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 15 42714754 42714754 + Missense_Mutation SNP C C T TCGA-ZF-A9R7-01A-11D-A38G-08 TCGA-ZF-A9R7-10A-01D-A38J-08 g.chr15:42714754C>T c.5249G>A c.(5248-5250)gGa>gAa p.G1750E BLCA 15 42717184 42717184 + Missense_Mutation SNP G G A TCGA-DK-A6B6-01A-11D-A30E-08 TCGA-DK-A6B6-10A-01D-A30H-08 g.chr15:42717184G>A c.4969C>T c.(4969-4971)Cgg>Tgg p.R1657W BLCA 15 42729493 42729493 + Missense_Mutation SNP C C G TCGA-XF-A9SJ-01A-11D-A391-08 TCGA-XF-A9SJ-10A-01D-A394-08 g.chr15:42729493C>G c.4614G>C c.(4612-4614)caG>caC p.Q1538H BLCA 15 42731243 42731243 + Missense_Mutation SNP C C T TCGA-CU-A0YR-01A-12D-A10S-08 TCGA-CU-A0YR-10A-01D-A10S-08 g.chr15:42731243C>T c.4463G>A c.(4462-4464)gGc>gAc p.G1488D BLCA 15 42731273 42731273 + Missense_Mutation SNP G G T TCGA-UY-A78N-01A-12D-A339-08 TCGA-UY-A78N-10A-01D-A339-08 g.chr15:42731273G>T c.4433C>A c.(4432-4434)aCc>aAc p.T1478N BLCA 15 42731931 42731931 + Missense_Mutation SNP C C T TCGA-FD-A5C1-01A-11D-A289-08 TCGA-FD-A5C1-10A-01D-A289-08 g.chr15:42731931C>T c.3775G>A c.(3775-3777)Gag>Aag p.E1259K BLCA 15 42734448 42734448 + Missense_Mutation SNP C C T TCGA-GC-A6I3-01A-11D-A31L-08 TCGA-GC-A6I3-10A-01D-A31J-08 g.chr15:42734448C>T c.3517G>A c.(3517-3519)Gga>Aga p.G1173R BLCA 15 42736437 42736437 + Silent SNP C C T TCGA-XF-AAMY-01A-11D-A42E-08 TCGA-XF-AAMY-10A-01D-A42H-08 g.chr15:42736437C>T c.3315G>A c.(3313-3315)ctG>ctA p.L1105L BLCA 15 42740283 42740283 + Missense_Mutation SNP C C T TCGA-XF-AAMJ-01A-11D-A42E-08 TCGA-XF-AAMJ-10A-01D-A42H-08 g.chr15:42740283C>T c.3053G>A c.(3052-3054)cGa>cAa p.R1018Q BLCA 15 42740304 42740305 + In_Frame_Ins INS - - CAT TCGA-GU-A42Q-01A-11D-A23U-08 TCGA-GU-A42Q-10A-01D-A23U-08 g.chr15:42740304_42740305insCAT c.3031_3032insATG c.(3031-3033)ggc>gATGgc p.1010_1011insD BLCA 15 42742330 42742330 + Missense_Mutation SNP T T G TCGA-UY-A8OB-01A-12D-A42E-08 TCGA-UY-A8OB-11A-12D-A42H-08 g.chr15:42742330T>G c.2071A>C c.(2071-2073)Aca>Cca p.T691P BLCA 15 42742632 42742632 + Missense_Mutation SNP C C G TCGA-XF-A9T0-01A-11D-A391-08 TCGA-XF-A9T0-10A-01D-A394-08 g.chr15:42742632C>G c.1769G>C c.(1768-1770)aGt>aCt p.S590T BLCA 15 42743140 42743140 + Missense_Mutation SNP C C G TCGA-XF-A9ST-01A-11D-A42E-08 TCGA-XF-A9ST-10A-01D-A42H-08 g.chr15:42743140C>G c.1261G>C c.(1261-1263)Gat>Cat p.D421H BLCA 15 42749375 42749375 + Missense_Mutation SNP G G A TCGA-S5-AA26-01A-11D-A38G-08 TCGA-S5-AA26-10A-01D-A38J-08 g.chr15:42749375G>A c.29C>T c.(28-30)tCa>tTa p.S10L BRCA 15 42710150 42710150 + Splice_Site SNP C C G TCGA-C8-A26Y-01A-11D-A16D-09 TCGA-C8-A26Y-10A-01D-A16D-09 g.chr15:42710150C>G c.e18-1 BRCA 15 42713309 42713309 + Missense_Mutation SNP C C A TCGA-E9-A1RD-01A-11D-A159-09 TCGA-E9-A1RD-10A-01D-A159-09 g.chr15:42713309C>A c.5398G>T c.(5398-5400)Ggc>Tgc p.G1800C BRCA 15 42729452 42729452 + Missense_Mutation SNP G G T TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr15:42729452G>T c.4655C>A c.(4654-4656)aCt>aAt p.T1552N BRCA 15 42730858 42730858 + Missense_Mutation SNP C C G TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr15:42730858C>G c.4483G>C c.(4483-4485)Gaa>Caa p.E1495Q BRCA 15 42734373 42734373 + Nonsense_Mutation SNP G G A TCGA-AN-A0FT-01A-11W-A050-09 TCGA-AN-A0FT-10A-01W-A055-09 g.chr15:42734373G>A c.3592C>T c.(3592-3594)Cag>Tag p.Q1198* BRCA 15 42740787 42740787 + Missense_Mutation SNP G G C TCGA-E2-A14X-01A-11D-A10Y-09 TCGA-E2-A14X-10A-01D-A110-09 g.chr15:42740787G>C c.2549C>G c.(2548-2550)tCg>tGg p.S850W BRCA 15 42742652 42742652 + Silent SNP C C T TCGA-BH-A0HF-01A-11W-A071-09 TCGA-BH-A0HF-10A-01W-A071-09 g.chr15:42742652C>T c.1749G>A c.(1747-1749)gtG>gtA p.V583V BRCA 15 42743220 42743220 + Missense_Mutation SNP G G T TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr15:42743220G>T c.1181C>A c.(1180-1182)aCt>aAt p.T394N BRCA 15 42743279 42743279 + Missense_Mutation SNP C C G TCGA-D8-A1JN-01A-11D-A13L-09 TCGA-D8-A1JN-10A-01D-A13O-09 g.chr15:42743279C>G c.1122G>C c.(1120-1122)atG>atC p.M374I BRCA 15 42743464 42743464 + Missense_Mutation SNP C C T TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr15:42743464C>T c.937G>A c.(937-939)Gac>Aac p.D313N BRCA 15 42743536 42743536 + Missense_Mutation SNP C C T TCGA-AO-A03R-01A-21W-A050-09 TCGA-AO-A03R-10A-01W-A055-09 g.chr15:42743536C>T c.865G>A c.(865-867)Ggt>Agt p.G289S BRCA 15 42743889 42743889 + Missense_Mutation SNP G G A TCGA-D8-A1JA-01A-11D-A13L-09 TCGA-D8-A1JA-10A-01W-A14R-09 g.chr15:42743889G>A c.512C>T c.(511-513)tCc>tTc p.S171F BRCA 15 42743987 42743987 + Silent SNP G G A TCGA-A2-A25D-01A-12D-A16D-09 TCGA-A2-A25D-10A-01D-A16D-09 g.chr15:42743987G>A c.414C>T c.(412-414)ggC>ggT p.G138G BRCA 15 42744120 42744120 + Missense_Mutation SNP A A G TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr15:42744120A>G c.281T>C c.(280-282)aTa>aCa p.I94T BRCA 15 42749157 42749157 + Splice_Site SNP G G A TCGA-C8-A12Q-01A-11D-A10Y-09 TCGA-C8-A12Q-10A-01D-A110-09 g.chr15:42749157G>A c.247C>T c.(247-249)Cga>Tga p.R83* CESC 15 42729566 42729566 + Nonsense_Mutation SNP G G C TCGA-EK-A3GK-01A-11D-A20U-09 TCGA-EK-A3GK-10A-01D-A20U-09 g.chr15:42729566G>C c.4541C>G c.(4540-4542)tCa>tGa p.S1514* CESC 15 42734469 42734469 + Missense_Mutation SNP G G A TCGA-DG-A2KM-01A-11D-A17W-09 TCGA-DG-A2KM-10A-01D-A17W-09 g.chr15:42734469G>A c.3496C>T c.(3496-3498)Cat>Tat p.H1166Y CHOL 15 42740764 42740764 + Silent SNP G G T TCGA-W5-AA2O-01A-11D-A417-09 TCGA-W5-AA2O-10A-01D-A41A-09 g.chr15:42740764G>T c.2572C>A c.(2572-2574)Cga>Aga p.R858R COAD 15 42709536 42709536 + Missense_Mutation SNP C C T TCGA-AA-3850-01A-01W-0995-10 TCGA-AA-3850-10A-01W-0995-10 g.chr15:42709536C>T c.5618G>A c.(5617-5619)cGa>cAa p.R1873Q COAD 15 42710089 42710089 + Missense_Mutation SNP C C T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr15:42710089C>T c.5509G>A c.(5509-5511)Gac>Aac p.D1837N COAD 15 42717101 42717101 + Silent SNP T T A TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr15:42717101T>A c.5052A>T c.(5050-5052)gtA>gtT p.V1684V COAD 15 42720269 42720269 + Nonsense_Mutation SNP G G A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr15:42720269G>A c.4876C>T c.(4876-4878)Cga>Tga p.R1626* COAD 15 42727684 42727684 + Silent SNP A A G TCGA-G4-6309-01A-21D-1835-10 TCGA-G4-6309-10A-01D-1835-10 g.chr15:42727684A>G c.4710T>C c.(4708-4710)caT>caC p.H1570H COAD 15 42729493 42729493 + Silent SNP C C T TCGA-AA-3697-01A-01D-1719-10 TCGA-AA-3697-11A-01D-1719-10 g.chr15:42729493C>T c.4614G>A c.(4612-4614)caG>caA p.Q1538Q COAD 15 42730815 42730815 + Missense_Mutation SNP G G T TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr15:42730815G>T c.4526C>A c.(4525-4527)tCt>tAt p.S1509Y COAD 15 42731492 42731492 + Missense_Mutation SNP C C A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr15:42731492C>A c.4214G>T c.(4213-4215)aGg>aTg p.R1405M COAD 15 42734269 42734269 + Splice_Site SNP A A G TCGA-DM-A1HB-01A-21D-A183-10 TCGA-DM-A1HB-10A-01D-A183-10 g.chr15:42734269A>G c.e7+1 COAD 15 42734425 42734425 + Silent SNP C C T TCGA-CK-5915-01A-11D-1650-10 TCGA-CK-5915-10A-01D-1650-10 g.chr15:42734425C>T c.3540G>A c.(3538-3540)acG>acA p.T1180T COAD 15 42736438 42736438 + Missense_Mutation SNP A A G TCGA-AA-A01Q-01A-01W-A005-10 TCGA-AA-A01Q-10A-01W-A005-10 g.chr15:42736438A>G c.3314T>C c.(3313-3315)cTg>cCg p.L1105P COAD 15 42738796 42738796 + Nonsense_Mutation SNP C C A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr15:42738796C>A c.3127G>T c.(3127-3129)Gga>Tga p.G1043* COAD 15 42740640 42740640 + Missense_Mutation SNP C C A TCGA-AA-3516-01A-02W-0833-10 TCGA-AA-3516-10A-01W-0833-10 g.chr15:42740640C>A c.2696G>T c.(2695-2697)aGg>aTg p.R899M COAD 15 42740764 42740764 + Nonsense_Mutation SNP G G A TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr15:42740764G>A c.2572C>T c.(2572-2574)Cga>Tga p.R858* COAD 15 42742266 42742266 + Missense_Mutation SNP G G A TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chr15:42742266G>A c.2135C>T c.(2134-2136)tCg>tTg p.S712L COAD 15 42742350 42742350 + Missense_Mutation SNP T T G TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr15:42742350T>G c.2051A>C c.(2050-2052)aAa>aCa p.K684T COAD 15 42742520 42742520 + Silent SNP C C T TCGA-CM-5349-01A-21D-1719-10 TCGA-CM-5349-10A-01D-1719-10 g.chr15:42742520C>T c.1881G>A c.(1879-1881)gaG>gaA p.E627E COAD 15 42742521 42742521 + Missense_Mutation SNP T T C TCGA-CM-5862-01A-01D-1650-10 TCGA-CM-5862-10A-01D-1650-10 g.chr15:42742521T>C c.1880A>G c.(1879-1881)gAg>gGg p.E627G COAD 15 42742522 42742522 + Nonsense_Mutation SNP C C A TCGA-AA-3496-01A-21D-1835-10 TCGA-AA-3496-11A-01D-1835-10 g.chr15:42742522C>A c.1879G>T c.(1879-1881)Gag>Tag p.E627* COAD 15 42742856 42742856 + Silent SNP T T C TCGA-AA-A00J-01A-02W-A005-10 TCGA-AA-A00J-10A-01W-A005-10 g.chr15:42742856T>C c.1545A>G c.(1543-1545)aaA>aaG p.K515K COAD 15 42742900 42742900 + Missense_Mutation SNP G G A TCGA-AA-3952-01A-01W-0995-10 TCGA-AA-3952-10A-01W-0995-10 g.chr15:42742900G>A c.1501C>T c.(1501-1503)Cct>Tct p.P501S COAD 15 42742965 42742965 + Missense_Mutation SNP T T A TCGA-D5-6538-01A-11D-1719-10 TCGA-D5-6538-10A-01D-1719-10 g.chr15:42742965T>A c.1436A>T c.(1435-1437)aAt>aTt p.N479I COAD 15 42743263 42743264 + Frame_Shift_Del DEL AG AG - TCGA-AA-3870-01A-01W-0995-10 TCGA-AA-3870-10A-01W-0995-10 g.chr15:42743263_42743264delAG c.1137_1138delCT c.(1135-1140)ctctttfs p.F380fs COAD 15 42743576 42743576 + Silent SNP G G A TCGA-AA-3845-01A-01W-0995-10 TCGA-AA-3845-10A-01W-0995-10 g.chr15:42743576G>A c.825C>T c.(823-825)caC>caT p.H275H COAD 15 42743992 42743993 + Frame_Shift_Ins INS - - T TCGA-AA-3518-01A-02W-0833-10 TCGA-AA-3518-10A-01W-0833-10 g.chr15:42743992_42743993insT c.408_409insA c.(406-411)aaagatfs p.D137fs COADREAD 15 42709536 42709536 + Missense_Mutation SNP C C T TCGA-AA-3850-01A-01W-0995-10 TCGA-AA-3850-10A-01W-0995-10 g.chr15:42709536C>T c.5618G>A c.(5617-5619)cGa>cAa p.R1873Q COADREAD 15 42710089 42710089 + Missense_Mutation SNP C C T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr15:42710089C>T c.5509G>A c.(5509-5511)Gac>Aac p.D1837N COADREAD 15 42717043 42717043 + Missense_Mutation SNP G G T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr15:42717043G>T c.5110C>A c.(5110-5112)Ctt>Att p.L1704I COADREAD 15 42717101 42717101 + Silent SNP T T A TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr15:42717101T>A c.5052A>T c.(5050-5052)gtA>gtT p.V1684V COADREAD 15 42720269 42720269 + Nonsense_Mutation SNP G G A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr15:42720269G>A c.4876C>T c.(4876-4878)Cga>Tga p.R1626* COADREAD 15 42727684 42727684 + Silent SNP A A G TCGA-G4-6309-01A-21D-1835-10 TCGA-G4-6309-10A-01D-1835-10 g.chr15:42727684A>G c.4710T>C c.(4708-4710)caT>caC p.H1570H COADREAD 15 42729493 42729493 + Silent SNP C C T TCGA-AA-3697-01A-01D-1719-10 TCGA-AA-3697-11A-01D-1719-10 g.chr15:42729493C>T c.4614G>A c.(4612-4614)caG>caA p.Q1538Q COADREAD 15 42730815 42730815 + Missense_Mutation SNP G G T TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr15:42730815G>T c.4526C>A c.(4525-4527)tCt>tAt p.S1509Y COADREAD 15 42731492 42731492 + Missense_Mutation SNP C C A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr15:42731492C>A c.4214G>T c.(4213-4215)aGg>aTg p.R1405M COADREAD 15 42734269 42734269 + Splice_Site SNP A A G TCGA-DM-A1HB-01A-21D-A183-10 TCGA-DM-A1HB-10A-01D-A183-10 g.chr15:42734269A>G c.e7+1 COADREAD 15 42734425 42734425 + Silent SNP C C T TCGA-CK-5915-01A-11D-1650-10 TCGA-CK-5915-10A-01D-1650-10 g.chr15:42734425C>T c.3540G>A c.(3538-3540)acG>acA p.T1180T COADREAD 15 42736438 42736438 + Missense_Mutation SNP A A G TCGA-AA-A01Q-01A-01W-A005-10 TCGA-AA-A01Q-10A-01W-A005-10 g.chr15:42736438A>G c.3314T>C c.(3313-3315)cTg>cCg p.L1105P COADREAD 15 42738796 42738796 + Nonsense_Mutation SNP C C A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr15:42738796C>A c.3127G>T c.(3127-3129)Gga>Tga p.G1043* COADREAD 15 42740640 42740640 + Missense_Mutation SNP C C A TCGA-AA-3516-01A-02W-0833-10 TCGA-AA-3516-10A-01W-0833-10 g.chr15:42740640C>A c.2696G>T c.(2695-2697)aGg>aTg p.R899M COADREAD 15 42740764 42740764 + Nonsense_Mutation SNP G G A TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr15:42740764G>A c.2572C>T c.(2572-2574)Cga>Tga p.R858* COADREAD 15 42742266 42742266 + Missense_Mutation SNP G G A TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chr15:42742266G>A c.2135C>T c.(2134-2136)tCg>tTg p.S712L COADREAD 15 42742302 42742302 + Missense_Mutation SNP T T C TCGA-AF-2691-01A-01W-0831-10 TCGA-AF-2691-10A-01W-0831-10 g.chr15:42742302T>C c.2099A>G c.(2098-2100)gAt>gGt p.D700G COADREAD 15 42742350 42742350 + Missense_Mutation SNP T T G TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr15:42742350T>G c.2051A>C c.(2050-2052)aAa>aCa p.K684T COADREAD 15 42742459 42742459 + Missense_Mutation SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr15:42742459G>A c.1942C>T c.(1942-1944)Cgc>Tgc p.R648C COADREAD 15 42742520 42742520 + Silent SNP C C T TCGA-CM-5349-01A-21D-1719-10 TCGA-CM-5349-10A-01D-1719-10 g.chr15:42742520C>T c.1881G>A c.(1879-1881)gaG>gaA p.E627E COADREAD 15 42742521 42742521 + Missense_Mutation SNP T T C TCGA-CM-5862-01A-01D-1650-10 TCGA-CM-5862-10A-01D-1650-10 g.chr15:42742521T>C c.1880A>G c.(1879-1881)gAg>gGg p.E627G COADREAD 15 42742522 42742522 + Nonsense_Mutation SNP C C A TCGA-AA-3496-01A-21D-1835-10 TCGA-AA-3496-11A-01D-1835-10 g.chr15:42742522C>A c.1879G>T c.(1879-1881)Gag>Tag p.E627* COADREAD 15 42742856 42742856 + Silent SNP T T C TCGA-AA-A00J-01A-02W-A005-10 TCGA-AA-A00J-10A-01W-A005-10 g.chr15:42742856T>C c.1545A>G c.(1543-1545)aaA>aaG p.K515K COADREAD 15 42742900 42742900 + Missense_Mutation SNP G G A TCGA-AA-3952-01A-01W-0995-10 TCGA-AA-3952-10A-01W-0995-10 g.chr15:42742900G>A c.1501C>T c.(1501-1503)Cct>Tct p.P501S COADREAD 15 42742965 42742965 + Missense_Mutation SNP T T A TCGA-D5-6538-01A-11D-1719-10 TCGA-D5-6538-10A-01D-1719-10 g.chr15:42742965T>A c.1436A>T c.(1435-1437)aAt>aTt p.N479I COADREAD 15 42743263 42743264 + Frame_Shift_Del DEL AG AG - TCGA-AA-3870-01A-01W-0995-10 TCGA-AA-3870-10A-01W-0995-10 g.chr15:42743263_42743264delAG c.1137_1138delCT c.(1135-1140)ctctttfs p.F380fs COADREAD 15 42743576 42743576 + Silent SNP G G A TCGA-AA-3845-01A-01W-0995-10 TCGA-AA-3845-10A-01W-0995-10 g.chr15:42743576G>A c.825C>T c.(823-825)caC>caT p.H275H COADREAD 15 42743992 42743993 + Frame_Shift_Ins INS - - T TCGA-AA-3518-01A-02W-0833-10 TCGA-AA-3518-10A-01W-0833-10 g.chr15:42743992_42743993insT c.408_409insA c.(406-411)aaagatfs p.D137fs DLBC 15 42743209 42743209 + Missense_Mutation SNP G G A TCGA-G8-6909-01A-11D-2210-10 TCGA-G8-6909-14A-01D-2210-10 g.chr15:42743209G>A c.1192C>T c.(1192-1194)Cgt>Tgt p.R398C ESCA 15 42730815 42730815 + Missense_Mutation SNP G G T TCGA-JY-A93D-01A-11D-A387-09 TCGA-JY-A93D-10A-01D-A38A-09 g.chr15:42730815G>T c.4526C>A c.(4525-4527)tCt>tAt p.S1509Y ESCA 15 42740536 42740536 + Frame_Shift_Del DEL T T - TCGA-2H-A9GR-01A-12D-A37C-09 TCGA-2H-A9GR-11A-11D-A37F-09 g.chr15:42740536delT c.2800delA c.(2800-2802)aggfs p.R935fs ESCA 15 42743781 42743781 + Missense_Mutation SNP G G A TCGA-X8-AAAR-01A-11D-A403-09 TCGA-X8-AAAR-10A-01D-A403-09 g.chr15:42743781G>A c.620C>T c.(619-621)tCt>tTt p.S207F ESCA 15 42749300 42749300 + Missense_Mutation SNP T T C TCGA-IG-A4P3-01A-11D-A27G-09 TCGA-IG-A4P3-10A-01D-A27G-09 g.chr15:42749300T>C c.104A>G c.(103-105)tAt>tGt p.Y35C GBMLGG 15 42714728 42714728 + Missense_Mutation SNP C C A TCGA-S9-A6WL-01A-21D-A33T-08 TCGA-S9-A6WL-10A-01D-A33W-08 g.chr15:42714728C>A c.5275G>T c.(5275-5277)Gat>Tat p.D1759Y GBMLGG 15 42731630 42731632 + In_Frame_Del DEL TTC TTC - TCGA-P5-A5ET-01A-11D-A27K-08 TCGA-P5-A5ET-10A-01D-A27N-08 g.chr15:42731630_42731632delTTC c.4074_4076delGAA c.(4072-4077)aagaaa>aaa p.1358_1359KK>K GBMLGG 15 42734288 42734288 + Missense_Mutation SNP T T C TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr15:42734288T>C c.3677A>G c.(3676-3678)gAa>gGa p.E1226G GBMLGG 15 42740426 42740426 + Silent SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr15:42740426G>T c.2910C>A c.(2908-2910)tcC>tcA p.S970S GBMLGG 15 42742995 42742995 + Missense_Mutation SNP G G A TCGA-DU-7006-01A-11D-2024-08 TCGA-DU-7006-10A-01D-2024-08 g.chr15:42742995G>A c.1406C>T c.(1405-1407)cCa>cTa p.P469L GBMLGG 15 42744114 42744114 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr15:42744114G>T c.287C>A c.(286-288)tCt>tAt p.S96Y HNSC 15 42720295 42720295 + Missense_Mutation SNP C C T TCGA-CQ-7064-01A-11D-2394-08 TCGA-CQ-7064-10A-01D-2394-08 g.chr15:42720295C>T c.4850G>A c.(4849-4851)cGg>cAg p.R1617Q HNSC 15 42729429 42729429 + Splice_Site SNP C C T TCGA-CN-A49C-01A-11D-A24D-08 TCGA-CN-A49C-10B-01D-A24F-08 g.chr15:42729429C>T c.e10+1 HNSC 15 42731746 42731746 + Silent SNP G G A TCGA-CV-7568-01A-11D-2229-08 TCGA-CV-7568-10A-01D-2229-08 g.chr15:42731746G>A c.3960C>T c.(3958-3960)acC>acT p.T1320T HNSC 15 42734335 42734335 + Silent SNP C C T TCGA-CV-5442-01A-01D-1512-08 TCGA-CV-5442-11A-01D-1512-08 g.chr15:42734335C>T c.3630G>A c.(3628-3630)gaG>gaA p.E1210E HNSC 15 42742071 42742071 + Missense_Mutation SNP G G A TCGA-CQ-A4CA-01A-11D-A25D-08 TCGA-CQ-A4CA-10A-01D-A25E-08 g.chr15:42742071G>A c.2330C>T c.(2329-2331)aCc>aTc p.T777I HNSC 15 42742338 42742338 + Missense_Mutation SNP G G A TCGA-CN-6011-01A-11D-1683-08 TCGA-CN-6011-10A-01D-1683-08 g.chr15:42742338G>A c.2063C>T c.(2062-2064)tCt>tTt p.S688F HNSC 15 42742378 42742378 + Missense_Mutation SNP C C T TCGA-CN-4723-01A-01D-1434-08 TCGA-CN-4723-10A-01D-1434-08 g.chr15:42742378C>T c.2023G>A c.(2023-2025)Gaa>Aaa p.E675K HNSC 15 42742624 42742624 + Missense_Mutation SNP C C G TCGA-CN-A63W-01A-11D-A30E-08 TCGA-CN-A63W-10A-01D-A30H-08 g.chr15:42742624C>G c.1777G>C c.(1777-1779)Gag>Cag p.E593Q HNSC 15 42743329 42743329 + Silent SNP G G A TCGA-BB-4227-01A-01D-1870-08 TCGA-BB-4227-10A-01D-1870-08 g.chr15:42743329G>A c.1072C>T c.(1072-1074)Ctg>Ttg p.L358L HNSC 15 42743338 42743338 + Missense_Mutation SNP G G C TCGA-BB-4227-01A-01D-1870-08 TCGA-BB-4227-10A-01D-1870-08 g.chr15:42743338G>C c.1063C>G c.(1063-1065)Cag>Gag p.Q355E HNSC 15 42743476 42743476 + Missense_Mutation SNP C C G TCGA-D6-A74Q-01A-11D-A34J-08 TCGA-D6-A74Q-10A-02D-A34M-08 g.chr15:42743476C>G c.925G>C c.(925-927)Gaa>Caa p.E309Q HNSC 15 42743875 42743875 + Missense_Mutation SNP G G C TCGA-BB-4227-01A-01D-1870-08 TCGA-BB-4227-10A-01D-1870-08 g.chr15:42743875G>C c.526C>G c.(526-528)Cac>Gac p.H176D HNSC 15 42749328 42749328 + Missense_Mutation SNP C C A TCGA-BA-5555-01A-01D-1512-08 TCGA-BA-5555-10A-01D-1512-08 g.chr15:42749328C>A c.76G>T c.(76-78)Ggg>Tgg p.G26W KICH 15 42720229 42720229 + Missense_Mutation SNP G G A TCGA-KO-8405-01A-11D-2310-10 TCGA-KO-8405-11A-01D-2311-10 g.chr15:42720229G>A c.4916C>T c.(4915-4917)aCc>aTc p.T1639I KICH 15 42734362 42734362 + Silent SNP T T C TCGA-KN-8426-01A-11D-2310-10 TCGA-KN-8426-11A-01D-2311-10 g.chr15:42734362T>C c.3603A>G c.(3601-3603)caA>caG p.Q1201Q KICH 15 42742931 42742931 + Silent SNP C C T TCGA-KL-8341-01A-11D-2310-10 TCGA-KL-8341-11A-01D-2310-10 g.chr15:42742931C>T c.1470G>A c.(1468-1470)tcG>tcA p.S490S KIPAN 15 42717056 42717056 + Missense_Mutation SNP A A C TCGA-EV-5901-01A-11D-1589-08 TCGA-EV-5901-10A-01D-1589-08 g.chr15:42717056A>C c.5097T>G c.(5095-5097)caT>caG p.H1699Q KIPAN 15 42720229 42720229 + Missense_Mutation SNP G G A TCGA-KO-8405-01A-11D-2310-10 TCGA-KO-8405-11A-01D-2311-10 g.chr15:42720229G>A c.4916C>T c.(4915-4917)aCc>aTc p.T1639I KIPAN 15 42734362 42734362 + Silent SNP T T C TCGA-KN-8426-01A-11D-2310-10 TCGA-KN-8426-11A-01D-2311-10 g.chr15:42734362T>C c.3603A>G c.(3601-3603)caA>caG p.Q1201Q KIPAN 15 42742117 42742117 + Missense_Mutation SNP C C A TCGA-DZ-6133-01A-11D-1961-08 TCGA-DZ-6133-10A-01D-1962-08 g.chr15:42742117C>A c.2284G>T c.(2284-2286)Ggt>Tgt p.G762C KIPAN 15 42742412 42742412 + Silent SNP G G A TCGA-CJ-5678-01A-11D-1534-10 TCGA-CJ-5678-11A-01D-1534-10 g.chr15:42742412G>A c.1989C>T c.(1987-1989)caC>caT p.H663H KIPAN 15 42742931 42742931 + Silent SNP C C T TCGA-KL-8341-01A-11D-2310-10 TCGA-KL-8341-11A-01D-2310-10 g.chr15:42742931C>T c.1470G>A c.(1468-1470)tcG>tcA p.S490S KIPAN 15 42743699 42743699 + Silent SNP A A G TCGA-B0-5705-01A-11D-1534-10 TCGA-B0-5705-11A-01D-1534-10 g.chr15:42743699A>G c.702T>C c.(700-702)aaT>aaC p.N234N KIPAN 15 42744055 42744055 + Missense_Mutation SNP T T A TCGA-CJ-4639-01A-02D-1386-10 TCGA-CJ-4639-11A-01D-1251-10 g.chr15:42744055T>A c.346A>T c.(346-348)Agt>Tgt p.S116C KIPAN 15 42749284 42749284 + Silent SNP A A G TCGA-CJ-4873-01A-01D-1373-10 TCGA-CJ-4873-11A-01D-1373-10 g.chr15:42749284A>G c.120T>C c.(118-120)tcT>tcC p.S40S KIRC 15 42742412 42742412 + Silent SNP G G A TCGA-CJ-5678-01A-11D-1534-10 TCGA-CJ-5678-11A-01D-1534-10 g.chr15:42742412G>A c.1989C>T c.(1987-1989)caC>caT p.H663H KIRC 15 42743699 42743699 + Silent SNP A A G TCGA-B0-5705-01A-11D-1534-10 TCGA-B0-5705-11A-01D-1534-10 g.chr15:42743699A>G c.702T>C c.(700-702)aaT>aaC p.N234N KIRC 15 42744055 42744055 + Missense_Mutation SNP T T A TCGA-CJ-4639-01A-02D-1386-10 TCGA-CJ-4639-11A-01D-1251-10 g.chr15:42744055T>A c.346A>T c.(346-348)Agt>Tgt p.S116C KIRC 15 42749284 42749284 + Silent SNP A A G TCGA-CJ-4873-01A-01D-1373-10 TCGA-CJ-4873-11A-01D-1373-10 g.chr15:42749284A>G c.120T>C c.(118-120)tcT>tcC p.S40S KIRP 15 42717056 42717056 + Missense_Mutation SNP A A C TCGA-EV-5901-01A-11D-1589-08 TCGA-EV-5901-10A-01D-1589-08 g.chr15:42717056A>C c.5097T>G c.(5095-5097)caT>caG p.H1699Q KIRP 15 42742117 42742117 + Missense_Mutation SNP C C A TCGA-DZ-6133-01A-11D-1961-08 TCGA-DZ-6133-10A-01D-1962-08 g.chr15:42742117C>A c.2284G>T c.(2284-2286)Ggt>Tgt p.G762C LGG 15 42714728 42714728 + Missense_Mutation SNP C C A TCGA-S9-A6WL-01A-21D-A33T-08 TCGA-S9-A6WL-10A-01D-A33W-08 g.chr15:42714728C>A c.5275G>T c.(5275-5277)Gat>Tat p.D1759Y LGG 15 42731630 42731632 + In_Frame_Del DEL TTC TTC - TCGA-P5-A5ET-01A-11D-A27K-08 TCGA-P5-A5ET-10A-01D-A27N-08 g.chr15:42731630_42731632delTTC c.4074_4076delGAA c.(4072-4077)aagaaa>aaa p.1358_1359KK>K LGG 15 42734288 42734288 + Missense_Mutation SNP T T C TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr15:42734288T>C c.3677A>G c.(3676-3678)gAa>gGa p.E1226G LGG 15 42740426 42740426 + Silent SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr15:42740426G>T c.2910C>A c.(2908-2910)tcC>tcA p.S970S LGG 15 42742995 42742995 + Missense_Mutation SNP G G A TCGA-DU-7006-01A-11D-2024-08 TCGA-DU-7006-10A-01D-2024-08 g.chr15:42742995G>A c.1406C>T c.(1405-1407)cCa>cTa p.P469L LGG 15 42744114 42744114 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr15:42744114G>T c.287C>A c.(286-288)tCt>tAt p.S96Y LIHC 15 42729475 42729475 + Silent SNP T T C TCGA-G3-A7M5-01A-11D-A33Q-10 TCGA-G3-A7M5-10A-01D-A33Q-10 g.chr15:42729475T>C c.4632A>G c.(4630-4632)ctA>ctG p.L1544L LIHC 15 42734378 42734378 + Missense_Mutation SNP G G A TCGA-BC-A10Z-01A-11D-A12Z-10 TCGA-BC-A10Z-11A-11D-A12Z-10 g.chr15:42734378G>A c.3587C>T c.(3586-3588)tCa>tTa p.S1196L LIHC 15 42742306 42742306 + Missense_Mutation SNP A A C TCGA-DD-A39X-01A-11D-A20W-10 TCGA-DD-A39X-11A-11D-A20W-10 g.chr15:42742306A>C c.2095T>G c.(2095-2097)Ttg>Gtg p.L699V LIHC 15 42742679 42742679 + Frame_Shift_Del DEL T T - TCGA-DD-A3A0-01A-11D-A20W-10 TCGA-DD-A3A0-11A-11D-A20W-10 g.chr15:42742679delT c.1722delA c.(1720-1722)aaafs p.K574fs LIHC 15 42743691 42743691 + Missense_Mutation SNP T T A TCGA-3K-AAZ8-01A-12D-A38X-10 TCGA-3K-AAZ8-10A-01D-A38X-10 g.chr15:42743691T>A c.710A>T c.(709-711)tAc>tTc p.Y237F LUAD 15 42714782 42714782 + Missense_Mutation SNP G G A TCGA-78-7148-01A-11D-2036-08 TCGA-78-7148-10A-01D-2036-08 g.chr15:42714782G>A c.5221C>T c.(5221-5223)Cat>Tat p.H1741Y LUAD 15 42727683 42727683 + Missense_Mutation SNP T T A TCGA-69-7765-01A-11D-2167-08 TCGA-69-7765-10A-01D-2167-08 g.chr15:42727683T>A c.4711A>T c.(4711-4713)Acc>Tcc p.T1571S LUAD 15 42729559 42729559 + Silent SNP T T G TCGA-05-4250-01A-01D-1105-08 TCGA-05-4250-10A-01D-1105-08 g.chr15:42729559T>G c.4548A>C c.(4546-4548)ccA>ccC p.P1516P LUAD 15 42731607 42731607 + Missense_Mutation SNP G G A TCGA-55-A48Y-01A-11D-A24D-08 TCGA-55-A48Y-10A-01D-A24F-08 g.chr15:42731607G>A c.4099C>T c.(4099-4101)Cct>Tct p.P1367S LUAD 15 42731855 42731855 + Missense_Mutation SNP G G A TCGA-55-A48Y-01A-11D-A24D-08 TCGA-55-A48Y-10A-01D-A24F-08 g.chr15:42731855G>A c.3851C>T c.(3850-3852)tCa>tTa p.S1284L LUAD 15 42731878 42731878 + Frame_Shift_Del DEL T T - TCGA-95-8039-01A-11D-2238-08 TCGA-95-8039-10A-01D-2238-08 g.chr15:42731878delT c.3828delA c.(3826-3828)agafs p.R1276fs LUAD 15 42734441 42734441 + Missense_Mutation SNP G G T TCGA-NJ-A4YI-01A-11D-A25L-08 TCGA-NJ-A4YI-10A-01D-A25L-08 g.chr15:42734441G>T c.3524C>A c.(3523-3525)tCt>tAt p.S1175Y LUAD 15 42742156 42742156 + Missense_Mutation SNP G G A TCGA-55-A48Z-01A-12D-A24P-08 TCGA-55-A48Z-10A-01D-A24P-08 g.chr15:42742156G>A c.2245C>T c.(2245-2247)Cca>Tca p.P749S LUAD 15 42742657 42742657 + Nonsense_Mutation SNP G G A TCGA-MP-A4TF-01A-11D-A25L-08 TCGA-MP-A4TF-10A-01D-A25L-08 g.chr15:42742657G>A c.1744C>T c.(1744-1746)Caa>Taa p.Q582* LUAD 15 42742934 42742934 + Silent SNP G G C TCGA-17-Z028-01A-01W-0746-08 TCGA-17-Z028-11A-01W-0746-08 g.chr15:42742934G>C c.1467C>G c.(1465-1467)ccC>ccG p.P489P LUAD 15 42743868 42743868 + Missense_Mutation SNP T T C TCGA-44-A4SS-01A-11D-A24P-08 TCGA-44-A4SS-10A-01D-A24P-08 g.chr15:42743868T>C c.533A>G c.(532-534)cAt>cGt p.H178R LUSC 15 42710039 42710039 + Silent SNP G G A TCGA-39-5030-01A-01D-1441-08 TCGA-39-5030-11A-01D-1441-08 g.chr15:42710039G>A c.5559C>T c.(5557-5559)tgC>tgT p.C1853C LUSC 15 42710095 42710095 + Silent SNP G G A TCGA-18-3409-01A-01D-0983-08 TCGA-18-3409-11A-01D-0983-08 g.chr15:42710095G>A c.5503C>T c.(5503-5505)Ctg>Ttg p.L1835L LUSC 15 42717087 42717087 + Missense_Mutation SNP T T A TCGA-18-3409-01A-01D-0983-08 TCGA-18-3409-11A-01D-0983-08 g.chr15:42717087T>A c.5066A>T c.(5065-5067)aAt>aTt p.N1689I LUSC 15 42720257 42720257 + Missense_Mutation SNP C C A TCGA-66-2742-01A-01D-0983-08 TCGA-66-2742-11A-01D-0983-08 g.chr15:42720257C>A c.4888G>T c.(4888-4890)Gcg>Tcg p.A1630S LUSC 15 42727711 42727711 + Silent SNP C C T TCGA-60-2698-01A-01D-1522-08 TCGA-60-2698-11A-01D-1522-08 g.chr15:42727711C>T c.4683G>A c.(4681-4683)cgG>cgA p.R1561R LUSC 15 42734294 42734294 + Missense_Mutation SNP G G A TCGA-18-3409-01A-01D-0983-08 TCGA-18-3409-11A-01D-0983-08 g.chr15:42734294G>A c.3671C>T c.(3670-3672)tCc>tTc p.S1224F LUSC 15 42742027 42742027 + Missense_Mutation SNP C C T TCGA-34-2600-01A-01D-1522-08 TCGA-34-2600-11A-01D-1522-08 g.chr15:42742027C>T c.2374G>A c.(2374-2376)Gaa>Aaa p.E792K LUSC 15 42742430 42742430 + Silent SNP T T C TCGA-66-2789-01A-01D-0983-08 TCGA-66-2789-11A-01D-0983-08 g.chr15:42742430T>C c.1971A>G c.(1969-1971)acA>acG p.T657T LUSC 15 42742495 42742495 + Nonsense_Mutation SNP T T A TCGA-22-4595-01A-01D-1267-08 TCGA-22-4595-11A-01D-1267-08 g.chr15:42742495T>A c.1906A>T c.(1906-1908)Aga>Tga p.R636* LUSC 15 42742724 42742724 + Silent SNP G G T TCGA-66-2734-01A-01D-0983-08 TCGA-66-2734-11A-01D-0983-08 g.chr15:42742724G>T c.1677C>A c.(1675-1677)acC>acA p.T559T LUSC 15 42742728 42742728 + Missense_Mutation SNP C C A TCGA-18-5595-01A-01D-1632-08 TCGA-18-5595-11A-01D-1632-08 g.chr15:42742728C>A c.1673G>T c.(1672-1674)aGt>aTt p.S558I LUSC 15 42743038 42743038 + Missense_Mutation SNP G G A TCGA-18-3409-01A-01D-0983-08 TCGA-18-3409-11A-01D-0983-08 g.chr15:42743038G>A c.1363C>T c.(1363-1365)Ctt>Ttt p.L455F OV 15 42734333 42734333 + Missense_Mutation SNP T T C TCGA-25-1317-01A-01W-0490-10 TCGA-25-1317-10A-01W-0490-10 g.chr15:42734333T>C c.3632A>G c.(3631-3633)aAt>aGt p.N1211S OV 15 42737062 42737062 + Missense_Mutation SNP T T G TCGA-09-1675-01B-01W-0633-09 TCGA-09-1675-10A-01W-0633-09 g.chr15:42737062T>G c.3254A>C c.(3253-3255)tAt>tCt p.Y1085S OV 15 42742522 42742522 + Missense_Mutation SNP C C T TCGA-13-1499-01A-01W-0549-09 TCGA-13-1499-10A-01W-0549-09 g.chr15:42742522C>T c.1879G>A c.(1879-1881)Gag>Aag p.E627K PAAD 15 42714807 42714807 + Silent SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr15:42714807G>A c.5196C>T c.(5194-5196)ctC>ctT p.L1732L PAAD 15 42717205 42717205 + Missense_Mutation SNP T T C TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr15:42717205T>C c.4948A>G c.(4948-4950)Atc>Gtc p.I1650V PAAD 15 42740566 42740566 + Missense_Mutation SNP C C A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr15:42740566C>A c.2770G>T c.(2770-2772)Ggt>Tgt p.G924C PCPG 15 42710138 42710145 + Frame_Shift_Del DEL GCAACCAT GCAACCAT - TCGA-QR-A70U-01A-11D-A35D-08 TCGA-QR-A70U-10A-01D-A35B-08 g.chr15:42710138_42710145delGCAACCAT c.5453_5460delATGGTTGC c.(5452-5460)catggttgcfs p.HGC1818fs PRAD 15 42720231 42720231 + Silent SNP G G T TCGA-J9-A8CP-01A-11D-A34U-08 TCGA-J9-A8CP-10A-01D-A34X-08 g.chr15:42720231G>T c.4914C>A c.(4912-4914)gtC>gtA p.V1638V PRAD 15 42731450 42731450 + Missense_Mutation SNP C C T TCGA-J9-A52D-01A-11D-A29Q-08 TCGA-J9-A52D-10A-01D-A29Q-08 g.chr15:42731450C>T c.4256G>A c.(4255-4257)aGt>aAt p.S1419N PRAD 15 42740292 42740292 + Missense_Mutation SNP C C A TCGA-J4-AATV-01A-11D-A41K-08 TCGA-J4-AATV-10A-01D-A41N-08 g.chr15:42740292C>A c.3044G>T c.(3043-3045)aGa>aTa p.R1015I PRAD 15 42740533 42740533 + Nonsense_Mutation SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr15:42740533G>A c.2803C>T c.(2803-2805)Cga>Tga p.R935* PRAD 15 42740885 42740885 + Silent SNP T T C TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr15:42740885T>C c.2451A>G c.(2449-2451)gtA>gtG p.V817V PRAD 15 42742890 42742890 + Missense_Mutation SNP G G A TCGA-HC-A6AQ-01A-11D-A30E-08 TCGA-HC-A6AQ-10A-01D-A30H-08 g.chr15:42742890G>A c.1511C>T c.(1510-1512)tCc>tTc p.S504F READ 15 42717043 42717043 + Missense_Mutation SNP G G T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr15:42717043G>T c.5110C>A c.(5110-5112)Ctt>Att p.L1704I READ 15 42742302 42742302 + Missense_Mutation SNP T T C TCGA-AF-2691-01A-01W-0831-10 TCGA-AF-2691-10A-01W-0831-10 g.chr15:42742302T>C c.2099A>G c.(2098-2100)gAt>gGt p.D700G READ 15 42742459 42742459 + Missense_Mutation SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr15:42742459G>A c.1942C>T c.(1942-1944)Cgc>Tgc p.R648C SARC 15 42727686 42727686 + Missense_Mutation SNP G G T TCGA-DX-A3U7-01A-11D-A29N-09 TCGA-DX-A3U7-10A-01D-A29N-09 g.chr15:42727686G>T c.4708C>A c.(4708-4710)Cat>Aat p.H1570N SKCM 15 42717175 42717175 + Missense_Mutation SNP T T C TCGA-RP-A693-06A-13D-A30X-08 TCGA-RP-A693-10A-01D-A30X-08 g.chr15:42717175T>C c.4978A>G c.(4978-4980)Agc>Ggc p.S1660G SKCM 15 42717188 42717188 + Silent SNP G G A TCGA-EE-A2GB-06A-11D-A197-08 TCGA-EE-A2GB-10A-01D-A199-08 g.chr15:42717188G>A c.4965C>T c.(4963-4965)ggC>ggT p.G1655G SKCM 15 42731497 42731497 + Missense_Mutation SNP G G T TCGA-ER-A19P-06A-11D-A196-08 TCGA-ER-A19P-10A-01D-A198-08 g.chr15:42731497G>T c.4209C>A c.(4207-4209)gaC>gaA p.D1403E SKCM 15 42742291 42742291 + Nonsense_Mutation SNP G G A TCGA-D9-A6EA-06A-11D-A30X-08 TCGA-D9-A6EA-10A-01D-A30X-08 g.chr15:42742291G>A c.2110C>T c.(2110-2112)Caa>Taa p.Q704* SKCM 15 42742955 42742955 + Silent SNP G G A TCGA-EE-A2MS-06A-11D-A197-08 TCGA-EE-A2MS-10A-01D-A199-08 g.chr15:42742955G>A c.1446C>T c.(1444-1446)tcC>tcT p.S482S SKCM 15 42742972 42742972 + Missense_Mutation SNP T T C TCGA-EE-A2MS-06A-11D-A197-08 TCGA-EE-A2MS-10A-01D-A199-08 g.chr15:42742972T>C c.1429A>G c.(1429-1431)Aaa>Gaa p.K477E SKCM 15 42743008 42743008 + Nonsense_Mutation SNP G G A TCGA-EE-A3JB-06A-11D-A21A-08 TCGA-EE-A3JB-10A-01D-A21A-08 g.chr15:42743008G>A c.1393C>T c.(1393-1395)Caa>Taa p.Q465* SKCM 15 42743035 42743035 + Missense_Mutation SNP G G A TCGA-EE-A2MJ-06A-11D-A197-08 TCGA-EE-A2MJ-10A-01D-A199-08 g.chr15:42743035G>A c.1366C>T c.(1366-1368)Cca>Tca p.P456S SKCM 15 42743105 42743105 + Silent SNP G G A TCGA-FS-A1ZB-06A-12D-A197-08 TCGA-FS-A1ZB-10A-01D-A199-08 g.chr15:42743105G>A c.1296C>T c.(1294-1296)tgC>tgT p.C432C SKCM 15 42743200 42743200 + Missense_Mutation SNP G G A TCGA-D3-A3CB-06A-11D-A196-08 TCGA-D3-A3CB-10A-01D-A198-08 g.chr15:42743200G>A c.1201C>T c.(1201-1203)Cca>Tca p.P401S SKCM 15 42743290 42743290 + Nonsense_Mutation SNP T T A TCGA-D3-A2JA-06A-11D-A196-08 TCGA-D3-A2JA-10A-01D-A198-08 g.chr15:42743290T>A c.1111A>T c.(1111-1113)Aag>Tag p.K371* SKCM 15 42743379 42743379 + Missense_Mutation SNP G G A TCGA-D3-A2JF-06A-11D-A196-08 TCGA-D3-A2JF-10A-01D-A198-08 g.chr15:42743379G>A c.1022C>T c.(1021-1023)gCg>gTg p.A341V SKCM 15 42743513 42743513 + Silent SNP A A C TCGA-EE-A2M5-06A-12D-A197-08 TCGA-EE-A2M5-10A-01D-A199-08 g.chr15:42743513A>C c.888T>G c.(886-888)ggT>ggG p.G296G SKCM 15 42743543 42743543 + Missense_Mutation SNP G G C TCGA-ER-A19S-06A-11D-A196-08 TCGA-ER-A19S-10A-01D-A198-08 g.chr15:42743543G>C c.858C>G c.(856-858)gaC>gaG p.D286E SKCM 15 42743614 42743614 + Missense_Mutation SNP A A G TCGA-FS-A1ZM-06A-12D-A197-08 TCGA-FS-A1ZM-10A-01D-A199-08 g.chr15:42743614A>G c.787T>C c.(787-789)Tgg>Cgg p.W263R SKCM 15 42743985 42743985 + Missense_Mutation SNP A A C TCGA-EE-A29L-06A-12D-A196-08 TCGA-EE-A29L-10A-01D-A198-08 g.chr15:42743985A>C c.416T>G c.(415-417)tTt>tGt p.F139C SKCM 15 42743992 42743992 + Missense_Mutation SNP C C T TCGA-EE-A2GR-06A-11D-A197-08 TCGA-EE-A2GR-10A-01D-A199-08 g.chr15:42743992C>T c.409G>A c.(409-411)Gat>Aat p.D137N SKCM 15 42744097 42744097 + Nonsense_Mutation SNP G G A TCGA-ER-A19P-06A-11D-A196-08 TCGA-ER-A19P-10A-01D-A198-08 g.chr15:42744097G>A c.304C>T c.(304-306)Caa>Taa p.Q102* ACC 5 121487769 121487769 + Missense_Mutation SNP C C G TCGA-P6-A5OH-01A-11D-A30A-10 TCGA-P6-A5OH-11A-01D-A30A-10 g.chr5:121487769C>G c.84C>G c.(82-84)aaC>aaG p.N28K BLCA 5 121488307 121488307 + Missense_Mutation SNP C C A TCGA-XF-A9SY-01A-21D-A42E-08 TCGA-XF-A9SY-10A-01D-A42H-08 g.chr5:121488307C>A c.622C>A c.(622-624)Ctc>Atc p.L208I BLCA 5 121488365 121488365 + Missense_Mutation SNP G G A TCGA-MV-A51V-01A-11D-A26M-08 TCGA-MV-A51V-10A-01D-A26K-08 g.chr5:121488365G>A c.680G>A c.(679-681)tGt>tAt p.C227Y BLCA 5 121488433 121488433 + Missense_Mutation SNP G G A TCGA-E7-A541-01A-11D-A26M-08 TCGA-E7-A541-10A-01D-A26K-08 g.chr5:121488433G>A c.748G>A c.(748-750)Gaa>Aaa p.E250K BLCA 5 121488577 121488577 + Missense_Mutation SNP C C A TCGA-UY-A78K-01A-11D-A339-08 TCGA-UY-A78K-10A-01D-A339-08 g.chr5:121488577C>A c.892C>A c.(892-894)Cgc>Agc p.R298S BRCA 5 121487948 121487948 + Missense_Mutation SNP C C T TCGA-AN-A0AK-01A-21W-A019-09 TCGA-AN-A0AK-10A-01W-A021-09 g.chr5:121487948C>T c.263C>T c.(262-264)cCg>cTg p.P88L CESC 5 121488160 121488160 + Nonsense_Mutation SNP C C T TCGA-IR-A3LB-01A-11D-A243-09 TCGA-IR-A3LB-10A-01D-A243-09 g.chr5:121488160C>T c.475C>T c.(475-477)Cag>Tag p.Q159* COAD 5 121487751 121487751 + Silent SNP A A G TCGA-D5-6540-01A-11D-1719-10 TCGA-D5-6540-10A-01D-1719-10 g.chr5:121487751A>G c.66A>G c.(64-66)gaA>gaG p.E22E COAD 5 121487761 121487761 + Missense_Mutation SNP C C T TCGA-AA-3845-01A-01W-0995-10 TCGA-AA-3845-10A-01W-0995-10 g.chr5:121487761C>T c.76C>T c.(76-78)Ctt>Ttt p.L26F COAD 5 121487990 121487990 + Missense_Mutation SNP G G A TCGA-AA-A022-01A-21W-A096-10 TCGA-AA-A022-11A-11W-A096-10 g.chr5:121487990G>A c.305G>A c.(304-306)cGa>cAa p.R102Q COAD 5 121488148 121488148 + Missense_Mutation SNP G G A TCGA-D5-6926-01A-11D-1924-10 TCGA-D5-6926-10A-01D-1924-10 g.chr5:121488148G>A c.463G>A c.(463-465)Gag>Aag p.E155K COAD 5 121488265 121488265 + Missense_Mutation SNP C C T TCGA-AA-3555-01A-01W-0831-10 TCGA-AA-3555-10A-01W-0831-10 g.chr5:121488265C>T c.580C>T c.(580-582)Ccc>Tcc p.P194S COAD 5 121488283 121488283 + Missense_Mutation SNP A A G TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr5:121488283A>G c.598A>G c.(598-600)Aac>Gac p.N200D COAD 5 121488383 121488383 + Missense_Mutation SNP C C A TCGA-AA-3672-01A-01W-0900-09 TCGA-AA-3672-10A-01W-0900-09 g.chr5:121488383C>A c.698C>A c.(697-699)aCc>aAc p.T233N COADREAD 5 121487751 121487751 + Silent SNP A A G TCGA-D5-6540-01A-11D-1719-10 TCGA-D5-6540-10A-01D-1719-10 g.chr5:121487751A>G c.66A>G c.(64-66)gaA>gaG p.E22E COADREAD 5 121487761 121487761 + Missense_Mutation SNP C C T TCGA-AA-3845-01A-01W-0995-10 TCGA-AA-3845-10A-01W-0995-10 g.chr5:121487761C>T c.76C>T c.(76-78)Ctt>Ttt p.L26F COADREAD 5 121487810 121487810 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr5:121487810C>T c.125C>T c.(124-126)tCc>tTc p.S42F COADREAD 5 121487990 121487990 + Missense_Mutation SNP G G A TCGA-AA-A022-01A-21W-A096-10 TCGA-AA-A022-11A-11W-A096-10 g.chr5:121487990G>A c.305G>A c.(304-306)cGa>cAa p.R102Q COADREAD 5 121488148 121488148 + Missense_Mutation SNP G G A TCGA-D5-6926-01A-11D-1924-10 TCGA-D5-6926-10A-01D-1924-10 g.chr5:121488148G>A c.463G>A c.(463-465)Gag>Aag p.E155K COADREAD 5 121488265 121488265 + Missense_Mutation SNP C C T TCGA-AA-3555-01A-01W-0831-10 TCGA-AA-3555-10A-01W-0831-10 g.chr5:121488265C>T c.580C>T c.(580-582)Ccc>Tcc p.P194S COADREAD 5 121488283 121488283 + Missense_Mutation SNP A A G TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr5:121488283A>G c.598A>G c.(598-600)Aac>Gac p.N200D COADREAD 5 121488383 121488383 + Missense_Mutation SNP C C A TCGA-AA-3672-01A-01W-0900-09 TCGA-AA-3672-10A-01W-0900-09 g.chr5:121488383C>A c.698C>A c.(697-699)aCc>aAc p.T233N COADREAD 5 121488577 121488577 + Missense_Mutation SNP C C T TCGA-AG-3890-01A-01W-1073-09 TCGA-AG-3890-10A-01W-1073-09 g.chr5:121488577C>T c.892C>T c.(892-894)Cgc>Tgc p.R298C DLBC 5 121487954 121487954 + Missense_Mutation SNP G G A TCGA-G8-6324-01A-11D-2210-10 TCGA-G8-6324-10A-01D-2210-10 g.chr5:121487954G>A c.269G>A c.(268-270)cGc>cAc p.R90H DLBC 5 121487969 121487969 + Missense_Mutation SNP G G A TCGA-G8-6909-01A-11D-2210-10 TCGA-G8-6909-14A-01D-2210-10 g.chr5:121487969G>A c.284G>A c.(283-285)cGg>cAg p.R95Q DLBC 5 121488255 121488255 + Missense_Mutation SNP G G T TCGA-FA-A6HN-01A-11D-A31X-10 TCGA-FA-A6HN-10A-01D-A31X-10 g.chr5:121488255G>T c.570G>T c.(568-570)aaG>aaT p.K190N ESCA 5 121487982 121487982 + Silent SNP C C T TCGA-2H-A9GH-01A-11D-A37C-09 TCGA-2H-A9GH-11A-11D-A37F-09 g.chr5:121487982C>T c.297C>T c.(295-297)atC>atT p.I99I GBMLGG 5 121487888 121487888 + Missense_Mutation SNP T T C TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr5:121487888T>C c.203T>C c.(202-204)cTa>cCa p.L68P HNSC 5 121488078 121488078 + Missense_Mutation SNP G G C TCGA-CV-6961-01A-21D-1912-08 TCGA-CV-6961-10A-01D-1912-08 g.chr5:121488078G>C c.393G>C c.(391-393)ttG>ttC p.L131F KIPAN 5 121487756 121487756 + Missense_Mutation SNP C C A TCGA-B1-A657-01A-11D-A31X-10 TCGA-B1-A657-10A-01D-A31X-10 g.chr5:121487756C>A c.71C>A c.(70-72)aCt>aAt p.T24N KIPAN 5 121488728 121488728 + Missense_Mutation SNP T T G TCGA-A3-3313-01A-01D-0966-08 TCGA-A3-3313-11A-01D-0966-08 g.chr5:121488728T>G c.1043T>G c.(1042-1044)aTt>aGt p.I348S KIRC 5 121488728 121488728 + Missense_Mutation SNP T T G TCGA-A3-3313-01A-01D-0966-08 TCGA-A3-3313-11A-01D-0966-08 g.chr5:121488728T>G c.1043T>G c.(1042-1044)aTt>aGt p.I348S KIRP 5 121487756 121487756 + Missense_Mutation SNP C C A TCGA-B1-A657-01A-11D-A31X-10 TCGA-B1-A657-10A-01D-A31X-10 g.chr5:121487756C>A c.71C>A c.(70-72)aCt>aAt p.T24N LGG 5 121487888 121487888 + Missense_Mutation SNP T T C TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr5:121487888T>C c.203T>C c.(202-204)cTa>cCa p.L68P LIHC 5 121487810 121487810 + Missense_Mutation SNP C C T TCGA-DD-A1EB-01A-11D-A12Z-10 TCGA-DD-A1EB-10A-01D-A12Z-10 g.chr5:121487810C>T c.125C>T c.(124-126)tCc>tTc p.S42F LIHC 5 121488330 121488330 + Silent SNP C C T TCGA-DD-AADR-01A-11D-A40R-10 TCGA-DD-AADR-10A-01D-A40U-10 g.chr5:121488330C>T c.645C>T c.(643-645)acC>acT p.T215T LUAD 5 121487812 121487812 + Missense_Mutation SNP C C A TCGA-50-5049-01A-01D-1625-08 TCGA-50-5049-10A-01D-1625-08 g.chr5:121487812C>A c.127C>A c.(127-129)Cca>Aca p.P43T LUAD 5 121487887 121487887 + Missense_Mutation SNP C C A TCGA-44-6147-01A-11D-1753-08 TCGA-44-6147-10A-01D-1753-08 g.chr5:121487887C>A c.202C>A c.(202-204)Cta>Ata p.L68I LUAD 5 121487999 121487999 + Missense_Mutation SNP G G T TCGA-62-A46R-01A-11D-A24D-08 TCGA-62-A46R-10A-01D-A24F-08 g.chr5:121487999G>T c.314G>T c.(313-315)gGg>gTg p.G105V LUAD 5 121488198 121488198 + Missense_Mutation SNP T T G TCGA-50-5936-01A-11D-1625-08 TCGA-50-5936-11A-01D-1625-08 g.chr5:121488198T>G c.513T>G c.(511-513)tgT>tgG p.C171W LUAD 5 121488214 121488214 + Missense_Mutation SNP C C T TCGA-L9-A444-01A-21D-A24D-08 TCGA-L9-A444-10A-01D-A24F-08 g.chr5:121488214C>T c.529C>T c.(529-531)Cca>Tca p.P177S LUAD 5 121488259 121488259 + Missense_Mutation SNP G G A TCGA-86-8358-01A-11D-2323-08 TCGA-86-8358-10A-01D-2323-08 g.chr5:121488259G>A c.574G>A c.(574-576)Gag>Aag p.E192K LUAD 5 121488479 121488479 + Missense_Mutation SNP A A C TCGA-38-4625-01A-01D-1553-08 TCGA-38-4625-11A-01D-1553-08 g.chr5:121488479A>C c.794A>C c.(793-795)aAg>aCg p.K265T LUSC 5 121487777 121487777 + Missense_Mutation SNP G G T TCGA-66-2785-01A-01D-1522-08 TCGA-66-2785-11A-01D-1522-08 g.chr5:121487777G>T c.92G>T c.(91-93)gGg>gTg p.G31V LUSC 5 121488583 121488583 + Silent SNP C C T TCGA-18-3409-01A-01D-0983-08 TCGA-18-3409-11A-01D-0983-08 g.chr5:121488583C>T c.898C>T c.(898-900)Ctg>Ttg p.L300L PAAD 5 121488445 121488445 + Missense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr5:121488445C>T c.760C>T c.(760-762)Ctc>Ttc p.L254F READ 5 121487810 121487810 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr5:121487810C>T c.125C>T c.(124-126)tCc>tTc p.S42F READ 5 121488577 121488577 + Missense_Mutation SNP C C T TCGA-AG-3890-01A-01W-1073-09 TCGA-AG-3890-10A-01W-1073-09 g.chr5:121488577C>T c.892C>T c.(892-894)Cgc>Tgc p.R298C SKCM 5 121487821 121487821 + Missense_Mutation SNP G G A TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr5:121487821G>A c.136G>A c.(136-138)Gag>Aag p.E46K SKCM 5 121487946 121487946 + Silent SNP C C T TCGA-EE-A29T-06A-11D-A197-08 TCGA-EE-A29T-10A-01D-A199-08 g.chr5:121487946C>T c.261C>T c.(259-261)atC>atT p.I87I SKCM 5 121487967 121487967 + Silent SNP C C T TCGA-FS-A1ZZ-06A-11D-A197-08 TCGA-FS-A1ZZ-10A-01D-A199-08 g.chr5:121487967C>T c.282C>T c.(280-282)ttC>ttT p.F94F SKCM 5 121488171 121488171 + Silent SNP G G A TCGA-EE-A2MS-06A-11D-A197-08 TCGA-EE-A2MS-10A-01D-A199-08 g.chr5:121488171G>A c.486G>A c.(484-486)caG>caA p.Q162Q SKCM 5 121488389 121488389 + Missense_Mutation SNP C C T TCGA-ER-A19P-06A-11D-A196-08 TCGA-ER-A19P-10A-01D-A198-08 g.chr5:121488389C>T c.704C>T c.(703-705)tCc>tTc p.S235F SKCM 5 121488390 121488390 + Silent SNP C C T TCGA-ER-A193-06A-12D-A197-08 TCGA-ER-A193-10A-01D-A199-08 g.chr5:121488390C>T c.705C>T c.(703-705)tcC>tcT p.S235S SKCM 5 121488400 121488400 + Missense_Mutation SNP C C T TCGA-D3-A3MR-06A-11D-A21A-08 TCGA-D3-A3MR-10A-01D-A21A-08 g.chr5:121488400C>T c.715C>T c.(715-717)Cat>Tat p.H239Y SKCM 5 121488406 121488406 + Missense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr5:121488406C>T c.721C>T c.(721-723)Ccc>Tcc p.P241S SKCM 5 121488488 121488488 + Missense_Mutation SNP C C T TCGA-DA-A1HW-06A-11D-A19A-08 TCGA-DA-A1HW-10A-01D-A19A-08 g.chr5:121488488C>T c.803C>T c.(802-804)cCc>cTc p.P268L SKCM 5 121488489 121488489 + Silent SNP C C T TCGA-EE-A2M5-06A-12D-A197-08 TCGA-EE-A2M5-10A-01D-A199-08 g.chr5:121488489C>T c.804C>T c.(802-804)ccC>ccT p.P268P SKCM 5 121488490 121488490 + Missense_Mutation SNP C C T TCGA-EE-A2M5-06A-12D-A197-08 TCGA-EE-A2M5-10A-01D-A199-08 g.chr5:121488490C>T c.805C>T c.(805-807)Ctt>Ttt p.L269F SKCM 5 121488495 121488495 + Silent SNP G G A TCGA-GF-A6C9-06A-11D-A30X-08 TCGA-GF-A6C9-10A-01D-A30X-08 g.chr5:121488495G>A c.810G>A c.(808-810)ccG>ccA p.P270P SKCM 5 121488633 121488633 + Silent SNP G G A TCGA-EE-A2MS-06A-11D-A197-08 TCGA-EE-A2MS-10A-01D-A199-08 g.chr5:121488633G>A c.948G>A c.(946-948)caG>caA p.Q316Q SKCM 5 121488712 121488712 + Missense_Mutation SNP G G A TCGA-D3-A1QA-06A-11D-A196-08 TCGA-D3-A1QA-10A-01D-A198-08 g.chr5:121488712G>A c.1027G>A c.(1027-1029)Gta>Ata p.V343I

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation ALL-US 15 42742679 42742679 single base substitution T C downstream_gene_variant ALL-US 15 42742679 42742679 single base substitution T C intron_variant ALL-US 15 42742679 42742679 single base substitution T C synonymous_variant K357K 1071A>G ALL-US 15 42742679 42742679 single base substitution T C synonymous_variant K574K 1722A>G ALL-US 15 42742679 42742679 single base substitution T C upstream_gene_variant BLCA-CN 15 42701503 42701503 single base substitution A G downstream_gene_variant BLCA-CN 15 42737093 42737093 single base substitution G C downstream_gene_variant BLCA-CN 15 42737093 42737093 single base substitution G C missense_variant L1075V 3223C>G BLCA-CN 15 42737093 42737093 single base substitution G C missense_variant L128V 382C>G BLCA-CN 15 42737093 42737093 single base substitution G C missense_variant L260V 778C>G BLCA-CN 15 42737093 42737093 single base substitution G C missense_variant L303V 907C>G BLCA-CN 15 42737093 42737093 single base substitution G C missense_variant L33V 97C>G BLCA-CN 15 42743992 42743992 single base substitution C G 5_prime_UTR_variant BLCA-CN 15 42743992 42743992 single base substitution C G intron_variant BLCA-CN 15 42743992 42743992 single base substitution C G missense_variant D137H 409G>C BLCA-CN 15 42743992 42743992 single base substitution C G missense_variant D160H 478G>C BLCA-CN 15 42743992 42743992 single base substitution C G upstream_gene_variant BLCA-CN 15 42744124 42744124 single base substitution C G 5_prime_UTR_variant BLCA-CN 15 42744124 42744124 single base substitution C G intron_variant BLCA-CN 15 42744124 42744124 single base substitution C G missense_variant E116Q 346G>C BLCA-CN 15 42744124 42744124 single base substitution C G missense_variant E93Q 277G>C BLCA-CN 15 42744124 42744124 single base substitution C G upstream_gene_variant BLCA-US 15 42702003 42702003 single base substitution G A downstream_gene_variant BLCA-US 15 42703108 42703108 single base substitution G C downstream_gene_variant BLCA-US 15 42703970 42703970 single base substitution G C downstream_gene_variant BOCA-FR 15 42741506 42741506 single base substitution G T downstream_gene_variant BOCA-FR 15 42741506 42741506 single base substitution G T intron_variant BOCA-FR 15 42741506 42741506 single base substitution G T upstream_gene_variant BRCA-EU 15 42700820 42700820 single base substitution G A downstream_gene_variant BRCA-EU 15 42702180 42702180 single base substitution T C downstream_gene_variant BRCA-EU 15 42703535 42703535 single base substitution G A downstream_gene_variant BRCA-EU 15 42704594 42704594 single base substitution C T downstream_gene_variant BRCA-EU 15 42707791 42707791 single base substitution G A 3_prime_UTR_variant BRCA-EU 15 42707791 42707791 single base substitution G A downstream_gene_variant BRCA-EU 15 42707791 42707791 single base substitution G A intron_variant BRCA-EU 15 42708235 42708235 single base substitution C G 3_prime_UTR_variant BRCA-EU 15 42708235 42708235 single base substitution C G downstream_gene_variant BRCA-EU 15 42708235 42708235 single base substitution C G intron_variant BRCA-EU 15 42708882 42708882 single base substitution A C 3_prime_UTR_variant BRCA-EU 15 42708882 42708882 single base substitution A C downstream_gene_variant BRCA-EU 15 42708882 42708882 single base substitution A C intron_variant BRCA-EU 15 42709412 42709412 single base substitution T A 3_prime_UTR_variant BRCA-EU 15 42709412 42709412 single base substitution T A downstream_gene_variant BRCA-EU 15 42709412 42709412 single base substitution T A intron_variant BRCA-EU 15 42710060 42710060 single base substitution C A downstream_gene_variant BRCA-EU 15 42710060 42710060 single base substitution C A intron_variant BRCA-EU 15 42710060 42710060 single base substitution C A synonymous_variant L1031L 3093G>T BRCA-EU 15 42710060 42710060 single base substitution C A synonymous_variant L1074L 3222G>T BRCA-EU 15 42710060 42710060 single base substitution C A synonymous_variant L1846L 5538G>T BRCA-EU 15 42710060 42710060 single base substitution C A synonymous_variant L812L 2436G>T BRCA-EU 15 42711760 42711760 single base substitution A G downstream_gene_variant BRCA-EU 15 42711760 42711760 single base substitution A G intron_variant BRCA-EU 15 42717844 42717844 single base substitution C A exon_variant BRCA-EU 15 42717844 42717844 single base substitution C A intron_variant BRCA-EU 15 42717844 42717844 single base substitution C A upstream_gene_variant BRCA-EU 15 42718608 42718608 single base substitution A G intron_variant BRCA-EU 15 42718608 42718608 single base substitution A G upstream_gene_variant BRCA-EU 15 42719817 42719817 single base substitution G A intron_variant BRCA-EU 15 42719817 42719817 single base substitution G A upstream_gene_variant BRCA-EU 15 42720432 42720432 single base substitution G A intron_variant BRCA-EU 15 42720432 42720432 single base substitution G A upstream_gene_variant BRCA-EU 15 42720465 42720465 single base substitution G T intron_variant BRCA-EU 15 42720465 42720465 single base substitution G T upstream_gene_variant BRCA-EU 15 42720720 42720720 single base substitution C G intron_variant BRCA-EU 15 42720720 42720720 single base substitution C G upstream_gene_variant BRCA-EU 15 42721897 42721897 single base substitution G C intron_variant BRCA-EU 15 42721897 42721897 single base substitution G C upstream_gene_variant BRCA-EU 15 42722728 42722728 single base substitution C T intron_variant BRCA-EU 15 42722728 42722728 single base substitution C T upstream_gene_variant BRCA-EU 15 42722773 42722773 single base substitution A G intron_variant BRCA-EU 15 42722773 42722773 single base substitution A G upstream_gene_variant BRCA-EU 15 42723003 42723003 deletion of <=200bp T - intron_variant BRCA-EU 15 42723003 42723003 deletion of <=200bp T - upstream_gene_variant BRCA-EU 15 42725554 42725554 single base substitution C T intron_variant BRCA-EU 15 42726270 42726270 single base substitution C G intron_variant BRCA-EU 15 42726494 42726494 single base substitution G A intron_variant BRCA-EU 15 42728183 42728183 single base substitution G T intron_variant BRCA-EU 15 42729546 42729546 single base substitution C A downstream_gene_variant BRCA-EU 15 42729546 42729546 single base substitution C A stop_gained E1521* 4561G>T BRCA-EU 15 42729546 42729546 single base substitution C A stop_gained E487* 1459G>T BRCA-EU 15 42729546 42729546 single base substitution C A stop_gained E706* 2116G>T BRCA-EU 15 42729546 42729546 single base substitution C A stop_gained E749* 2245G>T BRCA-EU 15 42730488 42730488 single base substitution C T downstream_gene_variant BRCA-EU 15 42730488 42730488 single base substitution C T intron_variant BRCA-EU 15 42732067 42732067 single base substitution C T downstream_gene_variant BRCA-EU 15 42732067 42732067 single base substitution C T intron_variant BRCA-EU 15 42732141 42732141 single base substitution C G downstream_gene_variant BRCA-EU 15 42732141 42732141 single base substitution C G intron_variant BRCA-EU 15 42732418 42732418 single base substitution G T downstream_gene_variant BRCA-EU 15 42732418 42732418 single base substitution G T intron_variant BRCA-EU 15 42736688 42736688 single base substitution T C downstream_gene_variant BRCA-EU 15 42736688 42736688 single base substitution T C intron_variant BRCA-EU 15 42737954 42737954 single base substitution G T downstream_gene_variant BRCA-EU 15 42737954 42737954 single base substitution G T intron_variant BRCA-EU 15 42738979 42738979 single base substitution T C downstream_gene_variant BRCA-EU 15 42738979 42738979 single base substitution T C intron_variant BRCA-EU 15 42738979 42738979 single base substitution T C upstream_gene_variant BRCA-EU 15 42740769 42740769 single base substitution C T downstream_gene_variant BRCA-EU 15 42740769 42740769 single base substitution C T missense_variant R41K 122G>A BRCA-EU 15 42740769 42740769 single base substitution C T missense_variant R639K 1916G>A BRCA-EU 15 42740769 42740769 single base substitution C T missense_variant R84K 251G>A BRCA-EU 15 42740769 42740769 single base substitution C T missense_variant R856K 2567G>A BRCA-EU 15 42740769 42740769 single base substitution C T upstream_gene_variant BRCA-EU 15 42744810 42744810 single base substitution C G intron_variant BRCA-EU 15 42744810 42744810 single base substitution C G upstream_gene_variant BRCA-EU 15 42746226 42746226 single base substitution C T intron_variant BRCA-EU 15 42746396 42746396 single base substitution G A intron_variant BRCA-EU 15 42746764 42746764 single base substitution A G intron_variant BRCA-EU 15 42746937 42746937 single base substitution A T intron_variant BRCA-EU 15 42747109 42747109 deletion of <=200bp G - intron_variant BRCA-EU 15 42751162 42751162 single base substitution C G intron_variant BRCA-EU 15 42751162 42751162 single base substitution C G upstream_gene_variant BRCA-EU 15 42751479 42751479 single base substitution C T intron_variant BRCA-EU 15 42751479 42751479 single base substitution C T upstream_gene_variant BRCA-EU 15 42753028 42753028 single base substitution A T intron_variant BRCA-EU 15 42753028 42753028 single base substitution A T upstream_gene_variant BRCA-EU 15 42753029 42753029 single base substitution G T intron_variant BRCA-EU 15 42753029 42753029 single base substitution G T upstream_gene_variant BRCA-EU 15 42761067 42761067 single base substitution G C intron_variant BRCA-EU 15 42761206 42761206 single base substitution G A intron_variant BRCA-EU 15 42761877 42761877 deletion of <=200bp A - intron_variant BRCA-EU 15 42764635 42764635 single base substitution C T intron_variant BRCA-EU 15 42764801 42764801 single base substitution C T intron_variant BRCA-EU 15 42766900 42766900 single base substitution G A intron_variant BRCA-EU 15 42767666 42767666 single base substitution C G intron_variant BRCA-EU 15 42767901 42767901 single base substitution G A intron_variant BRCA-EU 15 42768095 42768095 single base substitution T C intron_variant BRCA-EU 15 42768243 42768243 single base substitution C G intron_variant BRCA-EU 15 42768284 42768284 insertion of <=200bp - T intron_variant BRCA-EU 15 42769495 42769495 single base substitution A G intron_variant BRCA-EU 15 42770212 42770212 single base substitution C G intron_variant BRCA-EU 15 42770290 42770290 insertion of <=200bp - A intron_variant BRCA-EU 15 42772653 42772653 single base substitution T A intron_variant BRCA-EU 15 42773791 42773791 single base substitution C G intron_variant BRCA-EU 15 42774088 42774088 deletion of <=200bp G - intron_variant BRCA-EU 15 42775405 42775405 single base substitution A T intron_variant BRCA-EU 15 42778348 42778348 insertion of <=200bp - A intron_variant BRCA-EU 15 42780338 42780338 deletion of <=200bp T - intron_variant BRCA-EU 15 42780646 42780646 insertion of <=200bp - CA intron_variant BRCA-EU 15 42781412 42781412 single base substitution A C intron_variant BRCA-EU 15 42781924 42781924 single base substitution C G intron_variant BRCA-EU 15 42783048 42783048 deletion of <=200bp C - intron_variant BRCA-EU 15 42783048 42783048 deletion of <=200bp C - upstream_gene_variant BRCA-EU 15 42785958 42785958 single base substitution C G upstream_gene_variant BRCA-EU 15 42786585 42786585 single base substitution T G upstream_gene_variant BRCA-EU 15 42786950 42786954 deletion of <=200bp TGATC - upstream_gene_variant BRCA-EU 15 42786984 42786984 single base substitution A G upstream_gene_variant BRCA-EU 15 42787562 42787562 single base substitution G A upstream_gene_variant BRCA-FR 15 42707791 42707791 single base substitution G A 3_prime_UTR_variant BRCA-FR 15 42707791 42707791 single base substitution G A downstream_gene_variant BRCA-FR 15 42707791 42707791 single base substitution G A intron_variant BRCA-FR 15 42717844 42717844 single base substitution C A exon_variant BRCA-FR 15 42717844 42717844 single base substitution C A intron_variant BRCA-FR 15 42717844 42717844 single base substitution C A upstream_gene_variant BRCA-FR 15 42722773 42722773 single base substitution A G intron_variant BRCA-FR 15 42722773 42722773 single base substitution A G upstream_gene_variant BRCA-FR 15 42726270 42726270 single base substitution C G intron_variant BRCA-FR 15 42739853 42739853 single base substitution C G downstream_gene_variant BRCA-FR 15 42739853 42739853 single base substitution C G intron_variant BRCA-FR 15 42739853 42739853 single base substitution C G upstream_gene_variant BRCA-FR 15 42761206 42761206 single base substitution G A intron_variant BRCA-FR 15 42764801 42764801 single base substitution C T intron_variant BRCA-FR 15 42770212 42770212 single base substitution C G intron_variant BRCA-FR 15 42771085 42771085 single base substitution C A intron_variant BRCA-FR 15 42785320 42785320 single base substitution G A upstream_gene_variant BRCA-KR 15 42704376 42704376 single base substitution C A downstream_gene_variant BRCA-UK 15 42709585 42709585 single base substitution G C downstream_gene_variant BRCA-UK 15 42709585 42709585 single base substitution G C intron_variant BRCA-UK 15 42709612 42709612 single base substitution G C downstream_gene_variant BRCA-UK 15 42709612 42709612 single base substitution G C intron_variant BRCA-UK 15 42711029 42711029 single base substitution G C downstream_gene_variant BRCA-UK 15 42711029 42711029 single base substitution G C intron_variant BRCA-UK 15 42712875 42712875 single base substitution C T downstream_gene_variant BRCA-UK 15 42712875 42712875 single base substitution C T intron_variant BRCA-UK 15 42713830 42713830 single base substitution C G downstream_gene_variant BRCA-UK 15 42713830 42713830 single base substitution C G intron_variant BRCA-UK 15 42714688 42714688 single base substitution C G downstream_gene_variant BRCA-UK 15 42714688 42714688 single base substitution C G intron_variant BRCA-UK 15 42717097 42717097 single base substitution C T exon_variant BRCA-UK 15 42717097 42717097 single base substitution C T missense_variant D1686N 5056G>A BRCA-UK 15 42717097 42717097 single base substitution C T missense_variant D652N 1954G>A BRCA-UK 15 42717097 42717097 single base substitution C T missense_variant D72N 214G>A BRCA-UK 15 42717097 42717097 single base substitution C T missense_variant D871N 2611G>A BRCA-UK 15 42717097 42717097 single base substitution C T missense_variant D914N 2740G>A BRCA-UK 15 42717097 42717097 single base substitution C T upstream_gene_variant BRCA-UK 15 42732067 42732067 single base substitution C T downstream_gene_variant BRCA-UK 15 42732067 42732067 single base substitution C T intron_variant BRCA-UK 15 42736446 42736446 single base substitution C G downstream_gene_variant BRCA-UK 15 42736446 42736446 single base substitution C G missense_variant M1102I 3306G>C BRCA-UK 15 42736446 42736446 single base substitution C G missense_variant M155I 465G>C BRCA-UK 15 42736446 42736446 single base substitution C G missense_variant M287I 861G>C BRCA-UK 15 42736446 42736446 single base substitution C G missense_variant M330I 990G>C BRCA-UK 15 42736446 42736446 single base substitution C G missense_variant M60I 180G>C BRCA-UK 15 42736688 42736688 single base substitution T C downstream_gene_variant BRCA-UK 15 42736688 42736688 single base substitution T C intron_variant BRCA-UK 15 42737954 42737954 single base substitution G T downstream_gene_variant BRCA-UK 15 42737954 42737954 single base substitution G T intron_variant BRCA-UK 15 42749389 42749389 single base substitution T A intron_variant BRCA-UK 15 42749389 42749389 single base substitution T A missense_variant R5S 15A>T BRCA-UK 15 42753028 42753028 single base substitution A T intron_variant BRCA-UK 15 42753028 42753028 single base substitution A T upstream_gene_variant BRCA-UK 15 42753029 42753029 single base substitution G T intron_variant BRCA-UK 15 42753029 42753029 single base substitution G T upstream_gene_variant BRCA-UK 15 42773640 42773640 single base substitution C G intron_variant BRCA-UK 15 42774088 42774088 deletion of <=200bp G - intron_variant BRCA-UK 15 42775405 42775405 single base substitution A T intron_variant BRCA-US 15 42703522 42703522 single base substitution C T downstream_gene_variant BRCA-US 15 42710150 42710150 single base substitution C G downstream_gene_variant BRCA-US 15 42710150 42710150 single base substitution C G intron_variant BRCA-US 15 42710150 42710150 single base substitution C G splice_acceptor_variant BRCA-US 15 42713309 42713309 single base substitution C A downstream_gene_variant BRCA-US 15 42713309 42713309 single base substitution C A exon_variant BRCA-US 15 42713309 42713309 single base substitution C A missense_variant G1028C 3082G>T BRCA-US 15 42713309 42713309 single base substitution C A missense_variant G1800C 5398G>T BRCA-US 15 42713309 42713309 single base substitution C A missense_variant G186C 556G>T BRCA-US 15 42713309 42713309 single base substitution C A missense_variant G766C 2296G>T BRCA-US 15 42713309 42713309 single base substitution C A missense_variant G985C 2953G>T BRCA-US 15 42729452 42729452 single base substitution G T downstream_gene_variant BRCA-US 15 42729452 42729452 single base substitution G T missense_variant T1552N 4655C>A BRCA-US 15 42729452 42729452 single base substitution G T missense_variant T518N 1553C>A BRCA-US 15 42729452 42729452 single base substitution G T missense_variant T737N 2210C>A BRCA-US 15 42729452 42729452 single base substitution G T missense_variant T780N 2339C>A BRCA-US 15 42730858 42730858 single base substitution C G downstream_gene_variant BRCA-US 15 42730858 42730858 single base substitution C G missense_variant E1495Q 4483G>C BRCA-US 15 42730858 42730858 single base substitution C G missense_variant E461Q 1381G>C BRCA-US 15 42730858 42730858 single base substitution C G missense_variant E680Q 2038G>C BRCA-US 15 42730858 42730858 single base substitution C G missense_variant E723Q 2167G>C BRCA-US 15 42734373 42734373 single base substitution G A downstream_gene_variant BRCA-US 15 42734373 42734373 single base substitution G A stop_gained Q1198* 3592C>T BRCA-US 15 42734373 42734373 single base substitution G A stop_gained Q156* 466C>T BRCA-US 15 42734373 42734373 single base substitution G A stop_gained Q251* 751C>T BRCA-US 15 42734373 42734373 single base substitution G A stop_gained Q383* 1147C>T BRCA-US 15 42734373 42734373 single base substitution G A stop_gained Q426* 1276C>T BRCA-US 15 42740787 42740787 single base substitution G C downstream_gene_variant BRCA-US 15 42740787 42740787 single base substitution G C missense_variant S35W 104C>G BRCA-US 15 42740787 42740787 single base substitution G C missense_variant S633W 1898C>G BRCA-US 15 42740787 42740787 single base substitution G C missense_variant S78W 233C>G BRCA-US 15 42740787 42740787 single base substitution G C missense_variant S850W 2549C>G BRCA-US 15 42740787 42740787 single base substitution G C upstream_gene_variant BRCA-US 15 42742652 42742652 single base substitution C T downstream_gene_variant BRCA-US 15 42742652 42742652 single base substitution C T intron_variant BRCA-US 15 42742652 42742652 single base substitution C T synonymous_variant V366V 1098G>A BRCA-US 15 42742652 42742652 single base substitution C T synonymous_variant V583V 1749G>A BRCA-US 15 42742652 42742652 single base substitution C T upstream_gene_variant BRCA-US 15 42742957 42742957 deletion of <=200bp A - downstream_gene_variant BRCA-US 15 42742957 42742957 deletion of <=200bp A - frameshift_variant S265 BRCA-US 15 42742957 42742957 deletion of <=200bp A - frameshift_variant S482 BRCA-US 15 42742957 42742957 deletion of <=200bp A - intron_variant BRCA-US 15 42742957 42742957 deletion of <=200bp A - upstream_gene_variant BRCA-US 15 42743220 42743220 single base substitution G T downstream_gene_variant BRCA-US 15 42743220 42743220 single base substitution G T intron_variant BRCA-US 15 42743220 42743220 single base substitution G T missense_variant T177N 530C>A BRCA-US 15 42743220 42743220 single base substitution G T missense_variant T394N 1181C>A BRCA-US 15 42743220 42743220 single base substitution G T missense_variant T417N 1250C>A BRCA-US 15 42743220 42743220 single base substitution G T upstream_gene_variant BRCA-US 15 42743279 42743279 single base substitution C G downstream_gene_variant BRCA-US 15 42743279 42743279 single base substitution C G intron_variant BRCA-US 15 42743279 42743279 single base substitution C G missense_variant M157I 471G>C BRCA-US 15 42743279 42743279 single base substitution C G missense_variant M374I 1122G>C BRCA-US 15 42743279 42743279 single base substitution C G missense_variant M397I 1191G>C BRCA-US 15 42743279 42743279 single base substitution C G upstream_gene_variant BRCA-US 15 42743464 42743464 single base substitution C T downstream_gene_variant BRCA-US 15 42743464 42743464 single base substitution C T intron_variant BRCA-US 15 42743464 42743464 single base substitution C T missense_variant D313N 937G>A BRCA-US 15 42743464 42743464 single base substitution C T missense_variant D336N 1006G>A BRCA-US 15 42743464 42743464 single base substitution C T missense_variant D96N 286G>A BRCA-US 15 42743464 42743464 single base substitution C T upstream_gene_variant BRCA-US 15 42743536 42743536 single base substitution C T downstream_gene_variant BRCA-US 15 42743536 42743536 single base substitution C T intron_variant BRCA-US 15 42743536 42743536 single base substitution C T missense_variant G289S 865G>A BRCA-US 15 42743536 42743536 single base substitution C T missense_variant G312S 934G>A BRCA-US 15 42743536 42743536 single base substitution C T missense_variant G72S 214G>A BRCA-US 15 42743536 42743536 single base substitution C T upstream_gene_variant BRCA-US 15 42743889 42743889 single base substitution G A 5_prime_UTR_variant BRCA-US 15 42743889 42743889 single base substitution G A intron_variant BRCA-US 15 42743889 42743889 single base substitution G A missense_variant S171F 512C>T BRCA-US 15 42743889 42743889 single base substitution G A missense_variant S194F 581C>T BRCA-US 15 42743889 42743889 single base substitution G A upstream_gene_variant BRCA-US 15 42743987 42743987 single base substitution G A 5_prime_UTR_variant BRCA-US 15 42743987 42743987 single base substitution G A intron_variant BRCA-US 15 42743987 42743987 single base substitution G A synonymous_variant G138G 414C>T BRCA-US 15 42743987 42743987 single base substitution G A synonymous_variant G161G 483C>T BRCA-US 15 42743987 42743987 single base substitution G A upstream_gene_variant BRCA-US 15 42744120 42744120 single base substitution A G 5_prime_UTR_variant BRCA-US 15 42744120 42744120 single base substitution A G intron_variant BRCA-US 15 42744120 42744120 single base substitution A G missense_variant I117T 350T>C BRCA-US 15 42744120 42744120 single base substitution A G missense_variant I94T 281T>C BRCA-US 15 42744120 42744120 single base substitution A G upstream_gene_variant BRCA-US 15 42749157 42749157 single base substitution G A intron_variant BRCA-US 15 42749157 42749157 single base substitution G A stop_gained R106* 316C>T BRCA-US 15 42749157 42749157 single base substitution G A stop_gained R83* 247C>T BTCA-JP 15 42709536 42709536 single base substitution C T downstream_gene_variant BTCA-JP 15 42709536 42709536 single base substitution C T intron_variant BTCA-JP 15 42709536 42709536 single base substitution C T missense_variant R1058Q 3173G>A BTCA-JP 15 42709536 42709536 single base substitution C T missense_variant R1101Q 3302G>A BTCA-JP 15 42709536 42709536 single base substitution C T missense_variant R1873Q 5618G>A BTCA-JP 15 42709536 42709536 single base substitution C T missense_variant R839Q 2516G>A BTCA-JP 15 42709714 42709714 single base substitution T C downstream_gene_variant BTCA-JP 15 42709714 42709714 single base substitution T C intron_variant BTCA-JP 15 42738586 42738586 single base substitution C T downstream_gene_variant BTCA-JP 15 42738586 42738586 single base substitution C T intron_variant BTCA-JP 15 42738734 42738734 deletion of <=200bp A - downstream_gene_variant BTCA-JP 15 42738734 42738734 deletion of <=200bp A - intron_variant BTCA-JP 15 42740239 42740239 single base substitution T C downstream_gene_variant BTCA-JP 15 42740239 42740239 single base substitution T C intron_variant BTCA-JP 15 42740239 42740239 single base substitution T C upstream_gene_variant BTCA-JP 15 42742091 42742093 deletion of <=200bp CTT - downstream_gene_variant BTCA-JP 15 42742091 42742093 deletion of <=200bp CTT - inframe_deletion K553 BTCA-JP 15 42742091 42742093 deletion of <=200bp CTT - inframe_deletion K770 BTCA-JP 15 42742091 42742093 deletion of <=200bp CTT - intron_variant BTCA-JP 15 42742091 42742093 deletion of <=200bp CTT - upstream_gene_variant BTCA-JP 15 42749310 42749310 single base substitution G A intron_variant BTCA-JP 15 42749310 42749310 single base substitution G A missense_variant L32F 94C>T BTCA-JP 15 42749310 42749310 single base substitution G A missense_variant L55F 163C>T BTCA-JP 15 42749328 42749328 single base substitution C T intron_variant BTCA-JP 15 42749328 42749328 single base substitution C T missense_variant G26R 76G>A BTCA-JP 15 42749328 42749328 single base substitution C T missense_variant G49R 145G>A BTCA-JP 15 42758359 42758359 deletion of <=200bp A - intron_variant CESC-US 15 42729566 42729566 single base substitution G C downstream_gene_variant CESC-US 15 42729566 42729566 single base substitution G C stop_gained S1514* 4541C>G CESC-US 15 42729566 42729566 single base substitution G C stop_gained S480* 1439C>G CESC-US 15 42729566 42729566 single base substitution G C stop_gained S699* 2096C>G CESC-US 15 42729566 42729566 single base substitution G C stop_gained S742* 2225C>G CESC-US 15 42734469 42734469 single base substitution G A downstream_gene_variant CESC-US 15 42734469 42734469 single base substitution G A missense_variant H1166Y 3496C>T CESC-US 15 42734469 42734469 single base substitution G A missense_variant H124Y 370C>T CESC-US 15 42734469 42734469 single base substitution G A missense_variant H219Y 655C>T CESC-US 15 42734469 42734469 single base substitution G A missense_variant H351Y 1051C>T CESC-US 15 42734469 42734469 single base substitution G A missense_variant H394Y 1180C>T CLLE-ES 15 42703115 42703115 single base substitution T C downstream_gene_variant CLLE-ES 15 42764254 42764254 single base substitution A C intron_variant CLLE-ES 15 42777136 42777136 single base substitution C A intron_variant CLLE-ES 15 42781287 42781287 single base substitution A C intron_variant COAD-US 15 42700450 42700450 single base substitution G A downstream_gene_variant COAD-US 15 42717101 42717101 single base substitution T A exon_variant COAD-US 15 42717101 42717101 single base substitution T A synonymous_variant V1684V 5052A>T COAD-US 15 42717101 42717101 single base substitution T A synonymous_variant V650V 1950A>T COAD-US 15 42717101 42717101 single base substitution T A synonymous_variant V70V 210A>T COAD-US 15 42717101 42717101 single base substitution T A synonymous_variant V869V 2607A>T COAD-US 15 42717101 42717101 single base substitution T A synonymous_variant V912V 2736A>T COAD-US 15 42717101 42717101 single base substitution T A upstream_gene_variant COAD-US 15 42720269 42720269 single base substitution G A stop_gained R12* 34C>T COAD-US 15 42720269 42720269 single base substitution G A stop_gained R1626* 4876C>T COAD-US 15 42720269 42720269 single base substitution G A stop_gained R592* 1774C>T COAD-US 15 42720269 42720269 single base substitution G A stop_gained R811* 2431C>T COAD-US 15 42720269 42720269 single base substitution G A stop_gained R854* 2560C>T COAD-US 15 42720269 42720269 single base substitution G A upstream_gene_variant COAD-US 15 42729493 42729493 single base substitution C T downstream_gene_variant COAD-US 15 42729493 42729493 single base substitution C T synonymous_variant Q1538Q 4614G>A COAD-US 15 42729493 42729493 single base substitution C T synonymous_variant Q504Q 1512G>A COAD-US 15 42729493 42729493 single base substitution C T synonymous_variant Q723Q 2169G>A COAD-US 15 42729493 42729493 single base substitution C T synonymous_variant Q766Q 2298G>A COAD-US 15 42730815 42730815 single base substitution G T downstream_gene_variant COAD-US 15 42730815 42730815 single base substitution G T missense_variant S1509Y 4526C>A COAD-US 15 42730815 42730815 single base substitution G T missense_variant S475Y 1424C>A COAD-US 15 42730815 42730815 single base substitution G T missense_variant S694Y 2081C>A COAD-US 15 42730815 42730815 single base substitution G T missense_variant S737Y 2210C>A COAD-US 15 42731492 42731492 single base substitution C A downstream_gene_variant COAD-US 15 42731492 42731492 single base substitution C A missense_variant R1405M 4214G>T COAD-US 15 42731492 42731492 single base substitution C A missense_variant R371M 1112G>T COAD-US 15 42731492 42731492 single base substitution C A missense_variant R590M 1769G>T COAD-US 15 42731492 42731492 single base substitution C A missense_variant R633M 1898G>T COAD-US 15 42734425 42734425 single base substitution C T downstream_gene_variant COAD-US 15 42734425 42734425 single base substitution C T synonymous_variant T1180T 3540G>A COAD-US 15 42734425 42734425 single base substitution C T synonymous_variant T138T 414G>A COAD-US 15 42734425 42734425 single base substitution C T synonymous_variant T233T 699G>A COAD-US 15 42734425 42734425 single base substitution C T synonymous_variant T365T 1095G>A COAD-US 15 42734425 42734425 single base substitution C T synonymous_variant T408T 1224G>A COAD-US 15 42742965 42742965 single base substitution T A downstream_gene_variant COAD-US 15 42742965 42742965 single base substitution T A intron_variant COAD-US 15 42742965 42742965 single base substitution T A missense_variant N262I 785A>T COAD-US 15 42742965 42742965 single base substitution T A missense_variant N479I 1436A>T COAD-US 15 42742965 42742965 single base substitution T A upstream_gene_variant COCA-CN 15 42702885 42702885 single base substitution G A downstream_gene_variant COCA-CN 15 42703603 42703603 single base substitution C T downstream_gene_variant COCA-CN 15 42714198 42714198 single base substitution A C downstream_gene_variant COCA-CN 15 42714198 42714198 single base substitution A C intron_variant COCA-CN 15 42738742 42738742 single base substitution C A downstream_gene_variant COCA-CN 15 42738742 42738742 single base substitution C A intron_variant COCA-CN 15 42740643 42740643 single base substitution A G downstream_gene_variant COCA-CN 15 42740643 42740643 single base substitution A G missense_variant L126S 377T>C COCA-CN 15 42740643 42740643 single base substitution A G missense_variant L681S 2042T>C COCA-CN 15 42740643 42740643 single base substitution A G missense_variant L83S 248T>C COCA-CN 15 42740643 42740643 single base substitution A G missense_variant L898S 2693T>C COCA-CN 15 42740643 42740643 single base substitution A G upstream_gene_variant COCA-CN 15 42740657 42740657 single base substitution T C downstream_gene_variant COCA-CN 15 42740657 42740657 single base substitution T C synonymous_variant S121S 363A>G COCA-CN 15 42740657 42740657 single base substitution T C synonymous_variant S676S 2028A>G COCA-CN 15 42740657 42740657 single base substitution T C synonymous_variant S78S 234A>G COCA-CN 15 42740657 42740657 single base substitution T C synonymous_variant S893S 2679A>G COCA-CN 15 42740657 42740657 single base substitution T C upstream_gene_variant COCA-CN 15 42740744 42740744 single base substitution G A downstream_gene_variant COCA-CN 15 42740744 42740744 single base substitution G A synonymous_variant S49S 147C>T COCA-CN 15 42740744 42740744 single base substitution G A synonymous_variant S647S 1941C>T COCA-CN 15 42740744 42740744 single base substitution G A synonymous_variant S864S 2592C>T COCA-CN 15 42740744 42740744 single base substitution G A synonymous_variant S92S 276C>T COCA-CN 15 42740744 42740744 single base substitution G A upstream_gene_variant COCA-CN 15 42740883 42740883 single base substitution G A downstream_gene_variant COCA-CN 15 42740883 42740883 single base substitution G A missense_variant P3L 8C>T COCA-CN 15 42740883 42740883 single base substitution G A missense_variant P46L 137C>T COCA-CN 15 42740883 42740883 single base substitution G A missense_variant P601L 1802C>T COCA-CN 15 42740883 42740883 single base substitution G A missense_variant P818L 2453C>T COCA-CN 15 42740883 42740883 single base substitution G A upstream_gene_variant COCA-CN 15 42742459 42742459 single base substitution G A downstream_gene_variant COCA-CN 15 42742459 42742459 single base substitution G A intron_variant COCA-CN 15 42742459 42742459 single base substitution G A missense_variant R431C 1291C>T COCA-CN 15 42742459 42742459 single base substitution G A missense_variant R648C 1942C>T COCA-CN 15 42742459 42742459 single base substitution G A upstream_gene_variant COCA-CN 15 42743010 42743010 single base substitution G A downstream_gene_variant COCA-CN 15 42743010 42743010 single base substitution G A intron_variant COCA-CN 15 42743010 42743010 single base substitution G A missense_variant S247F 740C>T COCA-CN 15 42743010 42743010 single base substitution G A missense_variant S464F 1391C>T COCA-CN 15 42743010 42743010 single base substitution G A upstream_gene_variant COCA-CN 15 42749007 42749007 single base substitution C A intron_variant COCA-CN 15 42749235 42749235 single base substitution C T intron_variant COCA-CN 15 42749235 42749235 single base substitution C T missense_variant G57R 169G>A COCA-CN 15 42749235 42749235 single base substitution C T missense_variant G80R 238G>A COCA-CN 15 42764538 42764538 single base substitution A C intron_variant EOPC-DE 15 42768400 42768400 single base substitution A C intron_variant ESAD-UK 15 42700846 42700846 single base substitution C T downstream_gene_variant ESAD-UK 15 42702499 42702499 single base substitution G A downstream_gene_variant ESAD-UK 15 42703441 42703441 single base substitution G A downstream_gene_variant ESAD-UK 15 42704422 42704422 single base substitution G A downstream_gene_variant ESAD-UK 15 42706054 42706054 single base substitution T C 3_prime_UTR_variant ESAD-UK 15 42706054 42706054 single base substitution T C downstream_gene_variant ESAD-UK 15 42706859 42706859 single base substitution C T 3_prime_UTR_variant ESAD-UK 15 42706859 42706859 single base substitution C T downstream_gene_variant ESAD-UK 15 42707482 42707482 single base substitution G A 3_prime_UTR_variant ESAD-UK 15 42707482 42707482 single base substitution G A downstream_gene_variant ESAD-UK 15 42709577 42709577 single base substitution G C downstream_gene_variant ESAD-UK 15 42709577 42709577 single base substitution G C intron_variant ESAD-UK 15 42710865 42710865 single base substitution C G downstream_gene_variant ESAD-UK 15 42710865 42710865 single base substitution C G intron_variant ESAD-UK 15 42710992 42710992 single base substitution C T downstream_gene_variant ESAD-UK 15 42710992 42710992 single base substitution C T intron_variant ESAD-UK 15 42711239 42711239 single base substitution C T downstream_gene_variant ESAD-UK 15 42711239 42711239 single base substitution C T intron_variant ESAD-UK 15 42711411 42711411 single base substitution C T downstream_gene_variant ESAD-UK 15 42711411 42711411 single base substitution C T intron_variant ESAD-UK 15 42714672 42714672 single base substitution A C downstream_gene_variant ESAD-UK 15 42714672 42714672 single base substitution A C intron_variant ESAD-UK 15 42715501 42715501 single base substitution G C intron_variant ESAD-UK 15 42715751 42715751 single base substitution A T intron_variant ESAD-UK 15 42716372 42716372 single base substitution T C exon_variant ESAD-UK 15 42716372 42716372 single base substitution T C intron_variant ESAD-UK 15 42719997 42719997 deletion of <=200bp G - intron_variant ESAD-UK 15 42719997 42719997 deletion of <=200bp G - upstream_gene_variant ESAD-UK 15 42723002 42723002 single base substitution A T intron_variant ESAD-UK 15 42723002 42723002 single base substitution A T upstream_gene_variant ESAD-UK 15 42724309 42724309 single base substitution C A intron_variant ESAD-UK 15 42724309 42724309 single base substitution C A upstream_gene_variant ESAD-UK 15 42735257 42735257 single base substitution G C downstream_gene_variant ESAD-UK 15 42735257 42735257 single base substitution G C intron_variant ESAD-UK 15 42735542 42735542 single base substitution G T downstream_gene_variant ESAD-UK 15 42735542 42735542 single base substitution G T intron_variant ESAD-UK 15 42738136 42738136 single base substitution G A downstream_gene_variant ESAD-UK 15 42738136 42738136 single base substitution G A intron_variant ESAD-UK 15 42738399 42738399 single base substitution G A downstream_gene_variant ESAD-UK 15 42738399 42738399 single base substitution G A intron_variant ESAD-UK 15 42742534 42742534 single base substitution C T downstream_gene_variant ESAD-UK 15 42742534 42742534 single base substitution C T intron_variant ESAD-UK 15 42742534 42742534 single base substitution C T missense_variant D406N 1216G>A ESAD-UK 15 42742534 42742534 single base substitution C T missense_variant D623N 1867G>A ESAD-UK 15 42742534 42742534 single base substitution C T upstream_gene_variant ESAD-UK 15 42744388 42744388 single base substitution A C intron_variant ESAD-UK 15 42744388 42744388 single base substitution A C upstream_gene_variant ESAD-UK 15 42744399 42744399 single base substitution C T intron_variant ESAD-UK 15 42744399 42744399 single base substitution C T upstream_gene_variant ESAD-UK 15 42745225 42745225 single base substitution C T intron_variant ESAD-UK 15 42745225 42745225 single base substitution C T upstream_gene_variant ESAD-UK 15 42746381 42746381 single base substitution C G intron_variant ESAD-UK 15 42746395 42746395 single base substitution C T intron_variant ESAD-UK 15 42747672 42747672 single base substitution G C intron_variant ESAD-UK 15 42748268 42748268 deletion of <=200bp A - intron_variant ESAD-UK 15 42750946 42750946 single base substitution A C intron_variant ESAD-UK 15 42750946 42750946 single base substitution A C upstream_gene_variant ESAD-UK 15 42757174 42757174 single base substitution T C intron_variant ESAD-UK 15 42757368 42757368 single base substitution G A intron_variant ESAD-UK 15 42764801 42764801 single base substitution C A intron_variant ESAD-UK 15 42767338 42767338 single base substitution C A intron_variant ESAD-UK 15 42768313 42768313 single base substitution C T intron_variant ESAD-UK 15 42768620 42768620 single base substitution G A intron_variant ESAD-UK 15 42769372 42769372 single base substitution T C intron_variant ESAD-UK 15 42769569 42769569 single base substitution T C intron_variant ESAD-UK 15 42779112 42779112 single base substitution G C intron_variant ESAD-UK 15 42779319 42779319 single base substitution G A intron_variant ESAD-UK 15 42779523 42779523 single base substitution A G intron_variant ESAD-UK 15 42781019 42781019 insertion of <=200bp - A intron_variant ESAD-UK 15 42781617 42781617 single base substitution C T intron_variant ESAD-UK 15 42782385 42782385 single base substitution G A intron_variant ESCA-CN 15 42703406 42703406 single base substitution T C downstream_gene_variant ESCA-CN 15 42717141 42717141 single base substitution T G exon_variant ESCA-CN 15 42717141 42717141 single base substitution T G missense_variant K1671T 5012A>C ESCA-CN 15 42717141 42717141 single base substitution T G missense_variant K57T 170A>C ESCA-CN 15 42717141 42717141 single base substitution T G missense_variant K637T 1910A>C ESCA-CN 15 42717141 42717141 single base substitution T G missense_variant K856T 2567A>C ESCA-CN 15 42717141 42717141 single base substitution T G missense_variant K899T 2696A>C ESCA-CN 15 42717141 42717141 single base substitution T G upstream_gene_variant ESCA-CN 15 42731547 42731547 single base substitution C A downstream_gene_variant ESCA-CN 15 42731547 42731547 single base substitution C A missense_variant A1387S 4159G>T ESCA-CN 15 42731547 42731547 single base substitution C A missense_variant A353S 1057G>T ESCA-CN 15 42731547 42731547 single base substitution C A missense_variant A572S 1714G>T ESCA-CN 15 42731547 42731547 single base substitution C A missense_variant A615S 1843G>T ESCA-CN 15 42731575 42731575 single base substitution C G downstream_gene_variant ESCA-CN 15 42731575 42731575 single base substitution C G missense_variant L1377F 4131G>C ESCA-CN 15 42731575 42731575 single base substitution C G missense_variant L343F 1029G>C ESCA-CN 15 42731575 42731575 single base substitution C G missense_variant L562F 1686G>C ESCA-CN 15 42731575 42731575 single base substitution C G missense_variant L605F 1815G>C ESCA-CN 15 42734283 42734283 single base substitution G A downstream_gene_variant ESCA-CN 15 42734283 42734283 single base substitution G A synonymous_variant L1228L 3682C>T ESCA-CN 15 42734283 42734283 single base substitution G A synonymous_variant L186L 556C>T ESCA-CN 15 42734283 42734283 single base substitution G A synonymous_variant L281L 841C>T ESCA-CN 15 42734283 42734283 single base substitution G A synonymous_variant L413L 1237C>T ESCA-CN 15 42734283 42734283 single base substitution G A synonymous_variant L456L 1366C>T ESCA-CN 15 42743545 42743545 single base substitution C A downstream_gene_variant ESCA-CN 15 42743545 42743545 single base substitution C A intron_variant ESCA-CN 15 42743545 42743545 single base substitution C A missense_variant D286Y 856G>T ESCA-CN 15 42743545 42743545 single base substitution C A missense_variant D309Y 925G>T ESCA-CN 15 42743545 42743545 single base substitution C A missense_variant D69Y 205G>T ESCA-CN 15 42743545 42743545 single base substitution C A upstream_gene_variant ESCA-CN 15 42749013 42749013 single base substitution C T intron_variant ESCA-CN 15 42749023 42749023 single base substitution G A intron_variant GBM-US 15 42700426 42700426 single base substitution G A downstream_gene_variant KIRC-US 15 42701963 42701963 single base substitution C G downstream_gene_variant KIRC-US 15 42702005 42702005 single base substitution T G downstream_gene_variant KIRC-US 15 42742412 42742412 single base substitution G A downstream_gene_variant KIRC-US 15 42742412 42742412 single base substitution G A intron_variant KIRC-US 15 42742412 42742412 single base substitution G A synonymous_variant H446H 1338C>T KIRC-US 15 42742412 42742412 single base substitution G A synonymous_variant H663H 1989C>T KIRC-US 15 42742412 42742412 single base substitution G A upstream_gene_variant KIRC-US 15 42743699 42743699 single base substitution A G downstream_gene_variant KIRC-US 15 42743699 42743699 single base substitution A G intron_variant KIRC-US 15 42743699 42743699 single base substitution A G synonymous_variant N17N 51T>C KIRC-US 15 42743699 42743699 single base substitution A G synonymous_variant N234N 702T>C KIRC-US 15 42743699 42743699 single base substitution A G synonymous_variant N257N 771T>C KIRC-US 15 42743699 42743699 single base substitution A G upstream_gene_variant KIRC-US 15 42744055 42744055 single base substitution T A 5_prime_UTR_variant KIRC-US 15 42744055 42744055 single base substitution T A intron_variant KIRC-US 15 42744055 42744055 single base substitution T A missense_variant S116C 346A>T KIRC-US 15 42744055 42744055 single base substitution T A missense_variant S139C 415A>T KIRC-US 15 42744055 42744055 single base substitution T A upstream_gene_variant KIRC-US 15 42749284 42749284 single base substitution A G intron_variant KIRC-US 15 42749284 42749284 single base substitution A G synonymous_variant S40S 120T>C KIRC-US 15 42749284 42749284 single base substitution A G synonymous_variant S63S 189T>C KIRP-US 15 42717056 42717056 single base substitution A C exon_variant KIRP-US 15 42717056 42717056 single base substitution A C missense_variant H1699Q 5097T>G KIRP-US 15 42717056 42717056 single base substitution A C missense_variant H665Q 1995T>G KIRP-US 15 42717056 42717056 single base substitution A C missense_variant H85Q 255T>G KIRP-US 15 42717056 42717056 single base substitution A C missense_variant H884Q 2652T>G KIRP-US 15 42717056 42717056 single base substitution A C missense_variant H927Q 2781T>G KIRP-US 15 42717056 42717056 single base substitution A C upstream_gene_variant LAML-KR 15 42701688 42701688 single base substitution T C downstream_gene_variant LAML-KR 15 42703406 42703406 single base substitution T C downstream_gene_variant LAML-KR 15 42729508 42729508 single base substitution G A downstream_gene_variant LAML-KR 15 42729508 42729508 single base substitution G A synonymous_variant A1533A 4599C>T LAML-KR 15 42729508 42729508 single base substitution G A synonymous_variant A499A 1497C>T LAML-KR 15 42729508 42729508 single base substitution G A synonymous_variant A718A 2154C>T LAML-KR 15 42729508 42729508 single base substitution G A synonymous_variant A761A 2283C>T LAML-KR 15 42734833 42734833 single base substitution G T downstream_gene_variant LAML-KR 15 42734833 42734833 single base substitution G T intron_variant LAML-KR 15 42740369 42740369 single base substitution C T downstream_gene_variant LAML-KR 15 42740369 42740369 single base substitution C T synonymous_variant A174A 522G>A LAML-KR 15 42740369 42740369 single base substitution C T synonymous_variant A217A 651G>A LAML-KR 15 42740369 42740369 single base substitution C T synonymous_variant A42A 126G>A LAML-KR 15 42740369 42740369 single base substitution C T synonymous_variant A772A 2316G>A LAML-KR 15 42740369 42740369 single base substitution C T synonymous_variant A989A 2967G>A LAML-KR 15 42740369 42740369 single base substitution C T upstream_gene_variant LGG-US 15 42731630 42731632 deletion of <=200bp TTC - disruptive_inframe_deletion KK1358K LGG-US 15 42731630 42731632 deletion of <=200bp TTC - disruptive_inframe_deletion KK324K LGG-US 15 42731630 42731632 deletion of <=200bp TTC - disruptive_inframe_deletion KK543K LGG-US 15 42731630 42731632 deletion of <=200bp TTC - disruptive_inframe_deletion KK586K LGG-US 15 42731630 42731632 deletion of <=200bp TTC - downstream_gene_variant LGG-US 15 42742995 42742995 single base substitution G A downstream_gene_variant LGG-US 15 42742995 42742995 single base substitution G A intron_variant LGG-US 15 42742995 42742995 single base substitution G A missense_variant P252L 755C>T LGG-US 15 42742995 42742995 single base substitution G A missense_variant P469L 1406C>T LGG-US 15 42742995 42742995 single base substitution G A upstream_gene_variant LIAD-FR 15 42742033 42742033 single base substitution T C downstream_gene_variant LIAD-FR 15 42742033 42742033 single base substitution T C intron_variant LIAD-FR 15 42742033 42742033 single base substitution T C missense_variant N573D 1717A>G LIAD-FR 15 42742033 42742033 single base substitution T C missense_variant N790D 2368A>G LIAD-FR 15 42742033 42742033 single base substitution T C upstream_gene_variant LICA-FR 15 42727433 42727433 single base substitution T A intron_variant LICA-FR 15 42731276 42731276 single base substitution G C downstream_gene_variant LICA-FR 15 42731276 42731276 single base substitution G C missense_variant S1477C 4430C>G LICA-FR 15 42731276 42731276 single base substitution G C missense_variant S443C 1328C>G LICA-FR 15 42731276 42731276 single base substitution G C missense_variant S662C 1985C>G LICA-FR 15 42731276 42731276 single base substitution G C missense_variant S705C 2114C>G LICA-FR 15 42731968 42731968 single base substitution A G downstream_gene_variant LICA-FR 15 42731968 42731968 single base substitution A G intron_variant LICA-FR 15 42731968 42731968 single base substitution A G synonymous_variant A1246A 3738T>C LICA-FR 15 42731968 42731968 single base substitution A G synonymous_variant A431A 1293T>C LICA-FR 15 42731968 42731968 single base substitution A G synonymous_variant A474A 1422T>C LICA-FR 15 42740017 42740017 single base substitution T A downstream_gene_variant LICA-FR 15 42740017 42740017 single base substitution T A intron_variant LICA-FR 15 42740017 42740017 single base substitution T A upstream_gene_variant LICA-FR 15 42740310 42740310 single base substitution T C downstream_gene_variant LICA-FR 15 42740310 42740310 single base substitution T C missense_variant N1009S 3026A>G LICA-FR 15 42740310 42740310 single base substitution T C missense_variant N194S 581A>G LICA-FR 15 42740310 42740310 single base substitution T C missense_variant N237S 710A>G LICA-FR 15 42740310 42740310 single base substitution T C missense_variant N62S 185A>G LICA-FR 15 42740310 42740310 single base substitution T C missense_variant N792S 2375A>G LICA-FR 15 42740310 42740310 single base substitution T C upstream_gene_variant LICA-FR 15 42743629 42743629 single base substitution C G downstream_gene_variant LICA-FR 15 42743629 42743629 single base substitution C G intron_variant LICA-FR 15 42743629 42743629 single base substitution C G missense_variant D258H 772G>C LICA-FR 15 42743629 42743629 single base substitution C G missense_variant D281H 841G>C LICA-FR 15 42743629 42743629 single base substitution C G missense_variant D41H 121G>C LICA-FR 15 42743629 42743629 single base substitution C G upstream_gene_variant LICA-FR 15 42775647 42775647 single base substitution C T intron_variant LICA-FR 15 42778398 42778398 single base substitution C A intron_variant LIHC-US 15 42703132 42703132 single base substitution G A downstream_gene_variant LIHC-US 15 42720252 42720252 single base substitution T A synonymous_variant G1631G 4893A>T LIHC-US 15 42720252 42720252 single base substitution T A synonymous_variant G17G 51A>T LIHC-US 15 42720252 42720252 single base substitution T A synonymous_variant G597G 1791A>T LIHC-US 15 42720252 42720252 single base substitution T A synonymous_variant G816G 2448A>T LIHC-US 15 42720252 42720252 single base substitution T A synonymous_variant G859G 2577A>T LIHC-US 15 42720252 42720252 single base substitution T A upstream_gene_variant LIHC-US 15 42729475 42729475 single base substitution T C downstream_gene_variant LIHC-US 15 42729475 42729475 single base substitution T C synonymous_variant L1544L 4632A>G LIHC-US 15 42729475 42729475 single base substitution T C synonymous_variant L510L 1530A>G LIHC-US 15 42729475 42729475 single base substitution T C synonymous_variant L729L 2187A>G LIHC-US 15 42729475 42729475 single base substitution T C synonymous_variant L772L 2316A>G LIHC-US 15 42734378 42734378 single base substitution G A downstream_gene_variant LIHC-US 15 42734378 42734378 single base substitution G A missense_variant S1196L 3587C>T LIHC-US 15 42734378 42734378 single base substitution G A missense_variant S154L 461C>T LIHC-US 15 42734378 42734378 single base substitution G A missense_variant S249L 746C>T LIHC-US 15 42734378 42734378 single base substitution G A missense_variant S381L 1142C>T LIHC-US 15 42734378 42734378 single base substitution G A missense_variant S424L 1271C>T LIHC-US 15 42742306 42742306 single base substitution A C downstream_gene_variant LIHC-US 15 42742306 42742306 single base substitution A C intron_variant LIHC-US 15 42742306 42742306 single base substitution A C missense_variant L482V 1444T>G LIHC-US 15 42742306 42742306 single base substitution A C missense_variant L699V 2095T>G LIHC-US 15 42742306 42742306 single base substitution A C upstream_gene_variant LINC-JP 15 42702764 42702764 single base substitution T A downstream_gene_variant LINC-JP 15 42703007 42703007 single base substitution G A downstream_gene_variant LINC-JP 15 42703886 42703886 single base substitution C G downstream_gene_variant LINC-JP 15 42711571 42711571 single base substitution T A downstream_gene_variant LINC-JP 15 42711571 42711571 single base substitution T A intron_variant LINC-JP 15 42714171 42714171 single base substitution G A downstream_gene_variant LINC-JP 15 42714171 42714171 single base substitution G A exon_variant LINC-JP 15 42714171 42714171 single base substitution G A stop_gained Q1002* 3004C>T LINC-JP 15 42714171 42714171 single base substitution G A stop_gained Q160* 478C>T LINC-JP 15 42714171 42714171 single base substitution G A stop_gained Q1774* 5320C>T LINC-JP 15 42714171 42714171 single base substitution G A stop_gained Q740* 2218C>T LINC-JP 15 42714171 42714171 single base substitution G A stop_gained Q959* 2875C>T LINC-JP 15 42716139 42716139 single base substitution C A intron_variant LINC-JP 15 42717208 42717208 single base substitution C T exon_variant LINC-JP 15 42717208 42717208 single base substitution C T missense_variant E1649K 4945G>A LINC-JP 15 42717208 42717208 single base substitution C T missense_variant E35K 103G>A LINC-JP 15 42717208 42717208 single base substitution C T missense_variant E615K 1843G>A LINC-JP 15 42717208 42717208 single base substitution C T missense_variant E834K 2500G>A LINC-JP 15 42717208 42717208 single base substitution C T missense_variant E877K 2629G>A LINC-JP 15 42717208 42717208 single base substitution C T upstream_gene_variant LINC-JP 15 42725583 42725583 single base substitution G A intron_variant LINC-JP 15 42729704 42729704 single base substitution C T downstream_gene_variant LINC-JP 15 42729704 42729704 single base substitution C T intron_variant LINC-JP 15 42737260 42737260 single base substitution C T downstream_gene_variant LINC-JP 15 42737260 42737260 single base substitution C T intron_variant LINC-JP 15 42738734 42738734 single base substitution A C downstream_gene_variant LINC-JP 15 42738734 42738734 single base substitution A C intron_variant LINC-JP 15 42741506 42741506 single base substitution G C downstream_gene_variant LINC-JP 15 42741506 42741506 single base substitution G C intron_variant LINC-JP 15 42741506 42741506 single base substitution G C upstream_gene_variant LINC-JP 15 42743309 42743309 single base substitution C T downstream_gene_variant LINC-JP 15 42743309 42743309 single base substitution C T intron_variant LINC-JP 15 42743309 42743309 single base substitution C T synonymous_variant L147L 441G>A LINC-JP 15 42743309 42743309 single base substitution C T synonymous_variant L364L 1092G>A LINC-JP 15 42743309 42743309 single base substitution C T synonymous_variant L387L 1161G>A LINC-JP 15 42743309 42743309 single base substitution C T upstream_gene_variant LINC-JP 15 42743910 42743910 single base substitution T C 5_prime_UTR_variant LINC-JP 15 42743910 42743910 single base substitution T C intron_variant LINC-JP 15 42743910 42743910 single base substitution T C missense_variant H164R 491A>G LINC-JP 15 42743910 42743910 single base substitution T C missense_variant H187R 560A>G LINC-JP 15 42743910 42743910 single base substitution T C upstream_gene_variant LINC-JP 15 42743939 42743939 single base substitution A T 5_prime_UTR_variant LINC-JP 15 42743939 42743939 single base substitution A T intron_variant LINC-JP 15 42743939 42743939 single base substitution A T synonymous_variant G154G 462T>A LINC-JP 15 42743939 42743939 single base substitution A T synonymous_variant G177G 531T>A LINC-JP 15 42743939 42743939 single base substitution A T upstream_gene_variant LINC-JP 15 42747088 42747088 single base substitution C T intron_variant LINC-JP 15 42758276 42758276 single base substitution T A missense_variant R31W 91A>T LINC-JP 15 42770830 42770830 single base substitution C T intron_variant LIRI-JP 15 42700611 42700611 single base substitution A G downstream_gene_variant LIRI-JP 15 42701408 42701408 single base substitution T C downstream_gene_variant LIRI-JP 15 42701630 42701630 single base substitution T G downstream_gene_variant LIRI-JP 15 42701700 42701700 single base substitution G T downstream_gene_variant LIRI-JP 15 42702793 42702793 single base substitution T A downstream_gene_variant LIRI-JP 15 42704164 42704164 single base substitution A C downstream_gene_variant LIRI-JP 15 42705962 42705962 single base substitution T G 3_prime_UTR_variant LIRI-JP 15 42705962 42705962 single base substitution T G downstream_gene_variant LIRI-JP 15 42707302 42707302 insertion of <=200bp - T 3_prime_UTR_variant LIRI-JP 15 42707302 42707302 insertion of <=200bp - T downstream_gene_variant LIRI-JP 15 42710130 42710130 single base substitution A G downstream_gene_variant LIRI-JP 15 42710130 42710130 single base substitution A G exon_variant LIRI-JP 15 42710130 42710130 single base substitution A G intron_variant LIRI-JP 15 42710130 42710130 single base substitution A G missense_variant I1008T 3023T>C LIRI-JP 15 42710130 42710130 single base substitution A G missense_variant I1051T 3152T>C LIRI-JP 15 42710130 42710130 single base substitution A G missense_variant I1823T 5468T>C LIRI-JP 15 42710130 42710130 single base substitution A G missense_variant I789T 2366T>C LIRI-JP 15 42712238 42712238 single base substitution A G downstream_gene_variant LIRI-JP 15 42712238 42712238 single base substitution A G intron_variant LIRI-JP 15 42713857 42713857 deletion of <=200bp C - downstream_gene_variant LIRI-JP 15 42713857 42713857 deletion of <=200bp C - intron_variant LIRI-JP 15 42714853 42714853 single base substitution A C intron_variant LIRI-JP 15 42717618 42717618 single base substitution T C intron_variant LIRI-JP 15 42717618 42717618 single base substitution T C upstream_gene_variant LIRI-JP 15 42718300 42718300 single base substitution G T intron_variant LIRI-JP 15 42718300 42718300 single base substitution G T upstream_gene_variant LIRI-JP 15 42722067 42722067 single base substitution T C intron_variant LIRI-JP 15 42722067 42722067 single base substitution T C upstream_gene_variant LIRI-JP 15 42723176 42723176 single base substitution T C intron_variant LIRI-JP 15 42723176 42723176 single base substitution T C upstream_gene_variant LIRI-JP 15 42723444 42723444 single base substitution T C intron_variant LIRI-JP 15 42723444 42723444 single base substitution T C upstream_gene_variant LIRI-JP 15 42725904 42725904 single base substitution C A intron_variant LIRI-JP 15 42727911 42727911 single base substitution G T intron_variant LIRI-JP 15 42729410 42729410 single base substitution T C downstream_gene_variant LIRI-JP 15 42729410 42729410 single base substitution T C intron_variant LIRI-JP 15 42731532 42731532 single base substitution T C downstream_gene_variant LIRI-JP 15 42731532 42731532 single base substitution T C missense_variant K1392E 4174A>G LIRI-JP 15 42731532 42731532 single base substitution T C missense_variant K358E 1072A>G LIRI-JP 15 42731532 42731532 single base substitution T C missense_variant K577E 1729A>G LIRI-JP 15 42731532 42731532 single base substitution T C missense_variant K620E 1858A>G LIRI-JP 15 42731791 42731791 single base substitution T A downstream_gene_variant LIRI-JP 15 42731791 42731791 single base substitution T A intron_variant LIRI-JP 15 42731791 42731791 single base substitution T A missense_variant E1305D 3915A>T LIRI-JP 15 42731791 42731791 single base substitution T A missense_variant E490D 1470A>T LIRI-JP 15 42731791 42731791 single base substitution T A missense_variant E533D 1599A>T LIRI-JP 15 42731980 42731980 single base substitution T C downstream_gene_variant LIRI-JP 15 42731980 42731980 single base substitution T C intron_variant LIRI-JP 15 42731980 42731980 single base substitution T C synonymous_variant P1242P 3726A>G LIRI-JP 15 42731980 42731980 single base substitution T C synonymous_variant P427P 1281A>G LIRI-JP 15 42731980 42731980 single base substitution T C synonymous_variant P470P 1410A>G LIRI-JP 15 42732651 42732651 single base substitution T C downstream_gene_variant LIRI-JP 15 42732651 42732651 single base substitution T C intron_variant LIRI-JP 15 42734126 42734126 single base substitution T G 3_prime_UTR_variant LIRI-JP 15 42734126 42734126 single base substitution T G downstream_gene_variant LIRI-JP 15 42734126 42734126 single base substitution T G intron_variant LIRI-JP 15 42735344 42735344 single base substitution G C downstream_gene_variant LIRI-JP 15 42735344 42735344 single base substitution G C intron_variant LIRI-JP 15 42735423 42735423 single base substitution G A downstream_gene_variant LIRI-JP 15 42735423 42735423 single base substitution G A intron_variant LIRI-JP 15 42738378 42738378 single base substitution C T downstream_gene_variant LIRI-JP 15 42738378 42738378 single base substitution C T intron_variant LIRI-JP 15 42740369 42740369 single base substitution C A downstream_gene_variant LIRI-JP 15 42740369 42740369 single base substitution C A synonymous_variant A174A 522G>T LIRI-JP 15 42740369 42740369 single base substitution C A synonymous_variant A217A 651G>T LIRI-JP 15 42740369 42740369 single base substitution C A synonymous_variant A42A 126G>T LIRI-JP 15 42740369 42740369 single base substitution C A synonymous_variant A772A 2316G>T LIRI-JP 15 42740369 42740369 single base substitution C A synonymous_variant A989A 2967G>T LIRI-JP 15 42740369 42740369 single base substitution C A upstream_gene_variant LIRI-JP 15 42745592 42745594 deletion of <=200bp AGC - intron_variant LIRI-JP 15 42746734 42746734 single base substitution T C intron_variant LIRI-JP 15 42748278 42748278 single base substitution T C intron_variant LIRI-JP 15 42752620 42752620 single base substitution C T intron_variant LIRI-JP 15 42752620 42752620 single base substitution C T upstream_gene_variant LIRI-JP 15 42753419 42753419 single base substitution T C intron_variant LIRI-JP 15 42753419 42753419 single base substitution T C upstream_gene_variant LIRI-JP 15 42753540 42753551 deletion of <=200bp CTTGGCTAGCAA - intron_variant LIRI-JP 15 42753540 42753551 deletion of <=200bp CTTGGCTAGCAA - upstream_gene_variant LIRI-JP 15 42753562 42753562 single base substitution T C intron_variant LIRI-JP 15 42753562 42753562 single base substitution T C upstream_gene_variant LIRI-JP 15 42754261 42754261 single base substitution C A intron_variant LIRI-JP 15 42754261 42754261 single base substitution C A upstream_gene_variant LIRI-JP 15 42755184 42755184 single base substitution C A intron_variant LIRI-JP 15 42755608 42755608 single base substitution T C intron_variant LIRI-JP 15 42756824 42756824 single base substitution C T intron_variant LIRI-JP 15 42757287 42757287 single base substitution T C intron_variant LIRI-JP 15 42757333 42757333 single base substitution A C intron_variant LIRI-JP 15 42758142 42758142 single base substitution T C intron_variant LIRI-JP 15 42758630 42758630 single base substitution T C intron_variant LIRI-JP 15 42763040 42763040 single base substitution A G intron_variant LIRI-JP 15 42764798 42764798 single base substitution C T intron_variant LIRI-JP 15 42766587 42766587 single base substitution T C intron_variant LIRI-JP 15 42767219 42767219 single base substitution A C intron_variant LIRI-JP 15 42768828 42768828 single base substitution A C intron_variant LIRI-JP 15 42769054 42769054 single base substitution T C intron_variant LIRI-JP 15 42770281 42770281 single base substitution C T intron_variant LIRI-JP 15 42773086 42773086 single base substitution G C intron_variant LIRI-JP 15 42773491 42773491 single base substitution T C intron_variant LIRI-JP 15 42776755 42776755 single base substitution T C intron_variant LIRI-JP 15 42777997 42777997 single base substitution T A intron_variant LIRI-JP 15 42778629 42778629 single base substitution T A intron_variant LIRI-JP 15 42778738 42778738 single base substitution T C intron_variant LIRI-JP 15 42784228 42784228 single base substitution C A upstream_gene_variant LIRI-JP 15 42784736 42784736 single base substitution C T upstream_gene_variant LIRI-JP 15 42786375 42786375 single base substitution G A upstream_gene_variant LIRI-JP 15 42786538 42786538 single base substitution C A upstream_gene_variant LUSC-KR 15 42702496 42702496 single base substitution G T downstream_gene_variant LUSC-KR 15 42703277 42703277 single base substitution A G downstream_gene_variant LUSC-KR 15 42703406 42703406 single base substitution T C downstream_gene_variant LUSC-KR 15 42708310 42708310 single base substitution T A 3_prime_UTR_variant LUSC-KR 15 42708310 42708310 single base substitution T A downstream_gene_variant LUSC-KR 15 42708310 42708310 single base substitution T A intron_variant LUSC-KR 15 42714374 42714374 single base substitution C T downstream_gene_variant LUSC-KR 15 42714374 42714374 single base substitution C T intron_variant LUSC-KR 15 42715720 42715720 single base substitution C T intron_variant LUSC-KR 15 42716757 42716757 single base substitution C T exon_variant LUSC-KR 15 42716757 42716757 single base substitution C T intron_variant LUSC-KR 15 42716757 42716757 single base substitution C T upstream_gene_variant LUSC-KR 15 42719855 42719855 single base substitution T A intron_variant LUSC-KR 15 42719855 42719855 single base substitution T A upstream_gene_variant LUSC-KR 15 42723606 42723606 single base substitution C T intron_variant LUSC-KR 15 42723606 42723606 single base substitution C T upstream_gene_variant LUSC-KR 15 42728172 42728172 single base substitution G T intron_variant LUSC-KR 15 42735128 42735128 single base substitution C T downstream_gene_variant LUSC-KR 15 42735128 42735128 single base substitution C T intron_variant LUSC-KR 15 42743044 42743044 single base substitution G A downstream_gene_variant LUSC-KR 15 42743044 42743044 single base substitution G A intron_variant LUSC-KR 15 42743044 42743044 single base substitution G A missense_variant P236S 706C>T LUSC-KR 15 42743044 42743044 single base substitution G A missense_variant P453S 1357C>T LUSC-KR 15 42743044 42743044 single base substitution G A upstream_gene_variant LUSC-KR 15 42746140 42746140 single base substitution G A intron_variant LUSC-KR 15 42749697 42749697 single base substitution G T 5_prime_UTR_variant LUSC-KR 15 42749697 42749697 single base substitution G T intron_variant LUSC-KR 15 42751017 42751017 single base substitution G C intron_variant LUSC-KR 15 42751017 42751017 single base substitution G C upstream_gene_variant LUSC-KR 15 42753157 42753157 single base substitution C A intron_variant LUSC-KR 15 42753157 42753157 single base substitution C A upstream_gene_variant LUSC-KR 15 42754385 42754385 single base substitution A C intron_variant LUSC-KR 15 42754385 42754385 single base substitution A C upstream_gene_variant LUSC-KR 15 42755130 42755130 single base substitution C A intron_variant LUSC-KR 15 42756395 42756395 single base substitution G A intron_variant LUSC-KR 15 42759232 42759232 single base substitution G A intron_variant LUSC-KR 15 42759978 42759978 single base substitution G C intron_variant LUSC-KR 15 42763068 42763068 single base substitution C G intron_variant LUSC-KR 15 42763383 42763383 single base substitution C G intron_variant LUSC-KR 15 42765037 42765037 single base substitution G A intron_variant LUSC-KR 15 42770516 42770516 single base substitution C A intron_variant LUSC-KR 15 42770756 42770756 single base substitution C G intron_variant LUSC-KR 15 42774068 42774068 single base substitution A G intron_variant LUSC-KR 15 42775349 42775349 single base substitution C A intron_variant LUSC-KR 15 42775742 42775742 single base substitution C G intron_variant LUSC-KR 15 42775796 42775796 single base substitution C T intron_variant LUSC-KR 15 42775817 42775817 single base substitution C G intron_variant LUSC-KR 15 42784531 42784531 single base substitution T C upstream_gene_variant LUSC-KR 15 42787791 42787791 single base substitution G T upstream_gene_variant LUSC-US 15 42702161 42702161 single base substitution G C downstream_gene_variant LUSC-US 15 42702687 42702687 single base substitution C T downstream_gene_variant LUSC-US 15 42710039 42710039 single base substitution G A downstream_gene_variant LUSC-US 15 42710039 42710039 single base substitution G A intron_variant LUSC-US 15 42710039 42710039 single base substitution G A synonymous_variant C1038C 3114C>T LUSC-US 15 42710039 42710039 single base substitution G A synonymous_variant C1081C 3243C>T LUSC-US 15 42710039 42710039 single base substitution G A synonymous_variant C1853C 5559C>T LUSC-US 15 42710039 42710039 single base substitution G A synonymous_variant C819C 2457C>T LUSC-US 15 42710095 42710095 single base substitution G A downstream_gene_variant LUSC-US 15 42710095 42710095 single base substitution G A exon_variant LUSC-US 15 42710095 42710095 single base substitution G A intron_variant LUSC-US 15 42710095 42710095 single base substitution G A synonymous_variant L1020L 3058C>T LUSC-US 15 42710095 42710095 single base substitution G A synonymous_variant L1063L 3187C>T LUSC-US 15 42710095 42710095 single base substitution G A synonymous_variant L1835L 5503C>T LUSC-US 15 42710095 42710095 single base substitution G A synonymous_variant L801L 2401C>T LUSC-US 15 42717087 42717087 single base substitution T A exon_variant LUSC-US 15 42717087 42717087 single base substitution T A missense_variant N1689I 5066A>T LUSC-US 15 42717087 42717087 single base substitution T A missense_variant N655I 1964A>T LUSC-US 15 42717087 42717087 single base substitution T A missense_variant N75I 224A>T LUSC-US 15 42717087 42717087 single base substitution T A missense_variant N874I 2621A>T LUSC-US 15 42717087 42717087 single base substitution T A missense_variant N917I 2750A>T LUSC-US 15 42717087 42717087 single base substitution T A upstream_gene_variant LUSC-US 15 42720257 42720257 single base substitution C A missense_variant A1630S 4888G>T LUSC-US 15 42720257 42720257 single base substitution C A missense_variant A16S 46G>T LUSC-US 15 42720257 42720257 single base substitution C A missense_variant A596S 1786G>T LUSC-US 15 42720257 42720257 single base substitution C A missense_variant A815S 2443G>T LUSC-US 15 42720257 42720257 single base substitution C A missense_variant A858S 2572G>T LUSC-US 15 42720257 42720257 single base substitution C A upstream_gene_variant LUSC-US 15 42727711 42727711 single base substitution C T synonymous_variant R1561R 4683G>A LUSC-US 15 42727711 42727711 single base substitution C T synonymous_variant R527R 1581G>A LUSC-US 15 42727711 42727711 single base substitution C T synonymous_variant R746R 2238G>A LUSC-US 15 42727711 42727711 single base substitution C T synonymous_variant R789R 2367G>A LUSC-US 15 42734294 42734294 single base substitution G A downstream_gene_variant LUSC-US 15 42734294 42734294 single base substitution G A missense_variant S1224F 3671C>T LUSC-US 15 42734294 42734294 single base substitution G A missense_variant S182F 545C>T LUSC-US 15 42734294 42734294 single base substitution G A missense_variant S277F 830C>T LUSC-US 15 42734294 42734294 single base substitution G A missense_variant S409F 1226C>T LUSC-US 15 42734294 42734294 single base substitution G A missense_variant S452F 1355C>T LUSC-US 15 42742027 42742027 single base substitution C T downstream_gene_variant LUSC-US 15 42742027 42742027 single base substitution C T intron_variant LUSC-US 15 42742027 42742027 single base substitution C T missense_variant E575K 1723G>A LUSC-US 15 42742027 42742027 single base substitution C T missense_variant E792K 2374G>A LUSC-US 15 42742027 42742027 single base substitution C T upstream_gene_variant LUSC-US 15 42742430 42742430 single base substitution T C downstream_gene_variant LUSC-US 15 42742430 42742430 single base substitution T C intron_variant LUSC-US 15 42742430 42742430 single base substitution T C synonymous_variant T440T 1320A>G LUSC-US 15 42742430 42742430 single base substitution T C synonymous_variant T657T 1971A>G LUSC-US 15 42742430 42742430 single base substitution T C upstream_gene_variant LUSC-US 15 42742495 42742495 single base substitution T A downstream_gene_variant LUSC-US 15 42742495 42742495 single base substitution T A intron_variant LUSC-US 15 42742495 42742495 single base substitution T A stop_gained R419* 1255A>T LUSC-US 15 42742495 42742495 single base substitution T A stop_gained R636* 1906A>T LUSC-US 15 42742495 42742495 single base substitution T A upstream_gene_variant LUSC-US 15 42742724 42742724 single base substitution G T downstream_gene_variant LUSC-US 15 42742724 42742724 single base substitution G T intron_variant LUSC-US 15 42742724 42742724 single base substitution G T synonymous_variant T342T 1026C>A LUSC-US 15 42742724 42742724 single base substitution G T synonymous_variant T559T 1677C>A LUSC-US 15 42742724 42742724 single base substitution G T upstream_gene_variant LUSC-US 15 42742728 42742728 single base substitution C A downstream_gene_variant LUSC-US 15 42742728 42742728 single base substitution C A intron_variant LUSC-US 15 42742728 42742728 single base substitution C A missense_variant S341I 1022G>T LUSC-US 15 42742728 42742728 single base substitution C A missense_variant S558I 1673G>T LUSC-US 15 42742728 42742728 single base substitution C A upstream_gene_variant LUSC-US 15 42743038 42743038 single base substitution G A downstream_gene_variant LUSC-US 15 42743038 42743038 single base substitution G A intron_variant LUSC-US 15 42743038 42743038 single base substitution G A missense_variant L238F 712C>T LUSC-US 15 42743038 42743038 single base substitution G A missense_variant L455F 1363C>T LUSC-US 15 42743038 42743038 single base substitution G A upstream_gene_variant MALY-DE 15 42706308 42706308 single base substitution G T 3_prime_UTR_variant MALY-DE 15 42706308 42706308 single base substitution G T downstream_gene_variant MALY-DE 15 42712343 42712343 single base substitution C T downstream_gene_variant MALY-DE 15 42712343 42712343 single base substitution C T intron_variant MALY-DE 15 42713731 42713731 single base substitution C T downstream_gene_variant MALY-DE 15 42713731 42713731 single base substitution C T intron_variant MALY-DE 15 42716287 42716287 single base substitution T G exon_variant MALY-DE 15 42716287 42716287 single base substitution T G intron_variant MALY-DE 15 42718605 42718605 single base substitution A G intron_variant MALY-DE 15 42718605 42718605 single base substitution A G upstream_gene_variant MALY-DE 15 42728446 42728446 single base substitution C G intron_variant MALY-DE 15 42730561 42730561 single base substitution C T downstream_gene_variant MALY-DE 15 42730561 42730561 single base substitution C T intron_variant MALY-DE 15 42740410 42740410 single base substitution C A downstream_gene_variant MALY-DE 15 42740410 42740410 single base substitution C A stop_gained E161* 481G>T MALY-DE 15 42740410 42740410 single base substitution C A stop_gained E204* 610G>T MALY-DE 15 42740410 42740410 single base substitution C A stop_gained E29* 85G>T MALY-DE 15 42740410 42740410 single base substitution C A stop_gained E759* 2275G>T MALY-DE 15 42740410 42740410 single base substitution C A stop_gained E976* 2926G>T MALY-DE 15 42740410 42740410 single base substitution C A upstream_gene_variant MALY-DE 15 42748932 42748932 single base substitution T G intron_variant MALY-DE 15 42750278 42750278 single base substitution A T intron_variant MALY-DE 15 42750278 42750278 single base substitution A T upstream_gene_variant MALY-DE 15 42750306 42750306 single base substitution G C intron_variant MALY-DE 15 42750306 42750306 single base substitution G C upstream_gene_variant MALY-DE 15 42761243 42761243 single base substitution C T intron_variant MALY-DE 15 42762813 42762813 single base substitution T C intron_variant MALY-DE 15 42765402 42765402 single base substitution G A intron_variant MALY-DE 15 42773402 42773402 single base substitution C T intron_variant MALY-DE 15 42774897 42774897 single base substitution T G intron_variant MALY-DE 15 42778633 42778633 single base substitution A T intron_variant MALY-DE 15 42785546 42785546 single base substitution C A upstream_gene_variant MALY-DE 15 42785548 42785548 single base substitution C A upstream_gene_variant MELA-AU 15 42704246 42704246 single base substitution C T downstream_gene_variant MELA-AU 15 42705223 42705223 single base substitution C T 3_prime_UTR_variant MELA-AU 15 42705223 42705223 single base substitution C T downstream_gene_variant MELA-AU 15 42705496 42705496 single base substitution T C 3_prime_UTR_variant MELA-AU 15 42705496 42705496 single base substitution T C downstream_gene_variant MELA-AU 15 42705614 42705614 single base substitution C T 3_prime_UTR_variant MELA-AU 15 42705614 42705614 single base substitution C T downstream_gene_variant MELA-AU 15 42708497 42708497 single base substitution T G 3_prime_UTR_variant MELA-AU 15 42708497 42708497 single base substitution T G downstream_gene_variant MELA-AU 15 42708497 42708497 single base substitution T G intron_variant MELA-AU 15 42709425 42709425 single base substitution G A 3_prime_UTR_variant MELA-AU 15 42709425 42709425 single base substitution G A downstream_gene_variant MELA-AU 15 42709425 42709425 single base substitution G A intron_variant MELA-AU 15 42709488 42709488 single base substitution G A 3_prime_UTR_variant MELA-AU 15 42709488 42709488 single base substitution G A downstream_gene_variant MELA-AU 15 42709488 42709488 single base substitution G A intron_variant MELA-AU 15 42711136 42711136 single base substitution C T downstream_gene_variant MELA-AU 15 42711136 42711136 single base substitution C T intron_variant MELA-AU 15 42712899 42712899 single base substitution A G downstream_gene_variant MELA-AU 15 42712899 42712899 single base substitution A G intron_variant MELA-AU 15 42713225 42713225 single base substitution G A downstream_gene_variant MELA-AU 15 42713225 42713225 single base substitution G A intron_variant MELA-AU 15 42713443 42713443 single base substitution A G downstream_gene_variant MELA-AU 15 42713443 42713443 single base substitution A G intron_variant MELA-AU 15 42714427 42714427 single base substitution G A downstream_gene_variant MELA-AU 15 42714427 42714427 single base substitution G A intron_variant MELA-AU 15 42715062 42715062 single base substitution A T intron_variant MELA-AU 15 42715082 42715082 single base substitution G A intron_variant MELA-AU 15 42716063 42716063 single base substitution A G intron_variant MELA-AU 15 42717077 42717077 single base substitution G A exon_variant MELA-AU 15 42717077 42717077 single base substitution G A synonymous_variant L1692L 5076C>T MELA-AU 15 42717077 42717077 single base substitution G A synonymous_variant L658L 1974C>T MELA-AU 15 42717077 42717077 single base substitution G A synonymous_variant L78L 234C>T MELA-AU 15 42717077 42717077 single base substitution G A synonymous_variant L877L 2631C>T MELA-AU 15 42717077 42717077 single base substitution G A synonymous_variant L920L 2760C>T MELA-AU 15 42717077 42717077 single base substitution G A upstream_gene_variant MELA-AU 15 42717188 42717188 single base substitution G A exon_variant MELA-AU 15 42717188 42717188 single base substitution G A synonymous_variant G1655G 4965C>T MELA-AU 15 42717188 42717188 single base substitution G A synonymous_variant G41G 123C>T MELA-AU 15 42717188 42717188 single base substitution G A synonymous_variant G621G 1863C>T MELA-AU 15 42717188 42717188 single base substitution G A synonymous_variant G840G 2520C>T MELA-AU 15 42717188 42717188 single base substitution G A synonymous_variant G883G 2649C>T MELA-AU 15 42717188 42717188 single base substitution G A upstream_gene_variant MELA-AU 15 42717375 42717375 single base substitution C T intron_variant MELA-AU 15 42717375 42717375 single base substitution C T upstream_gene_variant MELA-AU 15 42718343 42718344 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 15 42718343 42718344 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 15 42718825 42718825 single base substitution C T intron_variant MELA-AU 15 42718825 42718825 single base substitution C T upstream_gene_variant MELA-AU 15 42718861 42718861 single base substitution C T intron_variant MELA-AU 15 42718861 42718861 single base substitution C T upstream_gene_variant MELA-AU 15 42719758 42719758 single base substitution G A intron_variant MELA-AU 15 42719758 42719758 single base substitution G A upstream_gene_variant MELA-AU 15 42719759 42719759 single base substitution G A intron_variant MELA-AU 15 42719759 42719759 single base substitution G A upstream_gene_variant MELA-AU 15 42720030 42720030 single base substitution G A intron_variant MELA-AU 15 42720030 42720030 single base substitution G A upstream_gene_variant MELA-AU 15 42720072 42720072 single base substitution G A intron_variant MELA-AU 15 42720072 42720072 single base substitution G A upstream_gene_variant MELA-AU 15 42720126 42720126 single base substitution G A intron_variant MELA-AU 15 42720126 42720126 single base substitution G A upstream_gene_variant MELA-AU 15 42720379 42720379 single base substitution G A intron_variant MELA-AU 15 42720379 42720379 single base substitution G A upstream_gene_variant MELA-AU 15 42720433 42720433 single base substitution G A intron_variant MELA-AU 15 42720433 42720433 single base substitution G A upstream_gene_variant MELA-AU 15 42720707 42720707 single base substitution T A intron_variant MELA-AU 15 42720707 42720707 single base substitution T A upstream_gene_variant MELA-AU 15 42720969 42720969 single base substitution G A intron_variant MELA-AU 15 42720969 42720969 single base substitution G A upstream_gene_variant MELA-AU 15 42721025 42721025 single base substitution G A intron_variant MELA-AU 15 42721025 42721025 single base substitution G A upstream_gene_variant MELA-AU 15 42721110 42721110 single base substitution C T intron_variant MELA-AU 15 42721110 42721110 single base substitution C T upstream_gene_variant MELA-AU 15 42721328 42721328 single base substitution G A intron_variant MELA-AU 15 42721328 42721328 single base substitution G A upstream_gene_variant MELA-AU 15 42721624 42721624 single base substitution G A intron_variant MELA-AU 15 42721624 42721624 single base substitution G A upstream_gene_variant MELA-AU 15 42722198 42722198 single base substitution G A intron_variant MELA-AU 15 42722198 42722198 single base substitution G A upstream_gene_variant MELA-AU 15 42722624 42722624 single base substitution C T intron_variant MELA-AU 15 42722624 42722624 single base substitution C T upstream_gene_variant MELA-AU 15 42722765 42722765 single base substitution G A intron_variant MELA-AU 15 42722765 42722765 single base substitution G A upstream_gene_variant MELA-AU 15 42723180 42723180 single base substitution T A intron_variant MELA-AU 15 42723180 42723180 single base substitution T A upstream_gene_variant MELA-AU 15 42723189 42723189 single base substitution G A intron_variant MELA-AU 15 42723189 42723189 single base substitution G A upstream_gene_variant MELA-AU 15 42723639 42723639 single base substitution G A intron_variant MELA-AU 15 42723639 42723639 single base substitution G A upstream_gene_variant MELA-AU 15 42725273 42725273 single base substitution C T intron_variant MELA-AU 15 42725273 42725273 single base substitution C T upstream_gene_variant MELA-AU 15 42725775 42725776 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 15 42727568 42727568 single base substitution C A intron_variant MELA-AU 15 42727770 42727770 single base substitution T C intron_variant MELA-AU 15 42729790 42729790 single base substitution G A downstream_gene_variant MELA-AU 15 42729790 42729790 single base substitution G A intron_variant MELA-AU 15 42731145 42731145 single base substitution G A downstream_gene_variant MELA-AU 15 42731145 42731145 single base substitution G A intron_variant MELA-AU 15 42731624 42731624 single base substitution A G downstream_gene_variant MELA-AU 15 42731624 42731624 single base substitution A G missense_variant L1361P 4082T>C MELA-AU 15 42731624 42731624 single base substitution A G missense_variant L327P 980T>C MELA-AU 15 42731624 42731624 single base substitution A G missense_variant L546P 1637T>C MELA-AU 15 42731624 42731624 single base substitution A G missense_variant L589P 1766T>C MELA-AU 15 42732801 42732801 single base substitution G A downstream_gene_variant MELA-AU 15 42732801 42732801 single base substitution G A intron_variant MELA-AU 15 42733917 42733917 single base substitution G A downstream_gene_variant MELA-AU 15 42733917 42733917 single base substitution G A intron_variant MELA-AU 15 42733984 42733984 single base substitution G A 3_prime_UTR_variant MELA-AU 15 42733984 42733984 single base substitution G A downstream_gene_variant MELA-AU 15 42733984 42733984 single base substitution G A intron_variant MELA-AU 15 42734496 42734496 single base substitution G A downstream_gene_variant MELA-AU 15 42734496 42734496 single base substitution G A missense_variant P1157S 3469C>T MELA-AU 15 42734496 42734496 single base substitution G A missense_variant P115S 343C>T MELA-AU 15 42734496 42734496 single base substitution G A missense_variant P210S 628C>T MELA-AU 15 42734496 42734496 single base substitution G A missense_variant P342S 1024C>T MELA-AU 15 42734496 42734496 single base substitution G A missense_variant P385S 1153C>T MELA-AU 15 42734497 42734497 single base substitution G A downstream_gene_variant MELA-AU 15 42734497 42734497 single base substitution G A synonymous_variant F114F 342C>T MELA-AU 15 42734497 42734497 single base substitution G A synonymous_variant F1156F 3468C>T MELA-AU 15 42734497 42734497 single base substitution G A synonymous_variant F209F 627C>T MELA-AU 15 42734497 42734497 single base substitution G A synonymous_variant F341F 1023C>T MELA-AU 15 42734497 42734497 single base substitution G A synonymous_variant F384F 1152C>T MELA-AU 15 42734503 42734503 single base substitution G A downstream_gene_variant MELA-AU 15 42734503 42734503 single base substitution G A synonymous_variant P112P 336C>T MELA-AU 15 42734503 42734503 single base substitution G A synonymous_variant P1154P 3462C>T MELA-AU 15 42734503 42734503 single base substitution G A synonymous_variant P207P 621C>T MELA-AU 15 42734503 42734503 single base substitution G A synonymous_variant P339P 1017C>T MELA-AU 15 42734503 42734503 single base substitution G A synonymous_variant P382P 1146C>T MELA-AU 15 42734568 42734568 single base substitution G A downstream_gene_variant MELA-AU 15 42734568 42734568 single base substitution G A missense_variant L1133F 3397C>T MELA-AU 15 42734568 42734568 single base substitution G A missense_variant L186F 556C>T MELA-AU 15 42734568 42734568 single base substitution G A missense_variant L318F 952C>T MELA-AU 15 42734568 42734568 single base substitution G A missense_variant L361F 1081C>T MELA-AU 15 42734568 42734568 single base substitution G A missense_variant L91F 271C>T MELA-AU 15 42735649 42735649 single base substitution G A downstream_gene_variant MELA-AU 15 42735649 42735649 single base substitution G A intron_variant MELA-AU 15 42735945 42735945 single base substitution G A downstream_gene_variant MELA-AU 15 42735945 42735945 single base substitution G A intron_variant MELA-AU 15 42736177 42736177 single base substitution G A downstream_gene_variant MELA-AU 15 42736177 42736177 single base substitution G A intron_variant MELA-AU 15 42736522 42736522 single base substitution C T downstream_gene_variant MELA-AU 15 42736522 42736522 single base substitution C T intron_variant MELA-AU 15 42738135 42738136 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 15 42738135 42738136 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 15 42738836 42738836 single base substitution G A downstream_gene_variant MELA-AU 15 42738836 42738836 single base substitution G A synonymous_variant L1029L 3087C>T MELA-AU 15 42738836 42738836 single base substitution G A synonymous_variant L214L 642C>T MELA-AU 15 42738836 42738836 single base substitution G A synonymous_variant L257L 771C>T MELA-AU 15 42738836 42738836 single base substitution G A synonymous_variant L812L 2436C>T MELA-AU 15 42738836 42738836 single base substitution G A synonymous_variant L82L 246C>T MELA-AU 15 42738836 42738836 single base substitution G A upstream_gene_variant MELA-AU 15 42738860 42738860 single base substitution G A downstream_gene_variant MELA-AU 15 42738860 42738860 single base substitution G A intron_variant MELA-AU 15 42738860 42738860 single base substitution G A splice_region_variant MELA-AU 15 42738860 42738860 single base substitution G A upstream_gene_variant MELA-AU 15 42739224 42739224 single base substitution G A downstream_gene_variant MELA-AU 15 42739224 42739224 single base substitution G A intron_variant MELA-AU 15 42739224 42739224 single base substitution G A upstream_gene_variant MELA-AU 15 42739356 42739356 single base substitution G A downstream_gene_variant MELA-AU 15 42739356 42739356 single base substitution G A intron_variant MELA-AU 15 42739356 42739356 single base substitution G A upstream_gene_variant MELA-AU 15 42740125 42740125 single base substitution G A downstream_gene_variant MELA-AU 15 42740125 42740125 single base substitution G A intron_variant MELA-AU 15 42740125 42740125 single base substitution G A upstream_gene_variant MELA-AU 15 42741089 42741089 single base substitution G A downstream_gene_variant MELA-AU 15 42741089 42741089 single base substitution G A intron_variant MELA-AU 15 42741089 42741089 single base substitution G A upstream_gene_variant MELA-AU 15 42741690 42741690 single base substitution G A downstream_gene_variant MELA-AU 15 42741690 42741690 single base substitution G A intron_variant MELA-AU 15 42741690 42741690 single base substitution G A upstream_gene_variant MELA-AU 15 42741917 42741917 single base substitution G A downstream_gene_variant MELA-AU 15 42741917 42741917 single base substitution G A intron_variant MELA-AU 15 42741917 42741917 single base substitution G A upstream_gene_variant MELA-AU 15 42742004 42742004 single base substitution G A downstream_gene_variant MELA-AU 15 42742004 42742004 single base substitution G A intron_variant MELA-AU 15 42742004 42742004 single base substitution G A synonymous_variant T582T 1746C>T MELA-AU 15 42742004 42742004 single base substitution G A synonymous_variant T799T 2397C>T MELA-AU 15 42742004 42742004 single base substitution G A upstream_gene_variant MELA-AU 15 42742383 42742383 single base substitution G A downstream_gene_variant MELA-AU 15 42742383 42742383 single base substitution G A intron_variant MELA-AU 15 42742383 42742383 single base substitution G A missense_variant S456F 1367C>T MELA-AU 15 42742383 42742383 single base substitution G A missense_variant S673F 2018C>T MELA-AU 15 42742383 42742383 single base substitution G A upstream_gene_variant MELA-AU 15 42742831 42742831 single base substitution G A downstream_gene_variant MELA-AU 15 42742831 42742831 single base substitution G A intron_variant MELA-AU 15 42742831 42742831 single base substitution G A stop_gained Q307* 919C>T MELA-AU 15 42742831 42742831 single base substitution G A stop_gained Q524* 1570C>T MELA-AU 15 42742831 42742831 single base substitution G A upstream_gene_variant MELA-AU 15 42743088 42743088 single base substitution G A downstream_gene_variant MELA-AU 15 42743088 42743088 single base substitution G A intron_variant MELA-AU 15 42743088 42743088 single base substitution G A missense_variant P221L 662C>T MELA-AU 15 42743088 42743088 single base substitution G A missense_variant P438L 1313C>T MELA-AU 15 42743088 42743088 single base substitution G A upstream_gene_variant MELA-AU 15 42743371 42743371 single base substitution C T downstream_gene_variant MELA-AU 15 42743371 42743371 single base substitution C T intron_variant MELA-AU 15 42743371 42743371 single base substitution C T missense_variant E127K 379G>A MELA-AU 15 42743371 42743371 single base substitution C T missense_variant E344K 1030G>A MELA-AU 15 42743371 42743371 single base substitution C T missense_variant E367K 1099G>A MELA-AU 15 42743371 42743371 single base substitution C T upstream_gene_variant MELA-AU 15 42743482 42743482 single base substitution G A downstream_gene_variant MELA-AU 15 42743482 42743482 single base substitution G A intron_variant MELA-AU 15 42743482 42743482 single base substitution G A missense_variant P307S 919C>T MELA-AU 15 42743482 42743482 single base substitution G A missense_variant P330S 988C>T MELA-AU 15 42743482 42743482 single base substitution G A missense_variant P90S 268C>T MELA-AU 15 42743482 42743482 single base substitution G A upstream_gene_variant MELA-AU 15 42743513 42743513 single base substitution A C downstream_gene_variant MELA-AU 15 42743513 42743513 single base substitution A C intron_variant MELA-AU 15 42743513 42743513 single base substitution A C synonymous_variant G296G 888T>G MELA-AU 15 42743513 42743513 single base substitution A C synonymous_variant G319G 957T>G MELA-AU 15 42743513 42743513 single base substitution A C synonymous_variant G79G 237T>G MELA-AU 15 42743513 42743513 single base substitution A C upstream_gene_variant MELA-AU 15 42743792 42743793 multiple base substitution (>=2bp and <=200bp) GG AA 5_prime_UTR_variant MELA-AU 15 42743792 42743793 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 15 42743792 42743793 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 15 42743792 42743793 multiple base substitution (>=2bp and <=200bp) GG AA missense_variant S203F 608CC>TT MELA-AU 15 42743792 42743793 multiple base substitution (>=2bp and <=200bp) GG AA missense_variant S226F 677CC>TT MELA-AU 15 42743792 42743793 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 15 42743816 42743816 single base substitution A C 5_prime_UTR_variant MELA-AU 15 42743816 42743816 single base substitution A C downstream_gene_variant MELA-AU 15 42743816 42743816 single base substitution A C intron_variant MELA-AU 15 42743816 42743816 single base substitution A C missense_variant N195K 585T>G MELA-AU 15 42743816 42743816 single base substitution A C missense_variant N218K 654T>G MELA-AU 15 42743816 42743816 single base substitution A C upstream_gene_variant MELA-AU 15 42743985 42743985 single base substitution A C 5_prime_UTR_premature_start_codon_gain_variant MELA-AU 15 42743985 42743985 single base substitution A C intron_variant MELA-AU 15 42743985 42743985 single base substitution A C missense_variant F139C 416T>G MELA-AU 15 42743985 42743985 single base substitution A C missense_variant F162C 485T>G MELA-AU 15 42743985 42743985 single base substitution A C upstream_gene_variant MELA-AU 15 42744414 42744414 single base substitution G A intron_variant MELA-AU 15 42744414 42744414 single base substitution G A upstream_gene_variant MELA-AU 15 42745558 42745558 single base substitution G A intron_variant MELA-AU 15 42746755 42746755 single base substitution G A intron_variant MELA-AU 15 42746756 42746756 single base substitution G A intron_variant MELA-AU 15 42747728 42747729 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 15 42748033 42748033 single base substitution G A intron_variant MELA-AU 15 42748210 42748210 single base substitution G A intron_variant MELA-AU 15 42748326 42748326 single base substitution A G intron_variant MELA-AU 15 42751136 42751136 single base substitution T A intron_variant MELA-AU 15 42751136 42751136 single base substitution T A upstream_gene_variant MELA-AU 15 42751842 42751842 single base substitution C T intron_variant MELA-AU 15 42751842 42751842 single base substitution C T upstream_gene_variant MELA-AU 15 42752686 42752686 single base substitution G A intron_variant MELA-AU 15 42752686 42752686 single base substitution G A upstream_gene_variant MELA-AU 15 42752878 42752878 single base substitution G A intron_variant MELA-AU 15 42752878 42752878 single base substitution G A upstream_gene_variant MELA-AU 15 42753730 42753731 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 15 42753730 42753731 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 15 42754361 42754361 single base substitution C T intron_variant MELA-AU 15 42754361 42754361 single base substitution C T upstream_gene_variant MELA-AU 15 42754850 42754850 single base substitution G A intron_variant MELA-AU 15 42756980 42756980 single base substitution A T intron_variant MELA-AU 15 42759303 42759303 single base substitution C T intron_variant MELA-AU 15 42759708 42759708 single base substitution G A intron_variant MELA-AU 15 42759872 42759872 single base substitution G A intron_variant MELA-AU 15 42760732 42760733 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 15 42760969 42760969 single base substitution G A intron_variant MELA-AU 15 42761150 42761150 single base substitution G A intron_variant MELA-AU 15 42761213 42761213 single base substitution C T intron_variant MELA-AU 15 42761435 42761435 single base substitution C A intron_variant MELA-AU 15 42761637 42761637 single base substitution A T intron_variant MELA-AU 15 42762207 42762208 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 15 42762723 42762723 single base substitution G A intron_variant MELA-AU 15 42763306 42763306 single base substitution C T intron_variant MELA-AU 15 42763700 42763700 single base substitution A C intron_variant MELA-AU 15 42763851 42763851 single base substitution C A intron_variant MELA-AU 15 42764982 42764982 single base substitution G A intron_variant MELA-AU 15 42765032 42765032 single base substitution A G intron_variant MELA-AU 15 42765344 42765344 single base substitution C T intron_variant MELA-AU 15 42765791 42765791 single base substitution G A intron_variant MELA-AU 15 42766500 42766500 single base substitution G A intron_variant MELA-AU 15 42768392 42768392 single base substitution G A intron_variant MELA-AU 15 42768473 42768473 single base substitution A C intron_variant MELA-AU 15 42770642 42770642 single base substitution G A intron_variant MELA-AU 15 42772117 42772117 single base substitution G A intron_variant MELA-AU 15 42772371 42772371 single base substitution T G intron_variant MELA-AU 15 42772905 42772906 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 15 42773786 42773786 single base substitution G A intron_variant MELA-AU 15 42774090 42774090 single base substitution G A intron_variant MELA-AU 15 42774568 42774568 single base substitution G A intron_variant MELA-AU 15 42775017 42775017 single base substitution G A intron_variant MELA-AU 15 42775565 42775565 single base substitution G A intron_variant MELA-AU 15 42776277 42776277 single base substitution A C intron_variant MELA-AU 15 42777129 42777129 single base substitution G A intron_variant MELA-AU 15 42777425 42777425 single base substitution C T intron_variant MELA-AU 15 42777443 42777443 single base substitution G A intron_variant MELA-AU 15 42777662 42777662 single base substitution G A intron_variant MELA-AU 15 42778159 42778159 single base substitution T C intron_variant MELA-AU 15 42781643 42781644 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 15 42781854 42781854 single base substitution G A intron_variant MELA-AU 15 42782846 42782846 single base substitution G A intron_variant MELA-AU 15 42782846 42782846 single base substitution G A upstream_gene_variant MELA-AU 15 42782859 42782859 single base substitution G A intron_variant MELA-AU 15 42782859 42782859 single base substitution G A upstream_gene_variant MELA-AU 15 42783572 42783572 single base substitution C T upstream_gene_variant MELA-AU 15 42784719 42784719 single base substitution C T upstream_gene_variant MELA-AU 15 42784971 42784971 single base substitution G A upstream_gene_variant MELA-AU 15 42785692 42785692 single base substitution G A upstream_gene_variant MELA-AU 15 42785935 42785935 single base substitution T C upstream_gene_variant MELA-AU 15 42786464 42786465 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 15 42786519 42786519 single base substitution G A upstream_gene_variant MELA-AU 15 42786743 42786743 single base substitution C T upstream_gene_variant MELA-AU 15 42787358 42787358 single base substitution C T upstream_gene_variant MELA-AU 15 42787773 42787773 single base substitution G A upstream_gene_variant MELA-AU 15 42787774 42787774 single base substitution G A upstream_gene_variant ORCA-IN 15 42703713 42703713 single base substitution T G downstream_gene_variant ORCA-IN 15 42735016 42735016 single base substitution C G downstream_gene_variant ORCA-IN 15 42735016 42735016 single base substitution C G intron_variant ORCA-IN 15 42742266 42742266 single base substitution G A downstream_gene_variant ORCA-IN 15 42742266 42742266 single base substitution G A intron_variant ORCA-IN 15 42742266 42742266 single base substitution G A missense_variant S495L 1484C>T ORCA-IN 15 42742266 42742266 single base substitution G A missense_variant S712L 2135C>T ORCA-IN 15 42742266 42742266 single base substitution G A upstream_gene_variant ORCA-IN 15 42743051 42743051 single base substitution C T downstream_gene_variant ORCA-IN 15 42743051 42743051 single base substitution C T intron_variant ORCA-IN 15 42743051 42743051 single base substitution C T synonymous_variant L233L 699G>A ORCA-IN 15 42743051 42743051 single base substitution C T synonymous_variant L450L 1350G>A ORCA-IN 15 42743051 42743051 single base substitution C T upstream_gene_variant ORCA-IN 15 42743988 42743988 single base substitution C T 5_prime_UTR_variant ORCA-IN 15 42743988 42743988 single base substitution C T intron_variant ORCA-IN 15 42743988 42743988 single base substitution C T missense_variant G138D 413G>A ORCA-IN 15 42743988 42743988 single base substitution C T missense_variant G161D 482G>A ORCA-IN 15 42743988 42743988 single base substitution C T upstream_gene_variant ORCA-IN 15 42757734 42757734 single base substitution C T intron_variant OV-AU 15 42715751 42715751 single base substitution A T intron_variant OV-AU 15 42720984 42720984 single base substitution C T intron_variant OV-AU 15 42720984 42720984 single base substitution C T upstream_gene_variant OV-AU 15 42723414 42723414 single base substitution T A intron_variant OV-AU 15 42723414 42723414 single base substitution T A upstream_gene_variant OV-AU 15 42732760 42732760 single base substitution C G downstream_gene_variant OV-AU 15 42732760 42732760 single base substitution C G intron_variant OV-AU 15 42738394 42738394 single base substitution A T downstream_gene_variant OV-AU 15 42738394 42738394 single base substitution A T intron_variant OV-AU 15 42742814 42742814 single base substitution A C downstream_gene_variant OV-AU 15 42742814 42742814 single base substitution A C intron_variant OV-AU 15 42742814 42742814 single base substitution A C missense_variant D312E 936T>G OV-AU 15 42742814 42742814 single base substitution A C missense_variant D529E 1587T>G OV-AU 15 42742814 42742814 single base substitution A C upstream_gene_variant OV-AU 15 42751810 42751810 single base substitution A C intron_variant OV-AU 15 42751810 42751810 single base substitution A C upstream_gene_variant OV-AU 15 42752551 42752551 single base substitution T G intron_variant OV-AU 15 42752551 42752551 single base substitution T G upstream_gene_variant OV-AU 15 42761737 42761737 single base substitution A T intron_variant OV-AU 15 42765380 42765380 single base substitution G A intron_variant OV-AU 15 42765723 42765723 single base substitution C T intron_variant OV-AU 15 42769239 42769239 single base substitution C T intron_variant OV-AU 15 42770064 42770064 single base substitution A C intron_variant OV-AU 15 42770852 42770852 single base substitution G A intron_variant OV-AU 15 42772981 42772981 single base substitution G C intron_variant OV-AU 15 42773558 42773558 single base substitution T G intron_variant OV-AU 15 42773683 42773683 single base substitution G T intron_variant OV-US 15 42742522 42742522 single base substitution C T downstream_gene_variant OV-US 15 42742522 42742522 single base substitution C T intron_variant OV-US 15 42742522 42742522 single base substitution C T missense_variant E410K 1228G>A OV-US 15 42742522 42742522 single base substitution C T missense_variant E627K 1879G>A OV-US 15 42742522 42742522 single base substitution C T upstream_gene_variant PACA-AU 15 42702670 42702670 single base substitution C G downstream_gene_variant PACA-AU 15 42717150 42717150 single base substitution C T exon_variant PACA-AU 15 42717150 42717150 single base substitution C T missense_variant G1668D 5003G>A PACA-AU 15 42717150 42717150 single base substitution C T missense_variant G54D 161G>A PACA-AU 15 42717150 42717150 single base substitution C T missense_variant G634D 1901G>A PACA-AU 15 42717150 42717150 single base substitution C T missense_variant G853D 2558G>A PACA-AU 15 42717150 42717150 single base substitution C T missense_variant G896D 2687G>A PACA-AU 15 42717150 42717150 single base substitution C T upstream_gene_variant PACA-AU 15 42724885 42724885 single base substitution A T intron_variant PACA-AU 15 42724885 42724885 single base substitution A T upstream_gene_variant PACA-AU 15 42725449 42725449 single base substitution G A intron_variant PACA-AU 15 42732544 42732544 single base substitution C T downstream_gene_variant PACA-AU 15 42732544 42732544 single base substitution C T intron_variant PACA-AU 15 42733674 42733674 single base substitution G A downstream_gene_variant PACA-AU 15 42733674 42733674 single base substitution G A intron_variant PACA-AU 15 42739698 42739698 single base substitution G A downstream_gene_variant PACA-AU 15 42739698 42739698 single base substitution G A intron_variant PACA-AU 15 42739698 42739698 single base substitution G A upstream_gene_variant PACA-AU 15 42743735 42743735 single base substitution G A downstream_gene_variant PACA-AU 15 42743735 42743735 single base substitution G A intron_variant PACA-AU 15 42743735 42743735 single base substitution G A synonymous_variant N222N 666C>T PACA-AU 15 42743735 42743735 single base substitution G A synonymous_variant N245N 735C>T PACA-AU 15 42743735 42743735 single base substitution G A synonymous_variant N5N 15C>T PACA-AU 15 42743735 42743735 single base substitution G A upstream_gene_variant PACA-AU 15 42759817 42759817 single base substitution C A intron_variant PACA-AU 15 42761070 42761070 single base substitution T C intron_variant PACA-AU 15 42763150 42763150 single base substitution C G intron_variant PACA-AU 15 42766653 42766653 single base substitution C A intron_variant PACA-AU 15 42769742 42769742 single base substitution G C intron_variant PACA-AU 15 42773037 42773037 single base substitution G A intron_variant PACA-AU 15 42785198 42785198 single base substitution T A upstream_gene_variant PACA-CA 15 42701641 42701641 single base substitution G T downstream_gene_variant PACA-CA 15 42704332 42704332 single base substitution A G downstream_gene_variant PACA-CA 15 42705188 42705188 insertion of <=200bp - A 3_prime_UTR_variant PACA-CA 15 42705188 42705188 insertion of <=200bp - A downstream_gene_variant PACA-CA 15 42710822 42710822 single base substitution C A downstream_gene_variant PACA-CA 15 42710822 42710822 single base substitution C A intron_variant PACA-CA 15 42712514 42712514 single base substitution G A downstream_gene_variant PACA-CA 15 42712514 42712514 single base substitution G A intron_variant PACA-CA 15 42716969 42716969 single base substitution C T exon_variant PACA-CA 15 42716969 42716969 single base substitution C T intron_variant PACA-CA 15 42716969 42716969 single base substitution C T upstream_gene_variant PACA-CA 15 42720214 42720214 single base substitution A T splice_donor_variant PACA-CA 15 42720214 42720214 single base substitution A T upstream_gene_variant PACA-CA 15 42723645 42723652 deletion of <=200bp CAGTGGTG - intron_variant PACA-CA 15 42723645 42723652 deletion of <=200bp CAGTGGTG - upstream_gene_variant PACA-CA 15 42726560 42726560 single base substitution G C intron_variant PACA-CA 15 42730073 42730073 single base substitution C G downstream_gene_variant PACA-CA 15 42730073 42730073 single base substitution C G intron_variant PACA-CA 15 42731305 42731305 single base substitution C T downstream_gene_variant PACA-CA 15 42731305 42731305 single base substitution C T synonymous_variant T1467T 4401G>A PACA-CA 15 42731305 42731305 single base substitution C T synonymous_variant T433T 1299G>A PACA-CA 15 42731305 42731305 single base substitution C T synonymous_variant T652T 1956G>A PACA-CA 15 42731305 42731305 single base substitution C T synonymous_variant T695T 2085G>A PACA-CA 15 42732667 42732667 single base substitution A C downstream_gene_variant PACA-CA 15 42732667 42732667 single base substitution A C intron_variant PACA-CA 15 42733649 42733649 single base substitution G A downstream_gene_variant PACA-CA 15 42733649 42733649 single base substitution G A intron_variant PACA-CA 15 42737010 42737010 single base substitution T C downstream_gene_variant PACA-CA 15 42737010 42737010 single base substitution T C intron_variant PACA-CA 15 42737954 42737954 single base substitution G C downstream_gene_variant PACA-CA 15 42737954 42737954 single base substitution G C intron_variant PACA-CA 15 42738890 42738890 single base substitution T C downstream_gene_variant PACA-CA 15 42738890 42738890 single base substitution T C intron_variant PACA-CA 15 42738890 42738890 single base substitution T C upstream_gene_variant PACA-CA 15 42745582 42745582 single base substitution A T intron_variant PACA-CA 15 42749610 42749610 single base substitution C T 5_prime_UTR_variant PACA-CA 15 42749610 42749610 single base substitution C T intron_variant PACA-CA 15 42750887 42750887 single base substitution T C intron_variant PACA-CA 15 42750887 42750887 single base substitution T C upstream_gene_variant PACA-CA 15 42751788 42751788 single base substitution G A intron_variant PACA-CA 15 42751788 42751788 single base substitution G A upstream_gene_variant PACA-CA 15 42762714 42762714 single base substitution A T intron_variant PACA-CA 15 42763601 42763601 single base substitution A C intron_variant PACA-CA 15 42763690 42763690 single base substitution G A intron_variant PACA-CA 15 42769213 42769213 single base substitution G C intron_variant PACA-CA 15 42770221 42770221 single base substitution A T intron_variant PACA-CA 15 42774198 42774198 single base substitution G A intron_variant PACA-CA 15 42774546 42774546 single base substitution A G intron_variant PACA-CA 15 42780485 42780485 single base substitution C A intron_variant PACA-CA 15 42781462 42781462 single base substitution G A intron_variant PACA-CA 15 42782257 42782257 single base substitution A T intron_variant PACA-CA 15 42784103 42784103 single base substitution G T upstream_gene_variant PACA-CA 15 42785550 42785550 single base substitution C A upstream_gene_variant PACA-CA 15 42786453 42786453 insertion of <=200bp - T upstream_gene_variant PACA-CA 15 42786735 42786735 single base substitution C T upstream_gene_variant PAEN-AU 15 42721678 42721678 single base substitution C T intron_variant PAEN-AU 15 42721678 42721678 single base substitution C T upstream_gene_variant PAEN-AU 15 42732874 42732874 single base substitution A C downstream_gene_variant PAEN-AU 15 42732874 42732874 single base substitution A C intron_variant PAEN-AU 15 42768844 42768845 deletion of <=200bp TA - intron_variant PAEN-IT 15 42750378 42750378 single base substitution C T intron_variant PAEN-IT 15 42750378 42750378 single base substitution C T upstream_gene_variant PBCA-DE 15 42702718 42702718 single base substitution G T downstream_gene_variant PBCA-DE 15 42702860 42702860 single base substitution C T downstream_gene_variant PBCA-DE 15 42713966 42713966 deletion of <=200bp G - downstream_gene_variant PBCA-DE 15 42713966 42713966 deletion of <=200bp G - intron_variant PBCA-DE 15 42732899 42732899 single base substitution G T downstream_gene_variant PBCA-DE 15 42732899 42732899 single base substitution G T intron_variant PBCA-DE 15 42736496 42736496 single base substitution C A downstream_gene_variant PBCA-DE 15 42736496 42736496 single base substitution C A intron_variant PBCA-DE 15 42739011 42739011 single base substitution C T downstream_gene_variant PBCA-DE 15 42739011 42739011 single base substitution C T intron_variant PBCA-DE 15 42739011 42739011 single base substitution C T upstream_gene_variant PBCA-DE 15 42762713 42762713 single base substitution T A intron_variant PBCA-DE 15 42768844 42768845 deletion of <=200bp TA - intron_variant PBCA-DE 15 42770098 42770098 insertion of <=200bp - A intron_variant PBCA-DE 15 42771674 42771674 single base substitution T C intron_variant PBCA-DE 15 42785548 42785548 single base substitution C A upstream_gene_variant PBCA-DE 15 42785550 42785550 single base substitution C A upstream_gene_variant PRAD-CA 15 42751661 42751661 single base substitution G A intron_variant PRAD-CA 15 42751661 42751661 single base substitution G A upstream_gene_variant PRAD-CA 15 42762496 42762496 single base substitution A C intron_variant PRAD-CA 15 42762713 42762713 single base substitution T A intron_variant PRAD-CA 15 42778221 42778221 single base substitution T C intron_variant PRAD-UK 15 42708104 42708104 single base substitution A G 3_prime_UTR_variant PRAD-UK 15 42708104 42708104 single base substitution A G downstream_gene_variant PRAD-UK 15 42708104 42708104 single base substitution A G intron_variant PRAD-UK 15 42711292 42711292 single base substitution C T downstream_gene_variant PRAD-UK 15 42711292 42711292 single base substitution C T intron_variant PRAD-UK 15 42715752 42715752 single base substitution T A intron_variant PRAD-UK 15 42725062 42725062 single base substitution G A intron_variant PRAD-UK 15 42725062 42725062 single base substitution G A upstream_gene_variant PRAD-UK 15 42730761 42730761 single base substitution A C downstream_gene_variant PRAD-UK 15 42730761 42730761 single base substitution A C intron_variant PRAD-UK 15 42731029 42731029 single base substitution G A downstream_gene_variant PRAD-UK 15 42731029 42731029 single base substitution G A intron_variant PRAD-UK 15 42742466 42742466 single base substitution G A downstream_gene_variant PRAD-UK 15 42742466 42742466 single base substitution G A intron_variant PRAD-UK 15 42742466 42742466 single base substitution G A synonymous_variant P428P 1284C>T PRAD-UK 15 42742466 42742466 single base substitution G A synonymous_variant P645P 1935C>T PRAD-UK 15 42742466 42742466 single base substitution G A upstream_gene_variant PRAD-UK 15 42762714 42762714 single base substitution A T intron_variant PRAD-UK 15 42769589 42769589 single base substitution A C intron_variant PRAD-UK 15 42781273 42781273 single base substitution C G intron_variant PRAD-US 15 42731450 42731450 single base substitution C T downstream_gene_variant PRAD-US 15 42731450 42731450 single base substitution C T missense_variant S1419N 4256G>A PRAD-US 15 42731450 42731450 single base substitution C T missense_variant S385N 1154G>A PRAD-US 15 42731450 42731450 single base substitution C T missense_variant S604N 1811G>A PRAD-US 15 42731450 42731450 single base substitution C T missense_variant S647N 1940G>A PRAD-US 15 42742890 42742890 single base substitution G A downstream_gene_variant PRAD-US 15 42742890 42742890 single base substitution G A intron_variant PRAD-US 15 42742890 42742890 single base substitution G A missense_variant S287F 860C>T PRAD-US 15 42742890 42742890 single base substitution G A missense_variant S504F 1511C>T PRAD-US 15 42742890 42742890 single base substitution G A upstream_gene_variant READ-US 15 42701572 42701574 deletion of <=200bp AGG - downstream_gene_variant READ-US 15 42714716 42714716 single base substitution G A downstream_gene_variant READ-US 15 42714716 42714716 single base substitution G A exon_variant READ-US 15 42714716 42714716 single base substitution G A missense_variant R149C 445C>T READ-US 15 42714716 42714716 single base substitution G A missense_variant R1763C 5287C>T READ-US 15 42714716 42714716 single base substitution G A missense_variant R729C 2185C>T READ-US 15 42714716 42714716 single base substitution G A missense_variant R948C 2842C>T READ-US 15 42714716 42714716 single base substitution G A missense_variant R991C 2971C>T READ-US 15 42717043 42717043 single base substitution G T exon_variant READ-US 15 42717043 42717043 single base substitution G T missense_variant L1704I 5110C>A READ-US 15 42717043 42717043 single base substitution G T missense_variant L670I 2008C>A READ-US 15 42717043 42717043 single base substitution G T missense_variant L889I 2665C>A READ-US 15 42717043 42717043 single base substitution G T missense_variant L90I 268C>A READ-US 15 42717043 42717043 single base substitution G T missense_variant L932I 2794C>A READ-US 15 42717043 42717043 single base substitution G T upstream_gene_variant READ-US 15 42742585 42742585 single base substitution T C downstream_gene_variant READ-US 15 42742585 42742585 single base substitution T C intron_variant READ-US 15 42742585 42742585 single base substitution T C missense_variant T389A 1165A>G READ-US 15 42742585 42742585 single base substitution T C missense_variant T606A 1816A>G READ-US 15 42742585 42742585 single base substitution T C upstream_gene_variant READ-US 15 42742849 42742849 single base substitution T C downstream_gene_variant READ-US 15 42742849 42742849 single base substitution T C intron_variant READ-US 15 42742849 42742849 single base substitution T C missense_variant K301E 901A>G READ-US 15 42742849 42742849 single base substitution T C missense_variant K518E 1552A>G READ-US 15 42742849 42742849 single base substitution T C upstream_gene_variant READ-US 15 42744102 42744102 single base substitution C T 5_prime_UTR_variant READ-US 15 42744102 42744102 single base substitution C T intron_variant READ-US 15 42744102 42744102 single base substitution C T missense_variant R100Q 299G>A READ-US 15 42744102 42744102 single base substitution C T missense_variant R123Q 368G>A READ-US 15 42744102 42744102 single base substitution C T upstream_gene_variant RECA-EU 15 42728416 42728416 single base substitution G T intron_variant RECA-EU 15 42783076 42783076 single base substitution A C intron_variant RECA-EU 15 42783076 42783076 single base substitution A C upstream_gene_variant SKCA-BR 15 42701008 42701027 deletion of <=200bp AGGGCCCCTCTTCTATCCGG - downstream_gene_variant SKCA-BR 15 42705243 42705243 single base substitution A G 3_prime_UTR_variant SKCA-BR 15 42705243 42705243 single base substitution A G downstream_gene_variant SKCA-BR 15 42705587 42705587 single base substitution T G 3_prime_UTR_variant SKCA-BR 15 42705587 42705587 single base substitution T G downstream_gene_variant SKCA-BR 15 42707320 42707320 insertion of <=200bp - CTT 3_prime_UTR_variant SKCA-BR 15 42707320 42707320 insertion of <=200bp - CTT downstream_gene_variant SKCA-BR 15 42709060 42709060 single base substitution C T 3_prime_UTR_variant SKCA-BR 15 42709060 42709060 single base substitution C T downstream_gene_variant SKCA-BR 15 42709060 42709060 single base substitution C T intron_variant SKCA-BR 15 42709570 42709570 single base substitution G A downstream_gene_variant SKCA-BR 15 42709570 42709570 single base substitution G A intron_variant SKCA-BR 15 42712582 42712582 single base substitution G A downstream_gene_variant SKCA-BR 15 42712582 42712582 single base substitution G A intron_variant SKCA-BR 15 42716300 42716300 single base substitution C T exon_variant SKCA-BR 15 42716300 42716300 single base substitution C T intron_variant SKCA-BR 15 42717706 42717706 insertion of <=200bp - CT exon_variant SKCA-BR 15 42717706 42717706 insertion of <=200bp - CT intron_variant SKCA-BR 15 42717706 42717706 insertion of <=200bp - CT upstream_gene_variant SKCA-BR 15 42720675 42720675 single base substitution G A intron_variant SKCA-BR 15 42720675 42720675 single base substitution G A upstream_gene_variant SKCA-BR 15 42721974 42721974 single base substitution G A intron_variant SKCA-BR 15 42721974 42721974 single base substitution G A upstream_gene_variant SKCA-BR 15 42723566 42723566 single base substitution C T intron_variant SKCA-BR 15 42723566 42723566 single base substitution C T upstream_gene_variant SKCA-BR 15 42724055 42724055 single base substitution A C intron_variant SKCA-BR 15 42724055 42724055 single base substitution A C upstream_gene_variant SKCA-BR 15 42725684 42725684 single base substitution C T intron_variant SKCA-BR 15 42728156 42728156 insertion of <=200bp - CT intron_variant SKCA-BR 15 42733195 42733220 deletion of <=200bp AAATATATATATATATATATATATAT - downstream_gene_variant SKCA-BR 15 42733195 42733220 deletion of <=200bp AAATATATATATATATATATATATAT - intron_variant SKCA-BR 15 42733371 42733371 insertion of <=200bp - TA downstream_gene_variant SKCA-BR 15 42733371 42733371 insertion of <=200bp - TA intron_variant SKCA-BR 15 42740573 42740573 single base substitution G A downstream_gene_variant SKCA-BR 15 42740573 42740573 single base substitution G A synonymous_variant L106L 318C>T SKCA-BR 15 42740573 42740573 single base substitution G A synonymous_variant L149L 447C>T SKCA-BR 15 42740573 42740573 single base substitution G A synonymous_variant L704L 2112C>T SKCA-BR 15 42740573 42740573 single base substitution G A synonymous_variant L921L 2763C>T SKCA-BR 15 42740573 42740573 single base substitution G A upstream_gene_variant SKCA-BR 15 42741310 42741310 single base substitution G A downstream_gene_variant SKCA-BR 15 42741310 42741310 single base substitution G A intron_variant SKCA-BR 15 42741310 42741310 single base substitution G A upstream_gene_variant SKCA-BR 15 42742954 42742954 single base substitution G A downstream_gene_variant SKCA-BR 15 42742954 42742954 single base substitution G A intron_variant SKCA-BR 15 42742954 42742954 single base substitution G A missense_variant P266S 796C>T SKCA-BR 15 42742954 42742954 single base substitution G A missense_variant P483S 1447C>T SKCA-BR 15 42742954 42742954 single base substitution G A upstream_gene_variant SKCA-BR 15 42743047 42743047 single base substitution A G downstream_gene_variant SKCA-BR 15 42743047 42743047 single base substitution A G intron_variant SKCA-BR 15 42743047 42743047 single base substitution A G missense_variant S235P 703T>C SKCA-BR 15 42743047 42743047 single base substitution A G missense_variant S452P 1354T>C SKCA-BR 15 42743047 42743047 single base substitution A G upstream_gene_variant SKCA-BR 15 42756678 42756678 single base substitution T A intron_variant SKCA-BR 15 42767802 42767802 single base substitution C T intron_variant SKCA-BR 15 42770734 42770736 deletion of <=200bp GAC - intron_variant SKCA-BR 15 42776276 42776276 single base substitution G A intron_variant SKCA-BR 15 42776540 42776540 single base substitution T A intron_variant SKCA-BR 15 42777957 42777957 single base substitution T C intron_variant SKCA-BR 15 42779388 42779388 single base substitution G A intron_variant SKCA-BR 15 42779735 42779735 single base substitution A C intron_variant SKCM-US 15 42702021 42702021 single base substitution C T downstream_gene_variant SKCM-US 15 42702858 42702858 single base substitution G A downstream_gene_variant SKCM-US 15 42703483 42703483 single base substitution A G downstream_gene_variant SKCM-US 15 42717175 42717175 single base substitution T C exon_variant SKCM-US 15 42717175 42717175 single base substitution T C missense_variant S1660G 4978A>G SKCM-US 15 42717175 42717175 single base substitution T C missense_variant S46G 136A>G SKCM-US 15 42717175 42717175 single base substitution T C missense_variant S626G 1876A>G SKCM-US 15 42717175 42717175 single base substitution T C missense_variant S845G 2533A>G SKCM-US 15 42717175 42717175 single base substitution T C missense_variant S888G 2662A>G SKCM-US 15 42717175 42717175 single base substitution T C upstream_gene_variant SKCM-US 15 42717188 42717188 single base substitution G A exon_variant SKCM-US 15 42717188 42717188 single base substitution G A synonymous_variant G1655G 4965C>T SKCM-US 15 42717188 42717188 single base substitution G A synonymous_variant G41G 123C>T SKCM-US 15 42717188 42717188 single base substitution G A synonymous_variant G621G 1863C>T SKCM-US 15 42717188 42717188 single base substitution G A synonymous_variant G840G 2520C>T SKCM-US 15 42717188 42717188 single base substitution G A synonymous_variant G883G 2649C>T SKCM-US 15 42717188 42717188 single base substitution G A upstream_gene_variant SKCM-US 15 42734577 42734577 single base substitution G A downstream_gene_variant SKCM-US 15 42734577 42734577 single base substitution G A missense_variant P1130S 3388C>T SKCM-US 15 42734577 42734577 single base substitution G A missense_variant P183S 547C>T SKCM-US 15 42734577 42734577 single base substitution G A missense_variant P315S 943C>T SKCM-US 15 42734577 42734577 single base substitution G A missense_variant P358S 1072C>T SKCM-US 15 42734577 42734577 single base substitution G A missense_variant P88S 262C>T SKCM-US 15 42742291 42742291 single base substitution G A downstream_gene_variant SKCM-US 15 42742291 42742291 single base substitution G A intron_variant SKCM-US 15 42742291 42742291 single base substitution G A stop_gained Q487* 1459C>T SKCM-US 15 42742291 42742291 single base substitution G A stop_gained Q704* 2110C>T SKCM-US 15 42742291 42742291 single base substitution G A upstream_gene_variant SKCM-US 15 42742899 42742899 single base substitution G A downstream_gene_variant SKCM-US 15 42742899 42742899 single base substitution G A intron_variant SKCM-US 15 42742899 42742899 single base substitution G A missense_variant P284L 851C>T SKCM-US 15 42742899 42742899 single base substitution G A missense_variant P501L 1502C>T SKCM-US 15 42742899 42742899 single base substitution G A upstream_gene_variant SKCM-US 15 42742955 42742955 single base substitution G A downstream_gene_variant SKCM-US 15 42742955 42742955 single base substitution G A intron_variant SKCM-US 15 42742955 42742955 single base substitution G A synonymous_variant S265S 795C>T SKCM-US 15 42742955 42742955 single base substitution G A synonymous_variant S482S 1446C>T SKCM-US 15 42742955 42742955 single base substitution G A upstream_gene_variant SKCM-US 15 42742972 42742972 single base substitution T C downstream_gene_variant SKCM-US 15 42742972 42742972 single base substitution T C intron_variant SKCM-US 15 42742972 42742972 single base substitution T C missense_variant K260E 778A>G SKCM-US 15 42742972 42742972 single base substitution T C missense_variant K477E 1429A>G SKCM-US 15 42742972 42742972 single base substitution T C upstream_gene_variant SKCM-US 15 42743008 42743008 single base substitution G A downstream_gene_variant SKCM-US 15 42743008 42743008 single base substitution G A intron_variant SKCM-US 15 42743008 42743008 single base substitution G A stop_gained Q248* 742C>T SKCM-US 15 42743008 42743008 single base substitution G A stop_gained Q465* 1393C>T SKCM-US 15 42743008 42743008 single base substitution G A upstream_gene_variant SKCM-US 15 42743035 42743035 single base substitution G A downstream_gene_variant SKCM-US 15 42743035 42743035 single base substitution G A intron_variant SKCM-US 15 42743035 42743035 single base substitution G A missense_variant P239S 715C>T SKCM-US 15 42743035 42743035 single base substitution G A missense_variant P456S 1366C>T SKCM-US 15 42743035 42743035 single base substitution G A upstream_gene_variant SKCM-US 15 42743105 42743105 single base substitution G A downstream_gene_variant SKCM-US 15 42743105 42743105 single base substitution G A intron_variant SKCM-US 15 42743105 42743105 single base substitution G A synonymous_variant C215C 645C>T SKCM-US 15 42743105 42743105 single base substitution G A synonymous_variant C432C 1296C>T SKCM-US 15 42743105 42743105 single base substitution G A upstream_gene_variant SKCM-US 15 42743200 42743200 single base substitution G A downstream_gene_variant SKCM-US 15 42743200 42743200 single base substitution G A intron_variant SKCM-US 15 42743200 42743200 single base substitution G A missense_variant P184S 550C>T SKCM-US 15 42743200 42743200 single base substitution G A missense_variant P401S 1201C>T SKCM-US 15 42743200 42743200 single base substitution G A missense_variant P424S 1270C>T SKCM-US 15 42743200 42743200 single base substitution G A upstream_gene_variant SKCM-US 15 42743290 42743290 single base substitution T A downstream_gene_variant SKCM-US 15 42743290 42743290 single base substitution T A intron_variant SKCM-US 15 42743290 42743290 single base substitution T A stop_gained K154* 460A>T SKCM-US 15 42743290 42743290 single base substitution T A stop_gained K371* 1111A>T SKCM-US 15 42743290 42743290 single base substitution T A stop_gained K394* 1180A>T SKCM-US 15 42743290 42743290 single base substitution T A upstream_gene_variant SKCM-US 15 42743379 42743379 single base substitution G A downstream_gene_variant SKCM-US 15 42743379 42743379 single base substitution G A intron_variant SKCM-US 15 42743379 42743379 single base substitution G A missense_variant A124V 371C>T SKCM-US 15 42743379 42743379 single base substitution G A missense_variant A341V 1022C>T SKCM-US 15 42743379 42743379 single base substitution G A missense_variant A364V 1091C>T SKCM-US 15 42743379 42743379 single base substitution G A upstream_gene_variant SKCM-US 15 42743513 42743513 single base substitution A C downstream_gene_variant SKCM-US 15 42743513 42743513 single base substitution A C intron_variant SKCM-US 15 42743513 42743513 single base substitution A C synonymous_variant G296G 888T>G SKCM-US 15 42743513 42743513 single base substitution A C synonymous_variant G319G 957T>G SKCM-US 15 42743513 42743513 single base substitution A C synonymous_variant G79G 237T>G SKCM-US 15 42743513 42743513 single base substitution A C upstream_gene_variant SKCM-US 15 42743543 42743543 single base substitution G C downstream_gene_variant SKCM-US 15 42743543 42743543 single base substitution G C intron_variant SKCM-US 15 42743543 42743543 single base substitution G C missense_variant D286E 858C>G SKCM-US 15 42743543 42743543 single base substitution G C missense_variant D309E 927C>G SKCM-US 15 42743543 42743543 single base substitution G C missense_variant D69E 207C>G SKCM-US 15 42743543 42743543 single base substitution G C upstream_gene_variant SKCM-US 15 42743614 42743614 single base substitution A G downstream_gene_variant SKCM-US 15 42743614 42743614 single base substitution A G intron_variant SKCM-US 15 42743614 42743614 single base substitution A G missense_variant W263R 787T>C SKCM-US 15 42743614 42743614 single base substitution A G missense_variant W286R 856T>C SKCM-US 15 42743614 42743614 single base substitution A G missense_variant W46R 136T>C SKCM-US 15 42743614 42743614 single base substitution A G upstream_gene_variant SKCM-US 15 42743985 42743985 single base substitution A C 5_prime_UTR_premature_start_codon_gain_variant SKCM-US 15 42743985 42743985 single base substitution A C intron_variant SKCM-US 15 42743985 42743985 single base substitution A C missense_variant F139C 416T>G SKCM-US 15 42743985 42743985 single base substitution A C missense_variant F162C 485T>G SKCM-US 15 42743985 42743985 single base substitution A C upstream_gene_variant SKCM-US 15 42743992 42743992 single base substitution C T 5_prime_UTR_variant SKCM-US 15 42743992 42743992 single base substitution C T intron_variant SKCM-US 15 42743992 42743992 single base substitution C T missense_variant D137N 409G>A SKCM-US 15 42743992 42743992 single base substitution C T missense_variant D160N 478G>A SKCM-US 15 42743992 42743992 single base substitution C T upstream_gene_variant STAD-US 15 42702149 42702149 single base substitution G A downstream_gene_variant STAD-US 15 42703095 42703095 single base substitution C T downstream_gene_variant STAD-US 15 42703188 42703188 single base substitution G T downstream_gene_variant STAD-US 15 42710116 42710116 single base substitution C A downstream_gene_variant STAD-US 15 42710116 42710116 single base substitution C A exon_variant STAD-US 15 42710116 42710116 single base substitution C A intron_variant STAD-US 15 42710116 42710116 single base substitution C A missense_variant D1013Y 3037G>T STAD-US 15 42710116 42710116 single base substitution C A missense_variant D1056Y 3166G>T STAD-US 15 42710116 42710116 single base substitution C A missense_variant D1828Y 5482G>T STAD-US 15 42710116 42710116 single base substitution C A missense_variant D794Y 2380G>T STAD-US 15 42717097 42717097 single base substitution C T exon_variant STAD-US 15 42717097 42717097 single base substitution C T missense_variant D1686N 5056G>A STAD-US 15 42717097 42717097 single base substitution C T missense_variant D652N 1954G>A STAD-US 15 42717097 42717097 single base substitution C T missense_variant D72N 214G>A STAD-US 15 42717097 42717097 single base substitution C T missense_variant D871N 2611G>A STAD-US 15 42717097 42717097 single base substitution C T missense_variant D914N 2740G>A STAD-US 15 42717097 42717097 single base substitution C T upstream_gene_variant STAD-US 15 42717190 42717190 single base substitution C A exon_variant STAD-US 15 42717190 42717190 single base substitution C A missense_variant G1655C 4963G>T STAD-US 15 42717190 42717190 single base substitution C A missense_variant G41C 121G>T STAD-US 15 42717190 42717190 single base substitution C A missense_variant G621C 1861G>T STAD-US 15 42717190 42717190 single base substitution C A missense_variant G840C 2518G>T STAD-US 15 42717190 42717190 single base substitution C A missense_variant G883C 2647G>T STAD-US 15 42717190 42717190 single base substitution C A upstream_gene_variant STAD-US 15 42731306 42731306 single base substitution G A downstream_gene_variant STAD-US 15 42731306 42731306 single base substitution G A missense_variant T1467M 4400C>T STAD-US 15 42731306 42731306 single base substitution G A missense_variant T433M 1298C>T STAD-US 15 42731306 42731306 single base substitution G A missense_variant T652M 1955C>T STAD-US 15 42731306 42731306 single base substitution G A missense_variant T695M 2084C>T STAD-US 15 42731697 42731697 single base substitution C T downstream_gene_variant STAD-US 15 42731697 42731697 single base substitution C T missense_variant A1337T 4009G>A STAD-US 15 42731697 42731697 single base substitution C T missense_variant A303T 907G>A STAD-US 15 42731697 42731697 single base substitution C T missense_variant A522T 1564G>A STAD-US 15 42731697 42731697 single base substitution C T missense_variant A565T 1693G>A STAD-US 15 42731731 42731731 single base substitution T C downstream_gene_variant STAD-US 15 42731731 42731731 single base substitution T C synonymous_variant E1325E 3975A>G STAD-US 15 42731731 42731731 single base substitution T C synonymous_variant E291E 873A>G STAD-US 15 42731731 42731731 single base substitution T C synonymous_variant E510E 1530A>G STAD-US 15 42731731 42731731 single base substitution T C synonymous_variant E553E 1659A>G STAD-US 15 42734448 42734448 single base substitution C T downstream_gene_variant STAD-US 15 42734448 42734448 single base substitution C T missense_variant G1173R 3517G>A STAD-US 15 42734448 42734448 single base substitution C T missense_variant G131R 391G>A STAD-US 15 42734448 42734448 single base substitution C T missense_variant G226R 676G>A STAD-US 15 42734448 42734448 single base substitution C T missense_variant G358R 1072G>A STAD-US 15 42734448 42734448 single base substitution C T missense_variant G401R 1201G>A STAD-US 15 42734523 42734523 single base substitution C T downstream_gene_variant STAD-US 15 42734523 42734523 single base substitution C T missense_variant A106T 316G>A STAD-US 15 42734523 42734523 single base substitution C T missense_variant A1148T 3442G>A STAD-US 15 42734523 42734523 single base substitution C T missense_variant A201T 601G>A STAD-US 15 42734523 42734523 single base substitution C T missense_variant A333T 997G>A STAD-US 15 42734523 42734523 single base substitution C T missense_variant A376T 1126G>A STAD-US 15 42734562 42734562 single base substitution G A downstream_gene_variant STAD-US 15 42734562 42734562 single base substitution G A stop_gained R1135* 3403C>T STAD-US 15 42734562 42734562 single base substitution G A stop_gained R188* 562C>T STAD-US 15 42734562 42734562 single base substitution G A stop_gained R320* 958C>T STAD-US 15 42734562 42734562 single base substitution G A stop_gained R363* 1087C>T STAD-US 15 42734562 42734562 single base substitution G A stop_gained R93* 277C>T STAD-US 15 42742066 42742066 single base substitution G A downstream_gene_variant STAD-US 15 42742066 42742066 single base substitution G A intron_variant STAD-US 15 42742066 42742066 single base substitution G A missense_variant R562W 1684C>T STAD-US 15 42742066 42742066 single base substitution G A missense_variant R779W 2335C>T STAD-US 15 42742066 42742066 single base substitution G A upstream_gene_variant STAD-US 15 42742247 42742247 single base substitution T G downstream_gene_variant STAD-US 15 42742247 42742247 single base substitution T G intron_variant STAD-US 15 42742247 42742247 single base substitution T G missense_variant E501D 1503A>C STAD-US 15 42742247 42742247 single base substitution T G missense_variant E718D 2154A>C STAD-US 15 42742247 42742247 single base substitution T G upstream_gene_variant STAD-US 15 42742591 42742591 insertion of <=200bp - T downstream_gene_variant STAD-US 15 42742591 42742591 insertion of <=200bp - T frameshift_variant I387N? STAD-US 15 42742591 42742591 insertion of <=200bp - T frameshift_variant I604N? STAD-US 15 42742591 42742591 insertion of <=200bp - T intron_variant STAD-US 15 42742591 42742591 insertion of <=200bp - T upstream_gene_variant STAD-US 15 42742969 42742969 insertion of <=200bp - T downstream_gene_variant STAD-US 15 42742969 42742969 insertion of <=200bp - T frameshift_variant T261N? STAD-US 15 42742969 42742969 insertion of <=200bp - T frameshift_variant T478N? STAD-US 15 42742969 42742969 insertion of <=200bp - T intron_variant STAD-US 15 42742969 42742969 insertion of <=200bp - T upstream_gene_variant STAD-US 15 42743249 42743249 single base substitution C A downstream_gene_variant STAD-US 15 42743249 42743249 single base substitution C A intron_variant STAD-US 15 42743249 42743249 single base substitution C A missense_variant L167F 501G>T STAD-US 15 42743249 42743249 single base substitution C A missense_variant L384F 1152G>T STAD-US 15 42743249 42743249 single base substitution C A missense_variant L407F 1221G>T STAD-US 15 42743249 42743249 single base substitution C A upstream_gene_variant STAD-US 15 42743354 42743354 single base substitution C T downstream_gene_variant STAD-US 15 42743354 42743354 single base substitution C T intron_variant STAD-US 15 42743354 42743354 single base substitution C T stop_gained W132* 396G>A STAD-US 15 42743354 42743354 single base substitution C T stop_gained W349* 1047G>A STAD-US 15 42743354 42743354 single base substitution C T stop_gained W372* 1116G>A STAD-US 15 42743354 42743354 single base substitution C T upstream_gene_variant STAD-US 15 42743379 42743379 single base substitution G A downstream_gene_variant STAD-US 15 42743379 42743379 single base substitution G A intron_variant STAD-US 15 42743379 42743379 single base substitution G A missense_variant A124V 371C>T STAD-US 15 42743379 42743379 single base substitution G A missense_variant A341V 1022C>T STAD-US 15 42743379 42743379 single base substitution G A missense_variant A364V 1091C>T STAD-US 15 42743379 42743379 single base substitution G A upstream_gene_variant STAD-US 15 42743481 42743481 single base substitution G T downstream_gene_variant STAD-US 15 42743481 42743481 single base substitution G T intron_variant STAD-US 15 42743481 42743481 single base substitution G T missense_variant P307H 920C>A STAD-US 15 42743481 42743481 single base substitution G T missense_variant P330H 989C>A STAD-US 15 42743481 42743481 single base substitution G T missense_variant P90H 269C>A STAD-US 15 42743481 42743481 single base substitution G T upstream_gene_variant STAD-US 15 42743616 42743616 single base substitution A G downstream_gene_variant STAD-US 15 42743616 42743616 single base substitution A G intron_variant STAD-US 15 42743616 42743616 single base substitution A G missense_variant L262P 785T>C STAD-US 15 42743616 42743616 single base substitution A G missense_variant L285P 854T>C STAD-US 15 42743616 42743616 single base substitution A G missense_variant L45P 134T>C STAD-US 15 42743616 42743616 single base substitution A G upstream_gene_variant STAD-US 15 42743622 42743622 single base substitution G A downstream_gene_variant STAD-US 15 42743622 42743622 single base substitution G A intron_variant STAD-US 15 42743622 42743622 single base substitution G A missense_variant T260I 779C>T STAD-US 15 42743622 42743622 single base substitution G A missense_variant T283I 848C>T STAD-US 15 42743622 42743622 single base substitution G A missense_variant T43I 128C>T STAD-US 15 42743622 42743622 single base substitution G A upstream_gene_variant STAD-US 15 42743712 42743712 single base substitution C T downstream_gene_variant STAD-US 15 42743712 42743712 single base substitution C T intron_variant STAD-US 15 42743712 42743712 single base substitution C T missense_variant R13H 38G>A STAD-US 15 42743712 42743712 single base substitution C T missense_variant R230H 689G>A STAD-US 15 42743712 42743712 single base substitution C T missense_variant R253H 758G>A STAD-US 15 42743712 42743712 single base substitution C T upstream_gene_variant STAD-US 15 42743714 42743714 single base substitution T C downstream_gene_variant STAD-US 15 42743714 42743714 single base substitution T C intron_variant STAD-US 15 42743714 42743714 single base substitution T C synonymous_variant V12V 36A>G STAD-US 15 42743714 42743714 single base substitution T C synonymous_variant V229V 687A>G STAD-US 15 42743714 42743714 single base substitution T C synonymous_variant V252V 756A>G STAD-US 15 42743714 42743714 single base substitution T C upstream_gene_variant STAD-US 15 42743852 42743852 single base substitution A G 5_prime_UTR_variant STAD-US 15 42743852 42743852 single base substitution A G downstream_gene_variant STAD-US 15 42743852 42743852 single base substitution A G intron_variant STAD-US 15 42743852 42743852 single base substitution A G synonymous_variant G183G 549T>C STAD-US 15 42743852 42743852 single base substitution A G synonymous_variant G206G 618T>C STAD-US 15 42743852 42743852 single base substitution A G upstream_gene_variant THCA-SA 15 42744094 42744094 single base substitution A G 5_prime_UTR_variant THCA-SA 15 42744094 42744094 single base substitution A G intron_variant THCA-SA 15 42744094 42744094 single base substitution A G missense_variant W103R 307T>C THCA-SA 15 42744094 42744094 single base substitution A G missense_variant W126R 376T>C THCA-SA 15 42744094 42744094 single base substitution A G upstream_gene_variant THCA-SA 15 42749476 42749476 single base substitution C T 5_prime_UTR_variant THCA-SA 15 42749476 42749476 single base substitution C T intron_variant UCEC-US 15 42702174 42702174 single base substitution G T downstream_gene_variant UCEC-US 15 42703158 42703158 single base substitution C T downstream_gene_variant UCEC-US 15 42714150 42714150 single base substitution C A downstream_gene_variant UCEC-US 15 42714150 42714150 single base substitution C A exon_variant UCEC-US 15 42714150 42714150 single base substitution C A missense_variant D1009Y 3025G>T UCEC-US 15 42714150 42714150 single base substitution C A missense_variant D167Y 499G>T UCEC-US 15 42714150 42714150 single base substitution C A missense_variant D1781Y 5341G>T UCEC-US 15 42714150 42714150 single base substitution C A missense_variant D747Y 2239G>T UCEC-US 15 42714150 42714150 single base substitution C A missense_variant D966Y 2896G>T UCEC-US 15 42714724 42714724 single base substitution T G downstream_gene_variant UCEC-US 15 42714724 42714724 single base substitution T G exon_variant UCEC-US 15 42714724 42714724 single base substitution T G missense_variant K146T 437A>C UCEC-US 15 42714724 42714724 single base substitution T G missense_variant K1760T 5279A>C UCEC-US 15 42714724 42714724 single base substitution T G missense_variant K726T 2177A>C UCEC-US 15 42714724 42714724 single base substitution T G missense_variant K945T 2834A>C UCEC-US 15 42714724 42714724 single base substitution T G missense_variant K988T 2963A>C UCEC-US 15 42720288 42720288 single base substitution G A synonymous_variant L1619L 4857C>T UCEC-US 15 42720288 42720288 single base substitution G A synonymous_variant L585L 1755C>T UCEC-US 15 42720288 42720288 single base substitution G A synonymous_variant L5L 15C>T UCEC-US 15 42720288 42720288 single base substitution G A synonymous_variant L804L 2412C>T UCEC-US 15 42720288 42720288 single base substitution G A synonymous_variant L847L 2541C>T UCEC-US 15 42720288 42720288 single base substitution G A upstream_gene_variant UCEC-US 15 42729447 42729447 single base substitution G A downstream_gene_variant UCEC-US 15 42729447 42729447 single base substitution G A missense_variant R1554W 4660C>T UCEC-US 15 42729447 42729447 single base substitution G A missense_variant R520W 1558C>T UCEC-US 15 42729447 42729447 single base substitution G A missense_variant R739W 2215C>T UCEC-US 15 42729447 42729447 single base substitution G A missense_variant R782W 2344C>T UCEC-US 15 42729505 42729505 single base substitution T C downstream_gene_variant UCEC-US 15 42729505 42729505 single base substitution T C synonymous_variant V1534V 4602A>G UCEC-US 15 42729505 42729505 single base substitution T C synonymous_variant V500V 1500A>G UCEC-US 15 42729505 42729505 single base substitution T C synonymous_variant V719V 2157A>G UCEC-US 15 42729505 42729505 single base substitution T C synonymous_variant V762V 2286A>G UCEC-US 15 42729518 42729518 single base substitution T C downstream_gene_variant UCEC-US 15 42729518 42729518 single base substitution T C missense_variant H1530R 4589A>G UCEC-US 15 42729518 42729518 single base substitution T C missense_variant H496R 1487A>G UCEC-US 15 42729518 42729518 single base substitution T C missense_variant H715R 2144A>G UCEC-US 15 42729518 42729518 single base substitution T C missense_variant H758R 2273A>G UCEC-US 15 42730815 42730815 single base substitution G T downstream_gene_variant UCEC-US 15 42730815 42730815 single base substitution G T missense_variant S1509Y 4526C>A UCEC-US 15 42730815 42730815 single base substitution G T missense_variant S475Y 1424C>A UCEC-US 15 42730815 42730815 single base substitution G T missense_variant S694Y 2081C>A UCEC-US 15 42730815 42730815 single base substitution G T missense_variant S737Y 2210C>A UCEC-US 15 42731344 42731344 single base substitution C A downstream_gene_variant UCEC-US 15 42731344 42731344 single base substitution C A missense_variant K1454N 4362G>T UCEC-US 15 42731344 42731344 single base substitution C A missense_variant K420N 1260G>T UCEC-US 15 42731344 42731344 single base substitution C A missense_variant K639N 1917G>T UCEC-US 15 42731344 42731344 single base substitution C A missense_variant K682N 2046G>T UCEC-US 15 42731630 42731630 single base substitution T C downstream_gene_variant UCEC-US 15 42731630 42731630 single base substitution T C missense_variant K1359R 4076A>G UCEC-US 15 42731630 42731630 single base substitution T C missense_variant K325R 974A>G UCEC-US 15 42731630 42731630 single base substitution T C missense_variant K544R 1631A>G UCEC-US 15 42731630 42731630 single base substitution T C missense_variant K587R 1760A>G UCEC-US 15 42731777 42731777 single base substitution G T downstream_gene_variant UCEC-US 15 42731777 42731777 single base substitution G T intron_variant UCEC-US 15 42731777 42731777 single base substitution G T missense_variant S1310Y 3929C>A UCEC-US 15 42731777 42731777 single base substitution G T missense_variant S495Y 1484C>A UCEC-US 15 42731777 42731777 single base substitution G T missense_variant S538Y 1613C>A UCEC-US 15 42736410 42736410 single base substitution C A downstream_gene_variant UCEC-US 15 42736410 42736410 single base substitution C A missense_variant Q1114H 3342G>T UCEC-US 15 42736410 42736410 single base substitution C A missense_variant Q167H 501G>T UCEC-US 15 42736410 42736410 single base substitution C A missense_variant Q299H 897G>T UCEC-US 15 42736410 42736410 single base substitution C A missense_variant Q342H 1026G>T UCEC-US 15 42736410 42736410 single base substitution C A missense_variant Q72H 216G>T UCEC-US 15 42742347 42742347 single base substitution G T downstream_gene_variant UCEC-US 15 42742347 42742347 single base substitution G T intron_variant UCEC-US 15 42742347 42742347 single base substitution G T missense_variant S468Y 1403C>A UCEC-US 15 42742347 42742347 single base substitution G T missense_variant S685Y 2054C>A UCEC-US 15 42742347 42742347 single base substitution G T upstream_gene_variant UCEC-US 15 42742479 42742479 single base substitution G T downstream_gene_variant UCEC-US 15 42742479 42742479 single base substitution G T intron_variant UCEC-US 15 42742479 42742479 single base substitution G T missense_variant S424Y 1271C>A UCEC-US 15 42742479 42742479 single base substitution G T missense_variant S641Y 1922C>A UCEC-US 15 42742479 42742479 single base substitution G T upstream_gene_variant UCEC-US 15 42742931 42742931 single base substitution C T downstream_gene_variant UCEC-US 15 42742931 42742931 single base substitution C T intron_variant UCEC-US 15 42742931 42742931 single base substitution C T synonymous_variant S273S 819G>A UCEC-US 15 42742931 42742931 single base substitution C T synonymous_variant S490S 1470G>A UCEC-US 15 42742931 42742931 single base substitution C T upstream_gene_variant UCEC-US 15 42743268 42743268 single base substitution G A downstream_gene_variant UCEC-US 15 42743268 42743268 single base substitution G A intron_variant UCEC-US 15 42743268 42743268 single base substitution G A missense_variant P161L 482C>T UCEC-US 15 42743268 42743268 single base substitution G A missense_variant P378L 1133C>T UCEC-US 15 42743268 42743268 single base substitution G A missense_variant P401L 1202C>T UCEC-US 15 42743268 42743268 single base substitution G A upstream_gene_variant UCEC-US 15 42743538 42743538 single base substitution A G downstream_gene_variant UCEC-US 15 42743538 42743538 single base substitution A G intron_variant UCEC-US 15 42743538 42743538 single base substitution A G missense_variant L288P 863T>C UCEC-US 15 42743538 42743538 single base substitution A G missense_variant L311P 932T>C UCEC-US 15 42743538 42743538 single base substitution A G missense_variant L71P 212T>C UCEC-US 15 42743538 42743538 single base substitution A G upstream_gene_variant

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand PT13 COSM5896271 c.442C>T p.P148S Substitution - Missense 15:42451761-42451761 - HCC123T COSM1608375 c.4945G>A p.E1649K Substitution - Missense 15:42425010-42425010 - TCGA-J9-A52D-01 COSM4877871 c.4256G>A p.S1419N Substitution - Missense 15:42439252-42439252 - CRC-1 COSM304237 c.5170G>A p.A1724T Substitution - Missense 15:42424012-42424012 - TCGA-CG-5728-01 COSM4054730 c.920C>A p.P307H Substitution - Missense 15:42451283-42451283 - TCGA-EB-A24D-01 COSM3607875 c.1039G>A p.V347I Substitution - Missense 5:122153029-122153029 + RK175_C01 COSM3744607 c.2967G>T p.A989A Substitution - coding silent 15:42448171-42448171 - NOKSI COSM1619357 c.776A>C p.H259P Substitution - Missense 5:122152766-122152766 + TCGA-BS-A0UJ-01 COSM961737 c.4076A>G p.K1359R Substitution - Missense 15:42439432-42439432 - DLBCL813 COSM1581971 c.233C>T p.S78L Substitution - Missense 5:122152223-122152223 + TCGA-BR-8361-01 COSM4054734 c.687A>G p.V229V Substitution - coding silent 15:42451516-42451516 - TCGA-EE-A2GB-06 COSM3501298 c.4965C>T p.G1655G Substitution - coding silent 15:42424990-42424990 - 2492700 COSM5600913 c.500C>T p.P167L Substitution - Missense 5:122152490-122152490 + TCGA-66-2789-01 COSM700565 c.1971A>G p.T657T Substitution - coding silent 15:42450232-42450232 - HCC54T COSM1608377 c.491A>G p.H164R Substitution - Missense 15:42451712-42451712 - TCGA-AA-3518-01 COSM265610 c.408_409insA p.D137fs*4 Insertion - Frameshift 15:42451794-42451795 - TCGA-AG-3890-01 COSM288632 c.892C>T p.R298C Substitution - Missense 5:122152882-122152882 + TCGA-AZ-4315-01 COSM1372931 c.4876C>T p.R1626* Substitution - Nonsense 15:42428071-42428071 - 2492703 COSM5600913 c.500C>T p.P167L Substitution - Missense 5:122152490-122152490 + PD5925a COSM5788359 c.5538G>T p.L1846L Substitution - coding silent 15:42417862-42417862 - WSU-HN13 COSM4601510 c.3512C>T p.P1171L Substitution - Missense 15:42442255-42442255 - T2932 COSM1372939 c.1444delT p.S482fs*33 Deletion - Frameshift 15:42450759-42450759 - 91603 COSM329636 c.551A>G p.H184R Substitution - Missense 5:122152541-122152541 + TCGA-AZ-4315-01 COSM1372934 c.4214G>T p.R1405M Substitution - Missense 15:42439294-42439294 - LUAD-NYU1051S COSM368907 c.1031C>G p.T344S Substitution - Missense 5:122153021-122153021 + TCGA-AA-A010-01 COSM286685 c.2051A>C p.K684T Substitution - Missense 15:42450152-42450152 - RK194_C01 COSM1629557 c.3915A>T p.E1305D Substitution - Missense 15:42439593-42439593 - TCGA-HC-A6AQ-01 COSM3782876 c.1511C>T p.S504F Substitution - Missense 15:42450692-42450692 - TCGA-AX-A0J0-01 COSM961738 c.3929C>A p.S1310Y Substitution - Missense 15:42439579-42439579 - CHC304T COSM4949658 c.4430C>G p.S1477C Substitution - Missense 15:42439078-42439078 - B109-Tumor COSM1749139 c.277G>C p.E93Q Substitution - Missense 15:42451926-42451926 - TCGA-EE-A2MS-06 COSM3501301 c.1446C>T p.S482S Substitution - coding silent 15:42450757-42450757 - TCGA-D1-A17Q-01 COSM1060050 c.941A>C p.K314T Substitution - Missense 5:122152931-122152931 + I2L-P31-Tumor-Organoid COSM5363050 c.3694+1G>C p.? Unknown 15:42442072-42442072 - Au1 COSM5597923 c.3771C>T p.F1257F Substitution - coding silent 15:42439737-42439737 - TCGA-BR-8368-01 COSM4127386 c.1094A>G p.*365W Nonstop extension 5:122153084-122153084 + CSCC-4-T COSM4565363 c.2015_2016CC>TT p.T672I Substitution - Missense 15:42450187-42450188 - S00827 COSM316817 c.883A>G p.T295A Substitution - Missense 5:122152873-122152873 + TCGA-F5-6814-01 COSM3420304 c.5287C>T p.R1763C Substitution - Missense 15:42422518-42422518 - MO_1277 COSM5560884 c.803A>G p.N268S Substitution - Missense 15:42451400-42451400 - TCGA-D3-A2JA-06 COSM3501306 c.1111A>T p.K371* Substitution - Nonsense 15:42451092-42451092 - CN-AML-08-T COSM5426035 c.2967G>A p.A989A Substitution - coding silent 15:42448171-42448171 - B106 COSM1749137 c.3223C>G p.L1075V Substitution - Missense 15:42444895-42444895 - TCGA-EE-A2GR-06 COSM3501312 c.409G>A p.D137N Substitution - Missense 15:42451794-42451794 - TCGA-EE-A29L-06 COSM3501311 c.416T>G p.F139C Substitution - Missense 15:42451787-42451787 - T407 COSM4742587 c.2116delA p.S706fs*14 Deletion - Frameshift 15:42450087-42450087 - TCGA-18-3409-01 COSM735911 c.898C>T p.L300L Substitution - coding silent 5:122152888-122152888 + 2492702 COSM5600913 c.500C>T p.P167L Substitution - Missense 5:122152490-122152490 + PCSI_0081_Pa_P_526 COSM3377565 c.4401G>A p.T1467T Substitution - coding silent 15:42439107-42439107 - TCGA-D3-A3CB-06 COSM3501305 c.1201C>T p.P401S Substitution - Missense 15:42451002-42451002 - 477 COSM4438674 c.3184G>A p.E1062K Substitution - Missense 15:42444934-42444934 - PT13 COSM5896272 c.5124G>C p.V1708V Substitution - coding silent 15:42424058-42424058 - S00947 COSM316818 c.986A>C p.Y329S Substitution - Missense 5:122152976-122152976 + TCGA-AA-3697-01 COSM1372933 c.4614G>A p.Q1538Q Substitution - coding silent 15:42437295-42437295 - TCGA-AA-A010-01 COSM286683 c.5509G>A p.D1837N Substitution - Missense 15:42417891-42417891 - TCGA-BR-8081-01 COSM4054735 c.549T>C p.G183G Substitution - coding silent 15:42451654-42451654 - TCGA-B0-5085-01 COSM1493445 c.2414T>C p.L805P Substitution - Missense 15:42449789-42449789 - 1604875 COSM141449 c.1240C>T p.L414F Substitution - Missense 15:42450963-42450963 - 3093_T COSM3946789 c.888A>C p.S296S Substitution - coding silent 5:122152878-122152878 + C086 COSM5291737 c.4099C>T p.P1367S Substitution - Missense 15:42439409-42439409 - SNU-C1 COSM2187359 c.2079C>G p.G693G Substitution - coding silent 15:42450124-42450124 - TCGA-D1-A16X-01 COSM1060044 c.224G>T p.R75I Substitution - Missense 5:122152214-122152214 + LOVO COSM1372939 c.1444delT p.S482fs*33 Deletion - Frameshift 15:42450759-42450759 - UM-SCC-17B COSM1619357 c.776A>C p.H259P Substitution - Missense 5:122152766-122152766 + PCSI_0081_Pa_X COSM3377565 c.4401G>A p.T1467T Substitution - coding silent 15:42439107-42439107 - TCGA-34-2600-01 COSM700566 c.2374G>A p.E792K Substitution - Missense 15:42449829-42449829 - 587376 COSM1233370 c.4060A>C p.K1354Q Substitution - Missense 15:42439448-42439448 - DLBCL833 COSM1581972 c.682G>A p.G228S Substitution - Missense 5:122152672-122152672 + GC_304T-GC_304N COSM4772826 c.5305-10delT p.? Unknown 15:42421998-42421998 - RK260_C01 COSM4944171 c.832G>A p.G278R Substitution - Missense 5:122152822-122152822 + T16 COSM5618900 c.4857C>G p.L1619L Substitution - coding silent 15:42428090-42428090 - T207 COSM1372939 c.1444delT p.S482fs*33 Deletion - Frameshift 15:42450759-42450759 - N744T COSM236619 c.1490A>G p.D497G Substitution - Missense 15:42450713-42450713 - LP6005334-DNA_E03 COSM4412889 c.1867G>A p.D623N Substitution - Missense 15:42450336-42450336 - TCGA-IR-A3LB-01 COSM4829401 c.475C>T p.Q159* Substitution - Nonsense 5:122152465-122152465 + PARBRK COSM5005576 c.1722A>G p.K574K Substitution - coding silent 15:42450481-42450481 - PD3985a COSM165698 c.15A>T p.R5S Substitution - Missense 15:42457191-42457191 - TCGA-BR-8487-01 COSM4054726 c.2335C>T p.R779W Substitution - Missense 15:42449868-42449868 - TCGA-EE-A2MJ-06 COSM3501303 c.1366C>T p.P456S Substitution - Missense 15:42450837-42450837 - Pat_41_B COSM5849185 c.4526C>T p.S1509F Substitution - Missense 15:42438617-42438617 - TCGA-EV-5901-01 COSM3987954 c.5097T>G p.H1699Q Substitution - Missense 15:42424858-42424858 - YUPROST COSM1696083 c.787C>T p.P263S Substitution - Missense 5:122152777-122152777 + TCGA-D3-A2JF-06 COSM3501307 c.1022C>T p.A341V Substitution - Missense 15:42451181-42451181 - Pat_41_B COSM5849188 c.2191G>A p.D731N Substitution - Missense 15:42450012-42450012 - TCGA-22-4595-01 COSM700564 c.1906A>T p.R636* Substitution - Nonsense 15:42450297-42450297 - SC_9097 COSM5551057 c.75C>T p.C25C Substitution - coding silent 15:42457131-42457131 - ESCC_157 COSM1432681 c.463G>A p.E155K Substitution - Missense 5:122152453-122152453 + CHC2110Tbis COSM360066 c.192G>T p.G64G Substitution - coding silent 5:122152182-122152182 + T3498 COSM4742590 c.1424delA p.N475fs*40 Deletion - Frameshift 15:42450779-42450779 - TCGA-D1-A17Q-01 COSM1060045 c.422C>A p.S141Y Substitution - Missense 5:122152412-122152412 + TCGA-13-1499-01 COSM77072 c.1879G>A p.E627K Substitution - Missense 15:42450324-42450324 - T2269 COSM4742582 c.4083A>G p.L1361L Substitution - coding silent 15:42439425-42439425 - TCGA-C8-A26Y-01 COSM3816074 c.5449-1G>C p.? Unknown 15:42417952-42417952 - TCGA-BR-A4QL-01 COSM4054723 c.3517G>A p.G1173R Substitution - Missense 15:42442250-42442250 - T2940 COSM4742585 c.3299T>C p.M1100T Substitution - Missense 15:42444255-42444255 - HCC123 COSM1608375 c.4945G>A p.E1649K Substitution - Missense 15:42425010-42425010 - LUAD-CHTN-MAD06-00668 COSM360066 c.192G>T p.G64G Substitution - coding silent 5:122152182-122152182 + RH18C COSM4985230 c.953T>G p.L318W Substitution - Missense 5:122152943-122152943 + CN-AML-08-T COSM5426034 c.4599C>T p.A1533A Substitution - coding silent 15:42437310-42437310 - Au4 COSM5605396 c.1030G>A p.E344K Substitution - Missense 15:42451173-42451173 - HCC140T COSM5823155 c.791A>G p.Q264R Substitution - Missense 5:122152781-122152781 + I2L-P24Ta-Tumor-Biopsy COSM5363003 c.1645C>G p.Q549E Substitution - Missense 15:42450558-42450558 - STC291 COSM961733 c.4602A>G p.V1534V Substitution - coding silent 15:42437307-42437307 - TCGA-F5-6814-01 COSM3420305 c.1816A>G p.T606A Substitution - Missense 15:42450387-42450387 - RK064_C01 COSM1629556 c.5468T>C p.I1823T Substitution - Missense 15:42417932-42417932 - TCGA-AC-A23H-01 COSM3816076 c.4483G>C p.E1495Q Substitution - Missense 15:42438660-42438660 - TCGA-D5-6540-01 COSM1432680 c.66A>G p.E22E Substitution - coding silent 5:122152056-122152056 + ORL-48 COSM4596855 c.5089G>T p.E1697* Substitution - Nonsense 15:42424866-42424866 - TCGA-BC-A10Z-01 COSM4936212 c.3587C>T p.S1196L Substitution - Missense 15:42442180-42442180 - TCGA-B1-A657-01 COSM4908223 c.71C>A p.T24N Substitution - Missense 5:122152061-122152061 + CN-AML-NR-08-Dx COSM5426034 c.4599C>T p.A1533A Substitution - coding silent 15:42437310-42437310 - YUKLAB COSM1708062 c.50A>G p.D17G Substitution - Missense 15:42457156-42457156 - 35M COSM5583188 c.227T>C p.I76T Substitution - Missense 5:122152217-122152217 + YURAY COSM5383305 c.5330G>A p.G1777E Substitution - Missense 15:42421963-42421963 - PD5003a COSM3719455 c.1738G>T p.E580* Substitution - Nonsense 15:42450465-42450465 - SNUH_G76_S1 COSM4003272 c.821C>G p.S274C Substitution - Missense 5:122152811-122152811 + PT19_1 COSM5899691 c.1042C>T p.R348C Substitution - Missense 15:42451161-42451161 - TCGA-CG-5726-01 COSM4054724 c.3442G>A p.A1148T Substitution - Missense 15:42442325-42442325 - CHC1052T COSM3667721 c.3738T>C p.A1246A Substitution - coding silent 15:42439770-42439770 - TCGA-FW-A3R5-06 COSM3918508 c.721C>T p.P241S Substitution - Missense 5:122152711-122152711 + BN36T COSM1608374 c.5320C>T p.Q1774* Substitution - Nonsense 15:42421973-42421973 - TCGA-AP-A051-01 COSM1060046 c.462C>T p.N154N Substitution - coding silent 5:122152452-122152452 + TCGA-BR-4368-01 COSM4054728 c.1152G>T p.L384F Substitution - Missense 15:42451051-42451051 - CSCC-49-T COSM4589803 c.265_266insT p.A89fs*25 Insertion - Frameshift 5:122152255-122152256 + Pat_46_A COSM5849186 c.3467_3468TC>AT p.F1156Y Substitution - Missense 15:42442299-42442300 - TCGA-A5-A0GP-01 COSM961729 c.5279A>C p.K1760T Substitution - Missense 15:42422526-42422526 - TCGA-ER-A19S-06 COSM3501309 c.858C>G p.D286E Substitution - Missense 15:42451345-42451345 - TCGA-AP-A059-01 COSM961743 c.1922C>A p.S641Y Substitution - Missense 15:42450281-42450281 - ESCC_4 COSM5622773 c.4346A>T p.D1449V Substitution - Missense 15:42439162-42439162 - OSCC-GB_01130111 COSM5954784 c.1350G>A p.L450L Substitution - coding silent 15:42450853-42450853 - TCGA-G3-A25S-01 COSM4927064 c.4893A>T p.G1631G Substitution - coding silent 15:42428054-42428054 - T3446 COSM1372939 c.1444delT p.S482fs*33 Deletion - Frameshift 15:42450759-42450759 - TCGA-AP-A059-01 COSM1060048 c.605C>T p.S202F Substitution - Missense 5:122152595-122152595 + SJDOSTEOS008 COSM5760007 c.252A>G p.Q84Q Substitution - coding silent 15:42451951-42451951 - Pat_04_A COSM5849190 c.508G>A p.G170S Substitution - Missense 15:42451695-42451695 - TCGA-BR-4201-01 COSM4054729 c.1047G>A p.W349* Substitution - Nonsense 15:42451156-42451156 - pfg122T COSM4753769 c.2107C>T p.L703F Substitution - Missense 15:42450096-42450096 - HCC95 COSM3706573 c.462T>A p.G154G Substitution - coding silent 15:42451741-42451741 - 93VU147T COSM1619357 c.776A>C p.H259P Substitution - Missense 5:122152766-122152766 + TCGA-FS-A1ZZ-06 COSM3607868 c.282C>T p.F94F Substitution - coding silent 5:122152272-122152272 + TCGA-18-3409-01 COSM700571 c.5503C>T p.L1835L Substitution - coding silent 15:42417897-42417897 - MOLT-4 COSM961730 c.5053C>T p.R1685C Substitution - Missense 15:42424902-42424902 - TCGA-A3-3380-01 COSM1493446 c.3123T>A p.I1041I Substitution - coding silent 15:42446602-42446602 - TCGA-AC-A23H-01 COSM3816081 c.281T>C p.I94T Substitution - Missense 15:42451922-42451922 - NCI-H23 COSM1678393 c.2138G>A p.G713D Substitution - Missense 15:42450065-42450065 - TCGA-EB-A5SE-01 COSM3501300 c.1502C>T p.P501L Substitution - Missense 15:42450701-42450701 - TCGA-BH-A0HF-01 COSM3816077 c.1749G>A p.V583V Substitution - coding silent 15:42450454-42450454 - 1517_PT COSM5754689 c.1567T>G p.S523A Substitution - Missense 15:42450636-42450636 - 3N24-VS-3T24 COSM4979709 c.5486A>G p.H1829R Substitution - Missense 15:42417914-42417914 - TCGA-E2-A14X-01 COSM433872 c.2549C>G p.S850W Substitution - Missense 15:42448589-42448589 - TCGA-GF-A6C9-06 COSM4900175 c.810G>A p.P270P Substitution - coding silent 5:122152800-122152800 + RMS10_ COSM4986006 c.436G>A p.G146R Substitution - Missense 5:122152426-122152426 + TCGA-CA-6718-01 COSM961735 c.4526C>A p.S1509Y Substitution - Missense 15:42438617-42438617 - Ly8 COSM1581971 c.233C>T p.S78L Substitution - Missense 5:122152223-122152223 + I2L-P19Ta-Tumor-Organoid COSM5362904 c.3703A>T p.S1235C Substitution - Missense 15:42439805-42439805 - TCGA-D1-A16E-01 COSM961741 c.2245C>A p.P749T Substitution - Missense 15:42449958-42449958 - HCC2998 COSM2187397 c.198T>A p.Y66* Substitution - Nonsense 15:42457008-42457008 - 46M COSM555026 c.4750G>T p.G1584W Substitution - Missense 15:42435446-42435446 - SNUH_G16_S1 COSM4003272 c.821C>G p.S274C Substitution - Missense 5:122152811-122152811 + TCGA-D8-A1JA-01 COSM3816080 c.512C>T p.S171F Substitution - Missense 15:42451691-42451691 - CRC-32T COSM5460667 c.169G>A p.G57R Substitution - Missense 15:42457037-42457037 - T3225 COSM4742586 c.2509A>G p.S837G Substitution - Missense 15:42448629-42448629 - TCGA-AN-A0FT-01 COSM433871 c.3592C>T p.Q1198* Substitution - Nonsense 15:42442175-42442175 - TCGA-CJ-4639-01 COSM3361390 c.346A>T p.S116C Substitution - Missense 15:42451857-42451857 - CSCC-29-T COSM4496846 c.483C>T p.S161S Substitution - coding silent 15:42451720-42451720 - ESCC_BICR_045T COSM5441582 c.5012A>C p.K1671T Substitution - Missense 15:42424943-42424943 - TCGA-B5-A0JY-01 COSM961744 c.1470G>A p.S490S Substitution - coding silent 15:42450733-42450733 - TCGA-F5-6814-01 COSM171617 c.5110C>A p.L1704I Substitution - Missense 15:42424845-42424845 - TCGA-DR-A0ZM-01 COSM459038 c.4074G>A p.K1358K Substitution - coding silent 15:42439434-42439434 - T3498 COSM4742592 c.60T>C p.H20H Substitution - coding silent 15:42457146-42457146 - TCGA-AN-A0AK-01 COSM3826619 c.263C>T p.P88L Substitution - Missense 5:122152253-122152253 + CHC1209T COSM4804532 c.772G>C p.D258H Substitution - Missense 15:42451431-42451431 - Pat_76_B COSM2187382 c.919C>T p.P307S Substitution - Missense 15:42451284-42451284 - TCGA-B5-A11E-01 COSM961734 c.4589A>G p.H1530R Substitution - Missense 15:42437320-42437320 - TCGA-DI-A0WH-01 COSM961740 c.3232C>T p.R1078C Substitution - Missense 15:42444886-42444886 - HCT8 COSM4633976 c.5121G>T p.K1707N Substitution - Missense 15:42424834-42424834 - YUGURT COSM5383306 c.3515C>T p.T1172I Substitution - Missense 15:42442252-42442252 - CHC470T COSM3667775 c.2368A>G p.N790D Substitution - Missense 15:42449835-42449835 - LIM2405 COSM4641923 c.5648C>T p.S1883L Substitution - Missense 15:42417308-42417308 - TCGA-18-3409-01 COSM700570 c.5066A>T p.N1689I Substitution - Missense 15:42424889-42424889 - Pat_26_A COSM5867116 c.1060G>A p.A354T Substitution - Missense 5:122153050-122153050 + SNUH_G22_S1 COSM4003271 c.773T>C p.L258P Substitution - Missense 5:122152763-122152763 + UD-SCC-2 COSM1619357 c.776A>C p.H259P Substitution - Missense 5:122152766-122152766 + TCGA-D1-A103-01 COSM961745 c.1133C>T p.P378L Substitution - Missense 15:42451070-42451070 - SNU-C4 COSM4615747 c.248_249insC p.V86fs*28 Insertion - Frameshift 5:122152238-122152239 + HCC137T COSM1608376 c.1092G>A p.L364L Substitution - coding silent 15:42451111-42451111 - TCGA-B5-A0JY-01 COSM961742 c.2054C>A p.S685Y Substitution - Missense 15:42450149-42450149 - TCGA-G4-6588-01 COSM1372930 c.5052A>T p.V1684V Substitution - coding silent 15:42424903-42424903 - P116 COSM1736546 c.1744C>T p.Q582* Substitution - Nonsense 15:42450459-42450459 - CCK81 COSM2187342 c.3135delA p.E1046fs*9 Deletion - Frameshift 15:42446590-42446590 - tumor_4105746 COSM5946354 c.2926G>T p.E976* Substitution - Nonsense 15:42448212-42448212 - WSU-HN6 COSM1619357 c.776A>C p.H259P Substitution - Missense 5:122152766-122152766 + I2L-P24Tb-Tumor-Organoid COSM5363003 c.1645C>G p.Q549E Substitution - Missense 15:42450558-42450558 - TCGA-D1-A16J-01 COSM961731 c.4857C>T p.L1619L Substitution - coding silent 15:42428090-42428090 - T2197 COSM1372939 c.1444delT p.S482fs*33 Deletion - Frameshift 15:42450759-42450759 - Pat_70_B COSM1372939 c.1444delT p.S482fs*33 Deletion - Frameshift 15:42450759-42450759 - HX16T COSM1619357 c.776A>C p.H259P Substitution - Missense 5:122152766-122152766 + TCGA-FP-8099-01 COSM4127385 c.851T>C p.L284P Substitution - Missense 5:122152841-122152841 + T613 COSM4742584 c.3477delT p.L1160fs*19 Deletion - Frameshift 15:42442290-42442290 - TCGA-D9-A6EC-06 COSM4400075 c.136G>A p.E46K Substitution - Missense 5:122152126-122152126 + 3N55-VS-3T55 COSM4983709 c.295A>G p.R99G Substitution - Missense 15:42451908-42451908 - C086 COSM5542024 c.4100C>T p.P1367L Substitution - Missense 15:42439408-42439408 - Pat_41_B COSM1372939 c.1444delT p.S482fs*33 Deletion - Frameshift 15:42450759-42450759 - CRC-06T COSM5456482 c.2453C>T p.P818L Substitution - Missense 15:42448685-42448685 - SW48 COSM2187355 c.2284G>A p.G762S Substitution - Missense 15:42449919-42449919 - TCGA-CU-A0YR-01 COSM416934 c.4463G>A p.G1488D Substitution - Missense 15:42439045-42439045 - Pat_06_B COSM5849187 c.3467delT p.F1156fs*23 Deletion - Frameshift 15:42442300-42442300 - CSCC-35-T COSM4492980 c.407C>T p.P136L Substitution - Missense 5:122152397-122152397 + TCGA-EK-A3GK-01 COSM4852866 c.4541C>G p.S1514* Substitution - Nonsense 15:42437368-42437368 - CHC304T COSM4949658 c.4430C>G p.S1477C Substitution - Missense 15:42439078-42439078 - S00935 COSM316674 c.294C>G p.D98E Substitution - Missense 15:42451909-42451909 - TCGA-B5-A11E-01 COSM961736 c.4362G>T p.K1454N Substitution - Missense 15:42439146-42439146 - TCGA-C8-A12Q-01 COSM433874 c.247C>T p.R83* Substitution - Nonsense 15:42456959-42456959 - Au4 COSM5605397 c.2397C>T p.T799T Substitution - coding silent 15:42449806-42449806 - YUROG COSM5402005 c.946C>T p.Q316* Substitution - Nonsense 5:122152936-122152936 + CSCC-44-T COSM4548627 c.4521G>C p.K1507N Substitution - Missense 15:42438622-42438622 - TCGA-66-2742-01 COSM700569 c.4888G>T p.A1630S Substitution - Missense 15:42428059-42428059 - pfg072T COSM4760745 c.824G>T p.S275I Substitution - Missense 5:122152814-122152814 + ESCC-233T COSM3936751 c.4159G>T p.A1387S Substitution - Missense 15:42439349-42439349 - C004 COSM5521989 c.763C>T p.P255S Substitution - Missense 5:122152753-122152753 + 234 COSM3730766 c.5305-11_5305-10delTT p.? Unknown 15:42421998-42421999 - STC297 COSM5054289 c.5546G>A p.R1849H Substitution - Missense 15:42417854-42417854 - SM-4B296 COSM5035654 c.983A>G p.E328G Substitution - Missense 5:122152973-122152973 + TCGA-BS-A0UV-01 COSM961746 c.863T>C p.L288P Substitution - Missense 15:42451340-42451340 - CSCC-18-T COSM4546092 c.3926G>T p.S1309I Substitution - Missense 15:42439582-42439582 - S00827 COSM316817 c.883A>G p.T295A Substitution - Missense 5:122152873-122152873 + 2492722 COSM5720367 c.451C>T p.Q151* Substitution - Nonsense 5:122152441-122152441 + TCGA-A4-A5DU-01 COSM3993918 c.253C>T p.P85S Substitution - Missense 5:122152243-122152243 + 3206A7_009_T COSM5040859 c.759C>G p.N253K Substitution - Missense 15:42451444-42451444 - TCGA-18-3409-01 COSM700567 c.3671C>T p.S1224F Substitution - Missense 15:42442096-42442096 - LUAD-5V8LT COSM402634 c.865C>T p.H289Y Substitution - Missense 5:122152855-122152855 + TCGA-25-2391-01 COSM119704 c.345G>T p.E115D Substitution - Missense 15:42451858-42451858 - CHC304T COSM4788507 c.3026A>G p.N1009S Substitution - Missense 15:42448112-42448112 - I2L-P7-Tumor-Organoid COSM5356922 c.377A>G p.K126R Substitution - Missense 5:122152367-122152367 + BD135T COSM5516692 c.2308_2310delAAG p.K770delK Deletion - In frame 15:42449893-42449895 - SH-0034 COSM4054726 c.2335C>T p.R779W Substitution - Missense 15:42449868-42449868 - CN-AML-NR-08-Dx COSM5426035 c.2967G>A p.A989A Substitution - coding silent 15:42448171-42448171 - TCGA-66-2734-01 COSM700563 c.1677C>A p.T559T Substitution - coding silent 15:42450526-42450526 - TCGA-DA-A1HW-06 COSM1696084 c.803C>T p.P268L Substitution - Missense 5:122152793-122152793 + CRC-19T COSM5481245 c.2679A>G p.S893S Substitution - coding silent 15:42448459-42448459 - HN_00761 COSM130318 c.1240C>G p.L414V Substitution - Missense 15:42450963-42450963 - TCGA-CG-5728-01 COSM4127384 c.621C>T p.G207G Substitution - coding silent 5:122152611-122152611 + 2492701 COSM5600913 c.500C>T p.P167L Substitution - Missense 5:122152490-122152490 + CSCC-31-T COSM4489368 c.3469C>T p.P1157S Substitution - Missense 15:42442298-42442298 - Au3 COSM5602654 c.3G>A p.M1I Substitution - Missense 5:122151993-122151993 + ESCC_120 COSM5650086 c.4950_4951insGAT p.I1650_F1651insD Insertion - In frame 15:42425004-42425005 - I2L-P24Ta-Tumor-Organoid COSM5363003 c.1645C>G p.Q549E Substitution - Missense 15:42450558-42450558 - PDA_057 COSM3134869 c.206C>T p.S69L Substitution - Missense 5:122152196-122152196 + TCGA-09-1675-01 COSM1323205 c.3254A>C p.Y1085S Substitution - Missense 15:42444864-42444864 - 2492721 COSM5720367 c.451C>T p.Q151* Substitution - Nonsense 5:122152441-122152441 + TCGA-EI-6917-01 COSM3420306 c.1552A>G p.K518E Substitution - Missense 15:42450651-42450651 - TCGA-FS-A1ZB-06 COSM3501304 c.1296C>T p.C432C Substitution - coding silent 15:42450907-42450907 - TCGA-18-5595-01 COSM700562 c.1673G>T p.S558I Substitution - Missense 15:42450530-42450530 - B109 COSM1749138 c.409G>C p.D137H Substitution - Missense 15:42451794-42451794 - LUAD-U6SJ7 COSM400168 c.2950G>T p.A984S Substitution - Missense 15:42448188-42448188 - RKO COSM2187398 c.192_194delAGA p.E64delE Deletion - In frame 15:42457012-42457014 - TCGA-CD-8526-01 COSM4054733 c.689G>A p.R230H Substitution - Missense 15:42451514-42451514 - PT08_2 COSM5893861 c.2909C>T p.S970F Substitution - Missense 15:42448229-42448229 - BD57T COSM5510727 c.76G>A p.G26R Substitution - Missense 15:42457130-42457130 - TCGA-BG-A0M7-01 COSM961730 c.5053C>T p.R1685C Substitution - Missense 15:42424902-42424902 - TCGA-EE-A2MS-06 COSM3607869 c.486G>A p.Q162Q Substitution - coding silent 5:122152476-122152476 + OSCC-GB_00040111 COSM3711806 c.413G>A p.G138D Substitution - Missense 15:42451790-42451790 - RKO COSM4647819 c.1560A>G p.T520T Substitution - coding silent 15:42450643-42450643 - LP2000104-DNA_A01 COSM5036900 c.563A>G p.K188R Substitution - Missense 5:122152553-122152553 + 2492723 COSM5720367 c.451C>T p.Q151* Substitution - Nonsense 5:122152441-122152441 + TCGA-E9-A1RD-01 COSM1478118 c.5398G>T p.G1800C Substitution - Missense 15:42421111-42421111 - TCGA-AA-A010-01 COSM286876 c.598A>G p.N200D Substitution - Missense 5:122152588-122152588 + HCC95T COSM3706573 c.462T>A p.G154G Substitution - coding silent 15:42451741-42451741 - pfg059T COSM4760744 c.146A>T p.N49I Substitution - Missense 5:122152136-122152136 + 9642_PT COSM5754688 c.2660A>G p.E887G Substitution - Missense 15:42448478-42448478 - TCGA-A3-3365-01 COSM1493444 c.2393T>A p.V798E Substitution - Missense 15:42449810-42449810 - TCGA-A3-3316-01 COSM1493444 c.2393T>A p.V798E Substitution - Missense 15:42449810-42449810 - TCGA-G3-A7M5-01 COSM4941856 c.4632A>G p.L1544L Substitution - coding silent 15:42437277-42437277 - TCGA-EE-A2MS-06 COSM3607873 c.948G>A p.Q316Q Substitution - coding silent 5:122152938-122152938 + TCGA-AA-A010-01 COSM286684 c.3127G>T p.G1043* Substitution - Nonsense 15:42446598-42446598 - YUGURT COSM5402004 c.934G>A p.G312R Substitution - Missense 5:122152924-122152924 + TCGA-66-2785-01 COSM735912 c.92G>T p.G31V Substitution - Missense 5:122152082-122152082 + TCGA-AA-3672-01 COSM267820 c.698C>A p.T233N Substitution - Missense 5:122152688-122152688 + TCGA-BR-6452-01 COSM4054722 c.3975A>G p.E1325E Substitution - coding silent 15:42439533-42439533 - Pat_76_B COSM5849189 c.569G>A p.G190E Substitution - Missense 15:42451634-42451634 - TCGA-AN-A046-01 COSM3816079 c.937G>A p.D313N Substitution - Missense 15:42451266-42451266 - 2290930 COSM4440384 c.609C>T p.S203S Substitution - coding silent 15:42451594-42451594 - sysucc-1317T COSM5448740 c.2592C>T p.S864S Substitution - coding silent 15:42448546-42448546 - WSU-HN8 COSM1619357 c.776A>C p.H259P Substitution - Missense 5:122152766-122152766 + TCGA-D9-A6EA-06 COSM4397860 c.2110C>T p.Q704* Substitution - Nonsense 15:42450093-42450093 - TCGA-AP-A059-01 COSM961739 c.3342G>T p.Q1114H Substitution - Missense 15:42444212-42444212 - TCGA-BR-7197-01 COSM589158 c.794A>C p.K265T Substitution - Missense 5:122152784-122152784 + TCGA-AX-A05Z-01 COSM961735 c.4526C>A p.S1509Y Substitution - Missense 15:42438617-42438617 - TCGA-BR-6452-01 COSM4054721 c.4009G>A p.A1337T Substitution - Missense 15:42439499-42439499 - PD22361a COSM5790629 c.331A>G p.I111V Substitution - Missense 5:122152321-122152321 + 8068554 COSM4781480 c.5003G>A p.G1668D Substitution - Missense 15:42424952-42424952 - 331 COSM3724294 c.184A>G p.R62G Substitution - Missense 5:122152174-122152174 + Gp5D COSM2187367 c.1725G>A p.G575G Substitution - coding silent 15:42450478-42450478 - T3182 COSM4742589 c.1607G>A p.R536Q Substitution - Missense 15:42450596-42450596 - 2492720 COSM5720367 c.451C>T p.Q151* Substitution - Nonsense 5:122152441-122152441 + 1517_CLM COSM5754689 c.1567T>G p.S523A Substitution - Missense 15:42450636-42450636 - sysucc-1240T COSM3826619 c.263C>T p.P88L Substitution - Missense 5:122152253-122152253 + HCC137 COSM1608376 c.1092G>A p.L364L Substitution - coding silent 15:42451111-42451111 - pfg008T COSM2187342 c.3135delA p.E1046fs*9 Deletion - Frameshift 15:42446590-42446590 - ESCC-100T COSM3936752 c.3682C>T p.L1228L Substitution - coding silent 15:42442085-42442085 - HCC54 COSM1608377 c.491A>G p.H164R Substitution - Missense 15:42451712-42451712 - 394 COSM3724295 c.134C>T p.T45I Substitution - Missense 5:122152124-122152124 + 587376 COSM1234122 c.957T>G p.N319K Substitution - Missense 5:122152947-122152947 + Pat_28_B COSM5849184 c.4960C>T p.H1654Y Substitution - Missense 15:42424995-42424995 - TCGA-AP-A059-01 COSM1060049 c.894C>T p.R298R Substitution - coding silent 5:122152884-122152884 + KM12 COSM1372939 c.1444delT p.S482fs*33 Deletion - Frameshift 15:42450759-42450759 - CSCC-41-T COSM4459725 c.1137C>T p.L379L Substitution - coding silent 15:42451066-42451066 - RKO COSM1372939 c.1444delT p.S482fs*33 Deletion - Frameshift 15:42450759-42450759 - STC252 COSM1581973 c.757C>T p.R253W Substitution - Missense 5:122152747-122152747 + S02299 COSM5690225 c.251A>T p.Q84L Substitution - Missense 15:42451952-42451952 - PD3992a COSM165699 c.5056G>A p.D1686N Substitution - Missense 15:42424899-42424899 - C608 COSM4442999 c.641G>A p.G214E Substitution - Missense 5:122152631-122152631 + TCGA-D8-A1XK-01 COSM1372939 c.1444delT p.S482fs*33 Deletion - Frameshift 15:42450759-42450759 - Gp2D COSM4628350 c.430A>G p.S144G Substitution - Missense 5:122152420-122152420 + TCGA-DG-A2KM-01 COSM4851614 c.3496C>T p.H1166Y Substitution - Missense 15:42442271-42442271 - 2250159 COSM5029304 c.711T>A p.P237P Substitution - coding silent 5:122152701-122152701 + YUSCA COSM5402003 c.183G>A p.K61K Substitution - coding silent 5:122152173-122152173 + TCGA-HC-7079-01 COSM3672047 c.2553C>A p.S851S Substitution - coding silent 15:42448585-42448585 - pfg008T COSM1372939 c.1444delT p.S482fs*33 Deletion - Frameshift 15:42450759-42450759 - TCGA-CJ-4873-01 COSM3361391 c.120T>C p.S40S Substitution - coding silent 15:42457086-42457086 - TCGA-RP-A693-06 COSM4896034 c.4978A>G p.S1660G Substitution - Missense 15:42424977-42424977 - pfg008T COSM1372939 c.1444delT p.S482fs*33 Deletion - Frameshift 15:42450759-42450759 - AOCS-113-1-5 COSM3981502 c.1587T>G p.D529E Substitution - Missense 15:42450616-42450616 - Gp2D COSM2187367 c.1725G>A p.G575G Substitution - coding silent 15:42450478-42450478 - TCGA-BR-4361-01 COSM4054731 c.785T>C p.L262P Substitution - Missense 15:42451418-42451418 - BN36 COSM1608374 c.5320C>T p.Q1774* Substitution - Nonsense 15:42421973-42421973 - 0051_CRUK_PC_0051_T1_DNA COSM5422187 c.1935C>T p.P645P Substitution - coding silent 15:42450268-42450268 - 43 COSM5734025 c.351G>T p.L117F Substitution - Missense 5:122152341-122152341 + 53M COSM2187382 c.919C>T p.P307S Substitution - Missense 15:42451284-42451284 - TCGA-EE-A2M5-06 COSM3501308 c.888T>G p.G296G Substitution - coding silent 15:42451315-42451315 - TCGA-AK-3447-01 COSM1493444 c.2393T>A p.V798E Substitution - Missense 15:42449810-42449810 - 587222 COSM961735 c.4526C>A p.S1509Y Substitution - Missense 15:42438617-42438617 - 234 COSM1372939 c.1444delT p.S482fs*33 Deletion - Frameshift 15:42450759-42450759 - TCGA-AN-A046-01 COSM3816075 c.4655C>A p.T1552N Substitution - Missense 15:42437254-42437254 - LU-1991 COSM5614218 c.467G>T p.G156V Substitution - Missense 15:42451736-42451736 - MO_1094 COSM5574140 c.5305-9_5305-8insT p.? Unknown 15:42421996-42421997 - TCGA-25-1317-01 COSM116240 c.3632A>G p.N1211S Substitution - Missense 15:42442135-42442135 - I2L-P19Ta-Tumor-Biopsy COSM5362904 c.3703A>T p.S1235C Substitution - Missense 15:42439805-42439805 - TCGA-D5-6538-01 COSM1372940 c.1436A>T p.N479I Substitution - Missense 15:42450767-42450767 - 19 COSM5747632 c.3667G>A p.V1223M Substitution - Missense 15:42442100-42442100 - Gp2D COSM2187371 c.1653A>G p.P551P Substitution - coding silent 15:42450550-42450550 - PDA_070 COSM4003272 c.821C>G p.S274C Substitution - Missense 5:122152811-122152811 + TCGA-DD-A39X-01 COSM4940653 c.2095T>G p.L699V Substitution - Missense 15:42450108-42450108 - ESCC_72 COSM5634289 c.2663C>T p.P888L Substitution - Missense 15:42448475-42448475 - LC_S15 COSM1188983 c.3563G>T p.G1188V Substitution - Missense 15:42442204-42442204 - TCGA-A3-3380-01 COSM1493444 c.2393T>A p.V798E Substitution - Missense 15:42449810-42449810 - 61 COSM5740307 c.224T>C p.I75T Substitution - Missense 15:42456982-42456982 - CSCC-27-T COSM4512915 c.920C>T p.P307L Substitution - Missense 15:42451283-42451283 - TCGA-BR-8487-01 COSM4054719 c.5482G>T p.D1828Y Substitution - Missense 15:42417918-42417918 - sysucc-1370T COSM5470348 c.2693T>C p.L898S Substitution - Missense 15:42448445-42448445 - OSCC-GB_00540111 COSM187882 c.2135C>T p.S712L Substitution - Missense 15:42450068-42450068 - SC_9047 COSM5551584 c.410A>G p.D137G Substitution - Missense 15:42451793-42451793 - pfg019T COSM1372939 c.1444delT p.S482fs*33 Deletion - Frameshift 15:42450759-42450759 - C008 COSM4742580 c.5022C>T p.V1674V Substitution - coding silent 15:42424933-42424933 - TCGA-CJ-5678-01 COSM470646 c.1989C>T p.H663H Substitution - coding silent 15:42450214-42450214 - T3225 COSM4742580 c.5022C>T p.V1674V Substitution - coding silent 15:42424933-42424933 - TCGA-39-5030-01 COSM700572 c.5559C>T p.C1853C Substitution - coding silent 15:42417841-42417841 - SC_9047 COSM5551492 c.339C>T p.D113D Substitution - coding silent 15:42451864-42451864 - 8057473 COSM3386868 c.666C>T p.N222N Substitution - coding silent 15:42451537-42451537 - HCT116 COSM1372939 c.1444delT p.S482fs*33 Deletion - Frameshift 15:42450759-42450759 - Single_Sample COSM1619357 c.776A>C p.H259P Substitution - Missense 5:122152766-122152766 + T1 COSM175407 c.1942C>T p.R648C Substitution - Missense 15:42450261-42450261 - CHC1209T COSM4804532 c.772G>C p.D258H Substitution - Missense 15:42451431-42451431 - ME029T COSM226761 c.5573C>T p.T1858I Substitution - Missense 15:42417827-42417827 - TCGA-D5-6926-01 COSM1432681 c.463G>A p.E155K Substitution - Missense 5:122152453-122152453 + 19M COSM5580050 c.399G>A p.R133R Substitution - coding silent 5:122152389-122152389 + T3174 COSM4742583 c.3483G>A p.E1161E Substitution - coding silent 15:42442284-42442284 - SCC-15 COSM1619357 c.776A>C p.H259P Substitution - Missense 5:122152766-122152766 + PT27 COSM5906009 c.5182C>T p.H1728Y Substitution - Missense 15:42424000-42424000 - ESCC_BICR_045T COSM5441583 c.856G>T p.D286Y Substitution - Missense 15:42451347-42451347 - TCGA-D8-A1JN-01 COSM1478119 c.1122G>C p.M374I Substitution - Missense 15:42451081-42451081 - T3145 COSM4742588 c.1742T>C p.F581S Substitution - Missense 15:42450461-42450461 - DLBCL797 COSM1581973 c.757C>T p.R253W Substitution - Missense 5:122152747-122152747 + TCGA-CG-4306-01 COSM4127383 c.493C>A p.L165M Substitution - Missense 5:122152483-122152483 + YUNOCA COSM1708061 c.5023G>A p.V1675M Substitution - Missense 15:42424932-42424932 - S00947 COSM316818 c.986A>C p.Y329S Substitution - Missense 5:122152976-122152976 + I2L-P24Tb-Tumor-Biopsy COSM5363003 c.1645C>G p.Q549E Substitution - Missense 15:42450558-42450558 - T3610 COSM4743967 c.578G>A p.G193D Substitution - Missense 5:122152568-122152568 + TCGA-ER-A19P-06 COSM3607870 c.704C>T p.S235F Substitution - Missense 5:122152694-122152694 + CSCC-54-T COSM4452192 c.164A>T p.K55M Substitution - Missense 5:122152154-122152154 + T2269 COSM1581973 c.757C>T p.R253W Substitution - Missense 5:122152747-122152747 + CAL33 COSM1619357 c.776A>C p.H259P Substitution - Missense 5:122152766-122152766 + PT37 COSM5920924 c.3353A>C p.E1118A Substitution - Missense 15:42442414-42442414 - RK262_C01 COSM4778747 c.4174A>G p.K1392E Substitution - Missense 15:42439334-42439334 - TCGA-FS-A1ZM-06 COSM3501310 c.787T>C p.W263R Substitution - Missense 15:42451416-42451416 - TCGA-CK-5915-01 COSM1372935 c.3540G>A p.T1180T Substitution - coding silent 15:42442227-42442227 - 587234 COSM1233369 c.2803C>T p.R935* Substitution - Nonsense 15:42448335-42448335 - LUAD-CHTN-MAD06-00668 COSM360067 c.624C>A p.L208L Substitution - coding silent 5:122152614-122152614 + TCGA-CD-A4MG-01 COSM4054732 c.779C>T p.T260I Substitution - Missense 15:42451424-42451424 - T469 COSM4742581 c.4262C>T p.S1421L Substitution - Missense 15:42439246-42439246 - PT08_1 COSM5893861 c.2909C>T p.S970F Substitution - Missense 15:42448229-42448229 - pfg001T COSM1640239 c.2290C>T p.R764* Substitution - Nonsense 15:42449913-42449913 - SNUH_G22_S1 COSM1619357 c.776A>C p.H259P Substitution - Missense 5:122152766-122152766 + TCGA-EE-A2MS-06 COSM3501302 c.1429A>G p.K477E Substitution - Missense 15:42450774-42450774 - Pat_76_A COSM5849189 c.569G>A p.G190E Substitution - Missense 15:42451634-42451634 - TCGA-AA-3870-01 COSM296344 c.1137_1138delCT p.F380fs*1 Deletion - Frameshift 15:42451065-42451066 - TCGA-B5-A0JY-01 COSM961728 c.5341G>T p.D1781Y Substitution - Missense 15:42421952-42421952 - J52_T COSM3946788 c.489T>G p.A163A Substitution - coding silent 5:122152479-122152479 + LUAD-YKER9 COSM351991 c.2898G>T p.E966D Substitution - Missense 15:42448240-42448240 - CSCC-27-T COSM4471582 c.1727C>T p.S576F Substitution - Missense 15:42450476-42450476 - TCGA-DU-7006-01 COSM3969111 c.1406C>T p.P469L Substitution - Missense 15:42450797-42450797 - PD11762a COSM5795672 c.2567G>A p.R856K Substitution - Missense 15:42448571-42448571 - SW48 COSM2187393 c.445C>T p.H149Y Substitution - Missense 15:42451758-42451758 - HCC039T COSM5809341 c.353A>G p.Q118R Substitution - Missense 5:122152343-122152343 + PT32 COSM5907663 c.1181C>T p.T394I Substitution - Missense 15:42451022-42451022 - ML4 COSM1165541 c.322C>T p.R108* Substitution - Nonsense 15:42451881-42451881 - 1N31-VS-1T31 COSM4974418 c.29C>G p.S10C Substitution - Missense 5:122152019-122152019 + S02237 COSM5676588 c.830C>T p.A277V Substitution - Missense 5:122152820-122152820 + TCGA-AN-A046-01 COSM3816078 c.1181C>A p.T394N Substitution - Missense 15:42451022-42451022 - TCGA-EI-6917-01 COSM3420307 c.299G>A p.R100Q Substitution - Missense 15:42451904-42451904 - Pat_76_A COSM2187382 c.919C>T p.P307S Substitution - Missense 15:42451284-42451284 - TCGA-BR-4362-01 COSM4054725 c.3403C>T p.R1135* Substitution - Nonsense 15:42442364-42442364 - I2L-P31-Tumor-Biopsy COSM5363050 c.3694+1G>C p.? Unknown 15:42442072-42442072 - LUAD-RT-S01487 COSM377957 c.278G>T p.G93V Substitution - Missense 5:122152268-122152268 + TCGA-D3-A1QA-06 COSM3607874 c.1027G>A p.V343I Substitution - Missense 5:122153017-122153017 + S00356 COSM318305 c.3043A>G p.R1015G Substitution - Missense 15:42448095-42448095 - S02342 COSM5692558 c.2034G>A p.Q678Q Substitution - coding silent 15:42450169-42450169 - TCGA-AO-A03R-01 COSM433873 c.865G>A p.G289S Substitution - Missense 15:42451338-42451338 - TCGA-D3-A3MR-06 COSM3607872 c.715C>T p.H239Y Substitution - Missense 5:122152705-122152705 + TCGA-18-3409-01 COSM700561 c.1363C>T p.L455F Substitution - Missense 15:42450840-42450840 - TCGA-B0-5705-01 COSM470647 c.702T>C p.N234N Substitution - coding silent 15:42451501-42451501 - D38 COSM1581971 c.233C>T p.S78L Substitution - Missense 5:122152223-122152223 + TCGA-60-2698-01 COSM700568 c.4683G>A p.R1561R Substitution - coding silent 15:42435513-42435513 - CH-52-T2 COSM5650887 c.208A>G p.K70E Substitution - Missense 5:122152198-122152198 + TCGA-HU-A4GU-01 COSM2187327 c.4400C>T p.T1467M Substitution - Missense 15:42439108-42439108 - 2290929 COSM4440384 c.609C>T p.S203S Substitution - coding silent 15:42451594-42451594 - TCGA-BR-4370-01 COSM165699 c.5056G>A p.D1686N Substitution - Missense 15:42424899-42424899 - pfg181T COSM187878 c.2572C>T p.R858* Substitution - Nonsense 15:42448566-42448566 - TCGA-DD-A1EB-01 COSM168163 c.125C>T p.S42F Substitution - Missense 5:122152115-122152115 + GC8_T COSM150900 c.951delT p.L318fs*1 Deletion - Frameshift 5:122152941-122152941 + Au2 COSM5600913 c.500C>T p.P167L Substitution - Missense 5:122152490-122152490 + 9642_CLM COSM5754688 c.2660A>G p.E887G Substitution - Missense 15:42448478-42448478 - HCT116 COSM2187402 c.149C>T p.A50V Substitution - Missense 15:42457057-42457057 - T3080 COSM4742591 c.284A>G p.N95S Substitution - Missense 15:42451919-42451919 - ESCC_56 COSM5632161 c.3827G>T p.R1276I Substitution - Missense 15:42439681-42439681 - BHY COSM1619357 c.776A>C p.H259P Substitution - Missense 5:122152766-122152766 + TCGA-B5-A0JY-01 COSM961732 c.4660C>T p.R1554W Substitution - Missense 15:42437249-42437249 - ESCC_BICR_061T COSM5430746 c.4131G>C p.L1377F Substitution - Missense 15:42439377-42439377 - YUSCA COSM5402002 c.10G>A p.G4R Substitution - Missense 5:122152000-122152000 + S00356 COSM318305 c.3043A>G p.R1015G Substitution - Missense 15:42448095-42448095 - YUJUBE COSM5383307 c.1818C>T p.T606T Substitution - coding silent 15:42450385-42450385 - TCGA-A5-A0GP-01 COSM1060047 c.542T>G p.L181R Substitution - Missense 5:122152532-122152532 + TCGA-BR-A4QL-01 COSM3501307 c.1022C>T p.A341V Substitution - Missense 15:42451181-42451181 - S02275 COSM5682772 c.311G>T p.R104I Substitution - Missense 15:42451892-42451892 - PTC-10C COSM4148769 c.1937T>C p.I646T Substitution - Missense 15:42450266-42450266 - UM-SCC-11B COSM1619357 c.776A>C p.H259P Substitution - Missense 5:122152766-122152766 + 4T COSM3711806 c.413G>A p.G138D Substitution - Missense 15:42451790-42451790 - TCGA-A2-A25D-01 COSM1478120 c.414C>T p.G138G Substitution - coding silent 15:42451789-42451789 - CHC2110Tbis COSM360066 c.192G>T p.G64G Substitution - coding silent 5:122152182-122152182 + TCGA-EB-A41A-01 COSM3501299 c.3388C>T p.P1130S Substitution - Missense 15:42442379-42442379 - PCSI_0208_Pa_P_526 COSM5031701 c.4929+2T>A p.? Unknown 15:42428016-42428016 - PD4203a COSM165700 c.3306G>C p.M1102I Substitution - Missense 15:42444248-42444248 - PD4106a COSM165839 c.145A>C p.N49H Substitution - Missense 5:122152135-122152135 + RKO COSM2187368 c.1722delA p.S576fs*2 Deletion - Frameshift 15:42450481-42450481 - CHC1052T COSM3667721 c.3738T>C p.A1246A Substitution - coding silent 15:42439770-42439770 - pfg143T COSM4753766 c.4480G>A p.A1494T Substitution - Missense 15:42438663-42438663 - TCGA-FP-7829-01 COSM4054727 c.2154A>C p.E718D Substitution - Missense 15:42450049-42450049 - TCGA-A3-3374-01 COSM1493443 c.1160C>G p.T387R Substitution - Missense 15:42451043-42451043 - LUAD-NYU201 COSM371437 c.982G>C p.E328Q Substitution - Missense 5:122152972-122152972 + CHC304T COSM4788507 c.3026A>G p.N1009S Substitution - Missense 15:42448112-42448112 - 587376 COSM1234123 c.1046A>G p.H349R Substitution - Missense 5:122153036-122153036 + TCGA-D1-A0ZO-01 COSM1060051 c.1031C>T p.T344I Substitution - Missense 5:122153021-122153021 + T3080 COSM1372939 c.1444delT p.S482fs*33 Deletion - Frameshift 15:42450759-42450759 - CSCC-16-T COSM4503579 c.642C>T p.S214S Substitution - coding silent 15:42451561-42451561 - B106-Tumor COSM1749137 c.3223C>G p.L1075V Substitution - Missense 15:42444895-42444895 - BD72T COSM187856 c.5618G>A p.R1873Q Substitution - Missense 15:42417338-42417338 - Gp5D COSM2187371 c.1653A>G p.P551P Substitution - coding silent 15:42450550-42450550 - T3090 COSM1372939 c.1444delT p.S482fs*33 Deletion - Frameshift 15:42450759-42450759 - TCGA-ER-A193-06 COSM3607871 c.705C>T p.S235S Substitution - coding silent 5:122152695-122152695 + TCGA-AP-A056-01 COSM961733 c.4602A>G p.V1534V Substitution - coding silent 15:42437307-42437307 - PD18280a COSM3770308 c.256G>T p.V86L Substitution - Missense 5:122152246-122152246 + B109 COSM1749139 c.277G>C p.E93Q Substitution - Missense 15:42451926-42451926 - PDA_015 COSM4998762 c.4313T>C p.I1438T Substitution - Missense 15:42439195-42439195 - TCGA-EE-A3JB-06 COSM4898744 c.1393C>T p.Q465* Substitution - Nonsense 15:42450810-42450810 - YUSUBA COSM1696084 c.803C>T p.P268L Substitution - Missense 5:122152793-122152793 + CSCC-19-T COSM4536725 c.2337G>T p.R779R Substitution - coding silent 15:42449866-42449866 - TCGA-HU-A4G9-01 COSM4054720 c.4963G>T p.G1655C Substitution - Missense 15:42424992-42424992 - UM-SCC-47 COSM1619357 c.776A>C p.H259P Substitution - Missense 5:122152766-122152766 + B109-Tumor COSM1749138 c.409G>C p.D137H Substitution - Missense 15:42451794-42451794 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.511143 15q15.1 Hs.729657;Hs.729659;Hs.729660;Hs.729664;Hs.729666;Hs.729668;Hs.729669;Hs.729670;Hs.729672;Hs.729673 5q23.2

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C Missense p.F139C c.416T>G 15 42743985 CM A C Missense p.L1807R c.5420T>G 15 42713287 THCA A C Synonymous p.G296G c.888T>G 15 42743513 CM A - Frameshift p.S482Pfs*33 c.1444delT 15 42742957 STAD AG - Frameshift p.F380*fs*1 c.1137_1138delCT 15 42743263 COREAD A G Missense p.F1155L c.3463T>C 15 42734502 THCA A G Missense p.W263R c.787T>C 15 42743614 CM A G Synonymous p.N234N c.702T>C 15 42743699 RCCC A G Synonymous p.S40S c.120T>C 15 42749284 RCCC A - IntronicDeletion . c.2432+30delT 15 42741939 STAD C A Missense p.A1630S c.4888G>T 15 42720257 LUSC C A Missense p.A585S c.1753G>T 15 42742648 HNSC C A Missense p.E115D c.345G>T 15 42744056 OV C A Missense p.G156V c.467G>T 15 42743934 NSCLC C A Missense p.G1584W c.4750G>T 15 42727644 CM C A Missense p.G1800C c.5398G>T 15 42713309 BRCA C A Missense p.G26W c.76G>T 15 42749328 HNSC C A Missense p.L384F c.1152G>T 15 42743249 STAD C A Missense p.R1647L c.4940G>T 15 42717213 LUAD C A Missense p.S558I c.1673G>T 15 42742728 LUSC CC AT Missense p.W174Y c.521_522delinsAT 15 42743879 CM C G Missense p.M1102I c.3306G>C 15 42736446 BRCA C G Missense p.M374I c.1122G>C 15 42743279 BRCA C T Missense p.D137N c.409G>A 15 42743992 CM C T Missense p.D1686N c.5056G>A 15 42717097 BRCA C T Missense p.D1686N c.5056G>A 15 42717097 STAD C T Missense p.E627K c.1879G>A 15 42742522 OV C T Missense p.E792K c.2374G>A 15 42742027 LUSC C T Missense p.G1488D c.4463G>A 15 42731243 BLCA C T Missense p.R1873Q c.5618G>A 15 42709536 COREAD C T Missense p.S1419N c.4256G>A 15 42731450 PRAD C T Nonsense p.W349* c.1047G>A 15 42743354 STAD C T Synonymous p.E1210E c.3630G>A 15 42734335 HNSC G A Missense p.A341V c.1022C>T 15 42743379 CM G A Missense p.P1239L c.3716C>T 15 42731990 CM G A Missense p.P401S c.1201C>T 15 42743200 CM G A Missense p.P453S c.1357C>T 15 42743044 CM G A Missense p.P456S c.1366C>T 15 42743035 CM G A Missense p.P469L c.1406C>T 15 42742995 LGG G A Missense p.P501S c.1501C>T 15 42742900 COREAD G A Missense p.S1057F c.3170C>T 15 42737146 CM G A Missense p.S419F c.1256C>T 15 42743145 CM G A Missense p.S504F c.1511C>T 15 42742890 PRAD G A Missense p.S688F c.2063C>T 15 42742338 HNSC G A Missense p.S970F c.2909C>T 15 42740427 CM G A Missense p.T1858I c.5573C>T 15 42710025 CM G A Missense p.T606I c.1817C>T 15 42742584 CM G A Nonsense p.Q1198* c.3592C>T 15 42734373 BRCA G A Nonsense p.Q465* c.1393C>T 15 42743008 CM G A Nonsense p.R764* c.2290C>T 15 42742111 STAD G A Nonsense p.R83* c.247C>T 15 42749157 BRCA G A Synonymous p.C1853C c.5559C>T 15 42710039 LUSC G A Synonymous p.C432C c.1296C>T 15 42743105 CM G A Synonymous p.G138G c.414C>T 15 42743987 BRCA G A Synonymous p.G1655G c.4965C>T 15 42717188 CM G A Synonymous p.H663H c.1989C>T 15 42742412 RCCC G A Synonymous p.L1619L c.4857C>T 15 42720288 UCEC G A Synonymous p.L358L c.1072C>T 15 42743329 HNSC G A Synonymous p.S482S c.1446C>T 15 42742955 CM G C Missense p.D286E c.858C>G 15 42743543 CM G C Missense p.D98E c.294C>G 15 42744107 SCLC G C Missense p.H176D c.526C>G 15 42743875 HNSC G C Missense p.L414V c.1240C>G 15 42743161 HNSC G C Missense p.Q355E c.1063C>G 15 42743338 HNSC G C Missense p.S850W c.2549C>G 15 42740787 BRCA G C Synonymous p.P489P c.1467C>G 15 42742934 LUAD GG AA Missense p.R922* c.2763_2764delinsTT 15 42740572 CM G T Missense p.P307H c.920C>A 15 42743481 STAD G T Synonymous p.S851S c.2553C>A 15 42740783 PRAD G T Synonymous p.T559T c.1677C>A 15 42742724 LUSC T A Missense p.R5S c.15A>T 15 42749389 BRCA T A Missense p.S116C c.346A>T 15 42744055 RCCC T A Nonsense p.K371* c.1111A>T 15 42743290 CM T A Nonsense p.R636* c.1906A>T 15 42742495 LUSC T C Missense p.D700G c.2099A>G 15 42742302 COREAD T C Missense p.K477E c.1429A>G 15 42742972 CM T C Missense p.N1211S c.3632A>G 15 42734333 OV T C Missense p.R1015G c.3043A>G 15 42740293 SCLC T C Synonymous p.K515K c.1545A>G 15 42742856 CM T C Synonymous p.T657T c.1971A>G 15 42742430 LUSC T G IntronicSNV . c.3694+145A>C 15 42734126 HC T G Missense p.K1760T c.5279A>C 15 42714724 UCEC T G Missense p.K417T c.1250A>C 15 42743151 MM T G Synonymous p.P1516P c.4548A>C 15 42729559 LUAD A C Missense p.K265T c.794A>C 5 121488479 LUAD A C Missense p.N49H c.145A>C 5 121487830 BRCA A C Missense p.Y329S c.986A>C 5 121488671 SCLC A G Missense p.T295A c.883A>G 5 121488568 SCLC C A 3-UTRSNV . c.1092+427C>A 5 121489204 MB C A Missense p.L165M c.493C>A 5 121488178 STAD C A Missense p.L68I c.202C>A 5 121487887 LUAD C A Missense p.P43T c.127C>A 5 121487812 LUAD CC TT Missense p.L269F c.804_805delinsTT 5 121488489 CM C T Missense p.H239Y c.715C>T 5 121488400 CM C T Missense p.P268L c.803C>T 5 121488488 CM C T Missense p.P50S c.148C>T 5 121487833 CM C T Missense p.R298C c.892C>T 5 121488577 COREAD C T Missense p.S235F c.704C>T 5 121488389 CM C T Synonymous p.G101G c.303C>T 5 121487988 CM C T Synonymous p.G207G c.621C>T 5 121488306 STAD C T Synonymous p.I87I c.261C>T 5 121487946 CM C T Synonymous p.L244L c.730C>T 5 121488415 CM C T Synonymous p.S235S c.705C>T 5 121488390 CM G A IntronicSNV . c.1-8757G>A 5 121478929 CLL G A Missense p.V343I c.1027G>A 5 121488712 CM G A Missense p.V347I c.1039G>A 5 121488724 CM G A Synonymous p.L244L c.732G>A 5 121488417 CM G A Synonymous p.Q162Q c.486G>A 5 121488171 CM G A Synonymous p.Q316Q c.948G>A 5 121488633 CM G C Missense p.L131F c.393G>C 5 121488078 HNSC T A Synonymous p.P310P c.930T>A 5 121488615 STAD T C 3-UTRSNV . c.1092+174T>C 5 121488951 MB T G Missense p.C171W c.513T>G 5 121488198 LUAD T G Missense p.L181R c.542T>G 5 121488227 UCEC TGTGGAGCTCCA - InFrameDeletion p.V256_H259delVELH c.765_776delTGTGGAGCTCCA 5 121488450 RCCC