Mutation - TCGA Type Chromosome Start Position End Position Strand Variant Classification Variant Type Reference Allele Tumor_seq Allele 1 Tumor_seq Allele 2 Tumor Sample Barcode Matched Norm Sample Barcode Genome Change cDNA Change Codon Change Protein Change BLCA 6 17616823 17616823 + Silent SNP G G T TCGA-E7-A6MD-01A-41D-A34U-08 TCGA-E7-A6MD-10B-01D-A34X-08 g.chr6:17616823G>T c.4278C>A c.(4276-4278)gcC>gcA p.A1426A BLCA 6 17616866 17616866 + Missense_Mutation SNP G G A TCGA-KQ-A41P-01A-12D-A339-08 TCGA-KQ-A41P-10F-01D-A339-08 g.chr6:17616866G>A c.4235C>T c.(4234-4236)tCa>tTa p.S1412L BLCA 6 17626341 17626341 + Missense_Mutation SNP G G A TCGA-DK-A3X1-01A-12D-A22Z-08 TCGA-DK-A3X1-10A-01D-A22Z-08 g.chr6:17626341G>A c.3599C>T c.(3598-3600)tCa>tTa p.S1200L BLCA 6 17628990 17628990 + Missense_Mutation SNP G G A TCGA-DK-A6B6-01A-11D-A30E-08 TCGA-DK-A6B6-10A-01D-A30H-08 g.chr6:17628990G>A c.3440C>T c.(3439-3441)tCa>tTa p.S1147L BLCA 6 17629115 17629115 + Missense_Mutation SNP C C A TCGA-DK-A6AW-01A-11D-A30E-08 TCGA-DK-A6AW-10A-01D-A30H-08 g.chr6:17629115C>A c.3315G>T c.(3313-3315)gaG>gaT p.E1105D BLCA 6 17629227 17629227 + Missense_Mutation SNP G G A TCGA-K4-A54R-01A-11D-A26M-08 TCGA-K4-A54R-10A-01D-A26K-08 g.chr6:17629227G>A c.3203C>T c.(3202-3204)tCa>tTa p.S1068L BLCA 6 17629422 17629422 + Missense_Mutation SNP G G T TCGA-XF-A9SP-01A-11D-A391-08 TCGA-XF-A9SP-10A-01D-A394-08 g.chr6:17629422G>T c.3008C>A c.(3007-3009)tCt>tAt p.S1003Y BLCA 6 17633031 17633031 + Silent SNP G G A TCGA-GU-A763-01A-11D-A32B-08 TCGA-GU-A763-10A-01D-A329-08 g.chr6:17633031G>A c.2509C>T c.(2509-2511)Ctg>Ttg p.L837L BLCA 6 17637526 17637526 + Silent SNP A A C TCGA-XF-A9SJ-01A-11D-A391-08 TCGA-XF-A9SJ-10A-01D-A394-08 g.chr6:17637526A>C c.2322T>G c.(2320-2322)tcT>tcG p.S774S BLCA 6 17649526 17649526 + Missense_Mutation SNP C C A TCGA-UY-A78M-01A-21D-A34U-08 TCGA-UY-A78M-10A-01D-A34X-08 g.chr6:17649526C>A c.1401G>T c.(1399-1401)atG>atT p.M467I BLCA 6 17669713 17669713 + Nonsense_Mutation SNP G G T TCGA-CF-A1HR-01A-11D-A13W-08 TCGA-CF-A1HR-10A-01D-A13W-08 g.chr6:17669713G>T c.917C>A c.(916-918)tCa>tAa p.S306* BLCA 6 17675190 17675190 + Silent SNP G G A TCGA-GC-A3WC-01A-31D-A22Z-08 TCGA-GC-A3WC-10A-01D-A22Z-08 g.chr6:17675190G>A c.798C>T c.(796-798)taC>taT p.Y266Y BLCA 6 17675473 17675473 + Missense_Mutation SNP C C T TCGA-YF-AA3L-01A-11D-A38G-08 TCGA-YF-AA3L-10A-01D-A38J-08 g.chr6:17675473C>T c.710G>A c.(709-711)gGa>gAa p.G237E BLCA 6 17675597 17675597 + Missense_Mutation SNP T T C TCGA-BL-A0C8-01A-11D-A10S-08 TCGA-BL-A0C8-10A-01D-A10S-08 g.chr6:17675597T>C c.586A>G c.(586-588)Ata>Gta p.I196V BLCA 6 17675821 17675821 + Missense_Mutation SNP G G C TCGA-G2-AA3B-01A-11D-A391-08 TCGA-G2-AA3B-10A-01D-A394-08 g.chr6:17675821G>C c.515C>G c.(514-516)tCt>tGt p.S172C BLCA 6 17675981 17675981 + Missense_Mutation SNP C C T TCGA-DK-A2I4-01A-11D-A21A-08 TCGA-DK-A2I4-10A-01D-A21A-08 g.chr6:17675981C>T c.355G>A c.(355-357)Gct>Act p.A119T BLCA 6 17688732 17688732 + Missense_Mutation SNP G G A TCGA-HQ-A5NE-01A-12D-A289-08 TCGA-HQ-A5NE-10A-01D-A289-08 g.chr6:17688732G>A c.229C>T c.(229-231)Cgc>Tgc p.R77C BRCA 6 17616916 17616916 + Missense_Mutation SNP G G C TCGA-D8-A27G-01A-11D-A16D-09 TCGA-D8-A27G-10A-01D-A16D-09 g.chr6:17616916G>C c.4185C>G c.(4183-4185)ttC>ttG p.F1395L BRCA 6 17629106 17629106 + Silent SNP T T C TCGA-AO-A0JD-01A-11W-A071-09 TCGA-AO-A0JD-10A-01W-A071-09 g.chr6:17629106T>C c.3324A>G c.(3322-3324)caA>caG p.Q1108Q BRCA 6 17629273 17629273 + Missense_Mutation SNP T T A TCGA-AN-A0G0-01A-11W-A050-09 TCGA-AN-A0G0-10A-01W-A055-09 g.chr6:17629273T>A c.3157A>T c.(3157-3159)Ata>Tta p.I1053L BRCA 6 17637546 17637546 + Missense_Mutation SNP C C G TCGA-BH-A0DZ-01A-11W-A019-09 TCGA-BH-A0DZ-10A-01W-A021-09 g.chr6:17637546C>G c.2302G>C c.(2302-2304)Gag>Cag p.E768Q BRCA 6 17637557 17637557 + Missense_Mutation SNP G G A TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr6:17637557G>A c.2291C>T c.(2290-2292)tCg>tTg p.S764L BRCA 6 17637763 17637763 + Silent SNP A A T TCGA-AC-A2BM-01A-11D-A21Q-09 TCGA-AC-A2BM-11A-13D-A21Q-09 g.chr6:17637763A>T c.2085T>A c.(2083-2085)acT>acA p.T695T BRCA 6 17637836 17637836 + Missense_Mutation SNP T T A TCGA-C8-A12P-01A-11D-A10Y-09 TCGA-C8-A12P-10A-01D-A110-09 g.chr6:17637836T>A c.2012A>T c.(2011-2013)aAc>aTc p.N671I BRCA 6 17669532 17669532 + Missense_Mutation SNP G G C TCGA-BH-A0BF-01A-21D-A12Q-09 TCGA-BH-A0BF-11A-31D-A12Q-09 g.chr6:17669532G>C c.1006C>G c.(1006-1008)Ctg>Gtg p.L336V BRCA 6 17675248 17675248 + Missense_Mutation SNP G G A TCGA-AO-A03M-01B-11D-A10M-09 TCGA-AO-A03M-10A-01D-A10M-09 g.chr6:17675248G>A c.740C>T c.(739-741)tCa>tTa p.S247L BRCA 6 17675939 17675939 + Missense_Mutation SNP G G A TCGA-AO-A12E-01A-11D-A10M-09 TCGA-AO-A12E-10A-01D-A10M-09 g.chr6:17675939G>A c.397C>T c.(397-399)Cgg>Tgg p.R133W BRCA 6 17688750 17688750 + Missense_Mutation SNP C C T TCGA-A2-A0YG-01A-21D-A10G-09 TCGA-A2-A0YG-10A-01D-A10G-09 g.chr6:17688750C>T c.211G>A c.(211-213)Gac>Aac p.D71N CESC 6 17626044 17626044 + Missense_Mutation SNP G G C TCGA-LP-A5U2-01A-11D-A28B-09 TCGA-LP-A5U2-10A-01D-A28E-09 g.chr6:17626044G>C c.3896C>G c.(3895-3897)tCt>tGt p.S1299C CESC 6 17632951 17632951 + Missense_Mutation SNP C C A TCGA-MY-A5BD-01A-11D-A26G-09 TCGA-MY-A5BD-10A-01D-A26G-09 g.chr6:17632951C>A c.2589G>T c.(2587-2589)caG>caT p.Q863H CESC 6 17665574 17665574 + Missense_Mutation SNP T T C TCGA-EA-A3HU-01A-11D-A20U-09 TCGA-EA-A3HU-10B-01D-A20U-09 g.chr6:17665574T>C c.1111A>G c.(1111-1113)Aag>Gag p.K371E CESC 6 17669684 17669684 + Missense_Mutation SNP C C G TCGA-JW-A5VL-01A-11D-A28B-09 TCGA-JW-A5VL-10A-01D-A28E-09 g.chr6:17669684C>G c.946G>C c.(946-948)Gag>Cag p.E316Q COAD 6 17616803 17616803 + Missense_Mutation SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr6:17616803G>A c.4298C>T c.(4297-4299)tCg>tTg p.S1433L COAD 6 17624928 17624928 + Silent SNP A A C TCGA-CK-6746-01A-11D-1835-10 TCGA-CK-6746-10A-01D-1835-10 g.chr6:17624928A>C c.4038T>G c.(4036-4038)tcT>tcG p.S1346S COAD 6 17629253 17629253 + Silent SNP T T G TCGA-AD-6964-01A-11D-1924-10 TCGA-AD-6964-10A-01D-1924-10 g.chr6:17629253T>G c.3177A>C c.(3175-3177)tcA>tcC p.S1059S COAD 6 17629371 17629371 + Missense_Mutation SNP G G T TCGA-AA-3821-01A-01W-0995-10 TCGA-AA-3821-10A-01W-0995-10 g.chr6:17629371G>T c.3059C>A c.(3058-3060)gCa>gAa p.A1020E COAD 6 17637424 17637424 + Silent SNP T T C TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr6:17637424T>C c.2424A>G c.(2422-2424)gcA>gcG p.A808A COAD 6 17637424 17637424 + Silent SNP T T C TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chr6:17637424T>C c.2424A>G c.(2422-2424)gcA>gcG p.A808A COAD 6 17637424 17637424 + Silent SNP T T C TCGA-AZ-6599-01A-11D-1771-10 TCGA-AZ-6599-11A-01D-1771-10 g.chr6:17637424T>C c.2424A>G c.(2422-2424)gcA>gcG p.A808A COAD 6 17637424 17637424 + Silent SNP T T C TCGA-G4-6310-01A-11D-1719-10 TCGA-G4-6310-10A-01D-1720-10 g.chr6:17637424T>C c.2424A>G c.(2422-2424)gcA>gcG p.A808A COAD 6 17637426 17637426 + Missense_Mutation SNP C C T TCGA-DM-A1DB-01A-11D-A152-10 TCGA-DM-A1DB-10A-01D-A152-10 g.chr6:17637426C>T c.2422G>A c.(2422-2424)Gca>Aca p.A808T COAD 6 17637604 17637604 + Silent SNP C C T TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr6:17637604C>T c.2244G>A c.(2242-2244)ccG>ccA p.P748P COAD 6 17637765 17637765 + Missense_Mutation SNP T T C TCGA-A6-6648-01A-11D-1771-10 TCGA-A6-6648-10A-01D-1771-10 g.chr6:17637765T>C c.2083A>G c.(2083-2085)Act>Gct p.T695A COAD 6 17637996 17637996 + Missense_Mutation SNP C C T TCGA-G4-6586-01A-11D-1771-10 TCGA-G4-6586-10A-01D-1771-10 g.chr6:17637996C>T c.1852G>A c.(1852-1854)Gca>Aca p.A618T COAD 6 17669527 17669527 + Missense_Mutation SNP A A T TCGA-AA-3966-01A-01W-1073-09 TCGA-AA-3966-10A-01W-1073-09 g.chr6:17669527A>T c.1011T>A c.(1009-1011)aaT>aaA p.N337K COAD 6 17669558 17669558 + Missense_Mutation SNP C C A TCGA-AA-3555-01A-01W-0831-10 TCGA-AA-3555-10A-01W-0831-10 g.chr6:17669558C>A c.980G>T c.(979-981)aGa>aTa p.R327I COAD 6 17675207 17675207 + Missense_Mutation SNP G G T TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chr6:17675207G>T c.781C>A c.(781-783)Cct>Act p.P261T COAD 6 17675210 17675210 + Frame_Shift_Del DEL A A - TCGA-AD-5900-01A-11D-1650-10 TCGA-AD-5900-10A-01D-1650-10 g.chr6:17675210delA c.778delT c.(778-780)tatfs p.Y260fs COAD 6 17675498 17675499 + Frame_Shift_Ins INS - - T TCGA-D5-6930-01A-11D-1924-10 TCGA-D5-6930-10A-01D-1924-10 g.chr6:17675498_17675499insT c.684_685insA c.(682-687)aaaccafs p.P229fs COAD 6 17706514 17706514 + Silent SNP C C T TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr6:17706514C>T c.105G>A c.(103-105)caG>caA p.Q35Q COADREAD 6 17616803 17616803 + Missense_Mutation SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr6:17616803G>A c.4298C>T c.(4297-4299)tCg>tTg p.S1433L COADREAD 6 17624928 17624928 + Silent SNP A A C TCGA-CK-6746-01A-11D-1835-10 TCGA-CK-6746-10A-01D-1835-10 g.chr6:17624928A>C c.4038T>G c.(4036-4038)tcT>tcG p.S1346S COADREAD 6 17629253 17629253 + Silent SNP T T G TCGA-AD-6964-01A-11D-1924-10 TCGA-AD-6964-10A-01D-1924-10 g.chr6:17629253T>G c.3177A>C c.(3175-3177)tcA>tcC p.S1059S COADREAD 6 17629371 17629371 + Missense_Mutation SNP G G T TCGA-AA-3821-01A-01W-0995-10 TCGA-AA-3821-10A-01W-0995-10 g.chr6:17629371G>T c.3059C>A c.(3058-3060)gCa>gAa p.A1020E COADREAD 6 17637424 17637424 + Silent SNP T T C TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr6:17637424T>C c.2424A>G c.(2422-2424)gcA>gcG p.A808A COADREAD 6 17637424 17637424 + Silent SNP T T C TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chr6:17637424T>C c.2424A>G c.(2422-2424)gcA>gcG p.A808A COADREAD 6 17637424 17637424 + Silent SNP T T C TCGA-AZ-6599-01A-11D-1771-10 TCGA-AZ-6599-11A-01D-1771-10 g.chr6:17637424T>C c.2424A>G c.(2422-2424)gcA>gcG p.A808A COADREAD 6 17637424 17637424 + Silent SNP T T C TCGA-G4-6310-01A-11D-1719-10 TCGA-G4-6310-10A-01D-1720-10 g.chr6:17637424T>C c.2424A>G c.(2422-2424)gcA>gcG p.A808A COADREAD 6 17637426 17637426 + Missense_Mutation SNP C C T TCGA-DM-A1DB-01A-11D-A152-10 TCGA-DM-A1DB-10A-01D-A152-10 g.chr6:17637426C>T c.2422G>A c.(2422-2424)Gca>Aca p.A808T COADREAD 6 17637604 17637604 + Silent SNP C C T TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr6:17637604C>T c.2244G>A c.(2242-2244)ccG>ccA p.P748P COADREAD 6 17637604 17637604 + Silent SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr6:17637604C>T c.2244G>A c.(2242-2244)ccG>ccA p.P748P COADREAD 6 17637765 17637765 + Missense_Mutation SNP T T C TCGA-A6-6648-01A-11D-1771-10 TCGA-A6-6648-10A-01D-1771-10 g.chr6:17637765T>C c.2083A>G c.(2083-2085)Act>Gct p.T695A COADREAD 6 17637996 17637996 + Missense_Mutation SNP C C T TCGA-G4-6586-01A-11D-1771-10 TCGA-G4-6586-10A-01D-1771-10 g.chr6:17637996C>T c.1852G>A c.(1852-1854)Gca>Aca p.A618T COADREAD 6 17669527 17669527 + Missense_Mutation SNP A A T TCGA-AA-3966-01A-01W-1073-09 TCGA-AA-3966-10A-01W-1073-09 g.chr6:17669527A>T c.1011T>A c.(1009-1011)aaT>aaA p.N337K COADREAD 6 17669558 17669558 + Missense_Mutation SNP C C A TCGA-AA-3555-01A-01W-0831-10 TCGA-AA-3555-10A-01W-0831-10 g.chr6:17669558C>A c.980G>T c.(979-981)aGa>aTa p.R327I COADREAD 6 17675207 17675207 + Missense_Mutation SNP G G T TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chr6:17675207G>T c.781C>A c.(781-783)Cct>Act p.P261T COADREAD 6 17675210 17675210 + Frame_Shift_Del DEL A A - TCGA-AD-5900-01A-11D-1650-10 TCGA-AD-5900-10A-01D-1650-10 g.chr6:17675210delA c.778delT c.(778-780)tatfs p.Y260fs COADREAD 6 17675498 17675499 + Frame_Shift_Ins INS - - T TCGA-D5-6930-01A-11D-1924-10 TCGA-D5-6930-10A-01D-1924-10 g.chr6:17675498_17675499insT c.684_685insA c.(682-687)aaaccafs p.P229fs COADREAD 6 17706514 17706514 + Silent SNP C C T TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr6:17706514C>T c.105G>A c.(103-105)caG>caA p.Q35Q DLBC 6 17629629 17629629 + Missense_Mutation SNP A A C TCGA-GS-A9TT-01A-11D-A382-10 TCGA-GS-A9TT-10A-01D-A385-10 g.chr6:17629629A>C c.2801T>G c.(2800-2802)aTa>aGa p.I934R DLBC 6 17706506 17706506 + Splice_Site SNP A A T TCGA-FF-8046-01A-11D-2210-10 TCGA-FF-8046-10A-01D-2210-10 g.chr6:17706506A>T c.e1+1 ESCA 6 17626152 17626152 + Missense_Mutation SNP G G T TCGA-L5-A8NI-01A-11D-A37C-09 TCGA-L5-A8NI-11A-11D-A37F-09 g.chr6:17626152G>T c.3788C>A c.(3787-3789)aCa>aAa p.T1263K ESCA 6 17629214 17629214 + Missense_Mutation SNP T T G TCGA-L5-A8NT-01A-11D-A37C-09 TCGA-L5-A8NT-11A-11D-A37F-09 g.chr6:17629214T>G c.3216A>C c.(3214-3216)aaA>aaC p.K1072N ESCA 6 17629455 17629455 + Missense_Mutation SNP G G T TCGA-V5-AASW-01A-11D-A403-09 TCGA-V5-AASW-10A-01D-A403-09 g.chr6:17629455G>T c.2975C>A c.(2974-2976)cCa>cAa p.P992Q ESCA 6 17633076 17633076 + Splice_Site SNP C C A TCGA-JY-A93D-01A-11D-A387-09 TCGA-JY-A93D-10A-01D-A38A-09 g.chr6:17633076C>A c.e17-1 ESCA 6 17649509 17649509 + Missense_Mutation SNP G G A TCGA-L5-A43I-01A-11D-A247-09 TCGA-L5-A43I-11A-11D-A247-09 g.chr6:17649509G>A c.1418C>T c.(1417-1419)cCg>cTg p.P473L ESCA 6 17661926 17661926 + Silent SNP T T C TCGA-LN-A49X-01A-31D-A27G-09 TCGA-LN-A49X-10A-01D-A27G-09 g.chr6:17661926T>C c.1353A>G c.(1351-1353)cgA>cgG p.R451R ESCA 6 17675153 17675153 + Nonsense_Mutation SNP G G A TCGA-L5-A88V-01A-11D-A351-09 TCGA-L5-A88V-11A-11D-A351-09 g.chr6:17675153G>A c.835C>T c.(835-837)Cga>Tga p.R279* ESCA 6 17675873 17675873 + Missense_Mutation SNP C C T TCGA-L5-A8NJ-01A-11D-A36J-09 TCGA-L5-A8NJ-11A-11D-A36M-09 g.chr6:17675873C>T c.463G>A c.(463-465)Gca>Aca p.A155T ESCA 6 17706534 17706534 + Missense_Mutation SNP A A C TCGA-LN-A9FO-01A-11D-A387-09 TCGA-LN-A9FO-10A-01D-A38A-09 g.chr6:17706534A>C c.85T>G c.(85-87)Tac>Gac p.Y29D GBM 6 17616339 17616339 + Missense_Mutation SNP G G A TCGA-14-0817-01A-01W-0424-08 TCGA-14-0817-10A-01W-0424-08 g.chr6:17616339G>A c.4417C>T c.(4417-4419)Cgc>Tgc p.R1473C GBM 6 17629357 17629357 + Missense_Mutation SNP C C T TCGA-06-2564-01A-01D-1494-08 TCGA-06-2564-10A-01D-1494-08 g.chr6:17629357C>T c.3073G>A c.(3073-3075)Ggt>Agt p.G1025S GBMLGG 6 17616339 17616339 + Missense_Mutation SNP G G A TCGA-14-0817-01A-01W-0424-08 TCGA-14-0817-10A-01W-0424-08 g.chr6:17616339G>A c.4417C>T c.(4417-4419)Cgc>Tgc p.R1473C GBMLGG 6 17624875 17624875 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr6:17624875G>A c.4091C>T c.(4090-4092)aCa>aTa p.T1364I GBMLGG 6 17629357 17629357 + Missense_Mutation SNP C C T TCGA-06-2564-01A-01D-1494-08 TCGA-06-2564-10A-01D-1494-08 g.chr6:17629357C>T c.3073G>A c.(3073-3075)Ggt>Agt p.G1025S GBMLGG 6 17629558 17629558 + Missense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr6:17629558C>A c.2872G>T c.(2872-2874)Gat>Tat p.D958Y GBMLGG 6 17629745 17629745 + Silent SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr6:17629745C>T c.2685G>A c.(2683-2685)tcG>tcA p.S895S GBMLGG 6 17629745 17629745 + Silent SNP C C T TCGA-P5-A5EV-01A-11D-A27K-08 TCGA-P5-A5EV-10A-01D-A27N-08 g.chr6:17629745C>T c.2685G>A c.(2683-2685)tcG>tcA p.S895S GBMLGG 6 17675524 17675524 + Missense_Mutation SNP T T C TCGA-TM-A84I-01A-11D-A36O-08 TCGA-TM-A84I-10A-01D-A367-08 g.chr6:17675524T>C c.659A>G c.(658-660)cAg>cGg p.Q220R GBMLGG 6 17688630 17688630 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr6:17688630C>T c.331G>A c.(331-333)Gaa>Aaa p.E111K GBMLGG 6 17706523 17706523 + Silent SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr6:17706523C>T c.96G>A c.(94-96)ggG>ggA p.G32G HNSC 6 17616845 17616845 + Missense_Mutation SNP G G T TCGA-UF-A7JO-01A-11D-A34J-08 TCGA-UF-A7JO-10A-01D-A34M-08 g.chr6:17616845G>T c.4256C>A c.(4255-4257)gCa>gAa p.A1419E HNSC 6 17626393 17626393 + Nonsense_Mutation SNP G G A TCGA-TN-A7HL-01A-11D-A34J-08 TCGA-TN-A7HL-10A-01D-A34M-08 g.chr6:17626393G>A c.3547C>T c.(3547-3549)Caa>Taa p.Q1183* HNSC 6 17629211 17629211 + Silent SNP T T C TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr6:17629211T>C c.3219A>G c.(3217-3219)gaA>gaG p.E1073E HNSC 6 17629246 17629246 + Missense_Mutation SNP G G C TCGA-TN-A7HL-01A-11D-A34J-08 TCGA-TN-A7HL-10A-01D-A34M-08 g.chr6:17629246G>C c.3184C>G c.(3184-3186)Cct>Gct p.P1062A HNSC 6 17637953 17637953 + Missense_Mutation SNP G G C TCGA-CR-6484-01A-11D-1870-08 TCGA-CR-6484-10A-01D-1870-08 g.chr6:17637953G>C c.1895C>G c.(1894-1896)aCa>aGa p.T632R HNSC 6 17649453 17649453 + Missense_Mutation SNP G G A TCGA-CV-5439-01A-01D-1683-08 TCGA-CV-5439-11B-01D-1683-08 g.chr6:17649453G>A c.1474C>T c.(1474-1476)Cct>Tct p.P492S HNSC 6 17669742 17669742 + Silent SNP G G C TCGA-CV-6938-01A-11D-1912-08 TCGA-CV-6938-10A-01D-1912-08 g.chr6:17669742G>C c.888C>G c.(886-888)ctC>ctG p.L296L HNSC 6 17675207 17675207 + Missense_Mutation SNP G G A TCGA-D6-6516-01A-11D-1870-08 TCGA-D6-6516-10A-01D-1870-08 g.chr6:17675207G>A c.781C>T c.(781-783)Cct>Tct p.P261S HNSC 6 17688742 17688742 + Silent SNP G G A TCGA-UF-A71B-01A-12D-A34J-08 TCGA-UF-A71B-10B-01D-A34M-08 g.chr6:17688742G>A c.219C>T c.(217-219)agC>agT p.S73S KIPAN 6 17624932 17624932 + Missense_Mutation SNP G G A TCGA-BP-4161-01A-02D-1386-10 TCGA-BP-4161-11A-01D-1251-10 g.chr6:17624932G>A c.4034C>T c.(4033-4035)tCa>tTa p.S1345L KIPAN 6 17637570 17637570 + Silent SNP A A G TCGA-BP-4346-01A-01D-1366-10 TCGA-BP-4346-11A-01D-1366-10 g.chr6:17637570A>G c.2278T>C c.(2278-2280)Ttg>Ctg p.L760L KIPAN 6 17688708 17688708 + Missense_Mutation SNP G G A TCGA-EV-5903-01A-11D-1589-08 TCGA-EV-5903-10A-01D-1589-08 g.chr6:17688708G>A c.253C>T c.(253-255)Cat>Tat p.H85Y KIPAN 6 17706532 17706532 + Nonsense_Mutation SNP G G C TCGA-B4-5838-01A-11D-1669-08 TCGA-B4-5838-10A-01D-1669-08 g.chr6:17706532G>C c.87C>G c.(85-87)taC>taG p.Y29* KIRC 6 17624932 17624932 + Missense_Mutation SNP G G A TCGA-BP-4161-01A-02D-1386-10 TCGA-BP-4161-11A-01D-1251-10 g.chr6:17624932G>A c.4034C>T c.(4033-4035)tCa>tTa p.S1345L KIRC 6 17637570 17637570 + Silent SNP A A G TCGA-BP-4346-01A-01D-1366-10 TCGA-BP-4346-11A-01D-1366-10 g.chr6:17637570A>G c.2278T>C c.(2278-2280)Ttg>Ctg p.L760L KIRC 6 17706532 17706532 + Nonsense_Mutation SNP G G C TCGA-B4-5838-01A-11D-1669-08 TCGA-B4-5838-10A-01D-1669-08 g.chr6:17706532G>C c.87C>G c.(85-87)taC>taG p.Y29* KIRP 6 17688708 17688708 + Missense_Mutation SNP G G A TCGA-EV-5903-01A-11D-1589-08 TCGA-EV-5903-10A-01D-1589-08 g.chr6:17688708G>A c.253C>T c.(253-255)Cat>Tat p.H85Y LGG 6 17624875 17624875 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr6:17624875G>A c.4091C>T c.(4090-4092)aCa>aTa p.T1364I LGG 6 17629558 17629558 + Missense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr6:17629558C>A c.2872G>T c.(2872-2874)Gat>Tat p.D958Y LGG 6 17629745 17629745 + Silent SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr6:17629745C>T c.2685G>A c.(2683-2685)tcG>tcA p.S895S LGG 6 17629745 17629745 + Silent SNP C C T TCGA-P5-A5EV-01A-11D-A27K-08 TCGA-P5-A5EV-10A-01D-A27N-08 g.chr6:17629745C>T c.2685G>A c.(2683-2685)tcG>tcA p.S895S LGG 6 17675524 17675524 + Missense_Mutation SNP T T C TCGA-TM-A84I-01A-11D-A36O-08 TCGA-TM-A84I-10A-01D-A367-08 g.chr6:17675524T>C c.659A>G c.(658-660)cAg>cGg p.Q220R LGG 6 17688630 17688630 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr6:17688630C>T c.331G>A c.(331-333)Gaa>Aaa p.E111K LGG 6 17706523 17706523 + Silent SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr6:17706523C>T c.96G>A c.(94-96)ggG>ggA p.G32G LIHC 6 17616802 17616802 + Silent SNP C C A TCGA-DD-AACQ-01A-11D-A40R-10 TCGA-DD-AACQ-10A-01D-A40U-10 g.chr6:17616802C>A c.4299G>T c.(4297-4299)tcG>tcT p.S1433S LIHC 6 17628999 17628999 + Missense_Mutation SNP T T C TCGA-DD-AAVY-01A-11D-A40R-10 TCGA-DD-AAVY-10A-01D-A40U-10 g.chr6:17628999T>C c.3431A>G c.(3430-3432)gAg>gGg p.E1144G LIHC 6 17629463 17629463 + Silent SNP T T C TCGA-WQ-A9G7-01A-11D-A36X-10 TCGA-WQ-A9G7-10A-01D-A370-10 g.chr6:17629463T>C c.2967A>G c.(2965-2967)ttA>ttG p.L989L LIHC 6 17637675 17637675 + Missense_Mutation SNP T T C TCGA-FV-A4ZQ-01A-11D-A25V-10 TCGA-FV-A4ZQ-10A-01D-A25V-10 g.chr6:17637675T>C c.2173A>G c.(2173-2175)Act>Gct p.T725A LIHC 6 17640200 17640200 + Missense_Mutation SNP C C G TCGA-DD-A11C-01A-11D-A12Z-10 TCGA-DD-A11C-11A-11D-A12Z-10 g.chr6:17640200C>G c.1816G>C c.(1816-1818)Gga>Cga p.G606R LIHC 6 17665533 17665533 + Frame_Shift_Del DEL T T - TCGA-DD-A1EG-01A-11D-A20W-10 TCGA-DD-A1EG-10A-01D-A20W-10 g.chr6:17665533delT c.1152delA c.(1150-1152)aaafs p.K384fs LIHC 6 17675798 17675798 + Missense_Mutation SNP T T G TCGA-DD-AAE7-01A-11D-A40R-10 TCGA-DD-AAE7-10A-01D-A40U-10 g.chr6:17675798T>G c.538A>C c.(538-540)Aac>Cac p.N180H LIHC 6 17706588 17706588 + Missense_Mutation SNP C C A TCGA-CC-A7IH-01A-11D-A33K-10 TCGA-CC-A7IH-10A-01D-A33K-10 g.chr6:17706588C>A c.31G>T c.(31-33)Ggc>Tgc p.G11C LUAD 6 17624952 17624952 + Silent SNP G G A TCGA-49-4505-01A-01D-1931-08 TCGA-49-4505-11A-01D-1265-08 g.chr6:17624952G>A c.4014C>T c.(4012-4014)ccC>ccT p.P1338P LUAD 6 17626174 17626174 + Missense_Mutation SNP G G C TCGA-55-8208-01A-11D-2238-08 TCGA-55-8208-10A-01D-2238-08 g.chr6:17626174G>C c.3766C>G c.(3766-3768)Caa>Gaa p.Q1256E LUAD 6 17629177 17629177 + Missense_Mutation SNP C C A TCGA-62-A46V-01A-11D-A24D-08 TCGA-62-A46V-10A-01D-A24F-08 g.chr6:17629177C>A c.3253G>T c.(3253-3255)Ggc>Tgc p.G1085C LUAD 6 17629326 17629326 + Missense_Mutation SNP G G A TCGA-NJ-A4YQ-01A-11D-A25L-08 TCGA-NJ-A4YQ-10A-01D-A25L-08 g.chr6:17629326G>A c.3104C>T c.(3103-3105)cCt>cTt p.P1035L LUAD 6 17629516 17629516 + Missense_Mutation SNP C C A TCGA-55-8299-01A-11D-2284-08 TCGA-55-8299-10B-01D-2323-08 g.chr6:17629516C>A c.2914G>T c.(2914-2916)Gtt>Ttt p.V972F LUAD 6 17632972 17632972 + Missense_Mutation SNP G G C TCGA-64-1677-01A-01W-0928-08 TCGA-64-1677-10A-01W-0928-08 g.chr6:17632972G>C c.2568C>G c.(2566-2568)gaC>gaG p.D856E LUAD 6 17632986 17632986 + Missense_Mutation SNP C C T TCGA-55-8511-01A-11D-2393-08 TCGA-55-8511-10A-01D-2393-08 g.chr6:17632986C>T c.2554G>A c.(2554-2556)Gag>Aag p.E852K LUAD 6 17633037 17633037 + Missense_Mutation SNP C C G TCGA-78-7220-01A-11D-2036-08 TCGA-78-7220-10A-01D-2036-08 g.chr6:17633037C>G c.2503G>C c.(2503-2505)Gtc>Ctc p.V835L LUAD 6 17688669 17688669 + Missense_Mutation SNP C C T TCGA-78-7147-01A-11D-2036-08 TCGA-78-7147-10A-01D-2036-08 g.chr6:17688669C>T c.292G>A c.(292-294)Gat>Aat p.D98N LUAD 6 17688767 17688767 + Missense_Mutation SNP A A T TCGA-35-5375-01A-01D-1625-08 TCGA-35-5375-10A-01D-1625-08 g.chr6:17688767A>T c.194T>A c.(193-195)gTa>gAa p.V65E LUAD 6 17688816 17688816 + Missense_Mutation SNP T T C TCGA-38-4631-01A-01D-1753-08 TCGA-38-4631-11A-01D-1753-08 g.chr6:17688816T>C c.145A>G c.(145-147)Aat>Gat p.N49D LUSC 6 17626107 17626107 + Missense_Mutation SNP C C G TCGA-66-2773-01A-01D-1267-08 TCGA-66-2773-11A-01D-1267-08 g.chr6:17626107C>G c.3833G>C c.(3832-3834)gGa>gCa p.G1278A LUSC 6 17637456 17637456 + Nonsense_Mutation SNP C C A TCGA-46-3769-01A-01D-0983-08 TCGA-46-3769-10A-01D-0983-08 g.chr6:17637456C>A c.2392G>T c.(2392-2394)Gag>Tag p.E798* LUSC 6 17640218 17640218 + Missense_Mutation SNP C C A TCGA-60-2715-01A-01D-1522-08 TCGA-60-2715-11A-01D-1522-08 g.chr6:17640218C>A c.1798G>T c.(1798-1800)Gca>Tca p.A600S LUSC 6 17640222 17640222 + Missense_Mutation SNP T T G TCGA-60-2715-01A-01D-1522-08 TCGA-60-2715-11A-01D-1522-08 g.chr6:17640222T>G c.1794A>C c.(1792-1794)agA>agC p.R598S LUSC 6 17648069 17648069 + Missense_Mutation SNP G G T TCGA-66-2768-01A-01D-1522-08 TCGA-66-2768-11A-01D-1522-08 g.chr6:17648069G>T c.1601C>A c.(1600-1602)tCt>tAt p.S534Y LUSC 6 17649457 17649457 + Silent SNP A A G TCGA-39-5037-01A-01D-1441-08 TCGA-39-5037-11A-01D-1441-08 g.chr6:17649457A>G c.1470T>C c.(1468-1470)agT>agC p.S490S LUSC 6 17661915 17661915 + Missense_Mutation SNP C C A TCGA-70-6722-01A-11D-1817-08 TCGA-70-6722-10A-01D-1817-08 g.chr6:17661915C>A c.1364G>T c.(1363-1365)cGc>cTc p.R455L LUSC 6 17669736 17669736 + Silent SNP T T A TCGA-66-2770-01A-01D-1522-08 TCGA-66-2770-11A-01D-1522-08 g.chr6:17669736T>A c.894A>T c.(892-894)gcA>gcT p.A298A LUSC 6 17675990 17675990 + Missense_Mutation SNP T T C TCGA-60-2719-01A-01D-1522-08 TCGA-60-2719-11A-01D-1522-08 g.chr6:17675990T>C c.346A>G c.(346-348)Act>Gct p.T116A LUSC 6 17688803 17688803 + Missense_Mutation SNP C C A TCGA-33-4566-01A-01D-1441-08 TCGA-33-4566-11A-01D-1441-08 g.chr6:17688803C>A c.158G>T c.(157-159)gGg>gTg p.G53V OV 6 17629080 17629080 + Missense_Mutation SNP A A T TCGA-13-2057-01A-02D-1526-09 TCGA-13-2057-10A-01D-1526-09 g.chr6:17629080A>T c.3350T>A c.(3349-3351)gTt>gAt p.V1117D OV 6 17637764 17637764 + Missense_Mutation SNP G G C TCGA-61-1998-01A-01W-0722-08 TCGA-61-1998-10A-01W-0722-08 g.chr6:17637764G>C c.2084C>G c.(2083-2085)aCt>aGt p.T695S PAAD 6 17626368 17626368 + Missense_Mutation SNP C C G TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr6:17626368C>G c.3572G>C c.(3571-3573)aGt>aCt p.S1191T PAAD 6 17661976 17661976 + Missense_Mutation SNP C C A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr6:17661976C>A c.1303G>T c.(1303-1305)Gcc>Tcc p.A435S PAAD 6 17669530 17669530 + Silent SNP C C T TCGA-3A-A9IB-01A-21D-A397-08 TCGA-3A-A9IB-10A-01D-A39A-08 g.chr6:17669530C>T c.1008G>A c.(1006-1008)ctG>ctA p.L336L PAAD 6 17688685 17688685 + Missense_Mutation SNP C C A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr6:17688685C>A c.276G>T c.(274-276)gaG>gaT p.E92D PAAD 6 17688753 17688753 + Missense_Mutation SNP T T C TCGA-FZ-5922-01A-11D-1609-08 TCGA-FZ-5922-11A-01D-1609-08 g.chr6:17688753T>C c.208A>G c.(208-210)Aca>Gca p.T70A PAAD 6 17706578 17706578 + Missense_Mutation SNP C C T TCGA-US-A77E-01A-11D-A32N-08 TCGA-US-A77E-11A-11D-A32N-08 g.chr6:17706578C>T c.41G>A c.(40-42)gGc>gAc p.G14D PRAD 6 17648120 17648120 + Missense_Mutation SNP G G A TCGA-KK-A7B4-01A-11D-A32B-08 TCGA-KK-A7B4-11A-11D-A329-08 g.chr6:17648120G>A c.1550C>T c.(1549-1551)cCg>cTg p.P517L PRAD 6 17662249 17662249 + Splice_Site SNP C C A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr6:17662249C>A c.1268G>T c.(1267-1269)aGt>aTt p.S423I READ 6 17637604 17637604 + Silent SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr6:17637604C>T c.2244G>A c.(2242-2244)ccG>ccA p.P748P SKCM 6 17629689 17629689 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr6:17629689G>A c.2741C>T c.(2740-2742)cCt>cTt p.P914L SKCM 6 17633028 17633028 + Missense_Mutation SNP G G A TCGA-EE-A20F-06A-21D-A196-08 TCGA-EE-A20F-10A-01D-A198-08 g.chr6:17633028G>A c.2512C>T c.(2512-2514)Cct>Tct p.P838S SKCM 6 17637499 17637499 + Silent SNP G G A TCGA-FS-A4F5-06A-11D-A25O-08 TCGA-FS-A4F5-10B-01D-A25O-08 g.chr6:17637499G>A c.2349C>T c.(2347-2349)acC>acT p.T783T SKCM 6 17637557 17637557 + Missense_Mutation SNP G G A TCGA-EE-A2MJ-06A-11D-A197-08 TCGA-EE-A2MJ-10A-01D-A199-08 g.chr6:17637557G>A c.2291C>T c.(2290-2292)tCg>tTg p.S764L SKCM 6 17637746 17637746 + Missense_Mutation SNP T T C TCGA-RP-A695-06A-11D-A30X-08 TCGA-RP-A695-10A-01D-A30X-08 g.chr6:17637746T>C c.2102A>G c.(2101-2103)aAt>aGt p.N701S SKCM 6 17637899 17637899 + Missense_Mutation SNP A A C TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr6:17637899A>C c.1949T>G c.(1948-1950)aTt>aGt p.I650S SKCM 6 17648081 17648081 + Missense_Mutation SNP G G A TCGA-EE-A29E-06A-11D-A197-08 TCGA-EE-A29E-10A-01D-A199-08 g.chr6:17648081G>A c.1589C>T c.(1588-1590)cCa>cTa p.P530L SKCM 6 17649455 17649455 + Missense_Mutation SNP G G A TCGA-ER-A19P-06A-11D-A196-08 TCGA-ER-A19P-10A-01D-A198-08 g.chr6:17649455G>A c.1472C>T c.(1471-1473)tCc>tTc p.S491F SKCM 6 17649490 17649490 + Silent SNP G G A TCGA-EE-A2MS-06A-11D-A197-08 TCGA-EE-A2MS-10A-01D-A199-08 g.chr6:17649490G>A c.1437C>T c.(1435-1437)atC>atT p.I479I SKCM 6 17665598 17665598 + Missense_Mutation SNP G G A TCGA-EE-A183-06A-11D-A196-08 TCGA-EE-A183-10A-01D-A198-08 g.chr6:17665598G>A c.1087C>T c.(1087-1089)Cct>Tct p.P363S SKCM 6 17669558 17669558 + Missense_Mutation SNP C C T TCGA-D3-A5GN-06A-11D-A27K-08 TCGA-D3-A5GN-10A-01D-A27N-08 g.chr6:17669558C>T c.980G>A c.(979-981)aGa>aAa p.R327K SKCM 6 17675216 17675216 + Missense_Mutation SNP G G A TCGA-D3-A2J8-06A-11D-A196-08 TCGA-D3-A2J8-10A-01D-A198-08 g.chr6:17675216G>A c.772C>T c.(772-774)Cct>Tct p.P258S SKCM 6 17675478 17675478 + Silent SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr6:17675478G>A c.705C>T c.(703-705)gcC>gcT p.A235A SKCM 6 17675575 17675575 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr6:17675575G>A c.608C>T c.(607-609)tCa>tTa p.S203L

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BLCA-CN 6 17640210 17640210 single base substitution G A synonymous_variant I602I 1806C>T BLCA-CN 6 17640210 17640210 single base substitution G A synonymous_variant I633I 1899C>T BLCA-US 6 17626341 17626341 single base substitution G A missense_variant S1200L 3599C>T BLCA-US 6 17626341 17626341 single base substitution G A missense_variant S1231L 3692C>T BLCA-US 6 17669713 17669713 single base substitution G T stop_gained S306* 917C>A BLCA-US 6 17675190 17675190 single base substitution G A synonymous_variant Y266Y 798C>T BLCA-US 6 17675597 17675597 single base substitution T C missense_variant I196V 586A>G BLCA-US 6 17675981 17675981 single base substitution C T missense_variant A119T 355G>A BOCA-FR 6 17632643 17632643 single base substitution C A intron_variant BOCA-FR 6 17638232 17638232 single base substitution C A intron_variant BOCA-FR 6 17643984 17643984 single base substitution C T intron_variant BOCA-FR 6 17670015 17670015 single base substitution C T intron_variant BRCA-EU 6 17610941 17610941 deletion of <=200bp A - downstream_gene_variant BRCA-EU 6 17611898 17611898 single base substitution G C downstream_gene_variant BRCA-EU 6 17611924 17611924 single base substitution C G downstream_gene_variant BRCA-EU 6 17612211 17612211 single base substitution A G downstream_gene_variant BRCA-EU 6 17612439 17612439 single base substitution A G downstream_gene_variant BRCA-EU 6 17615178 17615178 single base substitution C G downstream_gene_variant BRCA-EU 6 17615181 17615181 single base substitution C G downstream_gene_variant BRCA-EU 6 17615751 17615751 single base substitution G C 3_prime_UTR_variant BRCA-EU 6 17615751 17615751 single base substitution G C downstream_gene_variant BRCA-EU 6 17618137 17618137 single base substitution C G intron_variant BRCA-EU 6 17618706 17618706 single base substitution G C intron_variant BRCA-EU 6 17619226 17619226 single base substitution C A intron_variant BRCA-EU 6 17619286 17619286 single base substitution C A intron_variant BRCA-EU 6 17619685 17619685 single base substitution A G intron_variant BRCA-EU 6 17620557 17620557 single base substitution C T intron_variant BRCA-EU 6 17621845 17621845 single base substitution C G intron_variant BRCA-EU 6 17621859 17621860 deletion of <=200bp AT - intron_variant BRCA-EU 6 17622201 17622201 single base substitution A T intron_variant BRCA-EU 6 17622342 17622342 single base substitution T C intron_variant BRCA-EU 6 17623329 17623329 single base substitution C G intron_variant BRCA-EU 6 17624479 17624479 single base substitution G C intron_variant BRCA-EU 6 17625216 17625216 single base substitution T C intron_variant BRCA-EU 6 17626224 17626224 single base substitution G A missense_variant A1239V 3716C>T BRCA-EU 6 17626224 17626224 single base substitution G A missense_variant A1270V 3809C>T BRCA-EU 6 17627229 17627229 single base substitution G A intron_variant BRCA-EU 6 17628618 17628618 single base substitution G C intron_variant BRCA-EU 6 17631113 17631113 single base substitution T G intron_variant BRCA-EU 6 17633079 17633079 single base substitution A G splice_region_variant BRCA-EU 6 17633770 17633770 single base substitution G A intron_variant BRCA-EU 6 17635077 17635077 single base substitution C T intron_variant BRCA-EU 6 17636359 17636359 single base substitution G A intron_variant BRCA-EU 6 17636684 17636684 single base substitution C G intron_variant BRCA-EU 6 17637400 17637400 single base substitution A C missense_variant C816W 2448T>G BRCA-EU 6 17637400 17637400 single base substitution A C missense_variant C847W 2541T>G BRCA-EU 6 17639124 17639124 single base substitution A C intron_variant BRCA-EU 6 17639977 17639977 single base substitution C T intron_variant BRCA-EU 6 17641904 17641904 single base substitution G A intron_variant BRCA-EU 6 17643102 17643102 single base substitution G C intron_variant BRCA-EU 6 17643319 17643319 single base substitution A G intron_variant BRCA-EU 6 17643840 17643840 single base substitution C T intron_variant BRCA-EU 6 17644827 17644827 single base substitution A T intron_variant BRCA-EU 6 17647291 17647291 single base substitution A C intron_variant BRCA-EU 6 17648290 17648290 single base substitution G T intron_variant BRCA-EU 6 17648448 17648448 single base substitution G A intron_variant BRCA-EU 6 17648666 17648666 single base substitution G A intron_variant BRCA-EU 6 17648875 17648875 single base substitution A T intron_variant BRCA-EU 6 17652416 17652416 single base substitution C T intron_variant BRCA-EU 6 17652448 17652448 single base substitution G A intron_variant BRCA-EU 6 17653224 17653224 single base substitution T G intron_variant BRCA-EU 6 17653986 17653988 deletion of <=200bp AGG - intron_variant BRCA-EU 6 17653998 17653998 single base substitution G T intron_variant BRCA-EU 6 17655369 17655369 insertion of <=200bp - A intron_variant BRCA-EU 6 17656758 17656758 single base substitution A C intron_variant BRCA-EU 6 17657957 17657957 single base substitution A G intron_variant BRCA-EU 6 17658095 17658095 single base substitution A G intron_variant BRCA-EU 6 17659319 17659319 single base substitution G A intron_variant BRCA-EU 6 17660098 17660098 single base substitution G A intron_variant BRCA-EU 6 17661981 17661981 single base substitution G A missense_variant P433L 1298C>T BRCA-EU 6 17662877 17662877 single base substitution C T intron_variant BRCA-EU 6 17663662 17663662 insertion of <=200bp - T intron_variant BRCA-EU 6 17664178 17664178 single base substitution C A intron_variant BRCA-EU 6 17664608 17664608 single base substitution A G intron_variant BRCA-EU 6 17665279 17665279 single base substitution G A intron_variant BRCA-EU 6 17665280 17665280 single base substitution T A intron_variant BRCA-EU 6 17665742 17665745 deletion of <=200bp ACAA - intron_variant BRCA-EU 6 17665890 17665890 single base substitution T C intron_variant BRCA-EU 6 17666235 17666235 single base substitution A T intron_variant BRCA-EU 6 17668212 17668212 single base substitution A G intron_variant BRCA-EU 6 17668696 17668696 deletion of <=200bp A - intron_variant BRCA-EU 6 17668741 17668741 single base substitution G A intron_variant BRCA-EU 6 17670872 17670872 deletion of <=200bp T - intron_variant BRCA-EU 6 17671095 17671095 single base substitution G A intron_variant BRCA-EU 6 17674004 17674004 single base substitution A G intron_variant BRCA-EU 6 17676302 17676302 single base substitution A G intron_variant BRCA-EU 6 17676374 17676374 single base substitution C G intron_variant BRCA-EU 6 17676922 17676922 insertion of <=200bp - A intron_variant BRCA-EU 6 17679289 17679289 single base substitution T A intron_variant BRCA-EU 6 17679623 17679623 single base substitution C G intron_variant BRCA-EU 6 17680135 17680135 single base substitution T A intron_variant BRCA-EU 6 17680519 17680519 single base substitution G A intron_variant BRCA-EU 6 17680755 17680755 single base substitution G A intron_variant BRCA-EU 6 17680833 17680833 single base substitution G C intron_variant BRCA-EU 6 17681032 17681032 single base substitution G C intron_variant BRCA-EU 6 17681486 17681486 single base substitution G A intron_variant BRCA-EU 6 17683656 17683656 single base substitution C G intron_variant BRCA-EU 6 17685028 17685215 deletion of <=200bp AATACTGTCAGAGAATAGGGAGGCCCAGAAAGAGGGAGAAAAGAGGGGAATAGCCAGTTGGTGGAGCAGCTGGAACACACACAACATTTACTGATTAAGTTCATCATCTTATATGGGTGTGGCTCGTGGCACCCCAAAACAATTACAATAGTAATACCAAAGAGCACTGATCACCATGATAGATACAT - intron_variant BRCA-EU 6 17685229 17685229 single base substitution G A intron_variant BRCA-EU 6 17685441 17685441 single base substitution C A intron_variant BRCA-EU 6 17686951 17686951 single base substitution T A intron_variant BRCA-EU 6 17687070 17687070 single base substitution C G intron_variant BRCA-EU 6 17687541 17687541 single base substitution A C intron_variant BRCA-EU 6 17687913 17687913 single base substitution G C intron_variant BRCA-EU 6 17687975 17687975 single base substitution G C intron_variant BRCA-EU 6 17688091 17688091 single base substitution A G intron_variant BRCA-EU 6 17690753 17690753 single base substitution G A intron_variant BRCA-EU 6 17691382 17691382 deletion of <=200bp A - intron_variant BRCA-EU 6 17691918 17691918 single base substitution C T intron_variant BRCA-EU 6 17692432 17692436 deletion of <=200bp ACTAA - intron_variant BRCA-EU 6 17692819 17692819 single base substitution T A intron_variant BRCA-EU 6 17694192 17694192 single base substitution T C intron_variant BRCA-EU 6 17695193 17695193 single base substitution A C intron_variant BRCA-EU 6 17695324 17695324 single base substitution T G intron_variant BRCA-EU 6 17697535 17697535 single base substitution G C intron_variant BRCA-EU 6 17697801 17697801 single base substitution C T intron_variant BRCA-EU 6 17699159 17699159 single base substitution A T intron_variant BRCA-EU 6 17699839 17699839 single base substitution G C intron_variant BRCA-EU 6 17701266 17701266 single base substitution G A intron_variant BRCA-EU 6 17702967 17702967 single base substitution G A intron_variant BRCA-EU 6 17705104 17705104 single base substitution C A intron_variant BRCA-EU 6 17705152 17705152 single base substitution G T intron_variant BRCA-EU 6 17706709 17706709 single base substitution G A upstream_gene_variant BRCA-EU 6 17707819 17707819 single base substitution G A upstream_gene_variant BRCA-EU 6 17709949 17709949 single base substitution G C upstream_gene_variant BRCA-EU 6 17711574 17711574 single base substitution G T upstream_gene_variant BRCA-FR 6 17623329 17623329 single base substitution C G intron_variant BRCA-FR 6 17624479 17624479 single base substitution G C intron_variant BRCA-FR 6 17627229 17627229 single base substitution G A intron_variant BRCA-FR 6 17648290 17648290 single base substitution G T intron_variant BRCA-FR 6 17648666 17648666 single base substitution G A intron_variant BRCA-FR 6 17653224 17653224 single base substitution T G intron_variant BRCA-FR 6 17680833 17680833 single base substitution G C intron_variant BRCA-FR 6 17685229 17685229 single base substitution G A intron_variant BRCA-FR 6 17687913 17687913 single base substitution G C intron_variant BRCA-FR 6 17690753 17690753 single base substitution G A intron_variant BRCA-UK 6 17613717 17613717 single base substitution G A downstream_gene_variant BRCA-UK 6 17616370 17616370 single base substitution G C missense_variant F1462L 4386C>G BRCA-UK 6 17616370 17616370 single base substitution G C missense_variant F1493L 4479C>G BRCA-UK 6 17622342 17622342 single base substitution T C intron_variant BRCA-UK 6 17624938 17624938 single base substitution G C missense_variant S1343C 4028C>G BRCA-UK 6 17624938 17624938 single base substitution G C missense_variant S1374C 4121C>G BRCA-UK 6 17632905 17632905 single base substitution G A missense_variant P879S 2635C>T BRCA-UK 6 17632905 17632905 single base substitution G A missense_variant P910S 2728C>T BRCA-UK 6 17636684 17636684 single base substitution C G intron_variant BRCA-UK 6 17637550 17637550 single base substitution A G synonymous_variant S766S 2298T>C BRCA-UK 6 17637550 17637550 single base substitution A G synonymous_variant S797S 2391T>C BRCA-UK 6 17644831 17644831 single base substitution C T intron_variant BRCA-UK 6 17650498 17650498 single base substitution C T intron_variant BRCA-UK 6 17658095 17658095 single base substitution A G intron_variant BRCA-UK 6 17687975 17687975 single base substitution G C intron_variant BRCA-UK 6 17711574 17711574 single base substitution G T upstream_gene_variant BRCA-US 6 17616916 17616916 single base substitution G C missense_variant F1395L 4185C>G BRCA-US 6 17616916 17616916 single base substitution G C missense_variant F1426L 4278C>G BRCA-US 6 17629106 17629106 single base substitution T C synonymous_variant Q1108Q 3324A>G BRCA-US 6 17629106 17629106 single base substitution T C synonymous_variant Q1139Q 3417A>G BRCA-US 6 17629273 17629273 single base substitution T A missense_variant I1053L 3157A>T BRCA-US 6 17629273 17629273 single base substitution T A missense_variant I1084L 3250A>T BRCA-US 6 17637546 17637546 single base substitution C G missense_variant E768Q 2302G>C BRCA-US 6 17637546 17637546 single base substitution C G missense_variant E799Q 2395G>C BRCA-US 6 17637557 17637557 single base substitution G A missense_variant S764L 2291C>T BRCA-US 6 17637557 17637557 single base substitution G A missense_variant S795L 2384C>T BRCA-US 6 17637763 17637763 single base substitution A T synonymous_variant T695T 2085T>A BRCA-US 6 17637763 17637763 single base substitution A T synonymous_variant T726T 2178T>A BRCA-US 6 17637836 17637836 single base substitution T A missense_variant N671I 2012A>T BRCA-US 6 17637836 17637836 single base substitution T A missense_variant N702I 2105A>T BRCA-US 6 17669532 17669532 single base substitution G C missense_variant L336V 1006C>G BRCA-US 6 17675248 17675248 single base substitution G A missense_variant S247L 740C>T BRCA-US 6 17675939 17675939 single base substitution G A missense_variant R133W 397C>T BRCA-US 6 17688750 17688750 single base substitution C T missense_variant D71N 211G>A BTCA-JP 6 17616461 17616461 single base substitution T C intron_variant BTCA-JP 6 17624900 17624900 single base substitution G A stop_gained Q1356* 4066C>T BTCA-JP 6 17624900 17624900 single base substitution G A stop_gained Q1387* 4159C>T BTCA-JP 6 17628952 17628952 single base substitution C T missense_variant E1160K 3478G>A BTCA-JP 6 17628952 17628952 single base substitution C T missense_variant E1191K 3571G>A BTCA-JP 6 17629030 17629030 deletion of <=200bp A - frameshift_variant S1134 BTCA-JP 6 17629030 17629030 deletion of <=200bp A - frameshift_variant S1165 BTCA-JP 6 17632863 17632863 single base substitution T A intron_variant BTCA-JP 6 17632865 17632865 single base substitution A T intron_variant BTCA-JP 6 17640296 17640296 single base substitution C A splice_acceptor_variant BTCA-JP 6 17662255 17662255 single base substitution C T missense_variant R421Q 1262G>A BTCA-JP 6 17665722 17665722 single base substitution C T intron_variant BTCA-JP 6 17675405 17675405 single base substitution T A intron_variant BTCA-JP 6 17675842 17675842 single base substitution A G missense_variant L165P 494T>C CESC-US 6 17626044 17626044 single base substitution G C missense_variant S1299C 3896C>G CESC-US 6 17626044 17626044 single base substitution G C missense_variant S1330C 3989C>G CESC-US 6 17632951 17632951 single base substitution C A missense_variant Q863H 2589G>T CESC-US 6 17632951 17632951 single base substitution C A missense_variant Q894H 2682G>T CESC-US 6 17665574 17665574 single base substitution T C missense_variant K371E 1111A>G CESC-US 6 17669684 17669684 single base substitution C G missense_variant E316Q 946G>C CLLE-ES 6 17640796 17640796 single base substitution T G intron_variant CLLE-ES 6 17650640 17650640 single base substitution G A intron_variant CLLE-ES 6 17653706 17653706 single base substitution T C intron_variant CLLE-ES 6 17654583 17654583 single base substitution G T intron_variant CLLE-ES 6 17655194 17655194 single base substitution G A intron_variant CLLE-ES 6 17661193 17661193 single base substitution T C intron_variant CLLE-ES 6 17678802 17678802 single base substitution C G intron_variant CLLE-ES 6 17682278 17682278 single base substitution A T intron_variant CLLE-ES 6 17699434 17699434 single base substitution T A intron_variant COAD-US 6 17629253 17629253 single base substitution T G synonymous_variant S1059S 3177A>C COAD-US 6 17629253 17629253 single base substitution T G synonymous_variant S1090S 3270A>C COAD-US 6 17629745 17629745 single base substitution C T synonymous_variant S895S 2685G>A COAD-US 6 17629745 17629745 single base substitution C T synonymous_variant S926S 2778G>A COAD-US 6 17633061 17633061 single base substitution C T missense_variant A827T 2479G>A COAD-US 6 17633061 17633061 single base substitution C T missense_variant A858T 2572G>A COAD-US 6 17633077 17633077 insertion of <=200bp - A splice_acceptor_variant COAD-US 6 17633078 17633079 deletion of <=200bp AA - splice_region_variant COAD-US 6 17637996 17637996 single base substitution C T missense_variant A618T 1852G>A COAD-US 6 17637996 17637996 single base substitution C T missense_variant A649T 1945G>A COAD-US 6 17665479 17665479 single base substitution G C missense_variant N402K 1206C>G COAD-US 6 17669733 17669733 single base substitution T C synonymous_variant Q299Q 897A>G COAD-US 6 17675207 17675207 single base substitution G T missense_variant P261T 781C>A COAD-US 6 17675210 17675210 deletion of <=200bp A - frameshift_variant Y260 COAD-US 6 17675246 17675246 single base substitution T C missense_variant I248V 742A>G COAD-US 6 17675498 17675498 insertion of <=200bp - T frameshift_variant P229H? COCA-CN 6 17616256 17616256 single base substitution C T 3_prime_UTR_variant COCA-CN 6 17616256 17616256 single base substitution C T downstream_gene_variant COCA-CN 6 17617012 17617012 single base substitution G A intron_variant COCA-CN 6 17632262 17632262 single base substitution T C intron_variant COCA-CN 6 17633078 17633078 single base substitution A G splice_region_variant COCA-CN 6 17637626 17637626 single base substitution T G missense_variant K741T 2222A>C COCA-CN 6 17637626 17637626 single base substitution T G missense_variant K772T 2315A>C COCA-CN 6 17649563 17649563 single base substitution A G intron_variant COCA-CN 6 17657624 17657624 single base substitution T A intron_variant COCA-CN 6 17665549 17665549 single base substitution C T missense_variant R379Q 1136G>A COCA-CN 6 17669621 17669621 single base substitution T G intron_variant COCA-CN 6 17670323 17670323 single base substitution T C intron_variant COCA-CN 6 17672106 17672106 single base substitution G A intron_variant COCA-CN 6 17675708 17675708 single base substitution T G intron_variant COCA-CN 6 17676022 17676022 single base substitution A G intron_variant COCA-CN 6 17692516 17692516 single base substitution A G intron_variant COCA-CN 6 17705827 17705827 single base substitution A G intron_variant COCA-CN 6 17710675 17710675 single base substitution T C upstream_gene_variant EOPC-DE 6 17625194 17625194 single base substitution C T intron_variant ESAD-UK 6 17610664 17610664 single base substitution A G downstream_gene_variant ESAD-UK 6 17611415 17611415 single base substitution A G downstream_gene_variant ESAD-UK 6 17611833 17611833 single base substitution A C downstream_gene_variant ESAD-UK 6 17612410 17612410 single base substitution G C downstream_gene_variant ESAD-UK 6 17615227 17615227 single base substitution T C downstream_gene_variant ESAD-UK 6 17616247 17616247 single base substitution A C 3_prime_UTR_variant ESAD-UK 6 17616247 17616247 single base substitution A C downstream_gene_variant ESAD-UK 6 17620055 17620055 single base substitution G A intron_variant ESAD-UK 6 17622204 17622204 single base substitution G C intron_variant ESAD-UK 6 17622229 17622229 single base substitution T A intron_variant ESAD-UK 6 17622375 17622375 single base substitution G A intron_variant ESAD-UK 6 17624299 17624299 single base substitution A C intron_variant ESAD-UK 6 17626080 17626080 single base substitution G A missense_variant S1287F 3860C>T ESAD-UK 6 17626080 17626080 single base substitution G A missense_variant S1318F 3953C>T ESAD-UK 6 17630868 17630868 single base substitution C T intron_variant ESAD-UK 6 17633705 17633705 single base substitution T G intron_variant ESAD-UK 6 17635050 17635050 single base substitution G A intron_variant ESAD-UK 6 17639941 17639941 single base substitution C T intron_variant ESAD-UK 6 17643257 17643257 single base substitution G A intron_variant ESAD-UK 6 17651429 17651429 single base substitution G A intron_variant ESAD-UK 6 17659266 17659266 single base substitution C T intron_variant ESAD-UK 6 17660649 17660649 single base substitution C G intron_variant ESAD-UK 6 17662097 17662097 single base substitution A T intron_variant ESAD-UK 6 17662454 17662454 single base substitution T A intron_variant ESAD-UK 6 17666092 17666092 single base substitution T G intron_variant ESAD-UK 6 17666939 17666939 single base substitution A G intron_variant ESAD-UK 6 17668981 17668981 single base substitution C T intron_variant ESAD-UK 6 17669976 17669976 single base substitution T C intron_variant ESAD-UK 6 17670117 17670117 single base substitution G C intron_variant ESAD-UK 6 17673172 17673172 single base substitution T A intron_variant ESAD-UK 6 17674176 17674176 single base substitution G A intron_variant ESAD-UK 6 17675499 17675499 insertion of <=200bp - T frameshift_variant K228K? ESAD-UK 6 17676419 17676419 single base substitution C T intron_variant ESAD-UK 6 17678690 17678690 single base substitution A T intron_variant ESAD-UK 6 17681999 17681999 single base substitution T C intron_variant ESAD-UK 6 17685097 17685097 single base substitution C A intron_variant ESAD-UK 6 17686230 17686230 single base substitution T A intron_variant ESAD-UK 6 17687873 17687873 single base substitution C T intron_variant ESAD-UK 6 17688404 17688404 single base substitution A G intron_variant ESAD-UK 6 17690402 17690402 single base substitution T A intron_variant ESAD-UK 6 17690881 17690881 single base substitution G A intron_variant ESAD-UK 6 17691195 17691195 single base substitution C A intron_variant ESAD-UK 6 17695052 17695052 single base substitution A T intron_variant ESAD-UK 6 17699452 17699452 single base substitution G A intron_variant ESAD-UK 6 17701315 17701315 single base substitution G A intron_variant ESAD-UK 6 17701714 17701714 single base substitution G T intron_variant ESAD-UK 6 17702714 17702714 single base substitution G A intron_variant ESAD-UK 6 17704855 17704855 single base substitution T C intron_variant ESAD-UK 6 17705659 17705659 single base substitution G C intron_variant ESAD-UK 6 17707927 17707927 single base substitution G A upstream_gene_variant ESAD-UK 6 17709423 17709423 single base substitution A G upstream_gene_variant ESAD-UK 6 17709552 17709552 single base substitution T C upstream_gene_variant ESAD-UK 6 17711161 17711161 single base substitution A T upstream_gene_variant ESCA-CN 6 17629479 17629479 single base substitution C G missense_variant G1015A 3044G>C ESCA-CN 6 17629479 17629479 single base substitution C G missense_variant G984A 2951G>C ESCA-CN 6 17648103 17648103 single base substitution G T missense_variant P523T 1567C>A ESCA-CN 6 17648103 17648103 single base substitution G T missense_variant P554T 1660C>A ESCA-CN 6 17688691 17688691 single base substitution A G synonymous_variant D90D 270T>C GBM-US 6 17616339 17616339 single base substitution G A missense_variant R1473C 4417C>T GBM-US 6 17616339 17616339 single base substitution G A missense_variant R1504C 4510C>T GBM-US 6 17629357 17629357 single base substitution C T missense_variant G1025S 3073G>A GBM-US 6 17629357 17629357 single base substitution C T missense_variant G1056S 3166G>A KIRC-US 6 17624932 17624932 single base substitution G A missense_variant S1345L 4034C>T KIRC-US 6 17624932 17624932 single base substitution G A missense_variant S1376L 4127C>T KIRC-US 6 17637570 17637570 single base substitution A G synonymous_variant L760L 2278T>C KIRC-US 6 17637570 17637570 single base substitution A G synonymous_variant L791L 2371T>C KIRP-US 6 17688708 17688708 single base substitution G A missense_variant H85Y 253C>T LAML-KR 6 17616256 17616256 single base substitution C T 3_prime_UTR_variant LAML-KR 6 17616256 17616256 single base substitution C T downstream_gene_variant LAML-KR 6 17633078 17633078 single base substitution A G splice_region_variant LAML-KR 6 17676120 17676120 single base substitution G A intron_variant LGG-US 6 17629745 17629745 single base substitution C T synonymous_variant S895S 2685G>A LGG-US 6 17629745 17629745 single base substitution C T synonymous_variant S926S 2778G>A LICA-CN 6 17624973 17624973 single base substitution T A missense_variant Q1331H 3993A>T LICA-CN 6 17624973 17624973 single base substitution T A missense_variant Q1362H 4086A>T LICA-CN 6 17629658 17629658 single base substitution A C missense_variant F924L 2772T>G LICA-CN 6 17629658 17629658 single base substitution A C missense_variant F955L 2865T>G LICA-CN 6 17675512 17675512 single base substitution G C missense_variant T224S 671C>G LICA-FR 6 17623361 17623361 deletion of <=200bp A - intron_variant LICA-FR 6 17623589 17623589 deletion of <=200bp A - intron_variant LICA-FR 6 17629242 17629242 single base substitution A G missense_variant F1063S 3188T>C LICA-FR 6 17629242 17629242 single base substitution A G missense_variant F1094S 3281T>C LICA-FR 6 17629638 17629638 single base substitution C A missense_variant G931V 2792G>T LICA-FR 6 17629638 17629638 single base substitution C A missense_variant G962V 2885G>T LICA-FR 6 17646112 17646112 single base substitution T A intron_variant LICA-FR 6 17646374 17646374 single base substitution T C synonymous_variant T548T 1644A>G LICA-FR 6 17646374 17646374 single base substitution T C synonymous_variant T579T 1737A>G LICA-FR 6 17671366 17671366 single base substitution C T intron_variant LICA-FR 6 17689357 17689357 single base substitution C T intron_variant LICA-FR 6 17689366 17689366 single base substitution T C intron_variant LICA-FR 6 17696728 17696728 single base substitution T A intron_variant LICA-FR 6 17696822 17696822 single base substitution T C intron_variant LICA-FR 6 17702208 17702208 single base substitution T C intron_variant LICA-FR 6 17704436 17704436 single base substitution T C intron_variant LIHC-US 6 17637675 17637675 single base substitution T C missense_variant T725A 2173A>G LIHC-US 6 17637675 17637675 single base substitution T C missense_variant T756A 2266A>G LIHC-US 6 17640200 17640200 single base substitution C G missense_variant G606R 1816G>C LIHC-US 6 17640200 17640200 single base substitution C G missense_variant G637R 1909G>C LIHC-US 6 17706588 17706588 single base substitution C A missense_variant G11C 31G>T LINC-JP 6 17614099 17614099 single base substitution A C downstream_gene_variant LINC-JP 6 17617922 17617922 single base substitution C A intron_variant LINC-JP 6 17619856 17619856 single base substitution C A intron_variant LINC-JP 6 17624581 17624581 single base substitution T A intron_variant LINC-JP 6 17629341 17629341 single base substitution T C missense_variant N1030S 3089A>G LINC-JP 6 17629341 17629341 single base substitution T C missense_variant N1061S 3182A>G LINC-JP 6 17633094 17633094 single base substitution A C intron_variant LINC-JP 6 17633095 17633095 single base substitution C G intron_variant LINC-JP 6 17636200 17636200 single base substitution C A intron_variant LINC-JP 6 17640441 17640441 single base substitution T G intron_variant LINC-JP 6 17656309 17656309 single base substitution G T intron_variant LINC-JP 6 17662075 17662075 single base substitution A T intron_variant LINC-JP 6 17675335 17675335 single base substitution T C intron_variant LINC-JP 6 17679248 17679248 single base substitution T C intron_variant LINC-JP 6 17698753 17698753 single base substitution A G intron_variant LINC-JP 6 17699729 17699729 single base substitution G A intron_variant LINC-JP 6 17700281 17700281 single base substitution T C intron_variant LINC-JP 6 17702509 17702509 single base substitution C T intron_variant LINC-JP 6 17706422 17706422 single base substitution C T intron_variant LIRI-JP 6 17610888 17610888 single base substitution A G downstream_gene_variant LIRI-JP 6 17611249 17611249 deletion of <=200bp T - downstream_gene_variant LIRI-JP 6 17612135 17612135 single base substitution T C downstream_gene_variant LIRI-JP 6 17612350 17612350 single base substitution G A downstream_gene_variant LIRI-JP 6 17612637 17612637 deletion of <=200bp T - downstream_gene_variant LIRI-JP 6 17614363 17614363 single base substitution T C downstream_gene_variant LIRI-JP 6 17615044 17615044 single base substitution T C downstream_gene_variant LIRI-JP 6 17617494 17617494 single base substitution T C intron_variant LIRI-JP 6 17618074 17618074 single base substitution T G intron_variant LIRI-JP 6 17619054 17619054 single base substitution C T intron_variant LIRI-JP 6 17621228 17621228 single base substitution C T intron_variant LIRI-JP 6 17627541 17627541 single base substitution T C intron_variant LIRI-JP 6 17630565 17630565 single base substitution G A intron_variant LIRI-JP 6 17635286 17635286 single base substitution T C intron_variant LIRI-JP 6 17637035 17637035 single base substitution T C intron_variant LIRI-JP 6 17639504 17639504 single base substitution T G intron_variant LIRI-JP 6 17639537 17639537 single base substitution T G intron_variant LIRI-JP 6 17639628 17639628 single base substitution T A intron_variant LIRI-JP 6 17640131 17640131 single base substitution G T intron_variant LIRI-JP 6 17640275 17640275 single base substitution T C missense_variant N581D 1741A>G LIRI-JP 6 17640275 17640275 single base substitution T C missense_variant N612D 1834A>G LIRI-JP 6 17640420 17640420 single base substitution T G intron_variant LIRI-JP 6 17640935 17640935 single base substitution A T intron_variant LIRI-JP 6 17641484 17641484 single base substitution C T intron_variant LIRI-JP 6 17641614 17641614 single base substitution A C intron_variant LIRI-JP 6 17642878 17642878 single base substitution T C intron_variant LIRI-JP 6 17644191 17644191 single base substitution T C intron_variant LIRI-JP 6 17645618 17645618 single base substitution G A intron_variant LIRI-JP 6 17646046 17646046 single base substitution G A intron_variant LIRI-JP 6 17648050 17648050 single base substitution T C synonymous_variant L540L 1620A>G LIRI-JP 6 17648050 17648050 single base substitution T C synonymous_variant L571L 1713A>G LIRI-JP 6 17648427 17648427 single base substitution C T intron_variant LIRI-JP 6 17649378 17649378 single base substitution T C intron_variant LIRI-JP 6 17650823 17650823 single base substitution T C intron_variant LIRI-JP 6 17651356 17651356 single base substitution C A intron_variant LIRI-JP 6 17651496 17651496 single base substitution T C intron_variant LIRI-JP 6 17652476 17652476 single base substitution T C intron_variant LIRI-JP 6 17653129 17653129 single base substitution G A intron_variant LIRI-JP 6 17655086 17655086 single base substitution A C intron_variant LIRI-JP 6 17656273 17656273 single base substitution T C intron_variant LIRI-JP 6 17658387 17658387 single base substitution C A intron_variant LIRI-JP 6 17660271 17660271 single base substitution T C intron_variant LIRI-JP 6 17661161 17661161 single base substitution C T intron_variant LIRI-JP 6 17662869 17662869 single base substitution T C intron_variant LIRI-JP 6 17663193 17663193 single base substitution G T intron_variant LIRI-JP 6 17663975 17663975 single base substitution A G intron_variant LIRI-JP 6 17669002 17669002 single base substitution A G intron_variant LIRI-JP 6 17669114 17669114 single base substitution T C intron_variant LIRI-JP 6 17670820 17670820 single base substitution T C intron_variant LIRI-JP 6 17672402 17672402 single base substitution C T intron_variant LIRI-JP 6 17673328 17673328 single base substitution G C intron_variant LIRI-JP 6 17673699 17673699 single base substitution T C intron_variant LIRI-JP 6 17675492 17675492 single base substitution A G missense_variant F231L 691T>C LIRI-JP 6 17675530 17675530 single base substitution A T missense_variant L218H 653T>A LIRI-JP 6 17676060 17676060 single base substitution A G intron_variant LIRI-JP 6 17676743 17676750 deletion of <=200bp TTTCAGAA - intron_variant LIRI-JP 6 17677830 17677830 single base substitution T C intron_variant LIRI-JP 6 17677986 17677986 single base substitution A T intron_variant LIRI-JP 6 17679261 17679261 single base substitution T C intron_variant LIRI-JP 6 17682484 17682484 single base substitution C T intron_variant LIRI-JP 6 17683041 17683041 single base substitution C T intron_variant LIRI-JP 6 17684026 17684026 single base substitution G A intron_variant LIRI-JP 6 17685642 17685642 single base substitution T G intron_variant LIRI-JP 6 17686625 17686625 single base substitution T G intron_variant LIRI-JP 6 17689029 17689029 single base substitution T C intron_variant LIRI-JP 6 17689250 17689250 single base substitution C T intron_variant LIRI-JP 6 17689874 17689874 single base substitution T A intron_variant LIRI-JP 6 17691203 17691203 single base substitution T C intron_variant LIRI-JP 6 17692650 17692650 single base substitution C T intron_variant LIRI-JP 6 17694074 17694074 single base substitution G A intron_variant LIRI-JP 6 17695932 17695932 insertion of <=200bp - A intron_variant LIRI-JP 6 17696270 17696270 single base substitution A G intron_variant LIRI-JP 6 17698961 17698961 single base substitution T C intron_variant LIRI-JP 6 17699033 17699033 single base substitution G A intron_variant LIRI-JP 6 17700018 17700018 single base substitution A T intron_variant LIRI-JP 6 17703334 17703334 single base substitution C A intron_variant LIRI-JP 6 17703477 17703477 single base substitution A G intron_variant LIRI-JP 6 17704282 17704282 single base substitution G A intron_variant LIRI-JP 6 17707130 17707130 single base substitution G A upstream_gene_variant LIRI-JP 6 17708260 17708260 single base substitution G T upstream_gene_variant LIRI-JP 6 17710390 17710390 single base substitution A G upstream_gene_variant LIRI-JP 6 17711232 17711232 single base substitution C A upstream_gene_variant LUSC-KR 6 17612839 17612839 single base substitution C T downstream_gene_variant LUSC-KR 6 17616049 17616049 single base substitution T C 3_prime_UTR_variant LUSC-KR 6 17616049 17616049 single base substitution T C downstream_gene_variant LUSC-KR 6 17616256 17616256 single base substitution C T 3_prime_UTR_variant LUSC-KR 6 17616256 17616256 single base substitution C T downstream_gene_variant LUSC-KR 6 17617012 17617012 single base substitution G A intron_variant LUSC-KR 6 17619856 17619856 single base substitution C T intron_variant LUSC-KR 6 17628853 17628853 single base substitution T A intron_variant LUSC-KR 6 17629143 17629143 single base substitution G A missense_variant S1096L 3287C>T LUSC-KR 6 17629143 17629143 single base substitution G A missense_variant S1127L 3380C>T LUSC-KR 6 17629357 17629357 single base substitution C T missense_variant G1025S 3073G>A LUSC-KR 6 17629357 17629357 single base substitution C T missense_variant G1056S 3166G>A LUSC-KR 6 17635359 17635359 single base substitution G T intron_variant LUSC-KR 6 17635951 17635951 single base substitution C A intron_variant LUSC-KR 6 17640109 17640109 single base substitution A T intron_variant LUSC-KR 6 17645346 17645346 single base substitution G C intron_variant LUSC-KR 6 17653389 17653389 single base substitution C A intron_variant LUSC-KR 6 17657821 17657821 single base substitution T C intron_variant LUSC-KR 6 17664178 17664178 single base substitution C A intron_variant LUSC-KR 6 17665479 17665479 single base substitution G C missense_variant N402K 1206C>G LUSC-KR 6 17669563 17669563 single base substitution T A synonymous_variant A325A 975A>T LUSC-KR 6 17676120 17676120 single base substitution G A intron_variant LUSC-KR 6 17676721 17676721 single base substitution T C intron_variant LUSC-KR 6 17678424 17678424 single base substitution T C intron_variant LUSC-KR 6 17689785 17689785 single base substitution G T intron_variant LUSC-KR 6 17693960 17693960 single base substitution T C intron_variant LUSC-KR 6 17696314 17696314 single base substitution G C intron_variant LUSC-KR 6 17696752 17696752 single base substitution C A intron_variant LUSC-KR 6 17698583 17698583 single base substitution G C intron_variant LUSC-KR 6 17699216 17699216 single base substitution G C intron_variant LUSC-KR 6 17701853 17701853 single base substitution T C intron_variant LUSC-KR 6 17702269 17702269 single base substitution T C intron_variant LUSC-KR 6 17702504 17702504 single base substitution C T intron_variant LUSC-KR 6 17704353 17704353 single base substitution C G intron_variant LUSC-KR 6 17708599 17708599 single base substitution G C upstream_gene_variant LUSC-US 6 17626107 17626107 single base substitution C G missense_variant G1278A 3833G>C LUSC-US 6 17626107 17626107 single base substitution C G missense_variant G1309A 3926G>C LUSC-US 6 17637456 17637456 single base substitution C A stop_gained E798* 2392G>T LUSC-US 6 17637456 17637456 single base substitution C A stop_gained E829* 2485G>T LUSC-US 6 17640218 17640218 single base substitution C A missense_variant A600S 1798G>T LUSC-US 6 17640218 17640218 single base substitution C A missense_variant A631S 1891G>T LUSC-US 6 17640222 17640222 single base substitution T G missense_variant R598S 1794A>C LUSC-US 6 17640222 17640222 single base substitution T G missense_variant R629S 1887A>C LUSC-US 6 17648069 17648069 single base substitution G T missense_variant S534Y 1601C>A LUSC-US 6 17648069 17648069 single base substitution G T missense_variant S565Y 1694C>A LUSC-US 6 17649457 17649457 single base substitution A G synonymous_variant S490S 1470T>C LUSC-US 6 17649457 17649457 single base substitution A G synonymous_variant S521S 1563T>C LUSC-US 6 17661915 17661915 single base substitution C A missense_variant R455L 1364G>T LUSC-US 6 17669736 17669736 single base substitution T A synonymous_variant A298A 894A>T LUSC-US 6 17675990 17675990 single base substitution T C missense_variant T116A 346A>G LUSC-US 6 17688803 17688803 single base substitution C A missense_variant G53V 158G>T MALY-DE 6 17610416 17610416 single base substitution A T downstream_gene_variant MALY-DE 6 17613099 17613099 single base substitution T A downstream_gene_variant MALY-DE 6 17614316 17614316 single base substitution C A downstream_gene_variant MALY-DE 6 17615643 17615643 single base substitution G C 3_prime_UTR_variant MALY-DE 6 17615643 17615643 single base substitution G C downstream_gene_variant MALY-DE 6 17617619 17617619 single base substitution A G intron_variant MALY-DE 6 17620091 17620091 single base substitution G A intron_variant MALY-DE 6 17621771 17621774 deletion of <=200bp TCAT - intron_variant MALY-DE 6 17624521 17624521 single base substitution A G intron_variant MALY-DE 6 17630050 17630050 single base substitution G A intron_variant MALY-DE 6 17648012 17648012 single base substitution T C intron_variant MALY-DE 6 17648876 17648876 single base substitution T A intron_variant MALY-DE 6 17658788 17658788 single base substitution T C intron_variant MALY-DE 6 17662340 17662340 single base substitution T G intron_variant MALY-DE 6 17663375 17663375 single base substitution A G intron_variant MALY-DE 6 17663869 17663869 single base substitution T C intron_variant MALY-DE 6 17679450 17679450 insertion of <=200bp - A intron_variant MALY-DE 6 17685150 17685150 single base substitution C T intron_variant MALY-DE 6 17688270 17688270 single base substitution A T intron_variant MALY-DE 6 17689370 17689370 single base substitution A G intron_variant MALY-DE 6 17692234 17692234 single base substitution T G intron_variant MALY-DE 6 17699302 17699302 single base substitution T G intron_variant MALY-DE 6 17702826 17702826 single base substitution G A intron_variant MALY-DE 6 17707868 17707868 single base substitution T G upstream_gene_variant MELA-AU 6 17611466 17611467 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 6 17612497 17612497 single base substitution G A downstream_gene_variant MELA-AU 6 17612561 17612561 single base substitution C T downstream_gene_variant MELA-AU 6 17612781 17612781 single base substitution G A downstream_gene_variant MELA-AU 6 17613232 17613232 single base substitution T G downstream_gene_variant MELA-AU 6 17613741 17613741 single base substitution G A downstream_gene_variant MELA-AU 6 17614025 17614025 single base substitution C T downstream_gene_variant MELA-AU 6 17615039 17615039 single base substitution G C downstream_gene_variant MELA-AU 6 17616185 17616185 single base substitution G A 3_prime_UTR_variant MELA-AU 6 17616185 17616185 single base substitution G A downstream_gene_variant MELA-AU 6 17616238 17616238 single base substitution C T 3_prime_UTR_variant MELA-AU 6 17616238 17616238 single base substitution C T downstream_gene_variant MELA-AU 6 17616497 17616497 single base substitution G A intron_variant MELA-AU 6 17616670 17616670 single base substitution G A intron_variant MELA-AU 6 17616776 17616776 single base substitution G A missense_variant P1442L 4325C>T MELA-AU 6 17616776 17616776 single base substitution G A missense_variant P1473L 4418C>T MELA-AU 6 17617444 17617445 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 6 17617574 17617574 single base substitution G A intron_variant MELA-AU 6 17617616 17617616 deletion of <=200bp A - intron_variant MELA-AU 6 17618096 17618096 single base substitution G A intron_variant MELA-AU 6 17618341 17618341 single base substitution G A intron_variant MELA-AU 6 17618487 17618487 single base substitution G A intron_variant MELA-AU 6 17619018 17619018 single base substitution C T intron_variant MELA-AU 6 17619075 17619075 single base substitution G A intron_variant MELA-AU 6 17619689 17619689 single base substitution G A intron_variant MELA-AU 6 17620431 17620431 single base substitution A T intron_variant MELA-AU 6 17620432 17620432 single base substitution G A intron_variant MELA-AU 6 17620794 17620794 single base substitution C T intron_variant MELA-AU 6 17620899 17620900 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 6 17621821 17621821 deletion of <=200bp A - intron_variant MELA-AU 6 17622294 17622294 single base substitution G A intron_variant MELA-AU 6 17622472 17622472 single base substitution G A intron_variant MELA-AU 6 17623071 17623071 single base substitution G A intron_variant MELA-AU 6 17623273 17623273 single base substitution A G intron_variant MELA-AU 6 17623652 17623664 deletion of <=200bp CATATAAGAACTC - intron_variant MELA-AU 6 17623996 17623996 single base substitution G A intron_variant MELA-AU 6 17624603 17624603 single base substitution A G intron_variant MELA-AU 6 17624724 17624724 single base substitution G A intron_variant MELA-AU 6 17624911 17624911 single base substitution G A missense_variant P1352L 4055C>T MELA-AU 6 17624911 17624911 single base substitution G A missense_variant P1383L 4148C>T MELA-AU 6 17624953 17624953 single base substitution G A missense_variant P1338L 4013C>T MELA-AU 6 17624953 17624953 single base substitution G A missense_variant P1369L 4106C>T MELA-AU 6 17625065 17625065 single base substitution C T splice_acceptor_variant MELA-AU 6 17625197 17625197 single base substitution G A intron_variant MELA-AU 6 17625761 17625761 single base substitution G A intron_variant MELA-AU 6 17626293 17626293 single base substitution G A missense_variant T1216I 3647C>T MELA-AU 6 17626293 17626293 single base substitution G A missense_variant T1247I 3740C>T MELA-AU 6 17626700 17626700 single base substitution T G intron_variant MELA-AU 6 17627387 17627387 single base substitution G A intron_variant MELA-AU 6 17627642 17627642 single base substitution C T intron_variant MELA-AU 6 17628850 17628850 single base substitution A T intron_variant MELA-AU 6 17629085 17629085 single base substitution G A synonymous_variant S1115S 3345C>T MELA-AU 6 17629085 17629085 single base substitution G A synonymous_variant S1146S 3438C>T MELA-AU 6 17629813 17629813 single base substitution G A intron_variant MELA-AU 6 17630282 17630282 single base substitution A G intron_variant MELA-AU 6 17630435 17630435 single base substitution G A intron_variant MELA-AU 6 17630461 17630461 single base substitution G A intron_variant MELA-AU 6 17631238 17631238 single base substitution G A intron_variant MELA-AU 6 17631772 17631772 single base substitution G A intron_variant MELA-AU 6 17632128 17632128 single base substitution G A intron_variant MELA-AU 6 17632210 17632210 single base substitution A C intron_variant MELA-AU 6 17632555 17632555 single base substitution A C intron_variant MELA-AU 6 17632761 17632761 single base substitution T C intron_variant MELA-AU 6 17633097 17633097 single base substitution G A intron_variant MELA-AU 6 17633771 17633771 single base substitution G A intron_variant MELA-AU 6 17634245 17634245 single base substitution G A intron_variant MELA-AU 6 17634597 17634597 deletion of <=200bp A - intron_variant MELA-AU 6 17635084 17635084 single base substitution G A intron_variant MELA-AU 6 17635475 17635475 single base substitution G A intron_variant MELA-AU 6 17635600 17635600 single base substitution A G intron_variant MELA-AU 6 17635677 17635677 single base substitution G A intron_variant MELA-AU 6 17637529 17637529 single base substitution T A synonymous_variant S773S 2319A>T MELA-AU 6 17637529 17637529 single base substitution T A synonymous_variant S804S 2412A>T MELA-AU 6 17637557 17637557 single base substitution G A missense_variant S764L 2291C>T MELA-AU 6 17637557 17637557 single base substitution G A missense_variant S795L 2384C>T MELA-AU 6 17638671 17638671 single base substitution G A intron_variant MELA-AU 6 17639377 17639377 single base substitution C T intron_variant MELA-AU 6 17639442 17639442 single base substitution G A intron_variant MELA-AU 6 17641357 17641358 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 6 17641450 17641450 single base substitution G A intron_variant MELA-AU 6 17641802 17641802 single base substitution G A intron_variant MELA-AU 6 17641917 17641917 single base substitution T C intron_variant MELA-AU 6 17642462 17642462 single base substitution C T intron_variant MELA-AU 6 17643176 17643176 single base substitution C T intron_variant MELA-AU 6 17643244 17643244 single base substitution A T intron_variant MELA-AU 6 17643524 17643524 single base substitution G A intron_variant MELA-AU 6 17643630 17643630 single base substitution G A intron_variant MELA-AU 6 17643969 17643969 single base substitution C T intron_variant MELA-AU 6 17644149 17644149 single base substitution A C intron_variant MELA-AU 6 17644947 17644947 single base substitution G A intron_variant MELA-AU 6 17645107 17645107 single base substitution G A intron_variant MELA-AU 6 17645381 17645381 single base substitution G A intron_variant MELA-AU 6 17645660 17645660 single base substitution G A intron_variant MELA-AU 6 17646505 17646505 single base substitution C T intron_variant MELA-AU 6 17646792 17646792 single base substitution G A intron_variant MELA-AU 6 17646892 17646892 single base substitution T C intron_variant MELA-AU 6 17649110 17649110 single base substitution A G intron_variant MELA-AU 6 17649392 17649392 single base substitution A C splice_donor_variant MELA-AU 6 17649437 17649437 single base substitution G A missense_variant S497F 1490C>T MELA-AU 6 17649437 17649437 single base substitution G A missense_variant S528F 1583C>T MELA-AU 6 17649621 17649621 single base substitution A T intron_variant MELA-AU 6 17649722 17649722 single base substitution G A intron_variant MELA-AU 6 17649991 17649999 deletion of <=200bp TTGTTGTTG - intron_variant MELA-AU 6 17650449 17650450 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 6 17651657 17651657 single base substitution A G intron_variant MELA-AU 6 17651737 17651737 single base substitution G A intron_variant MELA-AU 6 17651800 17651800 single base substitution G A intron_variant MELA-AU 6 17652097 17652097 single base substitution G A intron_variant MELA-AU 6 17652097 17652097 single base substitution G A missense_variant P486S 1456C>T MELA-AU 6 17652625 17652625 single base substitution G A intron_variant MELA-AU 6 17652863 17652863 single base substitution G A intron_variant MELA-AU 6 17652892 17652892 single base substitution A G intron_variant MELA-AU 6 17653146 17653146 single base substitution G A intron_variant MELA-AU 6 17653391 17653391 single base substitution G A intron_variant MELA-AU 6 17653575 17653575 single base substitution G A intron_variant MELA-AU 6 17654543 17654543 single base substitution G A intron_variant MELA-AU 6 17655138 17655138 single base substitution C T intron_variant MELA-AU 6 17655496 17655496 single base substitution T C intron_variant MELA-AU 6 17656227 17656228 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 6 17656628 17656628 single base substitution G A intron_variant MELA-AU 6 17657292 17657292 single base substitution G A intron_variant MELA-AU 6 17657560 17657560 single base substitution G A intron_variant MELA-AU 6 17657566 17657566 single base substitution G A intron_variant MELA-AU 6 17657959 17657959 single base substitution G A intron_variant MELA-AU 6 17658001 17658001 single base substitution G A intron_variant MELA-AU 6 17658741 17658764 deletion of <=200bp CACTGGAAGTTGACAATAACCAGT - intron_variant MELA-AU 6 17658748 17658748 single base substitution A G intron_variant MELA-AU 6 17658888 17658888 single base substitution T C intron_variant MELA-AU 6 17658934 17658934 single base substitution G A intron_variant MELA-AU 6 17659431 17659431 single base substitution G A intron_variant MELA-AU 6 17659829 17659829 single base substitution G C intron_variant MELA-AU 6 17659909 17659909 single base substitution G A intron_variant MELA-AU 6 17659984 17659984 single base substitution G A intron_variant MELA-AU 6 17660001 17660001 single base substitution C T intron_variant MELA-AU 6 17660845 17660845 single base substitution G A intron_variant MELA-AU 6 17661026 17661026 single base substitution C T intron_variant MELA-AU 6 17661119 17661119 single base substitution C T intron_variant MELA-AU 6 17662898 17662898 single base substitution A G intron_variant MELA-AU 6 17663273 17663273 single base substitution G A intron_variant MELA-AU 6 17663463 17663463 single base substitution T C intron_variant MELA-AU 6 17663489 17663489 single base substitution C T intron_variant MELA-AU 6 17663495 17663495 single base substitution T C intron_variant MELA-AU 6 17665840 17665840 single base substitution T G intron_variant MELA-AU 6 17666075 17666075 single base substitution C G intron_variant MELA-AU 6 17667591 17667591 single base substitution A C intron_variant MELA-AU 6 17667675 17667675 single base substitution G A intron_variant MELA-AU 6 17667946 17667946 single base substitution C T intron_variant MELA-AU 6 17667966 17667966 single base substitution G A intron_variant MELA-AU 6 17668163 17668163 single base substitution G A intron_variant MELA-AU 6 17669049 17669049 single base substitution G A intron_variant MELA-AU 6 17669139 17669139 single base substitution A G intron_variant MELA-AU 6 17669931 17669931 single base substitution T C intron_variant MELA-AU 6 17670128 17670128 single base substitution C G intron_variant MELA-AU 6 17670316 17670316 single base substitution G A intron_variant MELA-AU 6 17670957 17670957 single base substitution G A intron_variant MELA-AU 6 17671167 17671167 single base substitution G A intron_variant MELA-AU 6 17671234 17671234 single base substitution G A intron_variant MELA-AU 6 17671242 17671242 single base substitution A C intron_variant MELA-AU 6 17671262 17671262 single base substitution G A intron_variant MELA-AU 6 17671427 17671427 single base substitution G A intron_variant MELA-AU 6 17672158 17672158 single base substitution G A intron_variant MELA-AU 6 17672287 17672287 single base substitution C A intron_variant MELA-AU 6 17674158 17674158 single base substitution G A intron_variant MELA-AU 6 17674658 17674658 single base substitution G A intron_variant MELA-AU 6 17674772 17674772 single base substitution G A intron_variant MELA-AU 6 17675004 17675004 single base substitution G A intron_variant MELA-AU 6 17676251 17676251 single base substitution T C intron_variant MELA-AU 6 17676959 17676959 single base substitution G A intron_variant MELA-AU 6 17677028 17677028 single base substitution A T intron_variant MELA-AU 6 17677228 17677228 single base substitution G A intron_variant MELA-AU 6 17677311 17677311 single base substitution A G intron_variant MELA-AU 6 17678484 17678485 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 6 17678897 17678897 single base substitution G A intron_variant MELA-AU 6 17679332 17679332 single base substitution A T intron_variant MELA-AU 6 17680322 17680322 single base substitution G T intron_variant MELA-AU 6 17680325 17680325 single base substitution A G intron_variant MELA-AU 6 17680473 17680473 single base substitution T C intron_variant MELA-AU 6 17681442 17681442 single base substitution T A intron_variant MELA-AU 6 17681586 17681586 single base substitution G A intron_variant MELA-AU 6 17681587 17681587 single base substitution G A intron_variant MELA-AU 6 17682218 17682218 single base substitution C T intron_variant MELA-AU 6 17682969 17682969 single base substitution G A intron_variant MELA-AU 6 17683152 17683152 single base substitution A G intron_variant MELA-AU 6 17683492 17683492 single base substitution G A intron_variant MELA-AU 6 17683906 17683906 single base substitution G A intron_variant MELA-AU 6 17683958 17683958 single base substitution A G intron_variant MELA-AU 6 17684184 17684184 single base substitution A T intron_variant MELA-AU 6 17684584 17684584 single base substitution C T intron_variant MELA-AU 6 17684963 17684963 single base substitution G A intron_variant MELA-AU 6 17685280 17685280 single base substitution G A intron_variant MELA-AU 6 17685485 17685485 single base substitution G A intron_variant MELA-AU 6 17685548 17685548 single base substitution G A intron_variant MELA-AU 6 17688030 17688030 single base substitution G A intron_variant MELA-AU 6 17688336 17688336 single base substitution G A intron_variant MELA-AU 6 17689022 17689022 single base substitution G A intron_variant MELA-AU 6 17689074 17689074 single base substitution G A intron_variant MELA-AU 6 17689131 17689131 single base substitution G A intron_variant MELA-AU 6 17689742 17689742 single base substitution T C intron_variant MELA-AU 6 17690608 17690608 single base substitution C T intron_variant MELA-AU 6 17690610 17690610 single base substitution C A intron_variant MELA-AU 6 17690815 17690815 single base substitution G A intron_variant MELA-AU 6 17690875 17690875 single base substitution G A intron_variant MELA-AU 6 17691425 17691425 insertion of <=200bp - T intron_variant MELA-AU 6 17691714 17691714 single base substitution G A intron_variant MELA-AU 6 17692275 17692275 single base substitution G A intron_variant MELA-AU 6 17692462 17692462 single base substitution G A intron_variant MELA-AU 6 17692582 17692582 single base substitution G A intron_variant MELA-AU 6 17693077 17693077 single base substitution G A intron_variant MELA-AU 6 17693135 17693135 single base substitution C T intron_variant MELA-AU 6 17694010 17694010 single base substitution G A intron_variant MELA-AU 6 17694573 17694573 single base substitution G A intron_variant MELA-AU 6 17694654 17694654 single base substitution C T intron_variant MELA-AU 6 17695076 17695076 single base substitution G A intron_variant MELA-AU 6 17695085 17695085 single base substitution C T intron_variant MELA-AU 6 17695483 17695483 single base substitution C T intron_variant MELA-AU 6 17695596 17695596 single base substitution A G intron_variant MELA-AU 6 17695958 17695958 single base substitution G A intron_variant MELA-AU 6 17696043 17696043 single base substitution A C intron_variant MELA-AU 6 17696216 17696217 multiple base substitution (>=2bp and <=200bp) GG AT intron_variant MELA-AU 6 17697161 17697163 multiple base substitution (>=2bp and <=200bp) GGC ATG intron_variant MELA-AU 6 17697392 17697392 single base substitution G A intron_variant MELA-AU 6 17697838 17697838 single base substitution G A intron_variant MELA-AU 6 17699087 17699087 single base substitution G A intron_variant MELA-AU 6 17699992 17699993 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 6 17700597 17700597 single base substitution A C intron_variant MELA-AU 6 17700670 17700670 single base substitution A G intron_variant MELA-AU 6 17701199 17701199 single base substitution C G intron_variant MELA-AU 6 17701708 17701708 single base substitution G A intron_variant MELA-AU 6 17702514 17702514 single base substitution G A intron_variant MELA-AU 6 17702830 17702830 single base substitution C T intron_variant MELA-AU 6 17702935 17702935 single base substitution A G intron_variant MELA-AU 6 17702939 17702939 single base substitution C T intron_variant MELA-AU 6 17703365 17703365 single base substitution G A intron_variant MELA-AU 6 17703416 17703416 single base substitution G A intron_variant MELA-AU 6 17704306 17704306 single base substitution G A intron_variant MELA-AU 6 17704431 17704431 single base substitution G A intron_variant MELA-AU 6 17704479 17704479 single base substitution C T intron_variant MELA-AU 6 17704572 17704572 single base substitution A G intron_variant MELA-AU 6 17704601 17704601 single base substitution C A intron_variant MELA-AU 6 17706364 17706364 single base substitution G A intron_variant MELA-AU 6 17706638 17706638 single base substitution C T 5_prime_UTR_variant MELA-AU 6 17706638 17706638 single base substitution C T upstream_gene_variant MELA-AU 6 17706978 17706979 multiple base substitution (>=2bp and <=200bp) GT AA upstream_gene_variant MELA-AU 6 17707222 17707222 single base substitution G A upstream_gene_variant MELA-AU 6 17707225 17707225 single base substitution G A upstream_gene_variant MELA-AU 6 17708104 17708104 single base substitution C T upstream_gene_variant MELA-AU 6 17708239 17708239 single base substitution C T upstream_gene_variant MELA-AU 6 17709392 17709392 single base substitution C T upstream_gene_variant MELA-AU 6 17710436 17710436 single base substitution G A upstream_gene_variant MELA-AU 6 17710808 17710808 single base substitution C T upstream_gene_variant MELA-AU 6 17711335 17711335 single base substitution G A upstream_gene_variant MELA-AU 6 17711555 17711555 single base substitution A G upstream_gene_variant ORCA-IN 6 17641973 17641973 single base substitution C T intron_variant ORCA-IN 6 17649971 17649971 single base substitution G A intron_variant ORCA-IN 6 17658745 17658745 single base substitution G A intron_variant ORCA-IN 6 17663047 17663047 single base substitution G A intron_variant ORCA-IN 6 17663493 17663493 single base substitution T C intron_variant ORCA-IN 6 17673073 17673073 single base substitution G C intron_variant ORCA-IN 6 17675874 17675874 single base substitution C A synonymous_variant S154S 462G>T ORCA-IN 6 17685155 17685155 single base substitution G A intron_variant ORCA-IN 6 17697070 17697070 single base substitution G A intron_variant OV-AU 6 17620472 17620472 single base substitution A T intron_variant OV-AU 6 17621499 17621499 single base substitution G C intron_variant OV-AU 6 17626463 17626463 single base substitution C G intron_variant OV-AU 6 17629723 17629723 single base substitution A C missense_variant F903V 2707T>G OV-AU 6 17629723 17629723 single base substitution A C missense_variant F934V 2800T>G OV-AU 6 17632551 17632551 single base substitution C A intron_variant OV-AU 6 17640169 17640169 single base substitution C G splice_donor_variant OV-AU 6 17641572 17641572 single base substitution C G intron_variant OV-AU 6 17647457 17647457 single base substitution G T intron_variant OV-AU 6 17654821 17654821 single base substitution G A intron_variant OV-AU 6 17684469 17684469 single base substitution G C intron_variant OV-AU 6 17688136 17688136 single base substitution G C intron_variant OV-AU 6 17699614 17699614 single base substitution T C intron_variant OV-AU 6 17703618 17703618 single base substitution A T intron_variant OV-AU 6 17705692 17705692 single base substitution T A intron_variant OV-AU 6 17706352 17706352 single base substitution C A intron_variant OV-AU 6 17707116 17707116 single base substitution T C upstream_gene_variant OV-AU 6 17707764 17707764 single base substitution G T upstream_gene_variant PACA-AU 6 17613190 17613190 single base substitution C A downstream_gene_variant PACA-AU 6 17625790 17625790 single base substitution T C intron_variant PACA-AU 6 17629155 17629155 single base substitution A T missense_variant L1092Q 3275T>A PACA-AU 6 17629155 17629155 single base substitution A T missense_variant L1123Q 3368T>A PACA-AU 6 17632551 17632551 single base substitution C A intron_variant PACA-AU 6 17638727 17638727 single base substitution G C intron_variant PACA-AU 6 17643884 17643884 single base substitution C T intron_variant PACA-AU 6 17643924 17643924 single base substitution C A intron_variant PACA-AU 6 17649449 17649449 single base substitution T A missense_variant E493V 1478A>T PACA-AU 6 17649449 17649449 single base substitution T A missense_variant E524V 1571A>T PACA-AU 6 17652982 17652982 single base substitution G A intron_variant PACA-AU 6 17660000 17660000 single base substitution C A intron_variant PACA-AU 6 17660589 17660589 single base substitution C T intron_variant PACA-AU 6 17664180 17664180 single base substitution A C intron_variant PACA-AU 6 17665382 17665382 single base substitution G C intron_variant PACA-AU 6 17667672 17667672 insertion of <=200bp - A intron_variant PACA-AU 6 17669065 17669065 single base substitution C T intron_variant PACA-AU 6 17670934 17670934 single base substitution A T intron_variant PACA-AU 6 17677961 17677961 single base substitution T C intron_variant PACA-AU 6 17683951 17683951 insertion of <=200bp - TTTA intron_variant PACA-AU 6 17686983 17686983 single base substitution C T intron_variant PACA-AU 6 17687301 17687301 single base substitution G A intron_variant PACA-AU 6 17692540 17692540 single base substitution C G intron_variant PACA-AU 6 17694183 17694183 single base substitution C A intron_variant PACA-AU 6 17694355 17694355 single base substitution C A intron_variant PACA-AU 6 17694979 17694979 single base substitution G C intron_variant PACA-AU 6 17700442 17700442 deletion of <=200bp T - intron_variant PACA-AU 6 17703345 17703352 deletion of <=200bp AATGAACC - intron_variant PACA-AU 6 17705158 17705158 deletion of <=200bp T - intron_variant PACA-AU 6 17705942 17705944 deletion of <=200bp GAG - intron_variant PACA-AU 6 17707185 17707185 insertion of <=200bp - C upstream_gene_variant PACA-AU 6 17711398 17711398 single base substitution T A upstream_gene_variant PACA-AU 6 17711399 17711399 single base substitution A T upstream_gene_variant PACA-CA 6 17610524 17610524 single base substitution C T downstream_gene_variant PACA-CA 6 17613905 17613905 single base substitution A G downstream_gene_variant PACA-CA 6 17615503 17615503 single base substitution A T 3_prime_UTR_variant PACA-CA 6 17615503 17615503 single base substitution A T downstream_gene_variant PACA-CA 6 17617364 17617364 single base substitution C G intron_variant PACA-CA 6 17618259 17618259 single base substitution G A intron_variant PACA-CA 6 17618262 17618262 single base substitution C A intron_variant PACA-CA 6 17618353 17618353 single base substitution T C intron_variant PACA-CA 6 17620201 17620201 single base substitution C T intron_variant PACA-CA 6 17621020 17621020 single base substitution G A intron_variant PACA-CA 6 17623306 17623306 single base substitution A G intron_variant PACA-CA 6 17628880 17628880 single base substitution A G splice_region_variant PACA-CA 6 17628919 17628919 single base substitution A T missense_variant F1171I 3511T>A PACA-CA 6 17628919 17628919 single base substitution A T missense_variant F1202I 3604T>A PACA-CA 6 17631012 17631012 single base substitution G C intron_variant PACA-CA 6 17631647 17631647 single base substitution C A intron_variant PACA-CA 6 17639326 17639326 single base substitution A T intron_variant PACA-CA 6 17639371 17639371 single base substitution C T intron_variant PACA-CA 6 17641425 17641425 single base substitution T C intron_variant PACA-CA 6 17643338 17643338 single base substitution C T intron_variant PACA-CA 6 17644877 17644877 insertion of <=200bp - A intron_variant PACA-CA 6 17648622 17648622 single base substitution C T intron_variant PACA-CA 6 17652000 17652000 single base substitution T C intron_variant PACA-CA 6 17661426 17661426 single base substitution T C intron_variant PACA-CA 6 17661615 17661615 single base substitution A G intron_variant PACA-CA 6 17661652 17661652 single base substitution T C intron_variant PACA-CA 6 17663508 17663508 single base substitution T A intron_variant PACA-CA 6 17670037 17670037 single base substitution A C intron_variant PACA-CA 6 17673053 17673053 single base substitution T A intron_variant PACA-CA 6 17682452 17682452 insertion of <=200bp - A intron_variant PACA-CA 6 17687880 17687880 single base substitution A C intron_variant PACA-CA 6 17688790 17688791 deletion of <=200bp TC - frameshift_variant R57 PACA-CA 6 17689496 17689496 single base substitution T C intron_variant PACA-CA 6 17698746 17698746 single base substitution G T intron_variant PACA-CA 6 17700710 17700710 single base substitution T G intron_variant PACA-CA 6 17704136 17704136 insertion of <=200bp - T intron_variant PACA-CA 6 17711607 17711607 single base substitution C T upstream_gene_variant PAEN-AU 6 17699429 17699429 single base substitution T A intron_variant PAEN-AU 6 17701387 17701387 single base substitution T G intron_variant PAEN-IT 6 17643154 17643154 single base substitution G A intron_variant PAEN-IT 6 17694331 17694331 single base substitution G A intron_variant PBCA-DE 6 17614614 17614614 deletion of <=200bp A - downstream_gene_variant PBCA-DE 6 17630655 17630655 single base substitution C A intron_variant PBCA-DE 6 17643071 17643071 single base substitution T C intron_variant PBCA-DE 6 17646163 17646163 single base substitution T C intron_variant PBCA-DE 6 17652112 17652112 single base substitution C T intron_variant PBCA-DE 6 17652112 17652112 single base substitution C T missense_variant A481T 1441G>A PBCA-DE 6 17659448 17659448 single base substitution C T intron_variant PBCA-DE 6 17663461 17663461 single base substitution A T intron_variant PBCA-DE 6 17663463 17663463 single base substitution T C intron_variant PBCA-DE 6 17670613 17670613 single base substitution C T intron_variant PBCA-DE 6 17672647 17672647 deletion of <=200bp A - intron_variant PBCA-DE 6 17686950 17686950 single base substitution A T intron_variant PBCA-DE 6 17689102 17689102 single base substitution C A intron_variant PBCA-DE 6 17691097 17691097 single base substitution G A intron_variant PBCA-DE 6 17696240 17696240 insertion of <=200bp - A intron_variant PBCA-DE 6 17705360 17705360 single base substitution C A intron_variant PRAD-CA 6 17613693 17613693 single base substitution A C downstream_gene_variant PRAD-CA 6 17620286 17620286 single base substitution A T intron_variant PRAD-CA 6 17628853 17628853 single base substitution T A intron_variant PRAD-CA 6 17656544 17656544 single base substitution C T intron_variant PRAD-CA 6 17663493 17663493 single base substitution T C intron_variant PRAD-CA 6 17679192 17679192 single base substitution A T intron_variant PRAD-CA 6 17683538 17683538 single base substitution G C intron_variant PRAD-CA 6 17691739 17691739 single base substitution T C intron_variant PRAD-UK 6 17615976 17615976 single base substitution C T 3_prime_UTR_variant PRAD-UK 6 17615976 17615976 single base substitution C T downstream_gene_variant PRAD-UK 6 17620873 17620873 single base substitution C A intron_variant PRAD-UK 6 17631021 17631021 insertion of <=200bp - GGGGAGAGGAGAGAAGAGAGC intron_variant PRAD-UK 6 17637222 17637222 single base substitution A G intron_variant PRAD-UK 6 17643903 17643903 single base substitution T A intron_variant PRAD-UK 6 17645953 17645953 single base substitution C T intron_variant PRAD-UK 6 17647515 17647515 single base substitution C A intron_variant READ-US 6 17637996 17637996 single base substitution C T missense_variant A618T 1852G>A READ-US 6 17637996 17637996 single base substitution C T missense_variant A649T 1945G>A READ-US 6 17675845 17675845 single base substitution G A missense_variant S164F 491C>T RECA-EU 6 17626147 17626147 single base substitution T A missense_variant S1265C 3793A>T RECA-EU 6 17626147 17626147 single base substitution T A missense_variant S1296C 3886A>T RECA-EU 6 17637057 17637057 single base substitution T A intron_variant RECA-EU 6 17663019 17663019 single base substitution C T intron_variant RECA-EU 6 17664259 17664259 single base substitution A G intron_variant RECA-EU 6 17667639 17667639 single base substitution G A intron_variant RECA-EU 6 17670934 17670934 single base substitution A G intron_variant RECA-EU 6 17677314 17677314 single base substitution A C intron_variant RECA-EU 6 17685779 17685779 single base substitution C A intron_variant SKCA-BR 6 17612806 17612806 single base substitution G T downstream_gene_variant SKCA-BR 6 17614870 17614870 single base substitution G C downstream_gene_variant SKCA-BR 6 17615248 17615248 single base substitution G A downstream_gene_variant SKCA-BR 6 17618793 17618795 deletion of <=200bp CTT - intron_variant SKCA-BR 6 17625930 17625930 single base substitution G A intron_variant SKCA-BR 6 17626334 17626334 single base substitution T G synonymous_variant T1202T 3606A>C SKCA-BR 6 17626334 17626334 single base substitution T G synonymous_variant T1233T 3699A>C SKCA-BR 6 17628482 17628482 single base substitution G A intron_variant SKCA-BR 6 17633077 17633077 insertion of <=200bp - TAA splice_acceptor_variant SKCA-BR 6 17635329 17635329 single base substitution G A intron_variant SKCA-BR 6 17637143 17637143 single base substitution G A intron_variant SKCA-BR 6 17638640 17638640 single base substitution A C intron_variant SKCA-BR 6 17638663 17638663 single base substitution A C intron_variant SKCA-BR 6 17645041 17645041 single base substitution G A intron_variant SKCA-BR 6 17649677 17649677 single base substitution G A intron_variant SKCA-BR 6 17650259 17650259 single base substitution C T intron_variant SKCA-BR 6 17650446 17650446 single base substitution C T intron_variant SKCA-BR 6 17654213 17654213 single base substitution A T intron_variant SKCA-BR 6 17657624 17657624 single base substitution T A intron_variant SKCA-BR 6 17660581 17660581 single base substitution T C intron_variant SKCA-BR 6 17663296 17663296 single base substitution G A intron_variant SKCA-BR 6 17663489 17663493 deletion of <=200bp CACAT - intron_variant SKCA-BR 6 17663493 17663493 single base substitution T C intron_variant SKCA-BR 6 17664410 17664410 single base substitution C T intron_variant SKCA-BR 6 17665341 17665341 single base substitution T A intron_variant SKCA-BR 6 17668300 17668302 deletion of <=200bp CTT - intron_variant SKCA-BR 6 17668405 17668405 single base substitution C A intron_variant SKCA-BR 6 17670314 17670314 single base substitution G A intron_variant SKCA-BR 6 17672256 17672256 single base substitution T C intron_variant SKCA-BR 6 17674001 17674001 single base substitution A C intron_variant SKCA-BR 6 17676489 17676489 single base substitution A G intron_variant SKCA-BR 6 17683494 17683494 single base substitution A G intron_variant SKCA-BR 6 17684075 17684075 single base substitution A T intron_variant SKCA-BR 6 17685135 17685135 single base substitution C T intron_variant SKCA-BR 6 17685399 17685400 deletion of <=200bp AC - intron_variant SKCA-BR 6 17687074 17687074 single base substitution C T intron_variant SKCA-BR 6 17690366 17690366 single base substitution G A intron_variant SKCA-BR 6 17691158 17691158 single base substitution C G intron_variant SKCA-BR 6 17692391 17692391 single base substitution G A intron_variant SKCA-BR 6 17692810 17692810 single base substitution G A intron_variant SKCA-BR 6 17693030 17693030 single base substitution C G intron_variant SKCA-BR 6 17694283 17694283 single base substitution C T intron_variant SKCA-BR 6 17697285 17697285 single base substitution G A intron_variant SKCA-BR 6 17697895 17697895 single base substitution G A intron_variant SKCA-BR 6 17698644 17698644 single base substitution G A intron_variant SKCA-BR 6 17701015 17701015 single base substitution G A intron_variant SKCA-BR 6 17702076 17702076 single base substitution A G intron_variant SKCA-BR 6 17704269 17704269 single base substitution A C intron_variant SKCA-BR 6 17705582 17705582 single base substitution C T intron_variant SKCA-BR 6 17707166 17707166 single base substitution C T upstream_gene_variant SKCA-BR 6 17707222 17707222 single base substitution G A upstream_gene_variant SKCA-BR 6 17707245 17707245 single base substitution C T upstream_gene_variant SKCA-BR 6 17708451 17708451 single base substitution T C upstream_gene_variant SKCA-BR 6 17708454 17708454 single base substitution A C upstream_gene_variant SKCA-BR 6 17709613 17709613 single base substitution G A upstream_gene_variant SKCM-US 6 17629689 17629689 single base substitution G A missense_variant P914L 2741C>T SKCM-US 6 17629689 17629689 single base substitution G A missense_variant P945L 2834C>T SKCM-US 6 17633028 17633028 single base substitution G A missense_variant P838S 2512C>T SKCM-US 6 17633028 17633028 single base substitution G A missense_variant P869S 2605C>T SKCM-US 6 17637499 17637499 single base substitution G A synonymous_variant T783T 2349C>T SKCM-US 6 17637499 17637499 single base substitution G A synonymous_variant T814T 2442C>T SKCM-US 6 17637557 17637557 single base substitution G A missense_variant S764L 2291C>T SKCM-US 6 17637557 17637557 single base substitution G A missense_variant S795L 2384C>T SKCM-US 6 17637606 17637606 single base substitution G A missense_variant P748S 2242C>T SKCM-US 6 17637606 17637606 single base substitution G A missense_variant P779S 2335C>T SKCM-US 6 17637746 17637746 single base substitution T C missense_variant N701S 2102A>G SKCM-US 6 17637746 17637746 single base substitution T C missense_variant N732S 2195A>G SKCM-US 6 17637899 17637899 single base substitution A C missense_variant I650S 1949T>G SKCM-US 6 17637899 17637899 single base substitution A C missense_variant I681S 2042T>G SKCM-US 6 17648081 17648081 single base substitution G A missense_variant P530L 1589C>T SKCM-US 6 17648081 17648081 single base substitution G A missense_variant P561L 1682C>T SKCM-US 6 17649490 17649490 single base substitution G A synonymous_variant I479I 1437C>T SKCM-US 6 17649490 17649490 single base substitution G A synonymous_variant I510I 1530C>T SKCM-US 6 17665598 17665598 single base substitution G A missense_variant P363S 1087C>T SKCM-US 6 17669558 17669558 single base substitution C T missense_variant R327K 980G>A SKCM-US 6 17675216 17675216 single base substitution G A missense_variant P258S 772C>T SKCM-US 6 17675478 17675478 single base substitution G A synonymous_variant A235A 705C>T SKCM-US 6 17675575 17675575 single base substitution G A missense_variant S203L 608C>T STAD-US 6 17624851 17624851 insertion of <=200bp - G frameshift_variant P1372P? STAD-US 6 17624851 17624851 insertion of <=200bp - G frameshift_variant P1403P? STAD-US 6 17626217 17626217 single base substitution A G synonymous_variant G1241G 3723T>C STAD-US 6 17626217 17626217 single base substitution A G synonymous_variant G1272G 3816T>C STAD-US 6 17626268 17626268 single base substitution A G synonymous_variant A1224A 3672T>C STAD-US 6 17626268 17626268 single base substitution A G synonymous_variant A1255A 3765T>C STAD-US 6 17628924 17628924 single base substitution G A missense_variant A1169V 3506C>T STAD-US 6 17628924 17628924 single base substitution G A missense_variant A1200V 3599C>T STAD-US 6 17629339 17629339 single base substitution A C missense_variant S1031A 3091T>G STAD-US 6 17629339 17629339 single base substitution A C missense_variant S1062A 3184T>G STAD-US 6 17629488 17629488 single base substitution A C missense_variant F1012C 3035T>G STAD-US 6 17629488 17629488 single base substitution A C missense_variant F981C 2942T>G STAD-US 6 17629497 17629497 single base substitution T C missense_variant N1009S 3026A>G STAD-US 6 17629497 17629497 single base substitution T C missense_variant N978S 2933A>G STAD-US 6 17629536 17629536 single base substitution G C missense_variant S965C 2894C>G STAD-US 6 17629536 17629536 single base substitution G C missense_variant S996C 2987C>G STAD-US 6 17629625 17629625 single base substitution A C synonymous_variant G935G 2805T>G STAD-US 6 17629625 17629625 single base substitution A C synonymous_variant G966G 2898T>G STAD-US 6 17629625 17629625 single base substitution A G synonymous_variant G935G 2805T>C STAD-US 6 17629625 17629625 single base substitution A G synonymous_variant G966G 2898T>C STAD-US 6 17632903 17632903 single base substitution T C synonymous_variant P879P 2637A>G STAD-US 6 17632903 17632903 single base substitution T C synonymous_variant P910P 2730A>G STAD-US 6 17632925 17632925 single base substitution A G missense_variant L872S 2615T>C STAD-US 6 17632925 17632925 single base substitution A G missense_variant L903S 2708T>C STAD-US 6 17637492 17637492 single base substitution A C missense_variant F786V 2356T>G STAD-US 6 17637492 17637492 single base substitution A C missense_variant F817V 2449T>G STAD-US 6 17637537 17637537 single base substitution T A missense_variant T771S 2311A>T STAD-US 6 17637537 17637537 single base substitution T A missense_variant T802S 2404A>T STAD-US 6 17637582 17637582 single base substitution G A stop_gained R756* 2266C>T STAD-US 6 17637582 17637582 single base substitution G A stop_gained R787* 2359C>T STAD-US 6 17637996 17637996 single base substitution C T missense_variant A618T 1852G>A STAD-US 6 17637996 17637996 single base substitution C T missense_variant A649T 1945G>A STAD-US 6 17640225 17640225 deletion of <=200bp A - frameshift_variant F597 STAD-US 6 17640225 17640225 deletion of <=200bp A - frameshift_variant F628 STAD-US 6 17648090 17648090 single base substitution A C missense_variant F527C 1580T>G STAD-US 6 17648090 17648090 single base substitution A C missense_variant F558C 1673T>G STAD-US 6 17665556 17665556 single base substitution T C missense_variant T377A 1129A>G STAD-US 6 17675564 17675564 single base substitution G C missense_variant L207V 619C>G STAD-US 6 17675805 17675822 deletion of <=200bp ATCATGCTGAGAGGTAGA - inframe_deletion STSQHD172 THCA-SA 6 17649515 17649515 insertion of <=200bp - T frameshift_variant V471V? THCA-SA 6 17649515 17649515 insertion of <=200bp - T frameshift_variant V502V? THCA-SA 6 17675553 17675553 single base substitution T C synonymous_variant P210P 630A>G UCEC-US 6 17616370 17616370 single base substitution G T missense_variant F1462L 4386C>A UCEC-US 6 17616370 17616370 single base substitution G T missense_variant F1493L 4479C>A UCEC-US 6 17624983 17624983 single base substitution C T missense_variant G1328E 3983G>A UCEC-US 6 17624983 17624983 single base substitution C T missense_variant G1359E 4076G>A UCEC-US 6 17628931 17628931 single base substitution C T missense_variant A1167T 3499G>A UCEC-US 6 17628931 17628931 single base substitution C T missense_variant A1198T 3592G>A UCEC-US 6 17628942 17628942 single base substitution G T missense_variant S1163Y 3488C>A UCEC-US 6 17628942 17628942 single base substitution G T missense_variant S1194Y 3581C>A UCEC-US 6 17629013 17629013 single base substitution C T synonymous_variant E1139E 3417G>A UCEC-US 6 17629013 17629013 single base substitution C T synonymous_variant E1170E 3510G>A UCEC-US 6 17629205 17629205 single base substitution C T missense_variant M1075I 3225G>A UCEC-US 6 17629205 17629205 single base substitution C T missense_variant M1106I 3318G>A UCEC-US 6 17629253 17629253 single base substitution T C synonymous_variant S1059S 3177A>G UCEC-US 6 17629253 17629253 single base substitution T C synonymous_variant S1090S 3270A>G UCEC-US 6 17629507 17629507 single base substitution C A missense_variant D1006Y 3016G>T UCEC-US 6 17629507 17629507 single base substitution C A missense_variant D975Y 2923G>T UCEC-US 6 17629522 17629522 single base substitution C T missense_variant E1001K 3001G>A UCEC-US 6 17629522 17629522 single base substitution C T missense_variant E970K 2908G>A UCEC-US 6 17629745 17629745 single base substitution C T synonymous_variant S895S 2685G>A UCEC-US 6 17629745 17629745 single base substitution C T synonymous_variant S926S 2778G>A UCEC-US 6 17637421 17637421 single base substitution T G missense_variant E809D 2427A>C UCEC-US 6 17637421 17637421 single base substitution T G missense_variant E840D 2520A>C UCEC-US 6 17637461 17637461 single base substitution G T missense_variant S796Y 2387C>A UCEC-US 6 17637461 17637461 single base substitution G T missense_variant S827Y 2480C>A UCEC-US 6 17637957 17637957 single base substitution C T missense_variant A631T 1891G>A UCEC-US 6 17637957 17637957 single base substitution C T missense_variant A662T 1984G>A UCEC-US 6 17637988 17637988 single base substitution C T synonymous_variant P620P 1860G>A UCEC-US 6 17637988 17637988 single base substitution C T synonymous_variant P651P 1953G>A UCEC-US 6 17648119 17648119 single base substitution C T synonymous_variant P517P 1551G>A UCEC-US 6 17648119 17648119 single base substitution C T synonymous_variant P548P 1644G>A UCEC-US 6 17665546 17665546 single base substitution C A missense_variant S380I 1139G>T UCEC-US 6 17665549 17665549 single base substitution C T missense_variant R379Q 1136G>A UCEC-US 6 17669229 17669229 single base substitution C A missense_variant D349Y 1045G>T UCEC-US 6 17669569 17669569 single base substitution C A splice_acceptor_variant UCEC-US 6 17669757 17669757 single base substitution C A missense_variant M291I 873G>T UCEC-US 6 17688743 17688743 single base substitution C T missense_variant S73N 218G>A UCEC-US 6 17688850 17688850 single base substitution C T splice_acceptor_variant UCEC-US 6 17706608 17706608 single base substitution C T missense_variant G4E 11G>A

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand TCGA-BR-8485-01 COSM3860595 c.2942T>G p.F981C Substitution - Missense 6:17629257-17629257 - CHC2351T COSM4801194 c.3281T>C p.F1094S Substitution - Missense 6:17629011-17629011 - TCGA-D3-A2J8-06 COSM4897907 c.772C>T p.P258S Substitution - Missense 6:17674985-17674985 - I2L-P19Tb-Tumor-Biopsy COSM5357034 c.4465_4467delTCT p.S1489delS Deletion - In frame 6:17616151-17616153 - PT40 COSM5943161 c.1015-3_1015-2insT p.? Unknown 6:17669030-17669031 - PTC-46C COSM4160390 c.3606A>C p.T1202T Substitution - coding silent 6:17626103-17626103 - Pat_01_A COSM5869821 c.2465-3_2465-2insTT p.? Unknown 6:17632846-17632847 - EV005-R5 COSM4410715 c.527A>G p.H176R Substitution - Missense 6:17675578-17675578 - T03 COSM5065071 c.2798C>A p.S933Y Substitution - Missense 6:17629494-17629494 - TCGA-AP-A051-01 COSM4872551 c.4076G>A p.G1359E Substitution - Missense 6:17624752-17624752 - 8012341 COSM4781652 c.1571A>T p.E524V Substitution - Missense 6:17649218-17649218 - TCGA-HU-8604-01 COSM3860597 c.2933A>G p.N978S Substitution - Missense 6:17629266-17629266 - TCGA-D5-6930-01 COSM4615772 c.684_685insA p.P229fs*22 Insertion - Frameshift 6:17675267-17675268 - PD4980a COSM5771635 c.2541T>G p.C847W Substitution - Missense 6:17637169-17637169 - PCSI_0083_Pa_P_526 COSM3782042 c.3637+6T>C p.? Unknown 6:17628649-17628649 - BZ08 COSM5758038 c.67C>A p.Q23K Substitution - Missense 6:17706321-17706321 - TCGA-EE-A2MS-06 COSM4904209 c.1530C>T p.I510I Substitution - coding silent 6:17649259-17649259 - SNUH_G76_S1 COSM4418219 c.268G>A p.D90N Substitution - Missense 6:17688462-17688462 - TCGA-AX-A05Z-01 COSM1076292 c.1551G>A p.P517P Substitution - coding silent 6:17647888-17647888 - COLO205 COSM4353175 c.994G>T p.V332F Substitution - Missense 6:17669313-17669313 - TCGA-F5-6814-01 COSM4782375 c.491C>T p.S164F Substitution - Missense 6:17675614-17675614 - TCGA-BP-4346-01 COSM4858291 c.2371T>C p.L791L Substitution - coding silent 6:17637339-17637339 - T22 COSM5345111 c.777T>A p.F259L Substitution - Missense 6:17674980-17674980 - T22 COSM5345109 c.778T>A p.Y260N Substitution - Missense 6:17674979-17674979 - T1154 COSM4708698 c.1239A>G p.T413T Substitution - coding silent 6:17662047-17662047 - 2334193 COSM322145 c.1307A>G p.N436S Substitution - Missense 6:17661741-17661741 - HCC2998 COSM1672256 c.2016A>C p.K672N Substitution - Missense 6:17637601-17637601 - TCGA-AM-5821-01 COSM3761704 c.1206C>G p.N402K Substitution - Missense 6:17665248-17665248 - TCGA-AP-A051-01 COSM4872326 c.1045G>T p.D349Y Substitution - Missense 6:17668998-17668998 - CN-AML-CR-30-Dx COSM4003803 c.2465-3T>C p.? Unknown 6:17632847-17632847 - TP_2060 COSM5573202 c.1725+1G>A p.? Unknown 6:17647806-17647806 - PD9004a COSM5785910 c.3716C>T p.A1239V Substitution - Missense 6:17625993-17625993 - S00836 COSM313420 c.2082G>T p.Q694H Substitution - Missense 6:17637535-17637535 - TCGA-LP-A5U2-01 COSM4833676 c.3896C>G p.S1299C Substitution - Missense 6:17625813-17625813 - RMS110_ COSM4985443 c.2558-1G>T p.? Unknown 6:17632845-17632845 - PCSI_0547_Pa_P_526 COSM5032006 c.3604T>A p.F1202I Substitution - Missense 6:17628688-17628688 - QC2-39-T2 COSM5655530 c.181A>G p.K61E Substitution - Missense 6:17688549-17688549 - HCT15 COSM4353176 c.968C>T p.A323V Substitution - Missense 6:17669431-17669431 - TCGA-FW-A3R5-06 COSM3921111 c.705C>T p.A235A Substitution - coding silent 6:17675247-17675247 - 2521249 COSM5895174 c.2465-2_2465-1insTT p.? Unknown 6:17632845-17632846 - 2246952 COSM4413503 c.2345G>T p.G782V Substitution - Missense 6:17637272-17637272 - TCGA-G4-6586-01 COSM3860615 c.1945G>A p.A649T Substitution - Missense 6:17637765-17637765 - TCGA-C8-A12P-01 COSM4814551 c.2105A>T p.N702I Substitution - Missense 6:17637605-17637605 - TCGA-66-2770-01 COSM4859399 c.894A>T p.A298A Substitution - coding silent 6:17669505-17669505 - TCGA-BH-A0BF-01 COSM4815133 c.1006C>G p.L336V Substitution - Missense 6:17669301-17669301 - TCGA-AN-A0G0-01 COSM4815664 c.3250A>T p.I1084L Substitution - Missense 6:17629042-17629042 - HCC058T COSM5804510 c.3993A>T p.Q1331H Substitution - Missense 6:17624742-17624742 - LUAD-YINHD COSM351355 c.2483C>T p.S828L Substitution - Missense 6:17632826-17632826 - TCGA-06-2564-01 COSM3948814 c.3166G>A p.G1056S Substitution - Missense 6:17629126-17629126 - 450 COSM4435674 c.3427G>T p.D1143Y Substitution - Missense 6:17628772-17628772 - I2L-P19Tb-Tumor-Biopsy COSM5357033 c.4372_4374delTCT p.S1458delS Deletion - In frame 6:17616151-17616153 - TCGA-61-1998-01 COSM71902 c.2084C>G p.T695S Substitution - Missense 6:17637533-17637533 - TCGA-AY-6197-01 COSM4948344 c.781C>A p.P261T Substitution - Missense 6:17674976-17674976 - PD4937a COSM163022 c.4028C>G p.S1343C Substitution - Missense 6:17624707-17624707 - TCGA-66-2773-01 COSM4861815 c.3926G>C p.G1309A Substitution - Missense 6:17625876-17625876 - TCGA-AX-A05Z-01 COSM1076296 c.1136G>A p.R379Q Substitution - Missense 6:17665318-17665318 - TCGA-AP-A0LE-01 COSM1076277 c.3177A>G p.S1059S Substitution - coding silent 6:17629022-17629022 - CHC793T COSM4801345 c.1644A>G p.T548T Substitution - coding silent 6:17646143-17646143 - CSCC-31-T COSM4480721 c.2445C>T p.S815S Substitution - coding silent 6:17637172-17637172 - Gp2D COSM2855865 c.805G>A p.A269T Substitution - Missense 6:17674952-17674952 - TCGA-B4-5838-01 COSM1496242 c.87C>G p.Y29* Substitution - Nonsense 6:17706301-17706301 - PDA_055 COSM4783709 c.742A>G p.I248V Substitution - Missense 6:17675015-17675015 - PD4000a COSM163020 c.4386C>G p.F1462L Substitution - Missense 6:17616139-17616139 - EV005-R2 COSM4410716 c.527A>G p.H176R Substitution - Missense 6:17675578-17675578 - BD242T COSM5495820 c.3478G>A p.E1160K Substitution - Missense 6:17628721-17628721 - TCGA-A5-A0GB-01 COSM4874125 c.3581C>A p.S1194Y Substitution - Missense 6:17628711-17628711 - TCGA-AO-A12E-01 COSM1218068 c.397C>T p.R133W Substitution - Missense 6:17675708-17675708 - TCGA-46-3769-01 COSM4859313 c.2485G>T p.E829* Substitution - Nonsense 6:17637225-17637225 - ccRCC-90 COSM1663178 c.4216T>A p.F1406I Substitution - Missense 6:17616654-17616654 - TCGA-EE-A29E-06 COSM4891859 c.1682C>T p.P561L Substitution - Missense 6:17647850-17647850 - TCGA-BR-6452-01 COSM3860610 c.2449T>G p.F817V Substitution - Missense 6:17637261-17637261 - PD4000a COSM4809850 c.4479C>G p.F1493L Substitution - Missense 6:17616139-17616139 - 31231321 COSM1582671 c.1964G>A p.S655N Substitution - Missense 6:17637653-17637653 - PD11745a COSM2855852 c.1298C>T p.P433L Substitution - Missense 6:17661750-17661750 - TCGA-B5-A11W-01 COSM1076283 c.2685G>A p.S895S Substitution - coding silent 6:17629514-17629514 - P125 COSM1735947 c.1015-4delT p.? Unknown 6:17669032-17669032 - TCGA-B5-A11E-01 COSM1076302 c.970-1G>T p.? Unknown 6:17669338-17669338 - TCGA-BR-6452-01 COSM3860609 c.2356T>G p.F786V Substitution - Missense 6:17637261-17637261 - CHEWS012 COSM1442380 c.1852G>A p.A618T Substitution - Missense 6:17637765-17637765 - TCGA-AP-A0LP-01 COSM1076308 c.112-1G>A p.? Unknown 6:17688619-17688619 - TCGA-BR-6565-01 COSM3860599 c.2894C>G p.S965C Substitution - Missense 6:17629305-17629305 - TCGA-HU-A4H4-01 COSM3860618 c.1129A>G p.T377A Substitution - Missense 6:17665325-17665325 - C0074T COSM4422421 c.3793A>T p.S1265C Substitution - Missense 6:17625916-17625916 - TCGA-AY-6197-01 COSM1442381 c.781C>A p.P261T Substitution - Missense 6:17674976-17674976 - TCGA-G4-6303-01 COSM5830349 c.2465-3_2465-2insT p.? Unknown 6:17632846-17632847 - TCGA-BS-A0UV-01 COSM1076281 c.2908G>A p.E970K Substitution - Missense 6:17629291-17629291 - Pat_40_B COSM4708702 c.684delA p.K228fs*46 Deletion - Frameshift 6:17675268-17675268 - T3503 COSM4708694 c.3458C>T p.A1153V Substitution - Missense 6:17628834-17628834 - TCGA-FW-A3R5-06 COSM3921110 c.2834C>T p.P945L Substitution - Missense 6:17629458-17629458 - 234 COSM3730671 c.1015-7_1015-4delTTTT p.? Unknown 6:17669032-17669035 - TCGA-BR-4184-01 COSM3860615 c.1945G>A p.A649T Substitution - Missense 6:17637765-17637765 - TCGA-DK-A2I4-01 COSM3777333 c.355G>A p.A119T Substitution - Missense 6:17675750-17675750 - TCGA-60-2715-01 COSM4860847 c.1887A>C p.R629S Substitution - Missense 6:17639991-17639991 - RMS110_ COSM4985442 c.2465-1G>T p.? Unknown 6:17632845-17632845 - PT20_1 COSM5943430 c.2558-3delT p.? Unknown 6:17632847-17632847 - TCGA-AX-A0J0-01 COSM1076285 c.2427A>C p.E809D Substitution - Missense 6:17637190-17637190 - CN-AML-NR-07-Dx COSM4003803 c.2465-3T>C p.? Unknown 6:17632847-17632847 - TCGA-EE-A183-06 COSM3623060 c.1087C>T p.P363S Substitution - Missense 6:17665367-17665367 - PD4197a COSM4810080 c.2391T>C p.S797S Substitution - coding silent 6:17637319-17637319 - TCGA-AD-6964-01 COSM1442377 c.3177A>C p.S1059S Substitution - coding silent 6:17629022-17629022 - EGC3 COSM5061657 c.2962G>A p.G988R Substitution - Missense 6:17629330-17629330 - TCGA-AC-A2BM-01 COSM3829714 c.2085T>A p.T695T Substitution - coding silent 6:17637532-17637532 - RD COSM4985443 c.2558-1G>T p.? Unknown 6:17632845-17632845 - AOCS-109-1-X COSM4149288 c.1939+1G>C p.? Unknown 6:17639938-17639938 - TCGA-AP-A0LM-01 COSM4873444 c.3510G>A p.E1170E Substitution - coding silent 6:17628782-17628782 - 61 COSM5737486 c.928C>T p.R310* Substitution - Nonsense 6:17669471-17669471 - 587376 COSM1218070 c.1567C>T p.P523S Substitution - Missense 6:17647872-17647872 - 61 COSM5737483 c.3337T>C p.F1113L Substitution - Missense 6:17628955-17628955 - S02292 COSM5688085 c.1068+3A>G p.? Unknown 6:17668972-17668972 - TCGA-CG-5721-01 COSM3860613 c.2266C>T p.R756* Substitution - Nonsense 6:17637351-17637351 - T03 COSM5065070 c.2705C>A p.S902Y Substitution - Missense 6:17629494-17629494 - MO_1128 COSM5567394 c.4178C>T p.S1393L Substitution - Missense 6:17616692-17616692 - ME032T COSM227268 c.4165C>T p.P1389S Substitution - Missense 6:17624570-17624570 - PT40 COSM5943162 c.1015-3_1015-2insT p.? Unknown 6:17669030-17669031 - 74 COSM4777914 c.710G>T p.G237V Substitution - Missense 6:17675242-17675242 - TCGA-AA-3821-01 COSM294633 c.3059C>A p.A1020E Substitution - Missense 6:17629140-17629140 - PD4937a COSM4810301 c.4121C>G p.S1374C Substitution - Missense 6:17624707-17624707 - CN-AML-CR-30-Dx COSM4003804 c.2558-3T>C p.? Unknown 6:17632847-17632847 - TCGA-AP-A051-01 COSM1076268 c.3983G>A p.G1328E Substitution - Missense 6:17624752-17624752 - TCGA-EI-6917-01 COSM3860615 c.1945G>A p.A649T Substitution - Missense 6:17637765-17637765 - CHEWS012 COSM3860615 c.1945G>A p.A649T Substitution - Missense 6:17637765-17637765 - BD124T COSM5492005 c.494T>C p.L165P Substitution - Missense 6:17675611-17675611 - TCGA-AP-A059-01 COSM4866815 c.3592G>A p.A1198T Substitution - Missense 6:17628700-17628700 - T3090 COSM4708701 c.999T>G p.S333S Substitution - coding silent 6:17669308-17669308 - TCGA-33-4566-01 COSM4860077 c.158G>T p.G53V Substitution - Missense 6:17688572-17688572 - TCGA-AD-6964-01 COSM4786437 c.3270A>C p.S1090S Substitution - coding silent 6:17629022-17629022 - Pat_37_B COSM5869814 c.4369G>A p.A1457T Substitution - Missense 6:17616594-17616594 - B74 COSM1754664 c.1806C>T p.I602I Substitution - coding silent 6:17639979-17639979 - CN-AML-07-T COSM4003803 c.2465-3T>C p.? Unknown 6:17632847-17632847 - TCGA-D1-A17Q-01 COSM1076287 c.2387C>A p.S796Y Substitution - Missense 6:17637230-17637230 - PDA_055 COSM3761706 c.742A>G p.I248V Substitution - Missense 6:17675015-17675015 - 3T COSM3715366 c.462G>T p.S154S Substitution - coding silent 6:17675643-17675643 - pfg016T COSM1642954 c.1232delA p.N411fs*2 Deletion - Frameshift 6:17662054-17662054 - TCGA-60-2715-01 COSM741047 c.1798G>T p.A600S Substitution - Missense 6:17639987-17639987 - HCC078T COSM5806165 c.671C>G p.T224S Substitution - Missense 6:17675281-17675281 - TCGA-AP-A0LM-01 COSM96089 c.3417G>A p.E1139E Substitution - coding silent 6:17628782-17628782 - TCGA-CD-8531-01 COSM3860602 c.2898T>G p.G966G Substitution - coding silent 6:17629394-17629394 - YUROC COSM5404850 c.3080G>A p.G1027D Substitution - Missense 6:17629119-17629119 - TCGA-EE-A183-06 COSM4905926 c.1087C>T p.P363S Substitution - Missense 6:17665367-17665367 - TCGA-39-5037-01 COSM741044 c.1470T>C p.S490S Substitution - coding silent 6:17649226-17649226 - 255 COSM3730671 c.1015-7_1015-4delTTTT p.? Unknown 6:17669032-17669035 - PD4197a COSM163023 c.2298T>C p.S766S Substitution - coding silent 6:17637319-17637319 - 4537_T COSM3948817 c.115A>T p.I39F Substitution - Missense 6:17688615-17688615 - HCC82T COSM1621226 c.3089A>G p.N1030S Substitution - Missense 6:17629110-17629110 - RH30SJ_ COSM4985443 c.2558-1G>T p.? Unknown 6:17632845-17632845 - EV005-R2 COSM4410715 c.527A>G p.H176R Substitution - Missense 6:17675578-17675578 - TCGA-DK-A2I4-01 COSM3777332 c.355G>A p.A119T Substitution - Missense 6:17675750-17675750 - ESCC-134T COSM3941651 c.3044G>C p.G1015A Substitution - Missense 6:17629248-17629248 - TCGA-D3-A5GN-06 COSM4894568 c.980G>A p.R327K Substitution - Missense 6:17669327-17669327 - SKCO-1 COSM4353186 c.462G>A p.S154S Substitution - coding silent 6:17675643-17675643 - I2L-P18-Tumor-Organoid COSM5357228 c.3110G>T p.G1037V Substitution - Missense 6:17629182-17629182 - TCGA-D7-6525-01 COSM3860620 c.619C>G p.L207V Substitution - Missense 6:17675333-17675333 - TCGA-BL-A0C8-01 COSM4811288 c.586A>G p.I196V Substitution - Missense 6:17675366-17675366 - TCGA-66-2768-01 COSM4863234 c.1694C>A p.S565Y Substitution - Missense 6:17647838-17647838 - QC2-39-T2 COSM5655531 c.181A>G p.K61E Substitution - Missense 6:17688549-17688549 - 61 COSM5737481 c.3496T>C p.F1166L Substitution - Missense 6:17628796-17628796 - EWS502 COSM4586494 c.220G>A p.E74K Substitution - Missense 6:17688510-17688510 - PT08_2 COSM5893155 c.1069-8C>T p.? Unknown 6:17665393-17665393 - Gp5D COSM4353180 c.805G>A p.A269T Substitution - Missense 6:17674952-17674952 - PT20_1 COSM5943429 c.2465-3delT p.? Unknown 6:17632847-17632847 - TCGA-66-2773-01 COSM741050 c.3833G>C p.G1278A Substitution - Missense 6:17625876-17625876 - ESCC-180T COSM3941653 c.270T>C p.D90D Substitution - coding silent 6:17688460-17688460 - 450 COSM4435675 c.3520G>T p.D1174Y Substitution - Missense 6:17628772-17628772 - CHC793T COSM4801345 c.1644A>G p.T548T Substitution - coding silent 6:17646143-17646143 - SNUH_G26_S1 COSM4003804 c.2558-3T>C p.? Unknown 6:17632847-17632847 - PT08_1 COSM5893155 c.1069-8C>T p.? Unknown 6:17665393-17665393 - TCGA-HU-A4H4-01 COSM3860619 c.1129A>G p.T377A Substitution - Missense 6:17665325-17665325 - B74-Tumor COSM4006214 c.1899C>T p.I633I Substitution - coding silent 6:17639979-17639979 - BD242T COSM5495821 c.3571G>A p.E1191K Substitution - Missense 6:17628721-17628721 - TCGA-P5-A5EV-01 COSM1076283 c.2685G>A p.S895S Substitution - coding silent 6:17629514-17629514 - CSCC-31-T COSM4480722 c.2538C>T p.S846S Substitution - coding silent 6:17637172-17637172 - CSCC-44-T COSM4566243 c.3437_3438CC>TT p.S1146F Substitution - Missense 6:17628854-17628855 - TCGA-B5-A11E-01 COSM4870185 c.970-1G>T p.? Unknown 6:17669338-17669338 - TCGA-14-0817-01 COSM2154817 c.4417C>T p.R1473C Substitution - Missense 6:17616108-17616108 - TCGA-AD-5900-01 COSM1442382 c.778delT p.Y260fs*14 Deletion - Frameshift 6:17674979-17674979 - M006 COSM1739227 c.2197G>C p.V733L Substitution - Missense 6:17637420-17637420 - PD24205a COSM5787284 c.2558-4T>C p.? Unknown 6:17632848-17632848 - TCGA-AP-A0LM-01 COSM1076266 c.4386C>A p.F1462L Substitution - Missense 6:17616139-17616139 - TCGA-AM-5821-01 COSM3761703 c.2479G>A p.A827T Substitution - Missense 6:17632830-17632830 - TCGA-AO-A03M-01 COSM3829717 c.740C>T p.S247L Substitution - Missense 6:17675017-17675017 - BD175T COSM5507783 c.4159C>T p.Q1387* Substitution - Nonsense 6:17624669-17624669 - TCGA-AP-A051-01 COSM1076298 c.1045G>T p.D349Y Substitution - Missense 6:17668998-17668998 - LUAD-RT-S01813 COSM383449 c.974C>G p.A325G Substitution - Missense 6:17669333-17669333 - TCGA-BR-6452-01 COSM3860607 c.2615T>C p.L872S Substitution - Missense 6:17632694-17632694 - TCGA-AP-A0LM-01 COSM4872975 c.1953G>A p.P651P Substitution - coding silent 6:17637757-17637757 - LUAD-NYU213 COSM371549 c.2444C>T p.S815F Substitution - Missense 6:17637173-17637173 - PASFXA COSM5005866 c.2521G>T p.G841C Substitution - Missense 6:17632788-17632788 - TCGA-AM-5821-01 COSM4783709 c.742A>G p.I248V Substitution - Missense 6:17675015-17675015 - TCGA-EE-A29E-06 COSM3623058 c.1589C>T p.P530L Substitution - Missense 6:17647850-17647850 - 587376 COSM1218069 c.2457G>T p.E819D Substitution - Missense 6:17637160-17637160 - Gp5D COSM2855865 c.805G>A p.A269T Substitution - Missense 6:17674952-17674952 - Pat_40_B COSM5869825 c.511G>A p.D171N Substitution - Missense 6:17675594-17675594 - CHC793T COSM4801346 c.1737A>G p.T579T Substitution - coding silent 6:17646143-17646143 - TCGA-AP-A059-01 COSM4866795 c.3318G>A p.M1106I Substitution - Missense 6:17628974-17628974 - TCGA-AX-A0J0-01 COSM4867221 c.11G>A p.G4E Substitution - Missense 6:17706377-17706377 - TCGA-A2-A0YG-01 COSM450945 c.211G>A p.D71N Substitution - Missense 6:17688519-17688519 - TCGA-CF-A1HR-01 COSM4812765 c.917C>A p.S306* Substitution - Nonsense 6:17669482-17669482 - TCGA-FW-A3R5-06 COSM3921109 c.2741C>T p.P914L Substitution - Missense 6:17629458-17629458 - TCGA-HU-8604-01 COSM3860598 c.3026A>G p.N1009S Substitution - Missense 6:17629266-17629266 - T22 COSM5345110 c.778T>A p.Y260N Substitution - Missense 6:17674979-17674979 - ESCC_BICR_051T COSM5444085 c.1660C>A p.P554T Substitution - Missense 6:17647872-17647872 - PD4980a COSM5771634 c.2448T>G p.C816W Substitution - Missense 6:17637169-17637169 - TCGA-BP-4161-01 COSM1137476 c.4034C>T p.S1345L Substitution - Missense 6:17624701-17624701 - TCGA-AD-5900-01 COSM5128237 c.778delT p.Y260fs*14 Deletion - Frameshift 6:17674979-17674979 - TCGA-B5-A0JY-01 COSM1076283 c.2685G>A p.S895S Substitution - coding silent 6:17629514-17629514 - BD177T COSM5517351 c.1721-1G>T p.? Unknown 6:17640065-17640065 - Pat_45_B COSM5869824 c.1211G>A p.C404Y Substitution - Missense 6:17665243-17665243 - J36_T COSM3948814 c.3166G>A p.G1056S Substitution - Missense 6:17629126-17629126 - TCGA-AX-A0J0-01 COSM4867339 c.1984G>A p.A662T Substitution - Missense 6:17637726-17637726 - Pat_40_B COSM5869826 c.511G>A p.D171N Substitution - Missense 6:17675594-17675594 - TCGA-66-2768-01 COSM741045 c.1601C>A p.S534Y Substitution - Missense 6:17647838-17647838 - COLO201 COSM2855862 c.994G>T p.V332F Substitution - Missense 6:17669313-17669313 - LS411 COSM4646772 c.4237G>A p.G1413R Substitution - Missense 6:17616633-17616633 - TCGA-AX-A05Z-01 COSM4708699 c.1136G>A p.R379Q Substitution - Missense 6:17665318-17665318 - TCGA-D3-A5GN-06 COSM3623061 c.980G>A p.R327K Substitution - Missense 6:17669327-17669327 - EV005-R4 COSM4410715 c.527A>G p.H176R Substitution - Missense 6:17675578-17675578 - J30_T COSM3948815 c.975A>T p.A325A Substitution - coding silent 6:17669332-17669332 - YUGURT COSM5404854 c.2825C>A p.S942Y Substitution - Missense 6:17629374-17629374 - NCI-H2087 COSM22100 c.2370C>G p.F790L Substitution - Missense 6:17637247-17637247 - BD236T COSM5518642 c.1262G>A p.R421Q Substitution - Missense 6:17662024-17662024 - TCGA-B5-A0JY-01 COSM4420464 c.2778G>A p.S926S Substitution - coding silent 6:17629514-17629514 - TCGA-FW-A3R5-06 COSM3921113 c.608C>T p.S203L Substitution - Missense 6:17675344-17675344 - TCGA-BH-A0DZ-01 COSM4813035 c.2395G>C p.E799Q Substitution - Missense 6:17637315-17637315 - TCGA-AN-A046-01 COSM3623056 c.2291C>T p.S764L Substitution - Missense 6:17637326-17637326 - CSCC-44-T COSM4566242 c.3344_3345CC>TT p.S1115F Substitution - Missense 6:17628854-17628855 - CHC2351T COSM4801194 c.3281T>C p.F1094S Substitution - Missense 6:17629011-17629011 - TCGA-BL-A0C8-01 COSM420972 c.586A>G p.I196V Substitution - Missense 6:17675366-17675366 - T3080 COSM4708702 c.684delA p.K228fs*46 Deletion - Frameshift 6:17675268-17675268 - T2932 COSM4708705 c.72delG p.P25fs*102 Deletion - Frameshift 6:17706316-17706316 - TCGA-CJ-6028-01 COSM483712 c.3706A>G p.S1236G Substitution - Missense 6:17626003-17626003 - PD4203a COSM4810150 c.2728C>T p.P910S Substitution - Missense 6:17632674-17632674 - PASFXA COSM5005867 c.2614G>T p.G872C Substitution - Missense 6:17632788-17632788 - I2L-P19Tb-Tumor-Organoid COSM5357034 c.4465_4467delTCT p.S1489delS Deletion - In frame 6:17616151-17616153 - EV005-R4 COSM4410716 c.527A>G p.H176R Substitution - Missense 6:17675578-17675578 - Pat_41_B COSM5869815 c.3661C>T p.P1221S Substitution - Missense 6:17626048-17626048 - TCGA-B7-5816-01 COSM3860606 c.2730A>G p.P910P Substitution - coding silent 6:17632672-17632672 - TCGA-DD-A11C-01 COSM4925645 c.1909G>C p.G637R Substitution - Missense 6:17639969-17639969 - PT46 COSM5928835 c.2777C>T p.S926L Substitution - Missense 6:17629515-17629515 - TCGA-BR-4362-01 COSM3860604 c.2898T>C p.G966G Substitution - coding silent 6:17629394-17629394 - TCGA-AP-A0LM-01 COSM4873654 c.4479C>A p.F1493L Substitution - Missense 6:17616139-17616139 - 85 COSM5016127 c.1529_1532delACAA p.N510fs*4 Deletion - Frameshift 6:17649164-17649167 - T1154 COSM4708697 c.1239A>G p.T413T Substitution - coding silent 6:17662047-17662047 - STC243 COSM5061659 c.2624G>A p.G875E Substitution - Missense 6:17632778-17632778 - TCGA-AP-A056-01 COSM1076279 c.2923G>T p.D975Y Substitution - Missense 6:17629276-17629276 - TCGA-FV-A4ZQ-01 COSM4921957 c.2173A>G p.T725A Substitution - Missense 6:17637444-17637444 - CN-AML-28-T COSM4003804 c.2558-3T>C p.? Unknown 6:17632847-17632847 - TCGA-AA-3510-01 COSM1076283 c.2685G>A p.S895S Substitution - coding silent 6:17629514-17629514 - TCGA-G4-6586-01 COSM1442380 c.1852G>A p.A618T Substitution - Missense 6:17637765-17637765 - TCGA-BR-6452-01 COSM3860608 c.2708T>C p.L903S Substitution - Missense 6:17632694-17632694 - CHC2351T COSM4801193 c.3188T>C p.F1063S Substitution - Missense 6:17629011-17629011 - TCGA-CC-A7IH-01 COSM4923341 c.31G>T p.G11C Substitution - Missense 6:17706357-17706357 - CHC1742T COSM4792251 c.2885G>T p.G962V Substitution - Missense 6:17629407-17629407 - PTC_221 COSM5960127 c.1504_1505insA p.V502fs*18 Insertion - Frameshift 6:17649284-17649285 - 19 COSM5746525 c.2961A>G p.I987M Substitution - Missense 6:17629331-17629331 - T3152 COSM4708695 c.1325T>C p.V442A Substitution - Missense 6:17661723-17661723 - TCGA-DK-A3X1-01 COSM3777328 c.3599C>T p.S1200L Substitution - Missense 6:17626110-17626110 - Gp2D COSM4353180 c.805G>A p.A269T Substitution - Missense 6:17674952-17674952 - CN-AML-07-T COSM4003804 c.2558-3T>C p.? Unknown 6:17632847-17632847 - 1960034 COSM1644181 c.2923G>C p.D975H Substitution - Missense 6:17629276-17629276 - T13 COSM5617820 c.3895T>C p.S1299P Substitution - Missense 6:17625814-17625814 - PTC-14C COSM4160393 c.1384C>A p.L462M Substitution - Missense 6:17661664-17661664 - PT46 COSM5928834 c.2684C>T p.S895L Substitution - Missense 6:17629515-17629515 - 75 COSM5014567 c.4436+1G>T p.? Unknown 6:17616526-17616526 - 74 COSM4777913 c.710G>T p.G237V Substitution - Missense 6:17675242-17675242 - S02293 COSM5688572 c.4351A>T p.N1451Y Substitution - Missense 6:17616612-17616612 - TCGA-BS-A0UV-01 COSM4865000 c.3001G>A p.E1001K Substitution - Missense 6:17629291-17629291 - 49M COSM3430359 c.491C>T p.S164F Substitution - Missense 6:17675614-17675614 - TCGA-BH-A0BF-01 COSM450944 c.1006C>G p.L336V Substitution - Missense 6:17669301-17669301 - TCGA-AM-5821-01 COSM4783673 c.2572G>A p.A858T Substitution - Missense 6:17632830-17632830 - COLO205 COSM2855862 c.994G>T p.V332F Substitution - Missense 6:17669313-17669313 - COLO201 COSM4353175 c.994G>T p.V332F Substitution - Missense 6:17669313-17669313 - TCGA-AP-A0LE-01 COSM4871049 c.3270A>G p.S1090S Substitution - coding silent 6:17629022-17629022 - T22 COSM5345112 c.777T>A p.F259L Substitution - Missense 6:17674980-17674980 - PCSI_0547_Pa_P_526 COSM5032005 c.3511T>A p.F1171I Substitution - Missense 6:17628688-17628688 - PD11745a COSM4353165 c.1298C>T p.P433L Substitution - Missense 6:17661750-17661750 - TCGA-P5-A5EV-01 COSM4420464 c.2778G>A p.S926S Substitution - coding silent 6:17629514-17629514 - TCGA-D1-A103-01 COSM4874897 c.1139G>T p.S380I Substitution - Missense 6:17665315-17665315 - TCGA-D9-A6EC-06 COSM4405920 c.1949T>G p.I650S Substitution - Missense 6:17637668-17637668 - TCGA-AX-A0J0-01 COSM483713 c.1891G>A p.A631T Substitution - Missense 6:17637726-17637726 - 111677 COSM96089 c.3417G>A p.E1139E Substitution - coding silent 6:17628782-17628782 - BD177T COSM5517352 c.1814-1G>T p.? Unknown 6:17640065-17640065 - Pat_01_A COSM5869822 c.2558-3_2558-2insTT p.? Unknown 6:17632846-17632847 - LP2000108-DNA_A01 COSM4408453 c.3953C>T p.S1318F Substitution - Missense 6:17625849-17625849 - T2940 COSM4708691 c.3378G>T p.E1126D Substitution - Missense 6:17628821-17628821 - TCGA-EE-A2MJ-06 COSM3623056 c.2291C>T p.S764L Substitution - Missense 6:17637326-17637326 - BD124T COSM5492006 c.494T>C p.L165P Substitution - Missense 6:17675611-17675611 - TCGA-AC-A2BM-01 COSM3829715 c.2178T>A p.T726T Substitution - coding silent 6:17637532-17637532 - TCGA-C8-A12P-01 COSM450943 c.2012A>T p.N671I Substitution - Missense 6:17637605-17637605 - ESCC-180T COSM3941652 c.270T>C p.D90D Substitution - coding silent 6:17688460-17688460 - TCGA-13-2057-01 COSM1329201 c.3350T>A p.V1117D Substitution - Missense 6:17628849-17628849 - ESCC_BICR_051T COSM5444084 c.1567C>A p.P523T Substitution - Missense 6:17647872-17647872 - TCGA-FS-A4F5-06 COSM3623055 c.2349C>T p.T783T Substitution - coding silent 6:17637268-17637268 - T2940 COSM4708692 c.3471G>T p.E1157D Substitution - Missense 6:17628821-17628821 - TCGA-AX-A0J0-01 COSM1076310 c.11G>A p.G4E Substitution - Missense 6:17706377-17706377 - TCGA-AM-5821-01 COSM3761706 c.742A>G p.I248V Substitution - Missense 6:17675015-17675015 - 2521249 COSM5895175 c.2558-2_2558-1insTT p.? Unknown 6:17632845-17632846 - EV005-R7 COSM4410715 c.527A>G p.H176R Substitution - Missense 6:17675578-17675578 - TCGA-GC-A3WC-01 COSM3777331 c.798C>T p.Y266Y Substitution - coding silent 6:17674959-17674959 - 2_RESISTANT COSM1722369 c.2271C>T p.A757A Substitution - coding silent 6:17637346-17637346 - Pat_41_B COSM5869819 c.2987C>T p.T996I Substitution - Missense 6:17629212-17629212 - I2L-P18-Tumor-Organoid COSM5357227 c.3017G>T p.G1006V Substitution - Missense 6:17629182-17629182 - RMS85_ COSM4985442 c.2465-1G>T p.? Unknown 6:17632845-17632845 - TCGA-B0-5692-01 COSM483715 c.997T>C p.S333P Substitution - Missense 6:17669310-17669310 - Pat_40_A COSM5869826 c.511G>A p.D171N Substitution - Missense 6:17675594-17675594 - TCGA-60-2715-01 COSM4860848 c.1891G>T p.A631S Substitution - Missense 6:17639987-17639987 - 65 COSM5011578 c.969+1G>A p.? Unknown 6:17669429-17669429 - 8012341 COSM3393986 c.1478A>T p.E493V Substitution - Missense 6:17649218-17649218 - TCGA-GC-A3WC-01 COSM3777330 c.798C>T p.Y266Y Substitution - coding silent 6:17674959-17674959 - HCC2998 COSM4353152 c.2109A>C p.K703N Substitution - Missense 6:17637601-17637601 - TCGA-RP-A695-06 COSM4897103 c.2102A>G p.N701S Substitution - Missense 6:17637515-17637515 - H1155 COSM1195803 c.954G>A p.M318I Substitution - Missense 6:17669445-17669445 - TCGA-BR-6452-01 COSM3860590 c.3765T>C p.A1255A Substitution - coding silent 6:17626037-17626037 - CSCC-56-T COSM4496805 c.482C>T p.S161L Substitution - Missense 6:17675623-17675623 - SCMC_RM2_ COSM4985443 c.2558-1G>T p.? Unknown 6:17632845-17632845 - TCGA-EV-5903-01 COSM3994734 c.253C>T p.H85Y Substitution - Missense 6:17688477-17688477 - EV005-R5 COSM4410716 c.527A>G p.H176R Substitution - Missense 6:17675578-17675578 - TCGA-D1-A17Q-01 COSM4865337 c.2480C>A p.S827Y Substitution - Missense 6:17637230-17637230 - HCC117T COSM5808556 c.2772T>G p.F924L Substitution - Missense 6:17629427-17629427 - T2932 COSM4708704 c.72delG p.P25fs*102 Deletion - Frameshift 6:17706316-17706316 - TCGA-14-0817 COSM2154817 c.4417C>T p.R1473C Substitution - Missense 6:17616108-17616108 - PTC-14C COSM4160392 c.1384C>A p.L462M Substitution - Missense 6:17661664-17661664 - 49M COSM4782375 c.491C>T p.S164F Substitution - Missense 6:17675614-17675614 - TCGA-39-5037-01 COSM4860655 c.1563T>C p.S521S Substitution - coding silent 6:17649226-17649226 - Pat_37_B COSM5869813 c.4276G>A p.A1426T Substitution - Missense 6:17616594-17616594 - 61 COSM5737482 c.3244T>C p.F1082L Substitution - Missense 6:17628955-17628955 - PT08_1 COSM5893154 c.1069-8C>T p.? Unknown 6:17665393-17665393 - TCGA-RP-A695-06 COSM4897104 c.2195A>G p.N732S Substitution - Missense 6:17637515-17637515 - TCGA-66-2770-01 COSM741042 c.894A>T p.A298A Substitution - coding silent 6:17669505-17669505 - TCGA-BS-A0UV-01 COSM4864903 c.873G>T p.M291I Substitution - Missense 6:17669526-17669526 - ML_79_T_01 COSM4160391 c.3699A>C p.T1233T Substitution - coding silent 6:17626103-17626103 - 19 COSM5746524 c.2868A>G p.I956M Substitution - Missense 6:17629331-17629331 - TCGA-BR-4257-01 COSM3860594 c.3184T>G p.S1062A Substitution - Missense 6:17629108-17629108 - RK190_C01 COSM3745071 c.691T>C p.F231L Substitution - Missense 6:17675261-17675261 - TCGA-BR-6457-01 COSM3860596 c.3035T>G p.F1012C Substitution - Missense 6:17629257-17629257 - TCGA-BR-4361-01 COSM3860587 c.3723T>C p.G1241G Substitution - coding silent 6:17625986-17625986 - TCGA-BR-6565-01 COSM3860600 c.2987C>G p.S996C Substitution - Missense 6:17629305-17629305 - SNU-C4 COSM4615772 c.684_685insA p.P229fs*22 Insertion - Frameshift 6:17675267-17675268 - CN-AML-28-T COSM4003803 c.2465-3T>C p.? Unknown 6:17632847-17632847 - TCGA-AP-A0LP-01 COSM4872180 c.112-1G>A p.? Unknown 6:17688619-17688619 - 61 COSM5737480 c.3403T>C p.F1135L Substitution - Missense 6:17628796-17628796 - CN-AML-NR-07-Dx COSM4003804 c.2558-3T>C p.? Unknown 6:17632847-17632847 - EWS502 COSM4586495 c.220G>A p.E74K Substitution - Missense 6:17688510-17688510 - CSCC-29-T COSM4490781 c.3693C>T p.S1231S Substitution - coding silent 6:17626016-17626016 - LUAD-CHTN-MAD06-00668 COSM360146 c.2136G>T p.G712G Substitution - coding silent 6:17637481-17637481 - TCGA-AM-5820-01 COSM3761705 c.897A>G p.Q299Q Substitution - coding silent 6:17669502-17669502 - BZ08 COSM5758037 c.67C>A p.Q23K Substitution - Missense 6:17706321-17706321 - TCGA-AA-A010-01 COSM283430 c.4298C>T p.S1433L Substitution - Missense 6:17616572-17616572 - BD236T COSM5518641 c.1262G>A p.R421Q Substitution - Missense 6:17662024-17662024 - BD175T COSM5507782 c.4066C>T p.Q1356* Substitution - Nonsense 6:17624669-17624669 - YUROC COSM5404853 c.3146C>T p.S1049F Substitution - Missense 6:17629146-17629146 - T578 COSM3860613 c.2266C>T p.R756* Substitution - Nonsense 6:17637351-17637351 - TCGA-LP-A5U2-01 COSM4833677 c.3989C>G p.S1330C Substitution - Missense 6:17625813-17625813 - TCGA-AP-A0LM-01 COSM1076290 c.1860G>A p.P620P Substitution - coding silent 6:17637757-17637757 - TCGA-EI-6917-01 COSM1442380 c.1852G>A p.A618T Substitution - Missense 6:17637765-17637765 - TCGA-FW-A3R5-06 COSM3921114 c.608C>T p.S203L Substitution - Missense 6:17675344-17675344 - H1155 COSM1196076 c.4360G>A p.V1454M Substitution - Missense 6:17616165-17616165 - Pat_28_B COSM5869818 c.3196C>T p.P1066S Substitution - Missense 6:17629096-17629096 - PD9004a COSM5785911 c.3809C>T p.A1270V Substitution - Missense 6:17625993-17625993 - TCGA-DD-A11C-01 COSM4925644 c.1816G>C p.G606R Substitution - Missense 6:17639969-17639969 - TCGA-G4-6303-01 COSM5830350 c.2558-3_2558-2insT p.? Unknown 6:17632846-17632847 - EV005-R7 COSM4410716 c.527A>G p.H176R Substitution - Missense 6:17675578-17675578 - TCGA-B5-A11W-01 COSM4420464 c.2778G>A p.S926S Substitution - coding silent 6:17629514-17629514 - MO_1128 COSM5567395 c.4271C>T p.S1424L Substitution - Missense 6:17616692-17616692 - TCGA-EE-A2MS-06 COSM3623059 c.1437C>T p.I479I Substitution - coding silent 6:17649259-17649259 - T578 COSM4708699 c.1136G>A p.R379Q Substitution - Missense 6:17665318-17665318 - TCGA-FV-A4ZQ-01 COSM4921958 c.2266A>G p.T756A Substitution - Missense 6:17637444-17637444 - 61 COSM5737485 c.2230A>T p.T744S Substitution - Missense 6:17637480-17637480 - TCGA-60-2715-01 COSM741046 c.1794A>C p.R598S Substitution - Missense 6:17639991-17639991 - TCGA-BS-A0V6-01 COSM1076300 c.1040T>C p.I347T Substitution - Missense 6:17669003-17669003 - TCGA-D7-6525-01 COSM3860621 c.619C>G p.L207V Substitution - Missense 6:17675333-17675333 - TCGA-CD-8531-01 COSM3860601 c.2805T>G p.G935G Substitution - coding silent 6:17629394-17629394 - TCGA-70-6722-01 COSM741043 c.1364G>T p.R455L Substitution - Missense 6:17661684-17661684 - TCGA-EE-A20F-06 COSM3623054 c.2512C>T p.P838S Substitution - Missense 6:17632797-17632797 - TCGA-06-2564-01 COSM2152933 c.3073G>A p.G1025S Substitution - Missense 6:17629126-17629126 - PCSI_0083_Pa_P_526 COSM3782041 c.3544+6T>C p.? Unknown 6:17628649-17628649 - CHC1742T COSM4792251 c.2885G>T p.G962V Substitution - Missense 6:17629407-17629407 - B74-Tumor COSM1754664 c.1806C>T p.I602I Substitution - coding silent 6:17639979-17639979 - STC243 COSM5061658 c.2531G>A p.G844E Substitution - Missense 6:17632778-17632778 - 2246952 COSM4413504 c.2438G>T p.G813V Substitution - Missense 6:17637272-17637272 - TCGA-FW-A3R5-06 COSM3921112 c.705C>T p.A235A Substitution - coding silent 6:17675247-17675247 - SNUH_G76_S1 COSM4418220 c.268G>A p.D90N Substitution - Missense 6:17688462-17688462 - I-01 COSM4767012 c.2165C>T p.T722I Substitution - Missense 6:17637545-17637545 - TCGA-46-3769-01 COSM741048 c.2392G>T p.E798* Substitution - Nonsense 6:17637225-17637225 - LAU63 COSM232923 c.1604C>T p.T535I Substitution - Missense 6:17647835-17647835 - TCGA-60-2719-01 COSM4861730 c.346A>G p.T116A Substitution - Missense 6:17675759-17675759 - TCGA-FS-A4F5-06 COSM4899467 c.2442C>T p.T814T Substitution - coding silent 6:17637268-17637268 - 65 COSM5011579 c.969+1G>A p.? Unknown 6:17669429-17669429 - T578 COSM3860614 c.2359C>T p.R787* Substitution - Nonsense 6:17637351-17637351 - pfg127T COSM4750544 c.1990T>C p.C664R Substitution - Missense 6:17637627-17637627 - TCGA-BP-4346-01 COSM3366394 c.2278T>C p.L760L Substitution - coding silent 6:17637339-17637339 - T3503 COSM4708693 c.3365C>T p.A1122V Substitution - Missense 6:17628834-17628834 - TCGA-14-0817-01 COSM4781908 c.4510C>T p.R1504C Substitution - Missense 6:17616108-17616108 - TCGA-AX-A05Z-01 COSM4863861 c.1644G>A p.P548P Substitution - coding silent 6:17647888-17647888 - 99042 COSM96090 c.2100A>G p.P700P Substitution - coding silent 6:17637517-17637517 - CP66-MEL COSM22105 c.1765C>T p.P589S Substitution - Missense 6:17640020-17640020 - TCGA-F5-6814-01 COSM3430359 c.491C>T p.S164F Substitution - Missense 6:17675614-17675614 - TCGA-EE-A20F-06 COSM4891840 c.2605C>T p.P869S Substitution - Missense 6:17632797-17632797 - Pat_41_B COSM5869816 c.3754C>T p.P1252S Substitution - Missense 6:17626048-17626048 - TCGA-AP-A059-01 COSM1076275 c.3225G>A p.M1075I Substitution - Missense 6:17628974-17628974 - TCGA-AX-A0J0-01 COSM4867333 c.2520A>C p.E840D Substitution - Missense 6:17637190-17637190 - J30_T COSM3948816 c.975A>T p.A325A Substitution - coding silent 6:17669332-17669332 - TCGA-B7-5816-01 COSM3860605 c.2637A>G p.P879P Substitution - coding silent 6:17632672-17632672 - sysucc-882T COSM4003803 c.2465-3T>C p.? Unknown 6:17632847-17632847 - AOCS-109-1-X COSM4149287 c.1846+1G>C p.? Unknown 6:17639938-17639938 - I-01 COSM4767011 c.2072C>T p.T691I Substitution - Missense 6:17637545-17637545 - Pat_40_B COSM4708703 c.684delA p.K228fs*46 Deletion - Frameshift 6:17675268-17675268 - TCGA-A2-A0YG-01 COSM4812845 c.211G>A p.D71N Substitution - Missense 6:17688519-17688519 - TCGA-BP-4161-01 COSM4858281 c.4127C>T p.S1376L Substitution - Missense 6:17624701-17624701 - EGC3 COSM5061656 c.2869G>A p.G957R Substitution - Missense 6:17629330-17629330 - ESCC-134T COSM3941650 c.2951G>C p.G984A Substitution - Missense 6:17629248-17629248 - TCGA-D1-A103-01 COSM1076294 c.1139G>T p.S380I Substitution - Missense 6:17665315-17665315 - TCGA-D8-A27G-01 COSM3829711 c.4185C>G p.F1395L Substitution - Missense 6:17616685-17616685 - TCGA-MY-A5BD-01 COSM4855723 c.2589G>T p.Q863H Substitution - Missense 6:17632720-17632720 - TCGA-BS-A0UV-01 COSM1076304 c.873G>T p.M291I Substitution - Missense 6:17669526-17669526 - TCGA-AO-A03M-01 COSM3829716 c.740C>T p.S247L Substitution - Missense 6:17675017-17675017 - C0074T COSM4422422 c.3886A>T p.S1296C Substitution - Missense 6:17625916-17625916 - TCGA-MY-A5BD-01 COSM4855724 c.2682G>T p.Q894H Substitution - Missense 6:17632720-17632720 - 4537_T COSM3948818 c.115A>T p.I39F Substitution - Missense 6:17688615-17688615 - RD COSM4985442 c.2465-1G>T p.? Unknown 6:17632845-17632845 - TCGA-AP-A056-01 COSM4868434 c.3016G>T p.D1006Y Substitution - Missense 6:17629276-17629276 - BD124T COSM5492004 c.3493delT p.S1165fs*22 Deletion - Frameshift 6:17628799-17628799 - 585260 COSM325990 c.1324G>T p.V442L Substitution - Missense 6:17661724-17661724 - TCGA-BR-8485-01 COSM3860596 c.3035T>G p.F1012C Substitution - Missense 6:17629257-17629257 - TCGA-CF-A1HR-01 COSM420973 c.917C>A p.S306* Substitution - Nonsense 6:17669482-17669482 - CN-AML-NR-28-Dx COSM4003803 c.2465-3T>C p.? Unknown 6:17632847-17632847 - TCGA-B5-A0JY-01 COSM4869132 c.218G>A p.S73N Substitution - Missense 6:17688512-17688512 - ML_79_T_01 COSM4160390 c.3606A>C p.T1202T Substitution - coding silent 6:17626103-17626103 - Pat_28_B COSM5869817 c.3103C>T p.P1035S Substitution - Missense 6:17629096-17629096 - OV207 COSM253041 c.1015-6_1015-4delTTT p.? Unknown 6:17669032-17669034 - TCGA-BR-4361-01 COSM3860588 c.3816T>C p.G1272G Substitution - coding silent 6:17625986-17625986 - CHC793T COSM4801346 c.1737A>G p.T579T Substitution - coding silent 6:17646143-17646143 - CSCC-29-T COSM4490782 c.3786C>T p.S1262S Substitution - coding silent 6:17626016-17626016 - T3080 COSM4708703 c.684delA p.K228fs*46 Deletion - Frameshift 6:17675268-17675268 - TCGA-33-4566-01 COSM741040 c.158G>T p.G53V Substitution - Missense 6:17688572-17688572 - Pat_40_A COSM5869825 c.511G>A p.D171N Substitution - Missense 6:17675594-17675594 - OSCC-GB_00030111 COSM4881187 c.462G>T p.S154S Substitution - coding silent 6:17675643-17675643 - NCI-H128 COSM22101 c.2422G>A p.A808T Substitution - Missense 6:17637195-17637195 - TCGA-BR-8680-01 COSM3860616 c.1580T>G p.F527C Substitution - Missense 6:17647859-17647859 - TCGA-JW-A5VL-01 COSM4847980 c.946G>C p.E316Q Substitution - Missense 6:17669453-17669453 - SC_9099 COSM5556968 c.541A>C p.I181L Substitution - Missense 6:17675564-17675564 - TCGA-BR-6452-01 COSM3860611 c.2311A>T p.T771S Substitution - Missense 6:17637306-17637306 - HCC82 COSM1621226 c.3089A>G p.N1030S Substitution - Missense 6:17629110-17629110 - TCGA-D5-6930-01 COSM1442383 c.684_685insA p.P229fs*22 Insertion - Frameshift 6:17675267-17675268 - PD4203a COSM163021 c.2635C>T p.P879S Substitution - Missense 6:17632674-17632674 - AOCS-152-1-X COSM4149286 c.2800T>G p.F934V Substitution - Missense 6:17629492-17629492 - TCGA-BR-8680-01 COSM3860617 c.1673T>G p.F558C Substitution - Missense 6:17647859-17647859 - 107582 COSM94882 c.2407T>C p.C803R Substitution - Missense 6:17637210-17637210 - HCT-15 COSM1672257 c.968C>T p.A323V Substitution - Missense 6:17669431-17669431 - YUROC COSM5404852 c.3053C>T p.S1018F Substitution - Missense 6:17629146-17629146 - RH30SJ_ COSM4985442 c.2465-1G>T p.? Unknown 6:17632845-17632845 - S02292 COSM5688086 c.1068+3A>G p.? Unknown 6:17668972-17668972 - PTC-46C COSM4160391 c.3699A>C p.T1233T Substitution - coding silent 6:17626103-17626103 - TCGA-AN-A0G0-01 COSM450941 c.3157A>T p.I1053L Substitution - Missense 6:17629042-17629042 - 8066446 COSM3784470 c.3368T>A p.L1123Q Substitution - Missense 6:17628924-17628924 - CHC2351T COSM4801193 c.3188T>C p.F1063S Substitution - Missense 6:17629011-17629011 - TCGA-BR-4257-01 COSM3860593 c.3091T>G p.S1031A Substitution - Missense 6:17629108-17629108 - EV005-R6 COSM4410716 c.527A>G p.H176R Substitution - Missense 6:17675578-17675578 - TCGA-CG-5721-01 COSM3860614 c.2359C>T p.R787* Substitution - Nonsense 6:17637351-17637351 - Pat_41_B COSM5869820 c.3080C>T p.T1027I Substitution - Missense 6:17629212-17629212 - SCMC_RM2_ COSM4985442 c.2465-1G>T p.? Unknown 6:17632845-17632845 - CHC1742T COSM4792250 c.2792G>T p.G931V Substitution - Missense 6:17629407-17629407 - TCGA-AM-5821-01 COSM4783683 c.1206C>G p.N402K Substitution - Missense 6:17665248-17665248 - 61 COSM5737487 c.928C>T p.R310* Substitution - Nonsense 6:17669471-17669471 - CN-AML-NR-28-Dx COSM4003804 c.2558-3T>C p.? Unknown 6:17632847-17632847 - TCGA-AO-A0JD-01 COSM450940 c.3324A>G p.Q1108Q Substitution - coding silent 6:17628875-17628875 - 587316 COSM1218068 c.397C>T p.R133W Substitution - Missense 6:17675708-17675708 - EV005-R3 COSM4410716 c.527A>G p.H176R Substitution - Missense 6:17675578-17675578 - RK035_C01 COSM1634649 c.1741A>G p.N581D Substitution - Missense 6:17640044-17640044 - EV005-R1 COSM4410716 c.527A>G p.H176R Substitution - Missense 6:17675578-17675578 - pfg127T COSM4750545 c.2083T>C p.C695R Substitution - Missense 6:17637627-17637627 - TCGA-70-6722-01 COSM4862534 c.1364G>T p.R455L Substitution - Missense 6:17661684-17661684 - TCGA-CG-5721-01 COSM3860592 c.3599C>T p.A1200V Substitution - Missense 6:17628693-17628693 - TCGA-AY-6197-01 COSM5830351 c.2465-4_2465-3delTT p.? Unknown 6:17632847-17632848 - RMS85_ COSM4985443 c.2558-1G>T p.? Unknown 6:17632845-17632845 - TCGA-EE-A2MJ-06 COSM3829713 c.2384C>T p.S795L Substitution - Missense 6:17637326-17637326 - TCGA-AP-A059-01 COSM1076270 c.3499G>A p.A1167T Substitution - Missense 6:17628700-17628700 - TCGA-AA-3510-01 COSM4420464 c.2778G>A p.S926S Substitution - coding silent 6:17629514-17629514 - SNUH_G26_S1 COSM4003803 c.2465-3T>C p.? Unknown 6:17632847-17632847 - ESCC_133 COSM5642600 c.1430C>T p.S477L Substitution - Missense 6:17651892-17651892 - YUROC COSM5404851 c.3173G>A p.G1058D Substitution - Missense 6:17629119-17629119 - OSCC-GB_00030111 COSM3715366 c.462G>T p.S154S Substitution - coding silent 6:17675643-17675643 - S02293 COSM5688571 c.4258A>T p.N1420Y Substitution - Missense 6:17616612-17616612 - 61 COSM5737484 c.2137A>T p.T713S Substitution - Missense 6:17637480-17637480 - RK308_C01 COSM3745070 c.1620A>G p.L540L Substitution - coding silent 6:17647819-17647819 - CHC1742T COSM4792250 c.2792G>T p.G931V Substitution - Missense 6:17629407-17629407 - HCT-15 COSM1672255 c.3550G>T p.G1184C Substitution - Missense 6:17626159-17626159 - T578 COSM1076296 c.1136G>A p.R379Q Substitution - Missense 6:17665318-17665318 - HCC2998 COSM1672256 c.2016A>C p.K672N Substitution - Missense 6:17637601-17637601 - HCT15 COSM1672257 c.968C>T p.A323V Substitution - Missense 6:17669431-17669431 - TCGA-EB-A431-01 COSM3623057 c.2242C>T p.P748S Substitution - Missense 6:17637375-17637375 - 101692 COSM96091 c.459C>G p.S153S Substitution - coding silent 6:17675646-17675646 - 8066446 COSM3784469 c.3275T>A p.L1092Q Substitution - Missense 6:17628924-17628924 - TCGA-D9-A6EC-06 COSM4405921 c.2042T>G p.I681S Substitution - Missense 6:17637668-17637668 - TCGA-A5-A0GB-01 COSM1076272 c.3488C>A p.S1163Y Substitution - Missense 6:17628711-17628711 - TCGA-JW-A5VL-01 COSM4847981 c.946G>C p.E316Q Substitution - Missense 6:17669453-17669453 - TCGA-AM-5820-01 COSM4785210 c.897A>G p.Q299Q Substitution - coding silent 6:17669502-17669502 - TCGA-BR-4184-01 COSM1442380 c.1852G>A p.A618T Substitution - Missense 6:17637765-17637765 - HCC058T COSM5804511 c.4086A>T p.Q1362H Substitution - Missense 6:17624742-17624742 - HCC117T COSM5808557 c.2865T>G p.F955L Substitution - Missense 6:17629427-17629427 - AOCS-152-1-X COSM4149285 c.2707T>G p.F903V Substitution - Missense 6:17629492-17629492 - EV005-R3 COSM4410715 c.527A>G p.H176R Substitution - Missense 6:17675578-17675578 - SKCO-1 COSM2855871 c.462G>A p.S154S Substitution - coding silent 6:17675643-17675643 - 86583 COSM94883 c.1549C>T p.P517S Substitution - Missense 6:17647890-17647890 - TCGA-AA-3966-01 COSM273032 c.1011T>A p.N337K Substitution - Missense 6:17669296-17669296 - PTC_221 COSM5960126 c.1411_1412insA p.V471fs*18 Insertion - Frameshift 6:17649284-17649285 - TCGA-AN-A046-01 COSM3829713 c.2384C>T p.S795L Substitution - Missense 6:17637326-17637326 - TCGA-BR-6452-01 COSM3860612 c.2404A>T p.T802S Substitution - Missense 6:17637306-17637306 - TCGA-B5-A0JY-01 COSM1076306 c.218G>A p.S73N Substitution - Missense 6:17688512-17688512 - HCC078T COSM5806164 c.671C>G p.T224S Substitution - Missense 6:17675281-17675281 - EV005-R1 COSM4410715 c.527A>G p.H176R Substitution - Missense 6:17675578-17675578 - TCGA-BR-4362-01 COSM3860603 c.2805T>C p.G935G Substitution - coding silent 6:17629394-17629394 - YUDEXA COSM1696950 c.4401A>G p.I1467M Substitution - Missense 6:17616124-17616124 - TCGA-AO-A0JD-01 COSM4813592 c.3417A>G p.Q1139Q Substitution - coding silent 6:17628875-17628875 - Pat_45_B COSM5869823 c.1211G>A p.C404Y Substitution - Missense 6:17665243-17665243 - TCGA-D8-A27G-01 COSM3829712 c.4278C>G p.F1426L Substitution - Missense 6:17616685-17616685 - CSCC-56-T COSM4496804 c.482C>T p.S161L Substitution - Missense 6:17675623-17675623 - TP_2060 COSM5573201 c.1632+1G>A p.? Unknown 6:17647806-17647806 - TCGA-AY-6197-01 COSM5830352 c.2558-4_2558-3delTT p.? Unknown 6:17632847-17632848 - TCGA-DK-A3X1-01 COSM3777329 c.3692C>T p.S1231L Substitution - Missense 6:17626110-17626110 - 75 COSM5014566 c.4343+1G>T p.? Unknown 6:17616526-17616526 - T13 COSM5617821 c.3988T>C p.S1330P Substitution - Missense 6:17625814-17625814 - TCGA-BR-6452-01 COSM3860589 c.3672T>C p.A1224A Substitution - coding silent 6:17626037-17626037 - TCGA-06-2564 COSM2152933 c.3073G>A p.G1025S Substitution - Missense 6:17629126-17629126 - TCGA-CC-A7IH-01 COSM4923342 c.31G>T p.G11C Substitution - Missense 6:17706357-17706357 - EV005-R6 COSM4410715 c.527A>G p.H176R Substitution - Missense 6:17675578-17675578 - TCGA-D3-A2J8-06 COSM3623062 c.772C>T p.P258S Substitution - Missense 6:17674985-17674985 - TCGA-BH-A0DZ-01 COSM450942 c.2302G>C p.E768Q Substitution - Missense 6:17637315-17637315 - SNU-C4 COSM1442383 c.684_685insA p.P229fs*22 Insertion - Frameshift 6:17675267-17675268 - PD24205a COSM5787283 c.2465-4T>C p.? Unknown 6:17632848-17632848 - TCGA-BR-6457-01 COSM3860595 c.2942T>G p.F981C Substitution - Missense 6:17629257-17629257 - J36_T COSM2152933 c.3073G>A p.G1025S Substitution - Missense 6:17629126-17629126 - ICGC_MB126 COSM3765251 c.1441G>A p.A481T Substitution - Missense 6:17651881-17651881 - sysucc-882T COSM4003804 c.2558-3T>C p.? Unknown 6:17632847-17632847 - TCGA-AO-A12E-01 COSM3829718 c.397C>T p.R133W Substitution - Missense 6:17675708-17675708 - TCGA-60-2719-01 COSM741041 c.346A>G p.T116A Substitution - Missense 6:17675759-17675759 - ccRCC-28 COSM1663179 c.4135A>G p.S1379G Substitution - Missense 6:17624600-17624600 - BD124T COSM5492003 c.3400delT p.S1134fs*22 Deletion - Frameshift 6:17628799-17628799 - PT08_2 COSM5893154 c.1069-8C>T p.? Unknown 6:17665393-17665393 - I2L-P19Tb-Tumor-Organoid COSM5357033 c.4372_4374delTCT p.S1458delS Deletion - In frame 6:17616151-17616153 - SC_9099 COSM5556967 c.541A>C p.I181L Substitution - Missense 6:17675564-17675564 - TCGA-EB-A431-01 COSM4892305 c.2335C>T p.P779S Substitution - Missense 6:17637375-17637375 - LUAD-S01357 COSM387633 c.2327G>T p.S776I Substitution - Missense 6:17637290-17637290 - YUGURT COSM5404855 c.2918C>A p.S973Y Substitution - Missense 6:17629374-17629374 - T3090 COSM4708700 c.999T>G p.S333S Substitution - coding silent 6:17669308-17669308 - 2_PRE-TREATMENT COSM1722369 c.2271C>T p.A757A Substitution - coding silent 6:17637346-17637346 - TCGA-CG-5721-01 COSM3860591 c.3506C>T p.A1169V Substitution - Missense 6:17628693-17628693 - HCC82T COSM4781289 c.3182A>G p.N1061S Substitution - Missense 6:17629110-17629110 - TCGA-EV-5903-01 COSM3994735 c.253C>T p.H85Y Substitution - Missense 6:17688477-17688477 - LP2000108-DNA_A01 COSM4408452 c.3860C>T p.S1287F Substitution - Missense 6:17625849-17625849 - LUAD-S01302 COSM396188 c.1957G>C p.G653R Substitution - Missense 6:17637660-17637660 - 85 COSM5016128 c.1622_1625delACAA p.N541fs*4 Deletion - Frameshift 6:17649164-17649167 - T3152 COSM4708696 c.1325T>C p.V442A Substitution - Missense 6:17661723-17661723 - LS411 COSM4646773 c.4330G>A p.G1444R Substitution - Missense 6:17616633-17616633 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.601580;Hs.601581;Hs.601582;Hs.601583;Hs.601584;Hs.601585;Hs.601586;Hs.601587;Hs.601588;Hs.601589;Hs.601590;Hs.601591 6p22.3 603948 2467974|CGAP|BC052965|A/G|non-coding||4851|Candidate Hs.718669;Hs.718680;Hs.718681;Hs.718686;Hs.718687;Hs.718690;Hs.718691;Hs.718695;Hs.718696;Hs.718702;Hs.718703 6p22.3 603948 2467974|CGAP|BC052965|A/G|non-coding||4851|Candidate

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C Missense p.F981C c.2942T>G 6 17629488 STAD A C Missense p.S1031A c.3091T>G 6 17629339 STAD A G Synonymous p.L760L c.2278T>C 6 17637570 RCCC A G Synonymous p.S490S c.1470T>C 6 17649457 LUSC A G Synonymous p.S766S c.2298T>C 6 17637550 BRCA A - IntronicDeletion . c.852+37delT 6 17675099 STAD A T IntronicSNV . c.335-6277T>A 6 17682278 CLL A T Missense p.V65E c.194T>A 6 17688767 LUAD C A Missense p.A600S c.1798G>T 6 17640218 LUSC C A Missense p.C681F c.2042G>T 6 17637806 CM C A Missense p.Q694H c.2082G>T 6 17637766 SCLC C A Missense p.R455L c.1364G>T 6 17661915 LUSC C A Missense p.V442L c.1324G>T 6 17661955 SCLC C A Nonsense p.E798* c.2392G>T 6 17637456 LUSC C G Missense p.G1278A c.3833G>C 6 17626107 LUSC C T IntronicSNV . c.1396-2581G>A 6 17652112 MB C T Missense p.A119T c.355G>A 6 17675981 BLCA C T Missense p.D71N c.211G>A 6 17688750 BRCA C T Missense p.E970K c.2908G>A 6 17629522 BRCA C T Missense p.G1025S c.3073G>A 6 17629357 GBM C T Missense p.S1178N c.3533G>A 6 17628897 CM C T SpliceAcceptorSNV . c.112-1G>A 6 17688850 UCEC C T Synonymous p.S895S c.2685G>A 6 17629745 UCEC G A Missense p.P1389S c.4165C>T 6 17624801 CM G A Missense p.P258S c.772C>T 6 17675216 CM G A Missense p.P282L c.845C>T 6 17675143 CM G A Missense p.P363S c.1087C>T 6 17665598 CM G A Missense p.P492S c.1474C>T 6 17649453 HNSC G A Missense p.P499L c.1496C>T 6 17649431 CM G A Missense p.P838S c.2512C>T 6 17633028 CM G A Missense p.P879S c.2635C>T 6 17632905 BRCA G A Missense p.R1473C c.4417C>T 6 17616339 GBM G A Missense p.S1345L c.4034C>T 6 17624932 RCCC G A Missense p.S764L c.2291C>T 6 17637557 CM G A Missense p.T783I c.2348C>T 6 17637500 STAD G A Synonymous p.F790F c.2370C>T 6 17637478 CM G A Synonymous p.I479I c.1437C>T 6 17649490 CM G A Synonymous p.P1338P c.4014C>T 6 17624952 LUAD G C Missense p.D856E c.2568C>G 6 17632972 LUAD G C Missense p.F1462L c.4386C>G 6 17616370 BRCA G C Missense p.L1005V c.3013C>G 6 17629417 HNSC G C Missense p.L207V c.619C>G 6 17675564 STAD G C Missense p.L336V c.1006C>G 6 17669532 BRCA G C Missense p.S1343C c.4028C>G 6 17624938 BRCA G C Missense p.S965C c.2894C>G 6 17629536 STAD G C Missense p.T632R c.1895C>G 6 17637953 HNSC G C Missense p.T695S c.2084C>G 6 17637764 OV G C Synonymous p.L296L c.888C>G 6 17669742 HNSC G T Missense p.S1163Y c.3488C>A 6 17628942 UCEC G T Missense p.S534Y c.1601C>A 6 17648069 LUSC G T Nonsense p.S306* c.917C>A 6 17669713 BLCA G T Synonymous p.T1271T c.3813C>A 6 17626127 STAD T A Missense p.I1053L c.3157A>T 6 17629273 BRCA T A Missense p.N671I c.2012A>T 6 17637836 BRCA T A Synonymous p.A298A c.894A>T 6 17669736 LUSC T C Missense p.I196V c.586A>G 6 17675597 BLCA T C Missense p.N436S c.1307A>G 6 17661972 SCLC T C Missense p.N49D c.145A>G 6 17688816 LUAD T C Missense p.N581D c.1741A>G 6 17640275 HC T C Missense p.T116A c.346A>G 6 17675990 LUSC T C Synonymous p.E419E c.1257A>G 6 17662260 RCCC T C Synonymous p.P879P c.2637A>G 6 17632903 STAD T C Synonymous p.Q1108Q c.3324A>G 6 17629106 BRCA T C Synonymous p.S1059S c.3177A>G 6 17629253 UCEC T - Frameshift p.N411Ifs*2 c.1232delA 6 17662285 STAD T G Missense p.R598S c.1794A>C 6 17640222 LUSC