Mutation - TCGA Type Chromosome Start Position End Position Strand Variant Classification Variant Type Reference Allele Tumor_seq Allele 1 Tumor_seq Allele 2 Tumor Sample Barcode Matched Norm Sample Barcode Genome Change cDNA Change Codon Change Protein Change BLCA 9 104302628 104302628 + Silent SNP G G A TCGA-LT-A5Z6-01A-11D-A289-08 TCGA-LT-A5Z6-10A-01D-A289-08 g.chr9:104302628G>A c.273G>A c.(271-273)ttG>ttA p.L91L BLCA 9 104302807 104302807 + Nonsense_Mutation SNP T T A TCGA-XF-A9T6-01A-11D-A42E-08 TCGA-XF-A9T6-10A-01D-A42H-08 g.chr9:104302807T>A c.333T>A c.(331-333)taT>taA p.Y111* BLCA 9 104303103 104303103 + Silent SNP C C T TCGA-ZF-AA51-01A-21D-A391-08 TCGA-ZF-AA51-10A-01D-A394-08 g.chr9:104303103C>T c.474C>T c.(472-474)ttC>ttT p.F158F BLCA 9 104309797 104309797 + Silent SNP G G A TCGA-DK-A1AB-01A-11D-A13W-08 TCGA-DK-A1AB-10A-01D-A13W-08 g.chr9:104309797G>A c.1089G>A c.(1087-1089)ctG>ctA p.L363L BLCA 9 104314697 104314697 + Silent SNP G G A TCGA-BT-A20W-01A-21D-A14W-08 TCGA-BT-A20W-11A-11D-A14W-08 g.chr9:104314697G>A c.1563G>A c.(1561-1563)caG>caA p.Q521Q BRCA 9 104302598 104302598 + Silent SNP A A C TCGA-BH-A0BR-01A-21W-A12T-09 TCGA-BH-A0BR-10A-01D-A110-09 g.chr9:104302598A>C c.243A>C c.(241-243)cgA>cgC p.R81R BRCA 9 104313065 104313065 + Missense_Mutation SNP G G A TCGA-A8-A09I-01A-22W-A050-09 TCGA-A8-A09I-10A-01W-A055-09 g.chr9:104313065G>A c.1270G>A c.(1270-1272)Gag>Aag p.E424K BRCA 9 104313984 104313984 + Missense_Mutation SNP C C T TCGA-BH-A0DZ-01A-11W-A019-09 TCGA-BH-A0DZ-10A-01W-A021-09 g.chr9:104313984C>T c.1291C>T c.(1291-1293)Cat>Tat p.H431Y BRCA 9 104314674 104314674 + Missense_Mutation SNP C C T TCGA-AN-A04C-01A-21W-A050-09 TCGA-AN-A04C-10A-01D-A047-09 g.chr9:104314674C>T c.1540C>T c.(1540-1542)Cgt>Tgt p.R514C BRCA 9 104314716 104314716 + Missense_Mutation SNP G G T TCGA-D8-A1XQ-01A-11D-A14K-09 TCGA-D8-A1XQ-10A-01D-A14K-09 g.chr9:104314716G>T c.1582G>T c.(1582-1584)Gac>Tac p.D528Y BRCA 9 104315014 104315014 + Missense_Mutation SNP A A G TCGA-E9-A243-01A-21D-A167-09 TCGA-E9-A243-10A-01D-A17G-09 g.chr9:104315014A>G c.1880A>G c.(1879-1881)aAa>aGa p.K627R BRCA 9 104323426 104323426 + Missense_Mutation SNP C C G TCGA-C8-A12Q-01A-11D-A10Y-09 TCGA-C8-A12Q-10A-01D-A110-09 g.chr9:104323426C>G c.2563C>G c.(2563-2565)Cag>Gag p.Q855E CESC 9 104312939 104312939 + Missense_Mutation SNP C C T TCGA-MY-A5BD-01A-11D-A26G-09 TCGA-MY-A5BD-10A-01D-A26G-09 g.chr9:104312939C>T c.1144C>T c.(1144-1146)Cgc>Tgc p.R382C COAD 9 104302787 104302787 + Missense_Mutation SNP C C T TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr9:104302787C>T c.313C>T c.(313-315)Cgt>Tgt p.R105C COAD 9 104303116 104303116 + Missense_Mutation SNP G G A TCGA-CM-6162-01A-11D-1650-10 TCGA-CM-6162-10A-01D-1650-10 g.chr9:104303116G>A c.487G>A c.(487-489)Gcc>Acc p.A163T COAD 9 104309213 104309213 + Nonsense_Mutation SNP C C T TCGA-A6-6780-01A-11D-1835-10 TCGA-A6-6780-10A-01D-1835-10 g.chr9:104309213C>T c.859C>T c.(859-861)Cga>Tga p.R287* COAD 9 104309234 104309234 + Nonsense_Mutation SNP G G T TCGA-AA-3543-01A-01W-0833-10 TCGA-AA-3543-10A-01W-0833-10 g.chr9:104309234G>T c.880G>T c.(880-882)Gaa>Taa p.E294* COAD 9 104312898 104312898 + Missense_Mutation SNP G G A TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr9:104312898G>A c.1103G>A c.(1102-1104)cGg>cAg p.R368Q COAD 9 104312898 104312898 + Missense_Mutation SNP G G A TCGA-AA-3680-01A-01W-0900-09 TCGA-AA-3680-10A-01W-0900-09 g.chr9:104312898G>A c.1103G>A c.(1102-1104)cGg>cAg p.R368Q COAD 9 104312932 104312932 + Silent SNP A A G TCGA-D5-5539-01A-01D-1650-10 TCGA-D5-5539-10A-01D-1650-10 g.chr9:104312932A>G c.1137A>G c.(1135-1137)ccA>ccG p.P379P COAD 9 104312951 104312951 + Missense_Mutation SNP T T C TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chr9:104312951T>C c.1156T>C c.(1156-1158)Tca>Cca p.S386P COAD 9 104312963 104312963 + Missense_Mutation SNP G G A TCGA-A6-6654-01A-21D-1835-10 TCGA-A6-6654-10A-01D-1835-10 g.chr9:104312963G>A c.1168G>A c.(1168-1170)Gtc>Atc p.V390I COAD 9 104314053 104314053 + Missense_Mutation SNP A A G TCGA-CM-6677-01A-11D-1835-10 TCGA-CM-6677-10A-01D-1835-10 g.chr9:104314053A>G c.1360A>G c.(1360-1362)Atg>Gtg p.M454V COAD 9 104314839 104314839 + Nonsense_Mutation SNP C C T TCGA-AA-3685-01A-02W-0900-09 TCGA-AA-3685-10A-01W-0900-09 g.chr9:104314839C>T c.1705C>T c.(1705-1707)Cga>Tga p.R569* COAD 9 104314845 104314845 + Nonsense_Mutation SNP C C T TCGA-AA-A01I-01A-02W-A00E-09 TCGA-AA-A01I-10A-01W-A00E-09 g.chr9:104314845C>T c.1711C>T c.(1711-1713)Cga>Tga p.R571* COAD 9 104316389 104316389 + Splice_Site SNP T T C TCGA-AU-6004-01A-11D-1719-10 TCGA-AU-6004-10A-01D-1719-10 g.chr9:104316389T>C c.e14+2 COAD 9 104323143 104323143 + Missense_Mutation SNP A A G TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr9:104323143A>G c.2443A>G c.(2443-2445)Aac>Gac p.N815D COAD 9 104323143 104323143 + Missense_Mutation SNP A A G TCGA-DM-A28H-01A-11D-A16V-10 TCGA-DM-A28H-10A-01D-A16V-10 g.chr9:104323143A>G c.2443A>G c.(2443-2445)Aac>Gac p.N815D COAD 9 104323144 104323144 + Missense_Mutation SNP A A G TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chr9:104323144A>G c.2444A>G c.(2443-2445)aAc>aGc p.N815S COAD 9 104323203 104323203 + Missense_Mutation SNP C C T TCGA-AD-6964-01A-11D-1924-10 TCGA-AD-6964-10A-01D-1924-10 g.chr9:104323203C>T c.2503C>T c.(2503-2505)Cgc>Tgc p.R835C COAD 9 104324193 104324193 + Splice_Site SNP A A G TCGA-CM-4746-01A-01D-1408-10 TCGA-CM-4746-10A-01D-1408-10 g.chr9:104324193A>G c.2651A>G c.(2650-2652)gAg>gGg p.E884G COAD 9 104324622 104324622 + Missense_Mutation SNP G G A TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chr9:104324622G>A c.2846G>A c.(2845-2847)cGc>cAc p.R949H COADREAD 9 104302787 104302787 + Missense_Mutation SNP C C T TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr9:104302787C>T c.313C>T c.(313-315)Cgt>Tgt p.R105C COADREAD 9 104303116 104303116 + Missense_Mutation SNP G G A TCGA-CM-6162-01A-11D-1650-10 TCGA-CM-6162-10A-01D-1650-10 g.chr9:104303116G>A c.487G>A c.(487-489)Gcc>Acc p.A163T COADREAD 9 104309213 104309213 + Nonsense_Mutation SNP C C T TCGA-A6-6780-01A-11D-1835-10 TCGA-A6-6780-10A-01D-1835-10 g.chr9:104309213C>T c.859C>T c.(859-861)Cga>Tga p.R287* COADREAD 9 104309234 104309234 + Nonsense_Mutation SNP G G T TCGA-AA-3543-01A-01W-0833-10 TCGA-AA-3543-10A-01W-0833-10 g.chr9:104309234G>T c.880G>T c.(880-882)Gaa>Taa p.E294* COADREAD 9 104309422 104309422 + Missense_Mutation SNP A A G TCGA-DY-A0XA-01A-11D-A152-10 TCGA-DY-A0XA-10A-01D-A152-10 g.chr9:104309422A>G c.898A>G c.(898-900)Aat>Gat p.N300D COADREAD 9 104309423 104309423 + Missense_Mutation SNP A A T TCGA-EI-6510-01A-11D-1733-10 TCGA-EI-6510-10A-01D-1733-10 g.chr9:104309423A>T c.899A>T c.(898-900)aAt>aTt p.N300I COADREAD 9 104312898 104312898 + Missense_Mutation SNP G G A TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr9:104312898G>A c.1103G>A c.(1102-1104)cGg>cAg p.R368Q COADREAD 9 104312898 104312898 + Missense_Mutation SNP G G A TCGA-AA-3680-01A-01W-0900-09 TCGA-AA-3680-10A-01W-0900-09 g.chr9:104312898G>A c.1103G>A c.(1102-1104)cGg>cAg p.R368Q COADREAD 9 104312932 104312932 + Silent SNP A A G TCGA-D5-5539-01A-01D-1650-10 TCGA-D5-5539-10A-01D-1650-10 g.chr9:104312932A>G c.1137A>G c.(1135-1137)ccA>ccG p.P379P COADREAD 9 104312951 104312951 + Missense_Mutation SNP T T C TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chr9:104312951T>C c.1156T>C c.(1156-1158)Tca>Cca p.S386P COADREAD 9 104312963 104312963 + Missense_Mutation SNP G G A TCGA-A6-6654-01A-21D-1835-10 TCGA-A6-6654-10A-01D-1835-10 g.chr9:104312963G>A c.1168G>A c.(1168-1170)Gtc>Atc p.V390I COADREAD 9 104314053 104314053 + Missense_Mutation SNP A A G TCGA-CM-6677-01A-11D-1835-10 TCGA-CM-6677-10A-01D-1835-10 g.chr9:104314053A>G c.1360A>G c.(1360-1362)Atg>Gtg p.M454V COADREAD 9 104314839 104314839 + Nonsense_Mutation SNP C C T TCGA-AA-3685-01A-02W-0900-09 TCGA-AA-3685-10A-01W-0900-09 g.chr9:104314839C>T c.1705C>T c.(1705-1707)Cga>Tga p.R569* COADREAD 9 104314845 104314845 + Nonsense_Mutation SNP C C T TCGA-AA-A01I-01A-02W-A00E-09 TCGA-AA-A01I-10A-01W-A00E-09 g.chr9:104314845C>T c.1711C>T c.(1711-1713)Cga>Tga p.R571* COADREAD 9 104316389 104316389 + Splice_Site SNP T T C TCGA-AU-6004-01A-11D-1719-10 TCGA-AU-6004-10A-01D-1719-10 g.chr9:104316389T>C c.e14+2 COADREAD 9 104323143 104323143 + Missense_Mutation SNP A A G TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr9:104323143A>G c.2443A>G c.(2443-2445)Aac>Gac p.N815D COADREAD 9 104323143 104323143 + Missense_Mutation SNP A A G TCGA-DM-A28H-01A-11D-A16V-10 TCGA-DM-A28H-10A-01D-A16V-10 g.chr9:104323143A>G c.2443A>G c.(2443-2445)Aac>Gac p.N815D COADREAD 9 104323144 104323144 + Missense_Mutation SNP A A G TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chr9:104323144A>G c.2444A>G c.(2443-2445)aAc>aGc p.N815S COADREAD 9 104323203 104323203 + Missense_Mutation SNP C C T TCGA-AD-6964-01A-11D-1924-10 TCGA-AD-6964-10A-01D-1924-10 g.chr9:104323203C>T c.2503C>T c.(2503-2505)Cgc>Tgc p.R835C COADREAD 9 104323505 104323505 + Missense_Mutation SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr9:104323505G>A c.2642G>A c.(2641-2643)cGa>cAa p.R881Q COADREAD 9 104324193 104324193 + Splice_Site SNP A A G TCGA-CM-4746-01A-01D-1408-10 TCGA-CM-4746-10A-01D-1408-10 g.chr9:104324193A>G c.2651A>G c.(2650-2652)gAg>gGg p.E884G COADREAD 9 104324622 104324622 + Missense_Mutation SNP G G A TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chr9:104324622G>A c.2846G>A c.(2845-2847)cGc>cAc p.R949H ESCA 9 104309733 104309733 + Missense_Mutation SNP G G A TCGA-L5-A8NM-01A-11D-A37C-09 TCGA-L5-A8NM-11A-12D-A37F-09 g.chr9:104309733G>A c.1025G>A c.(1024-1026)cGt>cAt p.R342H ESCA 9 104314938 104314938 + Nonsense_Mutation SNP A A T TCGA-IC-A6RE-01A-11D-A33E-09 TCGA-IC-A6RE-10A-01D-A33H-09 g.chr9:104314938A>T c.1804A>T c.(1804-1806)Aaa>Taa p.K602* GBMLGG 9 104307093 104307093 + Missense_Mutation SNP C C T TCGA-TQ-A7RF-01A-11D-A33T-08 TCGA-TQ-A7RF-10A-01D-A33W-08 g.chr9:104307093C>T c.673C>T c.(673-675)Ctc>Ttc p.L225F HNSC 9 104302630 104302630 + Missense_Mutation SNP T T C TCGA-CV-A6K1-01A-11D-A31L-08 TCGA-CV-A6K1-10A-01D-A31J-08 g.chr9:104302630T>C c.275T>C c.(274-276)aTt>aCt p.I92T HNSC 9 104302796 104302796 + Missense_Mutation SNP C C T TCGA-CN-A497-01A-11D-A24D-08 TCGA-CN-A497-10A-01D-A24F-08 g.chr9:104302796C>T c.322C>T c.(322-324)Ctt>Ttt p.L108F HNSC 9 104314536 104314536 + Missense_Mutation SNP C C G TCGA-CV-7245-01A-11D-2012-08 TCGA-CV-7245-10A-01D-2013-08 g.chr9:104314536C>G c.1522C>G c.(1522-1524)Ctg>Gtg p.L508V HNSC 9 104314951 104314951 + Missense_Mutation SNP C C G TCGA-P3-A6T7-01A-11D-A34J-08 TCGA-P3-A6T7-10A-01D-A34M-08 g.chr9:104314951C>G c.1817C>G c.(1816-1818)tCt>tGt p.S606C HNSC 9 104319794 104319794 + Silent SNP G G A TCGA-BA-4076-01A-01D-1434-08 TCGA-BA-4076-10A-01D-1434-08 g.chr9:104319794G>A c.2298G>A c.(2296-2298)gaG>gaA p.E766E HNSC 9 104319876 104319876 + Nonsense_Mutation SNP C C T TCGA-CN-6994-01A-11D-1912-08 TCGA-CN-6994-10A-01D-1912-08 g.chr9:104319876C>T c.2380C>T c.(2380-2382)Cag>Tag p.Q794* HNSC 9 104324544 104324544 + Missense_Mutation SNP C C T TCGA-IQ-A61E-01A-22D-A30E-08 TCGA-IQ-A61E-10A-01D-A30H-08 g.chr9:104324544C>T c.2768C>T c.(2767-2769)cCg>cTg p.P923L KIPAN 9 104302538 104302538 + Missense_Mutation SNP G G C TCGA-P4-A5EB-01A-11D-A28G-10 TCGA-P4-A5EB-11A-11D-A28G-10 g.chr9:104302538G>C c.183G>C c.(181-183)atG>atC p.M61I KIPAN 9 104302568 104302568 + Silent SNP A A G TCGA-SX-A71S-01A-11D-A33Q-10 TCGA-SX-A71S-10A-01D-A33Q-10 g.chr9:104302568A>G c.213A>G c.(211-213)gaA>gaG p.E71E KIPAN 9 104309714 104309714 + Missense_Mutation SNP A A G TCGA-UZ-A9PX-01A-11D-A42J-10 TCGA-UZ-A9PX-10A-01D-A42M-10 g.chr9:104309714A>G c.1006A>G c.(1006-1008)Aaa>Gaa p.K336E KIPAN 9 104316360 104316360 + Missense_Mutation SNP G G T TCGA-B0-5099-01A-01D-1421-08 TCGA-B0-5099-11A-01D-1421-08 g.chr9:104316360G>T c.1992G>T c.(1990-1992)atG>atT p.M664I KIPAN 9 104324630 104324630 + Missense_Mutation SNP A A C TCGA-A3-3385-01A-02D-1421-08 TCGA-A3-3385-11A-01D-1421-08 g.chr9:104324630A>C c.2854A>C c.(2854-2856)Acc>Ccc p.T952P KIRC 9 104316360 104316360 + Missense_Mutation SNP G G T TCGA-B0-5099-01A-01D-1421-08 TCGA-B0-5099-11A-01D-1421-08 g.chr9:104316360G>T c.1992G>T c.(1990-1992)atG>atT p.M664I KIRC 9 104324630 104324630 + Missense_Mutation SNP A A C TCGA-A3-3385-01A-02D-1421-08 TCGA-A3-3385-11A-01D-1421-08 g.chr9:104324630A>C c.2854A>C c.(2854-2856)Acc>Ccc p.T952P KIRP 9 104302538 104302538 + Missense_Mutation SNP G G C TCGA-P4-A5EB-01A-11D-A28G-10 TCGA-P4-A5EB-11A-11D-A28G-10 g.chr9:104302538G>C c.183G>C c.(181-183)atG>atC p.M61I KIRP 9 104302568 104302568 + Silent SNP A A G TCGA-SX-A71S-01A-11D-A33Q-10 TCGA-SX-A71S-10A-01D-A33Q-10 g.chr9:104302568A>G c.213A>G c.(211-213)gaA>gaG p.E71E KIRP 9 104309714 104309714 + Missense_Mutation SNP A A G TCGA-UZ-A9PX-01A-11D-A42J-10 TCGA-UZ-A9PX-10A-01D-A42M-10 g.chr9:104309714A>G c.1006A>G c.(1006-1008)Aaa>Gaa p.K336E LGG 9 104307093 104307093 + Missense_Mutation SNP C C T TCGA-TQ-A7RF-01A-11D-A33T-08 TCGA-TQ-A7RF-10A-01D-A33W-08 g.chr9:104307093C>T c.673C>T c.(673-675)Ctc>Ttc p.L225F LIHC 9 104303192 104303192 + Missense_Mutation SNP T T C TCGA-K7-A5RF-01A-11D-A28X-10 TCGA-K7-A5RF-10B-01D-A28X-10 g.chr9:104303192T>C c.563T>C c.(562-564)aTt>aCt p.I188T LIHC 9 104314807 104314807 + Missense_Mutation SNP A A G TCGA-DD-AAE3-01A-11D-A40R-10 TCGA-DD-AAE3-10A-01D-A40U-10 g.chr9:104314807A>G c.1673A>G c.(1672-1674)aAt>aGt p.N558S LIHC 9 104315030 104315030 + Missense_Mutation SNP A A T TCGA-G3-A25Y-01A-11D-A16V-10 TCGA-G3-A25Y-10A-01D-A16V-10 g.chr9:104315030A>T c.1896A>T c.(1894-1896)gaA>gaT p.E632D LIHC 9 104323165 104323165 + Missense_Mutation SNP A A G TCGA-DD-A39Y-01A-11D-A20W-10 TCGA-DD-A39Y-11A-11D-A20W-10 g.chr9:104323165A>G c.2465A>G c.(2464-2466)gAg>gGg p.E822G LUAD 9 104303159 104303159 + Missense_Mutation SNP G G T TCGA-NJ-A4YF-01A-12D-A25L-08 TCGA-NJ-A4YF-10A-01D-A25L-08 g.chr9:104303159G>T c.530G>T c.(529-531)cGt>cTt p.R177L LUAD 9 104303258 104303258 + Splice_Site SNP G G C TCGA-49-4488-01A-01D-1753-08 TCGA-49-4488-11A-01D-1753-08 g.chr9:104303258G>C c.e5+1 LUAD 9 104307066 104307066 + Missense_Mutation SNP G G C TCGA-55-8092-01A-11D-2238-08 TCGA-55-8092-10A-01D-2238-08 g.chr9:104307066G>C c.646G>C c.(646-648)Gaa>Caa p.E216Q LUAD 9 104307162 104307162 + Nonsense_Mutation SNP C C T TCGA-55-6972-01A-11D-1945-08 TCGA-55-6972-11A-01D-1945-08 g.chr9:104307162C>T c.742C>T c.(742-744)Cag>Tag p.Q248* LUAD 9 104309130 104309130 + Missense_Mutation SNP C C T TCGA-50-5066-01A-01D-1625-08 TCGA-50-5066-10A-01D-1625-08 g.chr9:104309130C>T c.776C>T c.(775-777)aCa>aTa p.T259I LUAD 9 104314008 104314009 + Frame_Shift_Ins INS - - T TCGA-97-8177-01A-11D-2284-08 TCGA-97-8177-10A-01D-2284-08 g.chr9:104314008_104314009insT c.1315_1316insT c.(1315-1317)attfs p.I439fs LUAD 9 104314043 104314043 + Missense_Mutation SNP G G T TCGA-NJ-A55R-01A-11D-A25L-08 TCGA-NJ-A55R-10A-01D-A25L-08 g.chr9:104314043G>T c.1350G>T c.(1348-1350)aaG>aaT p.K450N LUAD 9 104314667 104314667 + Silent SNP A A G TCGA-95-7567-01A-11D-2063-08 TCGA-95-7567-10A-01D-2063-08 g.chr9:104314667A>G c.1533A>G c.(1531-1533)acA>acG p.T511T LUAD 9 104314692 104314692 + Silent SNP C C T TCGA-17-Z052-01A-01W-0747-08 TCGA-17-Z052-11A-01W-0747-08 g.chr9:104314692C>T c.1558C>T c.(1558-1560)Ctg>Ttg p.L520L LUAD 9 104314736 104314736 + Silent SNP G G A TCGA-75-5122-01A-01D-1753-08 TCGA-75-5122-10A-01D-1753-08 g.chr9:104314736G>A c.1602G>A c.(1600-1602)gcG>gcA p.A534A LUAD 9 104316344 104316344 + Missense_Mutation SNP A A T TCGA-69-7978-01A-11D-2184-08 TCGA-69-7978-10A-01D-2184-08 g.chr9:104316344A>T c.1976A>T c.(1975-1977)gAc>gTc p.D659V LUAD 9 104317049 104317049 + Missense_Mutation SNP A A T TCGA-44-7662-01A-11D-2063-08 TCGA-44-7662-10A-01D-2063-08 g.chr9:104317049A>T c.2093A>T c.(2092-2094)gAg>gTg p.E698V LUAD 9 104317070 104317070 + Missense_Mutation SNP G G A TCGA-95-7043-01A-11D-1945-08 TCGA-95-7043-10A-01D-1946-08 g.chr9:104317070G>A c.2114G>A c.(2113-2115)cGg>cAg p.R705Q LUAD 9 104319708 104319708 + Missense_Mutation SNP G G T TCGA-17-Z059-01A-01W-0747-08 TCGA-17-Z059-11A-01W-0747-08 g.chr9:104319708G>T c.2212G>T c.(2212-2214)Gcc>Tcc p.A738S LUAD 9 104319803 104319803 + Missense_Mutation SNP G G T TCGA-44-4112-01A-01D-1105-08 TCGA-44-4112-10A-01D-1458-08 g.chr9:104319803G>T c.2307G>T c.(2305-2307)aaG>aaT p.K769N LUAD 9 104319843 104319843 + Missense_Mutation SNP G G C TCGA-05-4410-01A-21D-1855-08 TCGA-05-4410-10A-01D-1855-08 g.chr9:104319843G>C c.2347G>C c.(2347-2349)Gag>Cag p.E783Q LUAD 9 104323505 104323505 + Missense_Mutation SNP G G C TCGA-64-1677-01A-01W-0928-08 TCGA-64-1677-10A-01W-0928-08 g.chr9:104323505G>C c.2642G>C c.(2641-2643)cGa>cCa p.R881P LUAD 9 104324194 104324194 + Silent SNP G G A TCGA-86-8279-01A-11D-2284-08 TCGA-86-8279-10A-01D-2284-08 g.chr9:104324194G>A c.2652G>A c.(2650-2652)gaG>gaA p.E884E LUAD 9 104324547 104324547 + Missense_Mutation SNP G G T TCGA-50-5930-01A-11D-1753-08 TCGA-50-5930-11A-01D-1753-08 g.chr9:104324547G>T c.2771G>T c.(2770-2772)tGc>tTc p.C924F LUSC 9 104297792 104297792 + Silent SNP G G A TCGA-39-5016-01A-01D-1441-08 TCGA-39-5016-11A-01D-1441-08 g.chr9:104297792G>A c.87G>A c.(85-87)ggG>ggA p.G29G LUSC 9 104309471 104309471 + Missense_Mutation SNP G G A TCGA-22-5491-01A-01D-1632-08 TCGA-22-5491-11A-01D-1632-08 g.chr9:104309471G>A c.947G>A c.(946-948)gGc>gAc p.G316D LUSC 9 104309491 104309491 + Silent SNP C C A TCGA-85-6561-01A-11D-1817-08 TCGA-85-6561-10A-01D-1817-08 g.chr9:104309491C>A c.967C>A c.(967-969)Cgg>Agg p.R323R LUSC 9 104316311 104316311 + Missense_Mutation SNP A A T TCGA-60-2710-01A-01D-1522-08 TCGA-60-2710-11A-01D-1522-08 g.chr9:104316311A>T c.1943A>T c.(1942-1944)gAt>gTt p.D648V LUSC 9 104317101 104317101 + Silent SNP G G A TCGA-39-5036-01A-01D-1441-08 TCGA-39-5036-11A-01D-1441-08 g.chr9:104317101G>A c.2145G>A c.(2143-2145)caG>caA p.Q715Q LUSC 9 104324201 104324201 + Missense_Mutation SNP T T C TCGA-37-4133-01A-01D-1352-08 TCGA-37-4133-10A-01D-1352-08 g.chr9:104324201T>C c.2659T>C c.(2659-2661)Tct>Cct p.S887P LUSC 9 104324230 104324230 + Silent SNP A A G TCGA-43-6143-01A-11D-1817-08 TCGA-43-6143-11A-01D-1817-08 g.chr9:104324230A>G c.2688A>G c.(2686-2688)acA>acG p.T896T OV 9 104302596 104302596 + Nonsense_Mutation SNP C C T TCGA-29-1710-01A-02W-0633-09 TCGA-29-1710-10A-01W-0633-09 g.chr9:104302596C>T c.241C>T c.(241-243)Cga>Tga p.R81* OV 9 104307065 104307065 + Silent SNP G G A TCGA-24-2267-01A-01W-0799-08 TCGA-24-2267-11A-01W-0799-08 g.chr9:104307065G>A c.645G>A c.(643-645)gaG>gaA p.E215E OV 9 104309780 104309780 + Missense_Mutation SNP A A C TCGA-20-1683-01A-01W-0633-09 TCGA-20-1683-10A-01W-0633-09 g.chr9:104309780A>C c.1072A>C c.(1072-1074)Aca>Cca p.T358P OV 9 104312889 104312889 + Splice_Site SNP T T G TCGA-23-1117-01A-02W-0488-09 TCGA-23-1117-10A-01W-0488-09 g.chr9:104312889T>G c.1094T>G c.(1093-1095)gTg>gGg p.V365G OV 9 104313974 104313974 + Missense_Mutation SNP G G C TCGA-13-0893-01B-01W-0494-09 TCGA-13-0893-10A-01W-0494-09 g.chr9:104313974G>C c.1281G>C c.(1279-1281)gaG>gaC p.E427D OV 9 104323145 104323145 + Missense_Mutation SNP C C A TCGA-23-2079-01A-01W-0722-08 TCGA-23-2079-10A-01W-0722-08 g.chr9:104323145C>A c.2445C>A c.(2443-2445)aaC>aaA p.N815K PAAD 9 104303164 104303164 + Missense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr9:104303164G>A c.535G>A c.(535-537)Gag>Aag p.E179K PAAD 9 104312897 104312897 + Missense_Mutation SNP C C T TCGA-FB-AAPP-01A-12D-A40W-08 TCGA-FB-AAPP-11A-11D-A40W-08 g.chr9:104312897C>T c.1102C>T c.(1102-1104)Cgg>Tgg p.R368W PAAD 9 104324559 104324559 + Missense_Mutation SNP G G A TCGA-2J-AABR-01A-11D-A40W-08 TCGA-2J-AABR-10A-01D-A40W-08 g.chr9:104324559G>A c.2783G>A c.(2782-2784)cGt>cAt p.R928H PCPG 9 104307131 104307133 + In_Frame_Del DEL TCT TCT - TCGA-QR-A6GW-01A-11D-A35D-08 TCGA-QR-A6GW-10A-01D-A35B-08 g.chr9:104307131_104307133delTCT c.711_713delTCT c.(709-714)gatctt>gat p.L239del PRAD 9 104302620 104302620 + Missense_Mutation SNP T T A TCGA-TP-A8TT-01A-12D-A41K-08 TCGA-TP-A8TT-10A-01D-A41N-08 g.chr9:104302620T>A c.265T>A c.(265-267)Tca>Aca p.S89T PRAD 9 104309224 104309225 + Frame_Shift_Del DEL AC AC - TCGA-EJ-A8FS-01A-11D-A34U-08 TCGA-EJ-A8FS-10A-01D-A34X-08 g.chr9:104309224_104309225delAC c.870_871delAC c.(868-873)cgacacfs p.H291fs PRAD 9 104312963 104312963 + Missense_Mutation SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr9:104312963G>A c.1168G>A c.(1168-1170)Gtc>Atc p.V390I PRAD 9 104314097 104314097 + Silent SNP A A G TCGA-J4-A83I-01A-11D-A364-08 TCGA-J4-A83I-10B-01D-A362-08 g.chr9:104314097A>G c.1404A>G c.(1402-1404)caA>caG p.Q468Q PRAD 9 104314442 104314442 + Missense_Mutation SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr9:104314442G>A c.1428G>A c.(1426-1428)atG>atA p.M476I PRAD 9 104314514 104314514 + Missense_Mutation SNP A A T TCGA-EJ-5515-01A-01D-1576-08 TCGA-EJ-5515-10A-01D-1577-08 g.chr9:104314514A>T c.1500A>T c.(1498-1500)aaA>aaT p.K500N PRAD 9 104323384 104323384 + Missense_Mutation SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr9:104323384G>A c.2521G>A c.(2521-2523)Gcc>Acc p.A841T READ 9 104309422 104309422 + Missense_Mutation SNP A A G TCGA-DY-A0XA-01A-11D-A152-10 TCGA-DY-A0XA-10A-01D-A152-10 g.chr9:104309422A>G c.898A>G c.(898-900)Aat>Gat p.N300D READ 9 104309423 104309423 + Missense_Mutation SNP A A T TCGA-EI-6510-01A-11D-1733-10 TCGA-EI-6510-10A-01D-1733-10 g.chr9:104309423A>T c.899A>T c.(898-900)aAt>aTt p.N300I READ 9 104323505 104323505 + Missense_Mutation SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr9:104323505G>A c.2642G>A c.(2641-2643)cGa>cAa p.R881Q SKCM 9 104297796 104297796 + Missense_Mutation SNP A A G TCGA-GF-A3OT-06A-23D-A23B-08 TCGA-GF-A3OT-10A-01D-A23B-08 g.chr9:104297796A>G c.91A>G c.(91-93)Aca>Gca p.T31A SKCM 9 104302572 104302572 + Missense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr9:104302572C>T c.217C>T c.(217-219)Cgt>Tgt p.R73C SKCM 9 104302837 104302837 + Silent SNP C C T TCGA-EE-A29M-06A-11D-A196-08 TCGA-EE-A29M-10A-01D-A198-08 g.chr9:104302837C>T c.363C>T c.(361-363)ctC>ctT p.L121L SKCM 9 104303238 104303238 + Silent SNP C C T TCGA-EE-A29D-06A-11D-A197-08 TCGA-EE-A29D-10A-01D-A199-08 g.chr9:104303238C>T c.609C>T c.(607-609)tcC>tcT p.S203S SKCM 9 104309240 104309240 + Silent SNP C C T TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr9:104309240C>T c.886C>T c.(886-888)Cta>Tta p.L296L SKCM 9 104312939 104312939 + Missense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr9:104312939C>T c.1144C>T c.(1144-1146)Cgc>Tgc p.R382C SKCM 9 104312959 104312959 + Silent SNP C C T TCGA-EE-A2MJ-06A-11D-A197-08 TCGA-EE-A2MJ-10A-01D-A199-08 g.chr9:104312959C>T c.1164C>T c.(1162-1164)ttC>ttT p.F388F SKCM 9 104314989 104314989 + Missense_Mutation SNP C C T TCGA-EE-A184-06A-11D-A196-08 TCGA-EE-A184-10B-01D-A198-08 g.chr9:104314989C>T c.1855C>T c.(1855-1857)Cgg>Tgg p.R619W SKCM 9 104319679 104319679 + Missense_Mutation SNP T T C TCGA-GN-A4U7-06A-21D-A32N-08 TCGA-GN-A4U7-10B-01D-A32N-08 g.chr9:104319679T>C c.2183T>C c.(2182-2184)cTc>cCc p.L728P SKCM 9 104319879 104319879 + Splice_Site SNP G G A TCGA-EE-A2A6-06A-11D-A197-08 TCGA-EE-A2A6-10A-01D-A199-08 g.chr9:104319879G>A c.e16+1 SKCM 9 104324684 104324684 + Missense_Mutation SNP C C T TCGA-EE-A29E-06A-11D-A197-08 TCGA-EE-A29E-10A-01D-A199-08 g.chr9:104324684C>T c.2908C>T c.(2908-2910)Cat>Tat p.H970Y

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BLCA-US 9 104309797 104309797 single base substitution G A synonymous_variant L363L 1089G>A BLCA-US 9 104314697 104314697 single base substitution G A synonymous_variant Q521Q 1563G>A BOCA-FR 9 104327786 104327786 single base substitution T C downstream_gene_variant BOCA-UK 9 104319849 104319849 single base substitution G C missense_variant A785P 2353G>C BOCA-UK 9 104319849 104319849 single base substitution G C upstream_gene_variant BRCA-EU 9 104291258 104291259 deletion of <=200bp CT - upstream_gene_variant BRCA-EU 9 104292424 104292424 single base substitution C G upstream_gene_variant BRCA-EU 9 104294087 104294087 single base substitution A G upstream_gene_variant BRCA-EU 9 104294196 104294196 single base substitution T C upstream_gene_variant BRCA-EU 9 104296149 104296149 single base substitution C T 5_prime_UTR_variant BRCA-EU 9 104296149 104296149 single base substitution C T upstream_gene_variant BRCA-EU 9 104296178 104296178 single base substitution A G 5_prime_UTR_variant BRCA-EU 9 104296178 104296178 single base substitution A G upstream_gene_variant BRCA-EU 9 104297695 104297695 single base substitution C G 5_prime_UTR_premature_start_codon_gain_variant BRCA-EU 9 104297695 104297695 single base substitution C G exon_variant BRCA-EU 9 104298405 104298405 single base substitution G T intron_variant BRCA-EU 9 104300036 104300036 single base substitution G A intron_variant BRCA-EU 9 104301557 104301557 single base substitution G A intron_variant BRCA-EU 9 104301948 104301948 single base substitution C G intron_variant BRCA-EU 9 104304249 104304249 deletion of <=200bp A - downstream_gene_variant BRCA-EU 9 104304249 104304249 deletion of <=200bp A - intron_variant BRCA-EU 9 104305599 104305599 single base substitution C A downstream_gene_variant BRCA-EU 9 104305599 104305599 single base substitution C A intron_variant BRCA-EU 9 104305892 104305892 single base substitution G C downstream_gene_variant BRCA-EU 9 104305892 104305892 single base substitution G C intron_variant BRCA-EU 9 104306509 104306509 single base substitution G A downstream_gene_variant BRCA-EU 9 104306509 104306509 single base substitution G A intron_variant BRCA-EU 9 104307409 104307409 single base substitution A C downstream_gene_variant BRCA-EU 9 104307409 104307409 single base substitution A C intron_variant BRCA-EU 9 104309059 104309059 deletion of <=200bp T - intron_variant BRCA-EU 9 104309059 104309059 insertion of <=200bp - T intron_variant BRCA-EU 9 104312913 104312913 single base substitution A G missense_variant Q373R 1118A>G BRCA-EU 9 104315768 104315768 single base substitution G A intron_variant BRCA-EU 9 104316032 104316032 single base substitution C G intron_variant BRCA-EU 9 104316712 104316712 deletion of <=200bp A - intron_variant BRCA-EU 9 104317218 104317218 deletion of <=200bp T - intron_variant BRCA-EU 9 104317702 104317702 single base substitution C T intron_variant BRCA-EU 9 104317960 104317960 single base substitution G C intron_variant BRCA-EU 9 104318753 104318753 single base substitution C A intron_variant BRCA-EU 9 104318753 104318753 single base substitution C A upstream_gene_variant BRCA-EU 9 104318853 104318853 single base substitution A T intron_variant BRCA-EU 9 104318853 104318853 single base substitution A T upstream_gene_variant BRCA-EU 9 104325260 104325260 single base substitution T C 3_prime_UTR_variant BRCA-EU 9 104325260 104325260 single base substitution T C downstream_gene_variant BRCA-EU 9 104326107 104326107 single base substitution G C downstream_gene_variant BRCA-FR 9 104292424 104292424 single base substitution C G upstream_gene_variant BRCA-FR 9 104294196 104294196 single base substitution T C upstream_gene_variant BRCA-FR 9 104298483 104298483 single base substitution G A intron_variant BRCA-US 9 104302598 104302598 single base substitution A C downstream_gene_variant BRCA-US 9 104302598 104302598 single base substitution A C synonymous_variant R81R 243A>C BRCA-US 9 104313065 104313065 single base substitution G A missense_variant E424K 1270G>A BRCA-US 9 104313984 104313984 single base substitution C T missense_variant H431Y 1291C>T BRCA-US 9 104314674 104314674 single base substitution C T missense_variant R514C 1540C>T BRCA-US 9 104314716 104314716 single base substitution G T missense_variant D528Y 1582G>T BRCA-US 9 104315014 104315014 single base substitution A G missense_variant K627R 1880A>G BRCA-US 9 104323426 104323426 single base substitution C G exon_variant BRCA-US 9 104323426 104323426 single base substitution C G missense_variant Q855E 2563C>G BTCA-JP 9 104307162 104307162 single base substitution C T downstream_gene_variant BTCA-JP 9 104307162 104307162 single base substitution C T stop_gained Q248* 742C>T BTCA-JP 9 104309602 104309602 single base substitution C T intron_variant BTCA-JP 9 104309862 104309862 deletion of <=200bp A - intron_variant BTCA-JP 9 104314802 104314802 single base substitution T C synonymous_variant D556D 1668T>C CESC-US 9 104312939 104312939 single base substitution C T missense_variant R382C 1144C>T CLLE-ES 9 104324437 104324437 single base substitution G T downstream_gene_variant CLLE-ES 9 104324437 104324437 single base substitution G T intron_variant COAD-US 9 104302787 104302787 single base substitution C T downstream_gene_variant COAD-US 9 104302787 104302787 single base substitution C T missense_variant R105C 313C>T COAD-US 9 104303116 104303116 single base substitution G A downstream_gene_variant COAD-US 9 104303116 104303116 single base substitution G A missense_variant A163T 487G>A COAD-US 9 104309213 104309213 single base substitution C T stop_gained R287* 859C>T COAD-US 9 104312898 104312898 single base substitution G A missense_variant R368Q 1103G>A COAD-US 9 104316389 104316389 single base substitution T C splice_donor_variant COAD-US 9 104323203 104323203 single base substitution C T exon_variant COAD-US 9 104323203 104323203 single base substitution C T missense_variant R835C 2503C>T COAD-US 9 104324622 104324622 single base substitution G A downstream_gene_variant COAD-US 9 104324622 104324622 single base substitution G A missense_variant R949H 2846G>A COCA-CN 9 104293263 104293263 single base substitution C G upstream_gene_variant COCA-CN 9 104294530 104294530 single base substitution T C upstream_gene_variant COCA-CN 9 104300981 104300981 single base substitution G A intron_variant COCA-CN 9 104302932 104302932 single base substitution G T downstream_gene_variant COCA-CN 9 104302932 104302932 single base substitution G T intron_variant COCA-CN 9 104305716 104305716 single base substitution T C downstream_gene_variant COCA-CN 9 104305716 104305716 single base substitution T C intron_variant COCA-CN 9 104305824 104305824 single base substitution A C downstream_gene_variant COCA-CN 9 104305824 104305824 single base substitution A C intron_variant COCA-CN 9 104305865 104305865 single base substitution A G downstream_gene_variant COCA-CN 9 104305865 104305865 single base substitution A G intron_variant COCA-CN 9 104309639 104309639 single base substitution G T intron_variant COCA-CN 9 104310563 104310563 single base substitution A T intron_variant COCA-CN 9 104323041 104323041 single base substitution T A exon_variant COCA-CN 9 104323041 104323041 single base substitution T A intron_variant COCA-CN 9 104324233 104324233 single base substitution G T downstream_gene_variant COCA-CN 9 104324233 104324233 single base substitution G T missense_variant K897N 2691G>T ESAD-UK 9 104293890 104293890 single base substitution C T upstream_gene_variant ESAD-UK 9 104294901 104294901 single base substitution G A upstream_gene_variant ESAD-UK 9 104295379 104295379 single base substitution A T upstream_gene_variant ESAD-UK 9 104297440 104297440 single base substitution C T intron_variant ESAD-UK 9 104298260 104298260 single base substitution C A intron_variant ESAD-UK 9 104299456 104299456 single base substitution G A intron_variant ESAD-UK 9 104302775 104302775 single base substitution G T downstream_gene_variant ESAD-UK 9 104302775 104302775 single base substitution G T missense_variant D101Y 301G>T ESAD-UK 9 104304920 104304920 single base substitution G C downstream_gene_variant ESAD-UK 9 104304920 104304920 single base substitution G C intron_variant ESAD-UK 9 104306297 104306297 single base substitution T C downstream_gene_variant ESAD-UK 9 104306297 104306297 single base substitution T C intron_variant ESAD-UK 9 104307941 104307941 single base substitution A G downstream_gene_variant ESAD-UK 9 104307941 104307941 single base substitution A G intron_variant ESAD-UK 9 104313536 104313536 single base substitution G A intron_variant ESAD-UK 9 104315689 104315689 single base substitution G A intron_variant ESAD-UK 9 104315991 104315991 single base substitution A G intron_variant ESAD-UK 9 104316712 104316712 deletion of <=200bp A - intron_variant ESAD-UK 9 104319087 104319087 deletion of <=200bp A - intron_variant ESAD-UK 9 104319087 104319087 deletion of <=200bp A - upstream_gene_variant ESAD-UK 9 104319168 104319168 single base substitution G C intron_variant ESAD-UK 9 104319168 104319168 single base substitution G C upstream_gene_variant ESAD-UK 9 104323309 104323309 single base substitution A C intron_variant ESAD-UK 9 104323312 104323312 single base substitution T G intron_variant ESAD-UK 9 104323359 104323359 single base substitution A G intron_variant ESAD-UK 9 104325876 104325876 single base substitution T A downstream_gene_variant ESAD-UK 9 104325878 104325878 deletion of <=200bp C - downstream_gene_variant ESAD-UK 9 104329495 104329495 single base substitution A C downstream_gene_variant KIRC-US 9 104316360 104316360 single base substitution G T missense_variant M664I 1992G>T KIRC-US 9 104324630 104324630 single base substitution A C downstream_gene_variant KIRC-US 9 104324630 104324630 single base substitution A C missense_variant T952P 2854A>C KIRP-US 9 104302538 104302538 single base substitution G C exon_variant KIRP-US 9 104302538 104302538 single base substitution G C missense_variant M61I 183G>C LAML-KR 9 104305575 104305575 single base substitution G C downstream_gene_variant LAML-KR 9 104305575 104305575 single base substitution G C intron_variant LAML-KR 9 104305577 104305577 single base substitution G T downstream_gene_variant LAML-KR 9 104305577 104305577 single base substitution G T intron_variant LAML-KR 9 104325989 104325989 single base substitution G T downstream_gene_variant LICA-CN 9 104303261 104303261 single base substitution A T downstream_gene_variant LICA-CN 9 104303261 104303261 single base substitution A T splice_region_variant LICA-CN 9 104307060 104307060 single base substitution G A downstream_gene_variant LICA-CN 9 104307060 104307060 single base substitution G A missense_variant V214M 640G>A LICA-CN 9 104314455 104314455 single base substitution A T missense_variant S481C 1441A>T LICA-FR 9 104291436 104291436 deletion of <=200bp T - upstream_gene_variant LICA-FR 9 104314013 104314013 single base substitution G T missense_variant Q440H 1320G>T LICA-FR 9 104314494 104314494 single base substitution G A missense_variant V494I 1480G>A LICA-FR 9 104323398 104323398 single base substitution T C exon_variant LICA-FR 9 104323398 104323398 single base substitution T C synonymous_variant D845D 2535T>C LIHC-US 9 104303192 104303192 single base substitution T C downstream_gene_variant LIHC-US 9 104303192 104303192 single base substitution T C missense_variant I188T 563T>C LIHC-US 9 104315030 104315030 single base substitution A T missense_variant E632D 1896A>T LINC-JP 9 104295598 104295598 single base substitution C A upstream_gene_variant LINC-JP 9 104305614 104305614 deletion of <=200bp T - downstream_gene_variant LINC-JP 9 104305614 104305614 deletion of <=200bp T - intron_variant LINC-JP 9 104309645 104309645 single base substitution T A intron_variant LINC-JP 9 104316081 104316081 single base substitution A G intron_variant LINC-JP 9 104324193 104324193 single base substitution A T downstream_gene_variant LINC-JP 9 104324193 104324193 single base substitution A T missense_variant E884V 2651A>T LINC-JP 9 104328490 104328490 single base substitution A G downstream_gene_variant LIRI-JP 9 104294106 104294106 single base substitution C T upstream_gene_variant LIRI-JP 9 104301749 104301749 single base substitution A G intron_variant LIRI-JP 9 104304781 104304781 single base substitution G A downstream_gene_variant LIRI-JP 9 104304781 104304781 single base substitution G A intron_variant LIRI-JP 9 104306425 104306425 single base substitution C T downstream_gene_variant LIRI-JP 9 104306425 104306425 single base substitution C T intron_variant LIRI-JP 9 104312173 104312173 single base substitution A T intron_variant LIRI-JP 9 104313145 104313145 single base substitution T G intron_variant LIRI-JP 9 104314304 104314304 single base substitution A G intron_variant LIRI-JP 9 104315273 104315273 single base substitution A T intron_variant LIRI-JP 9 104317164 104317164 single base substitution A G intron_variant LIRI-JP 9 104317410 104317410 single base substitution T G intron_variant LIRI-JP 9 104318685 104318685 single base substitution A G intron_variant LIRI-JP 9 104318685 104318685 single base substitution A G upstream_gene_variant LIRI-JP 9 104319539 104319539 single base substitution A G intron_variant LIRI-JP 9 104319539 104319539 single base substitution A G upstream_gene_variant LIRI-JP 9 104322151 104322151 single base substitution A G intron_variant LIRI-JP 9 104322151 104322151 single base substitution A G upstream_gene_variant LIRI-JP 9 104324538 104324538 single base substitution C A downstream_gene_variant LIRI-JP 9 104324538 104324538 single base substitution C A missense_variant T921N 2762C>A LIRI-JP 9 104325332 104325332 single base substitution A G 3_prime_UTR_variant LIRI-JP 9 104325332 104325332 single base substitution A G downstream_gene_variant LIRI-JP 9 104325401 104325401 single base substitution T G 3_prime_UTR_variant LIRI-JP 9 104325401 104325401 single base substitution T G downstream_gene_variant LUSC-KR 9 104296078 104296078 single base substitution G T upstream_gene_variant LUSC-KR 9 104296768 104296768 single base substitution C G intron_variant LUSC-KR 9 104302856 104302856 single base substitution G T downstream_gene_variant LUSC-KR 9 104302856 104302856 single base substitution G T missense_variant V128F 382G>T LUSC-KR 9 104305577 104305577 single base substitution G T downstream_gene_variant LUSC-KR 9 104305577 104305577 single base substitution G T intron_variant LUSC-KR 9 104305700 104305700 single base substitution A G downstream_gene_variant LUSC-KR 9 104305700 104305700 single base substitution A G intron_variant LUSC-KR 9 104306577 104306577 single base substitution G A downstream_gene_variant LUSC-KR 9 104306577 104306577 single base substitution G A intron_variant LUSC-KR 9 104311285 104311285 single base substitution C G intron_variant LUSC-KR 9 104314334 104314334 single base substitution C G intron_variant LUSC-KR 9 104323600 104323600 single base substitution G C exon_variant LUSC-KR 9 104323600 104323600 single base substitution G C intron_variant LUSC-US 9 104297792 104297792 single base substitution G A exon_variant LUSC-US 9 104297792 104297792 single base substitution G A synonymous_variant G29G 87G>A LUSC-US 9 104309471 104309471 single base substitution G A missense_variant G316D 947G>A LUSC-US 9 104309491 104309491 single base substitution C A synonymous_variant R323R 967C>A LUSC-US 9 104316311 104316311 single base substitution A T missense_variant D648V 1943A>T LUSC-US 9 104317101 104317101 single base substitution G A synonymous_variant Q715Q 2145G>A LUSC-US 9 104324201 104324201 single base substitution T C downstream_gene_variant LUSC-US 9 104324201 104324201 single base substitution T C missense_variant S887P 2659T>C LUSC-US 9 104324230 104324230 single base substitution A G downstream_gene_variant LUSC-US 9 104324230 104324230 single base substitution A G synonymous_variant T896T 2688A>G MALY-DE 9 104296349 104296349 single base substitution C G 5_prime_UTR_premature_start_codon_gain_variant MALY-DE 9 104296349 104296349 single base substitution C G exon_variant MALY-DE 9 104296349 104296349 single base substitution C G intron_variant MALY-DE 9 104297025 104297025 single base substitution T A intron_variant MALY-DE 9 104302143 104302143 single base substitution A C intron_variant MALY-DE 9 104302538 104302538 single base substitution G T exon_variant MALY-DE 9 104302538 104302538 single base substitution G T missense_variant M61I 183G>T MALY-DE 9 104316920 104316920 single base substitution A G intron_variant MALY-DE 9 104318342 104318342 single base substitution T C intron_variant MALY-DE 9 104318342 104318342 single base substitution T C upstream_gene_variant MALY-DE 9 104324195 104324195 single base substitution G A downstream_gene_variant MALY-DE 9 104324195 104324195 single base substitution G A missense_variant D885N 2653G>A MELA-AU 9 104291258 104291259 deletion of <=200bp CT - upstream_gene_variant MELA-AU 9 104291632 104291632 single base substitution T C upstream_gene_variant MELA-AU 9 104291724 104291724 single base substitution A G upstream_gene_variant MELA-AU 9 104291826 104291826 single base substitution G C upstream_gene_variant MELA-AU 9 104292131 104292131 single base substitution G A upstream_gene_variant MELA-AU 9 104292181 104292181 single base substitution C T upstream_gene_variant MELA-AU 9 104292416 104292416 single base substitution C T upstream_gene_variant MELA-AU 9 104292645 104292645 single base substitution A T upstream_gene_variant MELA-AU 9 104292705 104292705 single base substitution C T upstream_gene_variant MELA-AU 9 104292849 104292849 single base substitution C T upstream_gene_variant MELA-AU 9 104292878 104292878 single base substitution G A upstream_gene_variant MELA-AU 9 104292938 104292938 single base substitution C T upstream_gene_variant MELA-AU 9 104293091 104293091 single base substitution T G upstream_gene_variant MELA-AU 9 104293236 104293236 single base substitution A G upstream_gene_variant MELA-AU 9 104293325 104293325 single base substitution C T upstream_gene_variant MELA-AU 9 104293744 104293744 single base substitution C T upstream_gene_variant MELA-AU 9 104294501 104294501 single base substitution G A upstream_gene_variant MELA-AU 9 104295173 104295173 single base substitution T C upstream_gene_variant MELA-AU 9 104296031 104296031 single base substitution C T upstream_gene_variant MELA-AU 9 104296044 104296044 single base substitution C T upstream_gene_variant MELA-AU 9 104296067 104296067 single base substitution C T upstream_gene_variant MELA-AU 9 104296091 104296092 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 9 104296092 104296092 single base substitution C T upstream_gene_variant MELA-AU 9 104296111 104296111 single base substitution C T upstream_gene_variant MELA-AU 9 104296112 104296112 single base substitution C T upstream_gene_variant MELA-AU 9 104296116 104296116 single base substitution C T upstream_gene_variant MELA-AU 9 104296130 104296130 single base substitution C T upstream_gene_variant MELA-AU 9 104296143 104296143 single base substitution C T 5_prime_UTR_variant MELA-AU 9 104296143 104296143 single base substitution C T upstream_gene_variant MELA-AU 9 104297233 104297233 single base substitution A G intron_variant MELA-AU 9 104297381 104297381 single base substitution G A intron_variant MELA-AU 9 104297488 104297488 single base substitution C T intron_variant MELA-AU 9 104299180 104299180 single base substitution G A intron_variant MELA-AU 9 104299778 104299778 insertion of <=200bp - GAGAG intron_variant MELA-AU 9 104300142 104300142 single base substitution G C intron_variant MELA-AU 9 104301181 104301182 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 9 104302150 104302150 single base substitution T G intron_variant MELA-AU 9 104302648 104302648 single base substitution G A downstream_gene_variant MELA-AU 9 104302648 104302648 single base substitution G A missense_variant S98N 293G>A MELA-AU 9 104302704 104302704 single base substitution C T downstream_gene_variant MELA-AU 9 104302704 104302704 single base substitution C T intron_variant MELA-AU 9 104303027 104303027 single base substitution C T downstream_gene_variant MELA-AU 9 104303027 104303027 single base substitution C T intron_variant MELA-AU 9 104303171 104303171 single base substitution C T downstream_gene_variant MELA-AU 9 104303171 104303171 single base substitution C T missense_variant S181F 542C>T MELA-AU 9 104305100 104305100 single base substitution G A downstream_gene_variant MELA-AU 9 104305100 104305100 single base substitution G A intron_variant MELA-AU 9 104306040 104306040 single base substitution G A downstream_gene_variant MELA-AU 9 104306040 104306040 single base substitution G A intron_variant MELA-AU 9 104306065 104306065 single base substitution C T downstream_gene_variant MELA-AU 9 104306065 104306065 single base substitution C T intron_variant MELA-AU 9 104306885 104306885 single base substitution G A downstream_gene_variant MELA-AU 9 104306885 104306885 single base substitution G A intron_variant MELA-AU 9 104306926 104306926 single base substitution T C downstream_gene_variant MELA-AU 9 104306926 104306926 single base substitution T C intron_variant MELA-AU 9 104308310 104308310 single base substitution C T intron_variant MELA-AU 9 104308323 104308323 single base substitution C T intron_variant MELA-AU 9 104308660 104308660 single base substitution C G intron_variant MELA-AU 9 104309484 104309484 single base substitution C T synonymous_variant I320I 960C>T MELA-AU 9 104309648 104309648 single base substitution T C intron_variant MELA-AU 9 104309675 104309675 single base substitution C T splice_region_variant MELA-AU 9 104309922 104309922 single base substitution C T intron_variant MELA-AU 9 104310044 104310044 single base substitution C T intron_variant MELA-AU 9 104310617 104310617 single base substitution C T intron_variant MELA-AU 9 104311511 104311511 single base substitution C T intron_variant MELA-AU 9 104311777 104311777 single base substitution C T intron_variant MELA-AU 9 104311992 104311992 single base substitution C T intron_variant MELA-AU 9 104312653 104312653 single base substitution A G intron_variant MELA-AU 9 104313721 104313721 single base substitution T A intron_variant MELA-AU 9 104313763 104313763 single base substitution C T intron_variant MELA-AU 9 104313779 104313779 single base substitution T A intron_variant MELA-AU 9 104313949 104313949 single base substitution C T intron_variant MELA-AU 9 104314044 104314044 single base substitution G A missense_variant E451K 1351G>A MELA-AU 9 104314288 104314288 single base substitution C T intron_variant MELA-AU 9 104314374 104314374 single base substitution C T intron_variant MELA-AU 9 104315500 104315500 single base substitution C A intron_variant MELA-AU 9 104316087 104316087 single base substitution C T intron_variant MELA-AU 9 104316445 104316445 single base substitution C T intron_variant MELA-AU 9 104316482 104316482 single base substitution C T intron_variant MELA-AU 9 104316824 104316824 single base substitution T C intron_variant MELA-AU 9 104316985 104316985 single base substitution C T synonymous_variant L677L 2029C>T MELA-AU 9 104317245 104317245 single base substitution C T intron_variant MELA-AU 9 104318710 104318710 single base substitution T A intron_variant MELA-AU 9 104318710 104318710 single base substitution T A upstream_gene_variant MELA-AU 9 104319652 104319652 single base substitution C T intron_variant MELA-AU 9 104319652 104319652 single base substitution C T upstream_gene_variant MELA-AU 9 104320313 104320313 single base substitution C T intron_variant MELA-AU 9 104320313 104320313 single base substitution C T upstream_gene_variant MELA-AU 9 104320575 104320575 single base substitution G A intron_variant MELA-AU 9 104320575 104320575 single base substitution G A upstream_gene_variant MELA-AU 9 104320608 104320608 single base substitution C T intron_variant MELA-AU 9 104320608 104320608 single base substitution C T upstream_gene_variant MELA-AU 9 104320945 104320945 single base substitution T A intron_variant MELA-AU 9 104320945 104320945 single base substitution T A upstream_gene_variant MELA-AU 9 104321118 104321118 single base substitution C T intron_variant MELA-AU 9 104321118 104321118 single base substitution C T upstream_gene_variant MELA-AU 9 104321424 104321424 single base substitution T A intron_variant MELA-AU 9 104321424 104321424 single base substitution T A upstream_gene_variant MELA-AU 9 104321621 104321621 single base substitution C T intron_variant MELA-AU 9 104321621 104321621 single base substitution C T upstream_gene_variant MELA-AU 9 104321826 104321826 single base substitution C T intron_variant MELA-AU 9 104321826 104321826 single base substitution C T upstream_gene_variant MELA-AU 9 104322030 104322030 single base substitution T A intron_variant MELA-AU 9 104322030 104322030 single base substitution T A upstream_gene_variant MELA-AU 9 104322366 104322366 single base substitution G T intron_variant MELA-AU 9 104322366 104322366 single base substitution G T upstream_gene_variant MELA-AU 9 104322827 104322827 single base substitution C T intron_variant MELA-AU 9 104322827 104322827 single base substitution C T upstream_gene_variant MELA-AU 9 104323363 104323363 single base substitution C T intron_variant MELA-AU 9 104324138 104324138 single base substitution C T downstream_gene_variant MELA-AU 9 104324138 104324138 single base substitution C T intron_variant MELA-AU 9 104324944 104324944 single base substitution C T 3_prime_UTR_variant MELA-AU 9 104324944 104324944 single base substitution C T downstream_gene_variant MELA-AU 9 104325081 104325081 single base substitution G T 3_prime_UTR_variant MELA-AU 9 104325081 104325081 single base substitution G T downstream_gene_variant MELA-AU 9 104325504 104325504 single base substitution G A 3_prime_UTR_variant MELA-AU 9 104325504 104325504 single base substitution G A downstream_gene_variant MELA-AU 9 104325800 104325800 single base substitution C T downstream_gene_variant MELA-AU 9 104326135 104326135 single base substitution C G downstream_gene_variant MELA-AU 9 104326139 104326139 deletion of <=200bp T - downstream_gene_variant MELA-AU 9 104327340 104327340 single base substitution C T downstream_gene_variant MELA-AU 9 104327649 104327649 single base substitution T C downstream_gene_variant MELA-AU 9 104328225 104328225 single base substitution C T downstream_gene_variant MELA-AU 9 104328518 104328518 single base substitution C T downstream_gene_variant MELA-AU 9 104328558 104328559 multiple base substitution (>=2bp and <=200bp) CT TA downstream_gene_variant MELA-AU 9 104329752 104329752 single base substitution C T downstream_gene_variant MELA-AU 9 104330085 104330085 single base substitution C T downstream_gene_variant ORCA-IN 9 104305842 104305842 single base substitution G A downstream_gene_variant ORCA-IN 9 104305842 104305842 single base substitution G A intron_variant ORCA-IN 9 104327205 104327205 single base substitution C T downstream_gene_variant OV-AU 9 104294657 104294657 single base substitution G C upstream_gene_variant OV-AU 9 104294744 104294744 single base substitution C G upstream_gene_variant OV-AU 9 104299509 104299509 single base substitution A C intron_variant OV-AU 9 104305577 104305577 single base substitution G T downstream_gene_variant OV-AU 9 104305577 104305577 single base substitution G T intron_variant OV-AU 9 104310151 104310151 single base substitution G C intron_variant OV-AU 9 104317192 104317192 single base substitution G T intron_variant OV-AU 9 104317640 104317640 single base substitution G C intron_variant OV-AU 9 104317985 104317985 single base substitution G A intron_variant OV-AU 9 104317985 104317985 single base substitution G A upstream_gene_variant OV-AU 9 104327780 104327780 single base substitution C T downstream_gene_variant OV-US 9 104312889 104312889 single base substitution T G missense_variant V365G 1094T>G OV-US 9 104313974 104313974 single base substitution G C missense_variant E427D 1281G>C PACA-AU 9 104295548 104295548 insertion of <=200bp - G upstream_gene_variant PACA-AU 9 104307428 104307428 single base substitution A T downstream_gene_variant PACA-AU 9 104307428 104307428 single base substitution A T intron_variant PACA-AU 9 104308966 104308966 single base substitution G C intron_variant PACA-AU 9 104312669 104312669 single base substitution G T intron_variant PACA-AU 9 104314678 104314678 single base substitution G A missense_variant S515N 1544G>A PACA-AU 9 104314801 104314801 single base substitution A T missense_variant D556V 1667A>T PACA-AU 9 104314873 104314873 single base substitution G A missense_variant R580Q 1739G>A PACA-AU 9 104322278 104322278 single base substitution C A intron_variant PACA-AU 9 104322278 104322278 single base substitution C A upstream_gene_variant PACA-AU 9 104329543 104329543 single base substitution A G downstream_gene_variant PACA-AU 9 104329879 104329879 single base substitution G C downstream_gene_variant PACA-CA 9 104304249 104304249 deletion of <=200bp A - downstream_gene_variant PACA-CA 9 104304249 104304249 deletion of <=200bp A - intron_variant PACA-CA 9 104305649 104305649 single base substitution G T downstream_gene_variant PACA-CA 9 104305649 104305649 single base substitution G T intron_variant PACA-CA 9 104309751 104309751 single base substitution A C missense_variant K348T 1043A>C PACA-CA 9 104310356 104310356 deletion of <=200bp A - intron_variant PACA-CA 9 104311699 104311699 single base substitution A T intron_variant PACA-CA 9 104315879 104315879 single base substitution C T intron_variant PACA-CA 9 104318396 104318396 single base substitution C G intron_variant PACA-CA 9 104318396 104318396 single base substitution C G upstream_gene_variant PACA-CA 9 104320479 104320479 single base substitution C T intron_variant PACA-CA 9 104320479 104320479 single base substitution C T upstream_gene_variant PACA-CA 9 104321962 104321962 single base substitution A T intron_variant PACA-CA 9 104321962 104321962 single base substitution A T upstream_gene_variant PACA-CA 9 104323967 104323967 single base substitution T C downstream_gene_variant PACA-CA 9 104323967 104323967 single base substitution T C intron_variant PACA-CA 9 104324613 104324613 single base substitution T G downstream_gene_variant PACA-CA 9 104324613 104324613 single base substitution T G missense_variant V946G 2837T>G PAEN-AU 9 104305577 104305577 single base substitution G T downstream_gene_variant PAEN-AU 9 104305577 104305577 single base substitution G T intron_variant PAEN-AU 9 104315905 104315905 single base substitution T C intron_variant PAEN-IT 9 104316967 104316967 single base substitution C T intron_variant PAEN-IT 9 104318023 104318023 single base substitution C T intron_variant PAEN-IT 9 104318023 104318023 single base substitution C T upstream_gene_variant PBCA-DE 9 104294417 104294422 deletion of <=200bp TGGCGT - upstream_gene_variant PBCA-DE 9 104300568 104300568 single base substitution G C intron_variant PBCA-DE 9 104305716 104305716 single base substitution T C downstream_gene_variant PBCA-DE 9 104305716 104305716 single base substitution T C intron_variant PBCA-DE 9 104318760 104318760 deletion of <=200bp A - intron_variant PBCA-DE 9 104318760 104318760 deletion of <=200bp A - upstream_gene_variant PBCA-DE 9 104319403 104319403 single base substitution G T intron_variant PBCA-DE 9 104319403 104319403 single base substitution G T upstream_gene_variant PRAD-CA 9 104305649 104305649 single base substitution G T downstream_gene_variant PRAD-CA 9 104305649 104305649 single base substitution G T intron_variant PRAD-CA 9 104306338 104306338 single base substitution G T downstream_gene_variant PRAD-CA 9 104306338 104306338 single base substitution G T intron_variant PRAD-UK 9 104297208 104297208 single base substitution G C intron_variant PRAD-UK 9 104299943 104299943 single base substitution C A intron_variant PRAD-UK 9 104316901 104316901 single base substitution C G intron_variant PRAD-UK 9 104317170 104317170 insertion of <=200bp - A intron_variant PRAD-UK 9 104319207 104319207 single base substitution C A intron_variant PRAD-UK 9 104319207 104319207 single base substitution C A upstream_gene_variant PRAD-UK 9 104320160 104320160 single base substitution T A intron_variant PRAD-UK 9 104320160 104320160 single base substitution T A upstream_gene_variant PRAD-US 9 104312897 104312897 single base substitution C T missense_variant R368W 1102C>T PRAD-US 9 104314514 104314514 single base substitution A T missense_variant K500N 1500A>T READ-US 9 104302597 104302597 single base substitution G A downstream_gene_variant READ-US 9 104302597 104302597 single base substitution G A missense_variant R81Q 242G>A READ-US 9 104314779 104314779 single base substitution G A missense_variant A549T 1645G>A READ-US 9 104323089 104323089 single base substitution G A exon_variant READ-US 9 104323089 104323089 single base substitution G A missense_variant A797T 2389G>A RECA-EU 9 104307166 104307166 single base substitution A C downstream_gene_variant RECA-EU 9 104307166 104307166 single base substitution A C missense_variant E249A 746A>C RECA-EU 9 104307812 104307812 single base substitution T C downstream_gene_variant RECA-EU 9 104307812 104307812 single base substitution T C intron_variant SKCA-BR 9 104291435 104291436 deletion of <=200bp CT - upstream_gene_variant SKCA-BR 9 104293289 104293289 single base substitution G A upstream_gene_variant SKCA-BR 9 104293477 104293479 deletion of <=200bp TAC - upstream_gene_variant SKCA-BR 9 104294881 104294881 single base substitution G A upstream_gene_variant SKCA-BR 9 104296091 104296091 single base substitution C T upstream_gene_variant SKCA-BR 9 104296951 104296951 single base substitution A G intron_variant SKCA-BR 9 104305715 104305716 deletion of <=200bp CT - downstream_gene_variant SKCA-BR 9 104305715 104305716 deletion of <=200bp CT - intron_variant SKCA-BR 9 104305723 104305723 single base substitution G A downstream_gene_variant SKCA-BR 9 104305723 104305723 single base substitution G A intron_variant SKCA-BR 9 104305727 104305727 single base substitution G A downstream_gene_variant SKCA-BR 9 104305727 104305727 single base substitution G A intron_variant SKCA-BR 9 104305781 104305791 deletion of <=200bp TCTAACCCTGC - downstream_gene_variant SKCA-BR 9 104305781 104305791 deletion of <=200bp TCTAACCCTGC - intron_variant SKCA-BR 9 104306988 104306988 insertion of <=200bp - TA downstream_gene_variant SKCA-BR 9 104306988 104306988 insertion of <=200bp - TA intron_variant SKCA-BR 9 104307875 104307875 single base substitution T A downstream_gene_variant SKCA-BR 9 104307875 104307875 single base substitution T A intron_variant SKCA-BR 9 104310556 104310556 single base substitution C A intron_variant SKCA-BR 9 104314850 104314850 single base substitution A G synonymous_variant E572E 1716A>G SKCA-BR 9 104315866 104315866 insertion of <=200bp - AT intron_variant SKCA-BR 9 104320958 104320958 single base substitution T G intron_variant SKCA-BR 9 104320958 104320958 single base substitution T G upstream_gene_variant SKCA-BR 9 104321117 104321117 single base substitution C T intron_variant SKCA-BR 9 104321117 104321117 single base substitution C T upstream_gene_variant SKCA-BR 9 104321179 104321179 single base substitution C T intron_variant SKCA-BR 9 104321179 104321179 single base substitution C T upstream_gene_variant SKCA-BR 9 104325962 104325962 insertion of <=200bp - TGTG downstream_gene_variant SKCA-BR 9 104328539 104328539 single base substitution C T downstream_gene_variant SKCA-BR 9 104330326 104330326 single base substitution T G downstream_gene_variant SKCM-US 9 104297796 104297796 single base substitution A G exon_variant SKCM-US 9 104297796 104297796 single base substitution A G missense_variant T31A 91A>G SKCM-US 9 104302572 104302572 single base substitution C T downstream_gene_variant SKCM-US 9 104302572 104302572 single base substitution C T missense_variant R73C 217C>T SKCM-US 9 104302837 104302837 single base substitution C T downstream_gene_variant SKCM-US 9 104302837 104302837 single base substitution C T synonymous_variant L121L 363C>T SKCM-US 9 104303238 104303238 single base substitution C T downstream_gene_variant SKCM-US 9 104303238 104303238 single base substitution C T synonymous_variant S203S 609C>T SKCM-US 9 104309240 104309240 single base substitution C T synonymous_variant L296L 886C>T SKCM-US 9 104312939 104312939 single base substitution C T missense_variant R382C 1144C>T SKCM-US 9 104312959 104312959 single base substitution C T synonymous_variant F388F 1164C>T SKCM-US 9 104314989 104314989 single base substitution C T missense_variant R619W 1855C>T SKCM-US 9 104319879 104319879 single base substitution G A splice_donor_variant SKCM-US 9 104319879 104319879 single base substitution G A upstream_gene_variant SKCM-US 9 104324684 104324684 single base substitution C T downstream_gene_variant SKCM-US 9 104324684 104324684 single base substitution C T missense_variant H970Y 2908C>T STAD-US 9 104302547 104302547 single base substitution G A exon_variant STAD-US 9 104302547 104302547 single base substitution G A synonymous_variant Q64Q 192G>A STAD-US 9 104302555 104302555 single base substitution C T exon_variant STAD-US 9 104302555 104302555 single base substitution C T missense_variant A67V 200C>T STAD-US 9 104309176 104309176 single base substitution G A synonymous_variant L274L 822G>A STAD-US 9 104312974 104312974 single base substitution T C synonymous_variant N393N 1179T>C STAD-US 9 104312994 104312994 single base substitution C T missense_variant A400V 1199C>T STAD-US 9 104317003 104317003 single base substitution G A missense_variant D683N 2047G>A STAD-US 9 104317113 104317113 single base substitution C A synonymous_variant A719A 2157C>A STAD-US 9 104324610 104324610 single base substitution G A downstream_gene_variant STAD-US 9 104324610 104324610 single base substitution G A missense_variant C945Y 2834G>A STAD-US 9 104324640 104324640 single base substitution G A downstream_gene_variant STAD-US 9 104324640 104324640 single base substitution G A missense_variant R955H 2864G>A UCEC-US 9 104302516 104302516 single base substitution A C exon_variant UCEC-US 9 104302516 104302516 single base substitution A C missense_variant K54T 161A>C UCEC-US 9 104302835 104302835 single base substitution C A downstream_gene_variant UCEC-US 9 104302835 104302835 single base substitution C A missense_variant L121I 361C>A UCEC-US 9 104302910 104302910 insertion of <=200bp - GA downstream_gene_variant UCEC-US 9 104302910 104302910 insertion of <=200bp - GA frameshift_variant ?146D? UCEC-US 9 104302910 104302910 insertion of <=200bp - GA frameshift_variant R146D? UCEC-US 9 104307102 104307102 single base substitution G A downstream_gene_variant UCEC-US 9 104307102 104307102 single base substitution G A missense_variant E228K 682G>A UCEC-US 9 104312896 104312896 single base substitution G A synonymous_variant L367L 1101G>A UCEC-US 9 104312993 104312993 single base substitution G A missense_variant A400T 1198G>A UCEC-US 9 104314443 104314443 single base substitution C T missense_variant R477C 1429C>T UCEC-US 9 104314501 104314501 single base substitution G T missense_variant R496I 1487G>T UCEC-US 9 104314675 104314675 single base substitution G A missense_variant R514H 1541G>A UCEC-US 9 104314839 104314839 single base substitution C T stop_gained R569* 1705C>T UCEC-US 9 104314967 104314967 single base substitution G T missense_variant E611D 1833G>T UCEC-US 9 104317023 104317023 single base substitution G T missense_variant K689N 2067G>T UCEC-US 9 104319831 104319831 single base substitution G T stop_gained E779* 2335G>T UCEC-US 9 104319831 104319831 single base substitution G T upstream_gene_variant UCEC-US 9 104323512 104323512 single base substitution G T exon_variant UCEC-US 9 104323512 104323512 single base substitution G T missense_variant Q883H 2649G>T UCEC-US 9 104324285 104324285 single base substitution G T downstream_gene_variant UCEC-US 9 104324285 104324285 single base substitution G T missense_variant D915Y 2743G>T UCEC-US 9 104324563 104324563 single base substitution A C downstream_gene_variant UCEC-US 9 104324563 104324563 single base substitution A C missense_variant K929N 2787A>C UCEC-US 9 104324596 104324596 single base substitution C A downstream_gene_variant UCEC-US 9 104324596 104324596 single base substitution C A synonymous_variant V940V 2820C>A

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand TCGA-BR-6452-01 COSM3902646 c.2834G>A p.C945Y Substitution - Missense 9:101562328-101562328 + TCGA-39-5036-01 COSM752258 c.2145G>A p.Q715Q Substitution - coding silent 9:101554819-101554819 + DLD1 COSM1674680 c.2488T>G p.L830V Substitution - Missense 9:101560906-101560906 + SNU-C4 COSM3167294 c.2912G>A p.R971H Substitution - Missense 9:101562406-101562406 + 951_T COSM3952133 c.463G>A p.A155T Substitution - Missense 9:101540810-101540810 + UD-SCC-2 COSM4369202 c.730C>T p.R244C Substitution - Missense 9:101544868-101544868 + TCGA-B5-A11G-01 COSM1103365 c.436_437insGA p.G149fs*42 Insertion - Frameshift 9:101540628-101540629 + TCGA-D5-6928-01 COSM1458986 c.313C>T p.R105C Substitution - Missense 9:101540505-101540505 + TCGA-BR-4201-01 COSM3902643 c.1199C>T p.A400V Substitution - Missense 9:101550712-101550712 + PR-3023 COSM247070 c.2444A>G p.N815S Substitution - Missense 9:101560862-101560862 + 587220 COSM1223955 c.130-1G>A p.? Unknown 9:101540202-101540202 + TCGA-MY-A5BD-01 COSM3925800 c.1144C>T p.R382C Substitution - Missense 9:101550657-101550657 + LUAD-RT-S01702 COSM379488 c.2260C>T p.R754W Substitution - Missense 9:101557474-101557474 + TCGA-B5-A11E-01 COSM1103364 c.361C>A p.L121I Substitution - Missense 9:101540553-101540553 + TCGA-C8-A12Q-01 COSM455063 c.2563C>G p.Q855E Substitution - Missense 9:101561144-101561144 + TCGA-D1-A160-01 COSM1103371 c.1541G>A p.R514H Substitution - Missense 9:101552393-101552393 + TCGA-EJ-5515-01 COSM1132647 c.1500A>T p.K500N Substitution - Missense 9:101552232-101552232 + TCGA-P4-A5EB-01 COSM3996208 c.183G>C p.M61I Substitution - Missense 9:101540256-101540256 + SA106 COSM213799 c.41G>T p.G14V Substitution - Missense 9:101535464-101535464 + TCGA-DK-A1AB-01 COSM422016 c.1089G>A p.L363L Substitution - coding silent 9:101547515-101547515 + Patient_4 COSM5414430 c.1014G>C p.L338F Substitution - Missense 9:101547440-101547440 + TCGA-AP-A051-01 COSM1103369 c.1429C>T p.R477C Substitution - Missense 9:101552161-101552161 + TCGA-AA-A01I-01 COSM299893 c.1711C>T p.R571* Substitution - Nonsense 9:101552563-101552563 + CCK81 COSM3167292 c.2861A>G p.Q954R Substitution - Missense 9:101562355-101562355 + HCT8 COSM3167268 c.1321C>A p.L441I Substitution - Missense 9:101551732-101551732 + TCGA-AP-A051-01 COSM1103374 c.2335G>T p.E779* Substitution - Nonsense 9:101557549-101557549 + 587222 COSM1103373 c.2067G>T p.K689N Substitution - Missense 9:101554741-101554741 + TCGA-39-5016-01 COSM752263 c.87G>A p.G29G Substitution - coding silent 9:101535510-101535510 + HCT15 COSM1674680 c.2488T>G p.L830V Substitution - Missense 9:101560906-101560906 + TCGA-EE-A29E-06 COSM3652391 c.2908C>T p.H970Y Substitution - Missense 9:101562402-101562402 + SNUH_G22_S1 COSM3982641 c.541T>C p.S181P Substitution - Missense 9:101540888-101540888 + TCGA-AX-A0J1-01 COSM1103366 c.682G>A p.E228K Substitution - Missense 9:101544820-101544820 + RK307_C01 COSM3703465 c.2762C>A p.T921N Substitution - Missense 9:101562256-101562256 + 6115219 COSM5557934 c.915G>A p.K305K Substitution - coding silent 9:101547157-101547157 + HCT-15 COSM1674680 c.2488T>G p.L830V Substitution - Missense 9:101560906-101560906 + PT23_2 COSM5410056 c.844C>T p.R282* Substitution - Nonsense 9:101546916-101546916 + P04-1243 COSM247069 c.1246C>A p.H416N Substitution - Missense 9:101550759-101550759 + TCGA-A3-3316-01 COSM1496924 c.1564T>C p.S522P Substitution - Missense 9:101552416-101552416 + pfg016T COSM1643687 c.1901+5G>T p.? Unknown 9:101552758-101552758 + TCGA-60-2710-01 COSM752259 c.1943A>T p.D648V Substitution - Missense 9:101554029-101554029 + TCGA-23-1117-01 COSM76263 c.1094T>G p.V365G Substitution - Missense 9:101550607-101550607 + TCGA-FC-7961-01 COSM486841 c.1102C>T p.R368W Substitution - Missense 9:101550615-101550615 + TCGA-EE-A2A6-06 COSM3652390 c.2382+1G>A p.? Unknown 9:101557597-101557597 + PT40 COSM5923862 c.629-5C>T p.? Unknown 9:101544762-101544762 + 8067203 COSM3786075 c.1544G>A p.S515N Substitution - Missense 9:101552396-101552396 + LOVO COSM3167290 c.2752G>C p.A918P Substitution - Missense 9:101562246-101562246 + 2492721 COSM5721367 c.1619C>T p.S540F Substitution - Missense 9:101552471-101552471 + CHC2200T COSM4953015 c.2535T>C p.D845D Substitution - coding silent 9:101561116-101561116 + HCC2998 COSM3167282 c.2027A>C p.D676A Substitution - Missense 9:101554701-101554701 + EGC15 COSM3167259 c.787C>T p.R263* Substitution - Nonsense 9:101546859-101546859 + Pat_70_A COSM3925799 c.217C>T p.R73C Substitution - Missense 9:101540290-101540290 + TCGA-AX-A0J1-01 COSM1103368 c.1198G>A p.A400T Substitution - Missense 9:101550711-101550711 + TCGA-AP-A0LM-01 COSM1103376 c.2743G>T p.D915Y Substitution - Missense 9:101562003-101562003 + TCGA-BH-A0DZ-01 COSM455061 c.1291C>T p.H431Y Substitution - Missense 9:101551702-101551702 + TCGA-AP-A051-01 COSM1103378 c.2820C>A p.V940V Substitution - coding silent 9:101562314-101562314 + SC_9092 COSM5564751 c.529C>T p.R177C Substitution - Missense 9:101540876-101540876 + LP6005500-DNA_E03 COSM5034671 c.301G>T p.D101Y Substitution - Missense 9:101540493-101540493 + HCC063T COSM5812650 c.628+4A>T p.? Unknown 9:101540979-101540979 + TCGA-D9-A6EC-06 COSM4402015 c.886C>T p.L296L Substitution - coding silent 9:101546958-101546958 + YUKAT COSM5410058 c.2074A>G p.N692D Substitution - Missense 9:101554748-101554748 + TCGA-BR-8680-01 COSM3902644 c.2047G>A p.D683N Substitution - Missense 9:101554721-101554721 + S00938 COSM5663533 c.1015G>T p.A339S Substitution - Missense 9:101547441-101547441 + CHC798T COSM4958241 c.1480G>A p.V494I Substitution - Missense 9:101552212-101552212 + NCI-H1770 COSM23467 c.900T>C p.N300N Substitution - coding silent 9:101547142-101547142 + TCGA-AA-3685-01 COSM268195 c.1705C>T p.R569* Substitution - Nonsense 9:101552557-101552557 + 2492722 COSM5721367 c.1619C>T p.S540F Substitution - Missense 9:101552471-101552471 + 587228 COSM1223957 c.2243G>A p.R748H Substitution - Missense 9:101557457-101557457 + LUAD-S01315 COSM346075 c.860G>A p.R287Q Substitution - Missense 9:101546932-101546932 + TCGA-B5-A0JY-01 COSM1103370 c.1487G>T p.R496I Substitution - Missense 9:101552219-101552219 + HCC2998 COSM3167291 c.2786A>C p.K929T Substitution - Missense 9:101562280-101562280 + PD1582a COSM28424 c.1136C>T p.P379L Substitution - Missense 9:101550649-101550649 + ESO-859 COSM1240078 c.2726T>C p.L909P Substitution - Missense 9:101561986-101561986 + TCGA-BR-4184-01 COSM3902640 c.200C>T p.A67V Substitution - Missense 9:101540273-101540273 + TCGA-BR-6452-01 COSM3902642 c.1179T>C p.N393N Substitution - coding silent 9:101550692-101550692 + TCGA-BR-4368-01 COSM3902647 c.2864G>A p.R955H Substitution - Missense 9:101562358-101562358 + TCGA-G3-A25Y-01 COSM4917774 c.1896A>T p.E632D Substitution - Missense 9:101552748-101552748 + PDA_105 COSM5003765 c.31delG p.G11fs*27 Deletion - Frameshift 9:101535454-101535454 + TCGA-BG-A0MQ-01 COSM1103367 c.1101G>A p.L367L Substitution - coding silent 9:101550614-101550614 + 8035693 COSM3395480 c.1667A>T p.D556V Substitution - Missense 9:101552519-101552519 + S00944 COSM314851 c.1441A>T p.S481C Substitution - Missense 9:101552173-101552173 + ME044T COSM229130 c.2741A>G p.K914R Substitution - Missense 9:101562001-101562001 + TCGA-22-5491-01 COSM752261 c.947G>A p.G316D Substitution - Missense 9:101547189-101547189 + TCGA-FW-A3R5-06 COSM3925800 c.1144C>T p.R382C Substitution - Missense 9:101550657-101550657 + TCGA-AU-6004-01 COSM1458991 c.2019+2T>C p.? Unknown 9:101554107-101554107 + HCT15 COSM3167268 c.1321C>A p.L441I Substitution - Missense 9:101551732-101551732 + 47 COSM5012053 c.1049G>T p.R350L Substitution - Missense 9:101547475-101547475 + 587228 COSM1223956 c.946G>A p.G316S Substitution - Missense 9:101547188-101547188 + 46M COSM5588829 c.1712G>A p.R571Q Substitution - Missense 9:101552564-101552564 + TCGA-EE-A29M-06 COSM3652386 c.363C>T p.L121L Substitution - coding silent 9:101540555-101540555 + 1428_T COSM3952134 c.478G>A p.A160T Substitution - Missense 9:101540825-101540825 + TCGA-20-1683-01 COSM1330836 c.1072A>C p.T358P Substitution - Missense 9:101547498-101547498 + Gp5D COSM3167261 c.833T>C p.I278T Substitution - Missense 9:101546905-101546905 + LC_S3 COSM1190813 c.1024_1032delCGTCTCTGT p.R342_C344delRLC Deletion - In frame 9:101547450-101547458 + 695T COSM5825036 c.2020-9C>T p.? Unknown 9:101554685-101554685 + TCGA-85-6561-01 COSM752260 c.967C>A p.R323R Substitution - coding silent 9:101547209-101547209 + TCGA-A8-A09I-01 COSM455060 c.1270G>A p.E424K Substitution - Missense 9:101550783-101550783 + TCGA-AN-A04C-01 COSM455062 c.1540C>T p.R514C Substitution - Missense 9:101552392-101552392 + QC2-20-T2 COSM5652825 c.194G>A p.R65Q Substitution - Missense 9:101540267-101540267 + TCGA-AY-6197-01 COSM1458994 c.2846G>A p.R949H Substitution - Missense 9:101562340-101562340 + CHC205T COSM4407135 c.921T>C p.Y307Y Substitution - coding silent 9:101547163-101547163 + CHC2200T COSM4953015 c.2535T>C p.D845D Substitution - coding silent 9:101561116-101561116 + TCGA-CM-6162-01 COSM1195579 c.487G>A p.A163T Substitution - Missense 9:101540834-101540834 + BN04 COSM3663981 c.2651A>T p.E884V Substitution - Missense 9:101561911-101561911 + TCGA-EI-6917-01 COSM3432718 c.1645G>A p.A549T Substitution - Missense 9:101552497-101552497 + 2292385 COSM4610554 c.2504G>A p.R835H Substitution - Missense 9:101560922-101560922 + TCGA-FP-A4BE-01 COSM3902639 c.192G>A p.Q64Q Substitution - coding silent 9:101540265-101540265 + T2269 COSM4722079 c.2788A>C p.K930Q Substitution - Missense 9:101562282-101562282 + Gp2D COSM3167261 c.833T>C p.I278T Substitution - Missense 9:101546905-101546905 + CHC2098T COSM4788337 c.1320G>T p.Q440H Substitution - Missense 9:101551731-101551731 + BD135T COSM5516491 c.1668T>C p.D556D Substitution - coding silent 9:101552520-101552520 + TCGA-24-2267-01 COSM80461 c.645G>A p.E215E Substitution - coding silent 9:101544783-101544783 + PT52 COSM5939964 c.1333T>A p.L445M Substitution - Missense 9:101551744-101551744 + ESO-887 COSM1264372 c.611G>A p.R204Q Substitution - Missense 9:101540958-101540958 + TCGA-23-2079-01 COSM72458 c.2445C>A p.N815K Substitution - Missense 9:101560863-101560863 + YUPAER COSM5410056 c.844C>T p.R282* Substitution - Nonsense 9:101546916-101546916 + TCGA-BR-A4J4-01 COSM3902645 c.2157C>A p.A719A Substitution - coding silent 9:101554831-101554831 + TCGA-CJ-4641-01 COSM1137925 c.924A>G p.G308G Substitution - coding silent 9:101547166-101547166 + TCGA-43-6143-01 COSM752256 c.2688A>G p.T896T Substitution - coding silent 9:101561948-101561948 + TCGA-BT-A20W-01 COSM422015 c.1563G>A p.Q521Q Substitution - coding silent 9:101552415-101552415 + Pat_70_B COSM3925799 c.217C>T p.R73C Substitution - Missense 9:101540290-101540290 + TCGA-BH-A0BR-01 COSM455059 c.243A>C p.R81R Substitution - coding silent 9:101540316-101540316 + TCGA-EE-A184-06 COSM3652389 c.1855C>T p.R619W Substitution - Missense 9:101552707-101552707 + 8064580 COSM4389016 c.1739G>A p.R580Q Substitution - Missense 9:101552591-101552591 + 12T COSM109508 c.2770T>G p.C924G Substitution - Missense 9:101562264-101562264 + ccRCC-49 COSM1663942 c.1454A>G p.N485S Substitution - Missense 9:101552186-101552186 + TCGA-E9-A243-01 COSM1489526 c.1880A>G p.K627R Substitution - Missense 9:101552732-101552732 + TCGA-AD-6964-01 COSM1458993 c.2503C>T p.R835C Substitution - Missense 9:101560921-101560921 + TCGA-E6-A1LZ-01 COSM1103374 c.2335G>T p.E779* Substitution - Nonsense 9:101557549-101557549 + TCGA-AP-A051-01 COSM1103375 c.2649G>T p.Q883H Substitution - Missense 9:101561230-101561230 + TCGA-EI-6917-01 COSM3432719 c.2389G>A p.A797T Substitution - Missense 9:101560807-101560807 + 2492729 COSM5729905 c.1761G>A p.E587E Substitution - coding silent 9:101552613-101552613 + SH-0622 COSM5017512 c.2752-2delA p.? Unknown 9:101562244-101562244 + 134430 COSM326380 c.1534C>T p.R512C Substitution - Missense 9:101552386-101552386 + TCGA-13-0893-01 COSM76264 c.1281G>C p.E427D Substitution - Missense 9:101551692-101551692 + HCC104T COSM5808261 c.640G>A p.V214M Substitution - Missense 9:101544778-101544778 + TCGA-F5-6814-01 COSM3432717 c.242G>A p.R81Q Substitution - Missense 9:101540315-101540315 + TCGA-EE-A29D-06 COSM3652387 c.609C>T p.S203S Substitution - coding silent 9:101540956-101540956 + MO_1336 COSM5566758 c.217C>G p.R73G Substitution - Missense 9:101540290-101540290 + TCGA-AA-3680-01 COSM268019 c.1103G>A p.R368Q Substitution - Missense 9:101550616-101550616 + HCC018T COSM314851 c.1441A>T p.S481C Substitution - Missense 9:101552173-101552173 + ccRCC-106 COSM1663941 c.476T>C p.L159P Substitution - Missense 9:101540823-101540823 + TCGA-BS-A0UV-01 COSM1103372 c.1833G>T p.E611D Substitution - Missense 9:101552685-101552685 + TCGA-BP-5170-01 COSM486841 c.1102C>T p.R368W Substitution - Missense 9:101550615-101550615 + TCGA-29-1710-01 COSM1330837 c.241C>T p.R81* Substitution - Nonsense 9:101540314-101540314 + YULAD COSM5410057 c.1829A>T p.K610I Substitution - Missense 9:101552681-101552681 + TCGA-AA-A010-01 COSM284626 c.748-3T>C p.? Unknown 9:101546817-101546817 + H1155 COSM1195579 c.487G>A p.A163T Substitution - Missense 9:101540834-101540834 + 3N23-VS-3T23 COSM4979643 c.2194A>G p.M732V Substitution - Missense 9:101557408-101557408 + T2932 COSM4722078 c.1578T>C p.T526T Substitution - coding silent 9:101552430-101552430 + 2492720 COSM5721367 c.1619C>T p.S540F Substitution - Missense 9:101552471-101552471 + TCGA-D1-A17M-01 COSM268195 c.1705C>T p.R569* Substitution - Nonsense 9:101552557-101552557 + H1155 COSM1196199 c.85G>A p.G29R Substitution - Missense 9:101535508-101535508 + XHDG20 COSM4768842 c.1531-1G>T p.? Unknown 9:101552382-101552382 + CSCC-18-T COSM4495765 c.460C>A p.P154T Substitution - Missense 9:101540807-101540807 + TCGA-A6-6781-01 COSM268019 c.1103G>A p.R368Q Substitution - Missense 9:101550616-101550616 + PD6355a COSM1637037 c.2353G>C p.A785P Substitution - Missense 9:101557567-101557567 + YUPAT COSM1701433 c.718C>T p.Q240* Substitution - Nonsense 9:101544856-101544856 + TCGA-B0-5099-01 COSM486842 c.1992G>T p.M664I Substitution - Missense 9:101554078-101554078 + Pat_01_B COSM5875253 c.437G>A p.R146Q Substitution - Missense 9:101540629-101540629 + TCGA-CJ-4641-01 COSM1137926 c.2610T>C p.V870V Substitution - coding silent 9:101561191-101561191 + CHC798T COSM4958241 c.1480G>A p.V494I Substitution - Missense 9:101552212-101552212 + QC2-22-T2 COSM3167259 c.787C>T p.R263* Substitution - Nonsense 9:101546859-101546859 + TCGA-D8-A1XQ-01 COSM3835326 c.1582G>T p.D528Y Substitution - Missense 9:101552434-101552434 + HCC1954 COSM23475 c.2651A>G p.E884G Substitution - Missense 9:101561911-101561911 + Ad1 COSM1553824 c.2114G>A p.R705Q Substitution - Missense 9:101554788-101554788 + TCGA-BS-A0UV-01 COSM1103377 c.2787A>C p.K929N Substitution - Missense 9:101562281-101562281 + tumor_4147081 COSM5949133 c.183G>T p.M61I Substitution - Missense 9:101540256-101540256 + TCGA-EE-A2MJ-06 COSM3652388 c.1164C>T p.F388F Substitution - coding silent 9:101550677-101550677 + TCGA-BS-A0UF-01 COSM1103363 c.161A>C p.K54T Substitution - Missense 9:101540234-101540234 + pfg121T COSM1330837 c.241C>T p.R81* Substitution - Nonsense 9:101540314-101540314 + TCGA-K7-A5RF-01 COSM4909458 c.563T>C p.I188T Substitution - Missense 9:101540910-101540910 + DLD1 COSM3167268 c.1321C>A p.L441I Substitution - Missense 9:101551732-101551732 + SNU-C2B COSM379488 c.2260C>T p.R754W Substitution - Missense 9:101557474-101557474 + TCGA-FW-A3R5-06 COSM3925799 c.217C>T p.R73C Substitution - Missense 9:101540290-101540290 + C086 COSM5538294 c.542C>G p.S181C Substitution - Missense 9:101540889-101540889 + 261T COSM1727076 c.658G>T p.E220* Substitution - Nonsense 9:101544796-101544796 + 15145 COSM752259 c.1943A>T p.D648V Substitution - Missense 9:101554029-101554029 + TCGA-BR-8487-01 COSM3902641 c.822G>A p.L274L Substitution - coding silent 9:101546894-101546894 + J9_T COSM3952132 c.382G>A p.V128I Substitution - Missense 9:101540574-101540574 + 2218463 COSM4421291 c.1957G>T p.A653S Substitution - Missense 9:101554043-101554043 + TCGA-BS-A0UA-01 COSM1103374 c.2335G>T p.E779* Substitution - Nonsense 9:101557549-101557549 + CHC2098T COSM4788337 c.1320G>T p.Q440H Substitution - Missense 9:101551731-101551731 + TCGA-A3-3385-01 COSM486843 c.2854A>C p.T952P Substitution - Missense 9:101562348-101562348 + HN_63081 COSM128653 c.1649delC p.S550fs*1 Deletion - Frameshift 9:101552501-101552501 + SC_9109 COSM5551818 c.628G>A p.D210N Substitution - Missense 9:101540975-101540975 + C0011T COSM4422704 c.746A>C p.E249A Substitution - Missense 9:101544884-101544884 + PT34 COSM5910659 c.1526A>G p.N509S Substitution - Missense 9:101552258-101552258 + BN04T COSM3663981 c.2651A>T p.E884V Substitution - Missense 9:101561911-101561911 + 2492723 COSM5721367 c.1619C>T p.S540F Substitution - Missense 9:101552471-101552471 + 1848_T COSM3952135 c.1504A>G p.R502G Substitution - Missense 9:101552236-101552236 + KM12 COSM3167266 c.1251G>A p.Q417Q Substitution - coding silent 9:101550764-101550764 + TCGA-AX-A05Z-01 COSM1103373 c.2067G>T p.K689N Substitution - Missense 9:101554741-101554741 + 587284 COSM1223958 c.1627T>G p.L543V Substitution - Missense 9:101552479-101552479 + TCGA-GF-A3OT-06 COSM3652385 c.91A>G p.T31A Substitution - Missense 9:101535514-101535514 + TCGA-37-4133-01 COSM752257 c.2659T>C p.S887P Substitution - Missense 9:101561919-101561919 + C658 COSM4443605 c.614A>C p.K205T Substitution - Missense 9:101540961-101540961 + pfg124T COSM4765370 c.217_218insC p.R73fs*2 Insertion - Frameshift 9:101540290-101540291 + TCGA-A6-6780-01 COSM1458987 c.859C>T p.R287* Substitution - Nonsense 9:101546931-101546931 + S00944 COSM314851 c.1441A>T p.S481C Substitution - Missense 9:101552173-101552173 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.729082;Hs.729085 9q22 607699

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C Missense p.T952P c.2854A>C 9 104324630 RCCC A C Synonymous p.R81R c.243A>C 9 104302598 BRCA A G 3-UTRSNV . c.2925+631A>G 9 104325332 HC A G Missense p.K627R c.1880A>G 9 104315014 BRCA A G Missense p.K914R c.2741A>G 9 104324283 CM A G Synonymous p.T896T c.2688A>G 9 104324230 LUSC A T Missense p.D648V c.1943A>T 9 104316311 LUSC A T Missense p.D648V c.1943A>T 9 104316311 NSCLC A T Missense p.K500N c.1500A>T 9 104314514 PRAD A T Missense p.S481C c.1441A>T 9 104314455 SCLC C A Missense p.N815K c.2445C>A 9 104323145 OV C A Missense p.P529Q c.1586C>A 9 104314720 CM C A Missense p.P529Q c.1586C>A 9 104314720 LUAD C A Missense p.R953S c.2857C>A 9 104324633 LUAD C A Synonymous p.P903P c.2709C>A 9 104324251 STAD C A Synonymous p.R323R c.967C>A 9 104309491 LUSC C G Missense p.L508V c.1522C>G 9 104314536 HNSC C G Missense p.Q855E c.2563C>G 9 104323426 BRCA C T Missense p.A400V c.1199C>T 9 104312994 STAD C T Missense p.L159F c.475C>T 9 104303104 CM C T Missense p.R512C c.1534C>T 9 104314668 SCLC C T Missense p.R514C c.1540C>T 9 104314674 BRCA C T Missense p.R619W c.1855C>T 9 104314989 CM C T Missense p.S203F c.608C>T 9 104303237 CM C T Missense p.S524F c.1571C>T 9 104314705 CM C T Missense p.T259I c.776C>T 9 104309130 LUAD C T Nonsense p.Q173* c.517C>T 9 104303146 MM C T Nonsense p.Q794* c.2380C>T 9 104319876 HNSC C T Nonsense p.R569* c.1705C>T 9 104314839 COREAD C T Nonsense p.R569* c.1705C>T 9 104314839 UCEC C T Nonsense p.R571* c.1711C>T 9 104314845 COREAD C T Synonymous p.F388F c.1164C>T 9 104312959 CM C T Synonymous p.F879F c.2637C>T 9 104323500 CM C T Synonymous p.L121L c.363C>T 9 104302837 CM C T Synonymous p.L479L c.1437C>T 9 104314451 CM C T Synonymous p.L520L c.1558C>T 9 104314692 LUAD - GA Frameshift p.E147Kfs*44 c.437_438insGA 9 104302911 UCEC G A Missense p.D906N c.2716G>A 9 104324258 STAD G A Missense p.E424K c.1270G>A 9 104313065 BRCA G A Missense p.G316D c.947G>A 9 104309471 LUSC G A Missense p.R204Q c.611G>A 9 104303240 ESCA G A Missense p.R368Q c.1103G>A 9 104312898 COREAD G A Missense p.R514H c.1541G>A 9 104314675 UCEC G A Missense p.R955H c.2864G>A 9 104324640 STAD G A SpliceDonorSNV . c.2382+1G>A 9 104319879 CM G A Synonymous p.A534A c.1602G>A 9 104314736 LUAD G A Synonymous p.E215E c.645G>A 9 104307065 OV G A Synonymous p.E766E c.2298G>A 9 104319794 HNSC G A Synonymous p.G29G c.87G>A 9 104297792 LUSC G A Synonymous p.L363L c.1089G>A 9 104309797 BLCA G A Synonymous p.L367L c.1101G>A 9 104312896 UCEC G A Synonymous p.Q521Q c.1563G>A 9 104314697 BLCA G A Synonymous p.Q715Q c.2145G>A 9 104317101 LUSC G C Missense p.E427D c.1281G>C 9 104313974 OV G C Missense p.E783Q c.2347G>C 9 104319843 LUAD G C Missense p.R881P c.2642G>C 9 104323505 LUAD G C SpliceDonorSNV . c.628+1G>C 9 104303258 LUAD G T IntronicSNV . c.1901+5G>T 9 104315040 STAD G T Missense p.A738S c.2212G>T 9 104319708 LUAD G T Missense p.G14V c.41G>T 9 104297746 BRCA G T Missense p.K769N c.2307G>T 9 104319803 LUAD G T Missense p.M664I c.1992G>T 9 104316360 RCCC G T Nonsense p.E294* c.880G>T 9 104309234 COREAD G T Nonsense p.E779* c.2335G>T 9 104319831 UCEC G T Synonymous p.L79L c.237G>T 9 104302592 STAD T C Missense p.L909P c.2726T>C 9 104324268 ESCA T C Missense p.S887P c.2659T>C 9 104324201 LUSC T G Missense p.V365G c.1094T>G 9 104312889 OV T - IntronicDeletion . c.446-17delT 9 104303052 STAD - T IntronicInsertion . c.2383-50dupT 9 104323026 HC