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 3 47036641 47036641 + Silent SNP G G A TCGA-OR-A5J5-01A-11D-A29I-10 TCGA-OR-A5J5-10A-01D-A29L-10 g.chr3:47036641G>A c.1416G>A c.(1414-1416)gcG>gcA p.A472A ACC 3 47036675 47036675 + Missense_Mutation SNP G G T TCGA-OR-A5L9-01A-11D-A29I-10 TCGA-OR-A5L9-10B-01D-A29L-10 g.chr3:47036675G>T c.1450G>T c.(1450-1452)Gcc>Tcc p.A484S ACC 3 47041809 47041809 + Missense_Mutation SNP C C A TCGA-PK-A5HB-01A-11D-A29I-10 TCGA-PK-A5HB-11A-11D-A29L-10 g.chr3:47041809C>A c.4220C>A c.(4219-4221)tCc>tAc p.S1407Y ACC 3 47043602 47043602 + Missense_Mutation SNP G G A TCGA-PA-A5YG-01A-11D-A29I-10 TCGA-PA-A5YG-10A-01D-A29L-10 g.chr3:47043602G>A c.4975G>A c.(4975-4977)Gag>Aag p.E1659K BLCA 3 47031020 47031020 + Missense_Mutation SNP G G A TCGA-KQ-A41O-01A-12D-A34U-08 TCGA-KQ-A41O-10D-01D-A34X-08 g.chr3:47031020G>A c.493G>A c.(493-495)Gag>Aag p.E165K BLCA 3 47033343 47033343 + Missense_Mutation SNP G G A TCGA-DK-A6B6-01A-11D-A30E-08 TCGA-DK-A6B6-10A-01D-A30H-08 g.chr3:47033343G>A c.939G>A c.(937-939)atG>atA p.M313I BLCA 3 47036911 47036911 + Silent SNP C C T TCGA-KQ-A41S-01A-12D-A339-08 TCGA-KQ-A41S-10C-01D-A339-08 g.chr3:47036911C>T c.1686C>T c.(1684-1686)atC>atT p.I562I BLCA 3 47037250 47037250 + Missense_Mutation SNP G G A TCGA-ZF-AA4W-01A-12D-A38G-08 TCGA-ZF-AA4W-10A-01D-A38J-08 g.chr3:47037250G>A c.1945G>A c.(1945-1947)Gcc>Acc p.A649T BLCA 3 47040207 47040207 + Splice_Site SNP C C T TCGA-ZF-A9RC-01A-11D-A38G-08 TCGA-ZF-A9RC-10A-01D-A38J-08 g.chr3:47040207C>T c.3222C>T c.(3220-3222)agC>agT p.S1074S BLCA 3 47040469 47040469 + Silent SNP G G A TCGA-FJ-A3ZF-01A-11D-A23M-08 TCGA-FJ-A3ZF-10A-01D-A23K-08 g.chr3:47040469G>A c.3405G>A c.(3403-3405)ctG>ctA p.L1135L BLCA 3 47044008 47044008 + Nonsense_Mutation SNP C C T TCGA-KQ-A41O-01A-12D-A34U-08 TCGA-KQ-A41O-10D-01D-A34X-08 g.chr3:47044008C>T c.5299C>T c.(5299-5301)Cag>Tag p.Q1767* BLCA 3 47044731 47044731 + Silent SNP G G A TCGA-DK-A1A3-01A-11D-A13W-08 TCGA-DK-A1A3-10A-01D-A13W-08 g.chr3:47044731G>A c.5652G>A c.(5650-5652)gtG>gtA p.V1884V BLCA 3 47045403 47045403 + Missense_Mutation SNP G G A TCGA-UY-A9PH-01A-11D-A38G-08 TCGA-UY-A9PH-10A-01D-A38J-08 g.chr3:47045403G>A c.5818G>A c.(5818-5820)Gag>Aag p.E1940K BLCA 3 47045451 47045451 + Missense_Mutation SNP G G A TCGA-KQ-A41O-01A-12D-A34U-08 TCGA-KQ-A41O-10D-01D-A34X-08 g.chr3:47045451G>A c.5866G>A c.(5866-5868)Gtg>Atg p.V1956M BLCA 3 47045650 47045650 + Missense_Mutation SNP G G C TCGA-UY-A9PH-01A-11D-A38G-08 TCGA-UY-A9PH-10A-01D-A38J-08 g.chr3:47045650G>C c.5965G>C c.(5965-5967)Gag>Cag p.E1989Q BLCA 3 47045991 47045991 + Missense_Mutation SNP G G A TCGA-GD-A6C6-01A-21D-A31L-08 TCGA-GD-A6C6-10A-01D-A31J-08 g.chr3:47045991G>A c.6205G>A c.(6205-6207)Gta>Ata p.V2069I BLCA 3 47047473 47047473 + Missense_Mutation SNP T T C TCGA-E7-A541-01A-11D-A26M-08 TCGA-E7-A541-10A-01D-A26K-08 g.chr3:47047473T>C c.6839T>C c.(6838-6840)aTc>aCc p.I2280T BLCA 3 47049918 47049918 + Missense_Mutation SNP G G A TCGA-XF-AAMZ-01A-11D-A42E-08 TCGA-XF-AAMZ-10A-01D-A42H-08 g.chr3:47049918G>A c.7865G>A c.(7864-7866)cGt>cAt p.R2622H BLCA 3 47050035 47050035 + Missense_Mutation SNP C C T TCGA-2F-A9KO-01A-11D-A38G-08 TCGA-2F-A9KO-11A-12D-A38J-08 g.chr3:47050035C>T c.7904C>T c.(7903-7905)tCa>tTa p.S2635L BRCA 3 47033996 47033996 + Missense_Mutation SNP G G C TCGA-A8-A07C-01A-11D-A045-09 TCGA-A8-A07C-10A-01W-A055-09 g.chr3:47033996G>C c.1064G>C c.(1063-1065)gGg>gCg p.G355A BRCA 3 47036011 47036011 + Missense_Mutation SNP A A C TCGA-A2-A0T5-01A-21D-A099-09 TCGA-A2-A0T5-10A-01D-A099-09 g.chr3:47036011A>C c.1264A>C c.(1264-1266)Acc>Ccc p.T422P BRCA 3 47037780 47037780 + Missense_Mutation SNP T T C TCGA-E2-A1LA-01A-11D-A142-09 TCGA-E2-A1LA-10A-01D-A142-09 g.chr3:47037780T>C c.2171T>C c.(2170-2172)aTc>aCc p.I724T BRCA 3 47038822 47038822 + Missense_Mutation SNP A A G TCGA-C8-A26Y-01A-11D-A16D-09 TCGA-C8-A26Y-10A-01D-A16D-09 g.chr3:47038822A>G c.2723A>G c.(2722-2724)gAg>gGg p.E908G BRCA 3 47041682 47041682 + Missense_Mutation SNP G G C TCGA-A8-A08F-01A-11W-A019-09 TCGA-A8-A08F-10A-01W-A021-09 g.chr3:47041682G>C c.4093G>C c.(4093-4095)Gta>Cta p.V1365L BRCA 3 47043228 47043228 + Missense_Mutation SNP A A C TCGA-A2-A0T5-01A-21D-A099-09 TCGA-A2-A0T5-10A-01D-A099-09 g.chr3:47043228A>C c.4694A>C c.(4693-4695)cAc>cCc p.H1565P BRCA 3 47045357 47045357 + Silent SNP C C T TCGA-A8-A097-01A-11W-A050-09 TCGA-A8-A097-10A-01D-A047-09 g.chr3:47045357C>T c.5772C>T c.(5770-5772)gcC>gcT p.A1924A BRCA 3 47045770 47045770 + Missense_Mutation SNP A A C TCGA-A8-A0A6-01A-12W-A071-09 TCGA-A8-A0A6-10A-01W-A071-09 g.chr3:47045770A>C c.6085A>C c.(6085-6087)Acc>Ccc p.T2029P BRCA 3 47045824 47045824 + Nonsense_Mutation SNP C C T TCGA-EW-A1PB-01A-11D-A142-09 TCGA-EW-A1PB-10A-01D-A142-09 g.chr3:47045824C>T c.6139C>T c.(6139-6141)Caa>Taa p.Q2047* BRCA 3 47045885 47045885 + Splice_Site SNP T T G TCGA-A2-A0T6-01A-11D-A099-09 TCGA-A2-A0T6-10A-01D-A099-09 g.chr3:47045885T>G c.e37+2 BRCA 3 47047285 47047285 + Missense_Mutation SNP C C A TCGA-BH-A0W7-01A-11D-A10Y-09 TCGA-BH-A0W7-10A-01D-A110-09 g.chr3:47047285C>A c.6749C>A c.(6748-6750)cCc>cAc p.P2250H BRCA 3 47047309 47047310 + Frame_Shift_Ins INS - - G TCGA-A8-A086-01A-11W-A019-09 TCGA-A8-A086-10A-01W-A021-09 g.chr3:47047309_47047310insG c.6773_6774insG c.(6772-6777)gacttcfs p.DF2258fs BRCA 3 47049023 47049023 + Missense_Mutation SNP G G A TCGA-AC-A3W7-01A-11D-A228-09 TCGA-AC-A3W7-10A-01D-A22A-09 g.chr3:47049023G>A c.7343G>A c.(7342-7344)cGa>cAa p.R2448Q CESC 3 47030778 47030778 + Missense_Mutation SNP G G A TCGA-EK-A2RK-01A-11D-A18J-09 TCGA-EK-A2RK-10A-01D-A18J-09 g.chr3:47030778G>A c.380G>A c.(379-381)cGa>cAa p.R127Q CESC 3 47033349 47033349 + Silent SNP G G T TCGA-Q1-A73O-01A-11D-A32I-09 TCGA-Q1-A73O-10B-01D-A32I-09 g.chr3:47033349G>T c.945G>T c.(943-945)ctG>ctT p.L315L CESC 3 47037080 47037080 + Missense_Mutation SNP A A G TCGA-C5-A7CG-01A-11D-A32I-09 TCGA-C5-A7CG-10A-01D-A32I-09 g.chr3:47037080A>G c.1855A>G c.(1855-1857)Acc>Gcc p.T619A CESC 3 47039707 47039707 + Missense_Mutation SNP G G T TCGA-EK-A2PL-01A-11D-A18J-09 TCGA-EK-A2PL-10A-01D-A18J-09 g.chr3:47039707G>T c.3109G>T c.(3109-3111)Gtg>Ttg p.V1037L CESC 3 47041727 47041727 + Missense_Mutation SNP C C G TCGA-EK-A2H1-01A-11D-A17W-09 TCGA-EK-A2H1-10A-01D-A17W-09 g.chr3:47041727C>G c.4138C>G c.(4138-4140)Ctt>Gtt p.L1380V CESC 3 47042572 47042572 + Missense_Mutation SNP G G A TCGA-DR-A0ZM-01A-12D-A10S-08 TCGA-DR-A0ZM-10A-01D-A10S-08 g.chr3:47042572G>A c.4387G>A c.(4387-4389)Gag>Aag p.E1463K CESC 3 47043554 47043554 + Missense_Mutation SNP G G A TCGA-C5-A2LZ-01A-11D-A20U-09 TCGA-C5-A2LZ-10B-01D-A20U-09 g.chr3:47043554G>A c.4927G>A c.(4927-4929)Gat>Aat p.D1643N CESC 3 47045644 47045644 + Missense_Mutation SNP G G A TCGA-Q1-A73R-01A-11D-A33O-09 TCGA-Q1-A73R-10B-01D-A33O-09 g.chr3:47045644G>A c.5959G>A c.(5959-5961)Gca>Aca p.A1987T CESC 3 47047475 47047475 + Missense_Mutation SNP G G A TCGA-FU-A3HZ-01A-11D-A20U-09 TCGA-FU-A3HZ-10A-01D-A20U-09 g.chr3:47047475G>A c.6841G>A c.(6841-6843)Gac>Aac p.D2281N CESC 3 47049617 47049617 + Missense_Mutation SNP G G A TCGA-C5-A2LZ-01A-11D-A20U-09 TCGA-C5-A2LZ-10B-01D-A20U-09 g.chr3:47049617G>A c.7660G>A c.(7660-7662)Gct>Act p.A2554T CESC 3 47049909 47049909 + Missense_Mutation SNP C C T TCGA-LP-A4AU-01A-32D-A243-09 TCGA-LP-A4AU-10A-01D-A243-09 g.chr3:47049909C>T c.7856C>T c.(7855-7857)gCg>gTg p.A2619V COAD 3 47030358 47030358 + Missense_Mutation SNP C C T TCGA-AA-3994-01A-01W-1073-09 TCGA-AA-3994-10A-01W-1073-09 g.chr3:47030358C>T c.167C>T c.(166-168)cCg>cTg p.P56L COAD 3 47030775 47030775 + Missense_Mutation SNP G G A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr3:47030775G>A c.377G>A c.(376-378)gGc>gAc p.G126D COAD 3 47032926 47032926 + Missense_Mutation SNP T T C TCGA-D5-6930-01A-11D-1924-10 TCGA-D5-6930-10A-01D-1924-10 g.chr3:47032926T>C c.673T>C c.(673-675)Tct>Cct p.S225P COAD 3 47033395 47033395 + Missense_Mutation SNP A A G TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chr3:47033395A>G c.991A>G c.(991-993)Aat>Gat p.N331D COAD 3 47036645 47036645 + Missense_Mutation SNP C C T TCGA-AD-6964-01A-11D-1924-10 TCGA-AD-6964-10A-01D-1924-10 g.chr3:47036645C>T c.1420C>T c.(1420-1422)Cgc>Tgc p.R474C COAD 3 47037015 47037015 + Missense_Mutation SNP G G A TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr3:47037015G>A c.1790G>A c.(1789-1791)cGa>cAa p.R597Q COAD 3 47037427 47037427 + Silent SNP C C T TCGA-F4-6856-01A-11D-1924-10 TCGA-F4-6856-10A-01D-1924-10 g.chr3:47037427C>T c.2037C>T c.(2035-2037)tgC>tgT p.C679C COAD 3 47039707 47039707 + Missense_Mutation SNP G G A TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr3:47039707G>A c.3109G>A c.(3109-3111)Gtg>Atg p.V1037M COAD 3 47040272 47040272 + Missense_Mutation SNP T T C TCGA-AD-6901-01A-11D-1924-10 TCGA-AD-6901-10A-01D-1924-10 g.chr3:47040272T>C c.3287T>C c.(3286-3288)cTg>cCg p.L1096P COAD 3 47040312 47040312 + Silent SNP C C T TCGA-AA-A022-01A-21W-A096-10 TCGA-AA-A022-11A-11W-A096-10 g.chr3:47040312C>T c.3327C>T c.(3325-3327)gaC>gaT p.D1109D COAD 3 47040812 47040812 + Missense_Mutation SNP G G A TCGA-CK-5913-01A-11D-1650-10 TCGA-CK-5913-10A-01D-1650-10 g.chr3:47040812G>A c.3551G>A c.(3550-3552)cGc>cAc p.R1184H COAD 3 47041439 47041439 + Missense_Mutation SNP T T C TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr3:47041439T>C c.3850T>C c.(3850-3852)Tgg>Cgg p.W1284R COAD 3 47041622 47041622 + Frame_Shift_Del DEL T T - TCGA-AA-3672-01A-01W-0900-09 TCGA-AA-3672-10A-01W-0900-09 g.chr3:47041622delT c.4033delT c.(4033-4035)tttfs p.F1345fs COAD 3 47041759 47041759 + Silent SNP G G A TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr3:47041759G>A c.4170G>A c.(4168-4170)tcG>tcA p.S1390S COAD 3 47042540 47042540 + Missense_Mutation SNP C C T TCGA-AA-A01R-01A-21W-A096-10 TCGA-AA-A01R-11A-12W-A096-10 g.chr3:47042540C>T c.4355C>T c.(4354-4356)tCg>tTg p.S1452L COAD 3 47043178 47043178 + Splice_Site SNP G G T TCGA-AA-3815-01A-01W-0995-10 TCGA-AA-3815-10A-01W-0995-10 g.chr3:47043178G>T c.e30-1 COAD 3 47043264 47043264 + Missense_Mutation SNP C C T TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chr3:47043264C>T c.4730C>T c.(4729-4731)gCg>gTg p.A1577V COAD 3 47043759 47043759 + Missense_Mutation SNP G G A TCGA-A6-6780-01A-11D-1835-10 TCGA-A6-6780-10A-01D-1835-10 g.chr3:47043759G>A c.5132G>A c.(5131-5133)cGc>cAc p.R1711H COAD 3 47045584 47045584 + Missense_Mutation SNP C C T TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr3:47045584C>T c.5899C>T c.(5899-5901)Cgg>Tgg p.R1967W COAD 3 47046044 47046044 + Silent SNP G G A TCGA-AA-3949-01A-01W-0995-10 TCGA-AA-3949-10A-01W-0995-10 g.chr3:47046044G>A c.6258G>A c.(6256-6258)gcG>gcA p.A2086A COAD 3 47048573 47048573 + Silent SNP A A G TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr3:47048573A>G c.7152A>G c.(7150-7152)gtA>gtG p.V2384V COAD 3 47048602 47048602 + Missense_Mutation SNP G G A TCGA-AA-3877-01A-01W-0995-10 TCGA-AA-3877-10A-01W-0995-10 g.chr3:47048602G>A c.7181G>A c.(7180-7182)cGg>cAg p.R2394Q COAD 3 47049804 47049804 + Missense_Mutation SNP G G A TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr3:47049804G>A c.7751G>A c.(7750-7752)cGc>cAc p.R2584H COADREAD 3 47030195 47030195 + Missense_Mutation SNP T T G TCGA-AG-A011-01A-01W-A00K-09 TCGA-AG-A011-10A-01W-A00K-09 g.chr3:47030195T>G c.88T>G c.(88-90)Ttt>Gtt p.F30V COADREAD 3 47030358 47030358 + Missense_Mutation SNP C C T TCGA-AA-3994-01A-01W-1073-09 TCGA-AA-3994-10A-01W-1073-09 g.chr3:47030358C>T c.167C>T c.(166-168)cCg>cTg p.P56L COADREAD 3 47030775 47030775 + Missense_Mutation SNP G G A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr3:47030775G>A c.377G>A c.(376-378)gGc>gAc p.G126D COADREAD 3 47032926 47032926 + Missense_Mutation SNP T T C TCGA-D5-6930-01A-11D-1924-10 TCGA-D5-6930-10A-01D-1924-10 g.chr3:47032926T>C c.673T>C c.(673-675)Tct>Cct p.S225P COADREAD 3 47033395 47033395 + Missense_Mutation SNP A A G TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chr3:47033395A>G c.991A>G c.(991-993)Aat>Gat p.N331D COADREAD 3 47036645 47036645 + Missense_Mutation SNP C C T TCGA-AD-6964-01A-11D-1924-10 TCGA-AD-6964-10A-01D-1924-10 g.chr3:47036645C>T c.1420C>T c.(1420-1422)Cgc>Tgc p.R474C COADREAD 3 47037015 47037015 + Missense_Mutation SNP G G A TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr3:47037015G>A c.1790G>A c.(1789-1791)cGa>cAa p.R597Q COADREAD 3 47037427 47037427 + Silent SNP C C T TCGA-F4-6856-01A-11D-1924-10 TCGA-F4-6856-10A-01D-1924-10 g.chr3:47037427C>T c.2037C>T c.(2035-2037)tgC>tgT p.C679C COADREAD 3 47039707 47039707 + Missense_Mutation SNP G G A TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr3:47039707G>A c.3109G>A c.(3109-3111)Gtg>Atg p.V1037M COADREAD 3 47039977 47039977 + Missense_Mutation SNP T T A TCGA-AG-A036-01A-12W-A096-10 TCGA-AG-A036-11A-11W-A096-10 g.chr3:47039977T>A c.3143T>A c.(3142-3144)aTa>aAa p.I1048K COADREAD 3 47040272 47040272 + Missense_Mutation SNP T T C TCGA-AD-6901-01A-11D-1924-10 TCGA-AD-6901-10A-01D-1924-10 g.chr3:47040272T>C c.3287T>C c.(3286-3288)cTg>cCg p.L1096P COADREAD 3 47040312 47040312 + Silent SNP C C T TCGA-AA-A022-01A-21W-A096-10 TCGA-AA-A022-11A-11W-A096-10 g.chr3:47040312C>T c.3327C>T c.(3325-3327)gaC>gaT p.D1109D COADREAD 3 47040812 47040812 + Missense_Mutation SNP G G A TCGA-CK-5913-01A-11D-1650-10 TCGA-CK-5913-10A-01D-1650-10 g.chr3:47040812G>A c.3551G>A c.(3550-3552)cGc>cAc p.R1184H COADREAD 3 47041439 47041439 + Missense_Mutation SNP T T C TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr3:47041439T>C c.3850T>C c.(3850-3852)Tgg>Cgg p.W1284R COADREAD 3 47041622 47041622 + Frame_Shift_Del DEL T T - TCGA-AA-3672-01A-01W-0900-09 TCGA-AA-3672-10A-01W-0900-09 g.chr3:47041622delT c.4033delT c.(4033-4035)tttfs p.F1345fs COADREAD 3 47041759 47041759 + Silent SNP G G A TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr3:47041759G>A c.4170G>A c.(4168-4170)tcG>tcA p.S1390S COADREAD 3 47042529 47042529 + Silent SNP C C T TCGA-CI-6624-01C-11D-1826-10 TCGA-CI-6624-10A-01D-1826-10 g.chr3:47042529C>T c.4344C>T c.(4342-4344)aaC>aaT p.N1448N COADREAD 3 47042540 47042540 + Missense_Mutation SNP C C T TCGA-AA-A01R-01A-21W-A096-10 TCGA-AA-A01R-11A-12W-A096-10 g.chr3:47042540C>T c.4355C>T c.(4354-4356)tCg>tTg p.S1452L COADREAD 3 47042866 47042866 + Missense_Mutation SNP C C T TCGA-AG-A02N-01A-11W-A096-10 TCGA-AG-A02N-11A-11W-A096-10 g.chr3:47042866C>T c.4582C>T c.(4582-4584)Cgt>Tgt p.R1528C COADREAD 3 47043178 47043178 + Splice_Site SNP G G T TCGA-AA-3815-01A-01W-0995-10 TCGA-AA-3815-10A-01W-0995-10 g.chr3:47043178G>T c.e30-1 COADREAD 3 47043264 47043264 + Missense_Mutation SNP C C T TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chr3:47043264C>T c.4730C>T c.(4729-4731)gCg>gTg p.A1577V COADREAD 3 47043759 47043759 + Missense_Mutation SNP G G A TCGA-A6-6780-01A-11D-1835-10 TCGA-A6-6780-10A-01D-1835-10 g.chr3:47043759G>A c.5132G>A c.(5131-5133)cGc>cAc p.R1711H COADREAD 3 47045584 47045584 + Missense_Mutation SNP C C T TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr3:47045584C>T c.5899C>T c.(5899-5901)Cgg>Tgg p.R1967W COADREAD 3 47046044 47046044 + Silent SNP G G A TCGA-AA-3949-01A-01W-0995-10 TCGA-AA-3949-10A-01W-0995-10 g.chr3:47046044G>A c.6258G>A c.(6256-6258)gcG>gcA p.A2086A COADREAD 3 47048573 47048573 + Silent SNP A A G TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr3:47048573A>G c.7152A>G c.(7150-7152)gtA>gtG p.V2384V COADREAD 3 47048602 47048602 + Missense_Mutation SNP G G A TCGA-AA-3877-01A-01W-0995-10 TCGA-AA-3877-10A-01W-0995-10 g.chr3:47048602G>A c.7181G>A c.(7180-7182)cGg>cAg p.R2394Q COADREAD 3 47049804 47049804 + Missense_Mutation SNP G G A TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr3:47049804G>A c.7751G>A c.(7750-7752)cGc>cAc p.R2584H DLBC 3 47033970 47033970 + Silent SNP C C T TCGA-G8-6907-01A-11D-2210-10 TCGA-G8-6907-14A-01D-2210-10 g.chr3:47033970C>T c.1038C>T c.(1036-1038)taC>taT p.Y346Y DLBC 3 47046485 47046485 + Silent SNP C C T TCGA-GR-7351-01A-11D-2210-10 TCGA-GR-7351-10A-01D-2210-10 g.chr3:47046485C>T c.6318C>T c.(6316-6318)taC>taT p.Y2106Y ESCA 3 47033032 47033032 + Missense_Mutation SNP T T C TCGA-L5-A8NM-01A-11D-A37C-09 TCGA-L5-A8NM-11A-12D-A37F-09 g.chr3:47033032T>C c.779T>C c.(778-780)gTc>gCc p.V260A ESCA 3 47036669 47036669 + Missense_Mutation SNP T T C TCGA-2H-A9GM-01A-11D-A37C-09 TCGA-2H-A9GM-11A-11D-A37F-09 g.chr3:47036669T>C c.1444T>C c.(1444-1446)Tgc>Cgc p.C482R ESCA 3 47037271 47037271 + Missense_Mutation SNP G G T TCGA-L5-A43C-01A-11D-A247-09 TCGA-L5-A43C-11A-11D-A247-09 g.chr3:47037271G>T c.1966G>T c.(1966-1968)Gtg>Ttg p.V656L ESCA 3 47039969 47039969 + Missense_Mutation SNP G G T TCGA-LN-A49L-01A-11D-A247-09 TCGA-LN-A49L-10A-01D-A247-09 g.chr3:47039969G>T c.3135G>T c.(3133-3135)atG>atT p.M1045I ESCA 3 47040003 47040003 + Missense_Mutation SNP C C T TCGA-L5-A8NM-01A-11D-A37C-09 TCGA-L5-A8NM-11A-12D-A37F-09 g.chr3:47040003C>T c.3169C>T c.(3169-3171)Cgg>Tgg p.R1057W ESCA 3 47040460 47040460 + Silent SNP G G A TCGA-L5-A4OW-01A-11D-A28B-09 TCGA-L5-A4OW-11A-11D-A28E-09 g.chr3:47040460G>A c.3396G>A c.(3394-3396)gcG>gcA p.A1132A ESCA 3 47041439 47041439 + Missense_Mutation SNP T T A TCGA-L5-A4OI-01A-11D-A27G-09 TCGA-L5-A4OI-11A-11D-A27G-09 g.chr3:47041439T>A c.3850T>A c.(3850-3852)Tgg>Agg p.W1284R ESCA 3 47044496 47044496 + Missense_Mutation SNP C C T TCGA-LN-A7HY-01A-12D-A351-09 TCGA-LN-A7HY-10A-01D-A351-09 g.chr3:47044496C>T c.5509C>T c.(5509-5511)Cgc>Tgc p.R1837C ESCA 3 47044771 47044771 + Missense_Mutation SNP G G A TCGA-L5-A4ON-01A-11D-A27G-09 TCGA-L5-A4ON-11A-21D-A27G-09 g.chr3:47044771G>A c.5692G>A c.(5692-5694)Gag>Aag p.E1898K ESCA 3 47045639 47045639 + Missense_Mutation SNP G G T TCGA-V5-AASV-01A-11D-A387-09 TCGA-V5-AASV-10A-01D-A38A-09 g.chr3:47045639G>T c.5954G>T c.(5953-5955)cGt>cTt p.R1985L ESCA 3 47049918 47049918 + Missense_Mutation SNP G G A TCGA-LN-A9FQ-01A-31D-A387-09 TCGA-LN-A9FQ-10A-01D-A38A-09 g.chr3:47049918G>A c.7865G>A c.(7864-7866)cGt>cAt p.R2622H GBM 3 47040042 47040042 + Missense_Mutation SNP C C T TCGA-06-5858-01A-01D-1696-08 TCGA-06-5858-10A-01D-1696-08 g.chr3:47040042C>T c.3208C>T c.(3208-3210)Cgc>Tgc p.R1070C GBM 3 47040321 47040321 + Silent SNP C C T TCGA-26-6173-01A-11D-1845-08 TCGA-26-6173-10A-01D-1845-08 g.chr3:47040321C>T c.3336C>T c.(3334-3336)gtC>gtT p.V1112V GBM 3 47041457 47041457 + Missense_Mutation SNP C C T TCGA-32-4211-01A-01D-1353-08 TCGA-32-4211-10A-01D-1353-08 g.chr3:47041457C>T c.3868C>T c.(3868-3870)Cgg>Tgg p.R1290W GBM 3 47041686 47041686 + Missense_Mutation SNP G G T TCGA-06-6697-01A-11D-1845-08 TCGA-06-6697-10A-01D-1845-08 g.chr3:47041686G>T c.4097G>T c.(4096-4098)gGa>gTa p.G1366V GBMLGG 3 47037063 47037063 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr3:47037063C>T c.1838C>T c.(1837-1839)cCt>cTt p.P613L GBMLGG 3 47038035 47038035 + Missense_Mutation SNP T T C TCGA-HT-7477-01B-11D-A289-08 TCGA-HT-7477-10A-01D-A289-08 g.chr3:47038035T>C c.2426T>C c.(2425-2427)tTt>tCt p.F809S GBMLGG 3 47040042 47040042 + Missense_Mutation SNP C C T TCGA-06-5858-01A-01D-1696-08 TCGA-06-5858-10A-01D-1696-08 g.chr3:47040042C>T c.3208C>T c.(3208-3210)Cgc>Tgc p.R1070C GBMLGG 3 47040321 47040321 + Silent SNP C C T TCGA-26-6173-01A-11D-1845-08 TCGA-26-6173-10A-01D-1845-08 g.chr3:47040321C>T c.3336C>T c.(3334-3336)gtC>gtT p.V1112V GBMLGG 3 47040555 47040555 + Frame_Shift_Del DEL C C - TCGA-E1-A7YJ-01A-11D-A34A-08 TCGA-E1-A7YJ-10A-01D-A34A-08 g.chr3:47040555delC c.3491delC c.(3490-3492)gccfs p.A1164fs GBMLGG 3 47041457 47041457 + Missense_Mutation SNP C C T TCGA-32-4211-01A-01D-1353-08 TCGA-32-4211-10A-01D-1353-08 g.chr3:47041457C>T c.3868C>T c.(3868-3870)Cgg>Tgg p.R1290W GBMLGG 3 47041457 47041457 + Missense_Mutation SNP C C T TCGA-DH-5144-01A-01D-1468-08 TCGA-DH-5144-10A-01D-1468-08 g.chr3:47041457C>T c.3868C>T c.(3868-3870)Cgg>Tgg p.R1290W GBMLGG 3 47041686 47041686 + Missense_Mutation SNP G G T TCGA-06-6697-01A-11D-1845-08 TCGA-06-6697-10A-01D-1845-08 g.chr3:47041686G>T c.4097G>T c.(4096-4098)gGa>gTa p.G1366V GBMLGG 3 47041884 47041884 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr3:47041884G>A c.4295G>A c.(4294-4296)aGc>aAc p.S1432N GBMLGG 3 47043273 47043273 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr3:47043273G>A c.4739G>A c.(4738-4740)gGc>gAc p.G1580D GBMLGG 3 47044503 47044503 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr3:47044503G>A c.5516G>A c.(5515-5517)cGt>cAt p.R1839H GBMLGG 3 47050155 47050155 + Missense_Mutation SNP A A G TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr3:47050155A>G c.8024A>G c.(8023-8025)aAc>aGc p.N2675S HNSC 3 47030591 47030591 + Missense_Mutation SNP G G C TCGA-CN-6011-01A-11D-1683-08 TCGA-CN-6011-10A-01D-1683-08 g.chr3:47030591G>C c.286G>C c.(286-288)Gag>Cag p.E96Q HNSC 3 47033992 47033992 + Missense_Mutation SNP G G A TCGA-CV-6936-01A-11D-1912-08 TCGA-CV-6936-10A-01D-1912-08 g.chr3:47033992G>A c.1060G>A c.(1060-1062)Gag>Aag p.E354K HNSC 3 47037517 47037517 + Silent SNP C C T TCGA-D6-6516-01A-11D-1870-08 TCGA-D6-6516-10A-01D-1870-08 g.chr3:47037517C>T c.2127C>T c.(2125-2127)ccC>ccT p.P709P HNSC 3 47037919 47037919 + Silent SNP C C T TCGA-CN-4730-01A-01D-1434-08 TCGA-CN-4730-10A-01D-1434-08 g.chr3:47037919C>T c.2310C>T c.(2308-2310)tcC>tcT p.S770S HNSC 3 47040353 47040353 + Missense_Mutation SNP C C T TCGA-QK-A6VB-01A-12D-A34J-08 TCGA-QK-A6VB-10B-01D-A34M-08 g.chr3:47040353C>T c.3368C>T c.(3367-3369)aCa>aTa p.T1123I HNSC 3 47041650 47041650 + Missense_Mutation SNP C C T TCGA-CV-7425-01A-11D-2078-08 TCGA-CV-7425-10A-01D-2078-08 g.chr3:47041650C>T c.4061C>T c.(4060-4062)aCg>aTg p.T1354M HNSC 3 47041666 47041666 + Silent SNP C C A TCGA-BA-A6DL-01A-21D-A30E-08 TCGA-BA-A6DL-10A-01D-A30H-08 g.chr3:47041666C>A c.4077C>A c.(4075-4077)ggC>ggA p.G1359G HNSC 3 47043455 47043455 + Missense_Mutation SNP G G A TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr3:47043455G>A c.4828G>A c.(4828-4830)Gca>Aca p.A1610T HNSC 3 47044464 47044464 + Missense_Mutation SNP G G A TCGA-CQ-5323-01A-01D-1683-08 TCGA-CQ-5323-10A-01D-1683-08 g.chr3:47044464G>A c.5477G>A c.(5476-5478)cGc>cAc p.R1826H HNSC 3 47045664 47045664 + Silent SNP C C T TCGA-CN-4723-01A-01D-1434-08 TCGA-CN-4723-10A-01D-1434-08 g.chr3:47045664C>T c.5979C>T c.(5977-5979)atC>atT p.I1993I HNSC 3 47049354 47049354 + Nonsense_Mutation SNP C C G TCGA-CR-7374-01A-11D-2012-08 TCGA-CR-7374-10A-01D-2013-08 g.chr3:47049354C>G c.7556C>G c.(7555-7557)tCa>tGa p.S2519* HNSC 3 47049787 47049787 + Missense_Mutation SNP C C G TCGA-CR-7374-01A-11D-2012-08 TCGA-CR-7374-10A-01D-2013-08 g.chr3:47049787C>G c.7734C>G c.(7732-7734)atC>atG p.I2578M KICH 3 47041771 47041771 + Silent SNP G G A TCGA-KM-8443-01A-11D-2310-10 TCGA-KM-8443-10A-01D-2311-10 g.chr3:47041771G>A c.4182G>A c.(4180-4182)ggG>ggA p.G1394G KICH 3 47042507 47042507 + Missense_Mutation SNP A A G TCGA-KN-8433-01A-11D-2310-10 TCGA-KN-8433-11A-01D-2311-10 g.chr3:47042507A>G c.4322A>G c.(4321-4323)gAg>gGg p.E1441G KIPAN 3 47032943 47032943 + Silent SNP G G T TCGA-BQ-5890-01A-11D-1589-08 TCGA-BQ-5890-11A-01D-1589-08 g.chr3:47032943G>T c.690G>T c.(688-690)ctG>ctT p.L230L KIPAN 3 47037324 47037324 + Silent SNP C C G TCGA-CZ-5458-01A-01D-1501-10 TCGA-CZ-5458-11A-01D-1501-10 g.chr3:47037324C>G c.2019C>G c.(2017-2019)gcC>gcG p.A673A KIPAN 3 47038048 47038048 + Silent SNP G G A TCGA-BP-4976-01A-01D-1462-08 TCGA-BP-4976-11A-01D-1462-08 g.chr3:47038048G>A c.2439G>A c.(2437-2439)ctG>ctA p.L813L KIPAN 3 47038846 47038846 + Missense_Mutation SNP C C T TCGA-Y8-A8RY-01A-11D-A36X-10 TCGA-Y8-A8RY-10A-01D-A370-10 g.chr3:47038846C>T c.2747C>T c.(2746-2748)aCg>aTg p.T916M KIPAN 3 47041771 47041771 + Silent SNP G G A TCGA-KM-8443-01A-11D-2310-10 TCGA-KM-8443-10A-01D-2311-10 g.chr3:47041771G>A c.4182G>A c.(4180-4182)ggG>ggA p.G1394G KIPAN 3 47042507 47042507 + Missense_Mutation SNP A A G TCGA-KN-8433-01A-11D-2310-10 TCGA-KN-8433-11A-01D-2311-10 g.chr3:47042507A>G c.4322A>G c.(4321-4323)gAg>gGg p.E1441G KIPAN 3 47043759 47043759 + Missense_Mutation SNP G G A TCGA-BP-4998-01A-01D-1462-08 TCGA-BP-4998-11A-01D-1462-08 g.chr3:47043759G>A c.5132G>A c.(5131-5133)cGc>cAc p.R1711H KIPAN 3 47049869 47049869 + Missense_Mutation SNP G G A TCGA-DZ-6133-01A-11D-1961-08 TCGA-DZ-6133-10A-01D-1962-08 g.chr3:47049869G>A c.7816G>A c.(7816-7818)Gca>Aca p.A2606T KIPAN 3 47050126 47050126 + Silent SNP C C A TCGA-BP-4158-01A-02D-1366-10 TCGA-BP-4158-11A-01D-1366-10 g.chr3:47050126C>A c.7995C>A c.(7993-7995)gcC>gcA p.A2665A KIRC 3 47037324 47037324 + Silent SNP C C G TCGA-CZ-5458-01A-01D-1501-10 TCGA-CZ-5458-11A-01D-1501-10 g.chr3:47037324C>G c.2019C>G c.(2017-2019)gcC>gcG p.A673A KIRC 3 47038048 47038048 + Silent SNP G G A TCGA-BP-4976-01A-01D-1462-08 TCGA-BP-4976-11A-01D-1462-08 g.chr3:47038048G>A c.2439G>A c.(2437-2439)ctG>ctA p.L813L KIRC 3 47043759 47043759 + Missense_Mutation SNP G G A TCGA-BP-4998-01A-01D-1462-08 TCGA-BP-4998-11A-01D-1462-08 g.chr3:47043759G>A c.5132G>A c.(5131-5133)cGc>cAc p.R1711H KIRC 3 47050126 47050126 + Silent SNP C C A TCGA-BP-4158-01A-02D-1366-10 TCGA-BP-4158-11A-01D-1366-10 g.chr3:47050126C>A c.7995C>A c.(7993-7995)gcC>gcA p.A2665A KIRP 3 47032943 47032943 + Silent SNP G G T TCGA-BQ-5890-01A-11D-1589-08 TCGA-BQ-5890-11A-01D-1589-08 g.chr3:47032943G>T c.690G>T c.(688-690)ctG>ctT p.L230L KIRP 3 47038846 47038846 + Missense_Mutation SNP C C T TCGA-Y8-A8RY-01A-11D-A36X-10 TCGA-Y8-A8RY-10A-01D-A370-10 g.chr3:47038846C>T c.2747C>T c.(2746-2748)aCg>aTg p.T916M KIRP 3 47049869 47049869 + Missense_Mutation SNP G G A TCGA-DZ-6133-01A-11D-1961-08 TCGA-DZ-6133-10A-01D-1962-08 g.chr3:47049869G>A c.7816G>A c.(7816-7818)Gca>Aca p.A2606T LGG 3 47037063 47037063 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr3:47037063C>T c.1838C>T c.(1837-1839)cCt>cTt p.P613L LGG 3 47038035 47038035 + Missense_Mutation SNP T T C TCGA-HT-7477-01B-11D-A289-08 TCGA-HT-7477-10A-01D-A289-08 g.chr3:47038035T>C c.2426T>C c.(2425-2427)tTt>tCt p.F809S LGG 3 47040555 47040555 + Frame_Shift_Del DEL C C - TCGA-E1-A7YJ-01A-11D-A34A-08 TCGA-E1-A7YJ-10A-01D-A34A-08 g.chr3:47040555delC c.3491delC c.(3490-3492)gccfs p.A1164fs LGG 3 47041457 47041457 + Missense_Mutation SNP C C T TCGA-DH-5144-01A-01D-1468-08 TCGA-DH-5144-10A-01D-1468-08 g.chr3:47041457C>T c.3868C>T c.(3868-3870)Cgg>Tgg p.R1290W LGG 3 47041884 47041884 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr3:47041884G>A c.4295G>A c.(4294-4296)aGc>aAc p.S1432N LGG 3 47043273 47043273 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr3:47043273G>A c.4739G>A c.(4738-4740)gGc>gAc p.G1580D LGG 3 47044503 47044503 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr3:47044503G>A c.5516G>A c.(5515-5517)cGt>cAt p.R1839H LGG 3 47050155 47050155 + Missense_Mutation SNP A A G TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr3:47050155A>G c.8024A>G c.(8023-8025)aAc>aGc p.N2675S LIHC 3 47030821 47030821 + Silent SNP C C G TCGA-BC-A217-01A-11D-A152-10 TCGA-BC-A217-10A-01D-A152-10 g.chr3:47030821C>G c.423C>G c.(421-423)ctC>ctG p.L141L LIHC 3 47037989 47037989 + Missense_Mutation SNP G G T TCGA-DD-A3A8-01A-11D-A22F-10 TCGA-DD-A3A8-11A-11D-A22F-10 g.chr3:47037989G>T c.2380G>T c.(2380-2382)Ggc>Tgc p.G794C LIHC 3 47040568 47040568 + Silent SNP G G T TCGA-ES-A2HT-01A-12D-A183-10 TCGA-ES-A2HT-11A-11D-A183-10 g.chr3:47040568G>T c.3504G>T c.(3502-3504)cgG>cgT p.R1168R LIHC 3 47042832 47042832 + Silent SNP G G T TCGA-CC-A7IH-01A-11D-A33K-10 TCGA-CC-A7IH-10A-01D-A33K-10 g.chr3:47042832G>T c.4548G>T c.(4546-4548)ctG>ctT p.L1516L LIHC 3 47043918 47043918 + Missense_Mutation SNP A A T TCGA-DD-A119-01A-11D-A12Z-10 TCGA-DD-A119-10A-01D-A12Z-10 g.chr3:47043918A>T c.5209A>T c.(5209-5211)Atg>Ttg p.M1737L LIHC 3 47043973 47043973 + Missense_Mutation SNP G G T TCGA-CC-A7IG-01A-11D-A33K-10 TCGA-CC-A7IG-10A-01D-A33K-10 g.chr3:47043973G>T c.5264G>T c.(5263-5265)cGc>cTc p.R1755L LIHC 3 47044767 47044767 + Silent SNP C C T TCGA-DD-AADS-01A-11D-A40R-10 TCGA-DD-AADS-10A-01D-A40U-10 g.chr3:47044767C>T c.5688C>T c.(5686-5688)ctC>ctT p.L1896L LIHC 3 47046023 47046023 + Missense_Mutation SNP G G T TCGA-EP-A2KA-01A-11D-A183-10 TCGA-EP-A2KA-10A-01D-A183-10 g.chr3:47046023G>T c.6237G>T c.(6235-6237)ttG>ttT p.L2079F LIHC 3 47046579 47046579 + Silent SNP A A C TCGA-2Y-A9GT-01A-11D-A382-10 TCGA-2Y-A9GT-10A-01D-A385-10 g.chr3:47046579A>C c.6412A>C c.(6412-6414)Agg>Cgg p.R2138R LIHC 3 47047032 47047032 + Missense_Mutation SNP G G T TCGA-4R-AA8I-01A-11D-A382-10 TCGA-4R-AA8I-10B-01D-A385-10 g.chr3:47047032G>T c.6614G>T c.(6613-6615)cGc>cTc p.R2205L LIHC 3 47049823 47049823 + Silent SNP A A G TCGA-WX-AA44-01A-11D-A38X-10 TCGA-WX-AA44-10A-01D-A38X-10 g.chr3:47049823A>G c.7770A>G c.(7768-7770)gcA>gcG p.A2590A LUAD 3 47030766 47030766 + Missense_Mutation SNP C C G TCGA-55-A490-01A-11D-A24D-08 TCGA-55-A490-10A-01D-A24F-08 g.chr3:47030766C>G c.368C>G c.(367-369)cCa>cGa p.P123R LUAD 3 47032756 47032756 + Missense_Mutation SNP C C T TCGA-67-4679-01B-01D-1753-08 TCGA-67-4679-10A-01D-1753-08 g.chr3:47032756C>T c.604C>T c.(604-606)Ctc>Ttc p.L202F LUAD 3 47037012 47037012 + Missense_Mutation SNP A A C TCGA-55-8089-01A-11D-2238-08 TCGA-55-8089-10A-01D-2238-08 g.chr3:47037012A>C c.1787A>C c.(1786-1788)cAg>cCg p.Q596P LUAD 3 47037035 47037035 + Missense_Mutation SNP A A T TCGA-86-A456-01A-11D-A24D-08 TCGA-86-A456-10A-01D-A24F-08 g.chr3:47037035A>T c.1810A>T c.(1810-1812)Acc>Tcc p.T604S LUAD 3 47037928 47037928 + Silent SNP G G T TCGA-55-8094-01A-11D-2238-08 TCGA-55-8094-10A-01D-2238-08 g.chr3:47037928G>T c.2319G>T c.(2317-2319)gtG>gtT p.V773V LUAD 3 47039673 47039673 + Silent SNP C C T TCGA-55-6972-01A-11D-1945-08 TCGA-55-6972-11A-01D-1945-08 g.chr3:47039673C>T c.3075C>T c.(3073-3075)ttC>ttT p.F1025F LUAD 3 47041640 47041640 + Missense_Mutation SNP C C G TCGA-91-8497-01A-11D-2393-08 TCGA-91-8497-10A-01D-2393-08 g.chr3:47041640C>G c.4051C>G c.(4051-4053)Cca>Gca p.P1351A LUAD 3 47042584 47042584 + Missense_Mutation SNP C C T TCGA-55-8620-01A-11D-2393-08 TCGA-55-8620-10A-01D-2393-08 g.chr3:47042584C>T c.4399C>T c.(4399-4401)Cgg>Tgg p.R1467W LUAD 3 47042821 47042821 + Missense_Mutation SNP G G A TCGA-55-7576-01A-11D-2063-08 TCGA-55-7576-10A-01D-2063-08 g.chr3:47042821G>A c.4537G>A c.(4537-4539)Gtg>Atg p.V1513M LUAD 3 47043987 47043987 + Missense_Mutation SNP G G T TCGA-05-4415-01A-22D-1855-08 TCGA-05-4415-10A-01D-1855-08 g.chr3:47043987G>T c.5278G>T c.(5278-5280)Gcc>Tcc p.A1760S LUAD 3 47044463 47044463 + Missense_Mutation SNP C C T TCGA-75-5126-01A-01D-1753-08 TCGA-75-5126-10A-01D-1753-08 g.chr3:47044463C>T c.5476C>T c.(5476-5478)Cgc>Tgc p.R1826C LUAD 3 47044544 47044544 + Nonsense_Mutation SNP G G T TCGA-95-7562-01A-11D-2238-08 TCGA-95-7562-10B-01D-2238-08 g.chr3:47044544G>T c.5557G>T c.(5557-5559)Gaa>Taa p.E1853* LUAD 3 47044777 47044777 + Missense_Mutation SNP G G A TCGA-05-5428-01A-01D-1625-08 TCGA-05-5428-10A-01D-1625-08 g.chr3:47044777G>A c.5698G>A c.(5698-5700)Gag>Aag p.E1900K LUAD 3 47047932 47047932 + Missense_Mutation SNP T T A TCGA-91-A4BC-01A-11D-A24D-08 TCGA-91-A4BC-10A-01D-A24F-08 g.chr3:47047932T>A c.7127T>A c.(7126-7128)tTc>tAc p.F2376Y LUSC 3 47030752 47030752 + Silent SNP G G T TCGA-18-3421-01A-01D-0983-08 TCGA-18-3421-11A-01D-0983-08 g.chr3:47030752G>T c.354G>T c.(352-354)ctG>ctT p.L118L LUSC 3 47037075 47037075 + Missense_Mutation SNP C C T TCGA-22-1016-01A-01D-1521-08 TCGA-22-1016-11A-01D-1521-08 g.chr3:47037075C>T c.1850C>T c.(1849-1851)gCa>gTa p.A617V LUSC 3 47043973 47043973 + Missense_Mutation SNP G G A TCGA-21-1076-01A-02D-1521-08 TCGA-21-1076-11A-01D-1521-08 g.chr3:47043973G>A c.5264G>A c.(5263-5265)cGc>cAc p.R1755H LUSC 3 47044477 47044477 + Silent SNP C C A TCGA-18-3409-01A-01D-0983-08 TCGA-18-3409-11A-01D-0983-08 g.chr3:47044477C>A c.5490C>A c.(5488-5490)tcC>tcA p.S1830S LUSC 3 47045732 47045732 + Missense_Mutation SNP A A G TCGA-22-4591-01A-01D-1267-08 TCGA-22-4591-11A-01D-1267-08 g.chr3:47045732A>G c.6047A>G c.(6046-6048)cAg>cGg p.Q2016R OV 3 47050489 47050489 + Missense_Mutation SNP G G A TCGA-24-1470-01A-01W-0553-09 TCGA-24-1470-10A-01W-0553-09 g.chr3:47050489G>A c.8038G>A c.(8038-8040)Gcc>Acc p.A2680T PAAD 3 47030423 47030423 + Missense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr3:47030423G>A c.232G>A c.(232-234)Gcc>Acc p.A78T PAAD 3 47040450 47040450 + Splice_Site SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr3:47040450C>T c.3386C>T c.(3385-3387)gCg>gTg p.A1129V PAAD 3 47041634 47041634 + Missense_Mutation SNP C C G TCGA-2J-AABK-01A-31D-A40W-08 TCGA-2J-AABK-10A-01D-A40W-08 g.chr3:47041634C>G c.4045C>G c.(4045-4047)Ctc>Gtc p.L1349V PAAD 3 47041693 47041693 + Silent SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr3:47041693C>T c.4104C>T c.(4102-4104)ggC>ggT p.G1368G PAAD 3 47042768 47042768 + Splice_Site SNP G G T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr3:47042768G>T c.e29-1 PAAD 3 47047546 47047546 + Silent SNP C C A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr3:47047546C>A c.6912C>A c.(6910-6912)acC>acA p.T2304T PAAD 3 47049628 47049628 + Silent SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr3:47049628C>T c.7671C>T c.(7669-7671)agC>agT p.S2557S PCPG 3 47041446 47041446 + Missense_Mutation SNP A A T TCGA-QR-A70R-01A-11D-A35D-08 TCGA-QR-A70R-10A-01D-A35B-08 g.chr3:47041446A>T c.3857A>T c.(3856-3858)gAt>gTt p.D1286V PCPG 3 47043265 47043265 + Silent SNP G G A TCGA-QT-A5XL-01A-11D-A35D-08 TCGA-QT-A5XL-10A-01D-A35B-08 g.chr3:47043265G>A c.4731G>A c.(4729-4731)gcG>gcA p.A1577A PRAD 3 47036899 47036899 + Silent SNP A A G TCGA-EJ-5507-01A-01D-1576-08 TCGA-EJ-5507-10A-01D-1577-08 g.chr3:47036899A>G c.1674A>G c.(1672-1674)gcA>gcG p.A558A PRAD 3 47037252 47037252 + Silent SNP C C T TCGA-XJ-A83H-01A-11D-A34U-08 TCGA-XJ-A83H-10A-01D-A34X-08 g.chr3:47037252C>T c.1947C>T c.(1945-1947)gcC>gcT p.A649A PRAD 3 47038461 47038461 + Silent SNP C C A TCGA-KK-A6E1-01A-11D-A30X-08 TCGA-KK-A6E1-11A-21D-A30X-08 g.chr3:47038461C>A c.2574C>A c.(2572-2574)atC>atA p.I858I PRAD 3 47041142 47041142 + Silent SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr3:47041142G>A c.3726G>A c.(3724-3726)ctG>ctA p.L1242L PRAD 3 47042568 47042568 + Silent SNP C C T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr3:47042568C>T c.4383C>T c.(4381-4383)agC>agT p.S1461S PRAD 3 47043455 47043455 + Missense_Mutation SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr3:47043455G>A c.4828G>A c.(4828-4830)Gca>Aca p.A1610T PRAD 3 47043892 47043892 + Missense_Mutation SNP A A G TCGA-EJ-5494-01A-01D-1576-08 TCGA-EJ-5494-10A-01D-1577-08 g.chr3:47043892A>G c.5183A>G c.(5182-5184)gAc>gGc p.D1728G PRAD 3 47047523 47047523 + Missense_Mutation SNP C C T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr3:47047523C>T c.6889C>T c.(6889-6891)Ctc>Ttc p.L2297F PRAD 3 47049635 47049635 + Missense_Mutation SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr3:47049635G>A c.7678G>A c.(7678-7680)Gcc>Acc p.A2560T PRAD 3 47049880 47049880 + Silent SNP C C T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr3:47049880C>T c.7827C>T c.(7825-7827)tcC>tcT p.S2609S READ 3 47030195 47030195 + Missense_Mutation SNP T T G TCGA-AG-A011-01A-01W-A00K-09 TCGA-AG-A011-10A-01W-A00K-09 g.chr3:47030195T>G c.88T>G c.(88-90)Ttt>Gtt p.F30V READ 3 47039977 47039977 + Missense_Mutation SNP T T A TCGA-AG-A036-01A-12W-A096-10 TCGA-AG-A036-11A-11W-A096-10 g.chr3:47039977T>A c.3143T>A c.(3142-3144)aTa>aAa p.I1048K READ 3 47042529 47042529 + Silent SNP C C T TCGA-CI-6624-01C-11D-1826-10 TCGA-CI-6624-10A-01D-1826-10 g.chr3:47042529C>T c.4344C>T c.(4342-4344)aaC>aaT p.N1448N READ 3 47042866 47042866 + Missense_Mutation SNP C C T TCGA-AG-A02N-01A-11W-A096-10 TCGA-AG-A02N-11A-11W-A096-10 g.chr3:47042866C>T c.4582C>T c.(4582-4584)Cgt>Tgt p.R1528C SARC 3 47045620 47045620 + Missense_Mutation SNP C C T TCGA-WP-A9GB-01A-11D-A37C-09 TCGA-WP-A9GB-10A-01D-A37F-09 g.chr3:47045620C>T c.5935C>T c.(5935-5937)Cgg>Tgg p.R1979W SARC 3 47047004 47047004 + Missense_Mutation SNP C C T TCGA-QC-A7B5-01A-11D-A33E-09 TCGA-QC-A7B5-11A-11D-A33H-09 g.chr3:47047004C>T c.6586C>T c.(6586-6588)Cac>Tac p.H2196Y SKCM 3 47030212 47030212 + Silent SNP G G A TCGA-EE-A29D-06A-11D-A197-08 TCGA-EE-A29D-10A-01D-A199-08 g.chr3:47030212G>A c.105G>A c.(103-105)aaG>aaA p.K35K SKCM 3 47030424 47030424 + Missense_Mutation SNP C C T TCGA-EE-A29D-06A-11D-A197-08 TCGA-EE-A29D-10A-01D-A199-08 g.chr3:47030424C>T c.233C>T c.(232-234)gCc>gTc p.A78V SKCM 3 47031040 47031040 + Silent SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr3:47031040C>T c.513C>T c.(511-513)ttC>ttT p.F171F SKCM 3 47033073 47033073 + Missense_Mutation SNP C C T TCGA-EE-A181-06A-11D-A196-08 TCGA-EE-A181-10A-01D-A198-08 g.chr3:47033073C>T c.820C>T c.(820-822)Cgt>Tgt p.R274C SKCM 3 47033334 47033334 + Silent SNP C C T TCGA-ER-A2NC-06A-11D-A197-08 TCGA-ER-A2NC-10A-01D-A199-08 g.chr3:47033334C>T c.930C>T c.(928-930)gcC>gcT p.A310A SKCM 3 47036849 47036849 + Nonsense_Mutation SNP G G T TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr3:47036849G>T c.1624G>T c.(1624-1626)Gga>Tga p.G542* SKCM 3 47036850 47036850 + Missense_Mutation SNP G G A TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr3:47036850G>A c.1625G>A c.(1624-1626)gGa>gAa p.G542E SKCM 3 47036851 47036851 + Silent SNP A A T TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr3:47036851A>T c.1626A>T c.(1624-1626)ggA>ggT p.G542G SKCM 3 47037099 47037099 + Missense_Mutation SNP C C T TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr3:47037099C>T c.1874C>T c.(1873-1875)cCa>cTa p.P625L SKCM 3 47037254 47037254 + Missense_Mutation SNP G G A TCGA-EE-A29M-06A-11D-A196-08 TCGA-EE-A29M-10A-01D-A198-08 g.chr3:47037254G>A c.1949G>A c.(1948-1950)gGg>gAg p.G650E SKCM 3 47038258 47038258 + Missense_Mutation SNP C C T TCGA-EE-A2MP-06A-11D-A197-08 TCGA-EE-A2MP-10A-01D-A199-08 g.chr3:47038258C>T c.2491C>T c.(2491-2493)Ccc>Tcc p.P831S SKCM 3 47039691 47039691 + Silent SNP C C T TCGA-GF-A3OT-06A-23D-A23B-08 TCGA-GF-A3OT-10A-01D-A23B-08 g.chr3:47039691C>T c.3093C>T c.(3091-3093)acC>acT p.T1031T SKCM 3 47039692 47039692 + Missense_Mutation SNP C C T TCGA-GF-A3OT-06A-23D-A23B-08 TCGA-GF-A3OT-10A-01D-A23B-08 g.chr3:47039692C>T c.3094C>T c.(3094-3096)Ctc>Ttc p.L1032F SKCM 3 47041163 47041163 + Silent SNP C C T TCGA-D3-A5GR-06A-11D-A27K-08 TCGA-D3-A5GR-10A-01D-A27N-08 g.chr3:47041163C>T c.3747C>T c.(3745-3747)tcC>tcT p.S1249S SKCM 3 47041164 47041164 + Missense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr3:47041164C>T c.3748C>T c.(3748-3750)Ctc>Ttc p.L1250F SKCM 3 47041551 47041551 + Missense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr3:47041551C>T c.3962C>T c.(3961-3963)cCc>cTc p.P1321L SKCM 3 47042819 47042819 + Missense_Mutation SNP C C T TCGA-EE-A3JA-06A-11D-A20D-08 TCGA-EE-A3JA-10A-01D-A20D-08 g.chr3:47042819C>T c.4535C>T c.(4534-4536)cCc>cTc p.P1512L SKCM 3 47042835 47042835 + Silent SNP C C T TCGA-EE-A2M5-06A-12D-A197-08 TCGA-EE-A2M5-10A-01D-A199-08 g.chr3:47042835C>T c.4551C>T c.(4549-4551)gcC>gcT p.A1517A SKCM 3 47043209 47043209 + Missense_Mutation SNP C C T TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr3:47043209C>T c.4675C>T c.(4675-4677)Cgc>Tgc p.R1559C SKCM 3 47043253 47043253 + Silent SNP C C T TCGA-GF-A6C9-06A-11D-A30X-08 TCGA-GF-A6C9-10A-01D-A30X-08 g.chr3:47043253C>T c.4719C>T c.(4717-4719)ctC>ctT p.L1573L SKCM 3 47043884 47043884 + Silent SNP C C T TCGA-D9-A1JW-06A-11D-A19A-08 TCGA-D9-A1JW-10A-01D-A19A-08 g.chr3:47043884C>T c.5175C>T c.(5173-5175)ttC>ttT p.F1725F SKCM 3 47043884 47043884 + Silent SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr3:47043884C>T c.5175C>T c.(5173-5175)ttC>ttT p.F1725F SKCM 3 47043969 47043969 + Missense_Mutation SNP C C T TCGA-EB-A44Q-06A-11D-A25O-08 TCGA-EB-A44Q-10A-01D-A25O-08 g.chr3:47043969C>T c.5260C>T c.(5260-5262)Cgg>Tgg p.R1754W SKCM 3 47044494 47044494 + Missense_Mutation SNP C C T TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr3:47044494C>T c.5507C>T c.(5506-5508)tCa>tTa p.S1836L SKCM 3 47045637 47045637 + Silent SNP C C T TCGA-D3-A5GN-06A-11D-A27K-08 TCGA-D3-A5GN-10A-01D-A27N-08 g.chr3:47045637C>T c.5952C>T c.(5950-5952)cgC>cgT p.R1984R SKCM 3 47045731 47045731 + Nonsense_Mutation SNP C C T TCGA-EE-A3AC-06A-11D-A196-08 TCGA-EE-A3AC-10A-01D-A198-08 g.chr3:47045731C>T c.6046C>T c.(6046-6048)Cag>Tag p.Q2016* SKCM 3 47045759 47045759 + Missense_Mutation SNP T T C TCGA-EB-A5UN-06A-11D-A30X-08 TCGA-EB-A5UN-10A-01D-A30X-08 g.chr3:47045759T>C c.6074T>C c.(6073-6075)aTc>aCc p.I2025T SKCM 3 47046037 47046037 + Missense_Mutation SNP C C T TCGA-D9-A3Z1-06A-11D-A23B-08 TCGA-D9-A3Z1-10A-01D-A23B-08 g.chr3:47046037C>T c.6251C>T c.(6250-6252)aCc>aTc p.T2084I SKCM 3 47046714 47046714 + Missense_Mutation SNP C C T TCGA-FS-A4FC-06A-11D-A24R-08 TCGA-FS-A4FC-10A-01D-A24R-08 g.chr3:47046714C>T c.6463C>T c.(6463-6465)Cac>Tac p.H2155Y SKCM 3 47047317 47047317 + Nonsense_Mutation SNP C C T TCGA-ER-A19W-06A-41D-A23B-08 TCGA-ER-A19W-10A-01D-A23B-08 g.chr3:47047317C>T c.6781C>T c.(6781-6783)Cag>Tag p.Q2261* SKCM 3 47049159 47049159 + Silent SNP G G A TCGA-FS-A1ZZ-06A-11D-A197-08 TCGA-FS-A1ZZ-10A-01D-A199-08 g.chr3:47049159G>A c.7479G>A c.(7477-7479)aaG>aaA p.K2493K SKCM 3 47049364 47049364 + Silent SNP G G A TCGA-D3-A3C3-06A-12D-A19A-08 TCGA-D3-A3C3-10A-01D-A19A-08 g.chr3:47049364G>A c.7566G>A c.(7564-7566)cgG>cgA p.R2522R SKCM 3 47049645 47049645 + Missense_Mutation SNP C C T TCGA-EE-A3J5-06A-11D-A20D-08 TCGA-EE-A3J5-10A-01D-A20D-08 g.chr3:47049645C>T c.7688C>T c.(7687-7689)aCt>aTt p.T2563I SKCM 3 47050061 47050061 + Silent SNP C C T TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr3:47050061C>T c.7930C>T c.(7930-7932)Ctg>Ttg p.L2644L SKCM 3 47050062 47050062 + Missense_Mutation SNP T T C TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr3:47050062T>C c.7931T>C c.(7930-7932)cTg>cCg p.L2644P

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation AML-US 3 47047872 47047872 single base substitution C T downstream_gene_variant AML-US 3 47047872 47047872 single base substitution C T missense_variant A1643V 4928C>T AML-US 3 47047872 47047872 single base substitution C T missense_variant A183V 548C>T AML-US 3 47047872 47047872 single base substitution C T missense_variant A2172V 6515C>T AML-US 3 47047872 47047872 single base substitution C T missense_variant A2356V 7067C>T AML-US 3 47047872 47047872 single base substitution C T missense_variant A635V 1904C>T AML-US 3 47047872 47047872 single base substitution C T missense_variant A724V 2171C>T AML-US 3 47047872 47047872 single base substitution C T upstream_gene_variant BLCA-US 3 47040469 47040469 single base substitution G A 5_prime_UTR_variant BLCA-US 3 47040469 47040469 single base substitution G A intron_variant BLCA-US 3 47040469 47040469 single base substitution G A synonymous_variant L1135L 3405G>A BLCA-US 3 47040469 47040469 single base substitution G A upstream_gene_variant BLCA-US 3 47044731 47044731 single base substitution G A downstream_gene_variant BLCA-US 3 47044731 47044731 single base substitution G A synonymous_variant V1171V 3513G>A BLCA-US 3 47044731 47044731 single base substitution G A synonymous_variant V163V 489G>A BLCA-US 3 47044731 47044731 single base substitution G A synonymous_variant V1700V 5100G>A BLCA-US 3 47044731 47044731 single base substitution G A synonymous_variant V1884V 5652G>A BLCA-US 3 47044731 47044731 single base substitution G A synonymous_variant V252V 756G>A BLCA-US 3 47044731 47044731 single base substitution G A upstream_gene_variant BOCA-FR 3 47033059 47033059 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant BOCA-FR 3 47033059 47033059 single base substitution G A missense_variant R269H 806G>A BOCA-FR 3 47033059 47033059 single base substitution G A upstream_gene_variant BRCA-EU 3 47018195 47018195 single base substitution G C upstream_gene_variant BRCA-EU 3 47019651 47019651 single base substitution G C upstream_gene_variant BRCA-EU 3 47020468 47020468 single base substitution G C upstream_gene_variant BRCA-EU 3 47022969 47022969 single base substitution G C intron_variant BRCA-EU 3 47023458 47023458 single base substitution G A intron_variant BRCA-EU 3 47025496 47025496 deletion of <=200bp A - intron_variant BRCA-EU 3 47025808 47025808 single base substitution A C intron_variant BRCA-EU 3 47025809 47025809 single base substitution C A intron_variant BRCA-EU 3 47026103 47026103 single base substitution C T intron_variant BRCA-EU 3 47026314 47026314 deletion of <=200bp G - intron_variant BRCA-EU 3 47026775 47026775 single base substitution G A intron_variant BRCA-EU 3 47027994 47027994 single base substitution A G intron_variant BRCA-EU 3 47029219 47029219 single base substitution G A intron_variant BRCA-EU 3 47029233 47029233 single base substitution G A intron_variant BRCA-EU 3 47031220 47031220 single base substitution G C intron_variant BRCA-EU 3 47032726 47032726 single base substitution G A 5_prime_UTR_variant BRCA-EU 3 47032726 47032726 single base substitution G A missense_variant D192N 574G>A BRCA-EU 3 47032726 47032726 single base substitution G A upstream_gene_variant BRCA-EU 3 47033805 47033805 single base substitution C T intron_variant BRCA-EU 3 47033805 47033805 single base substitution C T upstream_gene_variant BRCA-EU 3 47034319 47034319 single base substitution C G intron_variant BRCA-EU 3 47034319 47034319 single base substitution C G upstream_gene_variant BRCA-EU 3 47034657 47034657 single base substitution C T intron_variant BRCA-EU 3 47034657 47034657 single base substitution C T upstream_gene_variant BRCA-EU 3 47035229 47035229 single base substitution T A intron_variant BRCA-EU 3 47035229 47035229 single base substitution T A upstream_gene_variant BRCA-EU 3 47037081 47037081 single base substitution C T 5_prime_UTR_variant BRCA-EU 3 47037081 47037081 single base substitution C T missense_variant T619I 1856C>T BRCA-EU 3 47037081 47037081 single base substitution C T missense_variant T90I 269C>T BRCA-EU 3 47038165 47038165 single base substitution C G intron_variant BRCA-EU 3 47038165 47038165 single base substitution C G upstream_gene_variant BRCA-EU 3 47038249 47038249 single base substitution G A 5_prime_UTR_variant BRCA-EU 3 47038249 47038249 single base substitution G A missense_variant E299K 895G>A BRCA-EU 3 47038249 47038249 single base substitution G A missense_variant E828K 2482G>A BRCA-EU 3 47038249 47038249 single base substitution G A upstream_gene_variant BRCA-EU 3 47038467 47038467 single base substitution G A 5_prime_UTR_variant BRCA-EU 3 47038467 47038467 single base substitution G A synonymous_variant L331L 993G>A BRCA-EU 3 47038467 47038467 single base substitution G A synonymous_variant L860L 2580G>A BRCA-EU 3 47038467 47038467 single base substitution G A upstream_gene_variant BRCA-EU 3 47039295 47039295 single base substitution C G intron_variant BRCA-EU 3 47039295 47039295 single base substitution C G upstream_gene_variant BRCA-EU 3 47039329 47039329 single base substitution G A intron_variant BRCA-EU 3 47039329 47039329 single base substitution G A upstream_gene_variant BRCA-EU 3 47043426 47043426 single base substitution A G 5_prime_UTR_premature_start_codon_gain_variant BRCA-EU 3 47043426 47043426 single base substitution A G exon_variant BRCA-EU 3 47043426 47043426 single base substitution A G missense_variant Y1416C 4247A>G BRCA-EU 3 47043426 47043426 single base substitution A G missense_variant Y1600C 4799A>G BRCA-EU 3 47043426 47043426 single base substitution A G missense_variant Y887C 2660A>G BRCA-EU 3 47043426 47043426 single base substitution A G upstream_gene_variant BRCA-EU 3 47043519 47043519 single base substitution G A 5_prime_UTR_variant BRCA-EU 3 47043519 47043519 single base substitution G A downstream_gene_variant BRCA-EU 3 47043519 47043519 single base substitution G A missense_variant R1447Q 4340G>A BRCA-EU 3 47043519 47043519 single base substitution G A missense_variant R1631Q 4892G>A BRCA-EU 3 47043519 47043519 single base substitution G A missense_variant R918Q 2753G>A BRCA-EU 3 47043519 47043519 single base substitution G A upstream_gene_variant BRCA-EU 3 47043708 47043708 single base substitution G C 5_prime_UTR_variant BRCA-EU 3 47043708 47043708 single base substitution G C downstream_gene_variant BRCA-EU 3 47043708 47043708 single base substitution G C missense_variant S1510T 4529G>C BRCA-EU 3 47043708 47043708 single base substitution G C missense_variant S1694T 5081G>C BRCA-EU 3 47043708 47043708 single base substitution G C missense_variant S62T 185G>C BRCA-EU 3 47043708 47043708 single base substitution G C missense_variant S981T 2942G>C BRCA-EU 3 47043708 47043708 single base substitution G C upstream_gene_variant BRCA-EU 3 47044497 47044497 single base substitution G T downstream_gene_variant BRCA-EU 3 47044497 47044497 single base substitution G T missense_variant R1124L 3371G>T BRCA-EU 3 47044497 47044497 single base substitution G T missense_variant R116L 347G>T BRCA-EU 3 47044497 47044497 single base substitution G T missense_variant R1653L 4958G>T BRCA-EU 3 47044497 47044497 single base substitution G T missense_variant R1837L 5510G>T BRCA-EU 3 47044497 47044497 single base substitution G T missense_variant R205L 614G>T BRCA-EU 3 47044497 47044497 single base substitution G T upstream_gene_variant BRCA-EU 3 47044498 47044498 single base substitution C T downstream_gene_variant BRCA-EU 3 47044498 47044498 single base substitution C T synonymous_variant R1124R 3372C>T BRCA-EU 3 47044498 47044498 single base substitution C T synonymous_variant R116R 348C>T BRCA-EU 3 47044498 47044498 single base substitution C T synonymous_variant R1653R 4959C>T BRCA-EU 3 47044498 47044498 single base substitution C T synonymous_variant R1837R 5511C>T BRCA-EU 3 47044498 47044498 single base substitution C T synonymous_variant R205R 615C>T BRCA-EU 3 47044498 47044498 single base substitution C T upstream_gene_variant BRCA-EU 3 47048247 47048247 insertion of <=200bp - T downstream_gene_variant BRCA-EU 3 47048247 47048247 insertion of <=200bp - T intron_variant BRCA-EU 3 47048247 47048247 insertion of <=200bp - T upstream_gene_variant BRCA-EU 3 47048431 47048431 single base substitution G A downstream_gene_variant BRCA-EU 3 47048431 47048431 single base substitution G A intron_variant BRCA-EU 3 47048431 47048431 single base substitution G A upstream_gene_variant BRCA-EU 3 47048449 47048449 single base substitution C T downstream_gene_variant BRCA-EU 3 47048449 47048449 single base substitution C T intron_variant BRCA-EU 3 47048449 47048449 single base substitution C T upstream_gene_variant BRCA-EU 3 47048482 47048482 single base substitution G C downstream_gene_variant BRCA-EU 3 47048482 47048482 single base substitution G C intron_variant BRCA-EU 3 47048482 47048482 single base substitution G C upstream_gene_variant BRCA-EU 3 47049236 47049236 single base substitution C T downstream_gene_variant BRCA-EU 3 47049236 47049236 single base substitution C T intron_variant BRCA-EU 3 47049236 47049236 single base substitution C T upstream_gene_variant BRCA-EU 3 47050509 47050509 single base substitution G C downstream_gene_variant BRCA-EU 3 47050509 47050509 single base substitution G C exon_variant BRCA-EU 3 47050509 47050509 single base substitution G C missense_variant M1024I 3072G>C BRCA-EU 3 47050509 47050509 single base substitution G C missense_variant M1973I 5919G>C BRCA-EU 3 47050509 47050509 single base substitution G C missense_variant M2502I 7506G>C BRCA-EU 3 47050509 47050509 single base substitution G C missense_variant M2686I 8058G>C BRCA-EU 3 47050509 47050509 single base substitution G C missense_variant M935I 2805G>C BRCA-EU 3 47051742 47051742 single base substitution G A downstream_gene_variant BRCA-EU 3 47052078 47052078 single base substitution C A downstream_gene_variant BRCA-FR 3 47019603 47019603 single base substitution C A upstream_gene_variant BRCA-FR 3 47021079 47021079 single base substitution C G upstream_gene_variant BRCA-FR 3 47034657 47034657 single base substitution C T intron_variant BRCA-FR 3 47034657 47034657 single base substitution C T upstream_gene_variant BRCA-FR 3 47039329 47039329 single base substitution G A intron_variant BRCA-FR 3 47039329 47039329 single base substitution G A upstream_gene_variant BRCA-FR 3 47051742 47051742 single base substitution G A downstream_gene_variant BRCA-KR 3 47041645 47041645 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant BRCA-KR 3 47041645 47041645 single base substitution C T intron_variant BRCA-KR 3 47041645 47041645 single base substitution C T synonymous_variant F1352F 4056C>T BRCA-KR 3 47041645 47041645 single base substitution C T upstream_gene_variant BRCA-UK 3 47020468 47020468 single base substitution G C upstream_gene_variant BRCA-UK 3 47032135 47032135 single base substitution C G intron_variant BRCA-UK 3 47032135 47032135 single base substitution C G upstream_gene_variant BRCA-UK 3 47035975 47035975 single base substitution C T 5_prime_UTR_variant BRCA-UK 3 47035975 47035975 single base substitution C T missense_variant H410Y 1228C>T BRCA-UK 3 47035975 47035975 single base substitution C T upstream_gene_variant BRCA-UK 3 47039557 47039557 single base substitution G T missense_variant V458F 1372G>T BRCA-UK 3 47039557 47039557 single base substitution G T missense_variant V987F 2959G>T BRCA-UK 3 47039557 47039557 single base substitution G T splice_region_variant BRCA-UK 3 47039557 47039557 single base substitution G T upstream_gene_variant BRCA-US 3 47033996 47033996 single base substitution G C 5_prime_UTR_variant BRCA-US 3 47033996 47033996 single base substitution G C missense_variant G355A 1064G>C BRCA-US 3 47033996 47033996 single base substitution G C upstream_gene_variant BRCA-US 3 47036011 47036011 single base substitution A C 5_prime_UTR_variant BRCA-US 3 47036011 47036011 single base substitution A C missense_variant T422P 1264A>C BRCA-US 3 47036011 47036011 single base substitution A C upstream_gene_variant BRCA-US 3 47037780 47037780 single base substitution T C 5_prime_UTR_variant BRCA-US 3 47037780 47037780 single base substitution T C missense_variant I195T 584T>C BRCA-US 3 47037780 47037780 single base substitution T C missense_variant I724T 2171T>C BRCA-US 3 47037780 47037780 single base substitution T C upstream_gene_variant BRCA-US 3 47038822 47038822 single base substitution A G 5_prime_UTR_variant BRCA-US 3 47038822 47038822 single base substitution A G missense_variant E379G 1136A>G BRCA-US 3 47038822 47038822 single base substitution A G missense_variant E908G 2723A>G BRCA-US 3 47038822 47038822 single base substitution A G upstream_gene_variant BRCA-US 3 47041682 47041682 single base substitution G C 5_prime_UTR_variant BRCA-US 3 47041682 47041682 single base substitution G C missense_variant V1365L 4093G>C BRCA-US 3 47041682 47041682 single base substitution G C splice_region_variant BRCA-US 3 47041682 47041682 single base substitution G C upstream_gene_variant BRCA-US 3 47043228 47043228 single base substitution A C 5_prime_UTR_variant BRCA-US 3 47043228 47043228 single base substitution A C exon_variant BRCA-US 3 47043228 47043228 single base substitution A C missense_variant H1381P 4142A>C BRCA-US 3 47043228 47043228 single base substitution A C missense_variant H1565P 4694A>C BRCA-US 3 47043228 47043228 single base substitution A C missense_variant H852P 2555A>C BRCA-US 3 47043228 47043228 single base substitution A C upstream_gene_variant BRCA-US 3 47045357 47045357 single base substitution C T downstream_gene_variant BRCA-US 3 47045357 47045357 single base substitution C T synonymous_variant A1211A 3633C>T BRCA-US 3 47045357 47045357 single base substitution C T synonymous_variant A1740A 5220C>T BRCA-US 3 47045357 47045357 single base substitution C T synonymous_variant A1924A 5772C>T BRCA-US 3 47045357 47045357 single base substitution C T synonymous_variant A203A 609C>T BRCA-US 3 47045357 47045357 single base substitution C T synonymous_variant A292A 876C>T BRCA-US 3 47045357 47045357 single base substitution C T upstream_gene_variant BRCA-US 3 47045770 47045770 single base substitution A C downstream_gene_variant BRCA-US 3 47045770 47045770 single base substitution A C exon_variant BRCA-US 3 47045770 47045770 single base substitution A C missense_variant T1316P 3946A>C BRCA-US 3 47045770 47045770 single base substitution A C missense_variant T1845P 5533A>C BRCA-US 3 47045770 47045770 single base substitution A C missense_variant T2029P 6085A>C BRCA-US 3 47045770 47045770 single base substitution A C missense_variant T308P 922A>C BRCA-US 3 47045770 47045770 single base substitution A C missense_variant T397P 1189A>C BRCA-US 3 47045770 47045770 single base substitution A C upstream_gene_variant BRCA-US 3 47045824 47045824 single base substitution C T downstream_gene_variant BRCA-US 3 47045824 47045824 single base substitution C T exon_variant BRCA-US 3 47045824 47045824 single base substitution C T stop_gained Q1334* 4000C>T BRCA-US 3 47045824 47045824 single base substitution C T stop_gained Q1863* 5587C>T BRCA-US 3 47045824 47045824 single base substitution C T stop_gained Q2047* 6139C>T BRCA-US 3 47045824 47045824 single base substitution C T stop_gained Q326* 976C>T BRCA-US 3 47045824 47045824 single base substitution C T stop_gained Q415* 1243C>T BRCA-US 3 47045824 47045824 single base substitution C T upstream_gene_variant BRCA-US 3 47045885 47045885 single base substitution T G downstream_gene_variant BRCA-US 3 47045885 47045885 single base substitution T G splice_donor_variant BRCA-US 3 47045885 47045885 single base substitution T G upstream_gene_variant BRCA-US 3 47047285 47047285 single base substitution C A downstream_gene_variant BRCA-US 3 47047285 47047285 single base substitution C A exon_variant BRCA-US 3 47047285 47047285 single base substitution C A missense_variant P1537H 4610C>A BRCA-US 3 47047285 47047285 single base substitution C A missense_variant P2066H 6197C>A BRCA-US 3 47047285 47047285 single base substitution C A missense_variant P2250H 6749C>A BRCA-US 3 47047285 47047285 single base substitution C A missense_variant P529H 1586C>A BRCA-US 3 47047285 47047285 single base substitution C A missense_variant P618H 1853C>A BRCA-US 3 47047285 47047285 single base substitution C A missense_variant P77H 230C>A BRCA-US 3 47047285 47047285 single base substitution C A upstream_gene_variant BRCA-US 3 47047309 47047309 insertion of <=200bp - G downstream_gene_variant BRCA-US 3 47047309 47047309 insertion of <=200bp - G exon_variant BRCA-US 3 47047309 47047309 insertion of <=200bp - G frameshift_variant D1545G? BRCA-US 3 47047309 47047309 insertion of <=200bp - G frameshift_variant D2074G? BRCA-US 3 47047309 47047309 insertion of <=200bp - G frameshift_variant D2258G? BRCA-US 3 47047309 47047309 insertion of <=200bp - G frameshift_variant D537G? BRCA-US 3 47047309 47047309 insertion of <=200bp - G frameshift_variant D626G? BRCA-US 3 47047309 47047309 insertion of <=200bp - G frameshift_variant D85G? BRCA-US 3 47047309 47047309 insertion of <=200bp - G upstream_gene_variant BTCA-JP 3 47030311 47030311 single base substitution G A intron_variant BTCA-JP 3 47035961 47035961 single base substitution G A 5_prime_UTR_variant BTCA-JP 3 47035961 47035961 single base substitution G A missense_variant R405H 1214G>A BTCA-JP 3 47035961 47035961 single base substitution G A upstream_gene_variant BTCA-JP 3 47038022 47038022 single base substitution G A 5_prime_UTR_variant BTCA-JP 3 47038022 47038022 single base substitution G A missense_variant A276T 826G>A BTCA-JP 3 47038022 47038022 single base substitution G A missense_variant A805T 2413G>A BTCA-JP 3 47038022 47038022 single base substitution G A upstream_gene_variant BTCA-JP 3 47038148 47038148 single base substitution C T intron_variant BTCA-JP 3 47038148 47038148 single base substitution C T upstream_gene_variant BTCA-JP 3 47038270 47038270 single base substitution G C 5_prime_UTR_variant BTCA-JP 3 47038270 47038270 single base substitution G C missense_variant E306Q 916G>C BTCA-JP 3 47038270 47038270 single base substitution G C missense_variant E835Q 2503G>C BTCA-JP 3 47038270 47038270 single base substitution G C upstream_gene_variant BTCA-JP 3 47039549 47039549 single base substitution T C splice_region_variant BTCA-JP 3 47039549 47039549 single base substitution T C upstream_gene_variant BTCA-JP 3 47040989 47040989 single base substitution G T intron_variant BTCA-JP 3 47040989 47040989 single base substitution G T upstream_gene_variant BTCA-JP 3 47041181 47041181 single base substitution C T 5_prime_UTR_variant BTCA-JP 3 47041181 47041181 single base substitution C T intron_variant BTCA-JP 3 47041181 47041181 single base substitution C T synonymous_variant S1255S 3765C>T BTCA-JP 3 47041181 47041181 single base substitution C T upstream_gene_variant BTCA-JP 3 47041861 47041861 single base substitution C T 5_prime_UTR_variant BTCA-JP 3 47041861 47041861 single base substitution C T synonymous_variant S1240S 3720C>T BTCA-JP 3 47041861 47041861 single base substitution C T synonymous_variant S1424S 4272C>T BTCA-JP 3 47041861 47041861 single base substitution C T synonymous_variant S711S 2133C>T BTCA-JP 3 47041861 47041861 single base substitution C T upstream_gene_variant BTCA-JP 3 47043361 47043361 single base substitution G A intron_variant BTCA-JP 3 47043361 47043361 single base substitution G A upstream_gene_variant BTCA-JP 3 47043373 47043373 single base substitution A G intron_variant BTCA-JP 3 47043373 47043373 single base substitution A G upstream_gene_variant BTCA-JP 3 47044497 47044497 single base substitution G A downstream_gene_variant BTCA-JP 3 47044497 47044497 single base substitution G A missense_variant R1124H 3371G>A BTCA-JP 3 47044497 47044497 single base substitution G A missense_variant R116H 347G>A BTCA-JP 3 47044497 47044497 single base substitution G A missense_variant R1653H 4958G>A BTCA-JP 3 47044497 47044497 single base substitution G A missense_variant R1837H 5510G>A BTCA-JP 3 47044497 47044497 single base substitution G A missense_variant R205H 614G>A BTCA-JP 3 47044497 47044497 single base substitution G A upstream_gene_variant BTCA-JP 3 47047182 47047182 single base substitution C G downstream_gene_variant BTCA-JP 3 47047182 47047182 single base substitution C G intron_variant BTCA-JP 3 47047182 47047182 single base substitution C G upstream_gene_variant BTCA-JP 3 47050299 47050299 single base substitution G T downstream_gene_variant BTCA-JP 3 47050299 47050299 single base substitution G T intron_variant BTCA-JP 3 47050633 47050633 single base substitution T C downstream_gene_variant BTCA-JP 3 47050633 47050633 single base substitution T C intron_variant BTCA-JP 3 47050726 47050726 single base substitution C T downstream_gene_variant BTCA-JP 3 47050726 47050726 single base substitution C T synonymous_variant F1065F 3195C>T BTCA-JP 3 47050726 47050726 single base substitution C T synonymous_variant F2014F 6042C>T BTCA-JP 3 47050726 47050726 single base substitution C T synonymous_variant F2543F 7629C>T BTCA-JP 3 47050726 47050726 single base substitution C T synonymous_variant F2727F 8181C>T BTCA-JP 3 47050726 47050726 single base substitution C T synonymous_variant F976F 2928C>T BTCA-JP 3 47050984 47050984 single base substitution G T 3_prime_UTR_variant BTCA-JP 3 47050984 47050984 single base substitution G T downstream_gene_variant CESC-US 3 47018170 47018170 single base substitution C T upstream_gene_variant CESC-US 3 47030778 47030778 single base substitution G A 5_prime_UTR_variant CESC-US 3 47030778 47030778 single base substitution G A missense_variant R127Q 380G>A CESC-US 3 47033349 47033349 single base substitution G T 5_prime_UTR_premature_start_codon_gain_variant CESC-US 3 47033349 47033349 single base substitution G T synonymous_variant L315L 945G>T CESC-US 3 47033349 47033349 single base substitution G T upstream_gene_variant CESC-US 3 47037080 47037080 single base substitution A G 5_prime_UTR_premature_start_codon_gain_variant CESC-US 3 47037080 47037080 single base substitution A G missense_variant T619A 1855A>G CESC-US 3 47037080 47037080 single base substitution A G missense_variant T90A 268A>G CESC-US 3 47039707 47039707 single base substitution G T 5_prime_UTR_premature_start_codon_gain_variant CESC-US 3 47039707 47039707 single base substitution G T missense_variant V1037L 3109G>T CESC-US 3 47039707 47039707 single base substitution G T missense_variant V508L 1522G>T CESC-US 3 47039707 47039707 single base substitution G T upstream_gene_variant CESC-US 3 47041727 47041727 single base substitution C G 5_prime_UTR_premature_start_codon_gain_variant CESC-US 3 47041727 47041727 single base substitution C G missense_variant L1196V 3586C>G CESC-US 3 47041727 47041727 single base substitution C G missense_variant L1380V 4138C>G CESC-US 3 47041727 47041727 single base substitution C G missense_variant L667V 1999C>G CESC-US 3 47041727 47041727 single base substitution C G upstream_gene_variant CESC-US 3 47042572 47042572 single base substitution G A 5_prime_UTR_variant CESC-US 3 47042572 47042572 single base substitution G A exon_variant CESC-US 3 47042572 47042572 single base substitution G A missense_variant E1279K 3835G>A CESC-US 3 47042572 47042572 single base substitution G A missense_variant E1463K 4387G>A CESC-US 3 47042572 47042572 single base substitution G A missense_variant E750K 2248G>A CESC-US 3 47042572 47042572 single base substitution G A upstream_gene_variant CESC-US 3 47043554 47043554 single base substitution G A 5_prime_UTR_variant CESC-US 3 47043554 47043554 single base substitution G A downstream_gene_variant CESC-US 3 47043554 47043554 single base substitution G A missense_variant D11N 31G>A CESC-US 3 47043554 47043554 single base substitution G A missense_variant D1459N 4375G>A CESC-US 3 47043554 47043554 single base substitution G A missense_variant D1643N 4927G>A CESC-US 3 47043554 47043554 single base substitution G A missense_variant D930N 2788G>A CESC-US 3 47043554 47043554 single base substitution G A upstream_gene_variant CESC-US 3 47045644 47045644 single base substitution G A downstream_gene_variant CESC-US 3 47045644 47045644 single base substitution G A missense_variant A1274T 3820G>A CESC-US 3 47045644 47045644 single base substitution G A missense_variant A1803T 5407G>A CESC-US 3 47045644 47045644 single base substitution G A missense_variant A1987T 5959G>A CESC-US 3 47045644 47045644 single base substitution G A missense_variant A266T 796G>A CESC-US 3 47045644 47045644 single base substitution G A missense_variant A355T 1063G>A CESC-US 3 47045644 47045644 single base substitution G A upstream_gene_variant CESC-US 3 47047475 47047475 single base substitution G A downstream_gene_variant CESC-US 3 47047475 47047475 single base substitution G A exon_variant CESC-US 3 47047475 47047475 single base substitution G A missense_variant D108N 322G>A CESC-US 3 47047475 47047475 single base substitution G A missense_variant D1568N 4702G>A CESC-US 3 47047475 47047475 single base substitution G A missense_variant D2097N 6289G>A CESC-US 3 47047475 47047475 single base substitution G A missense_variant D2281N 6841G>A CESC-US 3 47047475 47047475 single base substitution G A missense_variant D560N 1678G>A CESC-US 3 47047475 47047475 single base substitution G A missense_variant D649N 1945G>A CESC-US 3 47047475 47047475 single base substitution G A upstream_gene_variant CESC-US 3 47049617 47049617 single base substitution G A downstream_gene_variant CESC-US 3 47049617 47049617 single base substitution G A exon_variant CESC-US 3 47049617 47049617 single base substitution G A missense_variant A1841T 5521G>A CESC-US 3 47049617 47049617 single base substitution G A missense_variant A2370T 7108G>A CESC-US 3 47049617 47049617 single base substitution G A missense_variant A2554T 7660G>A CESC-US 3 47049617 47049617 single base substitution G A missense_variant A803T 2407G>A CESC-US 3 47049617 47049617 single base substitution G A missense_variant A892T 2674G>A CESC-US 3 47049909 47049909 single base substitution C T downstream_gene_variant CESC-US 3 47049909 47049909 single base substitution C T exon_variant CESC-US 3 47049909 47049909 single base substitution C T missense_variant A1906V 5717C>T CESC-US 3 47049909 47049909 single base substitution C T missense_variant A2435V 7304C>T CESC-US 3 47049909 47049909 single base substitution C T missense_variant A2619V 7856C>T CESC-US 3 47049909 47049909 single base substitution C T missense_variant A868V 2603C>T CESC-US 3 47049909 47049909 single base substitution C T missense_variant A957V 2870C>T CLLE-ES 3 47043712 47043712 single base substitution C T 5_prime_UTR_variant CLLE-ES 3 47043712 47043712 single base substitution C T downstream_gene_variant CLLE-ES 3 47043712 47043712 single base substitution C T synonymous_variant P1511P 4533C>T CLLE-ES 3 47043712 47043712 single base substitution C T synonymous_variant P1695P 5085C>T CLLE-ES 3 47043712 47043712 single base substitution C T synonymous_variant P63P 189C>T CLLE-ES 3 47043712 47043712 single base substitution C T synonymous_variant P982P 2946C>T CLLE-ES 3 47043712 47043712 single base substitution C T upstream_gene_variant COAD-US 3 47018150 47018150 single base substitution G T upstream_gene_variant COAD-US 3 47030775 47030775 single base substitution G A 5_prime_UTR_variant COAD-US 3 47030775 47030775 single base substitution G A missense_variant G126D 377G>A COAD-US 3 47032926 47032926 single base substitution T C 5_prime_UTR_variant COAD-US 3 47032926 47032926 single base substitution T C missense_variant S225P 673T>C COAD-US 3 47032926 47032926 single base substitution T C upstream_gene_variant COAD-US 3 47033395 47033395 single base substitution A G 5_prime_UTR_variant COAD-US 3 47033395 47033395 single base substitution A G missense_variant N331D 991A>G COAD-US 3 47033395 47033395 single base substitution A G upstream_gene_variant COAD-US 3 47036645 47036645 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant COAD-US 3 47036645 47036645 single base substitution C T missense_variant R474C 1420C>T COAD-US 3 47036645 47036645 single base substitution C T upstream_gene_variant COAD-US 3 47036756 47036756 single base substitution C G 5_prime_UTR_variant COAD-US 3 47036756 47036756 single base substitution C G missense_variant R511G 1531C>G COAD-US 3 47036756 47036756 single base substitution C G upstream_gene_variant COAD-US 3 47037015 47037015 single base substitution G A 5_prime_UTR_variant COAD-US 3 47037015 47037015 single base substitution G A missense_variant R597Q 1790G>A COAD-US 3 47037015 47037015 single base substitution G A missense_variant R68Q 203G>A COAD-US 3 47037427 47037427 single base substitution C T 5_prime_UTR_variant COAD-US 3 47037427 47037427 single base substitution C T synonymous_variant C150C 450C>T COAD-US 3 47037427 47037427 single base substitution C T synonymous_variant C679C 2037C>T COAD-US 3 47038013 47038013 single base substitution G A 5_prime_UTR_variant COAD-US 3 47038013 47038013 single base substitution G A missense_variant E273K 817G>A COAD-US 3 47038013 47038013 single base substitution G A missense_variant E802K 2404G>A COAD-US 3 47038013 47038013 single base substitution G A upstream_gene_variant COAD-US 3 47039707 47039707 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant COAD-US 3 47039707 47039707 single base substitution G A missense_variant V1037M 3109G>A COAD-US 3 47039707 47039707 single base substitution G A missense_variant V508M 1522G>A COAD-US 3 47039707 47039707 single base substitution G A upstream_gene_variant COAD-US 3 47040272 47040272 single base substitution T C 5_prime_UTR_variant COAD-US 3 47040272 47040272 single base substitution T C missense_variant L1096P 3287T>C COAD-US 3 47040272 47040272 single base substitution T C missense_variant L567P 1700T>C COAD-US 3 47040272 47040272 single base substitution T C upstream_gene_variant COAD-US 3 47043622 47043622 single base substitution G A 5_prime_UTR_variant COAD-US 3 47043622 47043622 single base substitution G A downstream_gene_variant COAD-US 3 47043622 47043622 single base substitution G A synonymous_variant V1481V 4443G>A COAD-US 3 47043622 47043622 single base substitution G A synonymous_variant V1665V 4995G>A COAD-US 3 47043622 47043622 single base substitution G A synonymous_variant V33V 99G>A COAD-US 3 47043622 47043622 single base substitution G A synonymous_variant V952V 2856G>A COAD-US 3 47043622 47043622 single base substitution G A upstream_gene_variant COAD-US 3 47043759 47043759 single base substitution G A 5_prime_UTR_variant COAD-US 3 47043759 47043759 single base substitution G A downstream_gene_variant COAD-US 3 47043759 47043759 single base substitution G A missense_variant R1527H 4580G>A COAD-US 3 47043759 47043759 single base substitution G A missense_variant R1711H 5132G>A COAD-US 3 47043759 47043759 single base substitution G A missense_variant R79H 236G>A COAD-US 3 47043759 47043759 single base substitution G A missense_variant R998H 2993G>A COAD-US 3 47043759 47043759 single base substitution G A upstream_gene_variant COAD-US 3 47045584 47045584 single base substitution C T downstream_gene_variant COAD-US 3 47045584 47045584 single base substitution C T missense_variant R1254W 3760C>T COAD-US 3 47045584 47045584 single base substitution C T missense_variant R1783W 5347C>T COAD-US 3 47045584 47045584 single base substitution C T missense_variant R1967W 5899C>T COAD-US 3 47045584 47045584 single base substitution C T missense_variant R246W 736C>T COAD-US 3 47045584 47045584 single base substitution C T missense_variant R335W 1003C>T COAD-US 3 47045584 47045584 single base substitution C T upstream_gene_variant COAD-US 3 47045846 47045846 single base substitution C T downstream_gene_variant COAD-US 3 47045846 47045846 single base substitution C T exon_variant COAD-US 3 47045846 47045846 single base substitution C T missense_variant S1341F 4022C>T COAD-US 3 47045846 47045846 single base substitution C T missense_variant S1870F 5609C>T COAD-US 3 47045846 47045846 single base substitution C T missense_variant S2054F 6161C>T COAD-US 3 47045846 47045846 single base substitution C T missense_variant S333F 998C>T COAD-US 3 47045846 47045846 single base substitution C T missense_variant S422F 1265C>T COAD-US 3 47045846 47045846 single base substitution C T upstream_gene_variant COAD-US 3 47046759 47046759 single base substitution C T 3_prime_UTR_variant COAD-US 3 47046759 47046759 single base substitution C T downstream_gene_variant COAD-US 3 47046759 47046759 single base substitution C T exon_variant COAD-US 3 47046759 47046759 single base substitution C T missense_variant L1457F 4369C>T COAD-US 3 47046759 47046759 single base substitution C T missense_variant L1986F 5956C>T COAD-US 3 47046759 47046759 single base substitution C T missense_variant L2170F 6508C>T COAD-US 3 47046759 47046759 single base substitution C T missense_variant L449F 1345C>T COAD-US 3 47046759 47046759 single base substitution C T missense_variant L538F 1612C>T COAD-US 3 47046759 47046759 single base substitution C T upstream_gene_variant COAD-US 3 47048573 47048573 single base substitution A G downstream_gene_variant COAD-US 3 47048573 47048573 single base substitution A G exon_variant COAD-US 3 47048573 47048573 single base substitution A G intron_variant COAD-US 3 47048573 47048573 single base substitution A G synonymous_variant V1671V 5013A>G COAD-US 3 47048573 47048573 single base substitution A G synonymous_variant V2200V 6600A>G COAD-US 3 47048573 47048573 single base substitution A G synonymous_variant V2384V 7152A>G COAD-US 3 47048573 47048573 single base substitution A G upstream_gene_variant COCA-CN 3 47030927 47030927 single base substitution C T intron_variant COCA-CN 3 47032911 47032911 single base substitution G A 5_prime_UTR_variant COCA-CN 3 47032911 47032911 single base substitution G A missense_variant A220T 658G>A COCA-CN 3 47032911 47032911 single base substitution G A upstream_gene_variant COCA-CN 3 47033077 47033077 single base substitution C T 5_prime_UTR_variant COCA-CN 3 47033077 47033077 single base substitution C T missense_variant A275V 824C>T COCA-CN 3 47033077 47033077 single base substitution C T upstream_gene_variant COCA-CN 3 47034054 47034054 single base substitution C A intron_variant COCA-CN 3 47034054 47034054 single base substitution C A upstream_gene_variant COCA-CN 3 47036825 47036825 single base substitution C T 5_prime_UTR_variant COCA-CN 3 47036825 47036825 single base substitution C T missense_variant R534C 1600C>T COCA-CN 3 47036825 47036825 single base substitution C T missense_variant R5C 13C>T COCA-CN 3 47038363 47038363 single base substitution C G intron_variant COCA-CN 3 47038363 47038363 single base substitution C G upstream_gene_variant COCA-CN 3 47038787 47038787 single base substitution G A 5_prime_UTR_variant COCA-CN 3 47038787 47038787 single base substitution G A synonymous_variant L367L 1101G>A COCA-CN 3 47038787 47038787 single base substitution G A synonymous_variant L896L 2688G>A COCA-CN 3 47038787 47038787 single base substitution G A upstream_gene_variant COCA-CN 3 47040016 47040016 single base substitution G A 5_prime_UTR_variant COCA-CN 3 47040016 47040016 single base substitution G A missense_variant G1061D 3182G>A COCA-CN 3 47040016 47040016 single base substitution G A missense_variant G532D 1595G>A COCA-CN 3 47040016 47040016 single base substitution G A upstream_gene_variant COCA-CN 3 47041454 47041454 single base substitution A G 5_prime_UTR_variant COCA-CN 3 47041454 47041454 single base substitution A G intron_variant COCA-CN 3 47041454 47041454 single base substitution A G missense_variant T1289A 3865A>G COCA-CN 3 47041454 47041454 single base substitution A G upstream_gene_variant COCA-CN 3 47041546 47041546 single base substitution G A 5_prime_UTR_variant COCA-CN 3 47041546 47041546 single base substitution G A intron_variant COCA-CN 3 47041546 47041546 single base substitution G A synonymous_variant K1319K 3957G>A COCA-CN 3 47041546 47041546 single base substitution G A upstream_gene_variant COCA-CN 3 47042783 47042783 single base substitution T C 5_prime_UTR_variant COCA-CN 3 47042783 47042783 single base substitution T C exon_variant COCA-CN 3 47042783 47042783 single base substitution T C missense_variant M1316T 3947T>C COCA-CN 3 47042783 47042783 single base substitution T C missense_variant M1500T 4499T>C COCA-CN 3 47042783 47042783 single base substitution T C missense_variant M787T 2360T>C COCA-CN 3 47042783 47042783 single base substitution T C upstream_gene_variant COCA-CN 3 47043098 47043098 single base substitution C T intron_variant COCA-CN 3 47043098 47043098 single base substitution C T upstream_gene_variant COCA-CN 3 47043154 47043154 single base substitution G A intron_variant COCA-CN 3 47043154 47043154 single base substitution G A upstream_gene_variant COCA-CN 3 47043884 47043884 single base substitution C T downstream_gene_variant COCA-CN 3 47043884 47043884 single base substitution C T synonymous_variant F1012F 3036C>T COCA-CN 3 47043884 47043884 single base substitution C T synonymous_variant F1541F 4623C>T COCA-CN 3 47043884 47043884 single base substitution C T synonymous_variant F1725F 5175C>T COCA-CN 3 47043884 47043884 single base substitution C T synonymous_variant F4F 12C>T COCA-CN 3 47043884 47043884 single base substitution C T synonymous_variant F93F 279C>T COCA-CN 3 47043884 47043884 single base substitution C T upstream_gene_variant COCA-CN 3 47043936 47043936 single base substitution G A downstream_gene_variant COCA-CN 3 47043936 47043936 single base substitution G A missense_variant A1030T 3088G>A COCA-CN 3 47043936 47043936 single base substitution G A missense_variant A111T 331G>A COCA-CN 3 47043936 47043936 single base substitution G A missense_variant A1559T 4675G>A COCA-CN 3 47043936 47043936 single base substitution G A missense_variant A1743T 5227G>A COCA-CN 3 47043936 47043936 single base substitution G A missense_variant A22T 64G>A COCA-CN 3 47043936 47043936 single base substitution G A upstream_gene_variant COCA-CN 3 47045665 47045665 single base substitution G A downstream_gene_variant COCA-CN 3 47045665 47045665 single base substitution G A exon_variant COCA-CN 3 47045665 47045665 single base substitution G A missense_variant D1281N 3841G>A COCA-CN 3 47045665 47045665 single base substitution G A missense_variant D1810N 5428G>A COCA-CN 3 47045665 47045665 single base substitution G A missense_variant D1994N 5980G>A COCA-CN 3 47045665 47045665 single base substitution G A missense_variant D273N 817G>A COCA-CN 3 47045665 47045665 single base substitution G A missense_variant D362N 1084G>A COCA-CN 3 47045665 47045665 single base substitution G A upstream_gene_variant COCA-CN 3 47045898 47045898 single base substitution T C downstream_gene_variant COCA-CN 3 47045898 47045898 single base substitution T C intron_variant COCA-CN 3 47045898 47045898 single base substitution T C upstream_gene_variant COCA-CN 3 47047015 47047015 single base substitution G A 3_prime_UTR_variant COCA-CN 3 47047015 47047015 single base substitution G A downstream_gene_variant COCA-CN 3 47047015 47047015 single base substitution G A exon_variant COCA-CN 3 47047015 47047015 single base substitution G A synonymous_variant A1486A 4458G>A COCA-CN 3 47047015 47047015 single base substitution G A synonymous_variant A2015A 6045G>A COCA-CN 3 47047015 47047015 single base substitution G A synonymous_variant A2199A 6597G>A COCA-CN 3 47047015 47047015 single base substitution G A synonymous_variant A26A 78G>A COCA-CN 3 47047015 47047015 single base substitution G A synonymous_variant A478A 1434G>A COCA-CN 3 47047015 47047015 single base substitution G A synonymous_variant A567A 1701G>A COCA-CN 3 47047015 47047015 single base substitution G A upstream_gene_variant COCA-CN 3 47048802 47048802 single base substitution C T downstream_gene_variant COCA-CN 3 47048802 47048802 single base substitution C T exon_variant COCA-CN 3 47048802 47048802 single base substitution C T intron_variant COCA-CN 3 47048802 47048802 single base substitution C T synonymous_variant Y1719Y 5157C>T COCA-CN 3 47048802 47048802 single base substitution C T synonymous_variant Y2248Y 6744C>T COCA-CN 3 47048802 47048802 single base substitution C T synonymous_variant Y2432Y 7296C>T COCA-CN 3 47048802 47048802 single base substitution C T synonymous_variant Y681Y 2043C>T COCA-CN 3 47048802 47048802 single base substitution C T synonymous_variant Y770Y 2310C>T COCA-CN 3 47048802 47048802 single base substitution C T upstream_gene_variant COCA-CN 3 47049947 47049947 single base substitution G A downstream_gene_variant COCA-CN 3 47049947 47049947 single base substitution G A intron_variant COCA-CN 3 47050222 47050222 single base substitution C T downstream_gene_variant COCA-CN 3 47050222 47050222 single base substitution C T intron_variant COCA-CN 3 47050522 47050522 single base substitution C T downstream_gene_variant COCA-CN 3 47050522 47050522 single base substitution C T exon_variant COCA-CN 3 47050522 47050522 single base substitution C T missense_variant R1029C 3085C>T COCA-CN 3 47050522 47050522 single base substitution C T missense_variant R1978C 5932C>T COCA-CN 3 47050522 47050522 single base substitution C T missense_variant R2507C 7519C>T COCA-CN 3 47050522 47050522 single base substitution C T missense_variant R2691C 8071C>T COCA-CN 3 47050522 47050522 single base substitution C T missense_variant R940C 2818C>T COCA-CN 3 47054397 47054397 single base substitution T C downstream_gene_variant EOPC-DE 3 47049108 47049108 single base substitution C T downstream_gene_variant EOPC-DE 3 47049108 47049108 single base substitution C T exon_variant EOPC-DE 3 47049108 47049108 single base substitution C T intron_variant EOPC-DE 3 47049108 47049108 single base substitution C T missense_variant R237W 709C>T EOPC-DE 3 47049108 47049108 single base substitution C T synonymous_variant S1763S 5289C>T EOPC-DE 3 47049108 47049108 single base substitution C T synonymous_variant S2292S 6876C>T EOPC-DE 3 47049108 47049108 single base substitution C T synonymous_variant S2476S 7428C>T EOPC-DE 3 47049108 47049108 single base substitution C T synonymous_variant S725S 2175C>T EOPC-DE 3 47049108 47049108 single base substitution C T synonymous_variant S814S 2442C>T EOPC-DE 3 47049108 47049108 single base substitution C T upstream_gene_variant ESAD-UK 3 47019447 47019447 single base substitution C T upstream_gene_variant ESAD-UK 3 47020695 47020695 single base substitution T G upstream_gene_variant ESAD-UK 3 47027174 47027174 single base substitution G A intron_variant ESAD-UK 3 47029743 47029743 single base substitution G C intron_variant ESAD-UK 3 47031211 47031211 single base substitution A G intron_variant ESAD-UK 3 47032464 47032464 single base substitution G T intron_variant ESAD-UK 3 47032464 47032464 single base substitution G T upstream_gene_variant ESAD-UK 3 47035346 47035346 single base substitution C T intron_variant ESAD-UK 3 47035346 47035346 single base substitution C T upstream_gene_variant ESAD-UK 3 47035587 47035587 single base substitution C T intron_variant ESAD-UK 3 47035587 47035587 single base substitution C T upstream_gene_variant ESAD-UK 3 47035745 47035745 single base substitution A C intron_variant ESAD-UK 3 47035745 47035745 single base substitution A C upstream_gene_variant ESAD-UK 3 47038197 47038197 single base substitution G T intron_variant ESAD-UK 3 47038197 47038197 single base substitution G T upstream_gene_variant ESAD-UK 3 47038260 47038260 single base substitution C T 5_prime_UTR_variant ESAD-UK 3 47038260 47038260 single base substitution C T synonymous_variant P302P 906C>T ESAD-UK 3 47038260 47038260 single base substitution C T synonymous_variant P831P 2493C>T ESAD-UK 3 47038260 47038260 single base substitution C T upstream_gene_variant ESAD-UK 3 47038597 47038597 single base substitution C T intron_variant ESAD-UK 3 47038597 47038597 single base substitution C T upstream_gene_variant ESAD-UK 3 47038711 47038711 single base substitution C T intron_variant ESAD-UK 3 47038711 47038711 single base substitution C T upstream_gene_variant ESAD-UK 3 47040780 47040780 single base substitution C T intron_variant ESAD-UK 3 47040780 47040780 single base substitution C T upstream_gene_variant ESAD-UK 3 47041748 47041748 single base substitution G A 5_prime_UTR_variant ESAD-UK 3 47041748 47041748 single base substitution G A missense_variant G1203S 3607G>A ESAD-UK 3 47041748 47041748 single base substitution G A missense_variant G1387S 4159G>A ESAD-UK 3 47041748 47041748 single base substitution G A missense_variant G674S 2020G>A ESAD-UK 3 47041748 47041748 single base substitution G A upstream_gene_variant ESAD-UK 3 47042633 47042633 single base substitution C T 5_prime_UTR_variant ESAD-UK 3 47042633 47042633 single base substitution C T exon_variant ESAD-UK 3 47042633 47042633 single base substitution C T missense_variant A1299V 3896C>T ESAD-UK 3 47042633 47042633 single base substitution C T missense_variant A1483V 4448C>T ESAD-UK 3 47042633 47042633 single base substitution C T missense_variant A770V 2309C>T ESAD-UK 3 47042633 47042633 single base substitution C T upstream_gene_variant ESAD-UK 3 47043095 47043095 single base substitution C T intron_variant ESAD-UK 3 47043095 47043095 single base substitution C T upstream_gene_variant ESAD-UK 3 47043613 47043613 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant ESAD-UK 3 47043613 47043613 single base substitution C T downstream_gene_variant ESAD-UK 3 47043613 47043613 single base substitution C T synonymous_variant S1478S 4434C>T ESAD-UK 3 47043613 47043613 single base substitution C T synonymous_variant S1662S 4986C>T ESAD-UK 3 47043613 47043613 single base substitution C T synonymous_variant S30S 90C>T ESAD-UK 3 47043613 47043613 single base substitution C T synonymous_variant S949S 2847C>T ESAD-UK 3 47043613 47043613 single base substitution C T upstream_gene_variant ESAD-UK 3 47046839 47046839 single base substitution T G downstream_gene_variant ESAD-UK 3 47046839 47046839 single base substitution T G intron_variant ESAD-UK 3 47046839 47046839 single base substitution T G upstream_gene_variant ESAD-UK 3 47050665 47050665 single base substitution C T downstream_gene_variant ESAD-UK 3 47050665 47050665 single base substitution C T intron_variant ESAD-UK 3 47051367 47051367 single base substitution G T downstream_gene_variant ESAD-UK 3 47051481 47051481 single base substitution G A downstream_gene_variant ESAD-UK 3 47054733 47054733 single base substitution G C downstream_gene_variant ESCA-CN 3 47040141 47040141 single base substitution C A intron_variant ESCA-CN 3 47040141 47040141 single base substitution C A upstream_gene_variant ESCA-CN 3 47040315 47040315 single base substitution G A 5_prime_UTR_variant ESCA-CN 3 47040315 47040315 single base substitution G A synonymous_variant V1110V 3330G>A ESCA-CN 3 47040315 47040315 single base substitution G A synonymous_variant V581V 1743G>A ESCA-CN 3 47040315 47040315 single base substitution G A upstream_gene_variant ESCA-CN 3 47042597 47042597 single base substitution A T 5_prime_UTR_premature_start_codon_gain_variant ESCA-CN 3 47042597 47042597 single base substitution A T exon_variant ESCA-CN 3 47042597 47042597 single base substitution A T missense_variant Q1287L 3860A>T ESCA-CN 3 47042597 47042597 single base substitution A T missense_variant Q1471L 4412A>T ESCA-CN 3 47042597 47042597 single base substitution A T missense_variant Q758L 2273A>T ESCA-CN 3 47042597 47042597 single base substitution A T upstream_gene_variant ESCA-CN 3 47045450 47045450 single base substitution C T downstream_gene_variant ESCA-CN 3 47045450 47045450 single base substitution C T synonymous_variant R1242R 3726C>T ESCA-CN 3 47045450 47045450 single base substitution C T synonymous_variant R1771R 5313C>T ESCA-CN 3 47045450 47045450 single base substitution C T synonymous_variant R1955R 5865C>T ESCA-CN 3 47045450 47045450 single base substitution C T synonymous_variant R234R 702C>T ESCA-CN 3 47045450 47045450 single base substitution C T synonymous_variant R323R 969C>T ESCA-CN 3 47045450 47045450 single base substitution C T upstream_gene_variant ESCA-CN 3 47048971 47048971 single base substitution T C downstream_gene_variant ESCA-CN 3 47048971 47048971 single base substitution T C exon_variant ESCA-CN 3 47048971 47048971 single base substitution T C intron_variant ESCA-CN 3 47048971 47048971 single base substitution T C upstream_gene_variant GBM-US 3 47040042 47040042 single base substitution C T 5_prime_UTR_variant GBM-US 3 47040042 47040042 single base substitution C T missense_variant R1070C 3208C>T GBM-US 3 47040042 47040042 single base substitution C T missense_variant R541C 1621C>T GBM-US 3 47040042 47040042 single base substitution C T upstream_gene_variant GBM-US 3 47040321 47040321 single base substitution C T 5_prime_UTR_variant GBM-US 3 47040321 47040321 single base substitution C T synonymous_variant V1112V 3336C>T GBM-US 3 47040321 47040321 single base substitution C T synonymous_variant V583V 1749C>T GBM-US 3 47040321 47040321 single base substitution C T upstream_gene_variant GBM-US 3 47041457 47041457 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant GBM-US 3 47041457 47041457 single base substitution C T intron_variant GBM-US 3 47041457 47041457 single base substitution C T missense_variant R1290W 3868C>T GBM-US 3 47041457 47041457 single base substitution C T upstream_gene_variant GBM-US 3 47041686 47041686 single base substitution G T 5_prime_UTR_variant GBM-US 3 47041686 47041686 single base substitution G T missense_variant G1182V 3545G>T GBM-US 3 47041686 47041686 single base substitution G T missense_variant G1366V 4097G>T GBM-US 3 47041686 47041686 single base substitution G T missense_variant G653V 1958G>T GBM-US 3 47041686 47041686 single base substitution G T upstream_gene_variant KIRC-US 3 47037324 47037324 single base substitution C G 5_prime_UTR_variant KIRC-US 3 47037324 47037324 single base substitution C G synonymous_variant A144A 432C>G KIRC-US 3 47037324 47037324 single base substitution C G synonymous_variant A673A 2019C>G KIRC-US 3 47038048 47038048 single base substitution G A 5_prime_UTR_variant KIRC-US 3 47038048 47038048 single base substitution G A synonymous_variant L284L 852G>A KIRC-US 3 47038048 47038048 single base substitution G A synonymous_variant L813L 2439G>A KIRC-US 3 47038048 47038048 single base substitution G A upstream_gene_variant KIRC-US 3 47043759 47043759 single base substitution G A 5_prime_UTR_variant KIRC-US 3 47043759 47043759 single base substitution G A downstream_gene_variant KIRC-US 3 47043759 47043759 single base substitution G A missense_variant R1527H 4580G>A KIRC-US 3 47043759 47043759 single base substitution G A missense_variant R1711H 5132G>A KIRC-US 3 47043759 47043759 single base substitution G A missense_variant R79H 236G>A KIRC-US 3 47043759 47043759 single base substitution G A missense_variant R998H 2993G>A KIRC-US 3 47043759 47043759 single base substitution G A upstream_gene_variant KIRC-US 3 47050126 47050126 single base substitution C A downstream_gene_variant KIRC-US 3 47050126 47050126 single base substitution C A exon_variant KIRC-US 3 47050126 47050126 single base substitution C A synonymous_variant A1003A 3009C>A KIRC-US 3 47050126 47050126 single base substitution C A synonymous_variant A1952A 5856C>A KIRC-US 3 47050126 47050126 single base substitution C A synonymous_variant A2481A 7443C>A KIRC-US 3 47050126 47050126 single base substitution C A synonymous_variant A2665A 7995C>A KIRC-US 3 47050126 47050126 single base substitution C A synonymous_variant A914A 2742C>A KIRP-US 3 47030855 47030855 single base substitution C T 5_prime_UTR_variant KIRP-US 3 47030855 47030855 single base substitution C T missense_variant R153W 457C>T KIRP-US 3 47032943 47032943 single base substitution G T 5_prime_UTR_variant KIRP-US 3 47032943 47032943 single base substitution G T synonymous_variant L230L 690G>T KIRP-US 3 47032943 47032943 single base substitution G T upstream_gene_variant KIRP-US 3 47049869 47049869 single base substitution G A downstream_gene_variant KIRP-US 3 47049869 47049869 single base substitution G A exon_variant KIRP-US 3 47049869 47049869 single base substitution G A missense_variant A1893T 5677G>A KIRP-US 3 47049869 47049869 single base substitution G A missense_variant A2422T 7264G>A KIRP-US 3 47049869 47049869 single base substitution G A missense_variant A2606T 7816G>A KIRP-US 3 47049869 47049869 single base substitution G A missense_variant A855T 2563G>A KIRP-US 3 47049869 47049869 single base substitution G A missense_variant A944T 2830G>A LAML-KR 3 47017285 47017285 single base substitution T C upstream_gene_variant LAML-KR 3 47043622 47043622 single base substitution G A 5_prime_UTR_variant LAML-KR 3 47043622 47043622 single base substitution G A downstream_gene_variant LAML-KR 3 47043622 47043622 single base substitution G A synonymous_variant V1481V 4443G>A LAML-KR 3 47043622 47043622 single base substitution G A synonymous_variant V1665V 4995G>A LAML-KR 3 47043622 47043622 single base substitution G A synonymous_variant V33V 99G>A LAML-KR 3 47043622 47043622 single base substitution G A synonymous_variant V952V 2856G>A LAML-KR 3 47043622 47043622 single base substitution G A upstream_gene_variant LAML-KR 3 47048971 47048971 single base substitution T C downstream_gene_variant LAML-KR 3 47048971 47048971 single base substitution T C exon_variant LAML-KR 3 47048971 47048971 single base substitution T C intron_variant LAML-KR 3 47048971 47048971 single base substitution T C upstream_gene_variant LAML-KR 3 47049801 47049801 single base substitution G T downstream_gene_variant LAML-KR 3 47049801 47049801 single base substitution G T exon_variant LAML-KR 3 47049801 47049801 single base substitution G T missense_variant R1870L 5609G>T LAML-KR 3 47049801 47049801 single base substitution G T missense_variant R2399L 7196G>T LAML-KR 3 47049801 47049801 single base substitution G T missense_variant R2583L 7748G>T LAML-KR 3 47049801 47049801 single base substitution G T missense_variant R832L 2495G>T LAML-KR 3 47049801 47049801 single base substitution G T missense_variant R921L 2762G>T LGG-US 3 47038035 47038035 single base substitution T C 5_prime_UTR_variant LGG-US 3 47038035 47038035 single base substitution T C missense_variant F280S 839T>C LGG-US 3 47038035 47038035 single base substitution T C missense_variant F809S 2426T>C LGG-US 3 47038035 47038035 single base substitution T C upstream_gene_variant LGG-US 3 47041457 47041457 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant LGG-US 3 47041457 47041457 single base substitution C T intron_variant LGG-US 3 47041457 47041457 single base substitution C T missense_variant R1290W 3868C>T LGG-US 3 47041457 47041457 single base substitution C T upstream_gene_variant LICA-CN 3 47035982 47035982 single base substitution A T 5_prime_UTR_premature_start_codon_gain_variant LICA-CN 3 47035982 47035982 single base substitution A T missense_variant Q412L 1235A>T LICA-CN 3 47035982 47035982 single base substitution A T upstream_gene_variant LICA-CN 3 47043739 47043739 single base substitution T C 5_prime_UTR_premature_start_codon_gain_variant LICA-CN 3 47043739 47043739 single base substitution T C downstream_gene_variant LICA-CN 3 47043739 47043739 single base substitution T C synonymous_variant F1520F 4560T>C LICA-CN 3 47043739 47043739 single base substitution T C synonymous_variant F1704F 5112T>C LICA-CN 3 47043739 47043739 single base substitution T C synonymous_variant F72F 216T>C LICA-CN 3 47043739 47043739 single base substitution T C synonymous_variant F991F 2973T>C LICA-CN 3 47043739 47043739 single base substitution T C upstream_gene_variant LICA-CN 3 47043976 47043976 single base substitution A T downstream_gene_variant LICA-CN 3 47043976 47043976 single base substitution A T missense_variant Q1043L 3128A>T LICA-CN 3 47043976 47043976 single base substitution A T missense_variant Q124L 371A>T LICA-CN 3 47043976 47043976 single base substitution A T missense_variant Q1572L 4715A>T LICA-CN 3 47043976 47043976 single base substitution A T missense_variant Q1756L 5267A>T LICA-CN 3 47043976 47043976 single base substitution A T missense_variant Q35L 104A>T LICA-CN 3 47043976 47043976 single base substitution A T upstream_gene_variant LICA-CN 3 47048638 47048638 single base substitution A G downstream_gene_variant LICA-CN 3 47048638 47048638 single base substitution A G exon_variant LICA-CN 3 47048638 47048638 single base substitution A G intron_variant LICA-CN 3 47048638 47048638 single base substitution A G missense_variant D1693G 5078A>G LICA-CN 3 47048638 47048638 single base substitution A G missense_variant D2222G 6665A>G LICA-CN 3 47048638 47048638 single base substitution A G missense_variant D2406G 7217A>G LICA-CN 3 47048638 47048638 single base substitution A G upstream_gene_variant LICA-FR 3 47019994 47020112 deletion of <=200bp TGGGTCCCTGCCACCATCACCCCGTGCCCCTTTCCCCGTGTCCAGACTGTGAGGTAAGGGGATGGGGAAGGGGGCACGGGGTGATGGTGGCAGGGACCCAAAAAAGAGTCAGTCAAGCC - upstream_gene_variant LICA-FR 3 47021127 47021135 deletion of <=200bp GAAGTGCAG - upstream_gene_variant LICA-FR 3 47033010 47033010 single base substitution G A 5_prime_UTR_variant LICA-FR 3 47033010 47033010 single base substitution G A missense_variant A253T 757G>A LICA-FR 3 47033010 47033010 single base substitution G A upstream_gene_variant LICA-FR 3 47036712 47036712 single base substitution G T 5_prime_UTR_variant LICA-FR 3 47036712 47036712 single base substitution G T missense_variant G496V 1487G>T LICA-FR 3 47036712 47036712 single base substitution G T upstream_gene_variant LICA-FR 3 47037227 47037227 single base substitution G A 5_prime_UTR_variant LICA-FR 3 47037227 47037227 single base substitution G A missense_variant G112E 335G>A LICA-FR 3 47037227 47037227 single base substitution G A missense_variant G641E 1922G>A LICA-FR 3 47040452 47040452 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant LICA-FR 3 47040452 47040452 single base substitution G A intron_variant LICA-FR 3 47040452 47040452 single base substitution G A missense_variant V1130M 3388G>A LICA-FR 3 47040452 47040452 single base substitution G A upstream_gene_variant LICA-FR 3 47040596 47040596 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant LICA-FR 3 47040596 47040596 single base substitution C T intron_variant LICA-FR 3 47040596 47040596 single base substitution C T stop_gained R1178* 3532C>T LICA-FR 3 47040596 47040596 single base substitution C T upstream_gene_variant LICA-FR 3 47042587 47042587 single base substitution G A 5_prime_UTR_variant LICA-FR 3 47042587 47042587 single base substitution G A exon_variant LICA-FR 3 47042587 47042587 single base substitution G A missense_variant E1284K 3850G>A LICA-FR 3 47042587 47042587 single base substitution G A missense_variant E1468K 4402G>A LICA-FR 3 47042587 47042587 single base substitution G A missense_variant E755K 2263G>A LICA-FR 3 47042587 47042587 single base substitution G A upstream_gene_variant LICA-FR 3 47045765 47045765 single base substitution C A downstream_gene_variant LICA-FR 3 47045765 47045765 single base substitution C A exon_variant LICA-FR 3 47045765 47045765 single base substitution C A missense_variant P1314H 3941C>A LICA-FR 3 47045765 47045765 single base substitution C A missense_variant P1843H 5528C>A LICA-FR 3 47045765 47045765 single base substitution C A missense_variant P2027H 6080C>A LICA-FR 3 47045765 47045765 single base substitution C A missense_variant P306H 917C>A LICA-FR 3 47045765 47045765 single base substitution C A missense_variant P395H 1184C>A LICA-FR 3 47045765 47045765 single base substitution C A upstream_gene_variant LICA-FR 3 47047047 47047047 single base substitution C T 3_prime_UTR_variant LICA-FR 3 47047047 47047047 single base substitution C T downstream_gene_variant LICA-FR 3 47047047 47047047 single base substitution C T exon_variant LICA-FR 3 47047047 47047047 single base substitution C T missense_variant A1497V 4490C>T LICA-FR 3 47047047 47047047 single base substitution C T missense_variant A2026V 6077C>T LICA-FR 3 47047047 47047047 single base substitution C T missense_variant A2210V 6629C>T LICA-FR 3 47047047 47047047 single base substitution C T missense_variant A37V 110C>T LICA-FR 3 47047047 47047047 single base substitution C T missense_variant A489V 1466C>T LICA-FR 3 47047047 47047047 single base substitution C T missense_variant A578V 1733C>T LICA-FR 3 47047047 47047047 single base substitution C T upstream_gene_variant LICA-FR 3 47048757 47048757 single base substitution G T downstream_gene_variant LICA-FR 3 47048757 47048757 single base substitution G T exon_variant LICA-FR 3 47048757 47048757 single base substitution G T intron_variant LICA-FR 3 47048757 47048757 single base substitution G T synonymous_variant L1704L 5112G>T LICA-FR 3 47048757 47048757 single base substitution G T synonymous_variant L2233L 6699G>T LICA-FR 3 47048757 47048757 single base substitution G T synonymous_variant L2417L 7251G>T LICA-FR 3 47048757 47048757 single base substitution G T synonymous_variant L666L 1998G>T LICA-FR 3 47048757 47048757 single base substitution G T synonymous_variant L755L 2265G>T LICA-FR 3 47048757 47048757 single base substitution G T upstream_gene_variant LIHC-US 3 47030821 47030821 single base substitution C G 5_prime_UTR_premature_start_codon_gain_variant LIHC-US 3 47030821 47030821 single base substitution C G synonymous_variant L141L 423C>G LIHC-US 3 47037989 47037989 single base substitution G T 5_prime_UTR_variant LIHC-US 3 47037989 47037989 single base substitution G T missense_variant G265C 793G>T LIHC-US 3 47037989 47037989 single base substitution G T missense_variant G794C 2380G>T LIHC-US 3 47037989 47037989 single base substitution G T upstream_gene_variant LIHC-US 3 47040281 47040281 single base substitution A G 5_prime_UTR_variant LIHC-US 3 47040281 47040281 single base substitution A G missense_variant E1099G 3296A>G LIHC-US 3 47040281 47040281 single base substitution A G missense_variant E570G 1709A>G LIHC-US 3 47040281 47040281 single base substitution A G upstream_gene_variant LIHC-US 3 47042832 47042832 single base substitution G T 5_prime_UTR_premature_start_codon_gain_variant LIHC-US 3 47042832 47042832 single base substitution G T exon_variant LIHC-US 3 47042832 47042832 single base substitution G T synonymous_variant L1332L 3996G>T LIHC-US 3 47042832 47042832 single base substitution G T synonymous_variant L1516L 4548G>T LIHC-US 3 47042832 47042832 single base substitution G T synonymous_variant L803L 2409G>T LIHC-US 3 47042832 47042832 single base substitution G T upstream_gene_variant LIHC-US 3 47043918 47043918 single base substitution A T downstream_gene_variant LIHC-US 3 47043918 47043918 single base substitution A T missense_variant M1024L 3070A>T LIHC-US 3 47043918 47043918 single base substitution A T missense_variant M105L 313A>T LIHC-US 3 47043918 47043918 single base substitution A T missense_variant M1553L 4657A>T LIHC-US 3 47043918 47043918 single base substitution A T missense_variant M16L 46A>T LIHC-US 3 47043918 47043918 single base substitution A T missense_variant M1737L 5209A>T LIHC-US 3 47043918 47043918 single base substitution A T upstream_gene_variant LIHC-US 3 47043973 47043973 single base substitution G T downstream_gene_variant LIHC-US 3 47043973 47043973 single base substitution G T missense_variant R1042L 3125G>T LIHC-US 3 47043973 47043973 single base substitution G T missense_variant R123L 368G>T LIHC-US 3 47043973 47043973 single base substitution G T missense_variant R1571L 4712G>T LIHC-US 3 47043973 47043973 single base substitution G T missense_variant R1755L 5264G>T LIHC-US 3 47043973 47043973 single base substitution G T missense_variant R34L 101G>T LIHC-US 3 47043973 47043973 single base substitution G T upstream_gene_variant LIHC-US 3 47046023 47046023 single base substitution G T downstream_gene_variant LIHC-US 3 47046023 47046023 single base substitution G T exon_variant LIHC-US 3 47046023 47046023 single base substitution G T missense_variant L1366F 4098G>T LIHC-US 3 47046023 47046023 single base substitution G T missense_variant L1895F 5685G>T LIHC-US 3 47046023 47046023 single base substitution G T missense_variant L2079F 6237G>T LIHC-US 3 47046023 47046023 single base substitution G T missense_variant L358F 1074G>T LIHC-US 3 47046023 47046023 single base substitution G T missense_variant L447F 1341G>T LIHC-US 3 47046023 47046023 single base substitution G T upstream_gene_variant LINC-JP 3 47018374 47018374 single base substitution C T upstream_gene_variant LINC-JP 3 47021674 47021674 single base substitution T C intron_variant LINC-JP 3 47033863 47033863 single base substitution G A intron_variant LINC-JP 3 47033863 47033863 single base substitution G A upstream_gene_variant LINC-JP 3 47036877 47036877 single base substitution A T 5_prime_UTR_variant LINC-JP 3 47036877 47036877 single base substitution A T missense_variant E22V 65A>T LINC-JP 3 47036877 47036877 single base substitution A T missense_variant E551V 1652A>T LINC-JP 3 47043555 47043555 single base substitution A T 5_prime_UTR_premature_start_codon_gain_variant LINC-JP 3 47043555 47043555 single base substitution A T downstream_gene_variant LINC-JP 3 47043555 47043555 single base substitution A T missense_variant D11V 32A>T LINC-JP 3 47043555 47043555 single base substitution A T missense_variant D1459V 4376A>T LINC-JP 3 47043555 47043555 single base substitution A T missense_variant D1643V 4928A>T LINC-JP 3 47043555 47043555 single base substitution A T missense_variant D930V 2789A>T LINC-JP 3 47043555 47043555 single base substitution A T upstream_gene_variant LINC-JP 3 47044103 47044103 single base substitution G T downstream_gene_variant LINC-JP 3 47044103 47044103 single base substitution G T intron_variant LINC-JP 3 47044103 47044103 single base substitution G T upstream_gene_variant LINC-JP 3 47044248 47044248 single base substitution G T downstream_gene_variant LINC-JP 3 47044248 47044248 single base substitution G T synonymous_variant A1092A 3276G>T LINC-JP 3 47044248 47044248 single base substitution G T synonymous_variant A1621A 4863G>T LINC-JP 3 47044248 47044248 single base substitution G T synonymous_variant A173A 519G>T LINC-JP 3 47044248 47044248 single base substitution G T synonymous_variant A1805A 5415G>T LINC-JP 3 47044248 47044248 single base substitution G T synonymous_variant A84A 252G>T LINC-JP 3 47044248 47044248 single base substitution G T upstream_gene_variant LINC-JP 3 47044249 47044249 single base substitution C T downstream_gene_variant LINC-JP 3 47044249 47044249 single base substitution C T synonymous_variant L1093L 3277C>T LINC-JP 3 47044249 47044249 single base substitution C T synonymous_variant L1622L 4864C>T LINC-JP 3 47044249 47044249 single base substitution C T synonymous_variant L174L 520C>T LINC-JP 3 47044249 47044249 single base substitution C T synonymous_variant L1806L 5416C>T LINC-JP 3 47044249 47044249 single base substitution C T synonymous_variant L85L 253C>T LINC-JP 3 47044249 47044249 single base substitution C T upstream_gene_variant LINC-JP 3 47045432 47045432 single base substitution C T downstream_gene_variant LINC-JP 3 47045432 47045432 single base substitution C T synonymous_variant Y1236Y 3708C>T LINC-JP 3 47045432 47045432 single base substitution C T synonymous_variant Y1765Y 5295C>T LINC-JP 3 47045432 47045432 single base substitution C T synonymous_variant Y1949Y 5847C>T LINC-JP 3 47045432 47045432 single base substitution C T synonymous_variant Y228Y 684C>T LINC-JP 3 47045432 47045432 single base substitution C T synonymous_variant Y317Y 951C>T LINC-JP 3 47045432 47045432 single base substitution C T upstream_gene_variant LINC-JP 3 47047462 47047462 single base substitution A G downstream_gene_variant LINC-JP 3 47047462 47047462 single base substitution A G exon_variant LINC-JP 3 47047462 47047462 single base substitution A G synonymous_variant L103L 309A>G LINC-JP 3 47047462 47047462 single base substitution A G synonymous_variant L1563L 4689A>G LINC-JP 3 47047462 47047462 single base substitution A G synonymous_variant L2092L 6276A>G LINC-JP 3 47047462 47047462 single base substitution A G synonymous_variant L2276L 6828A>G LINC-JP 3 47047462 47047462 single base substitution A G synonymous_variant L555L 1665A>G LINC-JP 3 47047462 47047462 single base substitution A G synonymous_variant L644L 1932A>G LINC-JP 3 47047462 47047462 single base substitution A G upstream_gene_variant LINC-JP 3 47050859 47050859 single base substitution G T 3_prime_UTR_variant LINC-JP 3 47050859 47050859 single base substitution G T downstream_gene_variant LINC-JP 3 47050964 47050964 single base substitution C G 3_prime_UTR_variant LINC-JP 3 47050964 47050964 single base substitution C G downstream_gene_variant LIRI-JP 3 47016642 47016642 single base substitution C A upstream_gene_variant LIRI-JP 3 47017641 47017641 single base substitution T C upstream_gene_variant LIRI-JP 3 47017646 47017646 single base substitution T G upstream_gene_variant LIRI-JP 3 47019930 47019930 insertion of <=200bp - A upstream_gene_variant LIRI-JP 3 47027294 47027294 single base substitution G A intron_variant LIRI-JP 3 47027676 47027676 single base substitution C A intron_variant LIRI-JP 3 47030855 47030855 single base substitution C T 5_prime_UTR_variant LIRI-JP 3 47030855 47030855 single base substitution C T missense_variant R153W 457C>T LIRI-JP 3 47031419 47031419 single base substitution A G intron_variant LIRI-JP 3 47032784 47032784 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant LIRI-JP 3 47032784 47032784 single base substitution C T missense_variant A211V 632C>T LIRI-JP 3 47032784 47032784 single base substitution C T upstream_gene_variant LIRI-JP 3 47033737 47033737 single base substitution G T intron_variant LIRI-JP 3 47033737 47033737 single base substitution G T upstream_gene_variant LIRI-JP 3 47038078 47038078 single base substitution C G 5_prime_UTR_variant LIRI-JP 3 47038078 47038078 single base substitution C G synonymous_variant T294T 882C>G LIRI-JP 3 47038078 47038078 single base substitution C G synonymous_variant T823T 2469C>G LIRI-JP 3 47038078 47038078 single base substitution C G upstream_gene_variant LIRI-JP 3 47038484 47038484 single base substitution A T 5_prime_UTR_premature_start_codon_gain_variant LIRI-JP 3 47038484 47038484 single base substitution A T missense_variant H337L 1010A>T LIRI-JP 3 47038484 47038484 single base substitution A T missense_variant H866L 2597A>T LIRI-JP 3 47038484 47038484 single base substitution A T upstream_gene_variant LIRI-JP 3 47047527 47047527 single base substitution A G downstream_gene_variant LIRI-JP 3 47047527 47047527 single base substitution A G exon_variant LIRI-JP 3 47047527 47047527 single base substitution A G missense_variant N125S 374A>G LIRI-JP 3 47047527 47047527 single base substitution A G missense_variant N1585S 4754A>G LIRI-JP 3 47047527 47047527 single base substitution A G missense_variant N2114S 6341A>G LIRI-JP 3 47047527 47047527 single base substitution A G missense_variant N2298S 6893A>G LIRI-JP 3 47047527 47047527 single base substitution A G missense_variant N577S 1730A>G LIRI-JP 3 47047527 47047527 single base substitution A G missense_variant N666S 1997A>G LIRI-JP 3 47047527 47047527 single base substitution A G upstream_gene_variant LIRI-JP 3 47052271 47052271 single base substitution A C downstream_gene_variant LIRI-JP 3 47053575 47053575 single base substitution G A downstream_gene_variant LIRI-JP 3 47055148 47055148 single base substitution C T downstream_gene_variant LUSC-KR 3 47018432 47018432 single base substitution T G upstream_gene_variant LUSC-KR 3 47025200 47025200 single base substitution A T intron_variant LUSC-KR 3 47039583 47039583 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant LUSC-KR 3 47039583 47039583 single base substitution C T synonymous_variant N466N 1398C>T LUSC-KR 3 47039583 47039583 single base substitution C T synonymous_variant N995N 2985C>T LUSC-KR 3 47039583 47039583 single base substitution C T upstream_gene_variant LUSC-KR 3 47043605 47043605 single base substitution C T 5_prime_UTR_variant LUSC-KR 3 47043605 47043605 single base substitution C T downstream_gene_variant LUSC-KR 3 47043605 47043605 single base substitution C T missense_variant R1476C 4426C>T LUSC-KR 3 47043605 47043605 single base substitution C T missense_variant R1660C 4978C>T LUSC-KR 3 47043605 47043605 single base substitution C T missense_variant R28C 82C>T LUSC-KR 3 47043605 47043605 single base substitution C T missense_variant R947C 2839C>T LUSC-KR 3 47043605 47043605 single base substitution C T upstream_gene_variant LUSC-KR 3 47051547 47051547 single base substitution G A downstream_gene_variant LUSC-KR 3 47054869 47054869 single base substitution C A downstream_gene_variant LUSC-US 3 47030752 47030752 single base substitution G T splice_region_variant LUSC-US 3 47037075 47037075 single base substitution C T 5_prime_UTR_variant LUSC-US 3 47037075 47037075 single base substitution C T missense_variant A617V 1850C>T LUSC-US 3 47037075 47037075 single base substitution C T missense_variant A88V 263C>T LUSC-US 3 47043973 47043973 single base substitution G A downstream_gene_variant LUSC-US 3 47043973 47043973 single base substitution G A missense_variant R1042H 3125G>A LUSC-US 3 47043973 47043973 single base substitution G A missense_variant R123H 368G>A LUSC-US 3 47043973 47043973 single base substitution G A missense_variant R1571H 4712G>A LUSC-US 3 47043973 47043973 single base substitution G A missense_variant R1755H 5264G>A LUSC-US 3 47043973 47043973 single base substitution G A missense_variant R34H 101G>A LUSC-US 3 47043973 47043973 single base substitution G A upstream_gene_variant LUSC-US 3 47044477 47044477 single base substitution C A downstream_gene_variant LUSC-US 3 47044477 47044477 single base substitution C A synonymous_variant S109S 327C>A LUSC-US 3 47044477 47044477 single base substitution C A synonymous_variant S1117S 3351C>A LUSC-US 3 47044477 47044477 single base substitution C A synonymous_variant S1646S 4938C>A LUSC-US 3 47044477 47044477 single base substitution C A synonymous_variant S1830S 5490C>A LUSC-US 3 47044477 47044477 single base substitution C A synonymous_variant S198S 594C>A LUSC-US 3 47044477 47044477 single base substitution C A upstream_gene_variant LUSC-US 3 47045732 47045732 single base substitution A G downstream_gene_variant LUSC-US 3 47045732 47045732 single base substitution A G exon_variant LUSC-US 3 47045732 47045732 single base substitution A G missense_variant Q1303R 3908A>G LUSC-US 3 47045732 47045732 single base substitution A G missense_variant Q1832R 5495A>G LUSC-US 3 47045732 47045732 single base substitution A G missense_variant Q2016R 6047A>G LUSC-US 3 47045732 47045732 single base substitution A G missense_variant Q295R 884A>G LUSC-US 3 47045732 47045732 single base substitution A G missense_variant Q384R 1151A>G LUSC-US 3 47045732 47045732 single base substitution A G upstream_gene_variant MALY-DE 3 47017848 47017848 single base substitution C T upstream_gene_variant MALY-DE 3 47029756 47029756 deletion of <=200bp G - intron_variant MALY-DE 3 47037956 47037956 single base substitution T C 5_prime_UTR_variant MALY-DE 3 47037956 47037956 single base substitution T C missense_variant S254P 760T>C MALY-DE 3 47037956 47037956 single base substitution T C missense_variant S783P 2347T>C MALY-DE 3 47037956 47037956 single base substitution T C upstream_gene_variant MALY-DE 3 47042463 47042463 single base substitution C T exon_variant MALY-DE 3 47042463 47042463 single base substitution C T intron_variant MALY-DE 3 47042463 47042463 single base substitution C T upstream_gene_variant MALY-DE 3 47043577 47043598 deletion of <=200bp AGCTGCAGCAGCTGCAGCAGCT - 5_prime_UTR_variant MALY-DE 3 47043577 47043598 deletion of <=200bp AGCTGCAGCAGCTGCAGCAGCT - downstream_gene_variant MALY-DE 3 47043577 47043598 deletion of <=200bp AGCTGCAGCAGCTGCAGCAGCT - frameshift_variant AAAAAAAA1466 MALY-DE 3 47043577 47043598 deletion of <=200bp AGCTGCAGCAGCTGCAGCAGCT - frameshift_variant AAAAAAAA1650 MALY-DE 3 47043577 47043598 deletion of <=200bp AGCTGCAGCAGCTGCAGCAGCT - frameshift_variant AAAAAAAA18 MALY-DE 3 47043577 47043598 deletion of <=200bp AGCTGCAGCAGCTGCAGCAGCT - frameshift_variant AAAAAAAA937 MALY-DE 3 47043577 47043598 deletion of <=200bp AGCTGCAGCAGCTGCAGCAGCT - upstream_gene_variant MALY-DE 3 47049756 47049756 single base substitution A G downstream_gene_variant MALY-DE 3 47049756 47049756 single base substitution A G intron_variant MALY-DE 3 47056068 47056068 single base substitution G T downstream_gene_variant MELA-AU 3 47016225 47016225 single base substitution G A upstream_gene_variant MELA-AU 3 47016836 47016836 single base substitution G A upstream_gene_variant MELA-AU 3 47017330 47017330 single base substitution G A upstream_gene_variant MELA-AU 3 47017374 47017374 single base substitution T C upstream_gene_variant MELA-AU 3 47017974 47017974 single base substitution G A upstream_gene_variant MELA-AU 3 47019477 47019477 single base substitution C T upstream_gene_variant MELA-AU 3 47020240 47020240 single base substitution G A upstream_gene_variant MELA-AU 3 47021102 47021102 single base substitution G A upstream_gene_variant MELA-AU 3 47022983 47022984 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 3 47023646 47023646 single base substitution G A intron_variant MELA-AU 3 47023731 47023731 single base substitution G A intron_variant MELA-AU 3 47023790 47023790 single base substitution C T intron_variant MELA-AU 3 47023966 47023966 single base substitution C T intron_variant MELA-AU 3 47024049 47024049 single base substitution C T intron_variant MELA-AU 3 47024706 47024706 single base substitution C T intron_variant MELA-AU 3 47025153 47025153 single base substitution G A intron_variant MELA-AU 3 47025277 47025277 single base substitution C T intron_variant MELA-AU 3 47025539 47025539 single base substitution C T intron_variant MELA-AU 3 47025638 47025638 single base substitution A T intron_variant MELA-AU 3 47025912 47025912 single base substitution G A intron_variant MELA-AU 3 47026106 47026106 single base substitution C T intron_variant MELA-AU 3 47026269 47026269 single base substitution C T intron_variant MELA-AU 3 47026323 47026323 single base substitution T C intron_variant MELA-AU 3 47026599 47026599 single base substitution C T intron_variant MELA-AU 3 47026996 47026996 single base substitution C T intron_variant MELA-AU 3 47027026 47027026 single base substitution G A intron_variant MELA-AU 3 47027143 47027143 single base substitution C T intron_variant MELA-AU 3 47027200 47027200 single base substitution G A intron_variant MELA-AU 3 47027631 47027631 single base substitution C T intron_variant MELA-AU 3 47027697 47027697 insertion of <=200bp - A intron_variant MELA-AU 3 47027717 47027717 single base substitution G A intron_variant MELA-AU 3 47029283 47029283 single base substitution A G intron_variant MELA-AU 3 47029386 47029386 single base substitution C T intron_variant MELA-AU 3 47029550 47029550 single base substitution C T intron_variant MELA-AU 3 47030095 47030095 single base substitution T G intron_variant MELA-AU 3 47030319 47030319 single base substitution C T intron_variant MELA-AU 3 47030577 47030577 single base substitution A G missense_variant N91S 272A>G MELA-AU 3 47030577 47030577 single base substitution A G splice_region_variant MELA-AU 3 47030713 47030713 single base substitution C T intron_variant MELA-AU 3 47030970 47030970 single base substitution G A intron_variant MELA-AU 3 47031138 47031138 single base substitution C T intron_variant MELA-AU 3 47031395 47031395 single base substitution C T intron_variant MELA-AU 3 47031550 47031550 single base substitution C T intron_variant MELA-AU 3 47031556 47031556 single base substitution C T intron_variant MELA-AU 3 47031566 47031566 single base substitution C T intron_variant MELA-AU 3 47032044 47032044 single base substitution C T intron_variant MELA-AU 3 47032044 47032044 single base substitution C T upstream_gene_variant MELA-AU 3 47032055 47032055 single base substitution C T intron_variant MELA-AU 3 47032055 47032055 single base substitution C T upstream_gene_variant MELA-AU 3 47032131 47032131 single base substitution C T intron_variant MELA-AU 3 47032131 47032131 single base substitution C T upstream_gene_variant MELA-AU 3 47032983 47032983 single base substitution C T 5_prime_UTR_variant MELA-AU 3 47032983 47032983 single base substitution C T missense_variant P244S 730C>T MELA-AU 3 47032983 47032983 single base substitution C T upstream_gene_variant MELA-AU 3 47033056 47033056 single base substitution C T 5_prime_UTR_variant MELA-AU 3 47033056 47033056 single base substitution C T missense_variant P268L 803C>T MELA-AU 3 47033056 47033056 single base substitution C T upstream_gene_variant MELA-AU 3 47033068 47033068 single base substitution A G 5_prime_UTR_variant MELA-AU 3 47033068 47033068 single base substitution A G missense_variant E272G 815A>G MELA-AU 3 47033068 47033068 single base substitution A G upstream_gene_variant MELA-AU 3 47033114 47033114 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant MELA-AU 3 47033114 47033114 single base substitution C T synonymous_variant D287D 861C>T MELA-AU 3 47033114 47033114 single base substitution C T upstream_gene_variant MELA-AU 3 47033610 47033611 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 3 47033610 47033611 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 3 47033782 47033782 single base substitution C T intron_variant MELA-AU 3 47033782 47033782 single base substitution C T upstream_gene_variant MELA-AU 3 47033796 47033796 single base substitution C T intron_variant MELA-AU 3 47033796 47033796 single base substitution C T upstream_gene_variant MELA-AU 3 47034644 47034644 single base substitution C T intron_variant MELA-AU 3 47034644 47034644 single base substitution C T upstream_gene_variant MELA-AU 3 47034817 47034817 single base substitution C T intron_variant MELA-AU 3 47034817 47034817 single base substitution C T upstream_gene_variant MELA-AU 3 47034857 47034857 single base substitution C T intron_variant MELA-AU 3 47034857 47034857 single base substitution C T upstream_gene_variant MELA-AU 3 47034863 47034863 single base substitution G A intron_variant MELA-AU 3 47034863 47034863 single base substitution G A upstream_gene_variant MELA-AU 3 47035078 47035078 single base substitution C T intron_variant MELA-AU 3 47035078 47035078 single base substitution C T upstream_gene_variant MELA-AU 3 47035533 47035533 single base substitution T C intron_variant MELA-AU 3 47035533 47035533 single base substitution T C upstream_gene_variant MELA-AU 3 47035858 47035858 single base substitution T G intron_variant MELA-AU 3 47035858 47035858 single base substitution T G upstream_gene_variant MELA-AU 3 47036048 47036048 single base substitution G A splice_region_variant MELA-AU 3 47036048 47036048 single base substitution G A upstream_gene_variant MELA-AU 3 47037052 47037052 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant MELA-AU 3 47037052 47037052 single base substitution C T synonymous_variant L609L 1827C>T MELA-AU 3 47037052 47037052 single base substitution C T synonymous_variant L80L 240C>T MELA-AU 3 47037344 47037344 single base substitution C T splice_region_variant MELA-AU 3 47037983 47037983 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant MELA-AU 3 47037983 47037983 single base substitution C T missense_variant R263W 787C>T MELA-AU 3 47037983 47037983 single base substitution C T missense_variant R792W 2374C>T MELA-AU 3 47037983 47037983 single base substitution C T upstream_gene_variant MELA-AU 3 47038029 47038029 single base substitution C T 5_prime_UTR_variant MELA-AU 3 47038029 47038029 single base substitution C T missense_variant A278V 833C>T MELA-AU 3 47038029 47038029 single base substitution C T missense_variant A807V 2420C>T MELA-AU 3 47038029 47038029 single base substitution C T upstream_gene_variant MELA-AU 3 47038040 47038040 single base substitution G A 5_prime_UTR_variant MELA-AU 3 47038040 47038040 single base substitution G A missense_variant E282K 844G>A MELA-AU 3 47038040 47038040 single base substitution G A missense_variant E811K 2431G>A MELA-AU 3 47038040 47038040 single base substitution G A upstream_gene_variant MELA-AU 3 47038369 47038369 single base substitution C T intron_variant MELA-AU 3 47038369 47038369 single base substitution C T upstream_gene_variant MELA-AU 3 47039107 47039107 single base substitution C T 5_prime_UTR_variant MELA-AU 3 47039107 47039107 single base substitution C T missense_variant L432F 1294C>T MELA-AU 3 47039107 47039107 single base substitution C T missense_variant L961F 2881C>T MELA-AU 3 47039107 47039107 single base substitution C T upstream_gene_variant MELA-AU 3 47039688 47039688 single base substitution G A 5_prime_UTR_variant MELA-AU 3 47039688 47039688 single base substitution G A stop_gained W1030* 3090G>A MELA-AU 3 47039688 47039688 single base substitution G A stop_gained W501* 1503G>A MELA-AU 3 47039688 47039688 single base substitution G A upstream_gene_variant MELA-AU 3 47040330 47040330 single base substitution C T 5_prime_UTR_variant MELA-AU 3 47040330 47040330 single base substitution C T synonymous_variant T1115T 3345C>T MELA-AU 3 47040330 47040330 single base substitution C T synonymous_variant T586T 1758C>T MELA-AU 3 47040330 47040330 single base substitution C T upstream_gene_variant MELA-AU 3 47040870 47040870 single base substitution G A 5_prime_UTR_variant MELA-AU 3 47040870 47040870 single base substitution G A synonymous_variant R1150R 3450G>A MELA-AU 3 47040870 47040870 single base substitution G A synonymous_variant R1203R 3609G>A MELA-AU 3 47040870 47040870 single base substitution G A synonymous_variant R621R 1863G>A MELA-AU 3 47040870 47040870 single base substitution G A upstream_gene_variant MELA-AU 3 47041163 47041163 single base substitution C T 5_prime_UTR_variant MELA-AU 3 47041163 47041163 single base substitution C T intron_variant MELA-AU 3 47041163 47041163 single base substitution C T synonymous_variant S1249S 3747C>T MELA-AU 3 47041163 47041163 single base substitution C T upstream_gene_variant MELA-AU 3 47041508 47041508 single base substitution C T 5_prime_UTR_variant MELA-AU 3 47041508 47041508 single base substitution C T intron_variant MELA-AU 3 47041508 47041508 single base substitution C T missense_variant P1307S 3919C>T MELA-AU 3 47041508 47041508 single base substitution C T upstream_gene_variant MELA-AU 3 47042845 47042845 single base substitution C T 5_prime_UTR_variant MELA-AU 3 47042845 47042845 single base substitution C T exon_variant MELA-AU 3 47042845 47042845 single base substitution C T stop_gained Q1337* 4009C>T MELA-AU 3 47042845 47042845 single base substitution C T stop_gained Q1521* 4561C>T MELA-AU 3 47042845 47042845 single base substitution C T stop_gained Q808* 2422C>T MELA-AU 3 47042845 47042845 single base substitution C T upstream_gene_variant MELA-AU 3 47043116 47043116 single base substitution C T intron_variant MELA-AU 3 47043116 47043116 single base substitution C T upstream_gene_variant MELA-AU 3 47043118 47043118 single base substitution C T intron_variant MELA-AU 3 47043118 47043118 single base substitution C T upstream_gene_variant MELA-AU 3 47043196 47043196 single base substitution C A 5_prime_UTR_variant MELA-AU 3 47043196 47043196 single base substitution C A exon_variant MELA-AU 3 47043196 47043196 single base substitution C A stop_gained C1370* 4110C>A MELA-AU 3 47043196 47043196 single base substitution C A stop_gained C1554* 4662C>A MELA-AU 3 47043196 47043196 single base substitution C A stop_gained C841* 2523C>A MELA-AU 3 47043196 47043196 single base substitution C A upstream_gene_variant MELA-AU 3 47043798 47043798 single base substitution C T downstream_gene_variant MELA-AU 3 47043798 47043798 single base substitution C T intron_variant MELA-AU 3 47043798 47043798 single base substitution C T upstream_gene_variant MELA-AU 3 47044657 47044657 single base substitution C T downstream_gene_variant MELA-AU 3 47044657 47044657 single base substitution C T splice_region_variant MELA-AU 3 47044657 47044657 single base substitution C T upstream_gene_variant MELA-AU 3 47044715 47044715 single base substitution C T downstream_gene_variant MELA-AU 3 47044715 47044715 single base substitution C T missense_variant T1166I 3497C>T MELA-AU 3 47044715 47044715 single base substitution C T missense_variant T158I 473C>T MELA-AU 3 47044715 47044715 single base substitution C T missense_variant T1695I 5084C>T MELA-AU 3 47044715 47044715 single base substitution C T missense_variant T1879I 5636C>T MELA-AU 3 47044715 47044715 single base substitution C T missense_variant T247I 740C>T MELA-AU 3 47044715 47044715 single base substitution C T upstream_gene_variant MELA-AU 3 47044737 47044737 single base substitution C T downstream_gene_variant MELA-AU 3 47044737 47044737 single base substitution C T synonymous_variant T1173T 3519C>T MELA-AU 3 47044737 47044737 single base substitution C T synonymous_variant T165T 495C>T MELA-AU 3 47044737 47044737 single base substitution C T synonymous_variant T1702T 5106C>T MELA-AU 3 47044737 47044737 single base substitution C T synonymous_variant T1886T 5658C>T MELA-AU 3 47044737 47044737 single base substitution C T synonymous_variant T254T 762C>T MELA-AU 3 47044737 47044737 single base substitution C T upstream_gene_variant MELA-AU 3 47044852 47044852 single base substitution C A downstream_gene_variant MELA-AU 3 47044852 47044852 single base substitution C A intron_variant MELA-AU 3 47044852 47044852 single base substitution C A upstream_gene_variant MELA-AU 3 47044919 47044920 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 3 47044919 47044920 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 3 47044919 47044920 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 3 47044999 47044999 single base substitution G A downstream_gene_variant MELA-AU 3 47044999 47044999 single base substitution G A intron_variant MELA-AU 3 47044999 47044999 single base substitution G A upstream_gene_variant MELA-AU 3 47045390 47045390 single base substitution C T downstream_gene_variant MELA-AU 3 47045390 47045390 single base substitution C T synonymous_variant V1222V 3666C>T MELA-AU 3 47045390 47045390 single base substitution C T synonymous_variant V1751V 5253C>T MELA-AU 3 47045390 47045390 single base substitution C T synonymous_variant V1935V 5805C>T MELA-AU 3 47045390 47045390 single base substitution C T synonymous_variant V214V 642C>T MELA-AU 3 47045390 47045390 single base substitution C T synonymous_variant V303V 909C>T MELA-AU 3 47045390 47045390 single base substitution C T upstream_gene_variant MELA-AU 3 47045980 47045980 single base substitution C T downstream_gene_variant MELA-AU 3 47045980 47045980 single base substitution C T splice_region_variant MELA-AU 3 47045980 47045980 single base substitution C T upstream_gene_variant MELA-AU 3 47046090 47046090 single base substitution C T downstream_gene_variant MELA-AU 3 47046090 47046090 single base substitution C T intron_variant MELA-AU 3 47046090 47046090 single base substitution C T upstream_gene_variant MELA-AU 3 47046518 47046518 single base substitution C T downstream_gene_variant MELA-AU 3 47046518 47046518 single base substitution C T exon_variant MELA-AU 3 47046518 47046518 single base substitution C T intron_variant MELA-AU 3 47046518 47046518 single base substitution C T synonymous_variant A1404A 4212C>T MELA-AU 3 47046518 47046518 single base substitution C T synonymous_variant A1933A 5799C>T MELA-AU 3 47046518 47046518 single base substitution C T synonymous_variant A2117A 6351C>T MELA-AU 3 47046518 47046518 single base substitution C T synonymous_variant A396A 1188C>T MELA-AU 3 47046518 47046518 single base substitution C T synonymous_variant A485A 1455C>T MELA-AU 3 47046518 47046518 single base substitution C T upstream_gene_variant MELA-AU 3 47046609 47046609 single base substitution G A downstream_gene_variant MELA-AU 3 47046609 47046609 single base substitution G A intron_variant MELA-AU 3 47046609 47046609 single base substitution G A upstream_gene_variant MELA-AU 3 47046819 47046819 single base substitution C G downstream_gene_variant MELA-AU 3 47046819 47046819 single base substitution C G intron_variant MELA-AU 3 47046819 47046819 single base substitution C G splice_region_variant MELA-AU 3 47046819 47046819 single base substitution C G upstream_gene_variant MELA-AU 3 47047520 47047520 single base substitution G A downstream_gene_variant MELA-AU 3 47047520 47047520 single base substitution G A exon_variant MELA-AU 3 47047520 47047520 single base substitution G A missense_variant A123T 367G>A MELA-AU 3 47047520 47047520 single base substitution G A missense_variant A1583T 4747G>A MELA-AU 3 47047520 47047520 single base substitution G A missense_variant A2112T 6334G>A MELA-AU 3 47047520 47047520 single base substitution G A missense_variant A2296T 6886G>A MELA-AU 3 47047520 47047520 single base substitution G A missense_variant A575T 1723G>A MELA-AU 3 47047520 47047520 single base substitution G A missense_variant A664T 1990G>A MELA-AU 3 47047520 47047520 single base substitution G A upstream_gene_variant MELA-AU 3 47048023 47048023 single base substitution G A downstream_gene_variant MELA-AU 3 47048023 47048023 single base substitution G A intron_variant MELA-AU 3 47048023 47048023 single base substitution G A upstream_gene_variant MELA-AU 3 47048262 47048262 single base substitution C T downstream_gene_variant MELA-AU 3 47048262 47048262 single base substitution C T intron_variant MELA-AU 3 47048262 47048262 single base substitution C T upstream_gene_variant MELA-AU 3 47048678 47048678 single base substitution C T downstream_gene_variant MELA-AU 3 47048678 47048678 single base substitution C T exon_variant MELA-AU 3 47048678 47048678 single base substitution C T intron_variant MELA-AU 3 47048678 47048678 single base substitution C T upstream_gene_variant MELA-AU 3 47048952 47048952 single base substitution C T downstream_gene_variant MELA-AU 3 47048952 47048952 single base substitution C T exon_variant MELA-AU 3 47048952 47048952 single base substitution C T intron_variant MELA-AU 3 47048952 47048952 single base substitution C T upstream_gene_variant MELA-AU 3 47049505 47049505 single base substitution C G downstream_gene_variant MELA-AU 3 47049505 47049505 single base substitution C G exon_variant MELA-AU 3 47049505 47049505 single base substitution C G intron_variant MELA-AU 3 47049918 47049918 single base substitution G A downstream_gene_variant MELA-AU 3 47049918 47049918 single base substitution G A exon_variant MELA-AU 3 47049918 47049918 single base substitution G A missense_variant R1909H 5726G>A MELA-AU 3 47049918 47049918 single base substitution G A missense_variant R2438H 7313G>A MELA-AU 3 47049918 47049918 single base substitution G A missense_variant R2622H 7865G>A MELA-AU 3 47049918 47049918 single base substitution G A missense_variant R871H 2612G>A MELA-AU 3 47049918 47049918 single base substitution G A missense_variant R960H 2879G>A MELA-AU 3 47049928 47049928 single base substitution C T downstream_gene_variant MELA-AU 3 47049928 47049928 single base substitution C T exon_variant MELA-AU 3 47049928 47049928 single base substitution C T synonymous_variant A1912A 5736C>T MELA-AU 3 47049928 47049928 single base substitution C T synonymous_variant A2441A 7323C>T MELA-AU 3 47049928 47049928 single base substitution C T synonymous_variant A2625A 7875C>T MELA-AU 3 47049928 47049928 single base substitution C T synonymous_variant A874A 2622C>T MELA-AU 3 47049928 47049928 single base substitution C T synonymous_variant A963A 2889C>T MELA-AU 3 47050065 47050066 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 3 47050065 47050066 multiple base substitution (>=2bp and <=200bp) CC TT exon_variant MELA-AU 3 47050065 47050066 multiple base substitution (>=2bp and <=200bp) CC TT missense_variant P1932L 5795CC>TT MELA-AU 3 47050065 47050066 multiple base substitution (>=2bp and <=200bp) CC TT missense_variant P2461L 7382CC>TT MELA-AU 3 47050065 47050066 multiple base substitution (>=2bp and <=200bp) CC TT missense_variant P2645L 7934CC>TT MELA-AU 3 47050065 47050066 multiple base substitution (>=2bp and <=200bp) CC TT missense_variant P894L 2681CC>TT MELA-AU 3 47050065 47050066 multiple base substitution (>=2bp and <=200bp) CC TT missense_variant P983L 2948CC>TT MELA-AU 3 47052059 47052059 single base substitution G T downstream_gene_variant MELA-AU 3 47052304 47052304 single base substitution C T downstream_gene_variant MELA-AU 3 47053413 47053413 single base substitution G A downstream_gene_variant MELA-AU 3 47053469 47053469 single base substitution G A downstream_gene_variant MELA-AU 3 47053656 47053656 single base substitution G A downstream_gene_variant ORCA-IN 3 47032135 47032135 single base substitution C T intron_variant ORCA-IN 3 47032135 47032135 single base substitution C T upstream_gene_variant ORCA-IN 3 47036563 47036563 single base substitution C A 5_prime_UTR_variant ORCA-IN 3 47036563 47036563 single base substitution C A synonymous_variant I446I 1338C>A ORCA-IN 3 47036563 47036563 single base substitution C A upstream_gene_variant ORCA-IN 3 47036662 47036662 single base substitution T A 5_prime_UTR_variant ORCA-IN 3 47036662 47036662 single base substitution T A stop_gained C479* 1437T>A ORCA-IN 3 47036662 47036662 single base substitution T A upstream_gene_variant ORCA-IN 3 47046026 47046026 single base substitution G A downstream_gene_variant ORCA-IN 3 47046026 47046026 single base substitution G A exon_variant ORCA-IN 3 47046026 47046026 single base substitution G A missense_variant M1367I 4101G>A ORCA-IN 3 47046026 47046026 single base substitution G A missense_variant M1896I 5688G>A ORCA-IN 3 47046026 47046026 single base substitution G A missense_variant M2080I 6240G>A ORCA-IN 3 47046026 47046026 single base substitution G A missense_variant M359I 1077G>A ORCA-IN 3 47046026 47046026 single base substitution G A missense_variant M448I 1344G>A ORCA-IN 3 47046026 47046026 single base substitution G A upstream_gene_variant OV-AU 3 47019631 47019631 single base substitution C T upstream_gene_variant OV-AU 3 47025149 47025149 single base substitution A T intron_variant OV-AU 3 47030179 47030179 single base substitution G A 5_prime_UTR_variant OV-AU 3 47030179 47030179 single base substitution G A synonymous_variant Q24Q 72G>A OV-AU 3 47051732 47051732 single base substitution A T downstream_gene_variant OV-US 3 47050489 47050489 single base substitution G A downstream_gene_variant OV-US 3 47050489 47050489 single base substitution G A exon_variant OV-US 3 47050489 47050489 single base substitution G A missense_variant A1018T 3052G>A OV-US 3 47050489 47050489 single base substitution G A missense_variant A1967T 5899G>A OV-US 3 47050489 47050489 single base substitution G A missense_variant A2496T 7486G>A OV-US 3 47050489 47050489 single base substitution G A missense_variant A2680T 8038G>A OV-US 3 47050489 47050489 single base substitution G A missense_variant A929T 2785G>A PACA-AU 3 47023421 47023421 single base substitution C T intron_variant PACA-AU 3 47028365 47028365 single base substitution G A intron_variant PACA-AU 3 47028775 47028786 deletion of <=200bp GGAGCAGCCTGA - intron_variant PACA-AU 3 47030874 47030874 single base substitution G A splice_region_variant PACA-AU 3 47031131 47031131 single base substitution C T intron_variant PACA-AU 3 47035627 47035627 single base substitution C A intron_variant PACA-AU 3 47035627 47035627 single base substitution C A upstream_gene_variant PACA-AU 3 47036897 47036897 single base substitution G A 5_prime_UTR_variant PACA-AU 3 47036897 47036897 single base substitution G A missense_variant A29T 85G>A PACA-AU 3 47036897 47036897 single base substitution G A missense_variant A558T 1672G>A PACA-AU 3 47040285 47040285 deletion of <=200bp C - 5_prime_UTR_variant PACA-AU 3 47040285 47040285 deletion of <=200bp C - frameshift_variant F1100 PACA-AU 3 47040285 47040285 deletion of <=200bp C - frameshift_variant F571 PACA-AU 3 47040285 47040285 deletion of <=200bp C - upstream_gene_variant PACA-AU 3 47041342 47041342 single base substitution T C intron_variant PACA-AU 3 47041342 47041342 single base substitution T C upstream_gene_variant PACA-AU 3 47044451 47044451 single base substitution A C downstream_gene_variant PACA-AU 3 47044451 47044451 single base substitution A C missense_variant T101P 301A>C PACA-AU 3 47044451 47044451 single base substitution A C missense_variant T1109P 3325A>C PACA-AU 3 47044451 47044451 single base substitution A C missense_variant T1638P 4912A>C PACA-AU 3 47044451 47044451 single base substitution A C missense_variant T1822P 5464A>C PACA-AU 3 47044451 47044451 single base substitution A C missense_variant T190P 568A>C PACA-AU 3 47044451 47044451 single base substitution A C upstream_gene_variant PACA-AU 3 47046048 47046048 single base substitution C T downstream_gene_variant PACA-AU 3 47046048 47046048 single base substitution C T exon_variant PACA-AU 3 47046048 47046048 single base substitution C T missense_variant R1375W 4123C>T PACA-AU 3 47046048 47046048 single base substitution C T missense_variant R1904W 5710C>T PACA-AU 3 47046048 47046048 single base substitution C T missense_variant R2088W 6262C>T PACA-AU 3 47046048 47046048 single base substitution C T missense_variant R367W 1099C>T PACA-AU 3 47046048 47046048 single base substitution C T missense_variant R456W 1366C>T PACA-AU 3 47046048 47046048 single base substitution C T upstream_gene_variant PACA-AU 3 47047957 47047957 single base substitution C T downstream_gene_variant PACA-AU 3 47047957 47047957 single base substitution C T intron_variant PACA-AU 3 47047957 47047957 single base substitution C T upstream_gene_variant PACA-AU 3 47054694 47054694 single base substitution C A downstream_gene_variant PACA-AU 3 47056060 47056071 deletion of <=200bp AGAAAGCAGGGA - downstream_gene_variant PACA-CA 3 47019390 47019390 single base substitution G T upstream_gene_variant PACA-CA 3 47022593 47022593 single base substitution A T intron_variant PACA-CA 3 47024058 47024058 single base substitution C T intron_variant PACA-CA 3 47030883 47030883 single base substitution C T intron_variant PACA-CA 3 47035644 47035644 single base substitution G A intron_variant PACA-CA 3 47035644 47035644 single base substitution G A upstream_gene_variant PACA-CA 3 47037248 47037248 insertion of <=200bp - G 5_prime_UTR_variant PACA-CA 3 47037248 47037248 insertion of <=200bp - G frameshift_variant A119G? PACA-CA 3 47037248 47037248 insertion of <=200bp - G frameshift_variant A648G? PACA-CA 3 47037537 47037537 single base substitution G T 5_prime_UTR_premature_start_codon_gain_variant PACA-CA 3 47037537 47037537 single base substitution G T missense_variant S187I 560G>T PACA-CA 3 47037537 47037537 single base substitution G T missense_variant S716I 2147G>T PACA-CA 3 47037537 47037537 single base substitution G T upstream_gene_variant PACA-CA 3 47043826 47043826 single base substitution C T downstream_gene_variant PACA-CA 3 47043826 47043826 single base substitution C T intron_variant PACA-CA 3 47043826 47043826 single base substitution C T upstream_gene_variant PACA-CA 3 47045229 47045229 single base substitution G T downstream_gene_variant PACA-CA 3 47045229 47045229 single base substitution G T intron_variant PACA-CA 3 47045229 47045229 single base substitution G T upstream_gene_variant PACA-CA 3 47045645 47045645 single base substitution C T downstream_gene_variant PACA-CA 3 47045645 47045645 single base substitution C T missense_variant A1274V 3821C>T PACA-CA 3 47045645 47045645 single base substitution C T missense_variant A1803V 5408C>T PACA-CA 3 47045645 47045645 single base substitution C T missense_variant A1987V 5960C>T PACA-CA 3 47045645 47045645 single base substitution C T missense_variant A266V 797C>T PACA-CA 3 47045645 47045645 single base substitution C T missense_variant A355V 1064C>T PACA-CA 3 47045645 47045645 single base substitution C T upstream_gene_variant PACA-CA 3 47047109 47047109 single base substitution G A downstream_gene_variant PACA-CA 3 47047109 47047109 single base substitution G A missense_variant G1518S 4552G>A PACA-CA 3 47047109 47047109 single base substitution G A missense_variant G2047S 6139G>A PACA-CA 3 47047109 47047109 single base substitution G A missense_variant G2231S 6691G>A PACA-CA 3 47047109 47047109 single base substitution G A missense_variant G510S 1528G>A PACA-CA 3 47047109 47047109 single base substitution G A missense_variant G58S 172G>A PACA-CA 3 47047109 47047109 single base substitution G A missense_variant G599S 1795G>A PACA-CA 3 47047109 47047109 single base substitution G A splice_region_variant PACA-CA 3 47047109 47047109 single base substitution G A upstream_gene_variant PACA-CA 3 47051824 47051824 single base substitution C T downstream_gene_variant PACA-CA 3 47052932 47052933 deletion of <=200bp GA - downstream_gene_variant PAEN-AU 3 47038394 47038394 single base substitution A C intron_variant PAEN-AU 3 47038394 47038394 single base substitution A C upstream_gene_variant PAEN-IT 3 47035901 47035901 single base substitution G A intron_variant PAEN-IT 3 47035901 47035901 single base substitution G A upstream_gene_variant PAEN-IT 3 47049209 47049209 single base substitution G T downstream_gene_variant PAEN-IT 3 47049209 47049209 single base substitution G T intron_variant PAEN-IT 3 47049209 47049209 single base substitution G T upstream_gene_variant PBCA-DE 3 47030001 47030001 single base substitution A C intron_variant PBCA-DE 3 47030926 47030926 single base substitution G A intron_variant PBCA-DE 3 47038498 47038498 single base substitution C T 5_prime_UTR_variant PBCA-DE 3 47038498 47038498 single base substitution C T missense_variant R342C 1024C>T PBCA-DE 3 47038498 47038498 single base substitution C T missense_variant R871C 2611C>T PBCA-DE 3 47038498 47038498 single base substitution C T upstream_gene_variant PBCA-DE 3 47049824 47049824 single base substitution C T downstream_gene_variant PBCA-DE 3 47049824 47049824 single base substitution C T exon_variant PBCA-DE 3 47049824 47049824 single base substitution C T synonymous_variant L1878L 5632C>T PBCA-DE 3 47049824 47049824 single base substitution C T synonymous_variant L2407L 7219C>T PBCA-DE 3 47049824 47049824 single base substitution C T synonymous_variant L2591L 7771C>T PBCA-DE 3 47049824 47049824 single base substitution C T synonymous_variant L840L 2518C>T PBCA-DE 3 47049824 47049824 single base substitution C T synonymous_variant L929L 2785C>T PBCA-DE 3 47050633 47050633 single base substitution T G downstream_gene_variant PBCA-DE 3 47050633 47050633 single base substitution T G intron_variant PRAD-CA 3 47018460 47018460 single base substitution G A upstream_gene_variant PRAD-CA 3 47026505 47026505 single base substitution C T intron_variant PRAD-CA 3 47037695 47037695 single base substitution A G intron_variant PRAD-CA 3 47037695 47037695 single base substitution A G upstream_gene_variant PRAD-CA 3 47049688 47049688 single base substitution C T downstream_gene_variant PRAD-CA 3 47049688 47049688 single base substitution C T intron_variant PRAD-UK 3 47022526 47022526 single base substitution C G intron_variant PRAD-UK 3 47048701 47048701 deletion of <=200bp A - downstream_gene_variant PRAD-UK 3 47048701 47048701 deletion of <=200bp A - exon_variant PRAD-UK 3 47048701 47048701 deletion of <=200bp A - intron_variant PRAD-UK 3 47048701 47048701 deletion of <=200bp A - upstream_gene_variant PRAD-US 3 47036899 47036899 single base substitution A G 5_prime_UTR_variant PRAD-US 3 47036899 47036899 single base substitution A G synonymous_variant A29A 87A>G PRAD-US 3 47036899 47036899 single base substitution A G synonymous_variant A558A 1674A>G PRAD-US 3 47038461 47038461 single base substitution C A 5_prime_UTR_premature_start_codon_gain_variant PRAD-US 3 47038461 47038461 single base substitution C A synonymous_variant I329I 987C>A PRAD-US 3 47038461 47038461 single base substitution C A synonymous_variant I858I 2574C>A PRAD-US 3 47038461 47038461 single base substitution C A upstream_gene_variant READ-US 3 47037248 47037248 single base substitution C T 5_prime_UTR_variant READ-US 3 47037248 47037248 single base substitution C T missense_variant A119V 356C>T READ-US 3 47037248 47037248 single base substitution C T missense_variant A648V 1943C>T READ-US 3 47041754 47041754 single base substitution C T 5_prime_UTR_variant READ-US 3 47041754 47041754 single base substitution C T missense_variant P1205S 3613C>T READ-US 3 47041754 47041754 single base substitution C T missense_variant P1389S 4165C>T READ-US 3 47041754 47041754 single base substitution C T missense_variant P676S 2026C>T READ-US 3 47041754 47041754 single base substitution C T upstream_gene_variant READ-US 3 47042529 47042529 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant READ-US 3 47042529 47042529 single base substitution C T exon_variant READ-US 3 47042529 47042529 single base substitution C T synonymous_variant N1264N 3792C>T READ-US 3 47042529 47042529 single base substitution C T synonymous_variant N1448N 4344C>T READ-US 3 47042529 47042529 single base substitution C T synonymous_variant N735N 2205C>T READ-US 3 47042529 47042529 single base substitution C T upstream_gene_variant READ-US 3 47046044 47046044 single base substitution G A downstream_gene_variant READ-US 3 47046044 47046044 single base substitution G A exon_variant READ-US 3 47046044 47046044 single base substitution G A synonymous_variant A1373A 4119G>A READ-US 3 47046044 47046044 single base substitution G A synonymous_variant A1902A 5706G>A READ-US 3 47046044 47046044 single base substitution G A synonymous_variant A2086A 6258G>A READ-US 3 47046044 47046044 single base substitution G A synonymous_variant A365A 1095G>A READ-US 3 47046044 47046044 single base substitution G A synonymous_variant A454A 1362G>A READ-US 3 47046044 47046044 single base substitution G A upstream_gene_variant RECA-EU 3 47031384 47031384 single base substitution C G intron_variant RECA-EU 3 47038577 47038577 single base substitution A T intron_variant RECA-EU 3 47038577 47038577 single base substitution A T upstream_gene_variant SKCA-BR 3 47016948 47016948 single base substitution A C upstream_gene_variant SKCA-BR 3 47018202 47018202 single base substitution A C upstream_gene_variant SKCA-BR 3 47018412 47018412 single base substitution C T upstream_gene_variant SKCA-BR 3 47020368 47020368 single base substitution G A upstream_gene_variant SKCA-BR 3 47022302 47022302 single base substitution A G intron_variant SKCA-BR 3 47023428 47023428 single base substitution G A intron_variant SKCA-BR 3 47023935 47023935 single base substitution C T intron_variant SKCA-BR 3 47026669 47026669 single base substitution C T intron_variant SKCA-BR 3 47031325 47031325 single base substitution T C intron_variant SKCA-BR 3 47035048 47035048 single base substitution T G intron_variant SKCA-BR 3 47035048 47035048 single base substitution T G upstream_gene_variant SKCA-BR 3 47041413 47041413 single base substitution T G 5_prime_UTR_variant SKCA-BR 3 47041413 47041413 single base substitution T G intron_variant SKCA-BR 3 47041413 47041413 single base substitution T G missense_variant V1275G 3824T>G SKCA-BR 3 47041413 47041413 single base substitution T G upstream_gene_variant SKCA-BR 3 47043383 47043383 single base substitution T G intron_variant SKCA-BR 3 47043383 47043383 single base substitution T G upstream_gene_variant SKCA-BR 3 47045542 47045542 single base substitution C T downstream_gene_variant SKCA-BR 3 47045542 47045542 single base substitution C T intron_variant SKCA-BR 3 47045542 47045542 single base substitution C T upstream_gene_variant SKCA-BR 3 47046099 47046099 single base substitution A C downstream_gene_variant SKCA-BR 3 47046099 47046099 single base substitution A C intron_variant SKCA-BR 3 47046099 47046099 single base substitution A C upstream_gene_variant SKCA-BR 3 47046465 47046465 single base substitution C T downstream_gene_variant SKCA-BR 3 47046465 47046465 single base substitution C T exon_variant SKCA-BR 3 47046465 47046465 single base substitution C T intron_variant SKCA-BR 3 47046465 47046465 single base substitution C T missense_variant P1387S 4159C>T SKCA-BR 3 47046465 47046465 single base substitution C T missense_variant P1916S 5746C>T SKCA-BR 3 47046465 47046465 single base substitution C T missense_variant P2100S 6298C>T SKCA-BR 3 47046465 47046465 single base substitution C T missense_variant P379S 1135C>T SKCA-BR 3 47046465 47046465 single base substitution C T missense_variant P468S 1402C>T SKCA-BR 3 47046465 47046465 single base substitution C T upstream_gene_variant SKCA-BR 3 47048452 47048452 single base substitution T G downstream_gene_variant SKCA-BR 3 47048452 47048452 single base substitution T G intron_variant SKCA-BR 3 47048452 47048452 single base substitution T G upstream_gene_variant SKCA-BR 3 47049497 47049497 single base substitution G A downstream_gene_variant SKCA-BR 3 47049497 47049497 single base substitution G A exon_variant SKCA-BR 3 47049497 47049497 single base substitution G A intron_variant SKCA-BR 3 47050633 47050633 single base substitution T G downstream_gene_variant SKCA-BR 3 47050633 47050633 single base substitution T G intron_variant SKCA-BR 3 47050638 47050638 single base substitution A G downstream_gene_variant SKCA-BR 3 47050638 47050638 single base substitution A G intron_variant SKCA-BR 3 47051682 47051682 single base substitution G A downstream_gene_variant SKCA-BR 3 47051916 47051916 single base substitution A G downstream_gene_variant SKCA-BR 3 47052245 47052245 single base substitution G C downstream_gene_variant SKCM-US 3 47030212 47030212 single base substitution G A 5_prime_UTR_variant SKCM-US 3 47030212 47030212 single base substitution G A synonymous_variant K35K 105G>A SKCM-US 3 47030358 47030358 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant SKCM-US 3 47030358 47030358 single base substitution C T missense_variant P56L 167C>T SKCM-US 3 47030424 47030424 single base substitution C T 5_prime_UTR_variant SKCM-US 3 47030424 47030424 single base substitution C T missense_variant A78V 233C>T SKCM-US 3 47031040 47031040 single base substitution C T 5_prime_UTR_variant SKCM-US 3 47031040 47031040 single base substitution C T synonymous_variant F171F 513C>T SKCM-US 3 47033073 47033073 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant SKCM-US 3 47033073 47033073 single base substitution C T missense_variant R274C 820C>T SKCM-US 3 47033073 47033073 single base substitution C T upstream_gene_variant SKCM-US 3 47033334 47033334 single base substitution C T 5_prime_UTR_variant SKCM-US 3 47033334 47033334 single base substitution C T synonymous_variant A310A 930C>T SKCM-US 3 47033334 47033334 single base substitution C T upstream_gene_variant SKCM-US 3 47037099 47037099 single base substitution C T 5_prime_UTR_variant SKCM-US 3 47037099 47037099 single base substitution C T missense_variant P625L 1874C>T SKCM-US 3 47037099 47037099 single base substitution C T missense_variant P96L 287C>T SKCM-US 3 47037254 47037254 single base substitution G A 5_prime_UTR_variant SKCM-US 3 47037254 47037254 single base substitution G A missense_variant G121E 362G>A SKCM-US 3 47037254 47037254 single base substitution G A missense_variant G650E 1949G>A SKCM-US 3 47038258 47038258 single base substitution C T 5_prime_UTR_variant SKCM-US 3 47038258 47038258 single base substitution C T missense_variant P302S 904C>T SKCM-US 3 47038258 47038258 single base substitution C T missense_variant P831S 2491C>T SKCM-US 3 47038258 47038258 single base substitution C T upstream_gene_variant SKCM-US 3 47041163 47041163 single base substitution C T 5_prime_UTR_variant SKCM-US 3 47041163 47041163 single base substitution C T intron_variant SKCM-US 3 47041163 47041163 single base substitution C T synonymous_variant S1249S 3747C>T SKCM-US 3 47041163 47041163 single base substitution C T upstream_gene_variant SKCM-US 3 47041164 47041164 single base substitution C T 5_prime_UTR_variant SKCM-US 3 47041164 47041164 single base substitution C T intron_variant SKCM-US 3 47041164 47041164 single base substitution C T missense_variant L1250F 3748C>T SKCM-US 3 47041164 47041164 single base substitution C T upstream_gene_variant SKCM-US 3 47041551 47041551 single base substitution C T 5_prime_UTR_variant SKCM-US 3 47041551 47041551 single base substitution C T intron_variant SKCM-US 3 47041551 47041551 single base substitution C T missense_variant P1321L 3962C>T SKCM-US 3 47041551 47041551 single base substitution C T upstream_gene_variant SKCM-US 3 47042819 47042819 single base substitution C T 5_prime_UTR_variant SKCM-US 3 47042819 47042819 single base substitution C T exon_variant SKCM-US 3 47042819 47042819 single base substitution C T missense_variant P1328L 3983C>T SKCM-US 3 47042819 47042819 single base substitution C T missense_variant P1512L 4535C>T SKCM-US 3 47042819 47042819 single base substitution C T missense_variant P799L 2396C>T SKCM-US 3 47042819 47042819 single base substitution C T upstream_gene_variant SKCM-US 3 47042835 47042835 single base substitution C T 5_prime_UTR_variant SKCM-US 3 47042835 47042835 single base substitution C T exon_variant SKCM-US 3 47042835 47042835 single base substitution C T synonymous_variant A1333A 3999C>T SKCM-US 3 47042835 47042835 single base substitution C T synonymous_variant A1517A 4551C>T SKCM-US 3 47042835 47042835 single base substitution C T synonymous_variant A804A 2412C>T SKCM-US 3 47042835 47042835 single base substitution C T upstream_gene_variant SKCM-US 3 47043209 47043209 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant SKCM-US 3 47043209 47043209 single base substitution C T exon_variant SKCM-US 3 47043209 47043209 single base substitution C T missense_variant R1375C 4123C>T SKCM-US 3 47043209 47043209 single base substitution C T missense_variant R1559C 4675C>T SKCM-US 3 47043209 47043209 single base substitution C T missense_variant R846C 2536C>T SKCM-US 3 47043209 47043209 single base substitution C T upstream_gene_variant SKCM-US 3 47043253 47043253 single base substitution C T 5_prime_UTR_variant SKCM-US 3 47043253 47043253 single base substitution C T exon_variant SKCM-US 3 47043253 47043253 single base substitution C T synonymous_variant L1389L 4167C>T SKCM-US 3 47043253 47043253 single base substitution C T synonymous_variant L1573L 4719C>T SKCM-US 3 47043253 47043253 single base substitution C T synonymous_variant L860L 2580C>T SKCM-US 3 47043253 47043253 single base substitution C T upstream_gene_variant SKCM-US 3 47043884 47043884 single base substitution C T downstream_gene_variant SKCM-US 3 47043884 47043884 single base substitution C T synonymous_variant F1012F 3036C>T SKCM-US 3 47043884 47043884 single base substitution C T synonymous_variant F1541F 4623C>T SKCM-US 3 47043884 47043884 single base substitution C T synonymous_variant F1725F 5175C>T SKCM-US 3 47043884 47043884 single base substitution C T synonymous_variant F4F 12C>T SKCM-US 3 47043884 47043884 single base substitution C T synonymous_variant F93F 279C>T SKCM-US 3 47043884 47043884 single base substitution C T upstream_gene_variant SKCM-US 3 47043969 47043969 single base substitution C T downstream_gene_variant SKCM-US 3 47043969 47043969 single base substitution C T missense_variant R1041W 3121C>T SKCM-US 3 47043969 47043969 single base substitution C T missense_variant R122W 364C>T SKCM-US 3 47043969 47043969 single base substitution C T missense_variant R1570W 4708C>T SKCM-US 3 47043969 47043969 single base substitution C T missense_variant R1754W 5260C>T SKCM-US 3 47043969 47043969 single base substitution C T missense_variant R33W 97C>T SKCM-US 3 47043969 47043969 single base substitution C T upstream_gene_variant SKCM-US 3 47044494 47044494 single base substitution C T downstream_gene_variant SKCM-US 3 47044494 47044494 single base substitution C T missense_variant S1123L 3368C>T SKCM-US 3 47044494 47044494 single base substitution C T missense_variant S115L 344C>T SKCM-US 3 47044494 47044494 single base substitution C T missense_variant S1652L 4955C>T SKCM-US 3 47044494 47044494 single base substitution C T missense_variant S1836L 5507C>T SKCM-US 3 47044494 47044494 single base substitution C T missense_variant S204L 611C>T SKCM-US 3 47044494 47044494 single base substitution C T upstream_gene_variant SKCM-US 3 47044715 47044715 single base substitution C T downstream_gene_variant SKCM-US 3 47044715 47044715 single base substitution C T missense_variant T1166I 3497C>T SKCM-US 3 47044715 47044715 single base substitution C T missense_variant T158I 473C>T SKCM-US 3 47044715 47044715 single base substitution C T missense_variant T1695I 5084C>T SKCM-US 3 47044715 47044715 single base substitution C T missense_variant T1879I 5636C>T SKCM-US 3 47044715 47044715 single base substitution C T missense_variant T247I 740C>T SKCM-US 3 47044715 47044715 single base substitution C T upstream_gene_variant SKCM-US 3 47045637 47045637 single base substitution C T downstream_gene_variant SKCM-US 3 47045637 47045637 single base substitution C T synonymous_variant R1271R 3813C>T SKCM-US 3 47045637 47045637 single base substitution C T synonymous_variant R1800R 5400C>T SKCM-US 3 47045637 47045637 single base substitution C T synonymous_variant R1984R 5952C>T SKCM-US 3 47045637 47045637 single base substitution C T synonymous_variant R263R 789C>T SKCM-US 3 47045637 47045637 single base substitution C T synonymous_variant R352R 1056C>T SKCM-US 3 47045637 47045637 single base substitution C T upstream_gene_variant SKCM-US 3 47045731 47045731 single base substitution C T downstream_gene_variant SKCM-US 3 47045731 47045731 single base substitution C T exon_variant SKCM-US 3 47045731 47045731 single base substitution C T stop_gained Q1303* 3907C>T SKCM-US 3 47045731 47045731 single base substitution C T stop_gained Q1832* 5494C>T SKCM-US 3 47045731 47045731 single base substitution C T stop_gained Q2016* 6046C>T SKCM-US 3 47045731 47045731 single base substitution C T stop_gained Q295* 883C>T SKCM-US 3 47045731 47045731 single base substitution C T stop_gained Q384* 1150C>T SKCM-US 3 47045731 47045731 single base substitution C T upstream_gene_variant SKCM-US 3 47045759 47045759 single base substitution T C downstream_gene_variant SKCM-US 3 47045759 47045759 single base substitution T C exon_variant SKCM-US 3 47045759 47045759 single base substitution T C missense_variant I1312T 3935T>C SKCM-US 3 47045759 47045759 single base substitution T C missense_variant I1841T 5522T>C SKCM-US 3 47045759 47045759 single base substitution T C missense_variant I2025T 6074T>C SKCM-US 3 47045759 47045759 single base substitution T C missense_variant I304T 911T>C SKCM-US 3 47045759 47045759 single base substitution T C missense_variant I393T 1178T>C SKCM-US 3 47045759 47045759 single base substitution T C upstream_gene_variant SKCM-US 3 47045856 47045856 single base substitution G A downstream_gene_variant SKCM-US 3 47045856 47045856 single base substitution G A exon_variant SKCM-US 3 47045856 47045856 single base substitution G A synonymous_variant E1344E 4032G>A SKCM-US 3 47045856 47045856 single base substitution G A synonymous_variant E1873E 5619G>A SKCM-US 3 47045856 47045856 single base substitution G A synonymous_variant E2057E 6171G>A SKCM-US 3 47045856 47045856 single base substitution G A synonymous_variant E336E 1008G>A SKCM-US 3 47045856 47045856 single base substitution G A synonymous_variant E425E 1275G>A SKCM-US 3 47045856 47045856 single base substitution G A upstream_gene_variant SKCM-US 3 47046037 47046037 single base substitution C T downstream_gene_variant SKCM-US 3 47046037 47046037 single base substitution C T exon_variant SKCM-US 3 47046037 47046037 single base substitution C T missense_variant T1371I 4112C>T SKCM-US 3 47046037 47046037 single base substitution C T missense_variant T1900I 5699C>T SKCM-US 3 47046037 47046037 single base substitution C T missense_variant T2084I 6251C>T SKCM-US 3 47046037 47046037 single base substitution C T missense_variant T363I 1088C>T SKCM-US 3 47046037 47046037 single base substitution C T missense_variant T452I 1355C>T SKCM-US 3 47046037 47046037 single base substitution C T upstream_gene_variant SKCM-US 3 47046714 47046714 single base substitution C T 3_prime_UTR_variant SKCM-US 3 47046714 47046714 single base substitution C T downstream_gene_variant SKCM-US 3 47046714 47046714 single base substitution C T exon_variant SKCM-US 3 47046714 47046714 single base substitution C T missense_variant H1442Y 4324C>T SKCM-US 3 47046714 47046714 single base substitution C T missense_variant H1971Y 5911C>T SKCM-US 3 47046714 47046714 single base substitution C T missense_variant H2155Y 6463C>T SKCM-US 3 47046714 47046714 single base substitution C T missense_variant H434Y 1300C>T SKCM-US 3 47046714 47046714 single base substitution C T missense_variant H523Y 1567C>T SKCM-US 3 47046714 47046714 single base substitution C T upstream_gene_variant SKCM-US 3 47047317 47047317 single base substitution C T downstream_gene_variant SKCM-US 3 47047317 47047317 single base substitution C T exon_variant SKCM-US 3 47047317 47047317 single base substitution C T stop_gained Q1548* 4642C>T SKCM-US 3 47047317 47047317 single base substitution C T stop_gained Q2077* 6229C>T SKCM-US 3 47047317 47047317 single base substitution C T stop_gained Q2261* 6781C>T SKCM-US 3 47047317 47047317 single base substitution C T stop_gained Q540* 1618C>T SKCM-US 3 47047317 47047317 single base substitution C T stop_gained Q629* 1885C>T SKCM-US 3 47047317 47047317 single base substitution C T stop_gained Q88* 262C>T SKCM-US 3 47047317 47047317 single base substitution C T upstream_gene_variant SKCM-US 3 47049159 47049159 single base substitution G A downstream_gene_variant SKCM-US 3 47049159 47049159 single base substitution G A exon_variant SKCM-US 3 47049159 47049159 single base substitution G A intron_variant SKCM-US 3 47049159 47049159 single base substitution G A missense_variant A254T 760G>A SKCM-US 3 47049159 47049159 single base substitution G A synonymous_variant K1780K 5340G>A SKCM-US 3 47049159 47049159 single base substitution G A synonymous_variant K2309K 6927G>A SKCM-US 3 47049159 47049159 single base substitution G A synonymous_variant K2493K 7479G>A SKCM-US 3 47049159 47049159 single base substitution G A synonymous_variant K742K 2226G>A SKCM-US 3 47049159 47049159 single base substitution G A synonymous_variant K831K 2493G>A SKCM-US 3 47049159 47049159 single base substitution G A upstream_gene_variant SKCM-US 3 47049364 47049364 single base substitution G A downstream_gene_variant SKCM-US 3 47049364 47049364 single base substitution G A exon_variant SKCM-US 3 47049364 47049364 single base substitution G A synonymous_variant R1809R 5427G>A SKCM-US 3 47049364 47049364 single base substitution G A synonymous_variant R2338R 7014G>A SKCM-US 3 47049364 47049364 single base substitution G A synonymous_variant R2522R 7566G>A SKCM-US 3 47049364 47049364 single base substitution G A synonymous_variant R771R 2313G>A SKCM-US 3 47049364 47049364 single base substitution G A synonymous_variant R860R 2580G>A SKCM-US 3 47049645 47049645 single base substitution C T downstream_gene_variant SKCM-US 3 47049645 47049645 single base substitution C T exon_variant SKCM-US 3 47049645 47049645 single base substitution C T missense_variant T1850I 5549C>T SKCM-US 3 47049645 47049645 single base substitution C T missense_variant T2379I 7136C>T SKCM-US 3 47049645 47049645 single base substitution C T missense_variant T2563I 7688C>T SKCM-US 3 47049645 47049645 single base substitution C T missense_variant T812I 2435C>T SKCM-US 3 47049645 47049645 single base substitution C T missense_variant T901I 2702C>T STAD-US 3 47030358 47030358 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant STAD-US 3 47030358 47030358 single base substitution C T missense_variant P56L 167C>T STAD-US 3 47030391 47030391 single base substitution C T 5_prime_UTR_variant STAD-US 3 47030391 47030391 single base substitution C T missense_variant A67V 200C>T STAD-US 3 47033984 47033984 single base substitution C T 5_prime_UTR_variant STAD-US 3 47033984 47033984 single base substitution C T missense_variant A351V 1052C>T STAD-US 3 47033984 47033984 single base substitution C T upstream_gene_variant STAD-US 3 47036838 47036838 single base substitution G A 5_prime_UTR_variant STAD-US 3 47036838 47036838 single base substitution G A missense_variant R538H 1613G>A STAD-US 3 47036838 47036838 single base substitution G A missense_variant R9H 26G>A STAD-US 3 47037020 47037020 single base substitution C T 5_prime_UTR_variant STAD-US 3 47037020 47037020 single base substitution C T missense_variant P599S 1795C>T STAD-US 3 47037020 47037020 single base substitution C T missense_variant P70S 208C>T STAD-US 3 47037022 47037022 single base substitution A G 5_prime_UTR_variant STAD-US 3 47037022 47037022 single base substitution A G synonymous_variant P599P 1797A>G STAD-US 3 47037022 47037022 single base substitution A G synonymous_variant P70P 210A>G STAD-US 3 47037074 47037074 single base substitution G A 5_prime_UTR_variant STAD-US 3 47037074 47037074 single base substitution G A missense_variant A617T 1849G>A STAD-US 3 47037074 47037074 single base substitution G A missense_variant A88T 262G>A STAD-US 3 47037219 47037219 single base substitution C T 5_prime_UTR_variant STAD-US 3 47037219 47037219 single base substitution C T synonymous_variant S109S 327C>T STAD-US 3 47037219 47037219 single base substitution C T synonymous_variant S638S 1914C>T STAD-US 3 47037248 47037248 single base substitution C T 5_prime_UTR_variant STAD-US 3 47037248 47037248 single base substitution C T missense_variant A119V 356C>T STAD-US 3 47037248 47037248 single base substitution C T missense_variant A648V 1943C>T STAD-US 3 47037863 47037863 single base substitution C T 5_prime_UTR_variant STAD-US 3 47037863 47037863 single base substitution C T missense_variant P223S 667C>T STAD-US 3 47037863 47037863 single base substitution C T missense_variant P752S 2254C>T STAD-US 3 47037863 47037863 single base substitution C T upstream_gene_variant STAD-US 3 47040920 47040920 deletion of <=200bp C - 5_prime_UTR_variant STAD-US 3 47040920 47040920 deletion of <=200bp C - frameshift_variant S1167 STAD-US 3 47040920 47040920 deletion of <=200bp C - frameshift_variant S1220 STAD-US 3 47040920 47040920 deletion of <=200bp C - frameshift_variant S638 STAD-US 3 47040920 47040920 deletion of <=200bp C - upstream_gene_variant STAD-US 3 47041809 47041809 single base substitution C A 5_prime_UTR_variant STAD-US 3 47041809 47041809 single base substitution C A missense_variant S1223Y 3668C>A STAD-US 3 47041809 47041809 single base substitution C A missense_variant S1407Y 4220C>A STAD-US 3 47041809 47041809 single base substitution C A missense_variant S694Y 2081C>A STAD-US 3 47041809 47041809 single base substitution C A upstream_gene_variant STAD-US 3 47041836 47041836 single base substitution G A 5_prime_UTR_variant STAD-US 3 47041836 47041836 single base substitution G A missense_variant G1232D 3695G>A STAD-US 3 47041836 47041836 single base substitution G A missense_variant G1416D 4247G>A STAD-US 3 47041836 47041836 single base substitution G A missense_variant G703D 2108G>A STAD-US 3 47041836 47041836 single base substitution G A upstream_gene_variant STAD-US 3 47042669 47042669 single base substitution G C exon_variant STAD-US 3 47042669 47042669 single base substitution G C missense_variant S1311T 3932G>C STAD-US 3 47042669 47042669 single base substitution G C missense_variant S1495T 4484G>C STAD-US 3 47042669 47042669 single base substitution G C missense_variant S782T 2345G>C STAD-US 3 47042669 47042669 single base substitution G C splice_region_variant STAD-US 3 47042669 47042669 single base substitution G C upstream_gene_variant STAD-US 3 47042782 47042782 single base substitution A G 5_prime_UTR_variant STAD-US 3 47042782 47042782 single base substitution A G exon_variant STAD-US 3 47042782 47042782 single base substitution A G missense_variant M1316V 3946A>G STAD-US 3 47042782 47042782 single base substitution A G missense_variant M1500V 4498A>G STAD-US 3 47042782 47042782 single base substitution A G missense_variant M787V 2359A>G STAD-US 3 47042782 47042782 single base substitution A G upstream_gene_variant STAD-US 3 47042816 47042816 deletion of <=200bp C - 5_prime_UTR_variant STAD-US 3 47042816 47042816 deletion of <=200bp C - exon_variant STAD-US 3 47042816 47042816 deletion of <=200bp C - frameshift_variant A1327 STAD-US 3 47042816 47042816 deletion of <=200bp C - frameshift_variant A1511 STAD-US 3 47042816 47042816 deletion of <=200bp C - frameshift_variant A798 STAD-US 3 47042816 47042816 deletion of <=200bp C - upstream_gene_variant STAD-US 3 47042822 47042822 insertion of <=200bp - G 5_prime_UTR_variant STAD-US 3 47042822 47042822 insertion of <=200bp - G exon_variant STAD-US 3 47042822 47042822 insertion of <=200bp - G frameshift_variant V1329G? STAD-US 3 47042822 47042822 insertion of <=200bp - G frameshift_variant V1513G? STAD-US 3 47042822 47042822 insertion of <=200bp - G frameshift_variant V800G? STAD-US 3 47042822 47042822 insertion of <=200bp - G upstream_gene_variant STAD-US 3 47042823 47042823 insertion of <=200bp - G 5_prime_UTR_variant STAD-US 3 47042823 47042823 insertion of <=200bp - G exon_variant STAD-US 3 47042823 47042823 insertion of <=200bp - G frameshift_variant V1329V? STAD-US 3 47042823 47042823 insertion of <=200bp - G frameshift_variant V1513V? STAD-US 3 47042823 47042823 insertion of <=200bp - G frameshift_variant V800V? STAD-US 3 47042823 47042823 insertion of <=200bp - G upstream_gene_variant STAD-US 3 47043424 47043424 single base substitution C A 5_prime_UTR_variant STAD-US 3 47043424 47043424 single base substitution C A exon_variant STAD-US 3 47043424 47043424 single base substitution C A synonymous_variant A1415A 4245C>A STAD-US 3 47043424 47043424 single base substitution C A synonymous_variant A1599A 4797C>A STAD-US 3 47043424 47043424 single base substitution C A synonymous_variant A886A 2658C>A STAD-US 3 47043424 47043424 single base substitution C A upstream_gene_variant STAD-US 3 47043895 47043895 single base substitution C T downstream_gene_variant STAD-US 3 47043895 47043895 single base substitution C T missense_variant T1016M 3047C>T STAD-US 3 47043895 47043895 single base substitution C T missense_variant T1545M 4634C>T STAD-US 3 47043895 47043895 single base substitution C T missense_variant T1729M 5186C>T STAD-US 3 47043895 47043895 single base substitution C T missense_variant T8M 23C>T STAD-US 3 47043895 47043895 single base substitution C T missense_variant T97M 290C>T STAD-US 3 47043895 47043895 single base substitution C T upstream_gene_variant STAD-US 3 47043945 47043945 single base substitution G A downstream_gene_variant STAD-US 3 47043945 47043945 single base substitution G A missense_variant D1033N 3097G>A STAD-US 3 47043945 47043945 single base substitution G A missense_variant D114N 340G>A STAD-US 3 47043945 47043945 single base substitution G A missense_variant D1562N 4684G>A STAD-US 3 47043945 47043945 single base substitution G A missense_variant D1746N 5236G>A STAD-US 3 47043945 47043945 single base substitution G A missense_variant D25N 73G>A STAD-US 3 47043945 47043945 single base substitution G A upstream_gene_variant STAD-US 3 47045630 47045630 single base substitution A G downstream_gene_variant STAD-US 3 47045630 47045630 single base substitution A G missense_variant N1269S 3806A>G STAD-US 3 47045630 47045630 single base substitution A G missense_variant N1798S 5393A>G STAD-US 3 47045630 47045630 single base substitution A G missense_variant N1982S 5945A>G STAD-US 3 47045630 47045630 single base substitution A G missense_variant N261S 782A>G STAD-US 3 47045630 47045630 single base substitution A G missense_variant N350S 1049A>G STAD-US 3 47045630 47045630 single base substitution A G upstream_gene_variant STAD-US 3 47045639 47045639 single base substitution G A downstream_gene_variant STAD-US 3 47045639 47045639 single base substitution G A missense_variant R1272H 3815G>A STAD-US 3 47045639 47045639 single base substitution G A missense_variant R1801H 5402G>A STAD-US 3 47045639 47045639 single base substitution G A missense_variant R1985H 5954G>A STAD-US 3 47045639 47045639 single base substitution G A missense_variant R264H 791G>A STAD-US 3 47045639 47045639 single base substitution G A missense_variant R353H 1058G>A STAD-US 3 47045639 47045639 single base substitution G A upstream_gene_variant STAD-US 3 47045664 47045664 single base substitution C A downstream_gene_variant STAD-US 3 47045664 47045664 single base substitution C A exon_variant STAD-US 3 47045664 47045664 single base substitution C A synonymous_variant I1280I 3840C>A STAD-US 3 47045664 47045664 single base substitution C A synonymous_variant I1809I 5427C>A STAD-US 3 47045664 47045664 single base substitution C A synonymous_variant I1993I 5979C>A STAD-US 3 47045664 47045664 single base substitution C A synonymous_variant I272I 816C>A STAD-US 3 47045664 47045664 single base substitution C A synonymous_variant I361I 1083C>A STAD-US 3 47045664 47045664 single base substitution C A upstream_gene_variant STAD-US 3 47045860 47045860 single base substitution C A downstream_gene_variant STAD-US 3 47045860 47045860 single base substitution C A exon_variant STAD-US 3 47045860 47045860 single base substitution C A missense_variant L1346M 4036C>A STAD-US 3 47045860 47045860 single base substitution C A missense_variant L1875M 5623C>A STAD-US 3 47045860 47045860 single base substitution C A missense_variant L2059M 6175C>A STAD-US 3 47045860 47045860 single base substitution C A missense_variant L338M 1012C>A STAD-US 3 47045860 47045860 single base substitution C A missense_variant L427M 1279C>A STAD-US 3 47045860 47045860 single base substitution C A upstream_gene_variant STAD-US 3 47046018 47046018 single base substitution T C downstream_gene_variant STAD-US 3 47046018 47046018 single base substitution T C exon_variant STAD-US 3 47046018 47046018 single base substitution T C missense_variant Y1365H 4093T>C STAD-US 3 47046018 47046018 single base substitution T C missense_variant Y1894H 5680T>C STAD-US 3 47046018 47046018 single base substitution T C missense_variant Y2078H 6232T>C STAD-US 3 47046018 47046018 single base substitution T C missense_variant Y357H 1069T>C STAD-US 3 47046018 47046018 single base substitution T C missense_variant Y446H 1336T>C STAD-US 3 47046018 47046018 single base substitution T C upstream_gene_variant STAD-US 3 47046463 47046463 insertion of <=200bp - C downstream_gene_variant STAD-US 3 47046463 47046463 insertion of <=200bp - C exon_variant STAD-US 3 47046463 47046463 insertion of <=200bp - C frameshift_variant F1386S? STAD-US 3 47046463 47046463 insertion of <=200bp - C frameshift_variant F1915S? STAD-US 3 47046463 47046463 insertion of <=200bp - C frameshift_variant F2099S? STAD-US 3 47046463 47046463 insertion of <=200bp - C frameshift_variant F378S? STAD-US 3 47046463 47046463 insertion of <=200bp - C frameshift_variant F467S? STAD-US 3 47046463 47046463 insertion of <=200bp - C intron_variant STAD-US 3 47046463 47046463 insertion of <=200bp - C upstream_gene_variant STAD-US 3 47047069 47047069 single base substitution G A 3_prime_UTR_variant STAD-US 3 47047069 47047069 single base substitution G A downstream_gene_variant STAD-US 3 47047069 47047069 single base substitution G A exon_variant STAD-US 3 47047069 47047069 single base substitution G A synonymous_variant P1504P 4512G>A STAD-US 3 47047069 47047069 single base substitution G A synonymous_variant P2033P 6099G>A STAD-US 3 47047069 47047069 single base substitution G A synonymous_variant P2217P 6651G>A STAD-US 3 47047069 47047069 single base substitution G A synonymous_variant P44P 132G>A STAD-US 3 47047069 47047069 single base substitution G A synonymous_variant P496P 1488G>A STAD-US 3 47047069 47047069 single base substitution G A synonymous_variant P585P 1755G>A STAD-US 3 47047069 47047069 single base substitution G A upstream_gene_variant STAD-US 3 47049627 47049627 single base substitution G A downstream_gene_variant STAD-US 3 47049627 47049627 single base substitution G A exon_variant STAD-US 3 47049627 47049627 single base substitution G A missense_variant S1844N 5531G>A STAD-US 3 47049627 47049627 single base substitution G A missense_variant S2373N 7118G>A STAD-US 3 47049627 47049627 single base substitution G A missense_variant S2557N 7670G>A STAD-US 3 47049627 47049627 single base substitution G A missense_variant S806N 2417G>A STAD-US 3 47049627 47049627 single base substitution G A missense_variant S895N 2684G>A STAD-US 3 47049819 47049819 single base substitution C T downstream_gene_variant STAD-US 3 47049819 47049819 single base substitution C T exon_variant STAD-US 3 47049819 47049819 single base substitution C T missense_variant A1876V 5627C>T STAD-US 3 47049819 47049819 single base substitution C T missense_variant A2405V 7214C>T STAD-US 3 47049819 47049819 single base substitution C T missense_variant A2589V 7766C>T STAD-US 3 47049819 47049819 single base substitution C T missense_variant A838V 2513C>T STAD-US 3 47049819 47049819 single base substitution C T missense_variant A927V 2780C>T STAD-US 3 47049917 47049917 single base substitution C T downstream_gene_variant STAD-US 3 47049917 47049917 single base substitution C T exon_variant STAD-US 3 47049917 47049917 single base substitution C T missense_variant R1909C 5725C>T STAD-US 3 47049917 47049917 single base substitution C T missense_variant R2438C 7312C>T STAD-US 3 47049917 47049917 single base substitution C T missense_variant R2622C 7864C>T STAD-US 3 47049917 47049917 single base substitution C T missense_variant R871C 2611C>T STAD-US 3 47049917 47049917 single base substitution C T missense_variant R960C 2878C>T STAD-US 3 47050494 47050494 single base substitution G A downstream_gene_variant STAD-US 3 47050494 47050494 single base substitution G A exon_variant STAD-US 3 47050494 47050494 single base substitution G A synonymous_variant A1019A 3057G>A STAD-US 3 47050494 47050494 single base substitution G A synonymous_variant A1968A 5904G>A STAD-US 3 47050494 47050494 single base substitution G A synonymous_variant A2497A 7491G>A STAD-US 3 47050494 47050494 single base substitution G A synonymous_variant A2681A 8043G>A STAD-US 3 47050494 47050494 single base substitution G A synonymous_variant A930A 2790G>A THCA-SA 3 47036756 47036756 single base substitution C G 5_prime_UTR_variant THCA-SA 3 47036756 47036756 single base substitution C G missense_variant R511G 1531C>G THCA-SA 3 47036756 47036756 single base substitution C G upstream_gene_variant THCA-SA 3 47043622 47043622 single base substitution G A 5_prime_UTR_variant THCA-SA 3 47043622 47043622 single base substitution G A downstream_gene_variant THCA-SA 3 47043622 47043622 single base substitution G A synonymous_variant V1481V 4443G>A THCA-SA 3 47043622 47043622 single base substitution G A synonymous_variant V1665V 4995G>A THCA-SA 3 47043622 47043622 single base substitution G A synonymous_variant V33V 99G>A THCA-SA 3 47043622 47043622 single base substitution G A synonymous_variant V952V 2856G>A THCA-SA 3 47043622 47043622 single base substitution G A upstream_gene_variant THCA-SA 3 47045846 47045846 single base substitution C T downstream_gene_variant THCA-SA 3 47045846 47045846 single base substitution C T exon_variant THCA-SA 3 47045846 47045846 single base substitution C T missense_variant S1341F 4022C>T THCA-SA 3 47045846 47045846 single base substitution C T missense_variant S1870F 5609C>T THCA-SA 3 47045846 47045846 single base substitution C T missense_variant S2054F 6161C>T THCA-SA 3 47045846 47045846 single base substitution C T missense_variant S333F 998C>T THCA-SA 3 47045846 47045846 single base substitution C T missense_variant S422F 1265C>T THCA-SA 3 47045846 47045846 single base substitution C T upstream_gene_variant THCA-SA 3 47051029 47051029 single base substitution A C 3_prime_UTR_variant THCA-SA 3 47051029 47051029 single base substitution A C downstream_gene_variant THCA-SA 3 47054869 47054869 single base substitution C A downstream_gene_variant THCA-US 3 47030166 47030166 single base substitution T C 5_prime_UTR_variant THCA-US 3 47030166 47030166 single base substitution T C missense_variant L20P 59T>C THCA-US 3 47042545 47042545 single base substitution A G 5_prime_UTR_variant THCA-US 3 47042545 47042545 single base substitution A G exon_variant THCA-US 3 47042545 47042545 single base substitution A G missense_variant T1270A 3808A>G THCA-US 3 47042545 47042545 single base substitution A G missense_variant T1454A 4360A>G THCA-US 3 47042545 47042545 single base substitution A G missense_variant T741A 2221A>G THCA-US 3 47042545 47042545 single base substitution A G upstream_gene_variant UCEC-US 3 47030239 47030239 single base substitution G A 5_prime_UTR_variant UCEC-US 3 47030239 47030239 single base substitution G A synonymous_variant E44E 132G>A UCEC-US 3 47030652 47030652 single base substitution C T 5_prime_UTR_variant UCEC-US 3 47030652 47030652 single base substitution C T missense_variant A116V 347C>T UCEC-US 3 47030858 47030858 single base substitution C T 5_prime_UTR_variant UCEC-US 3 47030858 47030858 single base substitution C T missense_variant R154C 460C>T UCEC-US 3 47032927 47032927 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant UCEC-US 3 47032927 47032927 single base substitution C T missense_variant S225F 674C>T UCEC-US 3 47032927 47032927 single base substitution C T upstream_gene_variant UCEC-US 3 47036998 47036998 single base substitution G T 5_prime_UTR_premature_start_codon_gain_variant UCEC-US 3 47036998 47036998 single base substitution G T missense_variant M591I 1773G>T UCEC-US 3 47036998 47036998 single base substitution G T missense_variant M62I 186G>T UCEC-US 3 47037248 47037248 single base substitution C T 5_prime_UTR_variant UCEC-US 3 47037248 47037248 single base substitution C T missense_variant A119V 356C>T UCEC-US 3 47037248 47037248 single base substitution C T missense_variant A648V 1943C>T UCEC-US 3 47037427 47037427 single base substitution C T 5_prime_UTR_variant UCEC-US 3 47037427 47037427 single base substitution C T synonymous_variant C150C 450C>T UCEC-US 3 47037427 47037427 single base substitution C T synonymous_variant C679C 2037C>T UCEC-US 3 47037797 47037797 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant UCEC-US 3 47037797 47037797 single base substitution C T missense_variant R201C 601C>T UCEC-US 3 47037797 47037797 single base substitution C T missense_variant R730C 2188C>T UCEC-US 3 47037797 47037797 single base substitution C T upstream_gene_variant UCEC-US 3 47038872 47038872 single base substitution A G 5_prime_UTR_variant UCEC-US 3 47038872 47038872 single base substitution A G missense_variant T396A 1186A>G UCEC-US 3 47038872 47038872 single base substitution A G missense_variant T925A 2773A>G UCEC-US 3 47038872 47038872 single base substitution A G upstream_gene_variant UCEC-US 3 47039652 47039652 single base substitution A G 5_prime_UTR_premature_start_codon_gain_variant UCEC-US 3 47039652 47039652 single base substitution A G synonymous_variant L1018L 3054A>G UCEC-US 3 47039652 47039652 single base substitution A G synonymous_variant L489L 1467A>G UCEC-US 3 47039652 47039652 single base substitution A G upstream_gene_variant UCEC-US 3 47039982 47039982 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant UCEC-US 3 47039982 47039982 single base substitution C T missense_variant R1050W 3148C>T UCEC-US 3 47039982 47039982 single base substitution C T missense_variant R521W 1561C>T UCEC-US 3 47039982 47039982 single base substitution C T upstream_gene_variant UCEC-US 3 47040005 47040007 deletion of <=200bp GAA - 5_prime_UTR_variant UCEC-US 3 47040005 47040007 deletion of <=200bp GAA - inframe_deletion RK1057R UCEC-US 3 47040005 47040007 deletion of <=200bp GAA - inframe_deletion RK528R UCEC-US 3 47040005 47040007 deletion of <=200bp GAA - upstream_gene_variant UCEC-US 3 47040542 47040542 single base substitution G A 5_prime_UTR_variant UCEC-US 3 47040542 47040542 single base substitution G A intron_variant UCEC-US 3 47040542 47040542 single base substitution G A missense_variant E1160K 3478G>A UCEC-US 3 47040542 47040542 single base substitution G A upstream_gene_variant UCEC-US 3 47040917 47040917 single base substitution T C 5_prime_UTR_variant UCEC-US 3 47040917 47040917 single base substitution T C missense_variant V1166A 3497T>C UCEC-US 3 47040917 47040917 single base substitution T C missense_variant V1219A 3656T>C UCEC-US 3 47040917 47040917 single base substitution T C missense_variant V637A 1910T>C UCEC-US 3 47040917 47040917 single base substitution T C upstream_gene_variant UCEC-US 3 47041651 47041651 single base substitution G A 5_prime_UTR_variant UCEC-US 3 47041651 47041651 single base substitution G A intron_variant UCEC-US 3 47041651 47041651 single base substitution G A synonymous_variant T1354T 4062G>A UCEC-US 3 47041651 47041651 single base substitution G A upstream_gene_variant UCEC-US 3 47041733 47041733 single base substitution C T 5_prime_UTR_variant UCEC-US 3 47041733 47041733 single base substitution C T missense_variant P1198S 3592C>T UCEC-US 3 47041733 47041733 single base substitution C T missense_variant P1382S 4144C>T UCEC-US 3 47041733 47041733 single base substitution C T missense_variant P669S 2005C>T UCEC-US 3 47041733 47041733 single base substitution C T upstream_gene_variant UCEC-US 3 47041748 47041748 single base substitution G T 5_prime_UTR_premature_start_codon_gain_variant UCEC-US 3 47041748 47041748 single base substitution G T missense_variant G1203C 3607G>T UCEC-US 3 47041748 47041748 single base substitution G T missense_variant G1387C 4159G>T UCEC-US 3 47041748 47041748 single base substitution G T missense_variant G674C 2020G>T UCEC-US 3 47041748 47041748 single base substitution G T upstream_gene_variant UCEC-US 3 47042546 47042546 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant UCEC-US 3 47042546 47042546 single base substitution C T exon_variant UCEC-US 3 47042546 47042546 single base substitution C T missense_variant T1270M 3809C>T UCEC-US 3 47042546 47042546 single base substitution C T missense_variant T1454M 4361C>T UCEC-US 3 47042546 47042546 single base substitution C T missense_variant T741M 2222C>T UCEC-US 3 47042546 47042546 single base substitution C T upstream_gene_variant UCEC-US 3 47042644 47042644 single base substitution C T 5_prime_UTR_variant UCEC-US 3 47042644 47042644 single base substitution C T exon_variant UCEC-US 3 47042644 47042644 single base substitution C T missense_variant R1303C 3907C>T UCEC-US 3 47042644 47042644 single base substitution C T missense_variant R1487C 4459C>T UCEC-US 3 47042644 47042644 single base substitution C T missense_variant R774C 2320C>T UCEC-US 3 47042644 47042644 single base substitution C T upstream_gene_variant UCEC-US 3 47043999 47043999 single base substitution C T downstream_gene_variant UCEC-US 3 47043999 47043999 single base substitution C T missense_variant R1051W 3151C>T UCEC-US 3 47043999 47043999 single base substitution C T missense_variant R132W 394C>T UCEC-US 3 47043999 47043999 single base substitution C T missense_variant R1580W 4738C>T UCEC-US 3 47043999 47043999 single base substitution C T missense_variant R1764W 5290C>T UCEC-US 3 47043999 47043999 single base substitution C T missense_variant R43W 127C>T UCEC-US 3 47043999 47043999 single base substitution C T upstream_gene_variant UCEC-US 3 47045639 47045639 single base substitution G A downstream_gene_variant UCEC-US 3 47045639 47045639 single base substitution G A missense_variant R1272H 3815G>A UCEC-US 3 47045639 47045639 single base substitution G A missense_variant R1801H 5402G>A UCEC-US 3 47045639 47045639 single base substitution G A missense_variant R1985H 5954G>A UCEC-US 3 47045639 47045639 single base substitution G A missense_variant R264H 791G>A UCEC-US 3 47045639 47045639 single base substitution G A missense_variant R353H 1058G>A UCEC-US 3 47045639 47045639 single base substitution G A upstream_gene_variant UCEC-US 3 47045784 47045784 single base substitution C A downstream_gene_variant UCEC-US 3 47045784 47045784 single base substitution C A exon_variant UCEC-US 3 47045784 47045784 single base substitution C A missense_variant N1320K 3960C>A UCEC-US 3 47045784 47045784 single base substitution C A missense_variant N1849K 5547C>A UCEC-US 3 47045784 47045784 single base substitution C A missense_variant N2033K 6099C>A UCEC-US 3 47045784 47045784 single base substitution C A missense_variant N312K 936C>A UCEC-US 3 47045784 47045784 single base substitution C A missense_variant N401K 1203C>A UCEC-US 3 47045784 47045784 single base substitution C A upstream_gene_variant UCEC-US 3 47046765 47046765 single base substitution C T 3_prime_UTR_variant UCEC-US 3 47046765 47046765 single base substitution C T downstream_gene_variant UCEC-US 3 47046765 47046765 single base substitution C T exon_variant UCEC-US 3 47046765 47046765 single base substitution C T missense_variant R1459C 4375C>T UCEC-US 3 47046765 47046765 single base substitution C T missense_variant R1988C 5962C>T UCEC-US 3 47046765 47046765 single base substitution C T missense_variant R2172C 6514C>T UCEC-US 3 47046765 47046765 single base substitution C T missense_variant R451C 1351C>T UCEC-US 3 47046765 47046765 single base substitution C T missense_variant R540C 1618C>T UCEC-US 3 47046765 47046765 single base substitution C T upstream_gene_variant UCEC-US 3 47047508 47047508 single base substitution G A downstream_gene_variant UCEC-US 3 47047508 47047508 single base substitution G A exon_variant UCEC-US 3 47047508 47047508 single base substitution G A missense_variant A119T 355G>A UCEC-US 3 47047508 47047508 single base substitution G A missense_variant A1579T 4735G>A UCEC-US 3 47047508 47047508 single base substitution G A missense_variant A2108T 6322G>A UCEC-US 3 47047508 47047508 single base substitution G A missense_variant A2292T 6874G>A UCEC-US 3 47047508 47047508 single base substitution G A missense_variant A571T 1711G>A UCEC-US 3 47047508 47047508 single base substitution G A missense_variant A660T 1978G>A UCEC-US 3 47047508 47047508 single base substitution G A upstream_gene_variant UCEC-US 3 47047676 47047676 single base substitution T A downstream_gene_variant UCEC-US 3 47047676 47047676 single base substitution T A exon_variant UCEC-US 3 47047676 47047676 single base substitution T A missense_variant V141E 422T>A UCEC-US 3 47047676 47047676 single base substitution T A missense_variant V1601E 4802T>A UCEC-US 3 47047676 47047676 single base substitution T A missense_variant V2130E 6389T>A UCEC-US 3 47047676 47047676 single base substitution T A missense_variant V2314E 6941T>A UCEC-US 3 47047676 47047676 single base substitution T A missense_variant V593E 1778T>A UCEC-US 3 47047676 47047676 single base substitution T A missense_variant V682E 2045T>A UCEC-US 3 47047676 47047676 single base substitution T A upstream_gene_variant UCEC-US 3 47049305 47049305 single base substitution G T downstream_gene_variant UCEC-US 3 47049305 47049305 single base substitution G T exon_variant UCEC-US 3 47049305 47049305 single base substitution G T splice_acceptor_variant UCEC-US 3 47049339 47049339 single base substitution G A downstream_gene_variant UCEC-US 3 47049339 47049339 single base substitution G A exon_variant UCEC-US 3 47049339 47049339 single base substitution G A missense_variant G1801D 5402G>A UCEC-US 3 47049339 47049339 single base substitution G A missense_variant G2330D 6989G>A UCEC-US 3 47049339 47049339 single base substitution G A missense_variant G2514D 7541G>A UCEC-US 3 47049339 47049339 single base substitution G A missense_variant G763D 2288G>A UCEC-US 3 47049339 47049339 single base substitution G A missense_variant G852D 2555G>A UCEC-US 3 47049566 47049566 single base substitution C A downstream_gene_variant UCEC-US 3 47049566 47049566 single base substitution C A exon_variant UCEC-US 3 47049566 47049566 single base substitution C A missense_variant L1824M 5470C>A UCEC-US 3 47049566 47049566 single base substitution C A missense_variant L2353M 7057C>A UCEC-US 3 47049566 47049566 single base substitution C A missense_variant L2537M 7609C>A UCEC-US 3 47049566 47049566 single base substitution C A missense_variant L786M 2356C>A UCEC-US 3 47049566 47049566 single base substitution C A missense_variant L875M 2623C>A

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand TCGA-D9-A1JW-06 COSM1177394 c.3306C>T p.F1102F Substitution - coding silent 3:47002394-47002394 + TCGA-A2-A0T5-01 COSM3823990 c.4694A>C p.H1565P Substitution - Missense 3:47001738-47001738 + OSCC-GB_00250111 COSM3714551 c.4371G>A p.M1457I Substitution - Missense 3:47004536-47004536 + CSCC-27-T COSM4499742 c.549C>T p.F183F Substitution - coding silent 3:46989586-46989586 + HCC99 COSM3660580 c.5416C>T p.L1806L Substitution - coding silent 3:47002759-47002759 + TCGA-BR-8059-01 COSM4117972 c.6175C>A p.L2059M Substitution - Missense 3:47004370-47004370 + CSCC-27-T COSM4466396 c.115C>T p.L39F Substitution - Missense 3:46995167-46995167 + 1N05-VS-1T05 COSM4972877 c.2824+1G>T p.? Unknown 3:46997434-46997434 + T2950 COSM4705671 c.6884A>G p.E2295G Substitution - Missense 3:47006028-47006028 + TCGA-B5-A11E-01 COSM1045375 c.2188C>T p.R730C Substitution - Missense 3:46996307-46996307 + TCGA-AD-6964-01 COSM1423488 c.1420C>T p.R474C Substitution - Missense 3:46995155-46995155 + CSCC-31-T COSM4503919 c.6510C>T p.L2170L Substitution - coding silent 3:47005271-47005271 + pfg122T COSM4754396 c.6385G>A p.V2129M Substitution - Missense 3:47005062-47005062 + TCGA-02-0033 COSM2148950 c.294C>G p.G98G Substitution - coding silent 3:46989109-46989109 + C086 COSM5535219 c.3598C>T p.P1200S Substitution - Missense 3:47002964-47002964 + 587328 COSM1216724 c.5791G>T p.V1931L Substitution - Missense 3:47003886-47003886 + 417 COSM4431717 c.6366G>C p.E2122D Substitution - Missense 3:47009290-47009290 + WA25 COSM240829 c.5051-1G>T p.? Unknown 3:47006164-47006164 + TCGA-HU-A4GU-01 COSM4117975 c.4363T>C p.Y1455H Substitution - Missense 3:47004528-47004528 + PD18024a COSM5777314 c.539C>T p.T180I Substitution - Missense 3:46995591-46995591 + CHC1629T COSM4791740 c.6080C>A p.P2027H Substitution - Missense 3:47004275-47004275 + pfg181T COSM4754398 c.7069C>T p.R2357C Substitution - Missense 3:47006384-47006384 + CSCC-49-T COSM4539708 c.2722G>A p.E908K Substitution - Missense 3:46997331-46997331 + SNUH_G16_S1 COSM4002709 c.4704C>T p.N1568N Substitution - coding silent 3:47001748-47001748 + TCGA-A8-A0A6-01 COSM3823994 c.6085A>C p.T2029P Substitution - Missense 3:47004280-47004280 + SW620 COSM3068726 c.4866C>T p.G1622G Substitution - coding silent 3:47005781-47005781 + TCGA-EE-A2MR-06 COSM3594626 c.2806C>T p.R936C Substitution - Missense 3:47001719-47001719 + PCA25-2 COSM5415625 c.1180G>A p.D394N Substitution - Missense 3:46994003-46994003 + SC_9047 COSM5551410 c.1605C>T p.C535C Substitution - coding silent 3:46997658-46997658 + 2492722 COSM5720012 c.3936C>T p.S1312S Substitution - coding silent 3:47000035-47000035 + sysucc-783T COSM5484625 c.4499T>C p.M1500T Substitution - Missense 3:47001293-47001293 + CX-1 COSM3068697 c.6000C>T p.L2000L Substitution - coding silent 3:47004195-47004195 + TCGA-BP-4976-01 COSM480130 c.1122G>A p.L374L Substitution - coding silent 3:46996558-46996558 + 1 COSM1715968 c.2005G>A p.E669K Substitution - Missense 3:46995820-46995820 + TCGA-D3-A5GN-06 COSM3594633 c.5952C>T p.R1984R Substitution - coding silent 3:47004147-47004147 + TCGA-EE-A2M5-06 COSM3594623 c.4551C>T p.A1517A Substitution - coding silent 3:47001345-47001345 + PT32 COSM5907283 c.3604C>T p.P1202S Substitution - Missense 3:47002970-47002970 + TCGA-CC-A7IH-01 COSM4924049 c.4548G>T p.L1516L Substitution - coding silent 3:47001342-47001342 + TCGA-G3-A7M9-01 COSM4922609 c.1979A>G p.E660G Substitution - Missense 3:46998791-46998791 + C80 COSM3068613 c.1900T>G p.Y634D Substitution - Missense 3:46998561-46998561 + M021 COSM1738849 c.2528C>T p.T843I Substitution - Missense 3:46996805-46996805 + ATL007 COSM5708760 c.1766A>G p.H589R Substitution - Missense 3:46998191-46998191 + HCC020T COSM5809121 c.3398A>T p.Q1133L Substitution - Missense 3:47002486-47002486 + 1517_PT COSM5756285 c.3108C>T p.A1036A Substitution - coding silent 3:46998216-46998216 + 61 COSM5736587 c.2375G>A p.R792Q Substitution - Missense 3:46996494-46996494 + HCC089T COSM5822398 c.5348A>G p.D1783G Substitution - Missense 3:47007148-47007148 + CSCC-49-T COSM4477551 c.2162C>T p.S721F Substitution - Missense 3:46996281-46996281 + TCGA-GF-A6C9-06 COSM4902786 c.2850C>T p.L950L Substitution - coding silent 3:47001763-47001763 + T1154 COSM4705656 c.1025T>C p.I342T Substitution - Missense 3:46996461-46996461 + RMS105_ COSM4986221 c.1190G>A p.G397E Substitution - Missense 3:46996784-46996784 + TCGA-EE-A2MR-06 COSM3594629 c.5507C>T p.S1836L Substitution - Missense 3:47003004-47003004 + CSCC-27-T COSM4466395 c.1432C>T p.L478F Substitution - Missense 3:46995167-46995167 + TCGA-F4-6854-01 COSM3696117 c.4639C>T p.L1547F Substitution - Missense 3:47005269-47005269 + TCGA-B5-A11E-01 COSM1045410 c.6874G>A p.A2292T Substitution - Missense 3:47006018-47006018 + CHC892T COSM4794999 c.757G>A p.A253T Substitution - Missense 3:46991520-46991520 + 2492721 COSM5720010 c.2690C>T p.P897L Substitution - Missense 3:46997299-46997299 + PT49 COSM5934792 c.2141C>T p.S714F Substitution - Missense 3:46996041-46996041 + TCGA-21-1076-01 COSM730729 c.3395G>A p.R1132H Substitution - Missense 3:47002483-47002483 + TCGA-BS-A0WQ-01 COSM1045385 c.3171_3173delGAA p.K1059delK Deletion - In frame 3:46998515-46998517 + 587238 COSM1216716 c.5494G>A p.A1832T Substitution - Missense 3:47002991-47002991 + S00932 COSM5662422 c.2290A>G p.T764A Substitution - Missense 3:46996409-46996409 + 35M COSM5581806 c.5216C>T p.S1739L Substitution - Missense 3:47006400-47006400 + ESCC_11 COSM5624512 c.3256G>A p.E1086K Substitution - Missense 3:47002262-47002262 + ESCC_151 COSM5645225 c.2787C>A p.N929K Substitution - Missense 3:46997396-46997396 + SC_9081 COSM5567904 c.6207C>T p.S2069S Substitution - coding silent 3:47009037-47009037 + TCGA-BR-8677-01 COSM4117955 c.2351C>A p.S784Y Substitution - Missense 3:47000319-47000319 + PCSI_0073_Pa_P_526 COSM216642 c.4091C>T p.A1364V Substitution - Missense 3:47004155-47004155 + EGC15 COSM5059757 c.3824T>G p.V1275G Substitution - Missense 3:46999923-46999923 + TCGA-EM-A3FM-01 COSM3373195 c.4360A>G p.T1454A Substitution - Missense 3:47001055-47001055 + sysucc-311T COSM5465896 c.7296C>T p.Y2432Y Substitution - coding silent 3:47007312-47007312 + HCT8 COSM4625103 c.2022G>A p.T674T Substitution - coding silent 3:46998834-46998834 + T3024 COSM4705654 c.190C>T p.H64Y Substitution - Missense 3:46988891-46988891 + TCGA-AP-A051-01 COSM1045415 c.5639-1G>T p.? Unknown 3:47007815-47007815 + TCGA-BP-4158-01 COSM3365198 c.6126C>A p.A2042A Substitution - coding silent 3:47008636-47008636 + TCGA-22-1016-01 COSM730731 c.533C>T p.A178V Substitution - Missense 3:46995585-46995585 + CHC2215T COSM4790268 c.2533G>A p.E845K Substitution - Missense 3:47001097-47001097 + ME020T COSM225513 c.6667C>T p.P2223S Substitution - Missense 3:47005595-47005595 + TCGA-EI-6917-01 COSM1045371 c.1943C>T p.A648V Substitution - Missense 3:46995758-46995758 + PT15_1 COSM5897453 c.4138C>T p.P1380S Substitution - Missense 3:47004202-47004202 + ESO-859 COSM1239549 c.1613G>A p.R538H Substitution - Missense 3:46995348-46995348 + 587318 COSM1216721 c.6167C>T p.P2056L Substitution - Missense 3:47008997-47008997 + TCGA-EK-A2H1-01 COSM4822285 c.2269C>G p.L757V Substitution - Missense 3:47000237-47000237 + sysucc-1317T COSM5449881 c.824C>T p.A275V Substitution - Missense 3:46991587-46991587 + TCGA-LP-A4AU-01 COSM4855218 c.7856C>T p.A2619V Substitution - Missense 3:47008419-47008419 + TCGA-AA-3715-01 COSM269696 c.2301G>A p.S767S Substitution - coding silent 3:47000269-47000269 + LC_S12 COSM1186260 c.6220T>C p.S2074P Substitution - Missense 3:47004516-47004516 + CSCC-62-T COSM4506396 c.7193C>T p.S2398F Substitution - Missense 3:47007124-47007124 + TCGA-HF-7132-01 COSM4117941 c.200C>T p.A67V Substitution - Missense 3:46988901-46988901 + TCGA-ER-A19W-06 COSM4399049 c.6781C>T p.Q2261* Substitution - Nonsense 3:47005827-47005827 + ESO-859 COSM1239550 c.296G>A p.R99H Substitution - Missense 3:46995348-46995348 + HCC125T COSM1617672 c.4959A>G p.L1653L Substitution - coding silent 3:47005972-47005972 + TCGA-D5-6928-01 COSM1423492 c.3109G>A p.V1037M Substitution - Missense 3:46998217-46998217 + TCGA-BR-6452-01 COSM4117947 c.1849G>A p.A617T Substitution - Missense 3:46995584-46995584 + LS174T COSM3068761 c.5281G>A p.V1761I Substitution - Missense 3:47007081-47007081 + TCGA-HU-A4GU-01 COSM4117974 c.6232T>C p.Y2078H Substitution - Missense 3:47004528-47004528 + TCGA-HU-A4GN-01 COSM4117945 c.1797A>G p.P599P Substitution - coding silent 3:46995532-46995532 + TCGA-AZ-4615-01 COSM3760130 c.4995G>A p.V1665V Substitution - coding silent 3:47002132-47002132 + PCSI_0073_Pa_X COSM216642 c.4091C>T p.A1364V Substitution - Missense 3:47004155-47004155 + CLL086 COSM1291716 c.3623A>G p.Q1208R Substitution - Missense 3:46999394-46999394 + TCGA-AA-3713-01 COSM1423487 c.991A>G p.N331D Substitution - Missense 3:46991905-46991905 + S02375 COSM5696609 c.1632C>T p.D544D Substitution - coding silent 3:46995367-46995367 + 1N05-VS-1T05 COSM4972878 c.1507+1G>T p.? Unknown 3:46997434-46997434 + TCGA-EE-A3AA-06 COSM3594631 c.5636C>T p.T1879I Substitution - Missense 3:47003225-47003225 + ESO-0079 COSM1258756 c.1268delA p.H423fs*49 Deletion - Frameshift 3:46994525-46994525 + 2492723 COSM5720011 c.1373C>T p.P458L Substitution - Missense 3:46997299-46997299 + C135 COSM4117964 c.5186C>T p.T1729M Substitution - Missense 3:47002405-47002405 + LP6005935-DNA_F01 COSM4879737 c.4986C>T p.S1662S Substitution - coding silent 3:47002123-47002123 + LS411 COSM1045373 c.2037C>T p.C679C Substitution - coding silent 3:46995937-46995937 + CSCC-31-T COSM4544628 c.2132G>A p.R711Q Substitution - Missense 3:46999379-46999379 + ICGC_PA112 COSM3670322 c.2611C>T p.R871C Substitution - Missense 3:46997008-46997008 + TCGA-B5-A11U-01 COSM1045393 c.2275C>T p.P759S Substitution - Missense 3:47000243-47000243 + TCGA-FU-A23K-01 COSM460787 c.5886C>T p.I1962I Substitution - coding silent 3:47004081-47004081 + PT15_1 COSM5897450 c.5602C>T p.P1868S Substitution - Missense 3:47003191-47003191 + GC8_T COSM149374 c.4509C>T p.I1503I Substitution - coding silent 3:47005055-47005055 + TCGA-EW-A1PB-01 COSM1485234 c.6139C>T p.Q2047* Substitution - Nonsense 3:47004334-47004334 + SNUH_G16_S1 COSM3760133 c.4292C>T p.S1431F Substitution - Missense 3:47004356-47004356 + TCGA-BR-8289-01 COSM4117976 c.6651G>A p.P2217P Substitution - coding silent 3:47005579-47005579 + TARGET-20-PARJCR-09A-02D COSM5487641 c.5198C>T p.A1733V Substitution - Missense 3:47006382-47006382 + 2492722 COSM5720010 c.2690C>T p.P897L Substitution - Missense 3:46997299-46997299 + TCGA-ER-A2NC-06 COSM3594612 c.930C>T p.A310A Substitution - coding silent 3:46991844-46991844 + TCGA-EM-A3FM-01 COSM3373196 c.2491A>G p.T831A Substitution - Missense 3:47001055-47001055 + TCGA-EE-A29D-06 COSM3594609 c.105G>A p.K35K Substitution - coding silent 3:46988722-46988722 + TCGA-AA-3994-01 COSM273665 c.167C>T p.P56L Substitution - Missense 3:46988868-46988868 + BN24T COSM1617669 c.5847C>T p.Y1949Y Substitution - coding silent 3:47003942-47003942 + SW480 COSM4655885 c.2627G>A p.R876K Substitution - Missense 3:46997024-46997024 + CSCC-54-T COSM1258759 c.4541G>A p.G1514E Substitution - Missense 3:47001335-47001335 + WA48 COSM240827 c.4564G>C p.E1522Q Substitution - Missense 3:47005194-47005194 + YULONE COSM5399470 c.5259C>T p.F1753F Substitution - coding silent 3:47006443-47006443 + TCGA-EW-A1PB-01 COSM1485235 c.4270C>T p.Q1424* Substitution - Nonsense 3:47004334-47004334 + T3091 COSM4705679 c.8205G>A p.S2735S Substitution - coding silent 3:47009260-47009260 + CSCC-54-T COSM1258760 c.2672G>A p.G891E Substitution - Missense 3:47001335-47001335 + TCGA-BR-4188-01 COSM4117979 c.5801G>A p.S1934N Substitution - Missense 3:47008137-47008137 + CHC2215T COSM4790267 c.4402G>A p.E1468K Substitution - Missense 3:47001097-47001097 + TCGA-DZ-6133-01 COSM3993107 c.5947G>A p.A1983T Substitution - Missense 3:47008379-47008379 + HCC2998 COSM3068719 c.6579G>A p.R2193R Substitution - coding silent 3:47005507-47005507 + TCGA-Q1-A73O-01 COSM4835090 c.945G>T p.L315L Substitution - coding silent 3:46991859-46991859 + 587332 COSM1216733 c.788G>A p.G263D Substitution - Missense 3:46996005-46996005 + CSCC-55-T COSM4504405 c.6648C>T p.I2216I Substitution - coding silent 3:47005576-47005576 + TCGA-BR-6452-01 COSM4117960 c.4498A>G p.M1500V Substitution - Missense 3:47001292-47001292 + T3152 COSM4705661 c.5661delA p.E1889fs*41 Deletion - Frameshift 3:47003250-47003250 + 2250254 COSM5030357 c.806G>A p.R269H Substitution - Missense 3:46991569-46991569 + CHC917T COSM3669147 c.6629C>T p.A2210V Substitution - Missense 3:47005557-47005557 + HCC101 COSM1617666 c.335A>T p.E112V Substitution - Missense 3:46995387-46995387 + ESO-1163 COSM1258757 c.7752C>T p.R2584R Substitution - coding silent 3:47008315-47008315 + TCGA-D1-A103-01 COSM1045400 c.4459C>T p.R1487C Substitution - Missense 3:47001154-47001154 + TCGA-EK-A2H1-01 COSM4822284 c.4138C>G p.L1380V Substitution - Missense 3:47000237-47000237 + 1 COSM1715969 c.688G>A p.E230K Substitution - Missense 3:46995820-46995820 + TCGA-B5-A0JY-01 COSM1045367 c.674C>T p.S225F Substitution - Missense 3:46991437-46991437 + PD18285a COSM3770544 c.6919G>A p.G2307R Substitution - Missense 3:47006063-47006063 + TCGA-DD-A3A8-01 COSM4935000 c.1063G>T p.G355C Substitution - Missense 3:46996499-46996499 + LUAD-S01356 COSM398235 c.2930A>T p.Y977F Substitution - Missense 3:47001936-47001936 + T3091 COSM4705680 c.6336G>A p.S2112S Substitution - coding silent 3:47009260-47009260 + 25T COSM3714550 c.6240G>A p.M2080I Substitution - Missense 3:47004536-47004536 + TCGA-24-2280-01 COSM133506 c.4363_4364TA>CC p.Y1455P Substitution - Missense 3:47004528-47004529 + TCGA-AP-A051-01 COSM1045369 c.1773G>T p.M591I Substitution - Missense 3:46995508-46995508 + HCC101T COSM1617666 c.335A>T p.E112V Substitution - Missense 3:46995387-46995387 + T24 COSM4838925 c.4972G>A p.D1658N Substitution - Missense 3:47005985-47005985 + TCGA-HU-A4GN-01 COSM4117946 c.480A>G p.P160P Substitution - coding silent 3:46995532-46995532 + BD236T COSM5518425 c.5510G>A p.R1837H Substitution - Missense 3:47003007-47003007 + PT48 COSM5931344 c.4172C>T p.P1391L Substitution - Missense 3:47004236-47004236 + HCC99T COSM3660580 c.5416C>T p.L1806L Substitution - coding silent 3:47002759-47002759 + CSCC-35-T COSM4495336 c.4518C>G p.T1506T Substitution - coding silent 3:47001312-47001312 + SC_9081 COSM5567903 c.8076C>T p.S2692S Substitution - coding silent 3:47009037-47009037 + 25T COSM3714551 c.4371G>A p.M1457I Substitution - Missense 3:47004536-47004536 + 587278 COSM1216731 c.5489C>T p.P1830L Substitution - Missense 3:47007548-47007548 + TCGA-BR-4292-01 COSM4117985 c.6174G>A p.A2058A Substitution - coding silent 3:47009004-47009004 + sysucc-274T COSM5476459 c.3957G>A p.K1319K Substitution - coding silent 3:47000056-47000056 + CSCC-27-T COSM4492057 c.3905C>T p.P1302L Substitution - Missense 3:47000004-47000004 + 587224 COSM1216722 c.8144T>C p.V2715A Substitution - Missense 3:47009105-47009105 + RK117_C01 COSM3702439 c.6893A>G p.N2298S Substitution - Missense 3:47006037-47006037 + BD57T COSM5509923 c.4272C>T p.S1424S Substitution - coding silent 3:47000371-47000371 + OSCC-GB_01060111 COSM4882500 c.1437T>A p.C479* Substitution - Nonsense 3:46995172-46995172 + TCGA-AP-A059-01 COSM1045389 c.2180T>C p.V727A Substitution - Missense 3:46999427-46999427 + BRC11 COSM5025941 c.21C>G p.I7M Substitution - Missense 3:46995073-46995073 + LS174T COSM3068760 c.7150G>A p.V2384I Substitution - Missense 3:47007081-47007081 + TCGA-F5-6814-01 COSM3427658 c.2296C>T p.P766S Substitution - Missense 3:47000264-47000264 + DLD1 COSM4625102 c.3339G>A p.T1113T Substitution - coding silent 3:46998834-46998834 + TCGA-CD-A4MG-01 COSM1045404 c.5954G>A p.R1985H Substitution - Missense 3:47004149-47004149 + TCGA-G4-6588-01 COSM1423508 c.7152A>G p.V2384V Substitution - coding silent 3:47007083-47007083 + CHC301T COSM3669150 c.5382G>T p.L1794L Substitution - coding silent 3:47007267-47007267 + RK282_C01 COSM4964150 c.1152C>G p.T384T Substitution - coding silent 3:46996588-46996588 + HCC2998 COSM3068720 c.4710G>A p.R1570R Substitution - coding silent 3:47005507-47005507 + TCGA-BR-8289-01 COSM4117977 c.4782G>A p.P1594P Substitution - coding silent 3:47005579-47005579 + PD4112a COSM162810 c.1228C>T p.H410Y Substitution - Missense 3:46994485-46994485 + TCGA-25-1320-01 COSM118404 c.1620C>A p.I540I Substitution - coding silent 3:46997673-46997673 + TCGA-22-4591-01 COSM730725 c.4178A>G p.Q1393R Substitution - Missense 3:47004242-47004242 + sysucc-783T COSM5484626 c.2630T>C p.M877T Substitution - Missense 3:47001293-47001293 + 2492721 COSM5720011 c.1373C>T p.P458L Substitution - Missense 3:46997299-46997299 + SNU-175 COSM3068600 c.3025G>A p.A1009T Substitution - Missense 3:46998133-46998133 + TCGA-06-6697-01 COSM3408702 c.4097G>T p.G1366V Substitution - Missense 3:47000196-47000196 + TCGA-EE-A3JA-06 COSM3594621 c.4535C>T p.P1512L Substitution - Missense 3:47001329-47001329 + CN-AML-CR-11-Dx COSM3760131 c.3126G>A p.V1042V Substitution - coding silent 3:47002132-47002132 + T3658 COSM4705667 c.6550C>T p.Q2184* Substitution - Nonsense 3:47005311-47005311 + T3090 COSM4705659 c.4210C>T p.R1404C Substitution - Missense 3:47000309-47000309 + PD11372a COSM5767250 c.1263G>A p.L421L Substitution - coding silent 3:46996977-46996977 + TCGA-A2-A0T5-01 COSM3823987 c.1264A>C p.T422P Substitution - Missense 3:46994521-46994521 + CSCC-27-T COSM4518739 c.5957_5958CC>TT p.S1986F Substitution - Missense 3:47008389-47008390 + BCM567T COSM4950079 c.3532C>T p.R1178* Substitution - Nonsense 3:46999106-46999106 + sysucc-1397T COSM5474612 c.3358G>A p.A1120T Substitution - Missense 3:47002446-47002446 + TCGA-CI-6624-01 COSM1566759 c.2475C>T p.N825N Substitution - coding silent 3:47001039-47001039 + TCGA-EE-A2M5-06 COSM3594624 c.2682C>T p.A894A Substitution - coding silent 3:47001345-47001345 + Au1 COSM5597154 c.1218C>T p.I406I Substitution - coding silent 3:46994475-46994475 + TCGA-D1-A16X-01 COSM1045384 c.1831C>T p.R611W Substitution - Missense 3:46998492-46998492 + CN-AML-CR-22-Dx COSM5424969 c.7748G>T p.R2583L Substitution - Missense 3:47008311-47008311 + TCGA-AX-A0J1-01 COSM1045407 c.4230C>A p.N1410K Substitution - Missense 3:47004294-47004294 + TCGA-EE-A3AC-06 COSM3594636 c.4177C>T p.Q1393* Substitution - Nonsense 3:47004241-47004241 + TCGA-D3-A3C3-06 COSM3594647 c.7566G>A p.R2522R Substitution - coding silent 3:47007874-47007874 + PTC-7C COSM4158075 c.6054C>G p.P2018P Substitution - coding silent 3:47004249-47004249 + 35M COSM5581805 c.7085C>T p.S2362L Substitution - Missense 3:47006400-47006400 + PT21_2 COSM1045383 c.3148C>T p.R1050W Substitution - Missense 3:46998492-46998492 + HN_62854 COSM121288 c.5952G>A p.L1984L Substitution - coding silent 3:47008384-47008384 + CHC433T COSM446600 c.214C>G p.R72G Substitution - Missense 3:46995266-46995266 + TCGA-D1-A15X-01 COSM1045373 c.2037C>T p.C679C Substitution - coding silent 3:46995937-46995937 + Gp5D COSM3068519 c.270G>A p.R90R Substitution - coding silent 3:46995322-46995322 + TCGA-06-6697-01 COSM3408703 c.2228G>T p.G743V Substitution - Missense 3:47000196-47000196 + TCGA-C8-A26Y-01 COSM3823989 c.1406A>G p.E469G Substitution - Missense 3:46997332-46997332 + CAL33 COSM189782 c.7181G>A p.R2394Q Substitution - Missense 3:47007112-47007112 + J57_T COSM3945522 c.1668C>T p.N556N Substitution - coding silent 3:46998093-46998093 + CADO-ES1 COSM3068717 c.6540C>T p.H2180H Substitution - coding silent 3:47005301-47005301 + SNUH_G16_S1 COSM149373 c.2835C>T p.N945N Substitution - coding silent 3:47001748-47001748 + TCGA-AD-6964-01 COSM1423489 c.103C>T p.R35C Substitution - Missense 3:46995155-46995155 + TCGA-AD-6901-01 COSM1423494 c.3287T>C p.L1096P Substitution - Missense 3:46998782-46998782 + 438 COSM4434318 c.6029T>G p.L2010R Substitution - Missense 3:47008539-47008539 + sysucc-274T COSM5476457 c.1600C>T p.R534C Substitution - Missense 3:46995335-46995335 + PD8984a COSM5769322 c.5081G>C p.S1694T Substitution - Missense 3:47002218-47002218 + PD7248a COSM5792010 c.2930A>G p.Y977C Substitution - Missense 3:47001936-47001936 + CSCC-11-T COSM4569925 c.2167T>G p.C723G Substitution - Missense 3:46996286-46996286 + 2492722 COSM5720011 c.1373C>T p.P458L Substitution - Missense 3:46997299-46997299 + YUWIA COSM5399468 c.3896C>T p.A1299V Substitution - Missense 3:46999995-46999995 + STC252 COSM5059758 c.5950C>T p.R1984C Substitution - Missense 3:47004145-47004145 + TCGA-18-3421-01 COSM730732 c.354G>T p.L118L Substitution - coding silent 3:46989262-46989262 + TCGA-A6-6780-01 COSM480132 c.3263G>A p.R1088H Substitution - Missense 3:47002269-47002269 + TCGA-AZ-6601-01 COSM1423506 c.5899C>T p.R1967W Substitution - Missense 3:47004094-47004094 + ESCC_47 COSM5290687 c.4399C>T p.R1467W Substitution - Missense 3:47001094-47001094 + TCGA-BS-A0WQ-01 COSM1045386 c.1854_1856delGAA p.K620delK Deletion - In frame 3:46998515-46998517 + TCGA-DD-A119-01 COSM4919834 c.5209A>T p.M1737L Substitution - Missense 3:47002428-47002428 + TCGA-A5-A0GB-01 COSM1045412 c.6941T>A p.V2314E Substitution - Missense 3:47006186-47006186 + TCGA-AP-A059-01 COSM1045388 c.3656T>C p.V1219A Substitution - Missense 3:46999427-46999427 + TCGA-D9-A3Z1-06 COSM3594642 c.4382C>T p.T1461I Substitution - Missense 3:47004547-47004547 + ESO-0292 COSM1241470 c.4455C>T p.S1485S Substitution - coding silent 3:47005001-47005001 + PCSI0073 COSM216642 c.4091C>T p.A1364V Substitution - Missense 3:47004155-47004155 + LS411 COSM3068664 c.3210C>A p.G1070G Substitution - coding silent 3:47002216-47002216 + T3116 COSM4705682 c.6361G>C p.G2121R Substitution - Missense 3:47009285-47009285 + LUAD_E00623 COSM354365 c.7606G>A p.G2536S Substitution - Missense 3:47008073-47008073 + Pat_32_A COSM5864623 c.7658G>A p.G2553E Substitution - Missense 3:47008125-47008125 + TCGA-A8-A07C-01 COSM446598 c.1064G>C p.G355A Substitution - Missense 3:46992506-46992506 + TCGA-AP-A051-01 COSM1045414 c.7508-1G>T p.? Unknown 3:47007815-47007815 + TCGA-A2-A0T5-01 COSM3823991 c.2825A>C p.H942P Substitution - Missense 3:47001738-47001738 + SNUH_G76_S1 COSM4002709 c.4704C>T p.N1568N Substitution - coding silent 3:47001748-47001748 + TCGA-ET-A25O-01 COSM3373194 c.59T>C p.L20P Substitution - Missense 3:46988676-46988676 + 587226 COSM1216715 c.2977G>A p.E993K Substitution - Missense 3:47001983-47001983 + HCC90 COSM1617667 c.4928A>T p.D1643V Substitution - Missense 3:47002065-47002065 + ESCC_BICR_060T COSM5435090 c.5865C>T p.R1955R Substitution - coding silent 3:47003960-47003960 + CHC917T COSM3669147 c.6629C>T p.A2210V Substitution - Missense 3:47005557-47005557 + CHC1736T COSM4802256 c.3388G>A p.V1130M Substitution - Missense 3:46998962-46998962 + TCGA-B5-A11U-01 COSM1045392 c.4144C>T p.P1382S Substitution - Missense 3:47000243-47000243 + BD236T COSM5518427 c.8181C>T p.F2727F Substitution - coding silent 3:47009236-47009236 + TCGA-BR-6452-01 COSM4117971 c.4110C>A p.I1370I Substitution - coding silent 3:47004174-47004174 + TCGA-FW-A5DX-01 COSM3594639 c.6171G>A p.E2057E Substitution - coding silent 3:47004366-47004366 + HCC99 COSM3660578 c.5415G>T p.A1805A Substitution - coding silent 3:47002758-47002758 + A9 COSM5350987 c.1989G>C p.L663F Substitution - Missense 3:46995804-46995804 + TCGA-AA-3715-01 COSM269697 c.4170G>A p.S1390S Substitution - coding silent 3:47000269-47000269 + TCGA-AX-A0J1-01 COSM1045405 c.4085G>A p.R1362H Substitution - Missense 3:47004149-47004149 + DLD1 COSM4625103 c.2022G>A p.T674T Substitution - coding silent 3:46998834-46998834 + TCGA-F1-6874-01 COSM1239549 c.1613G>A p.R538H Substitution - Missense 3:46995348-46995348 + T521 COSM4705664 c.3979G>A p.D1327N Substitution - Missense 3:47003943-47003943 + TCGA-D9-A1JW-06 COSM1177393 c.5175C>T p.F1725F Substitution - coding silent 3:47002394-47002394 + TCGA-A5-A0GB-01 COSM1045413 c.5072T>A p.V1691E Substitution - Missense 3:47006186-47006186 + CHC1754T COSM4792823 c.170G>T p.G57V Substitution - Missense 3:46995222-46995222 + S00501 COSM5701059 c.3903_3904insC p.P1304fs*20 Insertion - Frameshift 3:47000002-47000003 + PCSI_0073_Pa_P COSM216642 c.4091C>T p.A1364V Substitution - Missense 3:47004155-47004155 + TCGA-25-2400-01 COSM119664 c.1421C>G p.P474R Substitution - Missense 3:46997347-46997347 + TCGA-FW-A3R5-06 COSM1177394 c.3306C>T p.F1102F Substitution - coding silent 3:47002394-47002394 + TCGA-D1-A0ZO-01 COSM1045372 c.626C>T p.A209V Substitution - Missense 3:46995758-46995758 + S00932 COSM5662423 c.973A>G p.T325A Substitution - Missense 3:46996409-46996409 + 1517_CLM COSM5756287 c.4372G>A p.V1458M Substitution - Missense 3:47001067-47001067 + LUAD-5V8LT COSM402306 c.2267C>A p.T756N Substitution - Missense 3:47000235-47000235 + LUAD-B02477 COSM335893 c.5538G>A p.P1846P Substitution - coding silent 3:47007597-47007597 + 2217539 COSM4421764 c.2549C>T p.S850L Substitution - Missense 3:46996826-46996826 + CSCC-55-T COSM4504406 c.4779C>T p.I1593I Substitution - coding silent 3:47005576-47005576 + TCGA-BR-6453-01 COSM4117983 c.5995C>T p.R1999C Substitution - Missense 3:47008427-47008427 + PD9844a COSM5792712 c.3642C>T p.R1214R Substitution - coding silent 3:47003008-47003008 + TCGA-BG-A0M4-01 COSM1045397 c.2492C>T p.T831M Substitution - Missense 3:47001056-47001056 + SNUH_G76_S1 COSM4417105 c.6919+9T>C p.? Unknown 3:47006072-47006072 + BD57T COSM5509924 c.2403C>T p.S801S Substitution - coding silent 3:47000371-47000371 + CHC1754T COSM4792822 c.1487G>T p.G496V Substitution - Missense 3:46995222-46995222 + 587238 COSM189784 c.7751G>A p.R2584H Substitution - Missense 3:47008314-47008314 + SS6003137 COSM3414440 c.6630C>T p.A2210A Substitution - coding silent 3:47005558-47005558 + TCGA-B1-A656-01 COSM4414053 c.457C>T p.R153W Substitution - Missense 3:46989365-46989365 + TCGA-CD-A4MI-01 COSM4117943 c.1795C>T p.P599S Substitution - Missense 3:46995530-46995530 + TCGA-LP-A4AU-01 COSM4855219 c.5987C>T p.A1996V Substitution - Missense 3:47008419-47008419 + HCT116 COSM4632340 c.6234C>T p.H2078H Substitution - coding silent 3:47009064-47009064 + TCGA-D1-A17B-01 COSM1045379 c.2773A>G p.T925A Substitution - Missense 3:46997382-46997382 + CHLA-258 COSM1216728 c.5276G>A p.R1759H Substitution - Missense 3:47002495-47002495 + CN-AML-CR-11-Dx COSM3760130 c.4995G>A p.V1665V Substitution - coding silent 3:47002132-47002132 + T3498 COSM4705670 c.5008G>A p.A1670T Substitution - Missense 3:47006021-47006021 + TCGA-AP-A051-01 COSM1045395 c.2290G>T p.G764C Substitution - Missense 3:47000258-47000258 + PCSI_0073_Pa_P_526 COSM216643 c.5960C>T p.A1987V Substitution - Missense 3:47004155-47004155 + LIM1899 COSM4640536 c.5561G>A p.G1854D Substitution - Missense 3:47007620-47007620 + 2492722 COSM5720009 c.87C>T p.A29A Substitution - coding silent 3:46988704-46988704 + 8067508 COSM3781640 c.473+3G>A p.? Unknown 3:46989384-46989384 + TCGA-BR-6453-01 COSM4117982 c.7864C>T p.R2622C Substitution - Missense 3:47008427-47008427 + C008 COSM5523235 c.2667C>T p.P889P Substitution - coding silent 3:47001330-47001330 + ESO-1163 COSM1258758 c.5883C>T p.R1961R Substitution - coding silent 3:47008315-47008315 + CHEWS036 COSM4584397 c.4614C>T p.G1538G Substitution - coding silent 3:47001408-47001408 + TCGA-CD-A4MG-01 COSM4117957 c.2378G>A p.G793D Substitution - Missense 3:47000346-47000346 + 1517_CLM COSM5756288 c.2503G>A p.V835M Substitution - Missense 3:47001067-47001067 + SJRHB004_D COSM3738409 c.5357C>T p.T1786M Substitution - Missense 3:47002700-47002700 + TCGA-EI-6512-01 COSM296928 c.6258G>A p.A2086A Substitution - coding silent 3:47004554-47004554 + pfg122T COSM4754397 c.4516G>A p.V1506M Substitution - Missense 3:47005062-47005062 + SNUH_G16_S1 COSM3760132 c.6161C>T p.S2054F Substitution - Missense 3:47004356-47004356 + BD236T COSM5518426 c.3641G>A p.R1214H Substitution - Missense 3:47003007-47003007 + TCGA-BR-8487-01 COSM4117968 c.5945A>G p.N1982S Substitution - Missense 3:47004140-47004140 + ESCC-083T COSM3940543 c.4412A>T p.Q1471L Substitution - Missense 3:47001107-47001107 + CSCC-62-T COSM4506397 c.5324C>T p.S1775F Substitution - Missense 3:47007124-47007124 + TCGA-DD-A3A8-01 COSM4934999 c.2380G>T p.G794C Substitution - Missense 3:46996499-46996499 + HCC99T COSM3660581 c.3547C>T p.L1183L Substitution - coding silent 3:47002759-47002759 + Gp5D COSM3068518 c.1587G>A p.R529R Substitution - coding silent 3:46995322-46995322 + TCGA-FU-A23K-01 COSM460788 c.4017C>T p.I1339I Substitution - coding silent 3:47004081-47004081 + 587318 COSM1216720 c.8036C>T p.P2679L Substitution - Missense 3:47008997-47008997 + CLL113 COSM1291718 c.7834C>G p.Q2612E Substitution - Missense 3:47008397-47008397 + CSCC-11-T COSM4556218 c.682G>A p.G228S Substitution - Missense 3:46991445-46991445 + 2492723 COSM5720010 c.2690C>T p.P897L Substitution - Missense 3:46997299-46997299 + TCGA-BR-7851-01 COSM4117942 c.1052C>T p.A351V Substitution - Missense 3:46992494-46992494 + HCT15 COSM4625103 c.2022G>A p.T674T Substitution - coding silent 3:46998834-46998834 + 1517_PT COSM5756288 c.2503G>A p.V835M Substitution - Missense 3:47001067-47001067 + T3454 COSM4705657 c.3372C>T p.G1124G Substitution - coding silent 3:46998867-46998867 + SJHGG045_A COSM4972056 c.4727_4728CG>AA p.A1576E Substitution - Missense 3:47005524-47005525 + TCGA-F4-6856-01 COSM1045374 c.720C>T p.C240C Substitution - coding silent 3:46995937-46995937 + 470 COSM4437723 c.1641A>C p.P547P Substitution - coding silent 3:46995376-46995376 + GC_342T_a-GC_342N COSM4771899 c.748C>T p.R250W Substitution - Missense 3:46995965-46995965 + pfg068T COSM1045400 c.4459C>T p.R1487C Substitution - Missense 3:47001154-47001154 + CLL121 COSM1291715 c.3430C>A p.L1144M Substitution - Missense 3:46999004-46999004 + ESO-0292 COSM1241469 c.6324C>T p.S2108S Substitution - coding silent 3:47005001-47005001 + CX-1 COSM3068698 c.4131C>T p.L1377L Substitution - coding silent 3:47004195-47004195 + TCGA-AM-5821-01 COSM3760133 c.4292C>T p.S1431F Substitution - Missense 3:47004356-47004356 + LIM1899 COSM4640535 c.7430G>A p.G2477D Substitution - Missense 3:47007620-47007620 + TCGA-BH-A0W7-01 COSM446606 c.6749C>A p.P2250H Substitution - Missense 3:47005795-47005795 + 2492720 COSM5720009 c.87C>T p.A29A Substitution - coding silent 3:46988704-46988704 + HCC125T COSM1617671 c.6828A>G p.L2276L Substitution - coding silent 3:47005972-47005972 + TCGA-G4-6320-01 COSM3696115 c.1087G>A p.E363K Substitution - Missense 3:46996523-46996523 + T3152 COSM4705662 c.3792delA p.E1266fs*41 Deletion - Frameshift 3:47003250-47003250 + TCGA-BR-6452-01 COSM4117948 c.532G>A p.A178T Substitution - Missense 3:46995584-46995584 + sysucc-311T COSM5465899 c.6202C>T p.R2068C Substitution - Missense 3:47009032-47009032 + EOPC-035_tumor_01 COSM5951051 c.5559C>T p.S1853S Substitution - coding silent 3:47007618-47007618 + HT115 COSM3068767 c.5421C>T p.S1807S Substitution - coding silent 3:47007306-47007306 + TCGA-24-1470-01 COSM75567 c.6169G>A p.A2057T Substitution - Missense 3:47008999-47008999 + TCGA-D1-A17B-01 COSM1045380 c.1456A>G p.T486A Substitution - Missense 3:46997382-46997382 + T3101 COSM4705675 c.7867C>T p.P2623S Substitution - Missense 3:47008430-47008430 + LS180 COSM3068760 c.7150G>A p.V2384I Substitution - Missense 3:47007081-47007081 + TCGA-BC-A217-01 COSM4936864 c.423C>G p.L141L Substitution - coding silent 3:46989331-46989331 + HCC066T COSM5821050 c.1235A>T p.Q412L Substitution - Missense 3:46994492-46994492 + TCGA-G4-6320-01 COSM3696114 c.2404G>A p.E802K Substitution - Missense 3:46996523-46996523 + PD11372a COSM5767267 c.1165G>A p.E389K Substitution - Missense 3:46996759-46996759 + Pat_06_A COSM5864619 c.4621G>A p.A1541T Substitution - Missense 3:47005251-47005251 + TCGA-BR-6452-01 COSM4117967 c.3367G>A p.D1123N Substitution - Missense 3:47002455-47002455 + TCGA-CZ-5458-01 COSM480127 c.2019C>G p.A673A Substitution - coding silent 3:46995834-46995834 + TCGA-D9-A3Z1-06 COSM3594641 c.6251C>T p.T2084I Substitution - Missense 3:47004547-47004547 + TCGA-AG-A011-01 COSM265268 c.88T>G p.F30V Substitution - Missense 3:46988705-46988705 + BD124T COSM5491641 c.3765C>T p.S1255S Substitution - coding silent 3:46999691-46999691 + 46M COSM5588414 c.1270C>T p.R424W Substitution - Missense 3:46994527-46994527 + SW620 COSM3068725 c.6735C>T p.G2245G Substitution - coding silent 3:47005781-47005781 + TCGA-CG-5726-01 COSM1045371 c.1943C>T p.A648V Substitution - Missense 3:46995758-46995758 + ESCC_11 COSM5624511 c.5125G>A p.E1709K Substitution - Missense 3:47002262-47002262 + TCGA-BP-4976-01 COSM480129 c.2439G>A p.L813L Substitution - coding silent 3:46996558-46996558 + TCGA-F1-6874-01 COSM1239550 c.296G>A p.R99H Substitution - Missense 3:46995348-46995348 + TCGA-BS-A0UL-01 COSM1045398 c.4367G>A p.R1456H Substitution - Missense 3:47001062-47001062 + TTC466 COSM4584396 c.1059G>A p.R353R Substitution - coding silent 3:46996495-46996495 + Au1 COSM5597153 c.3605C>T p.P1202L Substitution - Missense 3:47002971-47002971 + TCGA-CG-5726-01 COSM1045372 c.626C>T p.A209V Substitution - Missense 3:46995758-46995758 + YUFIT COSM5399464 c.628C>T p.L210F Substitution - Missense 3:46991290-46991290 + 2492721 COSM5720009 c.87C>T p.A29A Substitution - coding silent 3:46988704-46988704 + TCGA-DD-A119-01 COSM4919835 c.3340A>T p.M1114L Substitution - Missense 3:47002428-47002428 + TCGA-HT-7477-01 COSM3974431 c.2426T>C p.F809S Substitution - Missense 3:46996545-46996545 + LS180 COSM3068761 c.5281G>A p.V1761I Substitution - Missense 3:47007081-47007081 + TCGA-EB-A44Q-06 COSM3594627 c.5260C>T p.R1754W Substitution - Missense 3:47002479-47002479 + S02375 COSM5696610 c.315C>T p.D105D Substitution - coding silent 3:46995367-46995367 + PD9702a COSM5772623 c.6189G>C p.M2063I Substitution - Missense 3:47009019-47009019 + CHC917T COSM3669148 c.4760C>T p.A1587V Substitution - Missense 3:47005557-47005557 + CHC1736T COSM4802256 c.3388G>A p.V1130M Substitution - Missense 3:46998962-46998962 + TCGA-FS-A1ZZ-06 COSM3594646 c.5610G>A p.K1870K Substitution - coding silent 3:47007669-47007669 + pfg068T COSM1045401 c.2590C>T p.R864C Substitution - Missense 3:47001154-47001154 + ZZUFHECRKL-G014T COSM5437487 c.3330G>A p.V1110V Substitution - coding silent 3:46998825-46998825 + TCGA-F4-6856-01 COSM1045373 c.2037C>T p.C679C Substitution - coding silent 3:46995937-46995937 + TCGA-A2-A0T6-01 COSM3823997 c.4329+2T>G p.? Unknown 3:47004395-47004395 + CHC892T COSM4961420 c.605G>A p.G202E Substitution - Missense 3:46995737-46995737 + ESO-081 COSM1243424 c.2976C>T p.R992R Substitution - coding silent 3:47001982-47001982 + TCGA-EE-A3J5-06 COSM3594650 c.5819C>T p.T1940I Substitution - Missense 3:47008155-47008155 + HCT15 COSM3068556 c.2133C>T p.R711R Substitution - coding silent 3:46996033-46996033 + T24 COSM4838924 c.6841G>A p.D2281N Substitution - Missense 3:47005985-47005985 + TCGA-FJ-A3ZF-01 COSM3775073 c.3405G>A p.L1135L Substitution - coding silent 3:46998979-46998979 + T3090 COSM4705678 c.6313G>A p.A2105T Substitution - Missense 3:47009237-47009237 + M021 COSM1738850 c.1211C>T p.T404I Substitution - Missense 3:46996805-46996805 + RK211_C01 COSM3767454 c.1280A>T p.H427L Substitution - Missense 3:46996994-46996994 + RK282_C01 COSM4964149 c.2469C>G p.T823T Substitution - coding silent 3:46996588-46996588 + HCC99 COSM3660579 c.3546G>T p.A1182A Substitution - coding silent 3:47002758-47002758 + TCGA-D9-A6EC-06 COSM4403876 c.557C>T p.P186L Substitution - Missense 3:46995609-46995609 + ESCC_151 COSM5645226 c.1470C>A p.N490K Substitution - Missense 3:46997396-46997396 + LP6005334-DNA_D03 COSM5953140 c.2493C>T p.P831P Substitution - coding silent 3:46996770-46996770 + PT32 COSM5907282 c.5473C>T p.P1825S Substitution - Missense 3:47002970-47002970 + PT48 COSM5931343 c.6041C>T p.P2014L Substitution - Missense 3:47004236-47004236 + TCGA-FW-A3R5-06 COSM3916162 c.3962C>T p.P1321L Substitution - Missense 3:47000061-47000061 + Au3 COSM5601892 c.2584C>T p.L862L Substitution - coding silent 3:46996981-46996981 + LOVO COSM1045402 c.5290C>T p.R1764W Substitution - Missense 3:47002509-47002509 + MO_1176 COSM5550350 c.2017G>A p.A673T Substitution - Missense 3:46995832-46995832 + EGC15 COSM1242559 c.1184delC p.S397fs*75 Deletion - Frameshift 3:46994007-46994007 + C086 COSM5535220 c.6333G>A p.L2111L Substitution - coding silent 3:47005010-47005010 + Au1 COSM5597152 c.5474C>T p.P1825L Substitution - Missense 3:47002971-47002971 + 587224 COSM1216723 c.6275T>C p.V2092A Substitution - Missense 3:47009105-47009105 + TCGA-AP-A051-01 COSM1045391 c.4062G>A p.T1354T Substitution - coding silent 3:47000161-47000161 + TCGA-EE-A2MP-06 COSM3594615 c.2491C>T p.P831S Substitution - Missense 3:46996768-46996768 + STC252 COSM5059759 c.4081C>T p.R1361C Substitution - Missense 3:47004145-47004145 + ICGC_PA112 COSM3670323 c.1294C>T p.R432C Substitution - Missense 3:46997008-46997008 + CHLA-258 COSM4584394 c.860A>C p.D287A Substitution - Missense 3:46991623-46991623 + TCGA-B5-A11E-01 COSM1045418 c.7609C>A p.L2537M Substitution - Missense 3:47008076-47008076 + CHC892T COSM4961420 c.605G>A p.G202E Substitution - Missense 3:46995737-46995737 + C008 COSM5523234 c.4536C>T p.P1512P Substitution - coding silent 3:47001330-47001330 + CHEWS036 COSM4584398 c.2745C>T p.G915G Substitution - coding silent 3:47001408-47001408 + TCGA-GN-A26C-01 COSM273665 c.167C>T p.P56L Substitution - Missense 3:46988868-46988868 + CAL33 COSM189781 c.5312G>A p.R1771Q Substitution - Missense 3:47007112-47007112 + T3116 COSM4705681 c.8230G>C p.G2744R Substitution - Missense 3:47009285-47009285 + AD43 COSM5966523 c.1219_1221delCTC p.L408delL Deletion - In frame 3:46996813-46996815 + CHC301T COSM3669150 c.5382G>T p.L1794L Substitution - coding silent 3:47007267-47007267 + TCGA-D1-A15X-01 COSM1045382 c.1737A>G p.L579L Substitution - coding silent 3:46998162-46998162 + TCGA-AA-3712-01 COSM446600 c.214C>G p.R72G Substitution - Missense 3:46995266-46995266 + TCGA-BR-8361-01 COSM4117980 c.7766C>T p.A2589V Substitution - Missense 3:47008329-47008329 + TCGA-AA-3949-01 COSM296927 c.4389G>A p.A1463A Substitution - coding silent 3:47004554-47004554 + TCGA-AX-A0J1-01 COSM1045406 c.6099C>A p.N2033K Substitution - Missense 3:47004294-47004294 + TCGA-EJ-5507-01 COSM1131426 c.357A>G p.A119A Substitution - coding silent 3:46995409-46995409 + ACINAR04 COSM1734663 c.5540A>T p.D1847V Substitution - Missense 3:47007599-47007599 + A9 COSM5350988 c.672G>C p.L224F Substitution - Missense 3:46995804-46995804 + LOVO COSM1045403 c.3421C>T p.R1141W Substitution - Missense 3:47002509-47002509 + TCGA-BR-8487-01 COSM4117969 c.4076A>G p.N1359S Substitution - Missense 3:47004140-47004140 + TCGA-BP-4998-01 COSM480131 c.5132G>A p.R1711H Substitution - Missense 3:47002269-47002269 + PT35 COSM5911952 c.3191C>T p.S1064F Substitution - Missense 3:47002197-47002197 + OSCC-GB_00940111 COSM4891718 c.1338C>A p.I446I Substitution - coding silent 3:46995073-46995073 + TCGA-BG-A0M4-01 COSM1045396 c.4361C>T p.T1454M Substitution - Missense 3:47001056-47001056 + CLL086 COSM1291717 c.2147A>G p.Q716R Substitution - Missense 3:46999394-46999394 + TCGA-CA-6717-01 COSM1423485 c.377G>A p.G126D Substitution - Missense 3:46989285-46989285 + TCGA-D3-A3C3-06 COSM3594648 c.5697G>A p.R1899R Substitution - coding silent 3:47007874-47007874 + TCGA-BR-6452-01 COSM4117970 c.5979C>A p.I1993I Substitution - coding silent 3:47004174-47004174 + 8067541 COSM4387814 c.5464A>C p.T1822P Substitution - Missense 3:47002961-47002961 + 1517_CLM COSM5756286 c.1791C>T p.A597A Substitution - coding silent 3:46998216-46998216 + TCGA-CC-A7IG-01 COSM4943080 c.5264G>T p.R1755L Substitution - Missense 3:47002483-47002483 + AD43 COSM5966522 c.2536_2538delCTC p.L847delL Deletion - In frame 3:46996813-46996815 + TCGA-26-6173-01 COSM3408699 c.3336C>T p.V1112V Substitution - coding silent 3:46998831-46998831 + 8031133 COSM3392430 c.4393C>T p.R1465W Substitution - Missense 3:47004558-47004558 + PD9844a COSM5792709 c.5510G>T p.R1837L Substitution - Missense 3:47003007-47003007 + TCGA-06-5858-01 COSM3408697 c.3208C>T p.R1070C Substitution - Missense 3:46998552-46998552 + TARGET-30-PANWRR COSM1286491 c.2807C>T p.P936L Substitution - Missense 3:46997416-46997416 + T2950 COSM4705672 c.5015A>G p.E1672G Substitution - Missense 3:47006028-47006028 + TCGA-EP-A2KA-01 COSM4917475 c.4368G>T p.L1456F Substitution - Missense 3:47004533-47004533 + SW480 COSM4655886 c.1310G>A p.R437K Substitution - Missense 3:46997024-46997024 + TCGA-BR-4292-01 COSM4117984 c.8043G>A p.A2681A Substitution - coding silent 3:47009004-47009004 + RK099_C01 COSM1633194 c.632C>T p.A211V Substitution - Missense 3:46991294-46991294 + HCC101 COSM1617665 c.1652A>T p.E551V Substitution - Missense 3:46995387-46995387 + TARGET-30-PANWRR COSM1286492 c.1490C>T p.P497L Substitution - Missense 3:46997416-46997416 + LS174T COSM4646088 c.1191G>A p.S397S Substitution - coding silent 3:46994014-46994014 + CRC-06T COSM5457053 c.3865A>G p.T1289A Substitution - Missense 3:46999964-46999964 + Au3 COSM5601891 c.1185C>T p.S395S Substitution - coding silent 3:46994008-46994008 + TCGA-D9-A6EC-06 COSM4403875 c.1874C>T p.P625L Substitution - Missense 3:46995609-46995609 + SNUH_G76_S1 COSM149373 c.2835C>T p.N945N Substitution - coding silent 3:47001748-47001748 + PCSI0073 COSM216643 c.5960C>T p.A1987V Substitution - Missense 3:47004155-47004155 + tumor_4107137 COSM5947152 c.4950_4971del22 p.A1651fs*15 Deletion - Frameshift 3:47002087-47002108 + BD114T COSM5502690 c.2413G>A p.A805T Substitution - Missense 3:46996532-46996532 + BZ38 COSM5759297 c.2487G>A p.S829S Substitution - coding silent 3:47001051-47001051 + 587290 COSM1216739 c.1271G>A p.R424Q Substitution - Missense 3:46994528-46994528 + PD8984a COSM5769323 c.3212G>C p.S1071T Substitution - Missense 3:47002218-47002218 + TCGA-A6-6781-01 COSM1423490 c.1790G>A p.R597Q Substitution - Missense 3:46995525-46995525 + SJRHB004 COSM3738409 c.5357C>T p.T1786M Substitution - Missense 3:47002700-47002700 + LUAD-F00162 COSM366426 c.1197G>T p.K399N Substitution - Missense 3:46994020-46994020 + 470 COSM4437724 c.324A>C p.P108P Substitution - coding silent 3:46995376-46995376 + TCGA-HT-7477-01 COSM3974432 c.1109T>C p.F370S Substitution - Missense 3:46996545-46996545 + 587328 COSM1216725 c.3922G>T p.V1308L Substitution - Missense 3:47003886-47003886 + CSCC-11-T COSM4569926 c.850T>G p.C284G Substitution - Missense 3:46996286-46996286 + MD-335 COSM302726 c.935A>C p.H312P Substitution - Missense 3:46996371-46996371 + OLID02 COSM132808 c.1624G>A p.G542R Substitution - Missense 3:46997677-46997677 + TCGA-B5-A11E-01 COSM1045411 c.5005G>A p.A1669T Substitution - Missense 3:47006018-47006018 + TCGA-DK-A1A3-01 COSM419990 c.3783G>A p.V1261V Substitution - coding silent 3:47003241-47003241 + PCSI_0002_Pa_X COSM4964687 c.830G>T p.S277I Substitution - Missense 3:46996047-46996047 + HCC101T COSM1617665 c.1652A>T p.E551V Substitution - Missense 3:46995387-46995387 + TCGA-BP-4998-01 COSM480132 c.3263G>A p.R1088H Substitution - Missense 3:47002269-47002269 + HCC089T COSM5822397 c.7217A>G p.D2406G Substitution - Missense 3:47007148-47007148 + LUAD-RT-S01769 COSM380990 c.1288G>C p.D430H Substitution - Missense 3:46997002-46997002 + TCGA-A6-6781-01 COSM1423491 c.473G>A p.R158Q Substitution - Missense 3:46995525-46995525 + CHLA-258 COSM1216729 c.3407G>A p.R1136H Substitution - Missense 3:47002495-47002495 + TCGA-EE-A181-06 COSM3594611 c.820C>T p.R274C Substitution - Missense 3:46991583-46991583 + TCGA-FW-A3R5-06 COSM1177393 c.5175C>T p.F1725F Substitution - coding silent 3:47002394-47002394 + TCGA-G4-6588-01 COSM1423509 c.5283A>G p.V1761V Substitution - coding silent 3:47007083-47007083 + T3658 COSM4705668 c.4681C>T p.Q1561* Substitution - Nonsense 3:47005311-47005311 + SC_9047 COSM5551866 c.4974C>T p.D1658D Substitution - coding silent 3:47005987-47005987 + ACINAR04 COSM1734662 c.7409A>T p.D2470V Substitution - Missense 3:47007599-47007599 + TCGA-CI-6624-01 COSM1566758 c.4344C>T p.N1448N Substitution - coding silent 3:47001039-47001039 + 19M COSM5579048 c.4613G>A p.G1538D Substitution - Missense 3:47001407-47001407 + TCGA-FU-A3HZ-01 COSM4838924 c.6841G>A p.D2281N Substitution - Missense 3:47005985-47005985 + WA48 COSM240828 c.6433G>C p.E2145Q Substitution - Missense 3:47005194-47005194 + TCGA-KK-A6E1-01 COSM4876417 c.2574C>A p.I858I Substitution - coding silent 3:46996971-46996971 + YULONE COSM5399469 c.7128C>T p.F2376F Substitution - coding silent 3:47006443-47006443 + RK117_C01 COSM3702440 c.5024A>G p.N1675S Substitution - Missense 3:47006037-47006037 + 587376 COSM1216738 c.4006G>A p.E1336K Substitution - Missense 3:47003970-47003970 + C135 COSM4117965 c.3317C>T p.T1106M Substitution - Missense 3:47002405-47002405 + TCGA-AP-A056-01 COSM1045364 c.132G>A p.E44E Substitution - coding silent 3:46988749-46988749 + TCGA-06-5858-01 COSM3408698 c.1891C>T p.R631C Substitution - Missense 3:46998552-46998552 + BN24 COSM1617669 c.5847C>T p.Y1949Y Substitution - coding silent 3:47003942-47003942 + CSCC-7-T COSM4480160 c.1077C>T p.S359S Substitution - coding silent 3:46996513-46996513 + LP6005935-DNA_F01 COSM4879738 c.3117C>T p.S1039S Substitution - coding silent 3:47002123-47002123 + TCGA-A8-A086-01 COSM5834675 c.6773_6774insG p.D2258fs*49 Insertion - Frameshift 3:47005819-47005820 + Pat_32_A COSM5864624 c.5789G>A p.G1930E Substitution - Missense 3:47008125-47008125 + TCGA-EB-A5UN-06 COSM3594637 c.6074T>C p.I2025T Substitution - Missense 3:47004269-47004269 + TCGA-B5-A11E-01 COSM1045376 c.871C>T p.R291C Substitution - Missense 3:46996307-46996307 + SJRHB004_D COSM3738410 c.3488C>T p.T1163M Substitution - Missense 3:47002700-47002700 + TCGA-B5-A11S-01 COSM1045408 c.6514C>T p.R2172C Substitution - Missense 3:47005275-47005275 + HT115 COSM3068766 c.7290C>T p.S2430S Substitution - coding silent 3:47007306-47007306 + TCGA-EE-A3J5-06 COSM3594649 c.7688C>T p.T2563I Substitution - Missense 3:47008155-47008155 + T3262 COSM4705666 c.3994C>T p.R1332C Substitution - Missense 3:47003958-47003958 + C086 COSM5535221 c.4464G>A p.L1488L Substitution - coding silent 3:47005010-47005010 + TCGA-EE-A29D-06 COSM3594610 c.233C>T p.A78V Substitution - Missense 3:46988934-46988934 + PTC-54C COSM4158074 c.3916T>C p.S1306P Substitution - Missense 3:47000015-47000015 + TCGA-21-1076-01 COSM730728 c.5264G>A p.R1755H Substitution - Missense 3:47002483-47002483 + TCGA-BH-A0W7-01 COSM446607 c.4880C>A p.P1627H Substitution - Missense 3:47005795-47005795 + UM-SCC-47 COSM4600199 c.57G>T p.W19C Substitution - Missense 3:46995109-46995109 + KPOPBR-03-T COSM5965746 c.4056C>T p.F1352F Substitution - coding silent 3:47000155-47000155 + T3225 COSM4705684 c.6391C>T p.R2131C Substitution - Missense 3:47009315-47009315 + ICGC_MB15 COSM307083 c.7771C>T p.L2591L Substitution - coding silent 3:47008334-47008334 + TCGA-CD-A4MG-01 COSM4117956 c.4247G>A p.G1416D Substitution - Missense 3:47000346-47000346 + CSCC-27-T COSM4507058 c.736C>T p.L246L Substitution - coding silent 3:46991499-46991499 + 587238 COSM189783 c.5882G>A p.R1961H Substitution - Missense 3:47008314-47008314 + 1_PRE-TREATMENT COSM1719620 c.4084C>T p.R1362C Substitution - Missense 3:47004148-47004148 + TCGA-BR-8677-01 COSM4117954 c.4220C>A p.S1407Y Substitution - Missense 3:47000319-47000319 + TCGA-C8-A26Y-01 COSM3823988 c.2723A>G p.E908G Substitution - Missense 3:46997332-46997332 + AOCS-034-3-8 COSM4149934 c.72G>A p.Q24Q Substitution - coding silent 3:46988689-46988689 + SNUH_G76_S1 COSM4417106 c.5050+9T>C p.? Unknown 3:47006072-47006072 + HN_62506 COSM124677 c.6235G>A p.V2079M Substitution - Missense 3:47009065-47009065 + ME020T COSM225512 c.4798C>T p.P1600S Substitution - Missense 3:47005595-47005595 + 587284 COSM1216735 c.6277G>A p.A2093T Substitution - Missense 3:47009107-47009107 + TCGA-BR-6452-01 COSM4117966 c.5236G>A p.D1746N Substitution - Missense 3:47002455-47002455 + BN24T COSM1617670 c.3978C>T p.Y1326Y Substitution - coding silent 3:47003942-47003942 + TCGA-B5-A11E-01 COSM1045419 c.5740C>A p.L1914M Substitution - Missense 3:47008076-47008076 + CSCC-27-T COSM4569783 c.708T>C p.S236S Substitution - coding silent 3:46995840-46995840 + Pat_06_A COSM5864616 c.4306-1G>A p.? Unknown 3:47001000-47001000 + HCA7 COSM1216717 c.3625G>A p.A1209T Substitution - Missense 3:47002991-47002991 + 587238 COSM1216717 c.3625G>A p.A1209T Substitution - Missense 3:47002991-47002991 + PD9702a COSM5772622 c.8058G>C p.M2686I Substitution - Missense 3:47009019-47009019 + pfg222T COSM4754395 c.352C>T p.H118Y Substitution - Missense 3:46995404-46995404 + BCM567T COSM4950079 c.3532C>T p.R1178* Substitution - Nonsense 3:46999106-46999106 + PT15_1 COSM5897451 c.3733C>T p.P1245S Substitution - Missense 3:47003191-47003191 + TCGA-DK-A1A3-01 COSM419989 c.5652G>A p.V1884V Substitution - coding silent 3:47003241-47003241 + 438 COSM4434317 c.7898T>G p.L2633R Substitution - Missense 3:47008539-47008539 + TCGA-BR-6452-01 COSM4117949 c.2254C>T p.P752S Substitution - Missense 3:46996373-46996373 + sysucc-783T COSM5484624 c.1865G>A p.G622D Substitution - Missense 3:46998526-46998526 + ESO-512 COSM1258759 c.4541G>A p.G1514E Substitution - Missense 3:47001335-47001335 + TCGA-D1-A15X-01 COSM1045381 c.3054A>G p.L1018L Substitution - coding silent 3:46998162-46998162 + ESO-081 COSM1243423 c.4845C>T p.R1615R Substitution - coding silent 3:47001982-47001982 + LUAD_E00623 COSM354366 c.5737G>A p.G1913S Substitution - Missense 3:47008073-47008073 + TCGA-B5-A1MY-01 COSM1045402 c.5290C>T p.R1764W Substitution - Missense 3:47002509-47002509 + pfg181T COSM4754399 c.5200C>T p.R1734C Substitution - Missense 3:47006384-47006384 + BD236T COSM5518424 c.1214G>A p.R405H Substitution - Missense 3:46994471-46994471 + CHC301T COSM3669149 c.7251G>T p.L2417L Substitution - coding silent 3:47007267-47007267 + PT36 COSM5915192 c.7177C>T p.H2393Y Substitution - Missense 3:47007108-47007108 + PT21_2 COSM1045384 c.1831C>T p.R611W Substitution - Missense 3:46998492-46998492 + Au3 COSM5601893 c.1267C>T p.L423L Substitution - coding silent 3:46996981-46996981 + 417 COSM4431716 c.8235G>C p.E2745D Substitution - Missense 3:47009290-47009290 + TCGA-HU-A4GU-01 COSM3068540 c.1914C>T p.S638S Substitution - coding silent 3:46995729-46995729 + PT49 COSM5934791 c.799C>T p.P267S Substitution - Missense 3:46991562-46991562 + LIM2405 COSM1216736 c.794G>A p.R265H Substitution - Missense 3:46991557-46991557 + TCGA-FP-A4BE-01 COSM4117964 c.5186C>T p.T1729M Substitution - Missense 3:47002405-47002405 + 384 COSM4426786 c.5333C>T p.A1778V Substitution - Missense 3:47002676-47002676 + TCGA-BS-A0UV-01 COSM1045387 c.3478G>A p.E1160K Substitution - Missense 3:46999052-46999052 + sysucc-274T COSM5476458 c.283C>T p.R95C Substitution - Missense 3:46995335-46995335 + TCGA-FW-A3R5-06 COSM3916160 c.513C>T p.F171F Substitution - coding silent 3:46989550-46989550 + T3101 COSM4705676 c.5998C>T p.P2000S Substitution - Missense 3:47008430-47008430 + PDA_092 COSM5003121 c.5168C>A p.S1723Y Substitution - Missense 3:47002387-47002387 + PD18259a COSM5794226 c.3023G>A p.R1008Q Substitution - Missense 3:47002029-47002029 + T1154 COSM4705655 c.2342T>C p.I781T Substitution - Missense 3:46996461-46996461 + TCGA-E2-A1LA-01 COSM1485230 c.2171T>C p.I724T Substitution - Missense 3:46996290-46996290 + CSCC-35-T COSM4495337 c.2649C>G p.T883T Substitution - coding silent 3:47001312-47001312 + TCGA-D5-6930-01 COSM1423486 c.673T>C p.S225P Substitution - Missense 3:46991436-46991436 + TCGA-AP-A051-01 COSM1045394 c.4159G>T p.G1387C Substitution - Missense 3:47000258-47000258 + 384 COSM4426787 c.3464C>T p.A1155V Substitution - Missense 3:47002676-47002676 + T3503 COSM4705674 c.5089C>T p.R1697W Substitution - Missense 3:47006203-47006203 + PD18024a COSM5777313 c.1856C>T p.T619I Substitution - Missense 3:46995591-46995591 + RMS105_ COSM4986220 c.2507G>A p.G836E Substitution - Missense 3:46996784-46996784 + BD124T COSM5491640 c.1642-8T>C p.? Unknown 3:46998059-46998059 + TCGA-32-4211-01 COSM3408701 c.3868C>T p.R1290W Substitution - Missense 3:46999967-46999967 + LUAD-NYU263 COSM372238 c.2316G>T p.P772P Substitution - coding silent 3:47000284-47000284 + CHC892T COSM4794999 c.757G>A p.A253T Substitution - Missense 3:46991520-46991520 + 19M COSM5579049 c.2744G>A p.G915D Substitution - Missense 3:47001407-47001407 + TCGA-AP-A0LM-01 COSM1045366 c.460C>T p.R154C Substitution - Missense 3:46989368-46989368 + CSCC-49-T COSM4477552 c.845C>T p.S282F Substitution - Missense 3:46996281-46996281 + MO_1176 COSM5550351 c.700G>A p.A234T Substitution - Missense 3:46995832-46995832 + TCGA-EB-A44Q-06 COSM3594628 c.3391C>T p.R1131W Substitution - Missense 3:47002479-47002479 + CHC1629T COSM4791740 c.6080C>A p.P2027H Substitution - Missense 3:47004275-47004275 + PD7248a COSM5792009 c.4799A>G p.Y1600C Substitution - Missense 3:47001936-47001936 + CHC433T COSM446599 c.1531C>G p.R511G Substitution - Missense 3:46995266-46995266 + TCGA-FS-A4FC-06 COSM3594643 c.6463C>T p.H2155Y Substitution - Missense 3:47005224-47005224 + BD114T COSM5502691 c.1096G>A p.A366T Substitution - Missense 3:46996532-46996532 + CSCC-11-T COSM4552668 c.3796G>A p.E1266K Substitution - Missense 3:47003254-47003254 + TCGA-BR-7851-01 COSM4117963 c.2928C>A p.A976A Substitution - coding silent 3:47001934-47001934 + TCGA-D1-A15X-01 COSM1045374 c.720C>T p.C240C Substitution - coding silent 3:46995937-46995937 + 2492720 COSM5720012 c.3936C>T p.S1312S Substitution - coding silent 3:47000035-47000035 + TCGA-EU-5907-01 COSM480133 c.6780C>A p.I2260I Substitution - coding silent 3:47005826-47005826 + CHC917T COSM3669148 c.4760C>T p.A1587V Substitution - Missense 3:47005557-47005557 + sysucc-311T COSM5465898 c.8071C>T p.R2691C Substitution - Missense 3:47009032-47009032 + 587226 COSM1216714 c.4846G>A p.E1616K Substitution - Missense 3:47001983-47001983 + TCGA-AX-A0J1-01 COSM1045404 c.5954G>A p.R1985H Substitution - Missense 3:47004149-47004149 + HCC125 COSM1617671 c.6828A>G p.L2276L Substitution - coding silent 3:47005972-47005972 + AOCS-034-1-0 COSM4149934 c.72G>A p.Q24Q Substitution - coding silent 3:46988689-46988689 + TCGA-A8-A0A6-01 COSM3823995 c.4216A>C p.T1406P Substitution - Missense 3:47004280-47004280 + LUAD-B02477 COSM335892 c.7407G>A p.P2469P Substitution - coding silent 3:47007597-47007597 + TCGA-D1-A101-01 COSM1045368 c.731C>T p.P244L Substitution - Missense 3:46991494-46991494 + HCC99T COSM3660579 c.3546G>T p.A1182A Substitution - coding silent 3:47002758-47002758 + TCGA-F4-6854-01 COSM3696116 c.6508C>T p.L2170F Substitution - Missense 3:47005269-47005269 + TCGA-BR-6565-01 COSM4117959 c.2615G>C p.S872T Substitution - Missense 3:47001179-47001179 + BZ38 COSM5759296 c.4356G>A p.S1452S Substitution - coding silent 3:47001051-47001051 + TCGA-D3-A5GR-06 COSM3594620 c.3747C>T p.S1249S Substitution - coding silent 3:46999673-46999673 + BD236T COSM5518428 c.6312C>T p.F2104F Substitution - coding silent 3:47009236-47009236 + TCGA-CD-A4MG-01 COSM1045405 c.4085G>A p.R1362H Substitution - Missense 3:47004149-47004149 + 587376 COSM1216736 c.794G>A p.R265H Substitution - Missense 3:46991557-46991557 + J57_T COSM3945521 c.2985C>T p.N995N Substitution - coding silent 3:46998093-46998093 + CSCC-44-T COSM4458867 c.1101C>T p.P367P Substitution - coding silent 3:46992543-46992543 + HCT15 COSM4625102 c.3339G>A p.T1113T Substitution - coding silent 3:46998834-46998834 + CHC2215T COSM4790268 c.2533G>A p.E845K Substitution - Missense 3:47001097-47001097 + sysucc-783T COSM5484623 c.3182G>A p.G1061D Substitution - Missense 3:46998526-46998526 + T3262 COSM4705665 c.5863C>T p.R1955C Substitution - Missense 3:47003958-47003958 + TCGA-D1-A0ZO-01 COSM1045371 c.1943C>T p.A648V Substitution - Missense 3:46995758-46995758 + 2492723 COSM5720009 c.87C>T p.A29A Substitution - coding silent 3:46988704-46988704 + 8061109 COSM3392424 c.1672G>A p.A558T Substitution - Missense 3:46995407-46995407 + TCGA-A8-A097-01 COSM3823992 c.5772C>T p.A1924A Substitution - coding silent 3:47003867-47003867 + TCGA-18-3409-01 COSM730727 c.3621C>A p.S1207S Substitution - coding silent 3:47002987-47002987 + GC8_T COSM149373 c.2835C>T p.N945N Substitution - coding silent 3:47001748-47001748 + SNUH_G45_S1 COSM149373 c.2835C>T p.N945N Substitution - coding silent 3:47001748-47001748 + sysucc-1370T COSM5471744 c.4728G>A p.A1576A Substitution - coding silent 3:47005525-47005525 + HCC90T COSM1617668 c.3059A>T p.D1020V Substitution - Missense 3:47002065-47002065 + TCGA-EE-A3JA-06 COSM3594622 c.2666C>T p.P889L Substitution - Missense 3:47001329-47001329 + ATL007 COSM5708759 c.3083A>G p.H1028R Substitution - Missense 3:46998191-46998191 + TCGA-DH-5144-01 COSM3408701 c.3868C>T p.R1290W Substitution - Missense 3:46999967-46999967 + TCGA-D5-6928-01 COSM1423493 c.1792G>A p.V598M Substitution - Missense 3:46998217-46998217 + ACINAR01 COSM1734660 c.2486C>T p.T829M Substitution - Missense 3:46996763-46996763 + 3498_T COSM3945524 c.5791G>T p.A1931S Substitution - Missense 3:47008127-47008127 + Detroit_562 COSM3068777 c.5617A>T p.S1873C Substitution - Missense 3:47007676-47007676 + T3225 COSM4705683 c.8260C>T p.R2754C Substitution - Missense 3:47009315-47009315 + TCGA-AA-3672-01 COSM267000 c.4033delT p.Y1346fs*20 Deletion - Frameshift 3:47000132-47000132 + TCGA-HU-A4GU-01 COSM3068541 c.597C>T p.S199S Substitution - coding silent 3:46995729-46995729 + TCGA-AM-5821-01 COSM3760132 c.6161C>T p.S2054F Substitution - Missense 3:47004356-47004356 + ESCC_136 COSM5643054 c.2320_2321insC p.L776fs*27 Insertion - Frameshift 3:46996439-46996440 + YUROG COSM5399463 c.358G>A p.G120R Substitution - Missense 3:46989266-46989266 + UM-SCC-47 COSM4600198 c.1374G>T p.W458C Substitution - Missense 3:46995109-46995109 + CHC301T COSM3669149 c.7251G>T p.L2417L Substitution - coding silent 3:47007267-47007267 + 2217539 COSM4421765 c.1232C>T p.S411L Substitution - Missense 3:46996826-46996826 + OSCC-GB_00250111 COSM3714550 c.6240G>A p.M2080I Substitution - Missense 3:47004536-47004536 + 8061109 COSM3392425 c.355G>A p.A119T Substitution - Missense 3:46995407-46995407 + TCGA-ER-A19W-06 COSM4399050 c.4912C>T p.Q1638* Substitution - Nonsense 3:47005827-47005827 + GC_342T_a-GC_342N COSM4771898 c.2065C>T p.R689W Substitution - Missense 3:46995965-46995965 + LUAD-S01356 COSM398234 c.4799A>T p.Y1600F Substitution - Missense 3:47001936-47001936 + CHC1754T COSM4792822 c.1487G>T p.G496V Substitution - Missense 3:46995222-46995222 + TCGA-EE-A3AC-06 COSM3594635 c.6046C>T p.Q2016* Substitution - Nonsense 3:47004241-47004241 + YUMUL COSM5399465 c.1210G>A p.E404K Substitution - Missense 3:46994467-46994467 + TCGA-AZ-6601-01 COSM1423507 c.4030C>T p.R1344W Substitution - Missense 3:47004094-47004094 + TTC466 COSM4584395 c.2376G>A p.R792R Substitution - coding silent 3:46996495-46996495 + SC_9024 COSM3068527 c.327C>T p.G109G Substitution - coding silent 3:46995379-46995379 + TCGA-CC-A7IH-01 COSM4924050 c.2679G>T p.L893L Substitution - coding silent 3:47001342-47001342 + ATL046 COSM5708762 c.4540G>C p.V1514L Substitution - Missense 3:47005086-47005086 + T19 COSM5344486 c.5317C>T p.P1773S Substitution - Missense 3:47002660-47002660 + ACINAR01 COSM1734661 c.1169C>T p.T390M Substitution - Missense 3:46996763-46996763 + HCT8 COSM4625102 c.3339G>A p.T1113T Substitution - coding silent 3:46998834-46998834 + CSCC-31-T COSM4544627 c.3608G>A p.R1203Q Substitution - Missense 3:46999379-46999379 + 587376 COSM1216737 c.5875G>A p.E1959K Substitution - Missense 3:47003970-47003970 + sysucc-1397T COSM5474611 c.5227G>A p.A1743T Substitution - Missense 3:47002446-47002446 + 1517_PT COSM5756287 c.4372G>A p.V1458M Substitution - Missense 3:47001067-47001067 + CSCC-7-T COSM4480159 c.2394C>T p.S798S Substitution - coding silent 3:46996513-46996513 + TCGA-Q1-A73R-01 COSM4856050 c.5959G>A p.A1987T Substitution - Missense 3:47004154-47004154 + TCGA-FP-A4BE-01 COSM4117965 c.3317C>T p.T1106M Substitution - Missense 3:47002405-47002405 + TCGA-E2-A1LA-01 COSM1485231 c.854T>C p.I285T Substitution - Missense 3:46996290-46996290 + TCGA-AA-3715-01 COSM269695 c.3850T>C p.W1284R Substitution - Missense 3:46999949-46999949 + TCGA-EE-A2MR-06 COSM3594625 c.4675C>T p.R1559C Substitution - Missense 3:47001719-47001719 + TCGA-A8-A086-01 COSM5834676 c.4904_4905insG p.D1635fs*49 Insertion - Frameshift 3:47005819-47005820 + ATL046 COSM5708761 c.6409G>C p.V2137L Substitution - Missense 3:47005086-47005086 + EOPC-035_tumor_01 COSM5951050 c.7428C>T p.S2476S Substitution - coding silent 3:47007618-47007618 + TCGA-EJ-5507-01 COSM1131425 c.1674A>G p.A558A Substitution - coding silent 3:46995409-46995409 + TCGA-22-1016-01 COSM730730 c.1850C>T p.A617V Substitution - Missense 3:46995585-46995585 + Detroit_562 COSM3068776 c.7486A>T p.S2496C Substitution - Missense 3:47007676-47007676 + MD-335 COSM302727 c.2252A>C p.H751P Substitution - Missense 3:46996371-46996371 + TCGA-AP-A0LE-01 COSM1045417 c.5672G>A p.G1891D Substitution - Missense 3:47007849-47007849 + 2492720 COSM5720010 c.2690C>T p.P897L Substitution - Missense 3:46997299-46997299 + PT15_1 COSM5897452 c.6007C>T p.P2003S Substitution - Missense 3:47004202-47004202 + TCGA-EI-6917-01 COSM1045372 c.626C>T p.A209V Substitution - Missense 3:46995758-46995758 + TCGA-BR-6452-01 COSM4117961 c.2629A>G p.M877V Substitution - Missense 3:47001292-47001292 + T3503 COSM4705673 c.6958C>T p.R2320W Substitution - Missense 3:47006203-47006203 + TCGA-18-3409-01 COSM730726 c.5490C>A p.S1830S Substitution - coding silent 3:47002987-47002987 + TCGA-EE-A3AA-06 COSM3594632 c.3767C>T p.T1256I Substitution - Missense 3:47003225-47003225 + TCGA-Q1-A73R-01 COSM4856051 c.4090G>A p.A1364T Substitution - Missense 3:47004154-47004154 + HCC022T COSM5817584 c.5112T>C p.F1704F Substitution - coding silent 3:47002249-47002249 + 3498_T COSM3945523 c.7660G>T p.A2554S Substitution - Missense 3:47008127-47008127 + T3498 COSM4705669 c.6877G>A p.A2293T Substitution - Missense 3:47006021-47006021 + YUGATOR COSM5399467 c.1998C>T p.L666L Substitution - coding silent 3:46998810-46998810 + LUAD-NYU263 COSM372237 c.4185G>T p.P1395P Substitution - coding silent 3:47000284-47000284 + ESCC-083T COSM3940544 c.2543A>T p.Q848L Substitution - Missense 3:47001107-47001107 + 1517_CLM COSM5756285 c.3108C>T p.A1036A Substitution - coding silent 3:46998216-46998216 + TCGA-FW-A3R5-06 COSM3916161 c.3748C>T p.L1250F Substitution - Missense 3:46999674-46999674 + TCGA-AA-3712-01 COSM446599 c.1531C>G p.R511G Substitution - Missense 3:46995266-46995266 + 2492720 COSM5720011 c.1373C>T p.P458L Substitution - Missense 3:46997299-46997299 + ZZUFHECRKL-G014T COSM5437488 c.2013G>A p.V671V Substitution - coding silent 3:46998825-46998825 + WA25 COSM240830 c.6920-1G>T p.? Unknown 3:47006164-47006164 + CHC2215T COSM4790267 c.4402G>A p.E1468K Substitution - Missense 3:47001097-47001097 + PD11372a COSM5767249 c.2580G>A p.L860L Substitution - coding silent 3:46996977-46996977 + OSCC-GB_00940111 COSM4891719 c.21C>A p.I7I Substitution - coding silent 3:46995073-46995073 + TCGA-EK-A2PL-01 COSM4838300 c.1792G>T p.V598L Substitution - Missense 3:46998217-46998217 + TCGA-BS-A0UL-01 COSM1045399 c.2498G>A p.R833H Substitution - Missense 3:47001062-47001062 + TCGA-A8-A097-01 COSM3823993 c.3903C>T p.A1301A Substitution - coding silent 3:47003867-47003867 + ESO-717 COSM1242559 c.1184delC p.S397fs*75 Deletion - Frameshift 3:46994007-46994007 + ICGC_MB15 COSM307082 c.5902C>T p.L1968L Substitution - coding silent 3:47008334-47008334 + TCGA-AA-3949-01 COSM296928 c.6258G>A p.A2086A Substitution - coding silent 3:47004554-47004554 + 1_RESISTANT COSM1719620 c.4084C>T p.R1362C Substitution - Missense 3:47004148-47004148 + 61 COSM4426786 c.5333C>T p.A1778V Substitution - Missense 3:47002676-47002676 + SC_9076 COSM5559077 c.7504C>T p.L2502F Substitution - Missense 3:47007694-47007694 + TCGA-KK-A6E1-01 COSM4876418 c.1257C>A p.I419I Substitution - coding silent 3:46996971-46996971 + CSCC-1-T COSM4556225 c.4963G>T p.E1655* Substitution - Nonsense 3:47005976-47005976 + TCGA-A2-A0T6-01 COSM3823996 c.6198+2T>G p.? Unknown 3:47004395-47004395 + T521 COSM4705663 c.5848G>A p.D1950N Substitution - Missense 3:47003943-47003943 + TCGA-BR-8361-01 COSM4117981 c.5897C>T p.A1966V Substitution - Missense 3:47008329-47008329 + TCGA-DR-A0ZM-01 COSM460789 c.4387G>A p.E1463K Substitution - Missense 3:47001082-47001082 + HCT15 COSM3068557 c.816C>T p.R272R Substitution - coding silent 3:46996033-46996033 + PT49 COSM5934793 c.824C>T p.S275F Substitution - Missense 3:46996041-46996041 + SNUH_G45_S1 COSM4002709 c.4704C>T p.N1568N Substitution - coding silent 3:47001748-47001748 + TCGA-EU-5907-01 COSM480134 c.4911C>A p.I1637I Substitution - coding silent 3:47005826-47005826 + T155 COSM1177393 c.5175C>T p.F1725F Substitution - coding silent 3:47002394-47002394 + PT36 COSM5915193 c.5308C>T p.H1770Y Substitution - Missense 3:47007108-47007108 + PD18285a COSM3770545 c.5050G>A p.G1684R Substitution - Missense 3:47006063-47006063 + BN24 COSM1617670 c.3978C>T p.Y1326Y Substitution - coding silent 3:47003942-47003942 + BD124T COSM5491639 c.2959-8T>C p.? Unknown 3:46998059-46998059 + 587316 COSM1216727 c.721G>A p.V241M Substitution - Missense 3:46995938-46995938 + HCC125 COSM1617672 c.4959A>G p.L1653L Substitution - coding silent 3:47005972-47005972 + TCGA-BR-6565-01 COSM4117958 c.4484G>C p.S1495T Substitution - Missense 3:47001179-47001179 + C086 COSM5535218 c.5467C>T p.P1823S Substitution - Missense 3:47002964-47002964 + PD18259a COSM5794225 c.4892G>A p.R1631Q Substitution - Missense 3:47002029-47002029 + CSCC-11-T COSM4552667 c.5665G>A p.E1889K Substitution - Missense 3:47003254-47003254 + PD9844a COSM5792711 c.5511C>T p.R1837R Substitution - coding silent 3:47003008-47003008 + ESCC_47 COSM5290688 c.2530C>T p.R844W Substitution - Missense 3:47001094-47001094 + TCGA-AD-6901-01 COSM1423495 c.1970T>C p.L657P Substitution - Missense 3:46998782-46998782 + TCGA-EK-A2RK-01 COSM4828956 c.380G>A p.R127Q Substitution - Missense 3:46989288-46989288 + SJHYPO029 COSM4775567 c.3424G>A p.G1142S Substitution - Missense 3:46998998-46998998 + TCGA-BR-4188-01 COSM4117978 c.7670G>A p.S2557N Substitution - Missense 3:47008137-47008137 + YUGATOR COSM5399466 c.3315C>T p.L1105L Substitution - coding silent 3:46998810-46998810 + Pat_06_A COSM5864618 c.6490G>A p.A2164T Substitution - Missense 3:47005251-47005251 + TCGA-EP-A2KA-01 COSM4917474 c.6237G>T p.L2079F Substitution - Missense 3:47004533-47004533 + HCC99T COSM3660578 c.5415G>T p.A1805A Substitution - coding silent 3:47002758-47002758 + SC_9047 COSM5551865 c.6843C>T p.D2281D Substitution - coding silent 3:47005987-47005987 + 37M COSM5583824 c.3697G>C p.G1233R Substitution - Missense 3:46999468-46999468 + TCGA-EE-A29M-06 COSM3594613 c.1949G>A p.G650E Substitution - Missense 3:46995764-46995764 + CHC892T COSM4961419 c.1922G>A p.G641E Substitution - Missense 3:46995737-46995737 + tumor_4107137 COSM5947153 c.3081_3102del22 p.A1028fs*15 Deletion - Frameshift 3:47002087-47002108 + C008 COSM5523232 c.2743G>A p.E915K Substitution - Missense 3:46997352-46997352 + LS411 COSM3068663 c.5079C>A p.G1693G Substitution - coding silent 3:47002216-47002216 + CN-AML-CR-22-Dx COSM5424970 c.5879G>T p.R1960L Substitution - Missense 3:47008311-47008311 + TCGA-FU-A3HZ-01 COSM4838925 c.4972G>A p.D1658N Substitution - Missense 3:47005985-47005985 + SJRHB004 COSM3738410 c.3488C>T p.T1163M Substitution - Missense 3:47002700-47002700 + 875-01-3TD COSM5417669 c.3216C>T p.P1072P Substitution - coding silent 3:47002222-47002222 + 2492723 COSM5720012 c.3936C>T p.S1312S Substitution - coding silent 3:47000035-47000035 + TCGA-EE-A2MR-06 COSM3594630 c.3638C>T p.S1213L Substitution - Missense 3:47003004-47003004 + 587238 COSM1216719 c.4727C>T p.A1576V Substitution - Missense 3:47005524-47005524 + SC_9047 COSM5551409 c.2922C>T p.C974C Substitution - coding silent 3:46997658-46997658 + PD11372a COSM5767266 c.2482G>A p.E828K Substitution - Missense 3:46996759-46996759 + SNU-175 COSM3068601 c.1708G>A p.A570T Substitution - Missense 3:46998133-46998133 + PD4002a COSM162809 c.1642G>T p.V548F Substitution - Missense 3:46998067-46998067 + 1_RESISTANT COSM1719619 c.5953C>T p.R1985C Substitution - Missense 3:47004148-47004148 + LUAD-RT-S01769 COSM380989 c.2605G>C p.D869H Substitution - Missense 3:46997002-46997002 + PCSI_0073_Pa_X COSM216643 c.5960C>T p.A1987V Substitution - Missense 3:47004155-47004155 + HCA7 COSM1216716 c.5494G>A p.A1832T Substitution - Missense 3:47002991-47002991 + ESO-512 COSM1258760 c.2672G>A p.G891E Substitution - Missense 3:47001335-47001335 + TCGA-D1-A163-01 COSM1045390 c.4043C>A p.A1348D Substitution - Missense 3:47000142-47000142 + TCGA-FS-A4FC-06 COSM3594644 c.4594C>T p.H1532Y Substitution - Missense 3:47005224-47005224 + CSCC-31-T COSM4503920 c.4641C>T p.L1547L Substitution - coding silent 3:47005271-47005271 + PD9844a COSM5792710 c.3641G>T p.R1214L Substitution - Missense 3:47003007-47003007 + PT37 COSM5918175 c.3935C>T p.S1312F Substitution - Missense 3:47000034-47000034 + TCGA-D3-A5GN-06 COSM3594634 c.4083C>T p.R1361R Substitution - coding silent 3:47004147-47004147 + LUAD-FH5PJ COSM394514 c.1217T>A p.I406N Substitution - Missense 3:46994474-46994474 + TCGA-BR-8059-01 COSM4117973 c.4306C>A p.L1436M Substitution - Missense 3:47004370-47004370 + CHC1754T COSM4792823 c.170G>T p.G57V Substitution - Missense 3:46995222-46995222 + 1517_PT COSM5088615 c.3903delC p.P1303fs*63 Deletion - Frameshift 3:47000002-47000002 + CHC1629T COSM4791741 c.4211C>A p.P1404H Substitution - Missense 3:47004275-47004275 + TCGA-CC-A7IG-01 COSM4943081 c.3395G>T p.R1132L Substitution - Missense 3:47002483-47002483 + TCGA-DR-A0ZM-01 COSM460790 c.2518G>A p.E840K Substitution - Missense 3:47001082-47001082 + CSCC-49-T COSM4539709 c.1405G>A p.E469K Substitution - Missense 3:46997331-46997331 + 37M COSM5583825 c.2221G>C p.G741R Substitution - Missense 3:46999468-46999468 + 587316 COSM1216726 c.2038G>A p.V680M Substitution - Missense 3:46995938-46995938 + 875-01-3TD COSM5417668 c.5085C>T p.P1695P Substitution - coding silent 3:47002222-47002222 + OSCC-GB_01060111 COSM4882501 c.120T>A p.C40* Substitution - Nonsense 3:46995172-46995172 + SJHGG045_A COSM4972055 c.6596_6597CG>AA p.A2199E Substitution - Missense 3:47005524-47005525 + TCGA-D1-A103-01 COSM1045401 c.2590C>T p.R864C Substitution - Missense 3:47001154-47001154 + PCSI_0227_Pa_P_526 COSM4962321 c.4822G>A p.G1608S Substitution - Missense 3:47005619-47005619 + C008 COSM5523233 c.1426G>A p.E476K Substitution - Missense 3:46997352-46997352 + SNU-C4 COSM4653699 c.928G>A p.A310T Substitution - Missense 3:46991842-46991842 + RK211_C01 COSM3767453 c.2597A>T p.H866L Substitution - Missense 3:46996994-46996994 + HCC022T COSM5817585 c.3243T>C p.F1081F Substitution - coding silent 3:47002249-47002249 + T3090 COSM4705660 c.2341C>T p.R781C Substitution - Missense 3:47000309-47000309 + PDA_092 COSM5003122 c.3299C>A p.S1100Y Substitution - Missense 3:47002387-47002387 + TCGA-AP-A051-01 COSM1045370 c.456G>T p.M152I Substitution - Missense 3:46995508-46995508 + TCGA-CZ-5458-01 COSM480128 c.702C>G p.A234A Substitution - coding silent 3:46995834-46995834 + ESCC_136 COSM5643055 c.1003_1004insC p.L337fs*27 Insertion - Frameshift 3:46996439-46996440 + 61 COSM5736588 c.1058G>A p.R353Q Substitution - Missense 3:46996494-46996494 + TCGA-EE-A2MP-06 COSM3594616 c.1174C>T p.P392S Substitution - Missense 3:46996768-46996768 + TCGA-AP-A0LE-01 COSM1045416 c.7541G>A p.G2514D Substitution - Missense 3:47007849-47007849 + TCGA-F5-6814-01 COSM3427657 c.4165C>T p.P1389S Substitution - Missense 3:47000264-47000264 + TCGA-G3-A7M9-01 COSM4922608 c.3296A>G p.E1099G Substitution - Missense 3:46998791-46998791 + TCGA-BQ-5890-01 COSM3993105 c.690G>T p.L230L Substitution - coding silent 3:46991453-46991453 + TCGA-CD-A4MI-01 COSM4117944 c.478C>T p.P160S Substitution - Missense 3:46995530-46995530 + HCC90 COSM1617668 c.3059A>T p.D1020V Substitution - Missense 3:47002065-47002065 + 587332 COSM1216732 c.2105G>A p.G702D Substitution - Missense 3:46996005-46996005 + TCGA-EB-A5UN-06 COSM3594638 c.4205T>C p.I1402T Substitution - Missense 3:47004269-47004269 + LP6005334-DNA_D03 COSM5953141 c.1176C>T p.P392P Substitution - coding silent 3:46996770-46996770 + 587238 COSM1216718 c.6596C>T p.A2199V Substitution - Missense 3:47005524-47005524 + T155 COSM1177394 c.3306C>T p.F1102F Substitution - coding silent 3:47002394-47002394 + T3090 COSM4705677 c.8182G>A p.A2728T Substitution - Missense 3:47009237-47009237 + TCGA-B5-A1MY-01 COSM1045403 c.3421C>T p.R1141W Substitution - Missense 3:47002509-47002509 + PD24216a COSM5777915 c.574G>A p.D192N Substitution - Missense 3:46991236-46991236 + TCGA-EI-6512-01 COSM296927 c.4389G>A p.A1463A Substitution - coding silent 3:47004554-47004554 + TCGA-BR-6452-01 COSM4117950 c.937C>T p.P313S Substitution - Missense 3:46996373-46996373 + Pat_06_A COSM5864617 c.2437-1G>A p.? Unknown 3:47001000-47001000 + 8031133 COSM3392429 c.6262C>T p.R2088W Substitution - Missense 3:47004558-47004558 + HCT8 COSM4634996 c.631G>A p.A211T Substitution - Missense 3:46991293-46991293 + 587278 COSM1216729 c.3407G>A p.R1136H Substitution - Missense 3:47002495-47002495 + TCGA-D1-A103-01 COSM1045365 c.347C>T p.A116V Substitution - Missense 3:46989162-46989162 + TCGA-BP-4158-01 COSM3365197 c.7995C>A p.A2665A Substitution - coding silent 3:47008636-47008636 + TCGA-FS-A1ZZ-06 COSM3594645 c.7479G>A p.K2493K Substitution - coding silent 3:47007669-47007669 + CHC892T COSM4961419 c.1922G>A p.G641E Substitution - Missense 3:46995737-46995737 + T3454 COSM4705658 c.2055C>T p.G685G Substitution - coding silent 3:46998867-46998867 + CSCC-1-T COSM4556224 c.6832G>T p.E2278* Substitution - Nonsense 3:47005976-47005976 + CHC1629T COSM4791741 c.4211C>A p.P1404H Substitution - Missense 3:47004275-47004275 + TCGA-BR-7851-01 COSM4117962 c.4797C>A p.A1599A Substitution - coding silent 3:47001934-47001934 + SC_9024 COSM3068526 c.1644C>T p.G548G Substitution - coding silent 3:46995379-46995379 + LUAD-5V8LT COSM402305 c.4136C>A p.T1379N Substitution - Missense 3:47000235-47000235 + LS411 COSM1045374 c.720C>T p.C240C Substitution - coding silent 3:46995937-46995937 + PCSI_0073_Pa_P COSM216643 c.5960C>T p.A1987V Substitution - Missense 3:47004155-47004155 + CLL113 COSM1291719 c.5965C>G p.Q1989E Substitution - Missense 3:47008397-47008397 + TCGA-26-6173-01 COSM3408700 c.2019C>T p.V673V Substitution - coding silent 3:46998831-46998831 + CSCC-27-T COSM4569782 c.2025T>C p.S675S Substitution - coding silent 3:46995840-46995840 + HCC020T COSM5809120 c.5267A>T p.Q1756L Substitution - Missense 3:47002486-47002486 + CADO-ES1 COSM3068718 c.4671C>T p.H1557H Substitution - coding silent 3:47005301-47005301 + 587278 COSM1216728 c.5276G>A p.R1759H Substitution - Missense 3:47002495-47002495 + TCGA-EK-A2PL-01 COSM4838299 c.3109G>T p.V1037L Substitution - Missense 3:46998217-46998217 + ESCC_BICR_060T COSM5435091 c.3996C>T p.R1332R Substitution - coding silent 3:47003960-47003960 + 19 COSM5746115 c.796G>A p.A266T Substitution - Missense 3:46991559-46991559 + 8067541 COSM4387815 c.3595A>C p.T1199P Substitution - Missense 3:47002961-47002961 + TCGA-GF-A6C9-06 COSM4902785 c.4719C>T p.L1573L Substitution - coding silent 3:47001763-47001763 + 61 COSM4426787 c.3464C>T p.A1155V Substitution - Missense 3:47002676-47002676 + HCC90T COSM1617667 c.4928A>T p.D1643V Substitution - Missense 3:47002065-47002065 + 2492721 COSM5720012 c.3936C>T p.S1312S Substitution - coding silent 3:47000035-47000035 + pfg222T COSM4754394 c.1669C>T p.H557Y Substitution - Missense 3:46995404-46995404 + PCSI_0002_Pa_X COSM4964686 c.2147G>T p.S716I Substitution - Missense 3:46996047-46996047 + SC_9076 COSM5559078 c.5635C>T p.L1879F Substitution - Missense 3:47007694-47007694 + TCGA-BR-4362-01 COSM273665 c.167C>T p.P56L Substitution - Missense 3:46988868-46988868 + TCGA-A8-A08F-01 COSM446603 c.2228-4G>C p.? Unknown 3:47000192-47000192 + LC_S12 COSM1186261 c.4351T>C p.S1451P Substitution - Missense 3:47004516-47004516 + sysucc-1370T COSM5471742 c.1113+9C>A p.? Unknown 3:46992564-46992564 + 1517_PT COSM5756286 c.1791C>T p.A597A Substitution - coding silent 3:46998216-46998216 + T19 COSM5344487 c.3448C>T p.P1150S Substitution - Missense 3:47002660-47002660 + BRC11 COSM5025940 c.1338C>G p.I446M Substitution - Missense 3:46995073-46995073 + sysucc-1370T COSM5471743 c.6597G>A p.A2199A Substitution - coding silent 3:47005525-47005525 + TCGA-A6-6780-01 COSM480131 c.5132G>A p.R1711H Substitution - Missense 3:47002269-47002269 + TCGA-A8-A08F-01 COSM446602 c.4093G>C p.V1365L Substitution - Missense 3:47000192-47000192 + HCT116 COSM4632339 c.8103C>T p.H2701H Substitution - coding silent 3:47009064-47009064 + PCSI_0227_Pa_P_526 COSM4962320 c.6691G>A p.G2231S Substitution - Missense 3:47005619-47005619 + RH18C COSM4985064 c.872G>A p.G291D Substitution - Missense 3:46991635-46991635 + PT48 COSM5931345 c.141-7C>T p.? Unknown 3:46988835-46988835 + HCC99 COSM3660581 c.3547C>T p.L1183L Substitution - coding silent 3:47002759-47002759 + 587284 COSM1216734 c.8146G>A p.A2716T Substitution - Missense 3:47009107-47009107 + TCGA-EE-A29M-06 COSM3594614 c.632G>A p.G211E Substitution - Missense 3:46995764-46995764 + TCGA-DZ-6133-01 COSM3993106 c.7816G>A p.A2606T Substitution - Missense 3:47008379-47008379 + sysucc-311T COSM5465897 c.5427C>T p.Y1809Y Substitution - coding silent 3:47007312-47007312 + TCGA-B5-A11S-01 COSM1045409 c.4645C>T p.R1549C Substitution - Missense 3:47005275-47005275 + 587278 COSM1216730 c.7358C>T p.P2453L Substitution - Missense 3:47007548-47007548 + TARGET-20-PARJCR-09A-02D COSM5487640 c.7067C>T p.A2356V Substitution - Missense 3:47006382-47006382 + CSCC-27-T COSM4518738 c.7826_7827CC>TT p.S2609F Substitution - Missense 3:47008389-47008390 + T166 COSM307712 c.2955G>C p.Q985H Substitution - Missense 3:47001961-47001961 + PTC-7C COSM4158076 c.4185C>G p.P1395P Substitution - coding silent 3:47004249-47004249 + C80 COSM3068612 c.3217T>G p.Y1073D Substitution - Missense 3:46998561-46998561 + TCGA-AZ-4615-01 COSM3760131 c.3126G>A p.V1042V Substitution - coding silent 3:47002132-47002132 + TCGA-D1-A16X-01 COSM1045383 c.3148C>T p.R1050W Substitution - Missense 3:46998492-46998492 + SS6003137 COSM3414441 c.4761C>T p.A1587A Substitution - coding silent 3:47005558-47005558 + 1_PRE-TREATMENT COSM1719619 c.5953C>T p.R1985C Substitution - Missense 3:47004148-47004148 + TCGA-FW-A5DX-01 COSM3594640 c.4302G>A p.E1434E Substitution - coding silent 3:47004366-47004366 + TCGA-22-4591-01 COSM730724 c.6047A>G p.Q2016R Substitution - Missense 3:47004242-47004242 + PT35 COSM5911951 c.5060C>T p.S1687F Substitution - Missense 3:47002197-47002197 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.437043 3p21.31 614169

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A - Frameshift p.H423Lfs*49 c.1268delA 3 47036015 ESCA A G Missense p.Q1208R c.3623A>G 3 47040884 CLL A G Missense p.Q2016R c.6047A>G 3 47045732 LUSC A G Missense p.T1454A c.4360A>G 3 47042545 THCA A G Missense p.T925A c.2773A>G 3 47038872 UCEC A G Synonymous p.A558A c.1674A>G 3 47036899 PRAD C A Missense p.L1144M c.3430C>A 3 47040494 CLL C A Missense p.P2250H c.6749C>A 3 47047285 BRCA C A Missense p.P2593H c.7778C>A 3 47049831 STAD C A Synonymous p.A2665A c.7995C>A 3 47050126 RCCC C A Synonymous p.I858I c.2574C>A 3 47038461 PRAD C A Synonymous p.I979I c.2937C>A 3 47039163 OV C A Synonymous p.V2636V c.7908C>A 3 47050039 MM CC TT Missense p.P2209F c.6625_6626delinsTT 3 47047043 CM C G Missense p.I2578M c.7734C>G 3 47049787 HNSC C G Missense p.I446M c.1338C>G 3 47036563 BRCA C G Missense p.P913R c.2738C>G 3 47038837 OV C G Missense p.Q2612E c.7834C>G 3 47049887 CLL C G Nonsense p.S2519* c.7556C>G 3 47049354 HNSC C G Synonymous p.A673A c.2019C>G 3 47037324 RCCC C T Missense p.A1987V c.5960C>T 3 47045645 PAAD C T Missense p.A211V c.632C>T 3 47032784 HC C T Missense p.A617V c.1850C>T 3 47037075 LUSC C T Missense p.A648V c.1943C>T 3 47037248 STAD C T Missense p.A648V c.1943C>T 3 47037248 UCEC C T Missense p.H410Y c.1228C>T 3 47035975 BRCA C T Missense p.H684Y c.2050C>T 3 47037440 CM C T Missense p.L1250F c.3748C>T 3 47041164 CM C T Missense p.L202F c.604C>T 3 47032756 LUAD C T Missense p.P1382S c.4144C>T 3 47041733 UCEC C T Missense p.P1434L c.4301C>T 3 47041890 CM C T Missense p.P1512L c.4535C>T 3 47042819 CM C T Missense p.P2044L c.6131C>T 3 47045816 CM C T Missense p.P2223S c.6667C>T 3 47047085 CM C T Missense p.P56L c.167C>T 3 47030358 CM C T Missense p.P56L c.167C>T 3 47030358 COREAD C T Missense p.P831S c.2491C>T 3 47038258 CM C T Missense p.P936L c.2807C>T 3 47038906 NB C T Missense p.R1290W c.3868C>T 3 47041457 GBM C T Missense p.R1290W c.3868C>T 3 47041457 LGG C T Missense p.R1764W c.5290C>T 3 47043999 UCEC C T Missense p.R1826C c.5476C>T 3 47044463 LUAD C T Missense p.R2172C c.6514C>T 3 47046765 UCEC C T Missense p.R2622C c.7864C>T 3 47049917 STAD C T Missense p.S1306F c.3917C>T 3 47041506 CM C T Missense p.S757F c.2270C>T 3 47037879 CM C T Missense p.S798F c.2393C>T 3 47038002 CM C T Missense p.T1454M c.4361C>T 3 47042546 UCEC C T Missense p.T1879I c.5636C>T 3 47044715 CM C T Missense p.T2563I c.7688C>T 3 47049645 CM C T Nonsense p.Q2016* c.6046C>T 3 47045731 CM C T Nonsense p.Q2047* c.6139C>T 3 47045824 BRCA C T Synonymous p.A1517A c.4551C>T 3 47042835 CM C T Synonymous p.A310A c.930C>T 3 47033334 CM C T Synonymous p.F1725F c.5175C>T 3 47043884 CM C T Synonymous p.F1766F c.5298C>T 3 47044007 CM C T Synonymous p.F180F c.540C>T 3 47031067 CM C T Synonymous p.L2591L c.7771C>T 3 47049824 MB C T Synonymous p.L43L c.127C>T 3 47030234 CM C T Synonymous p.L935L c.2805C>T 3 47038904 CM C T Synonymous p.S770S c.2310C>T 3 47037919 HNSC C T Synonymous p.V1112V c.3336C>T 3 47040321 GBM CTTCT - Frameshift p.L1277Gfs*45 c.3829_3833delCTTCT 3 47041418 BRCA GAA - InFrameDeletion p.K1059delK c.3175_3177delAAG 3 47040005 UCEC G A IntronicSNV . c.51+3268G>A 3 47024670 PIA G A Missense p.A2680T c.8038G>A 3 47050489 OV G A Missense p.D1994N c.5980G>A 3 47045665 BRCA G A Missense p.E1900K c.5698G>A 3 47044777 LUAD G A Missense p.E354K c.1060G>A 3 47033992 HNSC G A Missense p.G1142S c.3424G>A 3 47040488 ALL G A Missense p.G1514E c.4541G>A 3 47042825 ESCA G A Missense p.G2514D c.7541G>A 3 47049339 UCEC G A Missense p.G650E c.1949G>A 3 47037254 CM G A Missense p.R1711H c.5132G>A 3 47043759 RCCC G A Missense p.R1755H c.5264G>A 3 47043973 LUSC G A Missense p.R1826H c.5477G>A 3 47044464 HNSC G A Missense p.R538H c.1613G>A 3 47036838 STAD G A Missense p.S2557N c.7670G>A 3 47049627 STAD G A Missense p.V2702M c.8104G>A 3 47050555 HNSC G A Synonymous p.A2086A c.6258G>A 3 47046044 STAD G A Synonymous p.A2681A c.8043G>A 3 47050494 STAD G A Synonymous p.G2149G c.6447G>A 3 47046698 CM G A Synonymous p.L2607L c.7821G>A 3 47049874 HNSC G A Synonymous p.L27L c.81G>A 3 47030188 CM G A Synonymous p.L813L c.2439G>A 3 47038048 RCCC G A Synonymous p.R2522R c.7566G>A 3 47049364 CM G A Synonymous p.V1884V c.5652G>A 3 47044731 BLCA G C Missense p.E96Q c.286G>C 3 47030591 HNSC G C Missense p.G355A c.1064G>C 3 47033996 BRCA G C Missense p.S1495T c.4484G>C 3 47042669 STAD G C Missense p.V1365L c.4093G>C 3 47041682 BRCA G T Missense p.A1760S c.5278G>T 3 47043987 LUAD G T Missense p.D358Y c.1072G>T 3 47034004 CM G T Missense p.G1366V c.4097G>T 3 47041686 GBM G T Missense p.V987F c.2959G>T 3 47039557 BRCA G T Synonymous p.L118L c.354G>T 3 47030752 LUSC TA CC Missense p.Y2078P c.6232_6233delinsCC 3 47046018 OV T A Missense p.I1048K c.3143T>A 3 47039977 COREAD T A Missense p.V2314E c.6941T>A 3 47047676 UCEC T C Missense p.I724T c.2171T>C 3 47037780 BRCA T C Missense p.L20P c.59T>C 3 47030166 THCA T G Missense p.F30V c.88T>G 3 47030195 COREAD