Mutation - TCGA Type Chromosome Start Position End Position Strand Variant Classification Variant Type Reference Allele Tumor_seq Allele 1 Tumor_seq Allele 2 Tumor Sample Barcode Matched Norm Sample Barcode Genome Change cDNA Change Codon Change Protein Change ACC 15 74315257 74315257 + Missense_Mutation SNP G G A TCGA-OR-A5LB-01A-11D-A29I-10 TCGA-OR-A5LB-10A-01D-A29L-10 g.chr15:74315257G>A c.691G>A c.(691-693)Gca>Aca p.A231T ACC 15 74315308 74315308 + Nonsense_Mutation SNP C C T TCGA-OR-A5LB-01A-11D-A29I-10 TCGA-OR-A5LB-10A-01D-A29L-10 g.chr15:74315308C>T c.742C>T c.(742-744)Cag>Tag p.Q248* ACC 15 74335395 74335395 + Silent SNP C C T TCGA-OR-A5LL-01A-11D-A29I-10 TCGA-OR-A5LL-10A-01D-A29L-10 g.chr15:74335395C>T c.1776C>T c.(1774-1776)acC>acT p.T592T BLCA 15 74290639 74290639 + Missense_Mutation SNP G G C TCGA-DK-A1A5-01A-11D-A13W-08 TCGA-DK-A1A5-10A-01D-A13W-08 g.chr15:74290639G>C c.424G>C c.(424-426)Gag>Cag p.E142Q BLCA 15 74290715 74290715 + Missense_Mutation SNP C C G TCGA-K4-A5RH-01A-11D-A30E-08 TCGA-K4-A5RH-10A-01D-A30H-08 g.chr15:74290715C>G c.500C>G c.(499-501)gCa>gGa p.A167G BLCA 15 74315653 74315653 + Missense_Mutation SNP G G A TCGA-DK-A1A7-01A-11D-A13W-08 TCGA-DK-A1A7-10A-01D-A13W-08 g.chr15:74315653G>A c.1087G>A c.(1087-1089)Gag>Aag p.E363K BLCA 15 74315653 74315653 + Missense_Mutation SNP G G A TCGA-XF-A9SY-01A-21D-A42E-08 TCGA-XF-A9SY-10A-01D-A42H-08 g.chr15:74315653G>A c.1087G>A c.(1087-1089)Gag>Aag p.E363K BLCA 15 74326907 74326908 + Intron INS - - T TCGA-4Z-AA7Q-01A-11D-A391-08 TCGA-4Z-AA7Q-10A-01D-A394-08 g.chr15:74326907_74326908insT BLCA 15 74327519 74327519 + Intron SNP G G A TCGA-XF-AAMG-01A-11D-A42E-08 TCGA-XF-AAMG-10A-01D-A42H-08 g.chr15:74327519G>A BLCA 15 74327530 74327530 + Intron SNP G G A TCGA-LT-A5Z6-01A-11D-A289-08 TCGA-LT-A5Z6-10A-01D-A289-08 g.chr15:74327530G>A BLCA 15 74327616 74327616 + Intron SNP G G C TCGA-XF-AAMQ-01A-11D-A42E-08 TCGA-XF-AAMQ-10A-01D-A42H-08 g.chr15:74327616G>C BLCA 15 74327888 74327888 + Intron SNP C C G TCGA-MV-A51V-01A-11D-A26M-08 TCGA-MV-A51V-10A-01D-A26K-08 g.chr15:74327888C>G BLCA 15 74328185 74328185 + Intron SNP C C G TCGA-MV-A51V-01A-11D-A26M-08 TCGA-MV-A51V-10A-01D-A26K-08 g.chr15:74328185C>G BLCA 15 74328369 74328369 + Intron SNP C C G TCGA-XF-A9T8-01A-11D-A391-08 TCGA-XF-A9T8-10A-01D-A394-08 g.chr15:74328369C>G BLCA 15 74336846 74336846 + Missense_Mutation SNP G G A TCGA-ZF-AA4N-01A-11D-A38G-08 TCGA-ZF-AA4N-10A-01D-A38J-08 g.chr15:74336846G>A c.2146G>A c.(2146-2148)Gag>Aag p.E716K BLCA 15 74336951 74336951 + Missense_Mutation SNP C C T TCGA-FD-A43X-01A-11D-A23U-08 TCGA-FD-A43X-10A-01D-A23U-08 g.chr15:74336951C>T c.2251C>T c.(2251-2253)Cgt>Tgt p.R751C BLCA 15 74336969 74336969 + Missense_Mutation SNP C C T TCGA-DK-A1A3-01A-11D-A13W-08 TCGA-DK-A1A3-10A-01D-A13W-08 g.chr15:74336969C>T c.2269C>T c.(2269-2271)Ctc>Ttc p.L757F BRCA 15 74317242 74317242 + Missense_Mutation SNP C C G TCGA-D8-A1JA-01A-11D-A13L-09 TCGA-D8-A1JA-10A-01W-A14R-09 g.chr15:74317242C>G c.1228C>G c.(1228-1230)Ccc>Gcc p.P410A BRCA 15 74324915 74324915 + Silent SNP C C T TCGA-AN-A0XW-01A-11D-A10G-09 TCGA-AN-A0XW-10A-01D-A10G-09 g.chr15:74324915C>T c.1257C>T c.(1255-1257)ccC>ccT p.P419P BRCA 15 74327676 74327676 + Intron SNP A A C TCGA-A8-A0A6-01A-12W-A071-09 TCGA-A8-A0A6-10A-01W-A071-09 g.chr15:74327676A>C BRCA 15 74328401 74328401 + Intron SNP A A G TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr15:74328401A>G CESC 15 74287202 74287202 + Missense_Mutation SNP C C T TCGA-Q1-A5R3-01A-11D-A28B-09 TCGA-Q1-A5R3-10B-01D-A28E-09 g.chr15:74287202C>T c.49C>T c.(49-51)Cgg>Tgg p.R17W CESC 15 74290717 74290717 + Missense_Mutation SNP G G A TCGA-JX-A3Q0-01A-11D-A21Q-09 TCGA-JX-A3Q0-10A-01D-A21Q-09 g.chr15:74290717G>A c.502G>A c.(502-504)Gag>Aag p.E168K CESC 15 74315241 74315241 + Silent SNP C C G TCGA-LP-A4AV-01A-11D-A243-09 TCGA-LP-A4AV-10A-01D-A243-09 g.chr15:74315241C>G c.675C>G c.(673-675)ctC>ctG p.L225L CESC 15 74315461 74315461 + Missense_Mutation SNP G G C TCGA-DR-A0ZM-01A-12D-A10S-08 TCGA-DR-A0ZM-10A-01D-A10S-08 g.chr15:74315461G>C c.895G>C c.(895-897)Gag>Cag p.E299Q CESC 15 74315539 74315539 + Missense_Mutation SNP C C T TCGA-C5-A1M5-01A-11D-A13W-08 TCGA-C5-A1M5-10A-01D-A13W-08 g.chr15:74315539C>T c.973C>T c.(973-975)Cgc>Tgc p.R325C CESC 15 74328176 74328176 + Intron SNP G G A TCGA-JW-A5VL-01A-11D-A28B-09 TCGA-JW-A5VL-10A-01D-A28E-09 g.chr15:74328176G>A CESC 15 74336918 74336918 + Missense_Mutation SNP G G A TCGA-MY-A5BD-01A-11D-A26G-09 TCGA-MY-A5BD-10A-01D-A26G-09 g.chr15:74336918G>A c.2218G>A c.(2218-2220)Gag>Aag p.E740K COAD 15 74290416 74290416 + Silent SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr15:74290416G>A c.201G>A c.(199-201)ccG>ccA p.P67P COAD 15 74290480 74290480 + Missense_Mutation SNP C C A TCGA-AA-3672-01A-01W-0900-09 TCGA-AA-3672-10A-01W-0900-09 g.chr15:74290480C>A c.265C>A c.(265-267)Ccc>Acc p.P89T COAD 15 74290566 74290566 + Silent SNP G G A TCGA-D5-6533-01A-11D-1719-10 TCGA-D5-6533-10A-01D-1719-10 g.chr15:74290566G>A c.351G>A c.(349-351)tcG>tcA p.S117S COAD 15 74290566 74290566 + Silent SNP G G T TCGA-DM-A1HB-01A-21D-A183-10 TCGA-DM-A1HB-10A-01D-A183-10 g.chr15:74290566G>T c.351G>T c.(349-351)tcG>tcT p.S117S COAD 15 74290573 74290573 + Missense_Mutation SNP C C T TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr15:74290573C>T c.358C>T c.(358-360)Cgg>Tgg p.R120W COAD 15 74290798 74290798 + Missense_Mutation SNP C C T TCGA-CA-6715-01A-21D-1835-10 TCGA-CA-6715-10A-01D-1835-10 g.chr15:74290798C>T c.583C>T c.(583-585)Cgc>Tgc p.R195C COAD 15 74315196 74315196 + Silent SNP G G T TCGA-AA-3844-01A-01W-0995-10 TCGA-AA-3844-10A-01W-0995-10 g.chr15:74315196G>T c.630G>T c.(628-630)ccG>ccT p.P210P COAD 15 74315644 74315644 + Missense_Mutation SNP C C T TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chr15:74315644C>T c.1078C>T c.(1078-1080)Cgc>Tgc p.R360C COAD 15 74315741 74315742 + Frame_Shift_Ins INS - - G TCGA-DM-A1HB-01A-21D-A183-10 TCGA-DM-A1HB-10A-01D-A183-10 g.chr15:74315741_74315742insG c.1175_1176insG c.(1174-1179)caggggfs p.QG392fs COAD 15 74317244 74317244 + Silent SNP C C T TCGA-AA-3680-01A-01W-0900-09 TCGA-AA-3680-10A-01W-0900-09 g.chr15:74317244C>T c.1230C>T c.(1228-1230)ccC>ccT p.P410P COAD 15 74324939 74324939 + Silent SNP C C T TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr15:74324939C>T c.1281C>T c.(1279-1281)gcC>gcT p.A427A COAD 15 74326826 74326826 + Silent SNP C C T TCGA-AU-6004-01A-11D-1719-10 TCGA-AU-6004-10A-01D-1719-10 g.chr15:74326826C>T c.1665C>T c.(1663-1665)cgC>cgT p.R555R COAD 15 74327568 74327568 + Intron SNP C C T TCGA-G4-6315-01A-11D-1719-10 TCGA-G4-6315-10A-01D-1720-10 g.chr15:74327568C>T COAD 15 74327802 74327802 + Intron SNP G G A TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr15:74327802G>A COAD 15 74336601 74336601 + Missense_Mutation SNP G G T TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr15:74336601G>T c.1901G>T c.(1900-1902)aGc>aTc p.S634I COAD 15 74336708 74336708 + Missense_Mutation SNP C C T TCGA-F4-6856-01A-11D-1924-10 TCGA-F4-6856-10A-01D-1924-10 g.chr15:74336708C>T c.2008C>T c.(2008-2010)Cgc>Tgc p.R670C COAD 15 74336903 74336903 + Missense_Mutation SNP G G A TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr15:74336903G>A c.2203G>A c.(2203-2205)Gcg>Acg p.A735T COADREAD 15 74290416 74290416 + Silent SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr15:74290416G>A c.201G>A c.(199-201)ccG>ccA p.P67P COADREAD 15 74290480 74290480 + Missense_Mutation SNP C C A TCGA-AA-3672-01A-01W-0900-09 TCGA-AA-3672-10A-01W-0900-09 g.chr15:74290480C>A c.265C>A c.(265-267)Ccc>Acc p.P89T COADREAD 15 74290566 74290566 + Silent SNP G G A TCGA-D5-6533-01A-11D-1719-10 TCGA-D5-6533-10A-01D-1719-10 g.chr15:74290566G>A c.351G>A c.(349-351)tcG>tcA p.S117S COADREAD 15 74290566 74290566 + Silent SNP G G T TCGA-DM-A1HB-01A-21D-A183-10 TCGA-DM-A1HB-10A-01D-A183-10 g.chr15:74290566G>T c.351G>T c.(349-351)tcG>tcT p.S117S COADREAD 15 74290573 74290573 + Missense_Mutation SNP C C T TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr15:74290573C>T c.358C>T c.(358-360)Cgg>Tgg p.R120W COADREAD 15 74290798 74290798 + Missense_Mutation SNP C C T TCGA-CA-6715-01A-21D-1835-10 TCGA-CA-6715-10A-01D-1835-10 g.chr15:74290798C>T c.583C>T c.(583-585)Cgc>Tgc p.R195C COADREAD 15 74315196 74315196 + Silent SNP G G T TCGA-AA-3844-01A-01W-0995-10 TCGA-AA-3844-10A-01W-0995-10 g.chr15:74315196G>T c.630G>T c.(628-630)ccG>ccT p.P210P COADREAD 15 74315644 74315644 + Missense_Mutation SNP C C T TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chr15:74315644C>T c.1078C>T c.(1078-1080)Cgc>Tgc p.R360C COADREAD 15 74315741 74315742 + Frame_Shift_Ins INS - - G TCGA-DM-A1HB-01A-21D-A183-10 TCGA-DM-A1HB-10A-01D-A183-10 g.chr15:74315741_74315742insG c.1175_1176insG c.(1174-1179)caggggfs p.QG392fs COADREAD 15 74317244 74317244 + Silent SNP C C T TCGA-AA-3680-01A-01W-0900-09 TCGA-AA-3680-10A-01W-0900-09 g.chr15:74317244C>T c.1230C>T c.(1228-1230)ccC>ccT p.P410P COADREAD 15 74324939 74324939 + Silent SNP C C T TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr15:74324939C>T c.1281C>T c.(1279-1281)gcC>gcT p.A427A COADREAD 15 74326826 74326826 + Silent SNP C C T TCGA-AU-6004-01A-11D-1719-10 TCGA-AU-6004-10A-01D-1719-10 g.chr15:74326826C>T c.1665C>T c.(1663-1665)cgC>cgT p.R555R COADREAD 15 74326969 74326969 + Intron SNP G G A TCGA-AG-3901-01A-01W-1073-09 TCGA-AG-3901-10A-01W-1073-09 g.chr15:74326969G>A COADREAD 15 74327568 74327568 + Intron SNP C C T TCGA-G4-6315-01A-11D-1719-10 TCGA-G4-6315-10A-01D-1720-10 g.chr15:74327568C>T COADREAD 15 74327802 74327802 + Intron SNP G G A TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr15:74327802G>A COADREAD 15 74336601 74336601 + Missense_Mutation SNP G G T TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr15:74336601G>T c.1901G>T c.(1900-1902)aGc>aTc p.S634I COADREAD 15 74336708 74336708 + Missense_Mutation SNP C C T TCGA-F4-6856-01A-11D-1924-10 TCGA-F4-6856-10A-01D-1924-10 g.chr15:74336708C>T c.2008C>T c.(2008-2010)Cgc>Tgc p.R670C COADREAD 15 74336903 74336903 + Missense_Mutation SNP G G A TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr15:74336903G>A c.2203G>A c.(2203-2205)Gcg>Acg p.A735T ESCA 15 74290730 74290730 + Missense_Mutation SNP A A T TCGA-XP-A8T8-01A-11D-A36J-09 TCGA-XP-A8T8-10A-01D-A36M-09 g.chr15:74290730A>T c.515A>T c.(514-516)cAg>cTg p.Q172L ESCA 15 74327656 74327656 + Intron DEL C C - TCGA-L5-A8NM-01A-11D-A37C-09 TCGA-L5-A8NM-11A-12D-A37F-09 g.chr15:74327656delC ESCA 15 74335355 74335355 + Missense_Mutation SNP G G T TCGA-VR-A8EQ-01A-11D-A36J-09 TCGA-VR-A8EQ-10A-01D-A36M-09 g.chr15:74335355G>T c.1736G>T c.(1735-1737)aGc>aTc p.S579I ESCA 15 74335396 74335396 + Missense_Mutation SNP C C A TCGA-L5-A43J-01A-12D-A247-09 TCGA-L5-A43J-11A-11D-A247-09 g.chr15:74335396C>A c.1777C>A c.(1777-1779)Ctc>Atc p.L593I ESCA 15 74335500 74335500 + Intron DEL C C - TCGA-S8-A6BV-01A-21D-A31U-09 TCGA-S8-A6BV-10A-01D-A31U-09 g.chr15:74335500delC ESCA 15 74336717 74336717 + Missense_Mutation SNP A A G TCGA-LN-A49N-01A-11D-A247-09 TCGA-LN-A49N-10A-01D-A247-09 g.chr15:74336717A>G c.2017A>G c.(2017-2019)Atc>Gtc p.I673V GBM 15 74315385 74315385 + Silent SNP C C T TCGA-06-0173-01A-01D-1491-08 TCGA-06-0173-10B-01D-1491-08 g.chr15:74315385C>T c.819C>T c.(817-819)gcC>gcT p.A273A GBMLGG 15 74290533 74290533 + Silent SNP C C T TCGA-HT-A5R9-01A-11D-A289-08 TCGA-HT-A5R9-10A-01D-A289-08 g.chr15:74290533C>T c.318C>T c.(316-318)aaC>aaT p.N106N GBMLGG 15 74290723 74290723 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr15:74290723C>T c.508C>T c.(508-510)Cgc>Tgc p.R170C GBMLGG 15 74315324 74315324 + Missense_Mutation SNP C C A TCGA-HT-8104-01A-11D-2395-08 TCGA-HT-8104-10A-01D-2396-08 g.chr15:74315324C>A c.758C>A c.(757-759)gCc>gAc p.A253D GBMLGG 15 74315385 74315385 + Silent SNP C C T TCGA-06-0173-01A-01D-1491-08 TCGA-06-0173-10B-01D-1491-08 g.chr15:74315385C>T c.819C>T c.(817-819)gcC>gcT p.A273A GBMLGG 15 74328199 74328199 + Intron SNP T T C TCGA-VM-A8CB-01A-11D-A36O-08 TCGA-VM-A8CB-10A-01D-A367-08 g.chr15:74328199T>C GBMLGG 15 74337240 74337240 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr15:74337240G>T c.2540G>T c.(2539-2541)gGc>gTc p.G847V HNSC 15 74290542 74290542 + Silent SNP C C T TCGA-CN-A49B-01A-31D-A24D-08 TCGA-CN-A49B-10A-01D-A24F-08 g.chr15:74290542C>T c.327C>T c.(325-327)ttC>ttT p.F109F HNSC 15 74325651 74325651 + Missense_Mutation SNP C C T TCGA-CV-7427-01A-11D-2078-08 TCGA-CV-7427-10A-01D-2078-08 g.chr15:74325651C>T c.1553C>T c.(1552-1554)tCa>tTa p.S518L HNSC 15 74327691 74327691 + Intron SNP A A T TCGA-BA-A6DL-01A-21D-A30E-08 TCGA-BA-A6DL-10A-01D-A30H-08 g.chr15:74327691A>T HNSC 15 74327717 74327717 + Intron SNP C C T TCGA-T3-A92N-01A-11D-A391-08 TCGA-T3-A92N-10A-01D-A394-08 g.chr15:74327717C>T HNSC 15 74327753 74327753 + Intron SNP G G A TCGA-UF-A719-01A-12D-A34J-08 TCGA-UF-A719-10A-01D-A34M-08 g.chr15:74327753G>A HNSC 15 74328064 74328064 + Intron SNP C C T TCGA-T3-A92N-01A-11D-A391-08 TCGA-T3-A92N-10A-01D-A394-08 g.chr15:74328064C>T HNSC 15 74328212 74328212 + Intron SNP C C G TCGA-T3-A92N-01A-11D-A391-08 TCGA-T3-A92N-10A-01D-A394-08 g.chr15:74328212C>G HNSC 15 74328369 74328369 + Intron SNP C C G TCGA-CQ-5334-01A-01D-1683-08 TCGA-CQ-5334-10A-01D-1683-08 g.chr15:74328369C>G KICH 15 74315583 74315583 + Silent SNP C C T TCGA-KN-8428-01A-11D-2310-10 TCGA-KN-8428-11A-01D-2311-10 g.chr15:74315583C>T c.1017C>T c.(1015-1017)taC>taT p.Y339Y KICH 15 74327978 74327978 + Intron SNP C C T TCGA-KN-8428-01A-11D-2310-10 TCGA-KN-8428-11A-01D-2311-10 g.chr15:74327978C>T KIPAN 15 74315345 74315345 + Missense_Mutation SNP A A C TCGA-P4-AAVM-01A-11D-A42J-10 TCGA-P4-AAVM-11A-11D-A42M-10 g.chr15:74315345A>C c.779A>C c.(778-780)cAg>cCg p.Q260P KIPAN 15 74315449 74315449 + Missense_Mutation SNP C C T TCGA-B0-5098-01A-01D-1421-08 TCGA-B0-5098-11A-01D-1421-08 g.chr15:74315449C>T c.883C>T c.(883-885)Cgc>Tgc p.R295C KIPAN 15 74315583 74315583 + Silent SNP C C T TCGA-KN-8428-01A-11D-2310-10 TCGA-KN-8428-11A-01D-2311-10 g.chr15:74315583C>T c.1017C>T c.(1015-1017)taC>taT p.Y339Y KIPAN 15 74325643 74325643 + Silent SNP G G A TCGA-B1-A657-01A-11D-A31X-10 TCGA-B1-A657-10A-01D-A31X-10 g.chr15:74325643G>A c.1545G>A c.(1543-1545)aaG>aaA p.K515K KIPAN 15 74327953 74327953 + Intron SNP G G A TCGA-GL-7773-01A-11D-2136-08 TCGA-GL-7773-10A-01D-2136-08 g.chr15:74327953G>A KIPAN 15 74327978 74327978 + Intron SNP C C T TCGA-KN-8428-01A-11D-2310-10 TCGA-KN-8428-11A-01D-2311-10 g.chr15:74327978C>T KIPAN 15 74336686 74336686 + Missense_Mutation SNP C C G TCGA-A3-3326-01A-01D-0966-08 TCGA-A3-3326-11A-01D-0966-08 g.chr15:74336686C>G c.1986C>G c.(1984-1986)ttC>ttG p.F662L KIRC 15 74315449 74315449 + Missense_Mutation SNP C C T TCGA-B0-5098-01A-01D-1421-08 TCGA-B0-5098-11A-01D-1421-08 g.chr15:74315449C>T c.883C>T c.(883-885)Cgc>Tgc p.R295C KIRC 15 74336686 74336686 + Missense_Mutation SNP C C G TCGA-A3-3326-01A-01D-0966-08 TCGA-A3-3326-11A-01D-0966-08 g.chr15:74336686C>G c.1986C>G c.(1984-1986)ttC>ttG p.F662L KIRP 15 74315345 74315345 + Missense_Mutation SNP A A C TCGA-P4-AAVM-01A-11D-A42J-10 TCGA-P4-AAVM-11A-11D-A42M-10 g.chr15:74315345A>C c.779A>C c.(778-780)cAg>cCg p.Q260P KIRP 15 74325643 74325643 + Silent SNP G G A TCGA-B1-A657-01A-11D-A31X-10 TCGA-B1-A657-10A-01D-A31X-10 g.chr15:74325643G>A c.1545G>A c.(1543-1545)aaG>aaA p.K515K KIRP 15 74327953 74327953 + Intron SNP G G A TCGA-GL-7773-01A-11D-2136-08 TCGA-GL-7773-10A-01D-2136-08 g.chr15:74327953G>A LGG 15 74290533 74290533 + Silent SNP C C T TCGA-HT-A5R9-01A-11D-A289-08 TCGA-HT-A5R9-10A-01D-A289-08 g.chr15:74290533C>T c.318C>T c.(316-318)aaC>aaT p.N106N LGG 15 74290723 74290723 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr15:74290723C>T c.508C>T c.(508-510)Cgc>Tgc p.R170C LGG 15 74315324 74315324 + Missense_Mutation SNP C C A TCGA-HT-8104-01A-11D-2395-08 TCGA-HT-8104-10A-01D-2396-08 g.chr15:74315324C>A c.758C>A c.(757-759)gCc>gAc p.A253D LGG 15 74328199 74328199 + Intron SNP T T C TCGA-VM-A8CB-01A-11D-A36O-08 TCGA-VM-A8CB-10A-01D-A367-08 g.chr15:74328199T>C LGG 15 74337240 74337240 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr15:74337240G>T c.2540G>T c.(2539-2541)gGc>gTc p.G847V LIHC 15 74324992 74324992 + Nonsense_Mutation SNP C C G TCGA-DD-AADI-01A-11D-A40R-10 TCGA-DD-AADI-10A-01D-A40U-10 g.chr15:74324992C>G c.1334C>G c.(1333-1335)tCa>tGa p.S445* LIHC 15 74327563 74327563 + Intron SNP C C A TCGA-EP-A2KA-01A-11D-A183-10 TCGA-EP-A2KA-10A-01D-A183-10 g.chr15:74327563C>A LIHC 15 74328285 74328285 + Intron SNP G G T TCGA-CC-A8HV-01A-11D-A35Z-10 TCGA-CC-A8HV-10A-01D-A35Z-10 g.chr15:74328285G>T LIHC 15 74337203 74337203 + Frame_Shift_Del DEL C C - TCGA-4R-AA8I-01A-11D-A382-10 TCGA-4R-AA8I-10B-01D-A385-10 g.chr15:74337203delC c.2503delC c.(2503-2505)cccfs p.P836fs LUAD 15 74290522 74290522 + Missense_Mutation SNP G G T TCGA-91-6828-01A-11D-1855-08 TCGA-91-6828-10A-01D-1855-08 g.chr15:74290522G>T c.307G>T c.(307-309)Gcc>Tcc p.A103S LUAD 15 74290568 74290568 + Missense_Mutation SNP T T A TCGA-17-Z031-01A-01W-0746-08 TCGA-17-Z031-11A-01W-0746-08 g.chr15:74290568T>A c.353T>A c.(352-354)gTg>gAg p.V118E LUAD 15 74290784 74290784 + Missense_Mutation SNP C C G TCGA-86-8073-01A-11D-2238-08 TCGA-86-8073-10A-01D-2238-08 g.chr15:74290784C>G c.569C>G c.(568-570)tCc>tGc p.S190C LUAD 15 74315342 74315342 + Missense_Mutation SNP C C T TCGA-55-A4DG-01A-11D-A24D-08 TCGA-55-A4DG-10A-01D-A24F-08 g.chr15:74315342C>T c.776C>T c.(775-777)gCg>gTg p.A259V LUAD 15 74315359 74315359 + Missense_Mutation SNP G G T TCGA-78-7155-01A-11D-2036-08 TCGA-78-7155-10A-01D-2036-08 g.chr15:74315359G>T c.793G>T c.(793-795)Gtc>Ttc p.V265F LUAD 15 74315475 74315475 + Silent SNP G G T TCGA-05-4427-01A-21D-1855-08 TCGA-05-4427-10A-01D-1855-08 g.chr15:74315475G>T c.909G>T c.(907-909)gcG>gcT p.A303A LUAD 15 74315631 74315631 + Silent SNP G G T TCGA-55-A492-01A-11D-A24D-08 TCGA-55-A492-10A-01D-A24F-08 g.chr15:74315631G>T c.1065G>T c.(1063-1065)gcG>gcT p.A355A LUAD 15 74315681 74315681 + Missense_Mutation SNP G G T TCGA-99-8028-01A-11D-2238-08 TCGA-99-8028-10A-01D-2238-08 g.chr15:74315681G>T c.1115G>T c.(1114-1116)cGc>cTc p.R372L LUAD 15 74324920 74324920 + Missense_Mutation SNP A A T TCGA-78-7220-01A-11D-2036-08 TCGA-78-7220-10A-01D-2036-08 g.chr15:74324920A>T c.1262A>T c.(1261-1263)gAg>gTg p.E421V LUAD 15 74325578 74325578 + Nonsense_Mutation SNP G G T TCGA-91-6840-01A-11D-1945-08 TCGA-91-6840-10A-01D-1946-08 g.chr15:74325578G>T c.1480G>T c.(1480-1482)Gag>Tag p.E494* LUAD 15 74326883 74326883 + Intron SNP A A G TCGA-97-7546-01A-11D-2036-08 TCGA-97-7546-10A-01D-2036-08 g.chr15:74326883A>G LUAD 15 74328003 74328003 + Intron SNP G G T TCGA-69-7974-01A-11D-2184-08 TCGA-69-7974-10A-01D-2184-08 g.chr15:74328003G>T LUAD 15 74328155 74328155 + Intron SNP G G T TCGA-50-5946-01A-11D-1753-08 TCGA-50-5946-10A-01D-1753-08 g.chr15:74328155G>T LUAD 15 74328242 74328242 + Intron SNP G G A TCGA-78-7158-01A-11D-2036-08 TCGA-78-7158-10A-01D-2036-08 g.chr15:74328242G>A LUAD 15 74337110 74337110 + Missense_Mutation SNP A A G TCGA-35-4122-01A-01D-1105-08 TCGA-35-4122-10A-01D-1105-08 g.chr15:74337110A>G c.2410A>G c.(2410-2412)Agc>Ggc p.S804G LUAD 15 74337262 74337262 + Missense_Mutation SNP G G C TCGA-17-Z049-01A-01W-0746-08 TCGA-17-Z049-11A-01W-0747-08 g.chr15:74337262G>C c.2562G>C c.(2560-2562)ttG>ttC p.L854F LUAD 15 74337270 74337270 + Missense_Mutation SNP C C T TCGA-50-5049-01A-01D-1625-08 TCGA-50-5049-10A-01D-1625-08 g.chr15:74337270C>T c.2570C>T c.(2569-2571)cCg>cTg p.P857L LUAD 15 74337282 74337282 + Missense_Mutation SNP G G T TCGA-55-7281-01A-11D-2036-08 TCGA-55-7281-10A-01D-2036-08 g.chr15:74337282G>T c.2582G>T c.(2581-2583)cGg>cTg p.R861L LUSC 15 74326832 74326832 + Silent SNP G G T TCGA-66-2734-01A-01D-0983-08 TCGA-66-2734-11A-01D-0983-08 g.chr15:74326832G>T c.1671G>T c.(1669-1671)gtG>gtT p.V557V PAAD 15 74315645 74315645 + Missense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr15:74315645G>A c.1079G>A c.(1078-1080)cGc>cAc p.R360H PAAD 15 74325728 74325728 + Missense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr15:74325728C>T c.1630C>T c.(1630-1632)Cac>Tac p.H544Y PCPG 15 74336715 74336715 + Missense_Mutation SNP C C G TCGA-SQ-A6I4-01A-11D-A35I-08 TCGA-SQ-A6I4-10A-01D-A35G-08 g.chr15:74336715C>G c.2015C>G c.(2014-2016)cCt>cGt p.P672R PRAD 15 74327550 74327550 + Intron SNP C C T TCGA-KK-A59V-01A-11D-A29Q-08 TCGA-KK-A59V-11A-11D-A29Q-08 g.chr15:74327550C>T PRAD 15 74335504 74335504 + Intron SNP C C T TCGA-KK-A59V-01A-11D-A29Q-08 TCGA-KK-A59V-11A-11D-A29Q-08 g.chr15:74335504C>T PRAD 15 74336765 74336765 + Missense_Mutation SNP C C T TCGA-KK-A6DY-01A-12D-A30X-08 TCGA-KK-A6DY-11A-11D-A30X-08 g.chr15:74336765C>T c.2065C>T c.(2065-2067)Cgg>Tgg p.R689W READ 15 74326969 74326969 + Intron SNP G G A TCGA-AG-3901-01A-01W-1073-09 TCGA-AG-3901-10A-01W-1073-09 g.chr15:74326969G>A SARC 15 74290386 74290386 + Silent SNP C C T TCGA-DX-A23R-01A-11D-A26G-09 TCGA-DX-A23R-10A-01D-A26G-09 g.chr15:74290386C>T c.171C>T c.(169-171)tgC>tgT p.C57C SARC 15 74315216 74315216 + Missense_Mutation SNP T T A TCGA-IS-A3K6-01A-11D-A21Q-09 TCGA-IS-A3K6-10A-01D-A21Q-09 g.chr15:74315216T>A c.650T>A c.(649-651)cTc>cAc p.L217H SKCM 15 74290467 74290467 + Silent SNP G G A TCGA-EE-A17X-06A-11D-A197-08 TCGA-EE-A17X-10A-01D-A199-08 g.chr15:74290467G>A c.252G>A c.(250-252)tcG>tcA p.S84S SKCM 15 74290542 74290542 + Silent SNP C C T TCGA-FS-A1ZC-06A-11D-A197-08 TCGA-FS-A1ZC-10A-01D-A199-08 g.chr15:74290542C>T c.327C>T c.(325-327)ttC>ttT p.F109F SKCM 15 74290560 74290560 + Silent SNP C C T TCGA-D9-A148-06A-11D-A19A-08 TCGA-D9-A148-10A-01D-A19A-08 g.chr15:74290560C>T c.345C>T c.(343-345)cgC>cgT p.R115R SKCM 15 74325046 74325046 + Missense_Mutation SNP C C T TCGA-DA-A1HV-06A-21D-A196-08 TCGA-DA-A1HV-10A-01D-A198-08 g.chr15:74325046C>T c.1388C>T c.(1387-1389)tCc>tTc p.S463F SKCM 15 74326911 74326911 + Intron SNP C C T TCGA-QB-A6FS-06A-11D-A30X-08 TCGA-QB-A6FS-10A-01D-A30X-08 g.chr15:74326911C>T SKCM 15 74326924 74326924 + Intron SNP C C T TCGA-GN-A266-06A-11D-A197-08 TCGA-GN-A266-10A-01D-A199-08 g.chr15:74326924C>T SKCM 15 74327537 74327537 + Intron SNP G G A TCGA-EE-A20C-06A-11D-A196-08 TCGA-EE-A20C-10A-01D-A198-08 g.chr15:74327537G>A SKCM 15 74327548 74327548 + Intron SNP C C T TCGA-FS-A1ZA-06A-11D-A197-08 TCGA-FS-A1ZA-10A-01D-A199-08 g.chr15:74327548C>T SKCM 15 74327577 74327577 + Intron SNP C C T TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr15:74327577C>T SKCM 15 74327596 74327596 + Intron SNP G G A TCGA-EE-A3JB-06A-11D-A21A-08 TCGA-EE-A3JB-10A-01D-A21A-08 g.chr15:74327596G>A SKCM 15 74327753 74327753 + Intron SNP G G A TCGA-EE-A184-06A-11D-A196-08 TCGA-EE-A184-10B-01D-A198-08 g.chr15:74327753G>A SKCM 15 74327936 74327936 + Intron SNP C C T TCGA-FS-A1Z3-06A-11D-A197-08 TCGA-FS-A1Z3-10A-01D-A199-08 g.chr15:74327936C>T SKCM 15 74327980 74327980 + Intron SNP A A G TCGA-EE-A3AB-06A-11D-A196-08 TCGA-EE-A3AB-10A-01D-A198-08 g.chr15:74327980A>G SKCM 15 74327994 74327994 + Intron SNP C C T TCGA-EE-A183-06A-11D-A196-08 TCGA-EE-A183-10A-01D-A198-08 g.chr15:74327994C>T SKCM 15 74328022 74328022 + Intron SNP C C T TCGA-EE-A3AA-06A-11D-A196-08 TCGA-EE-A3AA-10A-01D-A198-08 g.chr15:74328022C>T SKCM 15 74328055 74328055 + Intron SNP C C T TCGA-EE-A3J5-06A-11D-A20D-08 TCGA-EE-A3J5-10A-01D-A20D-08 g.chr15:74328055C>T SKCM 15 74328066 74328066 + Intron SNP C C T TCGA-EE-A2MQ-06A-11D-A197-08 TCGA-EE-A2MQ-10A-01D-A199-08 g.chr15:74328066C>T SKCM 15 74328096 74328096 + Intron SNP C C T TCGA-GF-A6C9-06A-11D-A30X-08 TCGA-GF-A6C9-10A-01D-A30X-08 g.chr15:74328096C>T SKCM 15 74328110 74328110 + Intron SNP G G T TCGA-DA-A1HY-06A-11D-A19A-08 TCGA-DA-A1HY-10A-01D-A19A-08 g.chr15:74328110G>T SKCM 15 74328124 74328124 + Intron SNP C C T TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr15:74328124C>T SKCM 15 74328125 74328125 + Intron SNP C C T TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr15:74328125C>T SKCM 15 74328256 74328256 + Intron SNP C C T TCGA-EE-A2MT-06A-11D-A197-08 TCGA-EE-A2MT-10A-01D-A199-08 g.chr15:74328256C>T SKCM 15 74336649 74336649 + Missense_Mutation SNP C C T TCGA-EE-A20C-06A-11D-A196-08 TCGA-EE-A20C-10A-01D-A198-08 g.chr15:74336649C>T c.1949C>T c.(1948-1950)tCc>tTc p.S650F SKCM 15 74337233 74337233 + Missense_Mutation SNP G G A TCGA-DA-A1I5-06A-11D-A197-08 TCGA-DA-A1I5-10A-01D-A199-08 g.chr15:74337233G>A c.2533G>A c.(2533-2535)Gct>Act p.A845T

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BLCA-CN 15 74328141 74328141 single base substitution G T 3_prime_UTR_variant BLCA-CN 15 74328141 74328141 single base substitution G T downstream_gene_variant BLCA-CN 15 74328141 74328141 single base substitution G T intron_variant BLCA-CN 15 74328141 74328141 single base substitution G T missense_variant G732V 2195G>T BLCA-CN 15 74328141 74328141 single base substitution G T missense_variant G780V 2339G>T BLCA-US 15 74290639 74290639 single base substitution G C exon_variant BLCA-US 15 74290639 74290639 single base substitution G C missense_variant E142Q 424G>C BLCA-US 15 74315653 74315653 single base substitution G A exon_variant BLCA-US 15 74315653 74315653 single base substitution G A missense_variant E111K 331G>A BLCA-US 15 74315653 74315653 single base substitution G A missense_variant E134K 400G>A BLCA-US 15 74315653 74315653 single base substitution G A missense_variant E363K 1087G>A BLCA-US 15 74315653 74315653 single base substitution G A missense_variant E6K 16G>A BLCA-US 15 74315653 74315653 single base substitution G A upstream_gene_variant BLCA-US 15 74336969 74336969 single base substitution C T downstream_gene_variant BLCA-US 15 74336969 74336969 single base substitution C T missense_variant L709F 2125C>T BLCA-US 15 74336969 74336969 single base substitution C T missense_variant L757F 2269C>T BRCA-EU 15 74282234 74282234 single base substitution C T upstream_gene_variant BRCA-EU 15 74283490 74283490 deletion of <=200bp A - upstream_gene_variant BRCA-EU 15 74283490 74283490 insertion of <=200bp - A upstream_gene_variant BRCA-EU 15 74284844 74284844 single base substitution C T upstream_gene_variant BRCA-EU 15 74284897 74284897 single base substitution C A upstream_gene_variant BRCA-EU 15 74286473 74286473 single base substitution C G upstream_gene_variant BRCA-EU 15 74286488 74286488 single base substitution G C upstream_gene_variant BRCA-EU 15 74287893 74287893 single base substitution C T intron_variant BRCA-EU 15 74287893 74287893 single base substitution C T upstream_gene_variant BRCA-EU 15 74289823 74289823 single base substitution A G intron_variant BRCA-EU 15 74289823 74289823 single base substitution A G upstream_gene_variant BRCA-EU 15 74292490 74292490 single base substitution G C intron_variant BRCA-EU 15 74293101 74293101 single base substitution G C intron_variant BRCA-EU 15 74293929 74293929 single base substitution G A intron_variant BRCA-EU 15 74294422 74294422 single base substitution G A intron_variant BRCA-EU 15 74295304 74295304 deletion of <=200bp A - intron_variant BRCA-EU 15 74299445 74299445 single base substitution C T intron_variant BRCA-EU 15 74299692 74299692 deletion of <=200bp G - intron_variant BRCA-EU 15 74300167 74300167 single base substitution C T intron_variant BRCA-EU 15 74300941 74300941 single base substitution G C intron_variant BRCA-EU 15 74302440 74302440 single base substitution G C intron_variant BRCA-EU 15 74302447 74302447 single base substitution C G intron_variant BRCA-EU 15 74302897 74302897 single base substitution C G intron_variant BRCA-EU 15 74303802 74303802 single base substitution A C intron_variant BRCA-EU 15 74304132 74304132 single base substitution G C intron_variant BRCA-EU 15 74305243 74305243 single base substitution C T intron_variant BRCA-EU 15 74305418 74305418 single base substitution G C intron_variant BRCA-EU 15 74311024 74311024 single base substitution G A intron_variant BRCA-EU 15 74311024 74311024 single base substitution G A upstream_gene_variant BRCA-EU 15 74311207 74311207 single base substitution C T intron_variant BRCA-EU 15 74311207 74311207 single base substitution C T upstream_gene_variant BRCA-EU 15 74312468 74312468 single base substitution C T intron_variant BRCA-EU 15 74312468 74312468 single base substitution C T upstream_gene_variant BRCA-EU 15 74312818 74312818 single base substitution A C intron_variant BRCA-EU 15 74312818 74312818 single base substitution A C upstream_gene_variant BRCA-EU 15 74313034 74313034 single base substitution C T intron_variant BRCA-EU 15 74313034 74313034 single base substitution C T upstream_gene_variant BRCA-EU 15 74313531 74313531 single base substitution T C intron_variant BRCA-EU 15 74313531 74313531 single base substitution T C upstream_gene_variant BRCA-EU 15 74313574 74313574 single base substitution C G intron_variant BRCA-EU 15 74313574 74313574 single base substitution C G upstream_gene_variant BRCA-EU 15 74315638 74315638 single base substitution C T exon_variant BRCA-EU 15 74315638 74315638 single base substitution C T missense_variant R106C 316C>T BRCA-EU 15 74315638 74315638 single base substitution C T missense_variant R129C 385C>T BRCA-EU 15 74315638 74315638 single base substitution C T missense_variant R1C 1C>T BRCA-EU 15 74315638 74315638 single base substitution C T missense_variant R358C 1072C>T BRCA-EU 15 74315638 74315638 single base substitution C T upstream_gene_variant BRCA-EU 15 74316597 74316597 single base substitution C A intron_variant BRCA-EU 15 74316597 74316597 single base substitution C A upstream_gene_variant BRCA-EU 15 74320720 74320720 single base substitution C G exon_variant BRCA-EU 15 74320720 74320720 single base substitution C G intron_variant BRCA-EU 15 74320720 74320720 single base substitution C G upstream_gene_variant BRCA-EU 15 74321486 74321486 single base substitution C T downstream_gene_variant BRCA-EU 15 74321486 74321486 single base substitution C T intron_variant BRCA-EU 15 74321486 74321486 single base substitution C T upstream_gene_variant BRCA-EU 15 74321526 74321526 single base substitution C T downstream_gene_variant BRCA-EU 15 74321526 74321526 single base substitution C T intron_variant BRCA-EU 15 74321526 74321526 single base substitution C T upstream_gene_variant BRCA-EU 15 74321610 74321610 single base substitution T A downstream_gene_variant BRCA-EU 15 74321610 74321610 single base substitution T A intron_variant BRCA-EU 15 74321610 74321610 single base substitution T A upstream_gene_variant BRCA-EU 15 74321654 74321654 single base substitution T C downstream_gene_variant BRCA-EU 15 74321654 74321654 single base substitution T C intron_variant BRCA-EU 15 74321654 74321654 single base substitution T C upstream_gene_variant BRCA-EU 15 74322194 74322194 single base substitution C A downstream_gene_variant BRCA-EU 15 74322194 74322194 single base substitution C A intron_variant BRCA-EU 15 74322194 74322194 single base substitution C A upstream_gene_variant BRCA-EU 15 74324632 74324632 single base substitution G T downstream_gene_variant BRCA-EU 15 74324632 74324632 single base substitution G T intron_variant BRCA-EU 15 74324632 74324632 single base substitution G T upstream_gene_variant BRCA-EU 15 74329387 74329387 single base substitution C G downstream_gene_variant BRCA-EU 15 74329387 74329387 single base substitution C G intron_variant BRCA-EU 15 74329387 74329387 single base substitution C G upstream_gene_variant BRCA-EU 15 74331895 74331895 single base substitution G A downstream_gene_variant BRCA-EU 15 74331895 74331895 single base substitution G A intron_variant BRCA-EU 15 74331895 74331895 single base substitution G A upstream_gene_variant BRCA-EU 15 74332517 74332517 single base substitution C G downstream_gene_variant BRCA-EU 15 74332517 74332517 single base substitution C G intron_variant BRCA-EU 15 74332517 74332517 single base substitution C G upstream_gene_variant BRCA-EU 15 74335143 74335143 single base substitution G A intron_variant BRCA-EU 15 74335145 74335145 single base substitution G A intron_variant BRCA-EU 15 74335581 74335581 single base substitution A C 3_prime_UTR_variant BRCA-EU 15 74335581 74335581 single base substitution A C exon_variant BRCA-EU 15 74335581 74335581 single base substitution A C intron_variant BRCA-EU 15 74336905 74336905 single base substitution G A downstream_gene_variant BRCA-EU 15 74336905 74336905 single base substitution G A synonymous_variant A687A 2061G>A BRCA-EU 15 74336905 74336905 single base substitution G A synonymous_variant A735A 2205G>A BRCA-EU 15 74339596 74339596 single base substitution G A 3_prime_UTR_variant BRCA-EU 15 74339596 74339596 single base substitution G A downstream_gene_variant BRCA-EU 15 74341249 74341249 single base substitution G C downstream_gene_variant BRCA-EU 15 74342303 74342303 single base substitution T C downstream_gene_variant BRCA-EU 15 74342773 74342773 single base substitution C G downstream_gene_variant BRCA-EU 15 74342873 74342873 single base substitution T C downstream_gene_variant BRCA-EU 15 74343524 74343524 single base substitution G C downstream_gene_variant BRCA-EU 15 74344616 74344616 single base substitution C T downstream_gene_variant BRCA-EU 15 74344854 74344854 single base substitution C T downstream_gene_variant BRCA-EU 15 74344908 74344908 single base substitution G A downstream_gene_variant BRCA-FR 15 74282234 74282234 single base substitution C T upstream_gene_variant BRCA-FR 15 74284897 74284897 single base substitution C A upstream_gene_variant BRCA-FR 15 74289823 74289823 single base substitution A G intron_variant BRCA-FR 15 74289823 74289823 single base substitution A G upstream_gene_variant BRCA-FR 15 74300167 74300167 single base substitution C T intron_variant BRCA-FR 15 74304132 74304132 single base substitution G C intron_variant BRCA-FR 15 74312468 74312468 single base substitution C T intron_variant BRCA-FR 15 74312468 74312468 single base substitution C T upstream_gene_variant BRCA-FR 15 74315638 74315638 single base substitution C T exon_variant BRCA-FR 15 74315638 74315638 single base substitution C T missense_variant R106C 316C>T BRCA-FR 15 74315638 74315638 single base substitution C T missense_variant R129C 385C>T BRCA-FR 15 74315638 74315638 single base substitution C T missense_variant R1C 1C>T BRCA-FR 15 74315638 74315638 single base substitution C T missense_variant R358C 1072C>T BRCA-FR 15 74315638 74315638 single base substitution C T upstream_gene_variant BRCA-FR 15 74322447 74322447 single base substitution C T downstream_gene_variant BRCA-FR 15 74322447 74322447 single base substitution C T intron_variant BRCA-FR 15 74322447 74322447 single base substitution C T upstream_gene_variant BRCA-FR 15 74327673 74327673 single base substitution C T 3_prime_UTR_variant BRCA-FR 15 74327673 74327673 single base substitution C T downstream_gene_variant BRCA-FR 15 74327673 74327673 single base substitution C T intron_variant BRCA-FR 15 74327673 74327673 single base substitution C T missense_variant P576L 1727C>T BRCA-FR 15 74327673 74327673 single base substitution C T missense_variant P624L 1871C>T BRCA-FR 15 74327673 74327673 single base substitution C T synonymous_variant S637S 1911C>T BRCA-FR 15 74343524 74343524 single base substitution G C downstream_gene_variant BRCA-UK 15 74320975 74320975 single base substitution C G downstream_gene_variant BRCA-UK 15 74320975 74320975 single base substitution C G intron_variant BRCA-UK 15 74320975 74320975 single base substitution C G upstream_gene_variant BRCA-US 15 74282711 74282711 single base substitution G T upstream_gene_variant BRCA-US 15 74317242 74317242 single base substitution C G exon_variant BRCA-US 15 74317242 74317242 single base substitution C G missense_variant P158A 472C>G BRCA-US 15 74317242 74317242 single base substitution C G missense_variant P181A 541C>G BRCA-US 15 74317242 74317242 single base substitution C G missense_variant P410A 1228C>G BRCA-US 15 74317242 74317242 single base substitution C G missense_variant P53A 157C>G BRCA-US 15 74317242 74317242 single base substitution C G missense_variant P8A 22C>G BRCA-US 15 74324915 74324915 single base substitution C T downstream_gene_variant BRCA-US 15 74324915 74324915 single base substitution C T exon_variant BRCA-US 15 74324915 74324915 single base substitution C T intron_variant BRCA-US 15 74324915 74324915 single base substitution C T splice_region_variant BRCA-US 15 74327676 74327676 single base substitution A C 3_prime_UTR_variant BRCA-US 15 74327676 74327676 single base substitution A C downstream_gene_variant BRCA-US 15 74327676 74327676 single base substitution A C intron_variant BRCA-US 15 74327676 74327676 single base substitution A C missense_variant H577P 1730A>C BRCA-US 15 74327676 74327676 single base substitution A C missense_variant H625P 1874A>C BRCA-US 15 74327676 74327676 single base substitution A C synonymous_variant P638P 1914A>C BRCA-US 15 74328401 74328401 single base substitution A G 3_prime_UTR_variant BRCA-US 15 74328401 74328401 single base substitution A G downstream_gene_variant BRCA-US 15 74328401 74328401 single base substitution A G intron_variant BRCA-US 15 74328401 74328401 single base substitution A G stop_retained_variant *240* 720A>G BRCA-US 15 74328401 74328401 single base substitution A G stop_retained_variant *436* 1308A>G BTCA-JP 15 74317043 74317043 single base substitution T C intron_variant BTCA-JP 15 74317043 74317043 single base substitution T C upstream_gene_variant BTCA-JP 15 74323497 74323497 single base substitution C T downstream_gene_variant BTCA-JP 15 74323497 74323497 single base substitution C T intron_variant BTCA-JP 15 74323497 74323497 single base substitution C T upstream_gene_variant BTCA-JP 15 74324882 74324882 single base substitution C A downstream_gene_variant BTCA-JP 15 74324882 74324882 single base substitution C A exon_variant BTCA-JP 15 74324882 74324882 single base substitution C A intron_variant BTCA-JP 15 74335469 74335469 single base substitution T G 3_prime_UTR_variant BTCA-JP 15 74335469 74335469 single base substitution T G exon_variant BTCA-JP 15 74335469 74335469 single base substitution T G missense_variant I569S 1706T>G BTCA-JP 15 74335469 74335469 single base substitution T G missense_variant I617S 1850T>G CESC-US 15 74287202 74287202 single base substitution C T missense_variant R17W 49C>T CESC-US 15 74287202 74287202 single base substitution C T upstream_gene_variant CESC-US 15 74290717 74290717 single base substitution G A exon_variant CESC-US 15 74290717 74290717 single base substitution G A missense_variant E168K 502G>A CESC-US 15 74315241 74315241 single base substitution C G exon_variant CESC-US 15 74315241 74315241 single base substitution C G synonymous_variant L225L 675C>G CESC-US 15 74315241 74315241 single base substitution C G upstream_gene_variant CESC-US 15 74315461 74315461 single base substitution G C exon_variant CESC-US 15 74315461 74315461 single base substitution G C missense_variant E299Q 895G>C CESC-US 15 74315461 74315461 single base substitution G C missense_variant E47Q 139G>C CESC-US 15 74315461 74315461 single base substitution G C missense_variant E70Q 208G>C CESC-US 15 74315461 74315461 single base substitution G C upstream_gene_variant CESC-US 15 74315539 74315539 single base substitution C T exon_variant CESC-US 15 74315539 74315539 single base substitution C T missense_variant R325C 973C>T CESC-US 15 74315539 74315539 single base substitution C T missense_variant R73C 217C>T CESC-US 15 74315539 74315539 single base substitution C T missense_variant R96C 286C>T CESC-US 15 74315539 74315539 single base substitution C T upstream_gene_variant CESC-US 15 74328176 74328176 single base substitution G A 3_prime_UTR_variant CESC-US 15 74328176 74328176 single base substitution G A downstream_gene_variant CESC-US 15 74328176 74328176 single base substitution G A intron_variant CESC-US 15 74328176 74328176 single base substitution G A missense_variant E744K 2230G>A CESC-US 15 74328176 74328176 single base substitution G A missense_variant E792K 2374G>A CESC-US 15 74336918 74336918 single base substitution G A downstream_gene_variant CESC-US 15 74336918 74336918 single base substitution G A missense_variant E692K 2074G>A CESC-US 15 74336918 74336918 single base substitution G A missense_variant E740K 2218G>A CLLE-ES 15 74290323 74290323 single base substitution A C intron_variant CLLE-ES 15 74290323 74290323 single base substitution A C upstream_gene_variant CLLE-ES 15 74292053 74292053 single base substitution T C intron_variant CLLE-ES 15 74298071 74298071 single base substitution C G intron_variant CLLE-ES 15 74324269 74324269 single base substitution G A downstream_gene_variant CLLE-ES 15 74324269 74324269 single base substitution G A intron_variant CLLE-ES 15 74324269 74324269 single base substitution G A upstream_gene_variant CLLE-ES 15 74344157 74344157 single base substitution C T downstream_gene_variant COAD-US 15 74290573 74290573 single base substitution C T exon_variant COAD-US 15 74290573 74290573 single base substitution C T missense_variant R120W 358C>T COAD-US 15 74315450 74315450 single base substitution G A exon_variant COAD-US 15 74315450 74315450 single base substitution G A missense_variant R295H 884G>A COAD-US 15 74315450 74315450 single base substitution G A missense_variant R43H 128G>A COAD-US 15 74315450 74315450 single base substitution G A missense_variant R66H 197G>A COAD-US 15 74315450 74315450 single base substitution G A upstream_gene_variant COAD-US 15 74315644 74315644 single base substitution C T exon_variant COAD-US 15 74315644 74315644 single base substitution C T missense_variant R108C 322C>T COAD-US 15 74315644 74315644 single base substitution C T missense_variant R131C 391C>T COAD-US 15 74315644 74315644 single base substitution C T missense_variant R360C 1078C>T COAD-US 15 74315644 74315644 single base substitution C T missense_variant R3C 7C>T COAD-US 15 74315644 74315644 single base substitution C T upstream_gene_variant COAD-US 15 74324939 74324939 single base substitution C T downstream_gene_variant COAD-US 15 74324939 74324939 single base substitution C T exon_variant COAD-US 15 74324939 74324939 single base substitution C T intron_variant COAD-US 15 74324939 74324939 single base substitution C T synonymous_variant A198A 594C>T COAD-US 15 74324939 74324939 single base substitution C T synonymous_variant A427A 1281C>T COAD-US 15 74324939 74324939 single base substitution C T synonymous_variant A70A 210C>T COAD-US 15 74326826 74326826 single base substitution C T 3_prime_UTR_variant COAD-US 15 74326826 74326826 single base substitution C T downstream_gene_variant COAD-US 15 74326826 74326826 single base substitution C T intron_variant COAD-US 15 74326826 74326826 single base substitution C T missense_variant A108V 323C>T COAD-US 15 74326826 74326826 single base substitution C T missense_variant A258V 773C>T COAD-US 15 74326826 74326826 single base substitution C T missense_variant A421V 1262C>T COAD-US 15 74326826 74326826 single base substitution C T missense_variant A558V 1673C>T COAD-US 15 74326826 74326826 single base substitution C T synonymous_variant R198R 594C>T COAD-US 15 74326826 74326826 single base substitution C T synonymous_variant R507R 1521C>T COAD-US 15 74326826 74326826 single base substitution C T synonymous_variant R555R 1665C>T COAD-US 15 74327568 74327568 single base substitution C T 3_prime_UTR_variant COAD-US 15 74327568 74327568 single base substitution C T downstream_gene_variant COAD-US 15 74327568 74327568 single base substitution C T intron_variant COAD-US 15 74327568 74327568 single base substitution C T missense_variant P541L 1622C>T COAD-US 15 74327568 74327568 single base substitution C T missense_variant P589L 1766C>T COAD-US 15 74327568 74327568 single base substitution C T synonymous_variant A602A 1806C>T COAD-US 15 74328116 74328116 single base substitution A G 3_prime_UTR_variant COAD-US 15 74328116 74328116 single base substitution A G downstream_gene_variant COAD-US 15 74328116 74328116 single base substitution A G intron_variant COAD-US 15 74328116 74328116 single base substitution A G missense_variant S724G 2170A>G COAD-US 15 74328116 74328116 single base substitution A G missense_variant S772G 2314A>G COAD-US 15 74336633 74336633 single base substitution T C downstream_gene_variant COAD-US 15 74336633 74336633 single base substitution T C missense_variant F597L 1789T>C COAD-US 15 74336633 74336633 single base substitution T C missense_variant F645L 1933T>C COAD-US 15 74336708 74336708 single base substitution C T downstream_gene_variant COAD-US 15 74336708 74336708 single base substitution C T missense_variant R622C 1864C>T COAD-US 15 74336708 74336708 single base substitution C T missense_variant R670C 2008C>T COCA-CN 15 74315343 74315343 single base substitution G A exon_variant COCA-CN 15 74315343 74315343 single base substitution G A synonymous_variant A259A 777G>A COCA-CN 15 74315343 74315343 single base substitution G A synonymous_variant A30A 90G>A COCA-CN 15 74315343 74315343 single base substitution G A synonymous_variant A7A 21G>A COCA-CN 15 74315343 74315343 single base substitution G A upstream_gene_variant COCA-CN 15 74317361 74317361 single base substitution C T exon_variant COCA-CN 15 74317361 74317361 single base substitution C T intron_variant COCA-CN 15 74325672 74325672 single base substitution C T downstream_gene_variant COCA-CN 15 74325672 74325672 single base substitution C T intron_variant COCA-CN 15 74325672 74325672 single base substitution C T missense_variant P168L 503C>T COCA-CN 15 74325672 74325672 single base substitution C T missense_variant P225L 674C>T COCA-CN 15 74325672 74325672 single base substitution C T missense_variant P477L 1430C>T COCA-CN 15 74325672 74325672 single base substitution C T missense_variant P525L 1574C>T COCA-CN 15 74325672 74325672 single base substitution C T missense_variant P75L 224C>T COCA-CN 15 74327697 74327697 single base substitution C T 3_prime_UTR_variant COCA-CN 15 74327697 74327697 single base substitution C T downstream_gene_variant COCA-CN 15 74327697 74327697 single base substitution C T intron_variant COCA-CN 15 74327697 74327697 single base substitution C T missense_variant A584V 1751C>T COCA-CN 15 74327697 74327697 single base substitution C T missense_variant A632V 1895C>T COCA-CN 15 74327955 74327955 single base substitution G T 3_prime_UTR_variant COCA-CN 15 74327955 74327955 single base substitution G T downstream_gene_variant COCA-CN 15 74327955 74327955 single base substitution G T intron_variant COCA-CN 15 74327955 74327955 single base substitution G T missense_variant G670V 2009G>T COCA-CN 15 74327955 74327955 single base substitution G T missense_variant G718V 2153G>T COCA-CN 15 74328272 74328272 single base substitution G A 3_prime_UTR_variant COCA-CN 15 74328272 74328272 single base substitution G A downstream_gene_variant COCA-CN 15 74328272 74328272 single base substitution G A intron_variant COCA-CN 15 74328272 74328272 single base substitution G A missense_variant A776T 2326G>A COCA-CN 15 74328272 74328272 single base substitution G A missense_variant A824T 2470G>A COCA-CN 15 74336712 74336712 single base substitution G A downstream_gene_variant COCA-CN 15 74336712 74336712 single base substitution G A missense_variant R623H 1868G>A COCA-CN 15 74336712 74336712 single base substitution G A missense_variant R671H 2012G>A EOPC-DE 15 74317960 74317960 single base substitution A G exon_variant EOPC-DE 15 74317960 74317960 single base substitution A G intron_variant ESAD-UK 15 74282047 74282047 single base substitution G C upstream_gene_variant ESAD-UK 15 74284595 74284595 single base substitution C T upstream_gene_variant ESAD-UK 15 74285747 74285747 single base substitution C T upstream_gene_variant ESAD-UK 15 74285802 74285802 single base substitution C T upstream_gene_variant ESAD-UK 15 74287053 74287053 single base substitution G C 5_prime_UTR_variant ESAD-UK 15 74287053 74287053 single base substitution G C upstream_gene_variant ESAD-UK 15 74287198 74287198 single base substitution C T synonymous_variant P15P 45C>T ESAD-UK 15 74287198 74287198 single base substitution C T upstream_gene_variant ESAD-UK 15 74287636 74287636 single base substitution A G intron_variant ESAD-UK 15 74287636 74287636 single base substitution A G upstream_gene_variant ESAD-UK 15 74290001 74290001 single base substitution C T intron_variant ESAD-UK 15 74290001 74290001 single base substitution C T upstream_gene_variant ESAD-UK 15 74290353 74290353 single base substitution C T synonymous_variant P46P 138C>T ESAD-UK 15 74290353 74290353 single base substitution C T upstream_gene_variant ESAD-UK 15 74291468 74291468 single base substitution C A intron_variant ESAD-UK 15 74292686 74292686 single base substitution G A intron_variant ESAD-UK 15 74293087 74293087 single base substitution G A intron_variant ESAD-UK 15 74297094 74297094 single base substitution T G intron_variant ESAD-UK 15 74303268 74303268 single base substitution A G intron_variant ESAD-UK 15 74307201 74307201 single base substitution G A intron_variant ESAD-UK 15 74307314 74307314 single base substitution G C intron_variant ESAD-UK 15 74307792 74307792 single base substitution T C intron_variant ESAD-UK 15 74309963 74309963 single base substitution T C intron_variant ESAD-UK 15 74310888 74310888 single base substitution C T intron_variant ESAD-UK 15 74310888 74310888 single base substitution C T upstream_gene_variant ESAD-UK 15 74311032 74311032 single base substitution T C intron_variant ESAD-UK 15 74311032 74311032 single base substitution T C upstream_gene_variant ESAD-UK 15 74311565 74311565 single base substitution G A intron_variant ESAD-UK 15 74311565 74311565 single base substitution G A upstream_gene_variant ESAD-UK 15 74313753 74313753 single base substitution C A intron_variant ESAD-UK 15 74313753 74313753 single base substitution C A upstream_gene_variant ESAD-UK 15 74313818 74313818 single base substitution C T intron_variant ESAD-UK 15 74313818 74313818 single base substitution C T upstream_gene_variant ESAD-UK 15 74319485 74319485 single base substitution G A exon_variant ESAD-UK 15 74319485 74319485 single base substitution G A intron_variant ESAD-UK 15 74320360 74320360 single base substitution G A exon_variant ESAD-UK 15 74320360 74320360 single base substitution G A intron_variant ESAD-UK 15 74320360 74320360 single base substitution G A upstream_gene_variant ESAD-UK 15 74321475 74321475 single base substitution A C downstream_gene_variant ESAD-UK 15 74321475 74321475 single base substitution A C intron_variant ESAD-UK 15 74321475 74321475 single base substitution A C upstream_gene_variant ESAD-UK 15 74321735 74321735 single base substitution C T downstream_gene_variant ESAD-UK 15 74321735 74321735 single base substitution C T intron_variant ESAD-UK 15 74321735 74321735 single base substitution C T upstream_gene_variant ESAD-UK 15 74323507 74323507 single base substitution C G downstream_gene_variant ESAD-UK 15 74323507 74323507 single base substitution C G intron_variant ESAD-UK 15 74323507 74323507 single base substitution C G upstream_gene_variant ESAD-UK 15 74324724 74324724 insertion of <=200bp - A downstream_gene_variant ESAD-UK 15 74324724 74324724 insertion of <=200bp - A intron_variant ESAD-UK 15 74324724 74324724 insertion of <=200bp - A upstream_gene_variant ESAD-UK 15 74327868 74327868 single base substitution A G 3_prime_UTR_variant ESAD-UK 15 74327868 74327868 single base substitution A G downstream_gene_variant ESAD-UK 15 74327868 74327868 single base substitution A G intron_variant ESAD-UK 15 74327868 74327868 single base substitution A G missense_variant H641R 1922A>G ESAD-UK 15 74327868 74327868 single base substitution A G missense_variant H689R 2066A>G ESAD-UK 15 74340773 74340773 single base substitution C T downstream_gene_variant ESAD-UK 15 74344907 74344907 single base substitution C T downstream_gene_variant ESAD-UK 15 74344929 74344929 single base substitution G A downstream_gene_variant ESCA-CN 15 74315601 74315601 single base substitution G A exon_variant ESCA-CN 15 74315601 74315601 single base substitution G A synonymous_variant V116V 348G>A ESCA-CN 15 74315601 74315601 single base substitution G A synonymous_variant V345V 1035G>A ESCA-CN 15 74315601 74315601 single base substitution G A synonymous_variant V93V 279G>A ESCA-CN 15 74315601 74315601 single base substitution G A upstream_gene_variant GBM-US 15 74315385 74315385 single base substitution C T exon_variant GBM-US 15 74315385 74315385 single base substitution C T synonymous_variant A21A 63C>T GBM-US 15 74315385 74315385 single base substitution C T synonymous_variant A273A 819C>T GBM-US 15 74315385 74315385 single base substitution C T synonymous_variant A44A 132C>T GBM-US 15 74315385 74315385 single base substitution C T upstream_gene_variant KIRC-US 15 74328116 74328116 single base substitution A G 3_prime_UTR_variant KIRC-US 15 74328116 74328116 single base substitution A G downstream_gene_variant KIRC-US 15 74328116 74328116 single base substitution A G intron_variant KIRC-US 15 74328116 74328116 single base substitution A G missense_variant S724G 2170A>G KIRC-US 15 74328116 74328116 single base substitution A G missense_variant S772G 2314A>G KIRC-US 15 74328141 74328141 single base substitution G T 3_prime_UTR_variant KIRC-US 15 74328141 74328141 single base substitution G T downstream_gene_variant KIRC-US 15 74328141 74328141 single base substitution G T intron_variant KIRC-US 15 74328141 74328141 single base substitution G T missense_variant G732V 2195G>T KIRC-US 15 74328141 74328141 single base substitution G T missense_variant G780V 2339G>T KIRC-US 15 74336686 74336686 single base substitution C G downstream_gene_variant KIRC-US 15 74336686 74336686 single base substitution C G missense_variant F614L 1842C>G KIRC-US 15 74336686 74336686 single base substitution C G missense_variant F662L 1986C>G KIRP-US 15 74325643 74325643 single base substitution G A downstream_gene_variant KIRP-US 15 74325643 74325643 single base substitution G A intron_variant KIRP-US 15 74325643 74325643 single base substitution G A synonymous_variant K158K 474G>A KIRP-US 15 74325643 74325643 single base substitution G A synonymous_variant K215K 645G>A KIRP-US 15 74325643 74325643 single base substitution G A synonymous_variant K467K 1401G>A KIRP-US 15 74325643 74325643 single base substitution G A synonymous_variant K515K 1545G>A KIRP-US 15 74325643 74325643 single base substitution G A synonymous_variant K65K 195G>A LAML-KR 15 74326711 74326711 single base substitution G A 3_prime_UTR_variant LAML-KR 15 74326711 74326711 single base substitution G A downstream_gene_variant LAML-KR 15 74326711 74326711 single base substitution G A intron_variant LAML-KR 15 74328116 74328116 single base substitution A G 3_prime_UTR_variant LAML-KR 15 74328116 74328116 single base substitution A G downstream_gene_variant LAML-KR 15 74328116 74328116 single base substitution A G intron_variant LAML-KR 15 74328116 74328116 single base substitution A G missense_variant S724G 2170A>G LAML-KR 15 74328116 74328116 single base substitution A G missense_variant S772G 2314A>G LAML-KR 15 74328141 74328141 single base substitution G T 3_prime_UTR_variant LAML-KR 15 74328141 74328141 single base substitution G T downstream_gene_variant LAML-KR 15 74328141 74328141 single base substitution G T intron_variant LAML-KR 15 74328141 74328141 single base substitution G T missense_variant G732V 2195G>T LAML-KR 15 74328141 74328141 single base substitution G T missense_variant G780V 2339G>T LGG-US 15 74290533 74290533 single base substitution C T exon_variant LGG-US 15 74290533 74290533 single base substitution C T synonymous_variant N106N 318C>T LGG-US 15 74315324 74315324 single base substitution C A exon_variant LGG-US 15 74315324 74315324 single base substitution C A missense_variant A1D 2C>A LGG-US 15 74315324 74315324 single base substitution C A missense_variant A24D 71C>A LGG-US 15 74315324 74315324 single base substitution C A missense_variant A253D 758C>A LGG-US 15 74315324 74315324 single base substitution C A upstream_gene_variant LICA-CN 15 74315224 74315224 single base substitution A T exon_variant LICA-CN 15 74315224 74315224 single base substitution A T missense_variant S220C 658A>T LICA-CN 15 74315224 74315224 single base substitution A T upstream_gene_variant LICA-CN 15 74325754 74325754 single base substitution A T downstream_gene_variant LICA-CN 15 74325754 74325754 single base substitution A T intron_variant LICA-CN 15 74325754 74325754 single base substitution A T splice_region_variant LICA-CN 15 74325754 74325754 single base substitution A T synonymous_variant A102A 306A>T LICA-CN 15 74325754 74325754 single base substitution A T synonymous_variant A252A 756A>T LICA-CN 15 74325754 74325754 single base substitution A T synonymous_variant A504A 1512A>T LICA-CN 15 74325754 74325754 single base substitution A T synonymous_variant A552A 1656A>T LICA-CN 15 74336850 74336850 single base substitution G A downstream_gene_variant LICA-CN 15 74336850 74336850 single base substitution G A missense_variant R669H 2006G>A LICA-CN 15 74336850 74336850 single base substitution G A missense_variant R717H 2150G>A LICA-CN 15 74337162 74337162 single base substitution A G downstream_gene_variant LICA-CN 15 74337162 74337162 single base substitution A G missense_variant K773R 2318A>G LICA-CN 15 74337162 74337162 single base substitution A G missense_variant K821R 2462A>G LICA-FR 15 74282216 74282216 single base substitution C A upstream_gene_variant LICA-FR 15 74284196 74284196 single base substitution A T upstream_gene_variant LICA-FR 15 74302944 74302944 single base substitution C G intron_variant LICA-FR 15 74315341 74315341 single base substitution G A exon_variant LICA-FR 15 74315341 74315341 single base substitution G A missense_variant A259T 775G>A LICA-FR 15 74315341 74315341 single base substitution G A missense_variant A30T 88G>A LICA-FR 15 74315341 74315341 single base substitution G A missense_variant A7T 19G>A LICA-FR 15 74315341 74315341 single base substitution G A upstream_gene_variant LICA-FR 15 74327795 74327795 single base substitution G A 3_prime_UTR_variant LICA-FR 15 74327795 74327795 single base substitution G A downstream_gene_variant LICA-FR 15 74327795 74327795 single base substitution G A intron_variant LICA-FR 15 74327795 74327795 single base substitution G A missense_variant A617T 1849G>A LICA-FR 15 74327795 74327795 single base substitution G A missense_variant A665T 1993G>A LICA-FR 15 74335390 74335390 single base substitution A T 3_prime_UTR_variant LICA-FR 15 74335390 74335390 single base substitution A T exon_variant LICA-FR 15 74335390 74335390 single base substitution A T missense_variant S543C 1627A>T LICA-FR 15 74335390 74335390 single base substitution A T missense_variant S591C 1771A>T LIHC-US 15 74290431 74290431 single base substitution T G exon_variant LIHC-US 15 74290431 74290431 single base substitution T G missense_variant C72W 216T>G LINC-JP 15 74283332 74283332 single base substitution G T upstream_gene_variant LINC-JP 15 74284889 74284889 single base substitution C A upstream_gene_variant LINC-JP 15 74284890 74284890 single base substitution C A upstream_gene_variant LINC-JP 15 74287098 74287098 single base substitution G C 5_prime_UTR_variant LINC-JP 15 74287098 74287098 single base substitution G C upstream_gene_variant LINC-JP 15 74292073 74292073 single base substitution T C intron_variant LINC-JP 15 74293082 74293082 single base substitution T A intron_variant LINC-JP 15 74297222 74297222 single base substitution A C intron_variant LINC-JP 15 74298752 74298752 single base substitution G A intron_variant LINC-JP 15 74299779 74299779 single base substitution A G intron_variant LINC-JP 15 74305984 74305984 single base substitution C G intron_variant LINC-JP 15 74309133 74309133 single base substitution C T intron_variant LINC-JP 15 74321976 74321976 single base substitution A G downstream_gene_variant LINC-JP 15 74321976 74321976 single base substitution A G intron_variant LINC-JP 15 74321976 74321976 single base substitution A G upstream_gene_variant LINC-JP 15 74325559 74325559 single base substitution G T downstream_gene_variant LINC-JP 15 74325559 74325559 single base substitution G T intron_variant LINC-JP 15 74325559 74325559 single base substitution G T missense_variant K130N 390G>T LINC-JP 15 74325559 74325559 single base substitution G T missense_variant K187N 561G>T LINC-JP 15 74325559 74325559 single base substitution G T missense_variant K37N 111G>T LINC-JP 15 74325559 74325559 single base substitution G T missense_variant K439N 1317G>T LINC-JP 15 74325559 74325559 single base substitution G T missense_variant K487N 1461G>T LINC-JP 15 74325887 74325887 single base substitution G T downstream_gene_variant LINC-JP 15 74325887 74325887 single base substitution G T intron_variant LINC-JP 15 74325887 74325887 single base substitution G T missense_variant G549W 1645G>T LINC-JP 15 74329869 74329869 single base substitution G C downstream_gene_variant LINC-JP 15 74329869 74329869 single base substitution G C intron_variant LINC-JP 15 74329869 74329869 single base substitution G C upstream_gene_variant LINC-JP 15 74329870 74329870 single base substitution G T downstream_gene_variant LINC-JP 15 74329870 74329870 single base substitution G T intron_variant LINC-JP 15 74329870 74329870 single base substitution G T upstream_gene_variant LINC-JP 15 74335355 74335355 single base substitution G T 3_prime_UTR_variant LINC-JP 15 74335355 74335355 single base substitution G T exon_variant LINC-JP 15 74335355 74335355 single base substitution G T missense_variant S531I 1592G>T LINC-JP 15 74335355 74335355 single base substitution G T missense_variant S579I 1736G>T LINC-JP 15 74336917 74336917 single base substitution C T downstream_gene_variant LINC-JP 15 74336917 74336917 single base substitution C T synonymous_variant S691S 2073C>T LINC-JP 15 74336917 74336917 single base substitution C T synonymous_variant S739S 2217C>T LINC-JP 15 74337298 74337298 single base substitution C T downstream_gene_variant LINC-JP 15 74337298 74337298 single base substitution C T synonymous_variant S818S 2454C>T LINC-JP 15 74337298 74337298 single base substitution C T synonymous_variant S866S 2598C>T LIRI-JP 15 74282258 74282258 single base substitution C A upstream_gene_variant LIRI-JP 15 74282635 74282635 single base substitution A G upstream_gene_variant LIRI-JP 15 74284162 74284162 single base substitution A C upstream_gene_variant LIRI-JP 15 74285243 74285243 single base substitution T C upstream_gene_variant LIRI-JP 15 74285245 74285245 single base substitution T C upstream_gene_variant LIRI-JP 15 74286621 74286621 single base substitution C T upstream_gene_variant LIRI-JP 15 74288127 74288127 single base substitution A G intron_variant LIRI-JP 15 74288127 74288127 single base substitution A G upstream_gene_variant LIRI-JP 15 74293296 74293296 single base substitution A G intron_variant LIRI-JP 15 74294753 74294753 single base substitution C T intron_variant LIRI-JP 15 74294772 74294775 deletion of <=200bp CTTT - intron_variant LIRI-JP 15 74298558 74298558 single base substitution C A intron_variant LIRI-JP 15 74299071 74299071 single base substitution A G intron_variant LIRI-JP 15 74300615 74300615 single base substitution G A intron_variant LIRI-JP 15 74301138 74301138 single base substitution A T intron_variant LIRI-JP 15 74303444 74303444 single base substitution T G intron_variant LIRI-JP 15 74303659 74303659 single base substitution A G intron_variant LIRI-JP 15 74304022 74304022 single base substitution G T intron_variant LIRI-JP 15 74304725 74304725 single base substitution C T intron_variant LIRI-JP 15 74305202 74305202 single base substitution A G intron_variant LIRI-JP 15 74305393 74305393 single base substitution A G intron_variant LIRI-JP 15 74306374 74306374 single base substitution A G intron_variant LIRI-JP 15 74308130 74308130 single base substitution A G intron_variant LIRI-JP 15 74308383 74308383 single base substitution G A intron_variant LIRI-JP 15 74309621 74309621 single base substitution T C intron_variant LIRI-JP 15 74309712 74309712 single base substitution G A intron_variant LIRI-JP 15 74311178 74311178 single base substitution A G intron_variant LIRI-JP 15 74311178 74311178 single base substitution A G upstream_gene_variant LIRI-JP 15 74313532 74313532 single base substitution A G intron_variant LIRI-JP 15 74313532 74313532 single base substitution A G upstream_gene_variant LIRI-JP 15 74313794 74313794 single base substitution C T intron_variant LIRI-JP 15 74313794 74313794 single base substitution C T upstream_gene_variant LIRI-JP 15 74314262 74314262 single base substitution A G intron_variant LIRI-JP 15 74314262 74314262 single base substitution A G upstream_gene_variant LIRI-JP 15 74315105 74315105 single base substitution A G intron_variant LIRI-JP 15 74315105 74315105 single base substitution A G upstream_gene_variant LIRI-JP 15 74315829 74315829 single base substitution C T intron_variant LIRI-JP 15 74315829 74315829 single base substitution C T upstream_gene_variant LIRI-JP 15 74317089 74317089 single base substitution A G intron_variant LIRI-JP 15 74317089 74317089 single base substitution A G upstream_gene_variant LIRI-JP 15 74317190 74317190 single base substitution T C intron_variant LIRI-JP 15 74317190 74317190 single base substitution T C splice_region_variant LIRI-JP 15 74317190 74317190 single base substitution T C upstream_gene_variant LIRI-JP 15 74317233 74317233 single base substitution G T exon_variant LIRI-JP 15 74317233 74317233 single base substitution G T missense_variant A155S 463G>T LIRI-JP 15 74317233 74317233 single base substitution G T missense_variant A178S 532G>T LIRI-JP 15 74317233 74317233 single base substitution G T missense_variant A407S 1219G>T LIRI-JP 15 74317233 74317233 single base substitution G T missense_variant A50S 148G>T LIRI-JP 15 74317233 74317233 single base substitution G T missense_variant A5S 13G>T LIRI-JP 15 74319390 74319390 single base substitution G T exon_variant LIRI-JP 15 74319390 74319390 single base substitution G T intron_variant LIRI-JP 15 74322287 74322287 single base substitution A G downstream_gene_variant LIRI-JP 15 74322287 74322287 single base substitution A G intron_variant LIRI-JP 15 74322287 74322287 single base substitution A G upstream_gene_variant LIRI-JP 15 74322314 74322314 single base substitution G A downstream_gene_variant LIRI-JP 15 74322314 74322314 single base substitution G A intron_variant LIRI-JP 15 74322314 74322314 single base substitution G A upstream_gene_variant LIRI-JP 15 74323009 74323009 single base substitution A G downstream_gene_variant LIRI-JP 15 74323009 74323009 single base substitution A G intron_variant LIRI-JP 15 74323009 74323009 single base substitution A G upstream_gene_variant LIRI-JP 15 74324061 74324061 single base substitution A G downstream_gene_variant LIRI-JP 15 74324061 74324061 single base substitution A G intron_variant LIRI-JP 15 74324061 74324061 single base substitution A G upstream_gene_variant LIRI-JP 15 74324621 74324621 single base substitution C G downstream_gene_variant LIRI-JP 15 74324621 74324621 single base substitution C G intron_variant LIRI-JP 15 74324621 74324621 single base substitution C G upstream_gene_variant LIRI-JP 15 74325171 74325171 single base substitution A G downstream_gene_variant LIRI-JP 15 74325171 74325171 single base substitution A G intron_variant LIRI-JP 15 74326073 74326073 single base substitution C G 3_prime_UTR_variant LIRI-JP 15 74326073 74326073 single base substitution C G downstream_gene_variant LIRI-JP 15 74326073 74326073 single base substitution C G intron_variant LIRI-JP 15 74331943 74331943 single base substitution G A downstream_gene_variant LIRI-JP 15 74331943 74331943 single base substitution G A intron_variant LIRI-JP 15 74331943 74331943 single base substitution G A upstream_gene_variant LIRI-JP 15 74333468 74333468 single base substitution C A downstream_gene_variant LIRI-JP 15 74333468 74333468 single base substitution C A intron_variant LIRI-JP 15 74333468 74333468 single base substitution C A upstream_gene_variant LIRI-JP 15 74336398 74336398 single base substitution A C downstream_gene_variant LIRI-JP 15 74336398 74336398 single base substitution A C intron_variant LIRI-JP 15 74339290 74339290 single base substitution A G 3_prime_UTR_variant LIRI-JP 15 74339290 74339290 single base substitution A G downstream_gene_variant LIRI-JP 15 74342545 74342545 single base substitution C A downstream_gene_variant LUSC-KR 15 74286903 74286903 single base substitution G C upstream_gene_variant LUSC-KR 15 74292194 74292194 single base substitution G T intron_variant LUSC-KR 15 74293784 74293784 single base substitution G T intron_variant LUSC-KR 15 74296252 74296252 single base substitution C G intron_variant LUSC-KR 15 74296600 74296600 single base substitution G A intron_variant LUSC-KR 15 74304611 74304611 single base substitution G T intron_variant LUSC-KR 15 74306316 74306316 single base substitution C A intron_variant LUSC-KR 15 74308410 74308410 single base substitution G C intron_variant LUSC-KR 15 74309327 74309327 single base substitution A G intron_variant LUSC-KR 15 74316581 74316581 single base substitution G T intron_variant LUSC-KR 15 74316581 74316581 single base substitution G T upstream_gene_variant LUSC-KR 15 74322721 74322721 single base substitution G T downstream_gene_variant LUSC-KR 15 74322721 74322721 single base substitution G T intron_variant LUSC-KR 15 74322721 74322721 single base substitution G T upstream_gene_variant LUSC-KR 15 74332156 74332156 single base substitution G A downstream_gene_variant LUSC-KR 15 74332156 74332156 single base substitution G A intron_variant LUSC-KR 15 74332156 74332156 single base substitution G A upstream_gene_variant LUSC-KR 15 74335273 74335273 single base substitution C A intron_variant LUSC-KR 15 74336539 74336539 single base substitution C A downstream_gene_variant LUSC-KR 15 74336539 74336539 single base substitution C A intron_variant LUSC-KR 15 74338574 74338574 single base substitution A C 3_prime_UTR_variant LUSC-KR 15 74338574 74338574 single base substitution A C downstream_gene_variant LUSC-KR 15 74342141 74342141 single base substitution C A downstream_gene_variant LUSC-US 15 74326832 74326832 single base substitution G T 3_prime_UTR_variant LUSC-US 15 74326832 74326832 single base substitution G T downstream_gene_variant LUSC-US 15 74326832 74326832 single base substitution G T intron_variant LUSC-US 15 74326832 74326832 single base substitution G T missense_variant W110L 329G>T LUSC-US 15 74326832 74326832 single base substitution G T missense_variant W260L 779G>T LUSC-US 15 74326832 74326832 single base substitution G T missense_variant W423L 1268G>T LUSC-US 15 74326832 74326832 single base substitution G T missense_variant W560L 1679G>T LUSC-US 15 74326832 74326832 single base substitution G T synonymous_variant V200V 600G>T LUSC-US 15 74326832 74326832 single base substitution G T synonymous_variant V509V 1527G>T LUSC-US 15 74326832 74326832 single base substitution G T synonymous_variant V557V 1671G>T MALY-DE 15 74283544 74283544 single base substitution G A upstream_gene_variant MALY-DE 15 74284558 74284558 single base substitution C G upstream_gene_variant MALY-DE 15 74294731 74294732 deletion of <=200bp TG - intron_variant MALY-DE 15 74308991 74308991 single base substitution T G intron_variant MALY-DE 15 74308993 74308993 single base substitution T A intron_variant MALY-DE 15 74309009 74309009 single base substitution T C intron_variant MALY-DE 15 74310457 74310457 single base substitution T C intron_variant MALY-DE 15 74310457 74310457 single base substitution T C upstream_gene_variant MALY-DE 15 74321971 74321971 single base substitution A G downstream_gene_variant MALY-DE 15 74321971 74321971 single base substitution A G intron_variant MALY-DE 15 74321971 74321971 single base substitution A G upstream_gene_variant MALY-DE 15 74336597 74336597 single base substitution G A downstream_gene_variant MALY-DE 15 74336597 74336597 single base substitution G A missense_variant E585K 1753G>A MALY-DE 15 74336597 74336597 single base substitution G A missense_variant E633K 1897G>A MELA-AU 15 74282189 74282189 single base substitution G A upstream_gene_variant MELA-AU 15 74282243 74282243 single base substitution C T upstream_gene_variant MELA-AU 15 74282780 74282780 single base substitution G A upstream_gene_variant MELA-AU 15 74283481 74283481 single base substitution A C upstream_gene_variant MELA-AU 15 74283993 74283993 single base substitution G A upstream_gene_variant MELA-AU 15 74284239 74284239 single base substitution G A upstream_gene_variant MELA-AU 15 74284701 74284701 single base substitution G A upstream_gene_variant MELA-AU 15 74284742 74284742 single base substitution C T upstream_gene_variant MELA-AU 15 74285364 74285364 single base substitution C T upstream_gene_variant MELA-AU 15 74285596 74285596 single base substitution C T upstream_gene_variant MELA-AU 15 74285833 74285833 single base substitution G A upstream_gene_variant MELA-AU 15 74286412 74286412 single base substitution G A upstream_gene_variant MELA-AU 15 74287253 74287253 single base substitution C T stop_gained Q34* 100C>T MELA-AU 15 74287253 74287253 single base substitution C T upstream_gene_variant MELA-AU 15 74287419 74287419 single base substitution G A intron_variant MELA-AU 15 74287419 74287419 single base substitution G A upstream_gene_variant MELA-AU 15 74287959 74287959 single base substitution T G intron_variant MELA-AU 15 74287959 74287959 single base substitution T G upstream_gene_variant MELA-AU 15 74288119 74288119 single base substitution G A intron_variant MELA-AU 15 74288119 74288119 single base substitution G A upstream_gene_variant MELA-AU 15 74288443 74288443 single base substitution C T intron_variant MELA-AU 15 74288443 74288443 single base substitution C T upstream_gene_variant MELA-AU 15 74288574 74288574 single base substitution G A intron_variant MELA-AU 15 74288574 74288574 single base substitution G A upstream_gene_variant MELA-AU 15 74289593 74289593 single base substitution C T intron_variant MELA-AU 15 74289593 74289593 single base substitution C T upstream_gene_variant MELA-AU 15 74289594 74289594 single base substitution C T intron_variant MELA-AU 15 74289594 74289594 single base substitution C T upstream_gene_variant MELA-AU 15 74290284 74290284 single base substitution G T intron_variant MELA-AU 15 74290284 74290284 single base substitution G T upstream_gene_variant MELA-AU 15 74290414 74290414 single base substitution C T exon_variant MELA-AU 15 74290414 74290414 single base substitution C T missense_variant P67S 199C>T MELA-AU 15 74291582 74291582 single base substitution C T intron_variant MELA-AU 15 74293312 74293312 single base substitution C T intron_variant MELA-AU 15 74293913 74293913 single base substitution C T intron_variant MELA-AU 15 74293923 74293923 single base substitution C T intron_variant MELA-AU 15 74294601 74294601 single base substitution C T intron_variant MELA-AU 15 74294706 74294706 single base substitution C T intron_variant MELA-AU 15 74294781 74294781 single base substitution T G intron_variant MELA-AU 15 74295093 74295093 single base substitution C T intron_variant MELA-AU 15 74295344 74295344 single base substitution C T intron_variant MELA-AU 15 74295601 74295601 single base substitution C T intron_variant MELA-AU 15 74295656 74295656 single base substitution C T intron_variant MELA-AU 15 74296886 74296886 single base substitution C T intron_variant MELA-AU 15 74297072 74297072 single base substitution T G intron_variant MELA-AU 15 74297380 74297380 single base substitution C T intron_variant MELA-AU 15 74297518 74297518 single base substitution C T intron_variant MELA-AU 15 74298287 74298287 single base substitution G A intron_variant MELA-AU 15 74299250 74299250 single base substitution C T intron_variant MELA-AU 15 74299485 74299485 single base substitution T C intron_variant MELA-AU 15 74301674 74301674 single base substitution C T intron_variant MELA-AU 15 74301903 74301903 single base substitution C T intron_variant MELA-AU 15 74302781 74302781 single base substitution C T intron_variant MELA-AU 15 74303209 74303209 single base substitution C T intron_variant MELA-AU 15 74303623 74303623 single base substitution G A intron_variant MELA-AU 15 74304764 74304764 single base substitution C T intron_variant MELA-AU 15 74304773 74304773 single base substitution C T intron_variant MELA-AU 15 74304949 74304950 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 15 74305858 74305858 single base substitution C T intron_variant MELA-AU 15 74306906 74306906 single base substitution G A intron_variant MELA-AU 15 74307453 74307453 single base substitution C T intron_variant MELA-AU 15 74308565 74308565 single base substitution C T intron_variant MELA-AU 15 74309222 74309222 single base substitution C T intron_variant MELA-AU 15 74311087 74311087 single base substitution T C intron_variant MELA-AU 15 74311087 74311087 single base substitution T C upstream_gene_variant MELA-AU 15 74311347 74311347 single base substitution C T intron_variant MELA-AU 15 74311347 74311347 single base substitution C T upstream_gene_variant MELA-AU 15 74311566 74311566 single base substitution C T intron_variant MELA-AU 15 74311566 74311566 single base substitution C T upstream_gene_variant MELA-AU 15 74311580 74311580 single base substitution T C intron_variant MELA-AU 15 74311580 74311580 single base substitution T C upstream_gene_variant MELA-AU 15 74312740 74312740 single base substitution C T intron_variant MELA-AU 15 74312740 74312740 single base substitution C T upstream_gene_variant MELA-AU 15 74313134 74313134 single base substitution C T intron_variant MELA-AU 15 74313134 74313134 single base substitution C T upstream_gene_variant MELA-AU 15 74314799 74314799 single base substitution C T intron_variant MELA-AU 15 74314799 74314799 single base substitution C T upstream_gene_variant MELA-AU 15 74315943 74315944 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 15 74315943 74315944 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 15 74316173 74316173 single base substitution C A intron_variant MELA-AU 15 74316173 74316173 single base substitution C A upstream_gene_variant MELA-AU 15 74317035 74317035 single base substitution C T intron_variant MELA-AU 15 74317035 74317035 single base substitution C T upstream_gene_variant MELA-AU 15 74317047 74317048 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 15 74317047 74317048 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 15 74317904 74317904 single base substitution T C exon_variant MELA-AU 15 74317904 74317904 single base substitution T C intron_variant MELA-AU 15 74318043 74318043 single base substitution T A exon_variant MELA-AU 15 74318043 74318043 single base substitution T A intron_variant MELA-AU 15 74321467 74321467 single base substitution C T downstream_gene_variant MELA-AU 15 74321467 74321467 single base substitution C T intron_variant MELA-AU 15 74321467 74321467 single base substitution C T upstream_gene_variant MELA-AU 15 74321622 74321622 single base substitution C T downstream_gene_variant MELA-AU 15 74321622 74321622 single base substitution C T intron_variant MELA-AU 15 74321622 74321622 single base substitution C T upstream_gene_variant MELA-AU 15 74321963 74321963 single base substitution C T downstream_gene_variant MELA-AU 15 74321963 74321963 single base substitution C T intron_variant MELA-AU 15 74321963 74321963 single base substitution C T upstream_gene_variant MELA-AU 15 74322600 74322600 single base substitution C T downstream_gene_variant MELA-AU 15 74322600 74322600 single base substitution C T intron_variant MELA-AU 15 74322600 74322600 single base substitution C T upstream_gene_variant MELA-AU 15 74323188 74323188 single base substitution C T downstream_gene_variant MELA-AU 15 74323188 74323188 single base substitution C T intron_variant MELA-AU 15 74323188 74323188 single base substitution C T upstream_gene_variant MELA-AU 15 74323484 74323484 single base substitution C T downstream_gene_variant MELA-AU 15 74323484 74323484 single base substitution C T intron_variant MELA-AU 15 74323484 74323484 single base substitution C T upstream_gene_variant MELA-AU 15 74323933 74323933 single base substitution C T downstream_gene_variant MELA-AU 15 74323933 74323933 single base substitution C T intron_variant MELA-AU 15 74323933 74323933 single base substitution C T upstream_gene_variant MELA-AU 15 74324032 74324032 single base substitution T A downstream_gene_variant MELA-AU 15 74324032 74324032 single base substitution T A intron_variant MELA-AU 15 74324032 74324032 single base substitution T A upstream_gene_variant MELA-AU 15 74324900 74324900 single base substitution C T downstream_gene_variant MELA-AU 15 74324900 74324900 single base substitution C T exon_variant MELA-AU 15 74324900 74324900 single base substitution C T intron_variant MELA-AU 15 74325083 74325083 single base substitution C T downstream_gene_variant MELA-AU 15 74325083 74325083 single base substitution C T intron_variant MELA-AU 15 74325202 74325202 single base substitution C T downstream_gene_variant MELA-AU 15 74325202 74325202 single base substitution C T intron_variant MELA-AU 15 74326306 74326306 single base substitution T C 3_prime_UTR_variant MELA-AU 15 74326306 74326306 single base substitution T C downstream_gene_variant MELA-AU 15 74326306 74326306 single base substitution T C intron_variant MELA-AU 15 74326743 74326743 single base substitution C T 3_prime_UTR_variant MELA-AU 15 74326743 74326743 single base substitution C T downstream_gene_variant MELA-AU 15 74326743 74326743 single base substitution C T intron_variant MELA-AU 15 74327338 74327338 single base substitution C T 3_prime_UTR_variant MELA-AU 15 74327338 74327338 single base substitution C T downstream_gene_variant MELA-AU 15 74327338 74327338 single base substitution C T intron_variant MELA-AU 15 74327380 74327380 single base substitution C T 3_prime_UTR_variant MELA-AU 15 74327380 74327380 single base substitution C T downstream_gene_variant MELA-AU 15 74327380 74327380 single base substitution C T intron_variant MELA-AU 15 74327535 74327535 single base substitution C T 3_prime_UTR_variant MELA-AU 15 74327535 74327535 single base substitution C T downstream_gene_variant MELA-AU 15 74327535 74327535 single base substitution C T intron_variant MELA-AU 15 74327535 74327535 single base substitution C T missense_variant A530V 1589C>T MELA-AU 15 74327535 74327535 single base substitution C T missense_variant A578V 1733C>T MELA-AU 15 74327535 74327535 single base substitution C T synonymous_variant R591R 1773C>T MELA-AU 15 74327537 74327537 single base substitution G A 3_prime_UTR_variant MELA-AU 15 74327537 74327537 single base substitution G A downstream_gene_variant MELA-AU 15 74327537 74327537 single base substitution G A intron_variant MELA-AU 15 74327537 74327537 single base substitution G A missense_variant E531K 1591G>A MELA-AU 15 74327537 74327537 single base substitution G A missense_variant E579K 1735G>A MELA-AU 15 74327537 74327537 single base substitution G A missense_variant R592Q 1775G>A MELA-AU 15 74327852 74327852 single base substitution C T 3_prime_UTR_variant MELA-AU 15 74327852 74327852 single base substitution C T downstream_gene_variant MELA-AU 15 74327852 74327852 single base substitution C T intron_variant MELA-AU 15 74327852 74327852 single base substitution C T missense_variant R636W 1906C>T MELA-AU 15 74327852 74327852 single base substitution C T missense_variant R684W 2050C>T MELA-AU 15 74328022 74328022 single base substitution C T 3_prime_UTR_variant MELA-AU 15 74328022 74328022 single base substitution C T downstream_gene_variant MELA-AU 15 74328022 74328022 single base substitution C T intron_variant MELA-AU 15 74328022 74328022 single base substitution C T synonymous_variant S692S 2076C>T MELA-AU 15 74328022 74328022 single base substitution C T synonymous_variant S740S 2220C>T MELA-AU 15 74328930 74328930 single base substitution C T downstream_gene_variant MELA-AU 15 74328930 74328930 single base substitution C T intron_variant MELA-AU 15 74328930 74328930 single base substitution C T upstream_gene_variant MELA-AU 15 74329061 74329061 single base substitution C T downstream_gene_variant MELA-AU 15 74329061 74329061 single base substitution C T intron_variant MELA-AU 15 74329061 74329061 single base substitution C T upstream_gene_variant MELA-AU 15 74329062 74329062 single base substitution C T downstream_gene_variant MELA-AU 15 74329062 74329062 single base substitution C T intron_variant MELA-AU 15 74329062 74329062 single base substitution C T upstream_gene_variant MELA-AU 15 74329259 74329259 single base substitution C T downstream_gene_variant MELA-AU 15 74329259 74329259 single base substitution C T intron_variant MELA-AU 15 74329259 74329259 single base substitution C T upstream_gene_variant MELA-AU 15 74329396 74329396 single base substitution C T downstream_gene_variant MELA-AU 15 74329396 74329396 single base substitution C T intron_variant MELA-AU 15 74329396 74329396 single base substitution C T upstream_gene_variant MELA-AU 15 74329700 74329700 single base substitution C T downstream_gene_variant MELA-AU 15 74329700 74329700 single base substitution C T intron_variant MELA-AU 15 74329700 74329700 single base substitution C T upstream_gene_variant MELA-AU 15 74329926 74329926 single base substitution C T downstream_gene_variant MELA-AU 15 74329926 74329926 single base substitution C T intron_variant MELA-AU 15 74329926 74329926 single base substitution C T upstream_gene_variant MELA-AU 15 74330395 74330395 single base substitution C T downstream_gene_variant MELA-AU 15 74330395 74330395 single base substitution C T intron_variant MELA-AU 15 74330395 74330395 single base substitution C T upstream_gene_variant MELA-AU 15 74330854 74330854 single base substitution C T downstream_gene_variant MELA-AU 15 74330854 74330854 single base substitution C T intron_variant MELA-AU 15 74330854 74330854 single base substitution C T upstream_gene_variant MELA-AU 15 74331263 74331263 single base substitution C T downstream_gene_variant MELA-AU 15 74331263 74331263 single base substitution C T intron_variant MELA-AU 15 74331263 74331263 single base substitution C T upstream_gene_variant MELA-AU 15 74331390 74331390 single base substitution C T downstream_gene_variant MELA-AU 15 74331390 74331390 single base substitution C T intron_variant MELA-AU 15 74331390 74331390 single base substitution C T upstream_gene_variant MELA-AU 15 74332195 74332195 single base substitution G A downstream_gene_variant MELA-AU 15 74332195 74332195 single base substitution G A intron_variant MELA-AU 15 74332195 74332195 single base substitution G A upstream_gene_variant MELA-AU 15 74332271 74332271 single base substitution C T downstream_gene_variant MELA-AU 15 74332271 74332271 single base substitution C T intron_variant MELA-AU 15 74332271 74332271 single base substitution C T upstream_gene_variant MELA-AU 15 74332517 74332517 single base substitution C T downstream_gene_variant MELA-AU 15 74332517 74332517 single base substitution C T intron_variant MELA-AU 15 74332517 74332517 single base substitution C T upstream_gene_variant MELA-AU 15 74332774 74332774 single base substitution C T downstream_gene_variant MELA-AU 15 74332774 74332774 single base substitution C T intron_variant MELA-AU 15 74332774 74332774 single base substitution C T upstream_gene_variant MELA-AU 15 74333067 74333068 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 15 74333067 74333068 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 15 74333067 74333068 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 15 74333565 74333565 single base substitution G A downstream_gene_variant MELA-AU 15 74333565 74333565 single base substitution G A intron_variant MELA-AU 15 74333565 74333565 single base substitution G A upstream_gene_variant MELA-AU 15 74334455 74334456 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 15 74334477 74334477 single base substitution G A intron_variant MELA-AU 15 74334510 74334510 single base substitution C T intron_variant MELA-AU 15 74334628 74334628 single base substitution C T intron_variant MELA-AU 15 74334696 74334696 single base substitution C T intron_variant MELA-AU 15 74334697 74334697 single base substitution C T intron_variant MELA-AU 15 74335321 74335321 single base substitution G A intron_variant MELA-AU 15 74335331 74335331 single base substitution C T missense_variant S523F 1568C>T MELA-AU 15 74335331 74335331 single base substitution C T missense_variant S571F 1712C>T MELA-AU 15 74335331 74335331 single base substitution C T splice_region_variant MELA-AU 15 74335875 74335875 single base substitution G A downstream_gene_variant MELA-AU 15 74335875 74335875 single base substitution G A intron_variant MELA-AU 15 74335927 74335927 single base substitution C T downstream_gene_variant MELA-AU 15 74335927 74335927 single base substitution C T intron_variant MELA-AU 15 74336649 74336649 single base substitution C T downstream_gene_variant MELA-AU 15 74336649 74336649 single base substitution C T missense_variant S602F 1805C>T MELA-AU 15 74336649 74336649 single base substitution C T missense_variant S650F 1949C>T MELA-AU 15 74336686 74336686 single base substitution C T downstream_gene_variant MELA-AU 15 74336686 74336686 single base substitution C T synonymous_variant F614F 1842C>T MELA-AU 15 74336686 74336686 single base substitution C T synonymous_variant F662F 1986C>T MELA-AU 15 74337086 74337086 single base substitution C T downstream_gene_variant MELA-AU 15 74337086 74337086 single base substitution C T missense_variant R748C 2242C>T MELA-AU 15 74337086 74337086 single base substitution C T missense_variant R796C 2386C>T MELA-AU 15 74337317 74337317 single base substitution G T downstream_gene_variant MELA-AU 15 74337317 74337317 single base substitution G T missense_variant G825C 2473G>T MELA-AU 15 74337317 74337317 single base substitution G T missense_variant G873C 2617G>T MELA-AU 15 74337324 74337324 single base substitution C A downstream_gene_variant MELA-AU 15 74337324 74337324 single base substitution C A missense_variant A827E 2480C>A MELA-AU 15 74337324 74337324 single base substitution C A missense_variant A875E 2624C>A MELA-AU 15 74337645 74337645 single base substitution T C 3_prime_UTR_variant MELA-AU 15 74337645 74337645 single base substitution T C downstream_gene_variant MELA-AU 15 74337966 74337966 single base substitution G A 3_prime_UTR_variant MELA-AU 15 74337966 74337966 single base substitution G A downstream_gene_variant MELA-AU 15 74338224 74338224 single base substitution C T 3_prime_UTR_variant MELA-AU 15 74338224 74338224 single base substitution C T downstream_gene_variant MELA-AU 15 74338365 74338365 single base substitution C T 3_prime_UTR_variant MELA-AU 15 74338365 74338365 single base substitution C T downstream_gene_variant MELA-AU 15 74338415 74338415 single base substitution C T 3_prime_UTR_variant MELA-AU 15 74338415 74338415 single base substitution C T downstream_gene_variant MELA-AU 15 74339026 74339026 single base substitution C T 3_prime_UTR_variant MELA-AU 15 74339026 74339026 single base substitution C T downstream_gene_variant MELA-AU 15 74339312 74339312 single base substitution G A 3_prime_UTR_variant MELA-AU 15 74339312 74339312 single base substitution G A downstream_gene_variant MELA-AU 15 74339443 74339443 single base substitution G A 3_prime_UTR_variant MELA-AU 15 74339443 74339443 single base substitution G A downstream_gene_variant MELA-AU 15 74339635 74339635 single base substitution C T 3_prime_UTR_variant MELA-AU 15 74339635 74339635 single base substitution C T downstream_gene_variant MELA-AU 15 74339768 74339768 single base substitution T C 3_prime_UTR_variant MELA-AU 15 74339768 74339768 single base substitution T C downstream_gene_variant MELA-AU 15 74339772 74339772 single base substitution C T 3_prime_UTR_variant MELA-AU 15 74339772 74339772 single base substitution C T downstream_gene_variant MELA-AU 15 74341237 74341237 single base substitution C T downstream_gene_variant MELA-AU 15 74341374 74341374 single base substitution G A downstream_gene_variant MELA-AU 15 74341964 74341964 single base substitution G A downstream_gene_variant MELA-AU 15 74342124 74342124 single base substitution G A downstream_gene_variant MELA-AU 15 74342357 74342357 single base substitution C T downstream_gene_variant MELA-AU 15 74342425 74342425 single base substitution G C downstream_gene_variant MELA-AU 15 74342870 74342870 single base substitution C T downstream_gene_variant MELA-AU 15 74342923 74342923 single base substitution A G downstream_gene_variant MELA-AU 15 74342945 74342945 single base substitution C T downstream_gene_variant MELA-AU 15 74342966 74342966 single base substitution G A downstream_gene_variant MELA-AU 15 74343140 74343140 single base substitution C T downstream_gene_variant MELA-AU 15 74343157 74343157 single base substitution C T downstream_gene_variant MELA-AU 15 74344184 74344184 single base substitution C T downstream_gene_variant MELA-AU 15 74344386 74344386 single base substitution C T downstream_gene_variant MELA-AU 15 74344540 74344540 single base substitution C T downstream_gene_variant MELA-AU 15 74344691 74344691 single base substitution T G downstream_gene_variant ORCA-IN 15 74305585 74305585 single base substitution C G intron_variant ORCA-IN 15 74313717 74313717 single base substitution C T intron_variant ORCA-IN 15 74313717 74313717 single base substitution C T upstream_gene_variant ORCA-IN 15 74315516 74315516 single base substitution G T exon_variant ORCA-IN 15 74315516 74315516 single base substitution G T missense_variant G317V 950G>T ORCA-IN 15 74315516 74315516 single base substitution G T missense_variant G65V 194G>T ORCA-IN 15 74315516 74315516 single base substitution G T missense_variant G88V 263G>T ORCA-IN 15 74315516 74315516 single base substitution G T upstream_gene_variant ORCA-IN 15 74320543 74320543 single base substitution G A exon_variant ORCA-IN 15 74320543 74320543 single base substitution G A intron_variant ORCA-IN 15 74320543 74320543 single base substitution G A upstream_gene_variant ORCA-IN 15 74321480 74321480 single base substitution C T downstream_gene_variant ORCA-IN 15 74321480 74321480 single base substitution C T intron_variant ORCA-IN 15 74321480 74321480 single base substitution C T upstream_gene_variant ORCA-IN 15 74336748 74336748 single base substitution G A downstream_gene_variant ORCA-IN 15 74336748 74336748 single base substitution G A missense_variant G635D 1904G>A ORCA-IN 15 74336748 74336748 single base substitution G A missense_variant G683D 2048G>A ORCA-IN 15 74336986 74336986 deletion of <=200bp C - downstream_gene_variant ORCA-IN 15 74336986 74336986 deletion of <=200bp C - frameshift_variant G714 ORCA-IN 15 74336986 74336986 deletion of <=200bp C - frameshift_variant G762 OV-AU 15 74285005 74285005 single base substitution G C upstream_gene_variant OV-AU 15 74290464 74290464 single base substitution G A exon_variant OV-AU 15 74290464 74290464 single base substitution G A synonymous_variant A83A 249G>A OV-AU 15 74296269 74296269 single base substitution G C intron_variant OV-AU 15 74305358 74305358 single base substitution C T intron_variant OV-AU 15 74307483 74307483 single base substitution C T intron_variant OV-AU 15 74313268 74313268 single base substitution G A intron_variant OV-AU 15 74313268 74313268 single base substitution G A upstream_gene_variant OV-AU 15 74313691 74313691 single base substitution G T intron_variant OV-AU 15 74313691 74313691 single base substitution G T upstream_gene_variant PACA-AU 15 74285207 74285207 single base substitution G A upstream_gene_variant PACA-AU 15 74287933 74287933 single base substitution C A intron_variant PACA-AU 15 74287933 74287933 single base substitution C A upstream_gene_variant PACA-AU 15 74290400 74290400 single base substitution C T exon_variant PACA-AU 15 74290400 74290400 single base substitution C T missense_variant A62V 185C>T PACA-AU 15 74293466 74293466 deletion of <=200bp T - intron_variant PACA-AU 15 74295965 74295965 single base substitution T G intron_variant PACA-AU 15 74296246 74296246 single base substitution G A intron_variant PACA-AU 15 74299050 74299050 single base substitution T G intron_variant PACA-AU 15 74304025 74304025 single base substitution A G intron_variant PACA-AU 15 74306876 74306876 single base substitution G A intron_variant PACA-AU 15 74311208 74311208 single base substitution G A intron_variant PACA-AU 15 74311208 74311208 single base substitution G A upstream_gene_variant PACA-AU 15 74312202 74312202 single base substitution C G intron_variant PACA-AU 15 74312202 74312202 single base substitution C G upstream_gene_variant PACA-AU 15 74314041 74314041 single base substitution G A intron_variant PACA-AU 15 74314041 74314041 single base substitution G A upstream_gene_variant PACA-AU 15 74314047 74314047 single base substitution T A intron_variant PACA-AU 15 74314047 74314047 single base substitution T A upstream_gene_variant PACA-AU 15 74315298 74315298 single base substitution G A exon_variant PACA-AU 15 74315298 74315298 single base substitution G A synonymous_variant T15T 45G>A PACA-AU 15 74315298 74315298 single base substitution G A synonymous_variant T244T 732G>A PACA-AU 15 74315298 74315298 single base substitution G A upstream_gene_variant PACA-AU 15 74333300 74333300 single base substitution C T downstream_gene_variant PACA-AU 15 74333300 74333300 single base substitution C T intron_variant PACA-AU 15 74333300 74333300 single base substitution C T upstream_gene_variant PACA-AU 15 74335432 74335432 single base substitution G T 3_prime_UTR_variant PACA-AU 15 74335432 74335432 single base substitution G T exon_variant PACA-AU 15 74335432 74335432 single base substitution G T missense_variant A557S 1669G>T PACA-AU 15 74335432 74335432 single base substitution G T missense_variant A605S 1813G>T PACA-AU 15 74337086 74337086 single base substitution C T downstream_gene_variant PACA-AU 15 74337086 74337086 single base substitution C T missense_variant R748C 2242C>T PACA-AU 15 74337086 74337086 single base substitution C T missense_variant R796C 2386C>T PACA-AU 15 74340659 74340661 deletion of <=200bp CTC - downstream_gene_variant PACA-AU 15 74345090 74345090 single base substitution C T downstream_gene_variant PACA-CA 15 74282582 74282582 single base substitution G T upstream_gene_variant PACA-CA 15 74285837 74285837 single base substitution T C upstream_gene_variant PACA-CA 15 74296179 74296179 single base substitution C A intron_variant PACA-CA 15 74296274 74296274 single base substitution A C intron_variant PACA-CA 15 74298586 74298586 single base substitution G A intron_variant PACA-CA 15 74299515 74299515 insertion of <=200bp - T intron_variant PACA-CA 15 74304848 74304848 single base substitution G A intron_variant PACA-CA 15 74314708 74314708 single base substitution C T intron_variant PACA-CA 15 74314708 74314708 single base substitution C T upstream_gene_variant PACA-CA 15 74315383 74315383 single base substitution G A exon_variant PACA-CA 15 74315383 74315383 single base substitution G A missense_variant A21T 61G>A PACA-CA 15 74315383 74315383 single base substitution G A missense_variant A273T 817G>A PACA-CA 15 74315383 74315383 single base substitution G A missense_variant A44T 130G>A PACA-CA 15 74315383 74315383 single base substitution G A upstream_gene_variant PACA-CA 15 74318580 74318580 single base substitution C T exon_variant PACA-CA 15 74318580 74318580 single base substitution C T intron_variant PACA-CA 15 74319336 74319336 single base substitution T C exon_variant PACA-CA 15 74319336 74319336 single base substitution T C intron_variant PACA-CA 15 74319538 74319538 single base substitution A T exon_variant PACA-CA 15 74319538 74319538 single base substitution A T intron_variant PACA-CA 15 74321638 74321638 single base substitution T C downstream_gene_variant PACA-CA 15 74321638 74321638 single base substitution T C intron_variant PACA-CA 15 74321638 74321638 single base substitution T C upstream_gene_variant PACA-CA 15 74324717 74324717 single base substitution T A downstream_gene_variant PACA-CA 15 74324717 74324717 single base substitution T A intron_variant PACA-CA 15 74324717 74324717 single base substitution T A upstream_gene_variant PACA-CA 15 74324999 74324999 single base substitution C T downstream_gene_variant PACA-CA 15 74324999 74324999 single base substitution C T exon_variant PACA-CA 15 74324999 74324999 single base substitution C T intron_variant PACA-CA 15 74324999 74324999 single base substitution C T synonymous_variant P218P 654C>T PACA-CA 15 74324999 74324999 single base substitution C T synonymous_variant P447P 1341C>T PACA-CA 15 74324999 74324999 single base substitution C T synonymous_variant P90P 270C>T PACA-CA 15 74325023 74325023 single base substitution C T downstream_gene_variant PACA-CA 15 74325023 74325023 single base substitution C T exon_variant PACA-CA 15 74325023 74325023 single base substitution C T intron_variant PACA-CA 15 74325023 74325023 single base substitution C T synonymous_variant Y226Y 678C>T PACA-CA 15 74325023 74325023 single base substitution C T synonymous_variant Y455Y 1365C>T PACA-CA 15 74325023 74325023 single base substitution C T synonymous_variant Y98Y 294C>T PACA-CA 15 74326068 74326068 single base substitution G C 3_prime_UTR_variant PACA-CA 15 74326068 74326068 single base substitution G C downstream_gene_variant PACA-CA 15 74326068 74326068 single base substitution G C intron_variant PACA-CA 15 74333300 74333300 single base substitution C T downstream_gene_variant PACA-CA 15 74333300 74333300 single base substitution C T intron_variant PACA-CA 15 74333300 74333300 single base substitution C T upstream_gene_variant PACA-CA 15 74334283 74334283 single base substitution C A intron_variant PACA-CA 15 74337896 74337896 single base substitution C A 3_prime_UTR_variant PACA-CA 15 74337896 74337896 single base substitution C A downstream_gene_variant PACA-CA 15 74341876 74341876 single base substitution G C downstream_gene_variant PACA-CA 15 74342308 74342308 insertion of <=200bp - C downstream_gene_variant PAEN-AU 15 74320783 74320783 single base substitution C A exon_variant PAEN-AU 15 74320783 74320783 single base substitution C A intron_variant PAEN-AU 15 74320783 74320783 single base substitution C A upstream_gene_variant PAEN-AU 15 74337109 74337109 single base substitution G T downstream_gene_variant PAEN-AU 15 74337109 74337109 single base substitution G T synonymous_variant V755V 2265G>T PAEN-AU 15 74337109 74337109 single base substitution G T synonymous_variant V803V 2409G>T PAEN-IT 15 74303973 74303973 single base substitution A T intron_variant PBCA-DE 15 74285761 74285761 single base substitution G A upstream_gene_variant PBCA-DE 15 74313927 74313927 insertion of <=200bp - A intron_variant PBCA-DE 15 74313927 74313927 insertion of <=200bp - A upstream_gene_variant PBCA-DE 15 74320428 74320428 single base substitution G T exon_variant PBCA-DE 15 74320428 74320428 single base substitution G T intron_variant PBCA-DE 15 74320428 74320428 single base substitution G T upstream_gene_variant PBCA-DE 15 74320429 74320429 single base substitution A T exon_variant PBCA-DE 15 74320429 74320429 single base substitution A T intron_variant PBCA-DE 15 74320429 74320429 single base substitution A T upstream_gene_variant PBCA-DE 15 74328116 74328116 single base substitution A G 3_prime_UTR_variant PBCA-DE 15 74328116 74328116 single base substitution A G downstream_gene_variant PBCA-DE 15 74328116 74328116 single base substitution A G intron_variant PBCA-DE 15 74328116 74328116 single base substitution A G missense_variant S724G 2170A>G PBCA-DE 15 74328116 74328116 single base substitution A G missense_variant S772G 2314A>G PBCA-DE 15 74334044 74334044 single base substitution C A intron_variant PBCA-DE 15 74334641 74334641 deletion of <=200bp G - intron_variant PBCA-DE 15 74337040 74337040 single base substitution C T downstream_gene_variant PBCA-DE 15 74337040 74337040 single base substitution C T synonymous_variant S732S 2196C>T PBCA-DE 15 74337040 74337040 single base substitution C T synonymous_variant S780S 2340C>T PBCA-DE 15 74339819 74339819 single base substitution C A 3_prime_UTR_variant PBCA-DE 15 74339819 74339819 single base substitution C A downstream_gene_variant PBCA-DE 15 74341815 74341815 single base substitution G T downstream_gene_variant PBCA-DE 15 74344735 74344735 insertion of <=200bp - CACA downstream_gene_variant PBCA-DE 15 74344736 74344736 insertion of <=200bp - CCCTC downstream_gene_variant PRAD-CA 15 74282517 74282517 single base substitution C T upstream_gene_variant PRAD-CA 15 74302873 74302873 single base substitution A G intron_variant PRAD-CA 15 74303804 74303804 single base substitution C T intron_variant PRAD-CA 15 74311576 74311576 single base substitution C T intron_variant PRAD-CA 15 74311576 74311576 single base substitution C T upstream_gene_variant PRAD-CA 15 74320556 74320556 single base substitution T C exon_variant PRAD-CA 15 74320556 74320556 single base substitution T C intron_variant PRAD-CA 15 74320556 74320556 single base substitution T C upstream_gene_variant PRAD-CA 15 74333406 74333406 single base substitution T C downstream_gene_variant PRAD-CA 15 74333406 74333406 single base substitution T C intron_variant PRAD-CA 15 74333406 74333406 single base substitution T C upstream_gene_variant PRAD-CA 15 74333674 74333674 single base substitution G A downstream_gene_variant PRAD-CA 15 74333674 74333674 single base substitution G A exon_variant PRAD-CA 15 74333674 74333674 single base substitution G A intron_variant PRAD-UK 15 74306257 74306257 single base substitution T C intron_variant PRAD-UK 15 74310996 74310996 single base substitution T G intron_variant PRAD-UK 15 74310996 74310996 single base substitution T G upstream_gene_variant PRAD-UK 15 74332443 74332443 single base substitution C T downstream_gene_variant PRAD-UK 15 74332443 74332443 single base substitution C T intron_variant PRAD-UK 15 74332443 74332443 single base substitution C T upstream_gene_variant PRAD-US 15 74327550 74327550 single base substitution C T 3_prime_UTR_variant PRAD-US 15 74327550 74327550 single base substitution C T downstream_gene_variant PRAD-US 15 74327550 74327550 single base substitution C T intron_variant PRAD-US 15 74327550 74327550 single base substitution C T missense_variant S535L 1604C>T PRAD-US 15 74327550 74327550 single base substitution C T missense_variant S583L 1748C>T PRAD-US 15 74327550 74327550 single base substitution C T synonymous_variant L596L 1788C>T PRAD-US 15 74335504 74335504 single base substitution C T 3_prime_UTR_variant PRAD-US 15 74335504 74335504 single base substitution C T exon_variant PRAD-US 15 74335504 74335504 single base substitution C T intron_variant PRAD-US 15 74335504 74335504 single base substitution C T missense_variant H581Y 1741C>T PRAD-US 15 74335504 74335504 single base substitution C T missense_variant H629Y 1885C>T PRAD-US 15 74336765 74336765 single base substitution C T downstream_gene_variant PRAD-US 15 74336765 74336765 single base substitution C T missense_variant R641W 1921C>T PRAD-US 15 74336765 74336765 single base substitution C T missense_variant R689W 2065C>T RECA-EU 15 74283301 74283301 single base substitution C T upstream_gene_variant RECA-EU 15 74283589 74283589 single base substitution C A upstream_gene_variant RECA-EU 15 74287092 74287092 single base substitution C T 5_prime_UTR_variant RECA-EU 15 74287092 74287092 single base substitution C T upstream_gene_variant RECA-EU 15 74295560 74295560 single base substitution G A intron_variant RECA-EU 15 74327822 74327822 single base substitution T A 3_prime_UTR_variant RECA-EU 15 74327822 74327822 single base substitution T A downstream_gene_variant RECA-EU 15 74327822 74327822 single base substitution T A intron_variant RECA-EU 15 74327822 74327822 single base substitution T A missense_variant L626M 1876T>A RECA-EU 15 74327822 74327822 single base substitution T A missense_variant L674M 2020T>A RECA-EU 15 74339047 74339047 single base substitution G A 3_prime_UTR_variant RECA-EU 15 74339047 74339047 single base substitution G A downstream_gene_variant RECA-EU 15 74339470 74339470 single base substitution A T 3_prime_UTR_variant RECA-EU 15 74339470 74339470 single base substitution A T downstream_gene_variant SKCA-BR 15 74288805 74288805 single base substitution T C intron_variant SKCA-BR 15 74288805 74288805 single base substitution T C upstream_gene_variant SKCA-BR 15 74289937 74289937 single base substitution T C intron_variant SKCA-BR 15 74289937 74289937 single base substitution T C upstream_gene_variant SKCA-BR 15 74299494 74299494 single base substitution T C intron_variant SKCA-BR 15 74301105 74301105 single base substitution C T intron_variant SKCA-BR 15 74303991 74303991 single base substitution G A intron_variant SKCA-BR 15 74310189 74310189 single base substitution C T intron_variant SKCA-BR 15 74312628 74312629 deletion of <=200bp CT - intron_variant SKCA-BR 15 74312628 74312629 deletion of <=200bp CT - upstream_gene_variant SKCA-BR 15 74314497 74314497 single base substitution C T intron_variant SKCA-BR 15 74314497 74314497 single base substitution C T upstream_gene_variant SKCA-BR 15 74318182 74318182 single base substitution T C exon_variant SKCA-BR 15 74318182 74318182 single base substitution T C intron_variant SKCA-BR 15 74323830 74323830 single base substitution C T downstream_gene_variant SKCA-BR 15 74323830 74323830 single base substitution C T intron_variant SKCA-BR 15 74323830 74323830 single base substitution C T upstream_gene_variant SKCA-BR 15 74325422 74325422 single base substitution C T downstream_gene_variant SKCA-BR 15 74325422 74325422 single base substitution C T intron_variant SKCA-BR 15 74325612 74325612 single base substitution C T downstream_gene_variant SKCA-BR 15 74325612 74325612 single base substitution C T intron_variant SKCA-BR 15 74325612 74325612 single base substitution C T missense_variant S148F 443C>T SKCA-BR 15 74325612 74325612 single base substitution C T missense_variant S205F 614C>T SKCA-BR 15 74325612 74325612 single base substitution C T missense_variant S457F 1370C>T SKCA-BR 15 74325612 74325612 single base substitution C T missense_variant S505F 1514C>T SKCA-BR 15 74325612 74325612 single base substitution C T missense_variant S55F 164C>T SKCA-BR 15 74325932 74325932 single base substitution C T downstream_gene_variant SKCA-BR 15 74325932 74325932 single base substitution C T intron_variant SKCA-BR 15 74325932 74325932 single base substitution C T missense_variant P564S 1690C>T SKCA-BR 15 74327214 74327214 single base substitution C T 3_prime_UTR_variant SKCA-BR 15 74327214 74327214 single base substitution C T downstream_gene_variant SKCA-BR 15 74327214 74327214 single base substitution C T intron_variant SKCA-BR 15 74327264 74327264 single base substitution C T 3_prime_UTR_variant SKCA-BR 15 74327264 74327264 single base substitution C T downstream_gene_variant SKCA-BR 15 74327264 74327264 single base substitution C T intron_variant SKCA-BR 15 74328916 74328916 single base substitution G A downstream_gene_variant SKCA-BR 15 74328916 74328916 single base substitution G A intron_variant SKCA-BR 15 74328916 74328916 single base substitution G A upstream_gene_variant SKCA-BR 15 74331385 74331385 single base substitution T C downstream_gene_variant SKCA-BR 15 74331385 74331385 single base substitution T C intron_variant SKCA-BR 15 74331385 74331385 single base substitution T C upstream_gene_variant SKCA-BR 15 74333983 74333983 single base substitution C T intron_variant SKCA-BR 15 74335805 74335805 single base substitution C T downstream_gene_variant SKCA-BR 15 74335805 74335805 single base substitution C T intron_variant SKCA-BR 15 74339113 74339113 single base substitution G A 3_prime_UTR_variant SKCA-BR 15 74339113 74339113 single base substitution G A downstream_gene_variant SKCA-BR 15 74340906 74340906 single base substitution G A downstream_gene_variant SKCM-US 15 74284463 74284463 single base substitution G A upstream_gene_variant SKCM-US 15 74284493 74284493 single base substitution G A upstream_gene_variant SKCM-US 15 74290467 74290467 single base substitution G A exon_variant SKCM-US 15 74290467 74290467 single base substitution G A synonymous_variant S84S 252G>A SKCM-US 15 74290542 74290542 single base substitution C T exon_variant SKCM-US 15 74290542 74290542 single base substitution C T synonymous_variant F109F 327C>T SKCM-US 15 74290560 74290560 single base substitution C T exon_variant SKCM-US 15 74290560 74290560 single base substitution C T synonymous_variant R115R 345C>T SKCM-US 15 74325046 74325046 single base substitution C T downstream_gene_variant SKCM-US 15 74325046 74325046 single base substitution C T exon_variant SKCM-US 15 74325046 74325046 single base substitution C T intron_variant SKCM-US 15 74325046 74325046 single base substitution C T missense_variant S106F 317C>T SKCM-US 15 74325046 74325046 single base substitution C T missense_variant S463F 1388C>T SKCM-US 15 74325046 74325046 single base substitution C T splice_region_variant SKCM-US 15 74336649 74336649 single base substitution C T downstream_gene_variant SKCM-US 15 74336649 74336649 single base substitution C T missense_variant S602F 1805C>T SKCM-US 15 74336649 74336649 single base substitution C T missense_variant S650F 1949C>T SKCM-US 15 74336704 74336704 single base substitution C T downstream_gene_variant SKCM-US 15 74336704 74336704 single base substitution C T synonymous_variant S620S 1860C>T SKCM-US 15 74336704 74336704 single base substitution C T synonymous_variant S668S 2004C>T SKCM-US 15 74337233 74337233 single base substitution G A downstream_gene_variant SKCM-US 15 74337233 74337233 single base substitution G A missense_variant A797T 2389G>A SKCM-US 15 74337233 74337233 single base substitution G A missense_variant A845T 2533G>A STAD-US 15 74290464 74290464 single base substitution G A exon_variant STAD-US 15 74290464 74290464 single base substitution G A synonymous_variant A83A 249G>A STAD-US 15 74290466 74290466 single base substitution C T exon_variant STAD-US 15 74290466 74290466 single base substitution C T missense_variant S84L 251C>T STAD-US 15 74290724 74290724 single base substitution G A exon_variant STAD-US 15 74290724 74290724 single base substitution G A missense_variant R170H 509G>A STAD-US 15 74290799 74290799 single base substitution G A exon_variant STAD-US 15 74290799 74290799 single base substitution G A missense_variant R195H 584G>A STAD-US 15 74315304 74315304 single base substitution G A exon_variant STAD-US 15 74315304 74315304 single base substitution G A synonymous_variant A17A 51G>A STAD-US 15 74315304 74315304 single base substitution G A synonymous_variant A246A 738G>A STAD-US 15 74315304 74315304 single base substitution G A upstream_gene_variant STAD-US 15 74315437 74315437 single base substitution C T exon_variant STAD-US 15 74315437 74315437 single base substitution C T missense_variant R291W 871C>T STAD-US 15 74315437 74315437 single base substitution C T missense_variant R39W 115C>T STAD-US 15 74315437 74315437 single base substitution C T missense_variant R62W 184C>T STAD-US 15 74315437 74315437 single base substitution C T upstream_gene_variant STAD-US 15 74315474 74315474 single base substitution C T exon_variant STAD-US 15 74315474 74315474 single base substitution C T missense_variant A303V 908C>T STAD-US 15 74315474 74315474 single base substitution C T missense_variant A51V 152C>T STAD-US 15 74315474 74315474 single base substitution C T missense_variant A74V 221C>T STAD-US 15 74315474 74315474 single base substitution C T upstream_gene_variant STAD-US 15 74315644 74315644 single base substitution C T exon_variant STAD-US 15 74315644 74315644 single base substitution C T missense_variant R108C 322C>T STAD-US 15 74315644 74315644 single base substitution C T missense_variant R131C 391C>T STAD-US 15 74315644 74315644 single base substitution C T missense_variant R360C 1078C>T STAD-US 15 74315644 74315644 single base substitution C T missense_variant R3C 7C>T STAD-US 15 74315644 74315644 single base substitution C T upstream_gene_variant STAD-US 15 74315664 74315664 single base substitution C A exon_variant STAD-US 15 74315664 74315664 single base substitution C A missense_variant S114R 342C>A STAD-US 15 74315664 74315664 single base substitution C A missense_variant S137R 411C>A STAD-US 15 74315664 74315664 single base substitution C A missense_variant S366R 1098C>A STAD-US 15 74315664 74315664 single base substitution C A missense_variant S9R 27C>A STAD-US 15 74315664 74315664 single base substitution C A upstream_gene_variant STAD-US 15 74315711 74315711 single base substitution G A exon_variant STAD-US 15 74315711 74315711 single base substitution G A intron_variant STAD-US 15 74315711 74315711 single base substitution G A missense_variant R130H 389G>A STAD-US 15 74315711 74315711 single base substitution G A missense_variant R153H 458G>A STAD-US 15 74315711 74315711 single base substitution G A missense_variant R25H 74G>A STAD-US 15 74315711 74315711 single base substitution G A missense_variant R382H 1145G>A STAD-US 15 74315711 74315711 single base substitution G A upstream_gene_variant STAD-US 15 74317252 74317252 single base substitution C T exon_variant STAD-US 15 74317252 74317252 single base substitution C T missense_variant P11L 32C>T STAD-US 15 74317252 74317252 single base substitution C T missense_variant P161L 482C>T STAD-US 15 74317252 74317252 single base substitution C T missense_variant P184L 551C>T STAD-US 15 74317252 74317252 single base substitution C T missense_variant P413L 1238C>T STAD-US 15 74317252 74317252 single base substitution C T missense_variant P56L 167C>T STAD-US 15 74325013 74325013 single base substitution T C downstream_gene_variant STAD-US 15 74325013 74325013 single base substitution T C exon_variant STAD-US 15 74325013 74325013 single base substitution T C intron_variant STAD-US 15 74325013 74325013 single base substitution T C missense_variant V223A 668T>C STAD-US 15 74325013 74325013 single base substitution T C missense_variant V452A 1355T>C STAD-US 15 74325013 74325013 single base substitution T C missense_variant V95A 284T>C STAD-US 15 74325745 74325745 single base substitution C T downstream_gene_variant STAD-US 15 74325745 74325745 single base substitution C T intron_variant STAD-US 15 74325745 74325745 single base substitution C T synonymous_variant A192A 576C>T STAD-US 15 74325745 74325745 single base substitution C T synonymous_variant A249A 747C>T STAD-US 15 74325745 74325745 single base substitution C T synonymous_variant A501A 1503C>T STAD-US 15 74325745 74325745 single base substitution C T synonymous_variant A549A 1647C>T STAD-US 15 74325745 74325745 single base substitution C T synonymous_variant A99A 297C>T STAD-US 15 74336586 74336586 single base substitution C T downstream_gene_variant STAD-US 15 74336586 74336586 single base substitution C T missense_variant A581V 1742C>T STAD-US 15 74336586 74336586 single base substitution C T missense_variant A629V 1886C>T STAD-US 15 74337044 74337044 single base substitution C T downstream_gene_variant STAD-US 15 74337044 74337044 single base substitution C T stop_gained Q734* 2200C>T STAD-US 15 74337044 74337044 single base substitution C T stop_gained Q782* 2344C>T THCA-SA 15 74327802 74327802 single base substitution G A 3_prime_UTR_variant THCA-SA 15 74327802 74327802 single base substitution G A downstream_gene_variant THCA-SA 15 74327802 74327802 single base substitution G A intron_variant THCA-SA 15 74327802 74327802 single base substitution G A missense_variant R619H 1856G>A THCA-SA 15 74327802 74327802 single base substitution G A missense_variant R667H 2000G>A THCA-SA 15 74328206 74328206 single base substitution G C 3_prime_UTR_variant THCA-SA 15 74328206 74328206 single base substitution G C downstream_gene_variant THCA-SA 15 74328206 74328206 single base substitution G C intron_variant THCA-SA 15 74328206 74328206 single base substitution G C missense_variant A754P 2260G>C THCA-SA 15 74328206 74328206 single base substitution G C missense_variant A802P 2404G>C THCA-SA 15 74336656 74336656 single base substitution C T downstream_gene_variant THCA-SA 15 74336656 74336656 single base substitution C T synonymous_variant A604A 1812C>T THCA-SA 15 74336656 74336656 single base substitution C T synonymous_variant A652A 1956C>T THCA-SA 15 74337281 74337281 single base substitution C A downstream_gene_variant THCA-SA 15 74337281 74337281 single base substitution C A synonymous_variant R813R 2437C>A THCA-SA 15 74337281 74337281 single base substitution C A synonymous_variant R861R 2581C>A THCA-US 15 74282792 74282792 single base substitution G A upstream_gene_variant UCEC-US 15 74290467 74290467 single base substitution G A exon_variant UCEC-US 15 74290467 74290467 single base substitution G A synonymous_variant S84S 252G>A UCEC-US 15 74290677 74290677 single base substitution A G exon_variant UCEC-US 15 74290677 74290677 single base substitution A G synonymous_variant A154A 462A>G UCEC-US 15 74315256 74315256 single base substitution C T exon_variant UCEC-US 15 74315256 74315256 single base substitution C T synonymous_variant S1S 3C>T UCEC-US 15 74315256 74315256 single base substitution C T synonymous_variant S230S 690C>T UCEC-US 15 74315256 74315256 single base substitution C T upstream_gene_variant UCEC-US 15 74315550 74315550 single base substitution G A exon_variant UCEC-US 15 74315550 74315550 single base substitution G A synonymous_variant T328T 984G>A UCEC-US 15 74315550 74315550 single base substitution G A synonymous_variant T76T 228G>A UCEC-US 15 74315550 74315550 single base substitution G A synonymous_variant T99T 297G>A UCEC-US 15 74315550 74315550 single base substitution G A upstream_gene_variant UCEC-US 15 74315776 74315776 single base substitution C T intron_variant UCEC-US 15 74315776 74315776 single base substitution C T upstream_gene_variant UCEC-US 15 74325012 74325012 single base substitution G A downstream_gene_variant UCEC-US 15 74325012 74325012 single base substitution G A exon_variant UCEC-US 15 74325012 74325012 single base substitution G A intron_variant UCEC-US 15 74325012 74325012 single base substitution G A missense_variant V223M 667G>A UCEC-US 15 74325012 74325012 single base substitution G A missense_variant V452M 1354G>A UCEC-US 15 74325012 74325012 single base substitution G A missense_variant V95M 283G>A UCEC-US 15 74325022 74325022 single base substitution A T downstream_gene_variant UCEC-US 15 74325022 74325022 single base substitution A T exon_variant UCEC-US 15 74325022 74325022 single base substitution A T intron_variant UCEC-US 15 74325022 74325022 single base substitution A T missense_variant Y226F 677A>T UCEC-US 15 74325022 74325022 single base substitution A T missense_variant Y455F 1364A>T UCEC-US 15 74325022 74325022 single base substitution A T missense_variant Y98F 293A>T UCEC-US 15 74325572 74325572 single base substitution G T downstream_gene_variant UCEC-US 15 74325572 74325572 single base substitution G T intron_variant UCEC-US 15 74325572 74325572 single base substitution G T stop_gained E135* 403G>T UCEC-US 15 74325572 74325572 single base substitution G T stop_gained E192* 574G>T UCEC-US 15 74325572 74325572 single base substitution G T stop_gained E42* 124G>T UCEC-US 15 74325572 74325572 single base substitution G T stop_gained E444* 1330G>T UCEC-US 15 74325572 74325572 single base substitution G T stop_gained E492* 1474G>T UCEC-US 15 74325601 74325601 single base substitution G T downstream_gene_variant UCEC-US 15 74325601 74325601 single base substitution G T intron_variant UCEC-US 15 74325601 74325601 single base substitution G T missense_variant L144F 432G>T UCEC-US 15 74325601 74325601 single base substitution G T missense_variant L201F 603G>T UCEC-US 15 74325601 74325601 single base substitution G T missense_variant L453F 1359G>T UCEC-US 15 74325601 74325601 single base substitution G T missense_variant L501F 1503G>T UCEC-US 15 74325601 74325601 single base substitution G T missense_variant L51F 153G>T UCEC-US 15 74326863 74326863 single base substitution G A 3_prime_UTR_variant UCEC-US 15 74326863 74326863 single base substitution G A downstream_gene_variant UCEC-US 15 74326863 74326863 single base substitution G A intron_variant UCEC-US 15 74326863 74326863 single base substitution G A missense_variant E211K 631G>A UCEC-US 15 74326863 74326863 single base substitution G A missense_variant E520K 1558G>A UCEC-US 15 74326863 74326863 single base substitution G A missense_variant E568K 1702G>A UCEC-US 15 74326969 74326969 single base substitution G T 3_prime_UTR_variant UCEC-US 15 74326969 74326969 single base substitution G T downstream_gene_variant UCEC-US 15 74326969 74326969 single base substitution G T intron_variant UCEC-US 15 74326969 74326969 single base substitution G T missense_variant R603L 1808G>T UCEC-US 15 74327546 74327560 deletion of <=200bp TCCTCGCCAGCCCAC - 3_prime_UTR_variant UCEC-US 15 74327546 74327560 deletion of <=200bp TCCTCGCCAGCCCAC - downstream_gene_variant UCEC-US 15 74327546 74327560 deletion of <=200bp TCCTCGCCAGCCCAC - inframe_deletion SSPAH534 UCEC-US 15 74327546 74327560 deletion of <=200bp TCCTCGCCAGCCCAC - inframe_deletion SSPAH582 UCEC-US 15 74327546 74327560 deletion of <=200bp TCCTCGCCAGCCCAC - inframe_deletion VLASPL595V UCEC-US 15 74327546 74327560 deletion of <=200bp TCCTCGCCAGCCCAC - intron_variant UCEC-US 15 74327566 74327566 single base substitution G A 3_prime_UTR_variant UCEC-US 15 74327566 74327566 single base substitution G A downstream_gene_variant UCEC-US 15 74327566 74327566 single base substitution G A intron_variant UCEC-US 15 74327566 74327566 single base substitution G A missense_variant A602T 1804G>A UCEC-US 15 74327566 74327566 single base substitution G A synonymous_variant S540S 1620G>A UCEC-US 15 74327566 74327566 single base substitution G A synonymous_variant S588S 1764G>A UCEC-US 15 74337160 74337162 deletion of <=200bp GAA - downstream_gene_variant UCEC-US 15 74337160 74337162 deletion of <=200bp GAA - inframe_deletion LK772L UCEC-US 15 74337160 74337162 deletion of <=200bp GAA - inframe_deletion LK820L

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand 1920_T COSM3956902 c.1335A>T p.S445S Substitution - coding silent 15:74032652-74032652 + I2L-P7-Tumor-Organoid COSM5363091 c.1910G>A p.R637H Substitution - Missense 15:74044269-74044269 + TCGA-AZ-6598-01 COSM1374493 c.2203G>A p.A735T Substitution - Missense 15:74044562-74044562 + 136T COSM5576025 c.1064C>T p.A355V Substitution - Missense 15:74023289-74023289 + CCC4T COSM3706724 c.2598C>T p.S866S Substitution - coding silent 15:74044957-74044957 + BN45T COSM1608665 c.2217C>T p.S739S Substitution - coding silent 15:74044576-74044576 + TCGA-AP-A054-01 COSM964753 c.2460_2462delGAA p.K822delK Deletion - In frame 15:74044819-74044821 + TCGA-NH-A5IV-01 COSM4335798 c.73delC p.E27fs*71 Deletion - Frameshift 15:73994885-73994885 + 8016470 COSM3387046 c.1813G>T p.A605S Substitution - Missense 15:74043091-74043091 + PT15_1 COSM5897897 c.1384C>T p.P462S Substitution - Missense 15:74032701-74032701 + BB65-RCC COSM21735 c.1259A>T p.E420V Substitution - Missense 15:74032576-74032576 + TCGA-FS-A1ZC-06 COSM3503806 c.327C>T p.F109F Substitution - coding silent 15:73998201-73998201 + HCC058T COSM5804391 c.658A>T p.S220C Substitution - Missense 15:74022883-74022883 + HCC24 COSM1608664 c.1736G>T p.S579I Substitution - Missense 15:74043014-74043014 + S01578 COSM5670338 c.810C>A p.R270R Substitution - coding silent 15:74023035-74023035 + 8051734 COSM4136300 c.2409G>T p.V803V Substitution - coding silent 15:74044768-74044768 + TCGA-CA-6715-01 COSM1374479 c.583C>T p.R195C Substitution - Missense 15:73998457-73998457 + RKO COSM4614762 c.72_73insC p.E27fs*5 Insertion - Frameshift 15:73994884-73994885 + YUDON COSM5383806 c.1743G>A p.E581E Substitution - coding silent 15:74043021-74043021 + LUAD-B02077 COSM335028 c.544C>T p.R182C Substitution - Missense 15:73998418-73998418 + SNU-C4 COSM4652627 c.998T>C p.V333A Substitution - Missense 15:74023223-74023223 + PD2184a COSM28025 c.351G>A p.S117S Substitution - coding silent 15:73998225-73998225 + T3503 COSM1937913 c.793G>A p.V265I Substitution - Missense 15:74023018-74023018 + PCSI_0083_Pa_X COSM3377645 c.1365C>T p.Y455Y Substitution - coding silent 15:74032682-74032682 + HCC070T COSM5818208 c.2462A>G p.K821R Substitution - Missense 15:74044821-74044821 + 3N46-VS-3T46 COSM4982467 c.1251C>T p.D417D Substitution - coding silent 15:74024924-74024924 + T2643 COSM4716085 c.809G>A p.R270H Substitution - Missense 15:74023034-74023034 + 255 COSM3731791 c.429C>T p.C143C Substitution - coding silent 15:73998303-73998303 + RMS105_ COSM3754465 c.1933T>C p.F645L Substitution - Missense 15:74044292-74044292 + 4_RESISTANT COSM1724220 c.916C>T p.Q306* Substitution - Nonsense 15:74023141-74023141 + BCM723T COSM4956565 c.775G>A p.A259T Substitution - Missense 15:74023000-74023000 + CHC2048T COSM4793177 c.1771A>T p.S591C Substitution - Missense 15:74043049-74043049 + TCGA-D1-A167-01 COSM964729 c.984G>A p.T328T Substitution - coding silent 15:74023209-74023209 + TCGA-AP-A059-01 COSM334000 c.1474G>T p.E492* Substitution - Nonsense 15:74033231-74033231 + 8015299 COSM3771884 c.2386C>T p.R796C Substitution - Missense 15:74044745-74044745 + 8033414 COSM3387036 c.185C>T p.A62V Substitution - Missense 15:73998059-73998059 + TCGA-JX-A3Q0-01 COSM4824028 c.502G>A p.E168K Substitution - Missense 15:73998376-73998376 + RD COSM3754465 c.1933T>C p.F645L Substitution - Missense 15:74044292-74044292 + TCGA-MY-A5BD-01 COSM4855506 c.2218G>A p.E740K Substitution - Missense 15:74044577-74044577 + TCGA-06-0173 COSM35843 c.819C>T p.A273A Substitution - coding silent 15:74023044-74023044 + UM-SCC-4 COSM4593342 c.851G>T p.R284L Substitution - Missense 15:74023076-74023076 + CRC-02T COSM1937993 c.1574C>T p.P525L Substitution - Missense 15:74033331-74033331 + KM12 COSM1678582 c.2131C>A p.L711M Substitution - Missense 15:74044490-74044490 + TCGA-B0-5098-01 COSM1493518 c.883C>T p.R295C Substitution - Missense 15:74023108-74023108 + PCSI_0083_Pa_P_526 COSM3377645 c.1365C>T p.Y455Y Substitution - coding silent 15:74032682-74032682 + PD7219a COSM5775139 c.2205G>A p.A735A Substitution - coding silent 15:74044564-74044564 + CCK81 COSM4335798 c.73delC p.E27fs*71 Deletion - Frameshift 15:73994885-73994885 + LUAD-NYU1051S COSM368611 c.344G>T p.R115L Substitution - Missense 15:73998218-73998218 + 3N50-VS-3T50 COSM4056763 c.251C>T p.S84L Substitution - Missense 15:73998125-73998125 + 2250185 COSM5029374 c.556A>G p.N186D Substitution - Missense 15:73998430-73998430 + 61 COSM5740398 c.2476T>C p.Y826H Substitution - Missense 15:74044835-74044835 + TCGA-AZ-6601-01 COSM3690525 c.884G>A p.R295H Substitution - Missense 15:74023109-74023109 + T3262 COSM4716094 c.1669_1671delGTG p.V558delV Deletion - In frame 15:74034489-74034491 + Pat_41_B COSM5849740 c.2014C>T p.P672S Substitution - Missense 15:74044373-74044373 + 8057484 COSM3387041 c.732G>A p.T244T Substitution - coding silent 15:74022957-74022957 + RH30SJ_ COSM3754465 c.1933T>C p.F645L Substitution - Missense 15:74044292-74044292 + RK308_C01 COSM3744743 c.1184-8T>C p.? Unknown 15:74024849-74024849 + HCC24T COSM1608664 c.1736G>T p.S579I Substitution - Missense 15:74043014-74043014 + RMS10_ COSM3754465 c.1933T>C p.F645L Substitution - Missense 15:74044292-74044292 + CHC2048T COSM4793177 c.1771A>T p.S591C Substitution - Missense 15:74043049-74043049 + ICC001T COSM5807258 c.2150G>A p.R717H Substitution - Missense 15:74044509-74044509 + cSCCP7 COSM140071 c.1406C>T p.S469F Substitution - Missense 15:74033163-74033163 + TCGA-BR-8679-01 COSM4056782 c.908C>T p.A303V Substitution - Missense 15:74023133-74023133 + ESCC-159T COSM3936844 c.1035G>A p.V345V Substitution - coding silent 15:74023260-74023260 + TCGA-QG-A5Z2-01 COSM5187183 c.508C>T p.R170C Substitution - Missense 15:73998382-73998382 + TCGA-BR-8360-01 COSM4056804 c.1355T>C p.V452A Substitution - Missense 15:74032672-74032672 + TCGA-A3-3326-01 COSM471044 c.1986C>G p.F662L Substitution - Missense 15:74044345-74044345 + ESO-081 COSM1243519 c.1089G>T p.E363D Substitution - Missense 15:74023314-74023314 + RKO COSM4647844 c.523C>T p.R175C Substitution - Missense 15:73998397-73998397 + TCGA-06-0173-01 COSM35843 c.819C>T p.A273A Substitution - coding silent 15:74023044-74023044 + TCGA-HU-A4G8-01 COSM4056763 c.251C>T p.S84L Substitution - Missense 15:73998125-73998125 + 436 COSM4433996 c.1632C>T p.H544H Substitution - coding silent 15:74033389-74033389 + TCGA-AX-A0J1-01 COSM964733 c.1354G>A p.V452M Substitution - Missense 15:74032671-74032671 + S02384 COSM5698267 c.677A>T p.K226M Substitution - Missense 15:74022902-74022902 + TCGA-HT-A5R9-01 COSM3969254 c.318C>T p.N106N Substitution - coding silent 15:73998192-73998192 + TCGA-AA-3672-01 COSM267209 c.265C>A p.P89T Substitution - Missense 15:73998139-73998139 + pfg143T COSM4757508 c.1043T>C p.M348T Substitution - Missense 15:74023268-74023268 + UM-SCC-2 COSM4599300 c.2573C>T p.A858V Substitution - Missense 15:74044932-74044932 + RK167_C01 COSM1629678 c.1219G>T p.A407S Substitution - Missense 15:74024892-74024892 + STC297 COSM5054467 c.143C>T p.S48L Substitution - Missense 15:73998017-73998017 + BB65-RCC COSM21735 c.1259A>T p.E420V Substitution - Missense 15:74032576-74032576 + TCGA-D9-A148-06 COSM3503811 c.345C>T p.R115R Substitution - coding silent 15:73998219-73998219 + YUDIVI COSM1374476 c.358C>T p.R120W Substitution - Missense 15:73998232-73998232 + PTC_20 COSM5959126 c.2581C>A p.R861R Substitution - coding silent 15:74044940-74044940 + HCT15 COSM4632672 c.2138T>G p.L713R Substitution - Missense 15:74044497-74044497 + SS6003109 COSM3983036 c.138C>T p.P46P Substitution - coding silent 15:73998012-73998012 + RMS110_ COSM3754465 c.1933T>C p.F645L Substitution - Missense 15:74044292-74044292 + 2203 COSM555984 c.2570C>T p.P857L Substitution - Missense 15:74044929-74044929 + HCC104 COSM1608661 c.1461G>T p.K487N Substitution - Missense 15:74033218-74033218 + TCGA-B1-A657-01 COSM4908203 c.1545G>A p.K515K Substitution - coding silent 15:74033302-74033302 + OSCC-GB_01060111 COSM4882557 c.950G>T p.G317V Substitution - Missense 15:74023175-74023175 + TCGA-HU-A4G9-01 COSM4056812 c.1886C>T p.A629V Substitution - Missense 15:74044245-74044245 + TCGA-AA-3710-01 COSM5104835 c.180C>T p.C60C Substitution - coding silent 15:73998054-73998054 + SC_9100 COSM4716098 c.2158G>A p.G720R Substitution - Missense 15:74044517-74044517 + PT13 COSM5896261 c.1876C>T p.Q626* Substitution - Nonsense 15:74044235-74044235 + TCGA-EE-A20C-06 COSM3503820 c.1949C>T p.S650F Substitution - Missense 15:74044308-74044308 + TCGA-KK-A6DY-01 COSM1938066 c.2065C>T p.R689W Substitution - Missense 15:74044424-74044424 + SC_9094 COSM1938070 c.2264G>A p.R755H Substitution - Missense 15:74044623-74044623 + 19 COSM5187183 c.508C>T p.R170C Substitution - Missense 15:73998382-73998382 + LUAD-RT-S01818 COSM383868 c.2238C>T p.A746A Substitution - coding silent 15:74044597-74044597 + TCGA-BR-A4CS-01 COSM4056799 c.1238C>T p.P413L Substitution - Missense 15:74024911-74024911 + CCC4 COSM3706724 c.2598C>T p.S866S Substitution - coding silent 15:74044957-74044957 + sysucc-923T COSM5463922 c.777G>A p.A259A Substitution - coding silent 15:74023002-74023002 + BICR_22 COSM4593342 c.851G>T p.R284L Substitution - Missense 15:74023076-74023076 + 61 COSM5740392 c.728T>C p.M243T Substitution - Missense 15:74022953-74022953 + TCGA-DM-A1HB-01 COSM5167936 c.1175_1176insG p.K394fs*22 Insertion - Frameshift 15:74023400-74023401 + PDA_067 COSM3754465 c.1933T>C p.F645L Substitution - Missense 15:74044292-74044292 + 462 COSM4436764 c.841G>A p.E281K Substitution - Missense 15:74023066-74023066 + KM12 COSM1937880 c.288C>T p.P96P Substitution - coding silent 15:73998162-73998162 + TCGA-BR-6802-01 COSM1374482 c.1078C>T p.R360C Substitution - Missense 15:74023303-74023303 + sysucc-274T COSM5475829 c.2012G>A p.R671H Substitution - Missense 15:74044371-74044371 + DLD1 COSM4623167 c.259C>T p.Q87* Substitution - Nonsense 15:73998133-73998133 + TCGA-DA-A1I5-06 COSM3503822 c.2533G>A p.A845T Substitution - Missense 15:74044892-74044892 + RMS88_ COSM3754465 c.1933T>C p.F645L Substitution - Missense 15:74044292-74044292 + LIM1899 COSM4640018 c.776C>T p.A259V Substitution - Missense 15:74023001-74023001 + LUAD-S01356 COSM398018 c.2623G>A p.A875T Substitution - Missense 15:74044982-74044982 + TCGA-A6-6781-01 COSM1374476 c.358C>T p.R120W Substitution - Missense 15:73998232-73998232 + S02285 COSM5684565 c.966G>C p.V322V Substitution - coding silent 15:74023191-74023191 + T3118 COSM4716098 c.2158G>A p.G720R Substitution - Missense 15:74044517-74044517 + LUAD-RT-S01487 COSM377873 c.208C>T p.L70L Substitution - coding silent 15:73998082-73998082 + TCGA-HU-8602-01 COSM4056770 c.584G>A p.R195H Substitution - Missense 15:73998458-73998458 + TCGA-HT-8104-01 COSM3969259 c.758C>A p.A253D Substitution - Missense 15:74022983-74022983 + 4_PRE-TREATMENT COSM1724220 c.916C>T p.Q306* Substitution - Nonsense 15:74023141-74023141 + TCGA-CG-5723-01 COSM1937910 c.738G>A p.A246A Substitution - coding silent 15:74022963-74022963 + 4_RESISTANT COSM1724614 c.2383_2384insC p.R796fs*20 Insertion - Frameshift 15:74044742-74044743 + HCC009T COSM5819679 c.1656A>T p.A552A Substitution - coding silent 15:74033413-74033413 + BN45 COSM1608665 c.2217C>T p.S739S Substitution - coding silent 15:74044576-74044576 + RMS112_ COSM3754465 c.1933T>C p.F645L Substitution - Missense 15:74044292-74044292 + TCGA-DK-A1A3-01 COSM416823 c.2269C>T p.L757F Substitution - Missense 15:74044628-74044628 + TCGA-GN-A26C-01 COSM3503821 c.2004C>T p.S668S Substitution - coding silent 15:74044363-74044363 + HN_62506 COSM121597 c.2200C>T p.L734L Substitution - coding silent 15:74044559-74044559 + BB65-RCC COSM21735 c.1259A>T p.E420V Substitution - Missense 15:74032576-74032576 + Gp5D COSM1938011 c.1672G>T p.V558L Substitution - Missense 15:74034492-74034492 + CHEWS014 COSM4578473 c.506T>C p.L169P Substitution - Missense 15:73998380-73998380 + TCGA-BR-8680-01 COSM1736534 c.509G>A p.R170H Substitution - Missense 15:73998383-73998383 + Pat_41_B COSM5849741 c.2451delG p.G819fs*2 Deletion - Frameshift 15:74044810-74044810 + LUAD-B01811 COSM334000 c.1474G>T p.E492* Substitution - Nonsense 15:74033231-74033231 + T578 COSM1736534 c.509G>A p.R170H Substitution - Missense 15:73998383-73998383 + TCGA-D7-8578-01 COSM4056808 c.1647C>T p.A549A Substitution - coding silent 15:74033404-74033404 + TCGA-BR-4292-01 COSM4056794 c.1145G>A p.R382H Substitution - Missense 15:74023370-74023370 + TCGA-AA-A010-01 COSM284108 c.201G>A p.P67P Substitution - coding silent 15:73998075-73998075 + S02287 COSM5685617 c.2135C>T p.P712L Substitution - Missense 15:74044494-74044494 + CSCC-15-T COSM4471389 c.1716C>T p.S572S Substitution - coding silent 15:74042994-74042994 + QC2-03-T2 COSM5651801 c.2441G>A p.R814H Substitution - Missense 15:74044800-74044800 + TCGA-HU-A4H0-01 COSM1937877 c.249G>A p.A83A Substitution - coding silent 15:73998123-73998123 + TCGA-AA-3680-01 COSM293016 c.1230C>T p.P410P Substitution - coding silent 15:74024903-74024903 + TCGA-AN-A0XW-01 COSM434264 c.1257C>T p.P419P Substitution - coding silent 15:74032574-74032574 + pfg092T COSM4757514 c.1670T>G p.V557G Substitution - Missense 15:74034490-74034490 + TCGA-BC-A10Q-01 COSM4927686 c.216T>G p.C72W Substitution - Missense 15:73998090-73998090 + LS411 COSM1938077 c.2499G>A p.T833T Substitution - coding silent 15:74044858-74044858 + TCGA-BR-8361-01 COSM4056789 c.1098C>A p.S366R Substitution - Missense 15:74023323-74023323 + AOCS-134-3-9 COSM1937877 c.249G>A p.A83A Substitution - coding silent 15:73998123-73998123 + PR-09-5700 COSM246682 c.1518G>A p.P506P Substitution - coding silent 15:74033275-74033275 + CCK81 COSM1937931 c.899C>T p.A300V Substitution - Missense 15:74023124-74023124 + SC_9022 COSM5560809 c.578A>G p.N193S Substitution - Missense 15:73998452-73998452 + BCM723T COSM4956565 c.775G>A p.A259T Substitution - Missense 15:74023000-74023000 + TCGA-DA-A1HV-06 COSM3503816 c.1388C>T p.S463F Substitution - Missense 15:74032705-74032705 + P0041 COSM5885286 c.? p.Q701H Substitution - Missense TCGA-Q1-A5R3-01 COSM4833982 c.49C>T p.R17W Substitution - Missense 15:73994861-73994861 + HX28T COSM1608664 c.1736G>T p.S579I Substitution - Missense 15:74043014-74043014 + 47T COSM1938070 c.2264G>A p.R755H Substitution - Missense 15:74044623-74044623 + T3610 COSM4716090 c.1617G>T p.L539L Substitution - coding silent 15:74033374-74033374 + TCGA-AA-3715-01 COSM269914 c.1901G>T p.S634I Substitution - Missense 15:74044260-74044260 + P116 COSM1736534 c.509G>A p.R170H Substitution - Missense 15:73998383-73998383 + TCGA-66-2734-01 COSM701260 c.1671G>T p.V557V Substitution - coding silent 15:74034491-74034491 + 587238 COSM1221319 c.2615G>A p.R872H Substitution - Missense 15:74044974-74044974 + TCGA-HU-8602-01 COSM4056777 c.871C>T p.R291W Substitution - Missense 15:74023096-74023096 + TCGA-D8-A1JA-01 COSM3816711 c.1228C>G p.P410A Substitution - Missense 15:74024901-74024901 + TCGA-DK-A1A7-01 COSM416824 c.1087G>A p.E363K Substitution - Missense 15:74023312-74023312 + TCGA-DR-A0ZM-01 COSM458967 c.895G>C p.E299Q Substitution - Missense 15:74023120-74023120 + PCSI_0083_Pa_P COSM3377645 c.1365C>T p.Y455Y Substitution - coding silent 15:74032682-74032682 + TCGA-D1-A17Q-01 COSM964742 c.1503G>T p.L501F Substitution - Missense 15:74033260-74033260 + OSCC-GB_00800111 COSM4887930 c.2048G>A p.G683D Substitution - Missense 15:74044407-74044407 + SW48 COSM4656191 c.850C>T p.R284C Substitution - Missense 15:74023075-74023075 + NB07C COSM1236512 c.564C>A p.F188L Substitution - Missense 15:73998438-73998438 + RMS77_ COSM3754465 c.1933T>C p.F645L Substitution - Missense 15:74044292-74044292 + 47T COSM5575780 c.344G>A p.R115H Substitution - Missense 15:73998218-73998218 + MedB-1 COSM5621552 c.2468A>G p.Y823C Substitution - Missense 15:74044827-74044827 + TCGA-AU-6004-01 COSM1374488 c.1665C>T p.R555R Substitution - coding silent 15:74034485-74034485 + 2293782 COSM4608558 c.772C>A p.H258N Substitution - Missense 15:74022997-74022997 + 107136 COSM95027 c.1A>G p.M1V Substitution - Missense 15:73994813-73994813 + KM12 COSM1678582 c.2131C>A p.L711M Substitution - Missense 15:74044490-74044490 + RMS109_ COSM3754465 c.1933T>C p.F645L Substitution - Missense 15:74044292-74044292 + LIM1215 COSM4335798 c.73delC p.E27fs*71 Deletion - Frameshift 15:73994885-73994885 + TCGA-B5-A11E-01 COSM964721 c.462A>G p.A154A Substitution - coding silent 15:73998336-73998336 + PD2184a COSM28025 c.351G>A p.S117S Substitution - coding silent 15:73998225-73998225 + G5 COSM1191776 c.1655C>T p.A552V Substitution - Missense 15:74033412-74033412 + HCC104T COSM1608661 c.1461G>T p.K487N Substitution - Missense 15:74033218-74033218 + 234 COSM3731165 c.2456G>A p.G819D Substitution - Missense 15:74044815-74044815 + ESCC_11 COSM5624305 c.2377G>C p.A793P Substitution - Missense 15:74044736-74044736 + 11M COSM5576957 c.1551C>T p.V517V Substitution - coding silent 15:74033308-74033308 + TCGA-EE-A17X-06 COSM964717 c.252G>A p.S84S Substitution - coding silent 15:73998126-73998126 + TCGA-AA-3489-01 COSM5096740 c.2535T>C p.A845A Substitution - coding silent 15:74044894-74044894 + 587350 COSM1221320 c.1448A>C p.Q483P Substitution - Missense 15:74033205-74033205 + TCGA-BR-7703-01 COSM4056813 c.2344C>T p.Q782* Substitution - Nonsense 15:74044703-74044703 + PTC-28C COSM3754465 c.1933T>C p.F645L Substitution - Missense 15:74044292-74044292 + PD2184a COSM28025 c.351G>A p.S117S Substitution - coding silent 15:73998225-73998225 + RMS85_ COSM3754465 c.1933T>C p.F645L Substitution - Missense 15:74044292-74044292 + TCGA-AA-3844-01 COSM295289 c.630G>T p.P210P Substitution - coding silent 15:74022855-74022855 + YUOMEGA COSM5383800 c.1012T>G p.C338G Substitution - Missense 15:74023237-74023237 + LUAD_E00623 COSM353889 c.184G>T p.A62S Substitution - Missense 15:73998058-73998058 + RMS111_ COSM3754465 c.1933T>C p.F645L Substitution - Missense 15:74044292-74044292 + ESCC_95 COSM5637484 c.76C>T p.P26S Substitution - Missense 15:73994888-73994888 + T3498 COSM4716080 c.783G>A p.M261I Substitution - Missense 15:74023008-74023008 + CCK81 COSM1938008 c.1648delG p.E551fs*8 Deletion - Frameshift 15:74033405-74033405 + EGC15 COSM1736534 c.509G>A p.R170H Substitution - Missense 15:73998383-73998383 + SJDES018-R COSM4578478 c.841G>T p.E281* Substitution - Nonsense 15:74023066-74023066 + BB65-RCC COSM21735 c.1259A>T p.E420V Substitution - Missense 15:74032576-74032576 + TCGA-DK-A1A5-01 COSM416827 c.424G>C p.E142Q Substitution - Missense 15:73998298-73998298 + TCGA-DM-A28M-01 COSM5171042 c.1097G>T p.S366I Substitution - Missense 15:74023322-74023322 + YUCHUFA COSM1708379 c.200C>T p.P67L Substitution - Missense 15:73998074-73998074 + TCGA-F4-6856-01 COSM1374492 c.2008C>T p.R670C Substitution - Missense 15:74044367-74044367 + TCGA-D1-A103-01 COSM964746 c.1702G>A p.E568K Substitution - Missense 15:74034522-74034522 + LC_C11 COSM1189058 c.848T>C p.V283A Substitution - Missense 15:74023073-74023073 + TCGA-AA-3510-01 COSM5099181 c.2181G>T p.K727N Substitution - Missense 15:74044540-74044540 + TCGA-LP-A4AV-01 COSM4825528 c.675C>G p.L225L Substitution - coding silent 15:74022900-74022900 + TCGA-AA-3713-01 COSM1374482 c.1078C>T p.R360C Substitution - Missense 15:74023303-74023303 + TCGA-AM-5820-01 COSM3754465 c.1933T>C p.F645L Substitution - Missense 15:74044292-74044292 + TCGA-AZ-6598-01 COSM1374485 c.1281C>T p.A427A Substitution - coding silent 15:74032598-74032598 + CLN2 COSM1517506 c.2582G>T p.R861L Substitution - Missense 15:74044941-74044941 + CRC-9 COSM304648 c.2097A>T p.E699D Substitution - Missense 15:74044456-74044456 + ESCC_31 COSM5627793 c.1675A>G p.I559V Substitution - Missense 15:74034495-74034495 + TCGA-C5-A1M5-01 COSM4830866 c.973C>T p.R325C Substitution - Missense 15:74023198-74023198 + CSCC-56-T COSM4454684 c.557A>G p.N186S Substitution - Missense 15:73998431-73998431 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.526464 15q22 102578 2419100|CGAP|BC000080|A/G|non-coding||2690|Validated; 2419100|CGAP|BC020994|A/G|non-coding||2690|Validated; 1527455|dbSNP|BC000080|C/T|non-coding||2693|Validated; 1527455|dbSNP|BC020994|C/T|non-coding||2693|Validated; 1527463|dbSNP|BC000080|C/T|non-coding||2761|Validated; 1527463|dbSNP|BC020994|C/T|non-coding||2761|Validated; 1527465|dbSNP|BC000080|C/T|non-coding||2771|Validated; 1527465|dbSNP|BC020994|C/T|non-coding||2771|Validated

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C IntronicSNV . c.1710+63A>C 15 74326934 RCCC A G Missense p.S804G c.2410A>G 15 74337110 LUAD - A IntronicInsertion . c.1710+688dupA 15 74327558 BRCA A T IntronicSNV . c.1710+978A>T 15 74327849 CM A T Missense p.Y455F c.1364A>T 15 74325022 UCEC C A Missense p.F188L c.564C>A 15 74290779 NB C A Missense p.P67Q c.200C>A 15 74290415 LUAD C A Synonymous p.R689R c.2065C>A 15 74336765 STAD C G Missense p.F662L c.1986C>G 15 74336686 RCCC C T IntronicSNV . c.1657+78C>T 15 74325833 CM C T IntronicSNV . c.1710+1396C>T 15 74328267 CM C T IntronicSNV . c.1710+677C>T 15 74327548 CM C T IntronicSNV . c.1710+726C>T 15 74327597 CM C T Missense p.L757F c.2269C>T 15 74336969 BLCA C T Missense p.P857L c.2570C>T 15 74337270 LUAD C T Missense p.R360C c.1078C>T 15 74315644 STAD C T Missense p.R689W c.2065C>T 15 74336765 PRAD C T Missense p.S463F c.1388C>T 15 74325046 CM C T Missense p.S518L c.1553C>T 15 74325651 HNSC C T Missense p.S650F c.1949C>T 15 74336649 CM C T Synonymous p.A273A c.819C>T 15 74315385 GBM C T Synonymous p.A743A c.2229C>T 15 74336929 CM C T Synonymous p.F109F c.327C>T 15 74290542 CM C T Synonymous p.I559I c.1677C>T 15 74326838 CM C T Synonymous p.L734L c.2200C>T 15 74336900 HNSC C T Synonymous p.P410P c.1230C>T 15 74317244 COREAD C T Synonymous p.P419P c.1257C>T 15 74324915 BRCA C T Synonymous p.R115R c.345C>T 15 74290560 CM C T Synonymous p.S230S c.690C>T 15 74315256 UCEC C T Synonymous p.S668S c.2004C>T 15 74336704 CM G A 3-UTRSNV . c.2646+11G>A 15 74337357 CM GAA - InFrameDeletion p.K822delK c.2464_2466delAAG 15 74337160 UCEC G A IntronicSNV . c.1657+67G>A 15 74325822 RCCC G A IntronicSNV . c.1710+98G>A 15 74326969 COREAD G A Missense p.A845T c.2533G>A 15 74337233 CM G A Missense p.E310K c.928G>A 15 74315494 LUAD G A Missense p.E363K c.1087G>A 15 74315653 BLCA G A Missense p.R382H c.1145G>A 15 74315711 STAD G A Synonymous p.S84S c.252G>A 15 74290467 CM G A Synonymous p.S84S c.252G>A 15 74290467 UCEC G C Missense p.E142Q c.424G>C 15 74290639 BLCA G C Missense p.L854F c.2562G>C 15 74337262 LUAD G T IntronicSNV . c.1710+98G>T 15 74326969 UCEC G T Missense p.A103S c.307G>T 15 74290522 LUAD G T Synonymous p.A303A c.909G>T 15 74315475 LUAD G T Synonymous p.P210P c.630G>T 15 74315196 COREAD G T Synonymous p.V557V c.1671G>T 15 74326832 LUSC TCCTCGCCAGCCCAC - IntronicDeletion . c.1710+715_1710+729delCCCACTCCTCGCCAG 15 74327546 UCEC