AGA - upstream_gene_variant ESAD-UK 16 23087621 23087621 single base substitution A G downstream_gene_variant ESAD-UK 16 23087621 23087621 single base substitution A G intron_variant ESAD-UK 16 23087621 23087621 single base substitution A G upstream_gene_variant ESAD-UK 16 23089068 23089068 single base substitution A C downstream_gene_variant ESAD-UK 16 23089068 23089068 single base substitution A C intron_variant ESAD-UK 16 23089068 23089068 single base substitution A C upstream_gene_variant ESAD-UK 16 23089135 23089135 single base substitution A G downstream_gene_variant ESAD-UK 16 23089135 23089135 single base substitution A G intron_variant ESAD-UK 16 23089135 23089135 single base substitution A G upstream_gene_variant ESAD-UK 16 23090088 23090088 single base substitution C A downstream_gene_variant ESAD-UK 16 23090088 23090088 single base substitution C A intron_variant ESAD-UK 16 23090088 23090088 single base substitution C A upstream_gene_variant ESAD-UK 16 23095705 23095705 single base substitution A G intron_variant ESAD-UK 16 23096932 23096932 single base substitution G A exon_variant ESAD-UK 16 23096932 23096932 single base substitution G A synonymous_variant V558V 1674C>T ESAD-UK 16 23100949 23100949 single base substitution C G intron_variant ESAD-UK 16 23100949 23100949 single base substitution C G upstream_gene_variant ESAD-UK 16 23101707 23101707 deletion of <=200bp A - intron_variant ESAD-UK 16 23101707 23101707 deletion of <=200bp A - upstream_gene_variant ESAD-UK 16 23105172 23105172 single base substitution C T intron_variant ESAD-UK 16 23109979 23109979 single base substitution A T intron_variant ESAD-UK 16 23111018 23111018 single base substitution A C intron_variant ESAD-UK 16 23111967 23111967 single base substitution G A intron_variant ESAD-UK 16 23112440 23112440 single base substitution A T intron_variant ESAD-UK 16 23113005 23113005 single base substitution G A intron_variant ESAD-UK 16 23117144 23117144 single base substitution G A intron_variant ESAD-UK 16 23119071 23119071 deletion of <=200bp G - intron_variant ESAD-UK 16 23119072 23119072 single base substitution C A intron_variant ESAD-UK 16 23119073 23119073 single base substitution T A intron_variant ESAD-UK 16 23119100 23119100 single base substitution C G intron_variant ESAD-UK 16 23119868 23119868 single base substitution T C intron_variant ESAD-UK 16 23121696 23121696 single base substitution G A intron_variant ESAD-UK 16 23122352 23122352 single base substitution G T intron_variant ESAD-UK 16 23124274 23124274 single base substitution G C intron_variant ESAD-UK 16 23124299 23124299 single base substitution A C intron_variant ESAD-UK 16 23124835 23124835 single base substitution T C intron_variant ESAD-UK 16 23125029 23125029 single base substitution C T intron_variant ESAD-UK 16 23125629 23125629 single base substitution A G intron_variant ESAD-UK 16 23130513 23130513 single base substitution G A intron_variant ESAD-UK 16 23133915 23133915 single base substitution T A intron_variant ESAD-UK 16 23133953 23133953 single base substitution G A intron_variant ESAD-UK 16 23135453 23135453 single base substitution G A intron_variant ESAD-UK 16 23135512 23135512 single base substitution A G intron_variant ESAD-UK 16 23139458 23139458 single base substitution G C intron_variant ESAD-UK 16 23139660 23139660 single base substitution C G intron_variant ESAD-UK 16 23144955 23144955 single base substitution T C intron_variant ESAD-UK 16 23145626 23145626 single base substitution T G intron_variant ESAD-UK 16 23148225 23148225 single base substitution G A intron_variant ESAD-UK 16 23149346 23149346 single base substitution A G intron_variant ESAD-UK 16 23152037 23152037 single base substitution G T intron_variant ESAD-UK 16 23154368 23154368 single base substitution G T intron_variant ESAD-UK 16 23155375 23155375 single base substitution G A intron_variant ESAD-UK 16 23157446 23157446 single base substitution A G intron_variant ESAD-UK 16 23158850 23158850 single base substitution G A intron_variant ESAD-UK 16 23160064 23160064 single base substitution C G synonymous_variant A176A 528G>C ESAD-UK 16 23162776 23162776 single base substitution C T upstream_gene_variant ESAD-UK 16 23162925 23162925 deletion of <=200bp A - upstream_gene_variant ESAD-UK 16 23165252 23165252 single base substitution A T upstream_gene_variant ESCA-CN 16 23073691 23073691 deletion of <=200bp T - 3_prime_UTR_variant ESCA-CN 16 23079455 23079455 single base substitution G A exon_variant ESCA-CN 16 23079455 23079455 single base substitution G A missense_variant P1324L 3971C>T ESCA-CN 16 23079455 23079455 single base substitution G A missense_variant P617L 1850C>T ESCA-CN 16 23080228 23080228 single base substitution G A exon_variant ESCA-CN 16 23080228 23080228 single base substitution G A synonymous_variant V1066V 3198C>T ESCA-CN 16 23080228 23080228 single base substitution G A synonymous_variant V359V 1077C>T ESCA-CN 16 23083540 23083540 single base substitution T C intron_variant ESCA-CN 16 23083540 23083540 single base substitution T C missense_variant M65V 193A>G ESCA-CN 16 23093798 23093798 single base substitution C A exon_variant ESCA-CN 16 23093798 23093798 single base substitution C A synonymous_variant L637L 1911G>T KIRC-US 16 23079995 23079995 single base substitution G T intron_variant KIRC-US 16 23079995 23079995 single base substitution G T missense_variant P1144H 3431C>A KIRC-US 16 23079995 23079995 single base substitution G T missense_variant P437H 1310C>A KIRP-US 16 23083424 23083424 single base substitution G T exon_variant KIRP-US 16 23083424 23083424 single base substitution G T synonymous_variant T103T 309C>A KIRP-US 16 23083424 23083424 single base substitution G T synonymous_variant T810T 2430C>A LAML-KR 16 23132354 23132354 single base substitution A G intron_variant LGG-US 16 23080559 23080559 single base substitution C T exon_variant LGG-US 16 23080559 23080559 single base substitution C T missense_variant R249H 746G>A LGG-US 16 23080559 23080559 single base substitution C T missense_variant R956H 2867G>A LGG-US 16 23085199 23085199 single base substitution A G exon_variant LGG-US 16 23085199 23085199 single base substitution A G missense_variant Y727H 2179T>C LGG-US 16 23085199 23085199 single base substitution A G upstream_gene_variant LIAD-FR 16 23160238 23160238 single base substitution A G synonymous_variant A118A 354T>C LICA-CN 16 23160132 23160132 single base substitution C A stop_gained E154* 460G>T LICA-FR 16 23069231 23069231 single base substitution T C downstream_gene_variant LICA-FR 16 23090457 23090457 single base substitution T C downstream_gene_variant LICA-FR 16 23090457 23090457 single base substitution T C intron_variant LICA-FR 16 23090457 23090457 single base substitution T C upstream_gene_variant LICA-FR 16 23116814 23116814 single base substitution A G missense_variant V346A 1037T>C LIHC-US 16 23080459 23080459 single base substitution G T exon_variant LIHC-US 16 23080459 23080459 single base substitution G T synonymous_variant I282I 846C>A LIHC-US 16 23080459 23080459 single base substitution G T synonymous_variant I989I 2967C>A LIHC-US 16 23080584 23080584 single base substitution C A exon_variant LIHC-US 16 23080584 23080584 single base substitution C A missense_variant V241L 721G>T LIHC-US 16 23080584 23080584 single base substitution C A missense_variant V948L 2842G>T LIHC-US 16 23091273 23091273 single base substitution A G exon_variant LIHC-US 16 23091273 23091273 single base substitution A G missense_variant Y724H 2170T>C LIHC-US 16 23093795 23093795 single base substitution A G exon_variant LIHC-US 16 23093795 23093795 single base substitution A G synonymous_variant P638P 1914T>C LIHC-US 16 23093878 23093878 single base substitution G C missense_variant L611V 1831C>G LIHC-US 16 23093878 23093878 single base substitution G C splice_region_variant LIHC-US 16 23117594 23117594 single base substitution T C missense_variant Q298R 893A>G LINC-JP 16 23068281 23068281 single base substitution G T downstream_gene_variant LINC-JP 16 23080169 23080169 single base substitution C T exon_variant LINC-JP 16 23080169 23080169 single base substitution C T missense_variant R1086Q 3257G>A LINC-JP 16 23080169 23080169 single base substitution C T missense_variant R379Q 1136G>A LINC-JP 16 23080825 23080825 single base substitution C T exon_variant LINC-JP 16 23080825 23080825 single base substitution C T stop_gained W160* 480G>A LINC-JP 16 23080825 23080825 single base substitution C T stop_gained W867* 2601G>A LINC-JP 16 23084019 23084019 insertion of <=200bp - T intron_variant LINC-JP 16 23084019 23084019 insertion of <=200bp - T upstream_gene_variant LINC-JP 16 23091540 23091540 single base substitution G T intron_variant LINC-JP 16 23093309 23093309 single base substitution T C intron_variant LINC-JP 16 23093729 23093729 single base substitution T C intron_variant LINC-JP 16 23093839 23093839 single base substitution G A exon_variant LINC-JP 16 23093839 23093839 single base substitution G A stop_gained Q624* 1870C>T LINC-JP 16 23094917 23094917 deletion of <=200bp A - intron_variant LINC-JP 16 23097881 23097881 single base substitution G A intron_variant LINC-JP 16 23102239 23102239 single base substitution T C intron_variant LINC-JP 16 23102239 23102239 single base substitution T C upstream_gene_variant LINC-JP 16 23104287 23104287 single base substitution G C intron_variant LINC-JP 16 23107895 23107895 single base substitution T C intron_variant LINC-JP 16 23108703 23108703 single base substitution C T intron_variant LINC-JP 16 23113540 23113540 insertion of <=200bp - A intron_variant LINC-JP 16 23131821 23131821 single base substitution T C intron_variant LINC-JP 16 23140516 23140516 single base substitution T C intron_variant LINC-JP 16 23158305 23158305 single base substitution T G intron_variant LIRI-JP 16 23071871 23071871 single base substitution A G downstream_gene_variant LIRI-JP 16 23072261 23072261 single base substitution T C downstream_gene_variant LIRI-JP 16 23073618 23073618 single base substitution G T 3_prime_UTR_variant LIRI-JP 16 23074339 23074339 single base substitution T C 3_prime_UTR_variant LIRI-JP 16 23074339 23074339 single base substitution T C downstream_gene_variant LIRI-JP 16 23076420 23076420 single base substitution G T 3_prime_UTR_variant LIRI-JP 16 23076420 23076420 single base substitution G T downstream_gene_variant LIRI-JP 16 23076544 23076544 single base substitution C G 3_prime_UTR_variant LIRI-JP 16 23076544 23076544 single base substitution C G downstream_gene_variant LIRI-JP 16 23079319 23079322 deletion of <=200bp TAAA - 3_prime_UTR_variant LIRI-JP 16 23079319 23079322 deletion of <=200bp TAAA - exon_variant LIRI-JP 16 23081211 23081211 single base substitution A C intron_variant LIRI-JP 16 23081569 23081569 single base substitution T C intron_variant LIRI-JP 16 23086982 23086982 single base substitution T C downstream_gene_variant LIRI-JP 16 23086982 23086982 single base substitution T C intron_variant LIRI-JP 16 23086982 23086982 single base substitution T C upstream_gene_variant LIRI-JP 16 23089553 23089553 single base substitution A T downstream_gene_variant LIRI-JP 16 23089553 23089553 single base substitution A T intron_variant LIRI-JP 16 23089553 23089553 single base substitution A T upstream_gene_variant LIRI-JP 16 23094867 23094867 single base substitution T C intron_variant LIRI-JP 16 23097917 23097917 single base substitution A G intron_variant LIRI-JP 16 23098780 23098780 single base substitution T C intron_variant LIRI-JP 16 23098780 23098780 single base substitution T C upstream_gene_variant LIRI-JP 16 23099573 23099573 single base substitution G A intron_variant LIRI-JP 16 23099573 23099573 single base substitution G A upstream_gene_variant LIRI-JP 16 23102760 23102760 single base substitution C A intron_variant LIRI-JP 16 23102760 23102760 single base substitution C A upstream_gene_variant LIRI-JP 16 23103248 23103248 single base substitution G A intron_variant LIRI-JP 16 23103248 23103248 single base substitution G A upstream_gene_variant LIRI-JP 16 23103987 23103987 single base substitution G A intron_variant LIRI-JP 16 23105585 23105585 single base substitution C A intron_variant LIRI-JP 16 23106056 23106056 single base substitution A T intron_variant LIRI-JP 16 23106198 23106198 single base substitution G T intron_variant LIRI-JP 16 23107546 23107546 single base substitution C A intron_variant LIRI-JP 16 23107918 23107918 single base substitution G T intron_variant LIRI-JP 16 23108499 23108499 single base substitution G T intron_variant LIRI-JP 16 23108980 23108980 single base substitution G C intron_variant LIRI-JP 16 23109710 23109710 single base substitution C T intron_variant LIRI-JP 16 23110559 23110559 single base substitution T C intron_variant LIRI-JP 16 23111911 23111911 single base substitution T C intron_variant LIRI-JP 16 23112710 23112710 single base substitution C A intron_variant LIRI-JP 16 23112973 23112973 single base substitution G C intron_variant LIRI-JP 16 23113552 23113552 single base substitution A G intron_variant LIRI-JP 16 23113862 23113862 single base substitution C A intron_variant LIRI-JP 16 23115773 23115776 deletion of <=200bp CTCG - intron_variant LIRI-JP 16 23115872 23115872 single base substitution C T intron_variant LIRI-JP 16 23116087 23116087 single base substitution T C intron_variant LIRI-JP 16 23118148 23118148 single base substitution T C intron_variant LIRI-JP 16 23121455 23121455 single base substitution C T intron_variant LIRI-JP 16 23121553 23121553 single base substitution T C intron_variant LIRI-JP 16 23123331 23123331 single base substitution A T intron_variant LIRI-JP 16 23126761 23126761 single base substitution T C intron_variant LIRI-JP 16 23126766 23126766 single base substitution C G intron_variant LIRI-JP 16 23127459 23127459 single base substitution C T intron_variant LIRI-JP 16 23129201 23129201 single base substitution C G intron_variant LIRI-JP 16 23129642 23129642 single base substitution G A intron_variant LIRI-JP 16 23133030 23133030 single base substitution T A intron_variant LIRI-JP 16 23133241 23133241 single base substitution T C intron_variant LIRI-JP 16 23134035 23134035 single base substitution A G intron_variant LIRI-JP 16 23136684 23136684 single base substitution C A intron_variant LIRI-JP 16 23136779 23136779 single base substitution G A intron_variant LIRI-JP 16 23139466 23139466 single base substitution A T intron_variant LIRI-JP 16 23143297 23143297 single base substitution C T intron_variant LIRI-JP 16 23145672 23145672 single base substitution A G intron_variant LIRI-JP 16 23149255 23149255 single base substitution C T intron_variant LIRI-JP 16 23151665 23151665 single base substitution A C intron_variant LIRI-JP 16 23153823 23153823 single base substitution T C intron_variant LIRI-JP 16 23154962 23154962 single base substitution T C intron_variant LIRI-JP 16 23155558 23155558 single base substitution T C intron_variant LIRI-JP 16 23156703 23156703 single base substitution T C intron_variant LIRI-JP 16 23156826 23156826 single base substitution T G intron_variant LIRI-JP 16 23158157 23158157 single base substitution T C intron_variant LIRI-JP 16 23158917 23158917 single base substitution C A intron_variant LIRI-JP 16 23158918 23158918 single base substitution C A intron_variant LIRI-JP 16 23160154 23160154 single base substitution G A synonymous_variant L146L 438C>T LIRI-JP 16 23160924 23160924 single base substitution G T upstream_gene_variant LIRI-JP 16 23163170 23163170 single base substitution C A upstream_gene_variant LIRI-JP 16 23163171 23163171 single base substitution C A upstream_gene_variant LIRI-JP 16 23163312 23163312 single base substitution C A upstream_gene_variant LIRI-JP 16 23164130 23164130 single base substitution C T upstream_gene_variant LUSC-KR 16 23068329 23068329 single base substitution C A downstream_gene_variant LUSC-KR 16 23082736 23082736 single base substitution C T intron_variant LUSC-KR 16 23085322 23085322 single base substitution G A exon_variant LUSC-KR 16 23085322 23085322 single base substitution G A intron_variant LUSC-KR 16 23085322 23085322 single base substitution G A upstream_gene_variant LUSC-KR 16 23086908 23086908 single base substitution T C downstream_gene_variant LUSC-KR 16 23086908 23086908 single base substitution T C intron_variant LUSC-KR 16 23086908 23086908 single base substitution T C upstream_gene_variant LUSC-KR 16 23088990 23088990 single base substitution C A downstream_gene_variant LUSC-KR 16 23088990 23088990 single base substitution C A intron_variant LUSC-KR 16 23088990 23088990 single base substitution C A upstream_gene_variant LUSC-KR 16 23096224 23096224 single base substitution C G exon_variant LUSC-KR 16 23096224 23096224 single base substitution C G missense_variant C596S 1787G>C LUSC-KR 16 23096749 23096749 single base substitution T C intron_variant LUSC-KR 16 23098953 23098953 single base substitution C A intron_variant LUSC-KR 16 23098953 23098953 single base substitution C A upstream_gene_variant LUSC-KR 16 23107788 23107788 single base substitution G C intron_variant LUSC-KR 16 23119402 23119402 single base substitution G A missense_variant H246Y 736C>T LUSC-KR 16 23119567 23119567 single base substitution T A intron_variant LUSC-KR 16 23122023 23122023 single base substitution T A intron_variant LUSC-KR 16 23126886 23126886 single base substitution T A intron_variant LUSC-KR 16 23128058 23128058 single base substitution C A intron_variant LUSC-KR 16 23133337 23133337 single base substitution T C intron_variant LUSC-KR 16 23134648 23134648 single base substitution C A intron_variant LUSC-KR 16 23137333 23137333 single base substitution G A intron_variant LUSC-KR 16 23137764 23137764 single base substitution T G intron_variant LUSC-KR 16 23137966 23137966 single base substitution T A intron_variant LUSC-KR 16 23140099 23140099 single base substitution C T intron_variant LUSC-KR 16 23143814 23143814 single base substitution C T intron_variant LUSC-KR 16 23153794 23153794 single base substitution T C intron_variant LUSC-KR 16 23155534 23155534 single base substitution G C intron_variant LUSC-KR 16 23160908 23160908 single base substitution G A upstream_gene_variant LUSC-KR 16 23161189 23161189 single base substitution G A upstream_gene_variant LUSC-KR 16 23164328 23164328 single base substitution G C upstream_gene_variant LUSC-US 16 23079455 23079455 single base substitution G A exon_variant LUSC-US 16 23079455 23079455 single base substitution G A missense_variant P1324L 3971C>T LUSC-US 16 23079455 23079455 single base substitution G A missense_variant P617L 1850C>T LUSC-US 16 23079561 23079561 single base substitution C A exon_variant LUSC-US 16 23079561 23079561 single base substitution C A stop_gained G1289* 3865G>T LUSC-US 16 23079561 23079561 single base substitution C A stop_gained G582* 1744G>T LUSC-US 16 23079989 23079989 single base substitution T C intron_variant LUSC-US 16 23079989 23079989 single base substitution T C missense_variant K1146R 3437A>G LUSC-US 16 23079989 23079989 single base substitution T C missense_variant K439R 1316A>G MALY-DE 16 23069351 23069351 single base substitution T G downstream_gene_variant MALY-DE 16 23070052 23070052 single base substitution C A downstream_gene_variant MALY-DE 16 23071914 23071914 single base substitution T C downstream_gene_variant MALY-DE 16 23079708 23079708 single base substitution G A exon_variant MALY-DE 16 23079708 23079708 single base substitution G A missense_variant R1240C 3718C>T MALY-DE 16 23079708 23079708 single base substitution G A missense_variant R533C 1597C>T MALY-DE 16 23088192 23088192 single base substitution G A downstream_gene_variant MALY-DE 16 23088192 23088192 single base substitution G A intron_variant MALY-DE 16 23088192 23088192 single base substitution G A upstream_gene_variant MALY-DE 16 23091477 23091477 single base substitution T G exon_variant MALY-DE 16 23091477 23091477 single base substitution T G missense_variant M656L 1966A>C MALY-DE 16 23093857 23093857 single base substitution G A exon_variant MALY-DE 16 23093857 23093857 single base substitution G A missense_variant R618C 1852C>T MALY-DE 16 23096515 23096515 single base substitution C A intron_variant MALY-DE 16 23111412 23111412 single base substitution G A intron_variant MALY-DE 16 23114399 23114399 single base substitution G A intron_variant MALY-DE 16 23122769 23122769 single base substitution T C intron_variant MALY-DE 16 23123679 23123679 single base substitution C T intron_variant MALY-DE 16 23135320 23135320 insertion of <=200bp - A intron_variant MALY-DE 16 23142092 23142092 single base substitution C G intron_variant MALY-DE 16 23146008 23146008 single base substitution A G intron_variant MALY-DE 16 23146363 23146363 single base substitution T C intron_variant MALY-DE 16 23150327 23150327 single base substitution G T intron_variant MALY-DE 16 23156204 23156204 insertion of <=200bp - G intron_variant MALY-DE 16 23162182 23162182 single base substitution G A upstream_gene_variant MALY-DE 16 23163230 23163230 deletion of <=200bp T - upstream_gene_variant MALY-DE 16 23165371 23165371 single base substitution C A upstream_gene_variant MELA-AU 16 23067875 23067875 single base substitution G A downstream_gene_variant MELA-AU 16 23067944 23067944 single base substitution G A downstream_gene_variant MELA-AU 16 23068189 23068189 single base substitution G A downstream_gene_variant MELA-AU 16 23068206 23068206 single base substitution G A downstream_gene_variant MELA-AU 16 23068361 23068361 single base substitution A C downstream_gene_variant MELA-AU 16 23068440 23068440 single base substitution A T downstream_gene_variant MELA-AU 16 23068584 23068584 single base substitution G A downstream_gene_variant MELA-AU 16 23068975 23068975 single base substitution G A downstream_gene_variant MELA-AU 16 23069025 23069025 single base substitution A C downstream_gene_variant MELA-AU 16 23069239 23069240 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 16 23069337 23069337 single base substitution G A downstream_gene_variant MELA-AU 16 23069460 23069460 single base substitution A C downstream_gene_variant MELA-AU 16 23069733 23069733 single base substitution G T downstream_gene_variant MELA-AU 16 23069773 23069773 single base substitution A C downstream_gene_variant MELA-AU 16 23069855 23069855 single base substitution A G downstream_gene_variant MELA-AU 16 23070238 23070238 single base substitution G A downstream_gene_variant MELA-AU 16 23070443 23070443 single base substitution G A downstream_gene_variant MELA-AU 16 23070796 23070796 single base substitution G A downstream_gene_variant MELA-AU 16 23071355 23071355 single base substitution G A downstream_gene_variant MELA-AU 16 23071387 23071387 single base substitution G A downstream_gene_variant MELA-AU 16 23071547 23071547 single base substitution G A downstream_gene_variant MELA-AU 16 23071761 23071761 single base substitution G A downstream_gene_variant MELA-AU 16 23071776 23071776 single base substitution G A downstream_gene_variant MELA-AU 16 23072184 23072184 single base substitution G A downstream_gene_variant MELA-AU 16 23072409 23072409 single base substitution A T downstream_gene_variant MELA-AU 16 23072554 23072554 single base substitution G A downstream_gene_variant MELA-AU 16 23072569 23072569 single base substitution A G downstream_gene_variant MELA-AU 16 23072717 23072717 single base substitution G A downstream_gene_variant MELA-AU 16 23073144 23073144 single base substitution G A 3_prime_UTR_variant MELA-AU 16 23073269 23073269 single base substitution G A 3_prime_UTR_variant MELA-AU 16 23074266 23074266 single base substitution G A 3_prime_UTR_variant MELA-AU 16 23074331 23074331 single base substitution C T 3_prime_UTR_variant MELA-AU 16 23074331 23074331 single base substitution C T downstream_gene_variant MELA-AU 16 23075169 23075169 single base substitution G A 3_prime_UTR_variant MELA-AU 16 23075169 23075169 single base substitution G A downstream_gene_variant MELA-AU 16 23075590 23075590 single base substitution G A 3_prime_UTR_variant MELA-AU 16 23075590 23075590 single base substitution G A downstream_gene_variant MELA-AU 16 23075948 23075948 single base substitution C T 3_prime_UTR_variant MELA-AU 16 23075948 23075948 single base substitution C T downstream_gene_variant MELA-AU 16 23076195 23076195 single base substitution G A 3_prime_UTR_variant MELA-AU 16 23076195 23076195 single base substitution G A downstream_gene_variant MELA-AU 16 23076637 23076637 single base substitution G A 3_prime_UTR_variant MELA-AU 16 23076637 23076637 single base substitution G A downstream_gene_variant MELA-AU 16 23077141 23077141 single base substitution G A 3_prime_UTR_variant MELA-AU 16 23077141 23077141 single base substitution G A downstream_gene_variant MELA-AU 16 23078401 23078401 single base substitution G A 3_prime_UTR_variant MELA-AU 16 23078401 23078401 single base substitution G A downstream_gene_variant MELA-AU 16 23079292 23079292 single base substitution G A 3_prime_UTR_variant MELA-AU 16 23079292 23079292 single base substitution G A downstream_gene_variant MELA-AU 16 23079464 23079464 single base substitution G A exon_variant MELA-AU 16 23079464 23079464 single base substitution G A missense_variant P1321L 3962C>T MELA-AU 16 23079464 23079464 single base substitution G A missense_variant P614L 1841C>T MELA-AU 16 23080158 23080158 single base substitution G A exon_variant MELA-AU 16 23080158 23080158 single base substitution G A missense_variant P1090S 3268C>T MELA-AU 16 23080158 23080158 single base substitution G A missense_variant P383S 1147C>T MELA-AU 16 23080245 23080245 single base substitution G A exon_variant MELA-AU 16 23080245 23080245 single base substitution G A missense_variant P1061S 3181C>T MELA-AU 16 23080245 23080245 single base substitution G A missense_variant P354S 1060C>T MELA-AU 16 23080348 23080348 single base substitution G T exon_variant MELA-AU 16 23080348 23080348 single base substitution G T synonymous_variant S1026S 3078C>A MELA-AU 16 23080348 23080348 single base substitution G T synonymous_variant S319S 957C>A MELA-AU 16 23080399 23080399 single base substitution G A exon_variant MELA-AU 16 23080399 23080399 single base substitution G A synonymous_variant P1009P 3027C>T MELA-AU 16 23080399 23080399 single base substitution G A synonymous_variant P302P 906C>T MELA-AU 16 23080872 23080872 single base substitution C A exon_variant MELA-AU 16 23080872 23080872 single base substitution C A missense_variant V145F 433G>T MELA-AU 16 23080872 23080872 single base substitution C A missense_variant V852F 2554G>T MELA-AU 16 23081119 23081119 single base substitution C A intron_variant MELA-AU 16 23081399 23081399 single base substitution G A intron_variant MELA-AU 16 23081593 23081593 single base substitution G A intron_variant MELA-AU 16 23081693 23081693 single base substitution G A intron_variant MELA-AU 16 23081782 23081782 single base substitution C T intron_variant MELA-AU 16 23081990 23081990 single base substitution G A intron_variant MELA-AU 16 23082090 23082090 single base substitution A C intron_variant MELA-AU 16 23082350 23082350 single base substitution T A intron_variant MELA-AU 16 23082610 23082610 single base substitution G A intron_variant MELA-AU 16 23082620 23082620 single base substitution C T intron_variant MELA-AU 16 23083164 23083164 single base substitution G A intron_variant MELA-AU 16 23083294 23083294 single base substitution G A intron_variant MELA-AU 16 23083446 23083446 single base substitution G A exon_variant MELA-AU 16 23083446 23083446 single base substitution G A missense_variant S803F 2408C>T MELA-AU 16 23083446 23083446 single base substitution G A missense_variant S96F 287C>T MELA-AU 16 23083506 23083506 single base substitution G A exon_variant MELA-AU 16 23083506 23083506 single base substitution G A missense_variant S76F 227C>T MELA-AU 16 23083506 23083506 single base substitution G A missense_variant S783F 2348C>T MELA-AU 16 23083663 23083663 single base substitution G C intron_variant MELA-AU 16 23083663 23083663 single base substitution G C missense_variant Q24E 70C>G MELA-AU 16 23083916 23083916 single base substitution G A intron_variant MELA-AU 16 23083916 23083916 single base substitution G A upstream_gene_variant MELA-AU 16 23083964 23083964 single base substitution G A intron_variant MELA-AU 16 23083964 23083964 single base substitution G A upstream_gene_variant MELA-AU 16 23084234 23084234 single base substitution G A intron_variant MELA-AU 16 23084234 23084234 single base substitution G A upstream_gene_variant MELA-AU 16 23084741 23084741 single base substitution G A intron_variant MELA-AU 16 23084741 23084741 single base substitution G A upstream_gene_variant MELA-AU 16 23085334 23085334 single base substitution G A exon_variant MELA-AU 16 23085334 23085334 single base substitution G A intron_variant MELA-AU 16 23085334 23085334 single base substitution G A upstream_gene_variant MELA-AU 16 23085472 23085472 single base substitution G A exon_variant MELA-AU 16 23085472 23085472 single base substitution G A intron_variant MELA-AU 16 23085472 23085472 single base substitution G A upstream_gene_variant MELA-AU 16 23086375 23086375 single base substitution G A downstream_gene_variant MELA-AU 16 23086375 23086375 single base substitution G A intron_variant MELA-AU 16 23086375 23086375 single base substitution G A upstream_gene_variant MELA-AU 16 23086804 23086804 single base substitution G A downstream_gene_variant MELA-AU 16 23086804 23086804 single base substitution G A intron_variant MELA-AU 16 23086804 23086804 single base substitution G A upstream_gene_variant MELA-AU 16 23086838 23086838 single base substitution G A downstream_gene_variant MELA-AU 16 23086838 23086838 single base substitution G A intron_variant MELA-AU 16 23086838 23086838 single base substitution G A upstream_gene_variant MELA-AU 16 23086883 23086883 single base substitution G A downstream_gene_variant MELA-AU 16 23086883 23086883 single base substitution G A intron_variant MELA-AU 16 23086883 23086883 single base substitution G A upstream_gene_variant MELA-AU 16 23087276 23087276 single base substitution G A downstream_gene_variant MELA-AU 16 23087276 23087276 single base substitution G A intron_variant MELA-AU 16 23087276 23087276 single base substitution G A upstream_gene_variant MELA-AU 16 23087357 23087357 single base substitution C G downstream_gene_variant MELA-AU 16 23087357 23087357 single base substitution C G intron_variant MELA-AU 16 23087357 23087357 single base substitution C G upstream_gene_variant MELA-AU 16 23087454 23087454 single base substitution G A downstream_gene_variant MELA-AU 16 23087454 23087454 single base substitution G A intron_variant MELA-AU 16 23087454 23087454 single base substitution G A upstream_gene_variant MELA-AU 16 23087754 23087754 single base substitution G A downstream_gene_variant MELA-AU 16 23087754 23087754 single base substitution G A intron_variant MELA-AU 16 23087754 23087754 single base substitution G A upstream_gene_variant MELA-AU 16 23088728 23088728 single base substitution A G downstream_gene_variant MELA-AU 16 23088728 23088728 single base substitution A G intron_variant MELA-AU 16 23088728 23088728 single base substitution A G upstream_gene_variant MELA-AU 16 23088795 23088795 single base substitution G A downstream_gene_variant MELA-AU 16 23088795 23088795 single base substitution G A intron_variant MELA-AU 16 23088795 23088795 single base substitution G A upstream_gene_variant MELA-AU 16 23089499 23089499 single base substitution G A downstream_gene_variant MELA-AU 16 23089499 23089499 single base substitution G A intron_variant MELA-AU 16 23089499 23089499 single base substitution G A upstream_gene_variant MELA-AU 16 23090012 23090012 single base substitution C T downstream_gene_variant MELA-AU 16 23090012 23090012 single base substitution C T intron_variant MELA-AU 16 23090012 23090012 single base substitution C T upstream_gene_variant MELA-AU 16 23090133 23090133 single base substitution T G downstream_gene_variant MELA-AU 16 23090133 23090133 single base substitution T G intron_variant MELA-AU 16 23090133 23090133 single base substitution T G upstream_gene_variant MELA-AU 16 23090139 23090139 single base substitution G A downstream_gene_variant MELA-AU 16 23090139 23090139 single base substitution G A intron_variant MELA-AU 16 23090139 23090139 single base substitution G A upstream_gene_variant MELA-AU 16 23090946 23090946 single base substitution G A downstream_gene_variant MELA-AU 16 23090946 23090946 single base substitution G A intron_variant MELA-AU 16 23090946 23090946 single base substitution G A upstream_gene_variant MELA-AU 16 23091049 23091049 single base substitution T C downstream_gene_variant MELA-AU 16 23091049 23091049 single base substitution T C intron_variant MELA-AU 16 23091049 23091049 single base substitution T C upstream_gene_variant MELA-AU 16 23091168 23091168 single base substitution C T exon_variant MELA-AU 16 23091168 23091168 single base substitution C T intron_variant MELA-AU 16 23091168 23091168 single base substitution C T upstream_gene_variant MELA-AU 16 23091169 23091170 multiple base substitution (>=2bp and <=200bp) GG AA exon_variant MELA-AU 16 23091169 23091170 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 16 23091169 23091170 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 16 23091588 23091588 single base substitution G A intron_variant MELA-AU 16 23091641 23091641 single base substitution G C intron_variant MELA-AU 16 23091667 23091667 single base substitution G A intron_variant MELA-AU 16 23091700 23091700 single base substitution G A intron_variant MELA-AU 16 23092181 23092181 single base substitution G A intron_variant MELA-AU 16 23092530 23092530 single base substitution G A intron_variant MELA-AU 16 23092847 23092847 single base substitution G A intron_variant MELA-AU 16 23093748 23093748 single base substitution G A intron_variant MELA-AU 16 23094058 23094058 single base substitution G A intron_variant MELA-AU 16 23094504 23094504 single base substitution G A intron_variant MELA-AU 16 23094518 23094518 single base substitution G A intron_variant MELA-AU 16 23094741 23094741 single base substitution G A intron_variant MELA-AU 16 23094753 23094753 single base substitution G A intron_variant MELA-AU 16 23095121 23095121 single base substitution G A intron_variant MELA-AU 16 23095667 23095667 single base substitution G A intron_variant MELA-AU 16 23096361 23096361 single base substitution G A intron_variant MELA-AU 16 23096362 23096362 single base substitution G A intron_variant MELA-AU 16 23097009 23097009 single base substitution G A intron_variant MELA-AU 16 23097590 23097590 single base substitution G A intron_variant MELA-AU 16 23097860 23097860 single base substitution G A intron_variant MELA-AU 16 23097888 23097888 single base substitution G A intron_variant MELA-AU 16 23098089 23098089 single base substitution G A intron_variant MELA-AU 16 23099263 23099263 single base substitution T A intron_variant MELA-AU 16 23099263 23099263 single base substitution T A upstream_gene_variant MELA-AU 16 23099292 23099292 single base substitution G A intron_variant MELA-AU 16 23099292 23099292 single base substitution G A upstream_gene_variant MELA-AU 16 23099333 23099333 single base substitution G A intron_variant MELA-AU 16 23099333 23099333 single base substitution G A upstream_gene_variant MELA-AU 16 23099350 23099350 single base substitution T C intron_variant MELA-AU 16 23099350 23099350 single base substitution T C upstream_gene_variant MELA-AU 16 23099483 23099483 single base substitution G A intron_variant MELA-AU 16 23099483 23099483 single base substitution G A upstream_gene_variant MELA-AU 16 23100229 23100229 single base substitution G A intron_variant MELA-AU 16 23100229 23100229 single base substitution G A upstream_gene_variant MELA-AU 16 23100845 23100845 single base substitution G A intron_variant MELA-AU 16 23100845 23100845 single base substitution G A upstream_gene_variant MELA-AU 16 23101634 23101634 single base substitution G A intron_variant MELA-AU 16 23101634 23101634 single base substitution G A upstream_gene_variant MELA-AU 16 23101701 23101701 single base substitution C T intron_variant MELA-AU 16 23101701 23101701 single base substitution C T upstream_gene_variant MELA-AU 16 23101784 23101784 single base substitution A G intron_variant MELA-AU 16 23101784 23101784 single base substitution A G upstream_gene_variant MELA-AU 16 23102205 23102205 single base substitution G A intron_variant MELA-AU 16 23102205 23102205 single base substitution G A upstream_gene_variant MELA-AU 16 23102817 23102818 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 16 23102817 23102818 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 16 23103076 23103076 single base substitution A G intron_variant MELA-AU 16 23103076 23103076 single base substitution A G upstream_gene_variant MELA-AU 16 23103572 23103573 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 16 23103728 23103728 single base substitution G A intron_variant MELA-AU 16 23104180 23104180 single base substitution C T intron_variant MELA-AU 16 23104209 23104209 single base substitution A T intron_variant MELA-AU 16 23104259 23104259 single base substitution G A intron_variant MELA-AU 16 23104604 23104604 single base substitution G A intron_variant MELA-AU 16 23105509 23105509 single base substitution G A intron_variant MELA-AU 16 23105752 23105752 single base substitution A G intron_variant MELA-AU 16 23106082 23106082 single base substitution G A intron_variant MELA-AU 16 23106217 23106217 single base substitution G A intron_variant MELA-AU 16 23106346 23106346 single base substitution A G intron_variant MELA-AU 16 23106558 23106558 single base substitution A G intron_variant MELA-AU 16 23106610 23106610 single base substitution G A intron_variant MELA-AU 16 23106660 23106660 single base substitution G A intron_variant MELA-AU 16 23106941 23106941 single base substitution G A intron_variant MELA-AU 16 23107483 23107483 single base substitution T C intron_variant MELA-AU 16 23108769 23108769 single base substitution A T intron_variant MELA-AU 16 23109129 23109129 single base substitution T C intron_variant MELA-AU 16 23109531 23109531 single base substitution A G intron_variant MELA-AU 16 23110437 23110437 single base substitution G A intron_variant MELA-AU 16 23110665 23110665 single base substitution A T intron_variant MELA-AU 16 23111005 23111005 single base substitution G A intron_variant MELA-AU 16 23111076 23111076 single base substitution G A intron_variant MELA-AU 16 23112143 23112143 single base substitution G A intron_variant MELA-AU 16 23112178 23112178 single base substitution G A intron_variant MELA-AU 16 23112758 23112758 single base substitution G A intron_variant MELA-AU 16 23112916 23112916 single base substitution G A intron_variant MELA-AU 16 23112979 23112979 single base substitution A T intron_variant MELA-AU 16 23113689 23113689 single base substitution G A synonymous_variant A395A 1185C>T MELA-AU 16 23113712 23113712 single base substitution G A missense_variant H388Y 1162C>T MELA-AU 16 23113873 23113873 single base substitution G A intron_variant MELA-AU 16 23113934 23113934 single base substitution A G intron_variant MELA-AU 16 23114033 23114033 single base substitution A T intron_variant MELA-AU 16 23114271 23114271 single base substitution T C intron_variant MELA-AU 16 23114339 23114339 single base substitution G A intron_variant MELA-AU 16 23115087 23115087 single base substitution T C intron_variant MELA-AU 16 23115286 23115286 single base substitution A T intron_variant MELA-AU 16 23115590 23115590 single base substitution G A intron_variant MELA-AU 16 23115799 23115799 single base substitution C T intron_variant MELA-AU 16 23116091 23116091 single base substitution G A intron_variant MELA-AU 16 23116821 23116821 single base substitution C T missense_variant G344R 1030G>A MELA-AU 16 23116977 23116977 single base substitution G A intron_variant MELA-AU 16 23117621 23117621 single base substitution G A missense_variant S289F 866C>T MELA-AU 16 23117638 23117638 single base substitution A T intron_variant MELA-AU 16 23118283 23118283 single base substitution A G intron_variant MELA-AU 16 23118300 23118300 single base substitution G C intron_variant MELA-AU 16 23118637 23118637 single base substitution G C intron_variant MELA-AU 16 23118741 23118741 single base substitution A C intron_variant MELA-AU 16 23118829 23118829 single base substitution G A intron_variant MELA-AU 16 23120495 23120495 single base substitution C T intron_variant MELA-AU 16 23120826 23120826 single base substitution G A intron_variant MELA-AU 16 23120864 23120864 single base substitution G A intron_variant MELA-AU 16 23120906 23120906 single base substitution A C intron_variant MELA-AU 16 23121712 23121712 single base substitution G A intron_variant MELA-AU 16 23121715 23121715 single base substitution G A intron_variant MELA-AU 16 23121920 23121920 single base substitution G A intron_variant MELA-AU 16 23122158 23122158 single base substitution G A intron_variant MELA-AU 16 23122167 23122167 single base substitution G A intron_variant MELA-AU 16 23122324 23122324 single base substitution C T intron_variant MELA-AU 16 23122436 23122436 single base substitution G A intron_variant MELA-AU 16 23122787 23122787 single base substitution G A intron_variant MELA-AU 16 23123155 23123155 single base substitution G A intron_variant MELA-AU 16 23123374 23123374 single base substitution G A intron_variant MELA-AU 16 23123414 23123414 single base substitution G A intron_variant MELA-AU 16 23123564 23123564 single base substitution C T intron_variant MELA-AU 16 23123823 23123823 single base substitution G T intron_variant MELA-AU 16 23124109 23124109 single base substitution G A intron_variant MELA-AU 16 23124140 23124140 single base substitution G A intron_variant MELA-AU 16 23124535 23124535 single base substitution G A intron_variant MELA-AU 16 23124674 23124674 single base substitution G A intron_variant MELA-AU 16 23125439 23125439 single base substitution T A intron_variant MELA-AU 16 23125771 23125771 single base substitution A G intron_variant MELA-AU 16 23126134 23126134 single base substitution G A intron_variant MELA-AU 16 23126343 23126343 single base substitution C T intron_variant MELA-AU 16 23128135 23128135 single base substitution G A intron_variant MELA-AU 16 23129057 23129057 single base substitution G A intron_variant MELA-AU 16 23129230 23129230 single base substitution C T intron_variant MELA-AU 16 23129654 23129654 single base substitution G A intron_variant MELA-AU 16 23129690 23129691 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 16 23130152 23130152 single base substitution G T intron_variant MELA-AU 16 23130221 23130221 single base substitution G A intron_variant MELA-AU 16 23130856 23130856 single base substitution T A intron_variant MELA-AU 16 23131475 23131475 single base substitution G A intron_variant MELA-AU 16 23131773 23131773 single base substitution C T intron_variant MELA-AU 16 23133296 23133296 single base substitution G A intron_variant MELA-AU 16 23133866 23133866 single base substitution G A intron_variant MELA-AU 16 23133980 23133980 single base substitution T C intron_variant MELA-AU 16 23134470 23134470 single base substitution G A intron_variant MELA-AU 16 23135547 23135547 single base substitution A G intron_variant MELA-AU 16 23135567 23135567 single base substitution A T intron_variant MELA-AU 16 23135644 23135644 single base substitution T C intron_variant MELA-AU 16 23136197 23136197 single base substitution G A intron_variant MELA-AU 16 23136358 23136358 single base substitution G A intron_variant MELA-AU 16 23136490 23136490 single base substitution C T intron_variant MELA-AU 16 23136557 23136558 multiple base substitution (>=2bp and <=200bp) GA AT intron_variant MELA-AU 16 23136648 23136648 single base substitution A T intron_variant MELA-AU 16 23137541 23137541 single base substitution G A intron_variant MELA-AU 16 23137605 23137605 single base substitution G A intron_variant MELA-AU 16 23137668 23137668 single base substitution G A intron_variant MELA-AU 16 23137754 23137754 single base substitution G T intron_variant MELA-AU 16 23138212 23138212 single base substitution G A intron_variant MELA-AU 16 23139791 23139791 single base substitution A G intron_variant MELA-AU 16 23140575 23140575 single base substitution A G intron_variant MELA-AU 16 23141560 23141560 single base substitution G A intron_variant MELA-AU 16 23141975 23141975 single base substitution A C intron_variant MELA-AU 16 23142274 23142274 single base substitution T C intron_variant MELA-AU 16 23143348 23143348 single base substitution G A intron_variant MELA-AU 16 23144104 23144104 single base substitution G A intron_variant MELA-AU 16 23145088 23145088 single base substitution T C intron_variant MELA-AU 16 23145236 23145237 multiple base substitution (>=2bp and <=200bp) AA GC intron_variant MELA-AU 16 23145643 23145643 single base substitution G A intron_variant MELA-AU 16 23146166 23146166 single base substitution G A intron_variant MELA-AU 16 23146491 23146491 single base substitution G A intron_variant MELA-AU 16 23146859 23146859 single base substitution C T intron_variant MELA-AU 16 23146953 23146953 single base substitution G A intron_variant MELA-AU 16 23146996 23146996 single base substitution G A intron_variant MELA-AU 16 23147531 23147531 single base substitution G A intron_variant MELA-AU 16 23147870 23147870 single base substitution G T intron_variant MELA-AU 16 23148293 23148293 single base substitution G A intron_variant MELA-AU 16 23148310 23148310 single base substitution G A intron_variant MELA-AU 16 23149023 23149023 single base substitution T C intron_variant MELA-AU 16 23150050 23150050 single base substitution T G intron_variant MELA-AU 16 23150602 23150603 multiple base substitution (>=2bp and <=200bp) AA TT intron_variant MELA-AU 16 23151030 23151030 single base substitution G A intron_variant MELA-AU 16 23151619 23151619 single base substitution G A intron_variant MELA-AU 16 23151671 23151671 single base substitution G A intron_variant MELA-AU 16 23152002 23152002 single base substitution G A intron_variant MELA-AU 16 23152853 23152853 single base substitution C T intron_variant MELA-AU 16 23153083 23153083 single base substitution G A intron_variant MELA-AU 16 23153084 23153084 single base substitution G A intron_variant MELA-AU 16 23153501 23153501 single base substitution C T intron_variant MELA-AU 16 23153860 23153860 single base substitution T C intron_variant MELA-AU 16 23154115 23154115 single base substitution G A intron_variant MELA-AU 16 23154986 23154986 single base substitution A C intron_variant MELA-AU 16 23155058 23155058 single base substitution A T intron_variant MELA-AU 16 23155267 23155267 single base substitution G A intron_variant MELA-AU 16 23155673 23155673 single base substitution G A intron_variant MELA-AU 16 23156309 23156309 single base substitution A C intron_variant MELA-AU 16 23156502 23156502 single base substitution T A intron_variant MELA-AU 16 23156575 23156575 single base substitution G A intron_variant MELA-AU 16 23156679 23156679 single base substitution T C intron_variant MELA-AU 16 23156754 23156754 single base substitution C T intron_variant MELA-AU 16 23157958 23157958 single base substitution G A intron_variant MELA-AU 16 23157997 23157997 single base substitution T C intron_variant MELA-AU 16 23158816 23158816 single base substitution A T intron_variant MELA-AU 16 23158869 23158869 single base substitution C T intron_variant MELA-AU 16 23160898 23160898 single base substitution G A upstream_gene_variant MELA-AU 16 23161085 23161085 single base substitution G A upstream_gene_variant MELA-AU 16 23162377 23162377 single base substitution C T upstream_gene_variant MELA-AU 16 23162929 23162929 single base substitution G A upstream_gene_variant MELA-AU 16 23163213 23163213 single base substitution C A upstream_gene_variant MELA-AU 16 23163869 23163869 single base substitution G A upstream_gene_variant MELA-AU 16 23164134 23164135 multiple base substitution (>=2bp and <=200bp) GG AT upstream_gene_variant MELA-AU 16 23164220 23164220 single base substitution A G upstream_gene_variant MELA-AU 16 23164614 23164614 single base substitution C T upstream_gene_variant MELA-AU 16 23164963 23164963 single base substitution C T upstream_gene_variant MELA-AU 16 23165109 23165109 single base substitution G A upstream_gene_variant MELA-AU 16 23165327 23165327 single base substitution G A upstream_gene_variant MELA-AU 16 23165360 23165360 single base substitution G A upstream_gene_variant MELA-AU 16 23165500 23165500 single base substitution C T upstream_gene_variant ORCA-IN 16 23080529 23080529 single base substitution T G exon_variant ORCA-IN 16 23080529 23080529 single base substitution T G missense_variant Q259P 776A>C ORCA-IN 16 23080529 23080529 single base substitution T G missense_variant Q966P 2897A>C ORCA-IN 16 23129808 23129808 single base substitution G A intron_variant ORCA-IN 16 23135421 23135421 single base substitution G A intron_variant ORCA-IN 16 23145443 23145443 single base substitution C A intron_variant ORCA-IN 16 23150363 23150363 single base substitution T C intron_variant ORCA-IN 16 23161070 23161070 single base substitution T A upstream_gene_variant OV-AU 16 23075855 23075855 single base substitution G C 3_prime_UTR_variant OV-AU 16 23075855 23075855 single base substitution G C downstream_gene_variant OV-AU 16 23079509 23079509 single base substitution A T exon_variant OV-AU 16 23079509 23079509 single base substitution A T missense_variant L1306Q 3917T>A OV-AU 16 23079509 23079509 single base substitution A T missense_variant L599Q 1796T>A OV-AU 16 23080102 23080102 single base substitution T C intron_variant OV-AU 16 23080102 23080102 single base substitution T C synonymous_variant S1108S 3324A>G OV-AU 16 23080102 23080102 single base substitution T C synonymous_variant S401S 1203A>G OV-AU 16 23091173 23091173 single base substitution G A exon_variant OV-AU 16 23091173 23091173 single base substitution G A intron_variant OV-AU 16 23099729 23099729 single base substitution G A intron_variant OV-AU 16 23099729 23099729 single base substitution G A upstream_gene_variant OV-AU 16 23100629 23100629 single base substitution T A intron_variant OV-AU 16 23100629 23100629 single base substitution T A upstream_gene_variant OV-AU 16 23115247 23115247 single base substitution A C intron_variant OV-AU 16 23116767 23116767 single base substitution C T missense_variant D362N 1084G>A OV-AU 16 23125370 23125370 single base substitution G T intron_variant OV-AU 16 23126953 23126953 single base substitution T C intron_variant OV-AU 16 23127714 23127714 single base substitution T C intron_variant OV-AU 16 23132078 23132078 single base substitution C T intron_variant OV-AU 16 23135944 23135944 single base substitution G A intron_variant OV-AU 16 23145815 23145815 single base substitution A C intron_variant OV-AU 16 23146775 23146775 single base substitution A T intron_variant OV-AU 16 23149617 23149617 single base substitution C A intron_variant OV-AU 16 23153746 23153746 single base substitution G C intron_variant OV-AU 16 23154318 23154318 single base substitution G A intron_variant OV-AU 16 23155362 23155362 single base substitution T C intron_variant OV-US 16 23080132 23080132 single base substitution C T intron_variant OV-US 16 23080132 23080132 single base substitution C T synonymous_variant E1098E 3294G>A OV-US 16 23080132 23080132 single base substitution C T synonymous_variant E391E 1173G>A PACA-AU 16 23071543 23071543 single base substitution A G downstream_gene_variant PACA-AU 16 23082173 23082173 single base substitution G A intron_variant PACA-AU 16 23086322 23086322 single base substitution G A downstream_gene_variant PACA-AU 16 23086322 23086322 single base substitution G A intron_variant PACA-AU 16 23086322 23086322 single base substitution G A upstream_gene_variant PACA-AU 16 23086996 23086996 single base substitution C A downstream_gene_variant PACA-AU 16 23086996 23086996 single base substitution C A intron_variant PACA-AU 16 23086996 23086996 single base substitution C A upstream_gene_variant PACA-AU 16 23090260 23090278 deletion of <=200bp ATTATGCTACATGAAATAA - downstream_gene_variant PACA-AU 16 23090260 23090278 deletion of <=200bp ATTATGCTACATGAAATAA - intron_variant PACA-AU 16 23090260 23090278 deletion of <=200bp ATTATGCTACATGAAATAA - upstream_gene_variant PACA-AU 16 23093777 23093777 single base substitution A G exon_variant PACA-AU 16 23093777 23093777 single base substitution A G synonymous_variant H644H 1932T>C PACA-AU 16 23096244 23096244 single base substitution A G exon_variant PACA-AU 16 23096244 23096244 single base substitution A G synonymous_variant R589R 1767T>C PACA-AU 16 23096261 23096261 single base substitution G A exon_variant PACA-AU 16 23096261 23096261 single base substitution G A missense_variant R584C 1750C>T PACA-AU 16 23096676 23096676 single base substitution C T intron_variant PACA-AU 16 23105276 23105276 single base substitution G A intron_variant PACA-AU 16 23106061 23106061 single base substitution C G intron_variant PACA-AU 16 23109137 23109137 single base substitution C T intron_variant PACA-AU 16 23118483 23118483 single base substitution C T intron_variant PACA-AU 16 23118511 23118511 single base substitution C T intron_variant PACA-AU 16 23118625 23118625 single base substitution C G intron_variant PACA-AU 16 23118742 23118742 single base substitution T A intron_variant PACA-AU 16 23118969 23118969 single base substitution C A intron_variant PACA-AU 16 23119361 23119361 single base substitution C T splice_region_variant PACA-AU 16 23120074 23120074 single base substitution C A intron_variant PACA-AU 16 23120683 23120683 single base substitution C G intron_variant PACA-AU 16 23120873 23120873 single base substitution C G intron_variant PACA-AU 16 23121161 23121161 deletion of <=200bp C - intron_variant PACA-AU 16 23123015 23123015 single base substitution C T intron_variant PACA-AU 16 23123639 23123639 single base substitution C T intron_variant PACA-AU 16 23125367 23125367 single base substitution A T intron_variant PACA-AU 16 23126341 23126341 deletion of <=200bp G - intron_variant PACA-AU 16 23128519 23128519 single base substitution G A intron_variant PACA-AU 16 23129602 23129602 single base substitution G T intron_variant PACA-AU 16 23130426 23130426 single base substitution C T intron_variant PACA-AU 16 23133649 23133649 single base substitution G A intron_variant PACA-AU 16 23136344 23136344 single base substitution G C intron_variant PACA-AU 16 23145414 23145414 single base substitution A T intron_variant PACA-AU 16 23151131 23151131 single base substitution C T intron_variant PACA-AU 16 23161196 23161196 single base substitution G A upstream_gene_variant PACA-AU 16 23163102 23163102 single base substitution G A upstream_gene_variant PACA-CA 16 23068105 23068105 single base substitution T G downstream_gene_variant PACA-CA 16 23069012 23069012 single base substitution G A downstream_gene_variant PACA-CA 16 23073720 23073720 single base substitution G T 3_prime_UTR_variant PACA-CA 16 23073747 23073747 insertion of <=200bp - A 3_prime_UTR_variant PACA-CA 16 23078096 23078096 single base substitution T A 3_prime_UTR_variant PACA-CA 16 23078096 23078096 single base substitution T A downstream_gene_variant PACA-CA 16 23084357 23084357 single base substitution G A intron_variant PACA-CA 16 23084357 23084357 single base substitution G A upstream_gene_variant PACA-CA 16 23085116 23085116 single base substitution C T exon_variant PACA-CA 16 23085116 23085116 single base substitution C T synonymous_variant T754T 2262G>A PACA-CA 16 23085116 23085116 single base substitution C T upstream_gene_variant PACA-CA 16 23090515 23090515 deletion of <=200bp A - downstream_gene_variant PACA-CA 16 23090515 23090515 deletion of <=200bp A - intron_variant PACA-CA 16 23090515 23090515 deletion of <=200bp A - upstream_gene_variant PACA-CA 16 23096972 23096972 single base substitution G A exon_variant PACA-CA 16 23096972 23096972 single base substitution G A missense_variant S545F 1634C>T PACA-CA 16 23098296 23098296 single base substitution G A intron_variant PACA-CA 16 23098848 23098848 single base substitution A C intron_variant PACA-CA 16 23098848 23098848 single base substitution A C upstream_gene_variant PACA-CA 16 23100046 23100046 single base substitution T A intron_variant PACA-CA 16 23100046 23100046 single base substitution T A upstream_gene_variant PACA-CA 16 23101751 23101751 single base substitution C A intron_variant PACA-CA 16 23101751 23101751 single base substitution C A upstream_gene_variant PACA-CA 16 23114180 23114180 single base substitution G A intron_variant PACA-CA 16 23116291 23116291 single base substitution G A intron_variant PACA-CA 16 23117767 23117767 single base substitution G A synonymous_variant F271F 813C>T PACA-CA 16 23117788 23117788 single base substitution C A missense_variant M264I 792G>T PACA-CA 16 23124124 23124124 single base substitution C A intron_variant PACA-CA 16 23129574 23129574 single base substitution G A intron_variant PACA-CA 16 23129904 23129904 single base substitution G A intron_variant PACA-CA 16 23131731 23131731 single base substitution A T intron_variant PACA-CA 16 23132279 23132279 single base substitution C T intron_variant PACA-CA 16 23139717 23139717 single base substitution C A intron_variant PACA-CA 16 23144179 23144179 single base substitution C T intron_variant PACA-CA 16 23145410 23145410 single base substitution T A intron_variant PACA-CA 16 23150633 23150633 single base substitution G C intron_variant PACA-CA 16 23152691 23152691 single base substitution T A intron_variant PACA-CA 16 23153343 23153343 single base substitution G A intron_variant PACA-CA 16 23154608 23154608 single base substitution T G intron_variant PACA-CA 16 23154915 23154917 deletion of <=200bp GGA - intron_variant PACA-CA 16 23155810 23155810 single base substitution C T intron_variant PACA-CA 16 23156670 23156670 single base substitution A G intron_variant PACA-CA 16 23161068 23161068 single base substitution G T upstream_gene_variant PACA-CA 16 23164698 23164698 insertion of <=200bp - TAT upstream_gene_variant PACA-CA 16 23164747 23164747 single base substitution G A upstream_gene_variant PAEN-AU 16 23127466 23127466 single base substitution C T intron_variant PAEN-IT 16 23096026 23096026 single base substitution G T intron_variant PBCA-DE 16 23067920 23067920 single base substitution C T downstream_gene_variant PBCA-DE 16 23077981 23077981 single base substitution A T 3_prime_UTR_variant PBCA-DE 16 23077981 23077981 single base substitution A T downstream_gene_variant PBCA-DE 16 23084318 23084318 single base substitution C T intron_variant PBCA-DE 16 23084318 23084318 single base substitution C T upstream_gene_variant PBCA-DE 16 23094712 23094713 deletion of <=200bp GG - intron_variant PBCA-DE 16 23096260 23096260 single base substitution C T exon_variant PBCA-DE 16 23096260 23096260 single base substitution C T missense_variant R584H 1751G>A PBCA-DE 16 23107491 23107491 deletion of <=200bp A - intron_variant PBCA-DE 16 23117811 23117811 deletion of <=200bp A - splice_region_variant PBCA-DE 16 23118280 23118280 insertion of <=200bp - A intron_variant PBCA-DE 16 23161629 23161629 single base substitution T C upstream_gene_variant PBCA-DE 16 23161923 23161923 insertion of <=200bp - A upstream_gene_variant PBCA-DE 16 23164699 23164699 insertion of <=200bp - TAT upstream_gene_variant PBCA-DE 16 23164699 23164701 deletion of <=200bp TAT - upstream_gene_variant PRAD-CA 16 23068361 23068361 single base substitution A C downstream_gene_variant PRAD-CA 16 23073145 23073145 single base substitution A G 3_prime_UTR_variant PRAD-CA 16 23099296 23099296 single base substitution T G intron_variant PRAD-CA 16 23099296 23099296 single base substitution T G upstream_gene_variant PRAD-UK 16 23077504 23077504 single base substitution G C 3_prime_UTR_variant PRAD-UK 16 23077504 23077504 single base substitution G C downstream_gene_variant PRAD-UK 16 23080211 23080211 single base substitution C T exon_variant PRAD-UK 16 23080211 23080211 single base substitution C T missense_variant R1072H 3215G>A PRAD-UK 16 23080211 23080211 single base substitution C T missense_variant R365H 1094G>A PRAD-UK 16 23082707 23082707 single base substitution G A intron_variant PRAD-UK 16 23094959 23094959 single base substitution G C intron_variant PRAD-UK 16 23097067 23097067 single base substitution A C intron_variant PRAD-UK 16 23126932 23126932 insertion of <=200bp - A intron_variant PRAD-UK 16 23132299 23132299 single base substitution C T intron_variant PRAD-UK 16 23133122 23133122 single base substitution A G intron_variant PRAD-UK 16 23146564 23146564 single base substitution G A intron_variant PRAD-UK 16 23158677 23158677 single base substitution G A intron_variant PRAD-UK 16 23161209 23161209 single base substitution G A upstream_gene_variant PRAD-US 16 23080212 23080212 single base substitution G A exon_variant PRAD-US 16 23080212 23080212 single base substitution G A missense_variant R1072C 3214C>T PRAD-US 16 23080212 23080212 single base substitution G A missense_variant R365C 1093C>T PRAD-US 16 23080883 23080883 single base substitution G A exon_variant PRAD-US 16 23080883 23080883 single base substitution G A missense_variant S141F 422C>T PRAD-US 16 23080883 23080883 single base substitution G A missense_variant S848F 2543C>T PRAD-US 16 23080918 23080918 deletion of <=200bp T - exon_variant PRAD-US 16 23080918 23080918 deletion of <=200bp T - frameshift_variant P129 PRAD-US 16 23080918 23080918 deletion of <=200bp T - frameshift_variant P836 READ-US 16 23091449 23091449 single base substitution G T exon_variant READ-US 16 23091449 23091449 single base substitution G T missense_variant P665H 1994C>A READ-US 16 23093844 23093844 single base substitution C A exon_variant READ-US 16 23093844 23093844 single base substitution C A missense_variant C622F 1865G>T READ-US 16 23116834 23116834 deletion of <=200bp G - frameshift_variant A339 RECA-EU 16 23068308 23068308 single base substitution A T downstream_gene_variant RECA-EU 16 23078936 23078936 single base substitution C G 3_prime_UTR_variant RECA-EU 16 23078936 23078936 single base substitution C G downstream_gene_variant RECA-EU 16 23084283 23084283 single base substitution C G intron_variant RECA-EU 16 23084283 23084283 single base substitution C G upstream_gene_variant RECA-EU 16 23085676 23085676 single base substitution G C exon_variant RECA-EU 16 23085676 23085676 single base substitution G C intron_variant RECA-EU 16 23085676 23085676 single base substitution G C upstream_gene_variant RECA-EU 16 23086681 23086681 single base substitution C G downstream_gene_variant RECA-EU 16 23086681 23086681 single base substitution C G intron_variant RECA-EU 16 23086681 23086681 single base substitution C G upstream_gene_variant RECA-EU 16 23087379 23087379 single base substitution C A downstream_gene_variant RECA-EU 16 23087379 23087379 single base substitution C A intron_variant RECA-EU 16 23087379 23087379 single base substitution C A upstream_gene_variant RECA-EU 16 23092490 23092490 single base substitution C T intron_variant RECA-EU 16 23106909 23106909 single base substitution C T intron_variant RECA-EU 16 23113638 23113638 single base substitution A T splice_donor_variant RECA-EU 16 23113639 23113639 single base substitution C G splice_donor_variant RECA-EU 16 23116353 23116353 single base substitution T C intron_variant RECA-EU 16 23123307 23123307 single base substitution A G intron_variant RECA-EU 16 23126180 23126180 single base substitution C A intron_variant RECA-EU 16 23128569 23128569 single base substitution T A intron_variant RECA-EU 16 23136054 23136054 single base substitution A T intron_variant RECA-EU 16 23145961 23145961 single base substitution A T intron_variant RECA-EU 16 23146377 23146377 single base substitution T C intron_variant RECA-EU 16 23148641 23148641 single base substitution C G intron_variant RECA-EU 16 23152652 23152652 single base substitution A G intron_variant SKCA-BR 16 23068434 23068434 single base substitution C A downstream_gene_variant SKCA-BR 16 23072833 23072833 single base substitution C T 3_prime_UTR_variant SKCA-BR 16 23073236 23073236 single base substitution G A 3_prime_UTR_variant SKCA-BR 16 23075635 23075635 single base substitution A T 3_prime_UTR_variant SKCA-BR 16 23075635 23075635 single base substitution A T downstream_gene_variant SKCA-BR 16 23078487 23078487 single base substitution A G 3_prime_UTR_variant SKCA-BR 16 23078487 23078487 single base substitution A G downstream_gene_variant SKCA-BR 16 23079893 23079893 single base substitution G A exon_variant SKCA-BR 16 23079893 23079893 single base substitution G A missense_variant S1178F 3533C>T SKCA-BR 16 23079893 23079893 single base substitution G A missense_variant S471F 1412C>T SKCA-BR 16 23083068 23083068 insertion of <=200bp - GA intron_variant SKCA-BR 16 23085242 23085242 single base substitution A C exon_variant SKCA-BR 16 23085242 23085242 single base substitution A C intron_variant SKCA-BR 16 23085242 23085242 single base substitution A C upstream_gene_variant SKCA-BR 16 23090218 23090218 single base substitution G A downstream_gene_variant SKCA-BR 16 23090218 23090218 single base substitution G A intron_variant SKCA-BR 16 23090218 23090218 single base substitution G A upstream_gene_variant SKCA-BR 16 23090229 23090229 single base substitution A C downstream_gene_variant SKCA-BR 16 23090229 23090229 single base substitution A C intron_variant SKCA-BR 16 23090229 23090229 single base substitution A C upstream_gene_variant SKCA-BR 16 23092890 23092890 single base substitution C G intron_variant SKCA-BR 16 23094126 23094126 single base substitution T G intron_variant SKCA-BR 16 23095100 23095101 deletion of <=200bp TG - intron_variant SKCA-BR 16 23095607 23095607 single base substitution C T intron_variant SKCA-BR 16 23096154 23096154 single base substitution A G intron_variant SKCA-BR 16 23096261 23096261 single base substitution G A exon_variant SKCA-BR 16 23096261 23096261 single base substitution G A missense_variant R584C 1750C>T SKCA-BR 16 23099715 23099715 single base substitution C A intron_variant SKCA-BR 16 23099715 23099715 single base substitution C A upstream_gene_variant SKCA-BR 16 23104408 23104408 single base substitution G A intron_variant SKCA-BR 16 23105653 23105653 single base substitution A C intron_variant SKCA-BR 16 23110437 23110437 single base substitution G A intron_variant SKCA-BR 16 23112717 23112717 single base substitution G A intron_variant SKCA-BR 16 23113795 23113795 single base substitution G A intron_variant SKCA-BR 16 23113838 23113838 single base substitution G A intron_variant SKCA-BR 16 23122784 23122784 single base substitution G C intron_variant SKCA-BR 16 23124094 23124094 single base substitution G A intron_variant SKCA-BR 16 23125425 23125425 insertion of <=200bp - CA intron_variant SKCA-BR 16 23125791 23125791 single base substitution G A intron_variant SKCA-BR 16 23127767 23127767 single base substitution G A intron_variant SKCA-BR 16 23130426 23130427 deletion of <=200bp CT - intron_variant SKCA-BR 16 23134683 23134683 single base substitution A C intron_variant SKCA-BR 16 23134696 23134696 single base substitution T A intron_variant SKCA-BR 16 23137628 23137628 single base substitution G A intron_variant SKCA-BR 16 23138652 23138652 insertion of <=200bp - GATCACTT intron_variant SKCA-BR 16 23145412 23145412 single base substitution A T intron_variant SKCA-BR 16 23145414 23145414 single base substitution A T intron_variant SKCA-BR 16 23147320 23147320 single base substitution G A intron_variant SKCA-BR 16 23147668 23147668 single base substitution G A intron_variant SKCA-BR 16 23148007 23148007 single base substitution G A intron_variant SKCA-BR 16 23148445 23148445 single base substitution G A intron_variant SKCA-BR 16 23148464 23148464 single base substitution G T intron_variant SKCA-BR 16 23149956 23149956 single base substitution T C intron_variant SKCA-BR 16 23150512 23150512 single base substitution T G intron_variant SKCA-BR 16 23152702 23152702 insertion of <=200bp - AT intron_variant SKCA-BR 16 23152702 23152702 insertion of <=200bp - ATT intron_variant SKCA-BR 16 23160468 23160468 single base substitution C G missense_variant G42R 124G>C SKCA-BR 16 23161767 23161767 single base substitution G A upstream_gene_variant SKCA-BR 16 23162104 23162104 single base substitution G A upstream_gene_variant SKCA-BR 16 23163657 23163657 single base substitution C T upstream_gene_variant SKCA-BR 16 23165501 23165501 single base substitution A C upstream_gene_variant SKCM-US 16 23079464 23079464 single base substitution G A exon_variant SKCM-US 16 23079464 23079464 single base substitution G A missense_variant P1321L 3962C>T SKCM-US 16 23079464 23079464 single base substitution G A missense_variant P614L 1841C>T SKCM-US 16 23079465 23079465 single base substitution G A exon_variant SKCM-US 16 23079465 23079465 single base substitution G A missense_variant P1321S 3961C>T SKCM-US 16 23079465 23079465 single base substitution G A missense_variant P614S 1840C>T SKCM-US 16 23079694 23079695 deletion of <=200bp AA - exon_variant SKCM-US 16 23079694 23079695 deletion of <=200bp AA - frameshift_variant L1244 SKCM-US 16 23079694 23079695 deletion of <=200bp AA - frameshift_variant L537 SKCM-US 16 23079830 23079830 single base substitution G A exon_variant SKCM-US 16 23079830 23079830 single base substitution G A missense_variant S1199F 3596C>T SKCM-US 16 23079830 23079830 single base substitution G A missense_variant S492F 1475C>T SKCM-US 16 23079890 23079890 single base substitution G A exon_variant SKCM-US 16 23079890 23079890 single base substitution G A missense_variant P1179L 3536C>T SKCM-US 16 23079890 23079890 single base substitution G A missense_variant P472L 1415C>T SKCM-US 16 23079893 23079893 single base substitution G A exon_variant SKCM-US 16 23079893 23079893 single base substitution G A missense_variant S1178F 3533C>T SKCM-US 16 23079893 23079893 single base substitution G A missense_variant S471F 1412C>T SKCM-US 16 23079959 23079959 single base substitution C T intron_variant SKCM-US 16 23079959 23079959 single base substitution C T missense_variant R1156K 3467G>A SKCM-US 16 23079959 23079959 single base substitution C T missense_variant R449K 1346G>A SKCM-US 16 23080094 23080094 single base substitution G A intron_variant SKCM-US 16 23080094 23080094 single base substitution G A missense_variant S1111L 3332C>T SKCM-US 16 23080094 23080094 single base substitution G A missense_variant S404L 1211C>T SKCM-US 16 23080169 23080169 single base substitution C T exon_variant SKCM-US 16 23080169 23080169 single base substitution C T missense_variant R1086Q 3257G>A SKCM-US 16 23080169 23080169 single base substitution C T missense_variant R379Q 1136G>A SKCM-US 16 23080218 23080218 single base substitution G A exon_variant SKCM-US 16 23080218 23080218 single base substitution G A missense_variant P1070S 3208C>T SKCM-US 16 23080218 23080218 single base substitution G A missense_variant P363S 1087C>T SKCM-US 16 23080226 23080226 single base substitution G A exon_variant SKCM-US 16 23080226 23080226 single base substitution G A missense_variant S1067F 3200C>T SKCM-US 16 23080226 23080226 single base substitution G A missense_variant S360F 1079C>T SKCM-US 16 23080255 23080255 single base substitution G A exon_variant SKCM-US 16 23080255 23080255 single base substitution G A synonymous_variant S1057S 3171C>T SKCM-US 16 23080255 23080255 single base substitution G A synonymous_variant S350S 1050C>T SKCM-US 16 23080496 23080496 single base substitution G A exon_variant SKCM-US 16 23080496 23080496 single base substitution G A missense_variant P270L 809C>T SKCM-US 16 23080496 23080496 single base substitution G A missense_variant P977L 2930C>T SKCM-US 16 23080528 23080528 single base substitution C G exon_variant SKCM-US 16 23080528 23080528 single base substitution C G missense_variant Q259H 777G>C SKCM-US 16 23080528 23080528 single base substitution C G missense_variant Q966H 2898G>C SKCM-US 16 23080546 23080546 single base substitution G A exon_variant SKCM-US 16 23080546 23080546 single base substitution G A synonymous_variant S253S 759C>T SKCM-US 16 23080546 23080546 single base substitution G A synonymous_variant S960S 2880C>T SKCM-US 16 23080670 23080670 single base substitution G A exon_variant SKCM-US 16 23080670 23080670 single base substitution G A missense_variant S212F 635C>T SKCM-US 16 23080670 23080670 single base substitution G A missense_variant S919F 2756C>T SKCM-US 16 23080766 23080766 single base substitution G A exon_variant SKCM-US 16 23080766 23080766 single base substitution G A missense_variant S180L 539C>T SKCM-US 16 23080766 23080766 single base substitution G A missense_variant S887L 2660C>T SKCM-US 16 23080775 23080775 single base substitution G A exon_variant SKCM-US 16 23080775 23080775 single base substitution G A missense_variant S177L 530C>T SKCM-US 16 23080775 23080775 single base substitution G A missense_variant S884L 2651C>T SKCM-US 16 23080856 23080856 single base substitution G A exon_variant SKCM-US 16 23080856 23080856 single base substitution G A missense_variant A150V 449C>T SKCM-US 16 23080856 23080856 single base substitution G A missense_variant A857V 2570C>T SKCM-US 16 23083400 23083400 single base substitution G A exon_variant SKCM-US 16 23083400 23083400 single base substitution G A synonymous_variant S111S 333C>T SKCM-US 16 23083400 23083400 single base substitution G A synonymous_variant S818S 2454C>T SKCM-US 16 23083503 23083503 single base substitution G A exon_variant SKCM-US 16 23083503 23083503 single base substitution G A missense_variant S77F 230C>T SKCM-US 16 23083503 23083503 single base substitution G A missense_variant S784F 2351C>T SKCM-US 16 23085073 23085073 single base substitution G A exon_variant SKCM-US 16 23085073 23085073 single base substitution G A missense_variant P769S 2305C>T SKCM-US 16 23085073 23085073 single base substitution G A upstream_gene_variant SKCM-US 16 23085100 23085100 single base substitution G A exon_variant SKCM-US 16 23085100 23085100 single base substitution G A missense_variant L760F 2278C>T SKCM-US 16 23085100 23085100 single base substitution G A upstream_gene_variant SKCM-US 16 23096193 23096193 single base substitution G A exon_variant SKCM-US 16 23096193 23096193 single base substitution G A synonymous_variant T606T 1818C>T SKCM-US 16 23099047 23099047 single base substitution G A stop_gained Q509* 1525C>T SKCM-US 16 23099047 23099047 single base substitution G A upstream_gene_variant SKCM-US 16 23117550 23117550 single base substitution G A missense_variant P313S 937C>T SKCM-US 16 23117572 23117572 single base substitution G A synonymous_variant F305F 915C>T SKCM-US 16 23117577 23117577 single base substitution G A missense_variant P304S 910C>T SKCM-US 16 23117767 23117767 single base substitution G A synonymous_variant F271F 813C>T STAD-US 16 23079695 23079695 single base substitution A C exon_variant STAD-US 16 23079695 23079695 single base substitution A C missense_variant L1244R 3731T>G STAD-US 16 23079695 23079695 single base substitution A C missense_variant L537R 1610T>G STAD-US 16 23079707 23079707 single base substitution C T exon_variant STAD-US 16 23079707 23079707 single base substitution C T missense_variant R1240H 3719G>A STAD-US 16 23079707 23079707 single base substitution C T missense_variant R533H 1598G>A STAD-US 16 23079803 23079803 single base substitution C A exon_variant STAD-US 16 23079803 23079803 single base substitution C A missense_variant S1208I 3623G>T STAD-US 16 23079803 23079803 single base substitution C A missense_variant S501I 1502G>T STAD-US 16 23079919 23079919 single base substitution G A intron_variant STAD-US 16 23079919 23079919 single base substitution G A synonymous_variant S1169S 3507C>T STAD-US 16 23079919 23079919 single base substitution G A synonymous_variant S462S 1386C>T STAD-US 16 23080168 23080168 single base substitution C T exon_variant STAD-US 16 23080168 23080168 single base substitution C T synonymous_variant R1086R 3258G>A STAD-US 16 23080168 23080168 single base substitution C T synonymous_variant R379R 1137G>A STAD-US 16 23080178 23080178 single base substitution C T exon_variant STAD-US 16 23080178 23080178 single base substitution C T missense_variant G1083D 3248G>A STAD-US 16 23080178 23080178 single base substitution C T missense_variant G376D 1127G>A STAD-US 16 23080245 23080245 single base substitution G C exon_variant STAD-US 16 23080245 23080245 single base substitution G C missense_variant P1061A 3181C>G STAD-US 16 23080245 23080245 single base substitution G C missense_variant P354A 1060C>G STAD-US 16 23080308 23080308 single base substitution G A exon_variant STAD-US 16 23080308 23080308 single base substitution G A missense_variant R1040W 3118C>T STAD-US 16 23080308 23080308 single base substitution G A missense_variant R333W 997C>T STAD-US 16 23080440 23080440 single base substitution C T exon_variant STAD-US 16 23080440 23080440 single base substitution C T missense_variant D289N 865G>A STAD-US 16 23080440 23080440 single base substitution C T missense_variant D996N 2986G>A STAD-US 16 23080493 23080493 single base substitution G A exon_variant STAD-US 16 23080493 23080493 single base substitution G A missense_variant P271L 812C>T STAD-US 16 23080493 23080493 single base substitution G A missense_variant P978L 2933C>T STAD-US 16 23080573 23080573 single base substitution G A exon_variant STAD-US 16 23080573 23080573 single base substitution G A synonymous_variant D244D 732C>T STAD-US 16 23080573 23080573 single base substitution G A synonymous_variant D951D 2853C>T STAD-US 16 23080714 23080714 single base substitution A G exon_variant STAD-US 16 23080714 23080714 single base substitution A G synonymous_variant D197D 591T>C STAD-US 16 23080714 23080714 single base substitution A G synonymous_variant D904D 2712T>C STAD-US 16 23080765 23080765 single base substitution C T exon_variant STAD-US 16 23080765 23080765 single base substitution C T synonymous_variant S180S 540G>A STAD-US 16 23080765 23080765 single base substitution C T synonymous_variant S887S 2661G>A STAD-US 16 23080800 23080800 single base substitution G A exon_variant STAD-US 16 23080800 23080800 single base substitution G A missense_variant R169C 505C>T STAD-US 16 23080800 23080800 single base substitution G A missense_variant R876C 2626C>T STAD-US 16 23091266 23091266 single base substitution C T exon_variant STAD-US 16 23091266 23091266 single base substitution C T splice_donor_variant STAD-US 16 23091276 23091276 single base substitution G A exon_variant STAD-US 16 23091276 23091276 single base substitution G A missense_variant H723Y 2167C>T STAD-US 16 23091344 23091344 single base substitution C A exon_variant STAD-US 16 23091344 23091344 single base substitution C A missense_variant R700M 2099G>T STAD-US 16 23091458 23091458 single base substitution A T exon_variant STAD-US 16 23091458 23091458 single base substitution A T missense_variant V662D 1985T>A STAD-US 16 23091492 23091492 single base substitution C A splice_region_variant STAD-US 16 23091492 23091492 single base substitution C A stop_gained E651* 1951G>T STAD-US 16 23096246 23096246 single base substitution G T exon_variant STAD-US 16 23096246 23096246 single base substitution G T missense_variant R589S 1765C>A STAD-US 16 23102071 23102071 single base substitution C T missense_variant R430K 1289G>A STAD-US 16 23102071 23102071 single base substitution C T upstream_gene_variant STAD-US 16 23119471 23119471 single base substitution C T missense_variant G223R 667G>A THCA-SA 16 23072833 23072833 single base substitution C T 3_prime_UTR_variant THCA-SA 16 23073531 23073531 single base substitution C G 3_prime_UTR_variant THCA-SA 16 23075259 23075259 single base substitution C G 3_prime_UTR_variant THCA-SA 16 23075259 23075259 single base substitution C G downstream_gene_variant THCA-SA 16 23075369 23075369 single base substitution G A 3_prime_UTR_variant THCA-SA 16 23075369 23075369 single base substitution G A downstream_gene_variant THCA-SA 16 23076172 23076172 single base substitution A G 3_prime_UTR_variant THCA-SA 16 23076172 23076172 single base substitution A G downstream_gene_variant THCA-SA 16 23076292 23076292 single base substitution C A 3_prime_UTR_variant THCA-SA 16 23076292 23076292 single base substitution C A downstream_gene_variant THCA-SA 16 23076410 23076410 single base substitution C T 3_prime_UTR_variant THCA-SA 16 23076410 23076410 single base substitution C T downstream_gene_variant THCA-SA 16 23077351 23077351 single base substitution G A 3_prime_UTR_variant THCA-SA 16 23077351 23077351 single base substitution G A downstream_gene_variant THCA-SA 16 23077748 23077748 single base substitution A G 3_prime_UTR_variant THCA-SA 16 23077748 23077748 single base substitution A G downstream_gene_variant THCA-SA 16 23078389 23078389 single base substitution C T 3_prime_UTR_variant THCA-SA 16 23078389 23078389 single base substitution C T downstream_gene_variant THCA-SA 16 23098422 23098422 single base substitution A G exon_variant THCA-SA 16 23098422 23098422 single base substitution A G missense_variant I538T 1613T>C UCEC-US 16 23079618 23079618 single base substitution C T exon_variant UCEC-US 16 23079618 23079618 single base substitution C T missense_variant E1270K 3808G>A UCEC-US 16 23079618 23079618 single base substitution C T missense_variant E563K 1687G>A UCEC-US 16 23080121 23080121 single base substitution T G intron_variant UCEC-US 16 23080121 23080121 single base substitution T G missense_variant K1102T 3305A>C UCEC-US 16 23080121 23080121 single base substitution T G missense_variant K395T 1184A>C UCEC-US 16 23080231 23080231 single base substitution T G exon_variant UCEC-US 16 23080231 23080231 single base substitution T G missense_variant K1065N 3195A>C UCEC-US 16 23080231 23080231 single base substitution T G missense_variant K358N 1074A>C UCEC-US 16 23080366 23080366 single base substitution C A exon_variant UCEC-US 16 23080366 23080366 single base substitution C A missense_variant E1020D 3060G>T UCEC-US 16 23080366 23080366 single base substitution C A missense_variant E313D 939G>T UCEC-US 16 23080434 23080434 single base substitution C T exon_variant UCEC-US 16 23080434 23080434 single base substitution C T missense_variant V291I 871G>A UCEC-US 16 23080434 23080434 single base substitution C T missense_variant V998I 2992G>A UCEC-US 16 23080567 23080567 single base substitution C T exon_variant UCEC-US 16 23080567 23080567 single base substitution C T synonymous_variant S246S 738G>A UCEC-US 16 23080567 23080567 single base substitution C T synonymous_variant S953S 2859G>A UCEC-US 16 23080765 23080765 single base substitution C T exon_variant UCEC-US 16 23080765 23080765 single base substitution C T synonymous_variant S180S 540G>A UCEC-US 16 23080765 23080765 single base substitution C T synonymous_variant S887S 2661G>A UCEC-US 16 23083394 23083394 single base substitution C A exon_variant UCEC-US 16 23083394 23083394 single base substitution C A missense_variant E113D 339G>T UCEC-US 16 23083394 23083394 single base substitution C A missense_variant E820D 2460G>T UCEC-US 16 23085117 23085117 single base substitution G A exon_variant UCEC-US 16 23085117 23085117 single base substitution G A missense_variant T754M 2261C>T UCEC-US 16 23085117 23085117 single base substitution G A upstream_gene_variant UCEC-US 16 23085182 23085183 deletion of <=200bp CA - exon_variant UCEC-US 16 23085182 23085183 deletion of <=200bp CA - frameshift_variant V732 UCEC-US 16 23085182 23085183 deletion of <=200bp CA - upstream_gene_variant UCEC-US 16 23091330 23091330 single base substitution A G exon_variant UCEC-US 16 23091330 23091330 single base substitution A G missense_variant Y705H 2113T>C UCEC-US 16 23091401 23091401 single base substitution C T exon_variant UCEC-US 16 23091401 23091401 single base substitution C T missense_variant S681N 2042G>A UCEC-US 16 23098488 23098488 single base substitution C T missense_variant R516H 1547G>A UCEC-US 16 23098488 23098488 single base substitution C T upstream_gene_variant UCEC-US 16 23102000 23102000 single base substitution C T missense_variant D454N 1360G>A UCEC-US 16 23102000 23102000 single base substitution C T upstream_gene_variant UCEC-US 16 23119456 23119456 single base substitution C T missense_variant D228N 682G>A UCEC-US 16 23119485 23119485 single base substitution G A missense_variant A218V 653C>T UCEC-US 16 23119490 23119490 single base substitution C A missense_variant K216N 648G>T

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand TCGA-CG-5723-01 COSM4059351 c.1765C>A p.R589S Substitution - Missense 16:23084925-23084925 - T1154 COSM4739759 c.2166delG p.H723fs*68 Deletion - Frameshift 16:23079956-23079956 - ccRCC-25 COSM1664919 c.2462T>A p.M821K Substitution - Missense 16:23072071-23072071 - TCGA-FW-A3R5-06 COSM3888205 c.3171C>T p.S1057S Substitution - coding silent 16:23068934-23068934 - COLO-205 COSM1678926 c.2782A>T p.S928C Substitution - Missense 16:23069323-23069323 - HCC145 COSM3706942 c.2601G>A p.W867* Substitution - Nonsense 16:23069504-23069504 - TCGA-FW-A5DY-06 COSM3507719 c.3961C>T p.P1321S Substitution - Missense 16:23068144-23068144 - OSCC-GB_01370111 COSM5955725 c.2897A>C p.Q966P Substitution - Missense 16:23069208-23069208 - TCGA-DA-A1I0-06 COSM3507728 c.2651C>T p.S884L Substitution - Missense 16:23069454-23069454 - TCGA-HI-7168-01 COSM3672189 c.2543C>T p.S848F Substitution - Missense 16:23069562-23069562 - TCGA-BP-5169-01 COSM471497 c.3431C>A p.P1144H Substitution - Missense 16:23068674-23068674 - Pat_60_A COSM5850479 c.2410G>T p.A804S Substitution - Missense 16:23072123-23072123 - CSCC-27-T COSM4459365 c.1122C>T p.F374F Substitution - coding silent 16:23102431-23102431 - TCGA-D1-A101-01 COSM968711 c.1360G>A p.D454N Substitution - Missense 16:23090679-23090679 - TCGA-EE-A29C-06 COSM3507718 c.3962C>T p.P1321L Substitution - Missense 16:23068143-23068143 - T3174 COSM968684 c.3303G>A p.P1101P Substitution - coding silent 16:23068802-23068802 - TCGA-B5-A0K2-01 COSM968713 c.682G>A p.D228N Substitution - Missense 16:23108135-23108135 - 49M COSM3507720 c.3533C>T p.S1178F Substitution - Missense 16:23068572-23068572 - RK089_C01 COSM1629831 c.438C>T p.L146L Substitution - coding silent 16:23148833-23148833 - TCGA-AP-A056-01 COSM968717 c.648G>T p.K216N Substitution - Missense 16:23108169-23108169 - TCGA-FU-A23L-01 COSM460581 c.843C>G p.L281L Substitution - coding silent 16:23106416-23106416 - CHC2052T COSM4790013 c.1037T>C p.V346A Substitution - Missense 16:23105493-23105493 - ESCC-008T COSM3936974 c.3198C>T p.V1066V Substitution - coding silent 16:23068907-23068907 - TCGA-AC-A23H-01 COSM3817553 c.1539C>T p.F513F Substitution - coding silent 16:23087175-23087175 - CSCC-15-T COSM4570607 c.2970T>C p.A990A Substitution - coding silent 16:23069135-23069135 - 18195 COSM1301747 c.2348C>T p.S783F Substitution - Missense 16:23072185-23072185 - SW48 COSM3279331 c.3462G>A p.L1154L Substitution - coding silent 16:23068643-23068643 - CSCC-38-T COSM4457146 c.1034C>T p.T345I Substitution - Missense 16:23105496-23105496 - TCGA-AH-6544-01 COSM1563187 c.1017delC p.V340fs*27 Deletion - Frameshift 16:23105513-23105513 - PCSI_0208_Pa_P_526 COSM5031690 c.2262G>A p.T754T Substitution - coding silent 16:23073795-23073795 - ESO-732 COSM1270076 c.1702T>G p.L568V Substitution - Missense 16:23084988-23084988 - YUWIA COSM5384521 c.3188C>T p.P1063L Substitution - Missense 16:23068917-23068917 - TCGA-A5-A0VO-01 COSM264605 c.2261C>T p.T754M Substitution - Missense 16:23073796-23073796 - TCGA-D5-6928-01 COSM968684 c.3303G>A p.P1101P Substitution - coding silent 16:23068802-23068802 - T25 COSM3765874 c.354T>C p.A118A Substitution - coding silent 16:23148917-23148917 - GC8_T COSM148049 c.3272C>T p.A1091V Substitution - Missense 16:23068833-23068833 - TCGA-DU-8165-01 COSM3969458 c.2179T>C p.Y727H Substitution - Missense 16:23073878-23073878 - TCGA-AP-A0LM-01 COSM968688 c.3195A>C p.K1065N Substitution - Missense 16:23068910-23068910 - TCGA-EB-A3Y7-01 COSM3507731 c.2305C>T p.P769S Substitution - Missense 16:23073752-23073752 - HT115 COSM4257693 c.1735G>A p.D579N Substitution - Missense 16:23084955-23084955 - TCGA-G4-6298-01 COSM3690857 c.531C>T p.G177G Substitution - coding silent 16:23148740-23148740 - CLL090 COSM303529 c.1049G>T p.R350L Substitution - Missense 16:23105481-23105481 - sysucc-1370T COSM4059346 c.2626C>T p.R876C Substitution - Missense 16:23069479-23069479 - TCGA-AC-A23H-01 COSM3817552 c.2309C>T p.S770L Substitution - Missense 16:23073748-23073748 - TCGA-BS-A0UF-01 COSM968682 c.3305A>C p.K1102T Substitution - Missense 16:23068800-23068800 - MD-051 COSM303529 c.1049G>T p.R350L Substitution - Missense 16:23105481-23105481 - CSCC-42-T COSM4486215 c.3024C>T p.A1008A Substitution - coding silent 16:23069081-23069081 - TCGA-EE-A3AE-06 COSM3507735 c.937C>T p.P313S Substitution - Missense 16:23106229-23106229 - TCGA-60-2711-01 COSM703009 c.3971C>T p.P1324L Substitution - Missense 16:23068134-23068134 - Pat_26_A COSM5850480 c.2072C>T p.P691L Substitution - Missense 16:23080050-23080050 - 2492722 COSM5722420 c.3087C>T p.S1029S Substitution - coding silent 16:23069018-23069018 - TCGA-B5-A11E-01 COSM968709 c.1547G>A p.R516H Substitution - Missense 16:23087167-23087167 - HCT15 COSM1678927 c.2742C>A p.S914R Substitution - Missense 16:23069363-23069363 - C086 COSM5541484 c.3328C>T p.P1110S Substitution - Missense 16:23068777-23068777 - TCGA-30-1891-01 COSM117815 c.2569G>A p.A857T Substitution - Missense 16:23069536-23069536 - TCGA-D7-6528-01 COSM4059341 c.3181C>G p.P1061A Substitution - Missense 16:23068924-23068924 - GHE0624 COSM5714372 c.2420C>G p.S807C Substitution - Missense 16:23072113-23072113 - TCGA-EB-A299-01 COSM3507732 c.2278C>T p.L760F Substitution - Missense 16:23073779-23073779 - YUMOOK COSM1708945 c.2083C>T p.P695S Substitution - Missense 16:23080039-23080039 - TCGA-EE-A20F-06 COSM109260 c.3536C>T p.P1179L Substitution - Missense 16:23068569-23068569 - TCGA-EP-A2KA-01 COSM4917446 c.2967C>A p.I989I Substitution - coding silent 16:23069138-23069138 - TCGA-BR-4368-01 COSM4059349 c.2099G>T p.R700M Substitution - Missense 16:23080023-23080023 - TCGA-EE-A2GI-06 COSM3507726 c.2880C>T p.S960S Substitution - coding silent 16:23069225-23069225 - TCGA-BR-7707-01 COSM4059344 c.2853C>T p.D951D Substitution - coding silent 16:23069252-23069252 - HCC137T COSM1609099 c.1870C>T p.Q624* Substitution - Nonsense 16:23082518-23082518 - TCGA-AG-A002-01 COSM264605 c.2261C>T p.T754M Substitution - Missense 16:23073796-23073796 - B104-0 COSM1756916 c.3345G>T p.Q1115H Substitution - Missense 16:23068760-23068760 - J90_T COSM3957337 c.736C>T p.H246Y Substitution - Missense 16:23108081-23108081 - ESCC_BICR_033T COSM5439705 c.1911G>T p.L637L Substitution - coding silent 16:23082477-23082477 - TCGA-A5-A0GI-01 COSM968701 c.2195_2196delTG p.V732fs*9 Deletion - Frameshift 16:23073861-23073862 - TCGA-FW-A3R5-06 COSM3888206 c.2660C>T p.S887L Substitution - Missense 16:23069445-23069445 - TCGA-BC-A3KF-01 COSM4927801 c.893A>G p.Q298R Substitution - Missense 16:23106273-23106273 - TCGA-E2-A14X-01 COSM434914 c.981A>G p.Q327Q Substitution - coding silent 16:23105549-23105549 - PD11326a COSM417106 c.1049G>C p.R350P Substitution - Missense 16:23105481-23105481 - TCGA-B5-A11E-01 COSM968707 c.2042G>A p.S681N Substitution - Missense 16:23080080-23080080 - TCGA-FS-A4F0-06 COSM3507725 c.2898G>C p.Q966H Substitution - Missense 16:23069207-23069207 - TCGA-BR-8680-01 COSM4059339 c.3258G>A p.R1086R Substitution - coding silent 16:23068847-23068847 - I2L-P19Tb-Tumor-Organoid COSM5363488 c.2003G>T p.G668V Substitution - Missense 16:23080119-23080119 - TCGA-C5-A7UC-01 COSM270528 c.1546C>T p.R516C Substitution - Missense 16:23087168-23087168 - TCGA-HU-A4GU-01 COSM4059345 c.2712T>C p.D904D Substitution - coding silent 16:23069393-23069393 - TCGA-EI-6514-01 COSM3420862 c.1865G>T p.C622F Substitution - Missense 16:23082523-23082523 - CRC-06T COSM5456531 c.2886C>T p.V962V Substitution - coding silent 16:23069219-23069219 - TCGA-04-1343-01 COSM81894 c.3294G>A p.E1098E Substitution - coding silent 16:23068811-23068811 - SNUH_G45_S1 COSM3999798 c.1333G>T p.D445Y Substitution - Missense 16:23090706-23090706 - 60 COSM5735182 c.1852C>G p.R618G Substitution - Missense 16:23082536-23082536 - ESO-147 COSM1270075 c.442A>G p.N148D Substitution - Missense 16:23148829-23148829 - Pa36X COSM84335 c.2717A>G p.K906R Substitution - Missense 16:23069388-23069388 - TCGA-G4-6628-01 COSM1376762 c.3422C>A p.P1141H Substitution - Missense 16:23068683-23068683 - TCGA-AA-3558-01 COSM292481 c.3319G>A p.V1107M Substitution - Missense 16:23068786-23068786 - TCGA-DK-A3X1-01 COSM3794694 c.732C>G p.L244L Substitution - coding silent 16:23108085-23108085 - TCGA-43-5668-01 COSM703008 c.3865G>T p.G1289* Substitution - Nonsense 16:23068240-23068240 - 113803 COSM95454 c.2699G>C p.G900A Substitution - Missense 16:23069406-23069406 - TCGA-EA-A44S-01 COSM384619 c.3613C>T p.R1205C Substitution - Missense 16:23068492-23068492 - CSCC-55-T COSM3507719 c.3961C>T p.P1321S Substitution - Missense 16:23068144-23068144 - sysucc-1370T COSM5470466 c.2858C>T p.S953L Substitution - Missense 16:23069247-23069247 - TCGA-G2-A2EO-01 COSM1301748 c.1796C>T p.S599F Substitution - Missense 16:23084894-23084894 - MB_Exm987 COSM215638 c.1751G>A p.R584H Substitution - Missense 16:23084939-23084939 - TCGA-DA-A3F8-06 COSM3507729 c.2570C>T p.A857V Substitution - Missense 16:23069535-23069535 - TCGA-G9-6343-01 COSM3672190 c.2382G>T p.P794P Substitution - coding silent 16:23072151-23072151 - AOCS-158-1-6 COSM3948385 c.3324A>G p.S1108S Substitution - coding silent 16:23068781-23068781 - SC_9022 COSM5550601 c.2438C>A p.A813E Substitution - Missense 16:23072095-23072095 - TCGA-E2-A14T-01 COSM215638 c.1751G>A p.R584H Substitution - Missense 16:23084939-23084939 - 8057783 COSM3387304 c.1932T>C p.H644H Substitution - coding silent 16:23082456-23082456 - 4000_T COSM3957335 c.1951-1G>T p.? Unknown 16:23080172-23080172 - 449 COSM4435408 c.1195C>A p.P399T Substitution - Missense 16:23102358-23102358 - HCC066T COSM5821543 c.460G>T p.E154* Substitution - Nonsense 16:23148811-23148811 - Gp2D COSM3279371 c.2055G>A p.L685L Substitution - coding silent 16:23080067-23080067 - B104-0-Tumor COSM1756916 c.3345G>T p.Q1115H Substitution - Missense 16:23068760-23068760 - TCGA-BR-6566-01 COSM4059343 c.2933C>T p.P978L Substitution - Missense 16:23069172-23069172 - CHEWS031 COSM4578831 c.1758A>G p.Q586Q Substitution - coding silent 16:23084932-23084932 - BD124T COSM5493404 c.1849T>C p.W617R Substitution - Missense 16:23082539-23082539 - 1N58-VS-1T58 COSM4977492 c.1415G>A p.R472K Substitution - Missense 16:23090624-23090624 - TCGA-CG-5726-01 COSM4059355 c.667G>A p.G223R Substitution - Missense 16:23108150-23108150 - TCGA-CD-A4MG-01 COSM4059335 c.3731T>G p.L1244R Substitution - Missense 16:23068374-23068374 - BD72T COSM5513173 c.2860G>A p.D954N Substitution - Missense 16:23069245-23069245 - TCGA-BR-8680-01 COSM3279380 c.1951G>T p.E651* Substitution - Nonsense 16:23080171-23080171 - TCGA-DK-A1A7-01 COSM417106 c.1049G>C p.R350P Substitution - Missense 16:23105481-23105481 - TCGA-HU-8602-01 COSM4059353 c.1289G>A p.R430K Substitution - Missense 16:23090750-23090750 - SJRHB012_S COSM3737388 c.2770G>A p.E924K Substitution - Missense 16:23069335-23069335 - HCT8 COSM1678927 c.2742C>A p.S914R Substitution - Missense 16:23069363-23069363 - TCGA-AP-A0LM-01 COSM968696 c.2661G>A p.S887S Substitution - coding silent 16:23069444-23069444 - PT37 COSM5921062 c.3317C>T p.S1106F Substitution - Missense 16:23068788-23068788 - TCGA-AA-A010-01 COSM183325 c.1171G>A p.D391N Substitution - Missense 16:23102382-23102382 - 12-P412 COSM4578830 c.2328G>A p.S776S Substitution - coding silent 16:23073729-23073729 - PT33 COSM5909546 c.4016C>T p.S1339F Substitution - Missense 16:23068089-23068089 - YUDEDE COSM1708944 c.2701G>A p.E901K Substitution - Missense 16:23069404-23069404 - TCGA-BR-6452-01 COSM4059338 c.3507C>T p.S1169S Substitution - coding silent 16:23068598-23068598 - LUAD-S01302 COSM395592 c.3179C>T p.S1060F Substitution - Missense 16:23068926-23068926 - 2492721 COSM5722421 c.2177-9C>T p.? Unknown 16:23073889-23073889 - EGC15 COSM5054747 c.2900G>A p.S967N Substitution - Missense 16:23069205-23069205 - TCGA-E5-A2PC-01 COSM1301747 c.2348C>T p.S783F Substitution - Missense 16:23072185-23072185 - TCGA-DD-A39Z-01 COSM4915883 c.1914T>C p.P638P Substitution - coding silent 16:23082474-23082474 - TCGA-A6-6653-01 COSM1376760 c.4034C>T p.A1345V Substitution - Missense 16:23068071-23068071 - 2492723 COSM5722421 c.2177-9C>T p.? Unknown 16:23073889-23073889 - BD183T COSM5508164 c.1087C>T p.Q363* Substitution - Nonsense 16:23105443-23105443 - sysucc-1370T COSM5470467 c.1921C>G p.L641V Substitution - Missense 16:23082467-23082467 - PCSI_0090_Pa_X COSM3377831 c.1634C>T p.S545F Substitution - Missense 16:23085651-23085651 - 587284 COSM1232024 c.2671A>C p.S891R Substitution - Missense 16:23069434-23069434 - J73_T COSM3957336 c.1787G>C p.C596S Substitution - Missense 16:23084903-23084903 - 9210_T COSM5038684 c.1037_1043delTCGCCAG p.V346fs*19 Deletion - Frameshift 16:23105487-23105493 - 2334192 COSM316406 c.3758A>C p.K1253T Substitution - Missense 16:23068347-23068347 - TCGA-AA-3511-01 COSM1376763 c.2617C>T p.L873L Substitution - coding silent 16:23069488-23069488 - COLO201 COSM1678926 c.2782A>T p.S928C Substitution - Missense 16:23069323-23069323 - TCGA-EE-A3AF-06 COSM3507737 c.813C>T p.F271F Substitution - coding silent 16:23106446-23106446 - TCGA-FW-A3R5-06 COSM3888207 c.2351C>T p.S784F Substitution - Missense 16:23072182-23072182 - 91112 COSM330326 c.1539C>G p.F513L Substitution - Missense 16:23087175-23087175 - TCGA-BR-6452-01 COSM1678925 c.3118C>T p.R1040W Substitution - Missense 16:23068987-23068987 - SJRHB012 COSM3737388 c.2770G>A p.E924K Substitution - Missense 16:23069335-23069335 - LUAD-RT-S01832 COSM384619 c.3613C>T p.R1205C Substitution - Missense 16:23068492-23068492 - LUAD_E01047 COSM390098 c.4045C>G p.Q1349E Substitution - Missense 16:23068060-23068060 - TCGA-CG-5723-01 COSM4059348 c.2167C>T p.H723Y Substitution - Missense 16:23079955-23079955 - 86748 COSM95455 c.2487T>A p.D829E Substitution - Missense 16:23072046-23072046 - TCGA-AA-A010-01 COSM286395 c.3850A>C p.N1284H Substitution - Missense 16:23068255-23068255 - Gp5D COSM3279371 c.2055G>A p.L685L Substitution - coding silent 16:23080067-23080067 - TCGA-AC-A62Y-01 COSM3817551 c.2380C>T p.P794S Substitution - Missense 16:23072153-23072153 - TCGA-A5-A0VP-01 COSM968703 c.2113T>C p.Y705H Substitution - Missense 16:23080009-23080009 - 234 COSM3731174 c.3763G>A p.G1255S Substitution - Missense 16:23068342-23068342 - TCGA-BS-A0UM-01 COSM968684 c.3303G>A p.P1101P Substitution - coding silent 16:23068802-23068802 - CSCC-11-T COSM4535608 c.2207G>A p.W736* Substitution - Nonsense 16:23073850-23073850 - ESCC-D7 COSM5046427 c.2020C>T p.H674Y Substitution - Missense 16:23080102-23080102 - 86507 COSM95456 c.1681G>T p.D561Y Substitution - Missense 16:23085604-23085604 - DLD1 COSM4623271 c.2557A>G p.T853A Substitution - Missense 16:23069548-23069548 - TCGA-AC-A23H-01 COSM3817549 c.2597C>T p.S866L Substitution - Missense 16:23069508-23069508 - TCGA-HU-A4GQ-01 COSM4059342 c.2986G>A p.D996N Substitution - Missense 16:23069119-23069119 - TCGA-D8-A1XK-01 COSM3817554 c.786T>G p.T262T Substitution - coding silent 16:23106473-23106473 - TCGA-A6-6141-01 COSM1376765 c.724G>T p.E242* Substitution - Nonsense 16:23108093-23108093 - TCGA-D1-A17Q-01 COSM968680 c.3808G>A p.E1270K Substitution - Missense 16:23068297-23068297 - C608 COSM4442757 c.3715C>T p.R1239W Substitution - Missense 16:23068390-23068390 - HCC137 COSM1609099 c.1870C>T p.Q624* Substitution - Nonsense 16:23082518-23082518 - SNUH_G76_S1 COSM4419537 c.1613T>C p.I538T Substitution - Missense 16:23087101-23087101 - Pat_70_A COSM5850481 c.1060T>A p.S354T Substitution - Missense 16:23105470-23105470 - TCGA-EE-A2MJ-06 COSM3507733 c.1818C>T p.T606T Substitution - coding silent 16:23084872-23084872 - 2521243 COSM5886938 c.3266C>T p.S1089F Substitution - Missense 16:23068839-23068839 - 8066437 COSM3772169 c.1767T>C p.R589R Substitution - coding silent 16:23084923-23084923 - BD166T COSM5494646 c.2662C>T p.P888S Substitution - Missense 16:23069443-23069443 - XHDG39 COSM4770010 c.459C>G p.A153A Substitution - coding silent 16:23148812-23148812 - tumor_4160100 COSM5949257 c.1966A>C p.M656L Substitution - Missense 16:23080156-23080156 - PT19_2 COSM5900332 c.2177-1G>A p.? Unknown 16:23073881-23073881 - PD9761a COSM5776103 c.1984G>A p.V662I Substitution - Missense 16:23080138-23080138 - sysucc-311T COSM5479061 c.1622+7A>C p.? Unknown 16:23087085-23087085 - TCGA-BR-6452-01 COSM4059337 c.3623G>T p.S1208I Substitution - Missense 16:23068482-23068482 - CHC517T COSM3765874 c.354T>C p.A118A Substitution - coding silent 16:23148917-23148917 - CSCC-52-T COSM4477063 c.2118C>T p.I706I Substitution - coding silent 16:23080004-23080004 - PR-03-870 COSM248243 c.962A>C p.Y321S Substitution - Missense 16:23105568-23105568 - TCGA-EB-A1NK-01 COSM3507727 c.2756C>T p.S919F Substitution - Missense 16:23069349-23069349 - TCGA-D3-A51R-06 COSM3507722 c.3208C>T p.P1070S Substitution - Missense 16:23068897-23068897 - Pat_70_B COSM5850481 c.1060T>A p.S354T Substitution - Missense 16:23105470-23105470 - 2492723 COSM5722420 c.3087C>T p.S1029S Substitution - coding silent 16:23069018-23069018 - TCGA-BR-8591-01 COSM4059347 c.2176+1G>A p.? Unknown 16:23079945-23079945 - TCGA-JW-A5VL-01 COSM4847495 c.716G>T p.R239L Substitution - Missense 16:23108101-23108101 - 60T COSM109260 c.3536C>T p.P1179L Substitution - Missense 16:23068569-23068569 - TCGA-FU-A3HZ-01 COSM4839613 c.838G>T p.E280* Substitution - Nonsense 16:23106421-23106421 - PD6728b COSM5795314 c.22G>C p.G8R Substitution - Missense 16:23149249-23149249 - LAU149 COSM235551 c.2967C>T p.I989I Substitution - coding silent 16:23069138-23069138 - TCGA-HT-7620-01 COSM3969457 c.2867G>A p.R956H Substitution - Missense 16:23069238-23069238 - C0050T COSM4151270 c.1234+2T>A p.? Unknown 16:23102317-23102317 - 1115153 COSM5558595 c.428T>G p.L143R Substitution - Missense 16:23148843-23148843 - YURAY COSM5384520 c.3237T>A p.S1079S Substitution - coding silent 16:23068868-23068868 - PCSI_0504_Pa_P_526 COSM3507737 c.813C>T p.F271F Substitution - coding silent 16:23106446-23106446 - 587234 COSM270528 c.1546C>T p.R516C Substitution - Missense 16:23087168-23087168 - TCGA-A8-A06Y-01 COSM434912 c.2254G>T p.V752F Substitution - Missense 16:23073803-23073803 - TCGA-AP-A0LT-01 COSM968686 c.3224G>A p.S1075N Substitution - Missense 16:23068881-23068881 - U2940 COSM5622119 c.3388G>A p.A1130T Substitution - Missense 16:23068717-23068717 - KYSE110 COSM5049500 c.2755T>C p.S919P Substitution - Missense 16:23069350-23069350 - STC297 COSM5054748 c.2139C>T p.C713C Substitution - coding silent 16:23079983-23079983 - ESCC_140 COSM1629831 c.438C>T p.L146L Substitution - coding silent 16:23148833-23148833 - P112 COSM1735895 c.772-3delT p.? Unknown 16:23106490-23106490 - 8015271 COSM3387304 c.1932T>C p.H644H Substitution - coding silent 16:23082456-23082456 - 2492720 COSM5722421 c.2177-9C>T p.? Unknown 16:23073889-23073889 - LUAD-B02515 COSM336057 c.1355G>T p.G452V Substitution - Missense 16:23090684-23090684 - B47-Tumor COSM1756917 c.2854G>A p.E952K Substitution - Missense 16:23069251-23069251 - RMS80_ COSM4988759 c.3961C>A p.P1321T Substitution - Missense 16:23068144-23068144 - TCGA-AM-5821-01 COSM3754799 c.2792G>T p.R931L Substitution - Missense 16:23069313-23069313 - CCRF-CEM COSM1678928 c.2375G>A p.R792Q Substitution - Missense 16:23072158-23072158 - TCGA-AA-A01D-01 COSM301515 c.3291_3292GG>AT p.E1098* Substitution - Nonsense 16:23068813-23068814 - S02352 COSM5695296 c.327G>C p.P109P Substitution - coding silent 16:23148944-23148944 - LUAD-NYU330 COSM373791 c.2669A>G p.H890R Substitution - Missense 16:23069436-23069436 - TCGA-60-2711-01 COSM703007 c.3437A>G p.K1146R Substitution - Missense 16:23068668-23068668 - T25 COSM5342726 c.155C>T p.P52L Substitution - Missense 16:23149116-23149116 - 2_PRE-TREATMENT COSM1722930 c.2564C>T p.P855L Substitution - Missense 16:23069541-23069541 - AOCS-147-1-1 COSM3948384 c.3917T>A p.L1306Q Substitution - Missense 16:23068188-23068188 - TCGA-HJ-7597-01 COSM4059340 c.3248G>A p.G1083D Substitution - Missense 16:23068857-23068857 - YUHAMA COSM5384522 c.3172C>T p.P1058S Substitution - Missense 16:23068933-23068933 - TCGA-AA-A00N-01 COSM215638 c.1751G>A p.R584H Substitution - Missense 16:23084939-23084939 - CSCC-19-T COSM4476866 c.2103C>T p.D701D Substitution - coding silent 16:23080019-23080019 - HCT15 COSM3279334 c.3409G>A p.A1137T Substitution - Missense 16:23068696-23068696 - sysucc-311T COSM3690856 c.1147G>A p.D383N Substitution - Missense 16:23102406-23102406 - CSCC-11-T COSM4515194 c.1094_1095TG>GT p.V365G Substitution - Missense 16:23102458-23102459 - 2492720 COSM5722420 c.3087C>T p.S1029S Substitution - coding silent 16:23069018-23069018 - Detroit_562 COSM3279372 c.2045G>C p.S682T Substitution - Missense 16:23080077-23080077 - TCGA-AP-A0LM-01 COSM968698 c.2460G>T p.E820D Substitution - Missense 16:23072073-23072073 - sysucc-311T COSM235551 c.2967C>T p.I989I Substitution - coding silent 16:23069138-23069138 - ccRCC-86 COSM1664918 c.3572G>T p.G1191V Substitution - Missense 16:23068533-23068533 - 0024_CRUK_PC_0024_T1_DNA COSM5422520 c.3215G>A p.R1072H Substitution - Missense 16:23068890-23068890 - TCGA-KK-A59V-01 COSM4878328 c.3214C>T p.R1072C Substitution - Missense 16:23068891-23068891 - 8035543 COSM3387305 c.1750C>T p.R584C Substitution - Missense 16:23084940-23084940 - HCC145T COSM3706942 c.2601G>A p.W867* Substitution - Nonsense 16:23069504-23069504 - PD9193a COSM5792448 c.1708G>A p.V570I Substitution - Missense 16:23084982-23084982 - 234 COSM3730544 c.459C>A p.A153A Substitution - coding silent 16:23148812-23148812 - YUWAND COSM95457 c.721C>T p.H241Y Substitution - Missense 16:23108096-23108096 - DLD1 COSM1678927 c.2742C>A p.S914R Substitution - Missense 16:23069363-23069363 - TCGA-EB-A3XB-01 COSM3507720 c.3533C>T p.S1178F Substitution - Missense 16:23068572-23068572 - TCGA-AP-A059-01 COSM968694 c.2859G>A p.S953S Substitution - coding silent 16:23069246-23069246 - B47 COSM1756917 c.2854G>A p.E952K Substitution - Missense 16:23069251-23069251 - TCGA-FW-A3R5-06 COSM3888204 c.3596C>T p.S1199F Substitution - Missense 16:23068509-23068509 - TCGA-Q1-A73O-01 COSM4835662 c.994C>T p.H332Y Substitution - Missense 16:23105536-23105536 - TCGA-UB-A7MB-01 COSM4931649 c.2842G>T p.V948L Substitution - Missense 16:23069263-23069263 - TCGA-10-0934-01 COSM73229 c.3871G>A p.E1291K Substitution - Missense 16:23068234-23068234 - NCI-H2126 COSM24328 c.2306C>T p.P769L Substitution - Missense 16:23073751-23073751 - HCC132 COSM1609098 c.3257G>A p.R1086Q Substitution - Missense 16:23068848-23068848 - PTC-50C COSM3765874 c.354T>C p.A118A Substitution - coding silent 16:23148917-23148917 - 2492721 COSM5722420 c.3087C>T p.S1029S Substitution - coding silent 16:23069018-23069018 - pfg043T COSM4751199 c.2186A>C p.K729T Substitution - Missense 16:23073871-23073871 - TCGA-EB-A431-01 COSM3507723 c.3200C>T p.S1067F Substitution - Missense 16:23068905-23068905 - TCGA-EI-7002-01 COSM3420861 c.1994C>A p.P665H Substitution - Missense 16:23080128-23080128 - CSCC-11-T COSM968684 c.3303G>A p.P1101P Substitution - coding silent 16:23068802-23068802 - RKO COSM3279361 c.2365T>C p.W789R Substitution - Missense 16:23072168-23072168 - PD6367a COSM1637425 c.3750C>T p.L1250L Substitution - coding silent 16:23068355-23068355 - 587290 COSM1232026 c.436C>G p.L146V Substitution - Missense 16:23148835-23148835 - ESCC-078T COSM703009 c.3971C>T p.P1324L Substitution - Missense 16:23068134-23068134 - PD10052a COSM3718968 c.3974G>A p.G1325D Substitution - Missense 16:23068131-23068131 - TCGA-BS-A0UV-01 COSM968690 c.3060G>T p.E1020D Substitution - Missense 16:23069045-23069045 - SA214 COSM212237 c.1304C>T p.T435I Substitution - Missense 16:23090735-23090735 - AOCS-001-1-7 COSM3948386 c.1084G>A p.D362N Substitution - Missense 16:23105446-23105446 - PD4266a COSM5784938 c.3722C>T p.S1241L Substitution - Missense 16:23068383-23068383 - 8064559 COSM3387304 c.1932T>C p.H644H Substitution - coding silent 16:23082456-23082456 - C0050T COSM4151271 c.1234+1G>C p.? Unknown 16:23102318-23102318 - 951_T COSM3957334 c.3147G>C p.Q1049H Substitution - Missense 16:23068958-23068958 - YUOMEGA COSM5384523 c.2280C>T p.L760L Substitution - coding silent 16:23073777-23073777 - PTC-14C COSM4128820 c.2317G>T p.A773S Substitution - Missense 16:23073740-23073740 - H1672 COSM316406 c.3758A>C p.K1253T Substitution - Missense 16:23068347-23068347 - TCGA-A3-3374-01 COSM1493572 c.3323C>T p.S1108L Substitution - Missense 16:23068782-23068782 - TCGA-EE-A181-06 COSM3507724 c.2930C>T p.P977L Substitution - Missense 16:23069175-23069175 - T45458580 COSM5715372 c.1078C>A p.P360T Substitution - Missense 16:23105452-23105452 - T1 COSM5617694 c.535G>A p.G179S Substitution - Missense 16:23148736-23148736 - T2269 COSM4739758 c.2227G>A p.D743N Substitution - Missense 16:23073830-23073830 - TCGA-EE-A2MR-06 COSM1609098 c.3257G>A p.R1086Q Substitution - Missense 16:23068848-23068848 - TCGA-AM-5820-01 COSM3754798 c.3925C>T p.R1309C Substitution - Missense 16:23068180-23068180 - COLO205 COSM1678926 c.2782A>T p.S928C Substitution - Missense 16:23069323-23069323 - SCMC_RM2_ COSM3279335 c.3407C>T p.P1136L Substitution - Missense 16:23068698-23068698 - CSCC-16-T COSM4516767 c.2291_2292GG>AA p.R764K Substitution - Missense 16:23073765-23073766 - TCGA-EE-A3JD-06 COSM4396059 c.3467G>A p.R1156K Substitution - Missense 16:23068638-23068638 - TCGA-AA-3715-01 COSM270528 c.1546C>T p.R516C Substitution - Missense 16:23087168-23087168 - T84 COSM3279333 c.3424T>A p.F1142I Substitution - Missense 16:23068681-23068681 - 103452 COSM95457 c.721C>T p.H241Y Substitution - Missense 16:23108096-23108096 - TCGA-EE-A29H-06 COSM3507736 c.910C>T p.P304S Substitution - Missense 16:23106256-23106256 - TCGA-AP-A051-01 COSM968715 c.653C>T p.A218V Substitution - Missense 16:23108164-23108164 - 587342 COSM1232025 c.3290A>G p.K1097R Substitution - Missense 16:23068815-23068815 - 387 COSM4427261 c.3451G>C p.D1151H Substitution - Missense 16:23068654-23068654 - TCGA-BR-4184-01 COSM4059336 c.3719G>A p.R1240H Substitution - Missense 16:23068386-23068386 - TCGA-D3-A51J-06 COSM3507734 c.1525C>T p.Q509* Substitution - Nonsense 16:23087726-23087726 - T2272 COSM4739757 c.2688_2689delGG p.K898fs*7 Deletion - Frameshift 16:23069416-23069417 - 2492722 COSM5722421 c.2177-9C>T p.? Unknown 16:23073889-23073889 - TCGA-BG-A18B-01 COSM968692 c.2992G>A p.V998I Substitution - Missense 16:23069113-23069113 - T40 COSM5342727 c.110G>C p.G37A Substitution - Missense 16:23149161-23149161 - TCGA-DI-A0WH-01 COSM968705 c.2061G>A p.S687S Substitution - coding silent 16:23080061-23080061 - UACC-257 COSM1678925 c.3118C>T p.R1040W Substitution - Missense 16:23068987-23068987 - 8031668 COSM3387306 c.771+6G>A p.? Unknown 16:23108040-23108040 - CSCC-18-T COSM4484301 c.2793C>T p.R931R Substitution - coding silent 16:23069312-23069312 - TCGA-EP-A2KA-01 COSM4917420 c.2170T>C p.Y724H Substitution - Missense 16:23079952-23079952 - TCGA-BR-7707-01 COSM4059346 c.2626C>T p.R876C Substitution - Missense 16:23069479-23069479 - HCT-15 COSM1678927 c.2742C>A p.S914R Substitution - Missense 16:23069363-23069363 - CSCC-18-T COSM3507720 c.3533C>T p.S1178F Substitution - Missense 16:23068572-23068572 - SJACT069_D COSM4968312 c.2713G>A p.D905N Substitution - Missense 16:23069392-23069392 - LUAD-D02185 COSM338526 c.2200G>T p.G734C Substitution - Missense 16:23073857-23073857 - TCGA-AG-A002-01 COSM264604 c.3765T>G p.G1255G Substitution - coding silent 16:23068340-23068340 - SJRHB012_R COSM3737388 c.2770G>A p.E924K Substitution - Missense 16:23069335-23069335 - TCGA-EE-A2MR-06 COSM3507721 c.3332C>T p.S1111L Substitution - Missense 16:23068773-23068773 - HCC132T COSM1609098 c.3257G>A p.R1086Q Substitution - Missense 16:23068848-23068848 - TCGA-FW-A3R5-06 COSM3888208 c.915C>T p.F305F Substitution - coding silent 16:23106251-23106251 - T3094 COSM4739760 c.1766G>A p.R589H Substitution - Missense 16:23084924-23084924 - TCGA-EE-A29D-06 COSM3507730 c.2454C>T p.S818S Substitution - coding silent 16:23072079-23072079 - TCGA-BR-8382-01 COSM4059350 c.1985T>A p.V662D Substitution - Missense 16:23080137-23080137 - 2_RESISTANT COSM1722930 c.2564C>T p.P855L Substitution - Missense 16:23069541-23069541 - TCGA-BQ-5890-01 COSM3988342 c.2430C>A p.T810T Substitution - coding silent 16:23072103-23072103 - CHC2052T COSM4790013 c.1037T>C p.V346A Substitution - Missense 16:23105493-23105493 - TCGA-AN-A046-01 COSM3817550 c.2504G>A p.R835Q Substitution - Missense 16:23069601-23069601 - 99815 COSM95453 c.3356C>T p.S1119L Substitution - Missense 16:23068749-23068749 - sysucc-1397T COSM5473714 c.3715C>A p.R1239R Substitution - coding silent 16:23068390-23068390 - 1346 COSM1645114 c.2341A>G p.T781A Substitution - Missense 16:23072192-23072192 - T1154 COSM1678925 c.3118C>T p.R1040W Substitution - Missense 16:23068987-23068987 - TCGA-BC-A112-01 COSM4936453 c.1831C>G p.L611V Substitution - Missense 16:23082557-23082557 - TCGA-HU-A4G8-01 COSM968696 c.2661G>A p.S887S Substitution - coding silent 16:23069444-23069444 - TCGA-AM-5820-01 COSM3690856 c.1147G>A p.D383N Substitution - Missense 16:23102406-23102406 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.183817 16p12.2

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer AA - Frameshift p.L1244Rfs*8 c.3731_3732delTT 16 23079694 CM A C Missense p.L568V c.1702T>G 16 23096309 ESCA A G Missense p.K906R c.2717A>G 16 23080709 PAAD A G Missense p.Y705H c.2113T>C 16 23091330 UCEC A G Missense p.Y727H c.2179T>C 16 23085199 LGG - A IntronicInsertion . c.1234+100dupT 16 23113540 ESCA CA - Frameshift p.V732Gfs*9 c.2195_2196delTG 16 23085182 UCEC C A Missense p.Q650H c.1950G>T 16 23093759 LUAD C A Missense p.R162L c.485G>T 16 23160107 LUAD C A Missense p.R350L c.1049G>T 16 23116802 CLL C A Missense p.R587M c.1760G>T 16 23096251 LUAD C A Missense p.R700M c.2099G>T 16 23091344 STAD C A Missense p.V752F c.2254G>T 16 23085124 BRCA C A Nonsense p.G1289* c.3865G>T 16 23079561 LUSC C A Synonymous p.P794P c.2382G>T 16 23083472 PRAD CC AT Missense p.E1098* c.3291_3292delinsAT 16 23080134 COREAD C G Missense p.D380H c.1138G>C 16 23113736 HNSC C G Missense p.R350P c.1049G>C 16 23116802 BLCA C G Synonymous p.G699G c.2097G>C 16 23091346 BRCA C G Synonymous p.L747L c.2241G>C 16 23085137 LUAD C T Missense p.A857T c.2569G>A 16 23080857 OV C T Missense p.D228N c.682G>A 16 23119456 UCEC C T Missense p.D454N c.1360G>A 16 23102000 UCEC C T Missense p.E1291K c.3871G>A 16 23079555 OV C T Missense p.E242K c.724G>A 16 23119414 LUAD C T Missense p.E588K c.1762G>A 16 23096249 CM C T Missense p.G223R c.667G>A 16 23119471 STAD C T Missense p.R1156K c.3467G>A 16 23079959 CM C T Missense p.R584H c.1751G>A 16 23096260 BRCA C T Missense p.R584H c.1751G>A 16 23096260 MB C T Missense p.R956H c.2867G>A 16 23080559 LGG C T Missense p.R975H c.2924G>A 16 23080502 LUAD C T Missense p.V1107M c.3319G>A 16 23080107 COREAD C T Missense p.V998I c.2992G>A 16 23080434 UCEC C T Synonymous p.E1098E c.3294G>A 16 23080132 OV C T Synonymous p.R694R c.2082G>A 16 23091361 CM C T Synonymous p.S887S c.2661G>A 16 23080765 CM G A IntronicSNV . c.2336-97C>T 16 23083615 CM G A Missense p.A857V c.2570C>T 16 23080856 CM G A Missense p.L760F c.2278C>T 16 23085100 CM G A Missense p.P1179L c.3536C>T 16 23079890 CM G A Missense p.P1321L c.3962C>T 16 23079464 CM G A Missense p.P1324L c.3971C>T 16 23079455 LUSC G A Missense p.P304S c.910C>T 16 23117577 CM G A Missense p.P313L c.938C>T 16 23117549 HNSC G A Missense p.P313S c.937C>T 16 23117550 CM G A Missense p.P977L c.2930C>T 16 23080496 CM G A Missense p.S309F c.926C>T 16 23117561 HNSC G A Missense p.S599F c.1796C>T 16 23096215 BLCA G A Missense p.S783F c.2348C>T 16 23083506 BLCA G A Missense p.S811F c.2432C>T 16 23083422 CM G A Missense p.S848F c.2543C>T 16 23080883 PRAD G A Missense p.S884L c.2651C>T 16 23080775 CM G A Missense p.S919F c.2756C>T 16 23080670 CM G A Missense p.T435I c.1304C>T 16 23102056 BRCA G A Missense p.T754M c.2261C>T 16 23085117 UCEC G A Synonymous p.F271F c.813C>T 16 23117767 CM G A Synonymous p.F567F c.1701C>T 16 23096310 MM G A Synonymous p.L146L c.438C>T 16 23160154 HC G A Synonymous p.L320L c.960C>T 16 23116891 HNSC G A Synonymous p.S960S c.2880C>T 16 23080546 CM G A Synonymous p.T606T c.1818C>T 16 23096193 CM G A Synonymous p.V346V c.1038C>T 16 23116813 STAD G C Missense p.H332D c.994C>G 16 23116857 HNSC G C Missense p.P1061A c.3181C>G 16 23080245 STAD G C Synonymous p.S1029S c.3087C>G 16 23080339 LUAD - G IntronicInsertion . c.2336-95dupC 16 23083613 COREAD - G IntronicInsertion . c.634-12485dupC 16 23131989 CM G T 3-UTRSNV . c.4056+5752C>A 16 23073618 HC G T Missense p.P1144H c.3431C>A 16 23079995 RCCC G T Missense p.T1022K c.3065C>A 16 23080361 STAD G T Synonymous p.R222R c.664C>A 16 23119474 CM T A Synonymous p.V998V c.2994A>T 16 23080432 LUAD T C Missense p.H429R c.1286A>G 16 23102074 COREAD T C Missense p.K1146R c.3437A>G 16 23079989 LUSC T C Missense p.N148D c.442A>G 16 23160150 ESCA T C Synonymous p.Q327Q c.981A>G 16 23116870 BRCA T - Frameshift p.F837Lfs*2 c.2508delA 16 23080918 PRAD T G Missense p.K1253T c.3758A>C 16 23079668 SCLC TTAAA - IntronicDeletion . c.633+13498_633+13502delTTTAA 16 23146457 CLL