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 32541498 32541498 + Missense_Mutation SNP C C T TCGA-DK-A2I4-01A-11D-A21A-08 TCGA-DK-A2I4-10A-01D-A21A-08 g.chr9:32541498C>T c.3025G>A c.(3025-3027)Gag>Aag p.E1009K BLCA 9 32542506 32542506 + Missense_Mutation SNP G G T TCGA-DK-AA77-01A-11D-A391-08 TCGA-DK-AA77-10A-01D-A394-08 g.chr9:32542506G>T c.2017C>A c.(2017-2019)Cgt>Agt p.R673S BLCA 9 32542637 32542637 + Missense_Mutation SNP G G T TCGA-XF-A9T5-01A-11D-A42E-08 TCGA-XF-A9T5-10A-01D-A42H-08 g.chr9:32542637G>T c.1886C>A c.(1885-1887)tCc>tAc p.S629Y BLCA 9 32542984 32542984 + Silent SNP C C T TCGA-ZF-AA4V-01A-11D-A38G-08 TCGA-ZF-AA4V-10A-01D-A38J-08 g.chr9:32542984C>T c.1539G>A c.(1537-1539)gtG>gtA p.V513V BLCA 9 32543021 32543021 + Missense_Mutation SNP G G A TCGA-BT-A20J-01A-11D-A14W-08 TCGA-BT-A20J-11A-11D-A14W-08 g.chr9:32543021G>A c.1502C>T c.(1501-1503)tCt>tTt p.S501F BLCA 9 32543099 32543099 + Nonsense_Mutation SNP G G T TCGA-UY-A78K-01A-11D-A339-08 TCGA-UY-A78K-10A-01D-A339-08 g.chr9:32543099G>T c.1424C>A c.(1423-1425)tCa>tAa p.S475* BLCA 9 32543241 32543241 + Missense_Mutation SNP A A C TCGA-GD-A3OQ-01A-32D-A21Z-08 TCGA-GD-A3OQ-10A-01D-A21Z-08 g.chr9:32543241A>C c.1282T>G c.(1282-1284)Tca>Gca p.S428A BLCA 9 32544000 32544000 + Missense_Mutation SNP C C T TCGA-FD-A3B3-01A-12D-A202-08 TCGA-FD-A3B3-10A-01D-A202-08 g.chr9:32544000C>T c.523G>A c.(523-525)Gat>Aat p.D175N BLCA 9 32544067 32544067 + Silent SNP C C T TCGA-GV-A3QI-01A-11D-A21Z-08 TCGA-GV-A3QI-10A-01D-A21Z-08 g.chr9:32544067C>T c.456G>A c.(454-456)gtG>gtA p.V152V BLCA 9 32544192 32544192 + Missense_Mutation SNP C C G TCGA-BT-A20J-01A-11D-A14W-08 TCGA-BT-A20J-11A-11D-A14W-08 g.chr9:32544192C>G c.331G>C c.(331-333)Gat>Cat p.D111H BLCA 9 32544237 32544237 + Missense_Mutation SNP C C T TCGA-BL-A0C8-01A-11D-A10S-08 TCGA-BL-A0C8-10A-01D-A10S-08 g.chr9:32544237C>T c.286G>A c.(286-288)Gat>Aat p.D96N BLCA 9 32544239 32544239 + Missense_Mutation SNP G G A TCGA-BL-A0C8-01A-11D-A10S-08 TCGA-BL-A0C8-10A-01D-A10S-08 g.chr9:32544239G>A c.284C>T c.(283-285)gCt>gTt p.A95V BRCA 9 32541997 32541997 + Silent SNP G G T TCGA-BH-A0EB-01A-11W-A050-09 TCGA-BH-A0EB-10A-01W-A055-09 g.chr9:32541997G>T c.2526C>A c.(2524-2526)acC>acA p.T842T BRCA 9 32542676 32542676 + Missense_Mutation SNP C C T TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr9:32542676C>T c.1847G>A c.(1846-1848)aGa>aAa p.R616K BRCA 9 32543678 32543678 + Missense_Mutation SNP G G A TCGA-A8-A06Q-01A-11W-A050-09 TCGA-A8-A06Q-10A-01W-A055-09 g.chr9:32543678G>A c.845C>T c.(844-846)tCa>tTa p.S282L BRCA 9 32544087 32544087 + Missense_Mutation SNP C C G TCGA-AN-A0AJ-01A-11W-A019-09 TCGA-AN-A0AJ-10A-01W-A021-09 g.chr9:32544087C>G c.436G>C c.(436-438)Gat>Cat p.D146H CESC 9 32542047 32542047 + Nonsense_Mutation SNP G G A TCGA-EK-A2RC-01A-11D-A18J-09 TCGA-EK-A2RC-10A-01D-A18J-09 g.chr9:32542047G>A c.2476C>T c.(2476-2478)Caa>Taa p.Q826* CESC 9 32542367 32542367 + Missense_Mutation SNP G G A TCGA-Q1-A73O-01A-11D-A32I-09 TCGA-Q1-A73O-10B-01D-A32I-09 g.chr9:32542367G>A c.2156C>T c.(2155-2157)tCt>tTt p.S719F CESC 9 32542823 32542823 + Nonsense_Mutation SNP G G C TCGA-EK-A2RK-01A-11D-A18J-09 TCGA-EK-A2RK-10A-01D-A18J-09 g.chr9:32542823G>C c.1700C>G c.(1699-1701)tCa>tGa p.S567* COAD 9 32541757 32541757 + Silent SNP C C T TCGA-D5-6932-01A-11D-1924-10 TCGA-D5-6932-10A-01D-1924-10 g.chr9:32541757C>T c.2766G>A c.(2764-2766)gaG>gaA p.E922E COAD 9 32541758 32541758 + Missense_Mutation SNP T T C TCGA-G4-6307-01A-11D-1719-10 TCGA-G4-6307-10A-01D-1720-10 g.chr9:32541758T>C c.2765A>G c.(2764-2766)gAg>gGg p.E922G COAD 9 32542034 32542034 + Missense_Mutation SNP G G A TCGA-DM-A28F-01A-11D-A16V-10 TCGA-DM-A28F-10A-01D-A16V-10 g.chr9:32542034G>A c.2489C>T c.(2488-2490)tCa>tTa p.S830L COAD 9 32542035 32542035 + Missense_Mutation SNP A A G TCGA-AY-4071-01A-01W-1073-09 TCGA-AY-4071-10A-01W-1073-09 g.chr9:32542035A>G c.2488T>C c.(2488-2490)Tca>Cca p.S830P COAD 9 32542101 32542101 + Missense_Mutation SNP C C T TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr9:32542101C>T c.2422G>A c.(2422-2424)Gaa>Aaa p.E808K COAD 9 32542101 32542101 + Missense_Mutation SNP C C T TCGA-G4-6323-01A-11D-1719-10 TCGA-G4-6323-10A-01D-1720-10 g.chr9:32542101C>T c.2422G>A c.(2422-2424)Gaa>Aaa p.E808K COAD 9 32542177 32542177 + Silent SNP G G A TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr9:32542177G>A c.2346C>T c.(2344-2346)acC>acT p.T782T COAD 9 32542375 32542375 + Silent SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr9:32542375G>A c.2148C>T c.(2146-2148)taC>taT p.Y716Y COAD 9 32542463 32542463 + Missense_Mutation SNP C C A TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr9:32542463C>A c.2060G>T c.(2059-2061)aGa>aTa p.R687I COAD 9 32542995 32542995 + Missense_Mutation SNP T T C TCGA-AY-5543-01A-01D-1650-10 TCGA-AY-5543-10A-01D-1650-10 g.chr9:32542995T>C c.1528A>G c.(1528-1530)Atg>Gtg p.M510V COAD 9 32543159 32543159 + Missense_Mutation SNP G G A TCGA-AA-3966-01A-01W-1073-09 TCGA-AA-3966-10A-01W-1073-09 g.chr9:32543159G>A c.1364C>T c.(1363-1365)aCg>aTg p.T455M COAD 9 32543329 32543329 + Silent SNP C C T TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr9:32543329C>T c.1194G>A c.(1192-1194)gaG>gaA p.E398E COAD 9 32543408 32543408 + Missense_Mutation SNP G G A TCGA-AA-3815-01A-01W-0995-10 TCGA-AA-3815-10A-01W-0995-10 g.chr9:32543408G>A c.1115C>T c.(1114-1116)gCc>gTc p.A372V COAD 9 32543484 32543484 + Nonsense_Mutation SNP G G A TCGA-AA-A024-01A-02W-A00E-09 TCGA-AA-A024-10A-01W-A00E-09 g.chr9:32543484G>A c.1039C>T c.(1039-1041)Cga>Tga p.R347* COAD 9 32543744 32543744 + Missense_Mutation SNP C C T TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr9:32543744C>T c.779G>A c.(778-780)cGa>cAa p.R260Q COAD 9 32543969 32543969 + Missense_Mutation SNP G G A TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chr9:32543969G>A c.554C>T c.(553-555)aCa>aTa p.T185I COAD 9 32543970 32543970 + Missense_Mutation SNP T T C TCGA-CM-5862-01A-01D-1650-10 TCGA-CM-5862-10A-01D-1650-10 g.chr9:32543970T>C c.553A>G c.(553-555)Aca>Gca p.T185A COAD 9 32544014 32544014 + Missense_Mutation SNP G G T TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr9:32544014G>T c.509C>A c.(508-510)tCt>tAt p.S170Y COAD 9 32544122 32544122 + Frame_Shift_Del DEL T T - TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chr9:32544122delT c.401delA c.(400-402)aacfs p.N134fs COAD 9 32544139 32544139 + Silent SNP T T C TCGA-CK-5914-01A-11D-1650-10 TCGA-CK-5914-10A-01D-1650-10 g.chr9:32544139T>C c.384A>G c.(382-384)gtA>gtG p.V128V COAD 9 32544140 32544140 + Missense_Mutation SNP A A T TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chr9:32544140A>T c.383T>A c.(382-384)gTa>gAa p.V128E COAD 9 32544141 32544141 + Missense_Mutation SNP C C T TCGA-AY-5543-01A-01D-1650-10 TCGA-AY-5543-10A-01D-1650-10 g.chr9:32544141C>T c.382G>A c.(382-384)Gta>Ata p.V128I COADREAD 9 32541757 32541757 + Silent SNP C C T TCGA-D5-6932-01A-11D-1924-10 TCGA-D5-6932-10A-01D-1924-10 g.chr9:32541757C>T c.2766G>A c.(2764-2766)gaG>gaA p.E922E COADREAD 9 32541757 32541757 + Silent SNP C C T TCGA-DY-A1H8-01A-21D-A152-10 TCGA-DY-A1H8-10A-01D-A152-10 g.chr9:32541757C>T c.2766G>A c.(2764-2766)gaG>gaA p.E922E COADREAD 9 32541758 32541758 + Missense_Mutation SNP T T C TCGA-DC-5869-01A-01D-1657-10 TCGA-DC-5869-10A-01D-1657-10 g.chr9:32541758T>C c.2765A>G c.(2764-2766)gAg>gGg p.E922G COADREAD 9 32541758 32541758 + Missense_Mutation SNP T T C TCGA-G4-6307-01A-11D-1719-10 TCGA-G4-6307-10A-01D-1720-10 g.chr9:32541758T>C c.2765A>G c.(2764-2766)gAg>gGg p.E922G COADREAD 9 32542034 32542034 + Missense_Mutation SNP G G A TCGA-DM-A28F-01A-11D-A16V-10 TCGA-DM-A28F-10A-01D-A16V-10 g.chr9:32542034G>A c.2489C>T c.(2488-2490)tCa>tTa p.S830L COADREAD 9 32542035 32542035 + Missense_Mutation SNP A A G TCGA-AY-4071-01A-01W-1073-09 TCGA-AY-4071-10A-01W-1073-09 g.chr9:32542035A>G c.2488T>C c.(2488-2490)Tca>Cca p.S830P COADREAD 9 32542101 32542101 + Missense_Mutation SNP C C T TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr9:32542101C>T c.2422G>A c.(2422-2424)Gaa>Aaa p.E808K COADREAD 9 32542101 32542101 + Missense_Mutation SNP C C T TCGA-AF-6655-01A-11D-1826-10 TCGA-AF-6655-10A-01D-1826-10 g.chr9:32542101C>T c.2422G>A c.(2422-2424)Gaa>Aaa p.E808K COADREAD 9 32542101 32542101 + Missense_Mutation SNP C C T TCGA-G4-6323-01A-11D-1719-10 TCGA-G4-6323-10A-01D-1720-10 g.chr9:32542101C>T c.2422G>A c.(2422-2424)Gaa>Aaa p.E808K COADREAD 9 32542177 32542177 + Silent SNP G G A TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr9:32542177G>A c.2346C>T c.(2344-2346)acC>acT p.T782T COADREAD 9 32542375 32542375 + Silent SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr9:32542375G>A c.2148C>T c.(2146-2148)taC>taT p.Y716Y COADREAD 9 32542463 32542463 + Missense_Mutation SNP C C A TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr9:32542463C>A c.2060G>T c.(2059-2061)aGa>aTa p.R687I COADREAD 9 32542526 32542526 + Missense_Mutation SNP C C T TCGA-AG-3892-01A-01W-1073-09 TCGA-AG-3892-10A-01W-1073-09 g.chr9:32542526C>T c.1997G>A c.(1996-1998)aGc>aAc p.S666N COADREAD 9 32542594 32542594 + Missense_Mutation SNP T T G TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr9:32542594T>G c.1929A>C c.(1927-1929)aaA>aaC p.K643N COADREAD 9 32542995 32542995 + Missense_Mutation SNP T T C TCGA-AY-5543-01A-01D-1650-10 TCGA-AY-5543-10A-01D-1650-10 g.chr9:32542995T>C c.1528A>G c.(1528-1530)Atg>Gtg p.M510V COADREAD 9 32543159 32543159 + Missense_Mutation SNP G G A TCGA-AA-3966-01A-01W-1073-09 TCGA-AA-3966-10A-01W-1073-09 g.chr9:32543159G>A c.1364C>T c.(1363-1365)aCg>aTg p.T455M COADREAD 9 32543329 32543329 + Silent SNP C C T TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr9:32543329C>T c.1194G>A c.(1192-1194)gaG>gaA p.E398E COADREAD 9 32543404 32543404 + Missense_Mutation SNP A A C TCGA-AG-A014-01A-02W-A00K-09 TCGA-AG-A014-10A-01W-A00K-09 g.chr9:32543404A>C c.1119T>G c.(1117-1119)aaT>aaG p.N373K COADREAD 9 32543408 32543408 + Missense_Mutation SNP G G A TCGA-AA-3815-01A-01W-0995-10 TCGA-AA-3815-10A-01W-0995-10 g.chr9:32543408G>A c.1115C>T c.(1114-1116)gCc>gTc p.A372V COADREAD 9 32543427 32543427 + Missense_Mutation SNP C C A TCGA-EI-6507-01A-11D-1733-10 TCGA-EI-6507-10A-01D-1733-10 g.chr9:32543427C>A c.1096G>T c.(1096-1098)Gca>Tca p.A366S COADREAD 9 32543484 32543484 + Nonsense_Mutation SNP G G A TCGA-AA-A024-01A-02W-A00E-09 TCGA-AA-A024-10A-01W-A00E-09 g.chr9:32543484G>A c.1039C>T c.(1039-1041)Cga>Tga p.R347* COADREAD 9 32543744 32543744 + Missense_Mutation SNP C C T TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr9:32543744C>T c.779G>A c.(778-780)cGa>cAa p.R260Q COADREAD 9 32543969 32543969 + Missense_Mutation SNP G G A TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chr9:32543969G>A c.554C>T c.(553-555)aCa>aTa p.T185I COADREAD 9 32543970 32543970 + Missense_Mutation SNP T T C TCGA-AG-3732-01A-11D-1657-10 TCGA-AG-3732-11A-01D-1657-10 g.chr9:32543970T>C c.553A>G c.(553-555)Aca>Gca p.T185A COADREAD 9 32543970 32543970 + Missense_Mutation SNP T T C TCGA-CM-5862-01A-01D-1650-10 TCGA-CM-5862-10A-01D-1650-10 g.chr9:32543970T>C c.553A>G c.(553-555)Aca>Gca p.T185A COADREAD 9 32543970 32543970 + Missense_Mutation SNP T T C TCGA-G5-6235-01A-11D-1733-10 TCGA-G5-6235-10A-01D-1733-10 g.chr9:32543970T>C c.553A>G c.(553-555)Aca>Gca p.T185A COADREAD 9 32544014 32544014 + Missense_Mutation SNP G G T TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr9:32544014G>T c.509C>A c.(508-510)tCt>tAt p.S170Y COADREAD 9 32544122 32544122 + Frame_Shift_Del DEL T T - TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chr9:32544122delT c.401delA c.(400-402)aacfs p.N134fs COADREAD 9 32544139 32544139 + Silent SNP T T C TCGA-CK-5914-01A-11D-1650-10 TCGA-CK-5914-10A-01D-1650-10 g.chr9:32544139T>C c.384A>G c.(382-384)gtA>gtG p.V128V COADREAD 9 32544140 32544140 + Missense_Mutation SNP A A T TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chr9:32544140A>T c.383T>A c.(382-384)gTa>gAa p.V128E COADREAD 9 32544141 32544141 + Missense_Mutation SNP C C T TCGA-AY-5543-01A-01D-1650-10 TCGA-AY-5543-10A-01D-1650-10 g.chr9:32544141C>T c.382G>A c.(382-384)Gta>Ata p.V128I DLBC 9 32542793 32542793 + Missense_Mutation SNP G G T TCGA-G8-6914-01A-11D-2210-10 TCGA-G8-6914-14A-01D-2210-10 g.chr9:32542793G>T c.1730C>A c.(1729-1731)tCt>tAt p.S577Y DLBC 9 32543801 32543801 + Missense_Mutation SNP G G A TCGA-G8-6914-01A-11D-2210-10 TCGA-G8-6914-14A-01D-2210-10 g.chr9:32543801G>A c.722C>T c.(721-723)aCg>aTg p.T241M ESCA 9 32543529 32543529 + Missense_Mutation SNP C C T TCGA-L5-A4OW-01A-11D-A28B-09 TCGA-L5-A4OW-11A-11D-A28E-09 g.chr9:32543529C>T c.994G>A c.(994-996)Gag>Aag p.E332K ESCA 9 32543771 32543771 + Missense_Mutation SNP T T A TCGA-VR-AA4G-01A-11D-A37C-09 TCGA-VR-AA4G-10A-01D-A37F-09 g.chr9:32543771T>A c.752A>T c.(751-753)cAa>cTa p.Q251L GBM 9 32543467 32543467 + Missense_Mutation SNP T T C TCGA-26-6174-01A-21D-1845-08 TCGA-26-6174-10A-01D-1845-08 g.chr9:32543467T>C c.1056A>G c.(1054-1056)atA>atG p.I352M GBMLGG 9 32541485 32541485 + Missense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr9:32541485C>A c.3038G>T c.(3037-3039)aGt>aTt p.S1013I GBMLGG 9 32542146 32542146 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr9:32542146C>T c.2377G>A c.(2377-2379)Gga>Aga p.G793R GBMLGG 9 32543467 32543467 + Missense_Mutation SNP T T C TCGA-26-6174-01A-21D-1845-08 TCGA-26-6174-10A-01D-1845-08 g.chr9:32543467T>C c.1056A>G c.(1054-1056)atA>atG p.I352M HNSC 9 32541770 32541770 + Missense_Mutation SNP G G A TCGA-CR-6472-01A-11D-1870-08 TCGA-CR-6472-10A-01D-1870-08 g.chr9:32541770G>A c.2753C>T c.(2752-2754)tCt>tTt p.S918F HNSC 9 32542338 32542338 + Missense_Mutation SNP G G A TCGA-CR-6492-01A-12D-2078-08 TCGA-CR-6492-10A-01D-2078-08 g.chr9:32542338G>A c.2185C>T c.(2185-2187)Cat>Tat p.H729Y HNSC 9 32542340 32542340 + Missense_Mutation SNP G G C TCGA-UF-A71A-01A-22D-A34J-08 TCGA-UF-A71A-10A-01D-A34M-08 g.chr9:32542340G>C c.2183C>G c.(2182-2184)gCt>gGt p.A728G HNSC 9 32542374 32542374 + Missense_Mutation SNP C C T TCGA-BA-A6DL-01A-21D-A30E-08 TCGA-BA-A6DL-10A-01D-A30H-08 g.chr9:32542374C>T c.2149G>A c.(2149-2151)Gaa>Aaa p.E717K HNSC 9 32542604 32542604 + Missense_Mutation SNP C C T TCGA-CV-6961-01A-21D-1912-08 TCGA-CV-6961-10A-01D-1912-08 g.chr9:32542604C>T c.1919G>A c.(1918-1920)aGa>aAa p.R640K HNSC 9 32542610 32542610 + Missense_Mutation SNP C C G TCGA-HD-8635-01A-11D-2394-08 TCGA-HD-8635-10A-01D-2394-08 g.chr9:32542610C>G c.1913G>C c.(1912-1914)aGa>aCa p.R638T HNSC 9 32542793 32542793 + Missense_Mutation SNP G G T TCGA-QK-A6IJ-01A-11D-A31L-08 TCGA-QK-A6IJ-10A-01D-A31J-08 g.chr9:32542793G>T c.1730C>A c.(1729-1731)tCt>tAt p.S577Y HNSC 9 32543994 32543994 + Nonsense_Mutation SNP G G A TCGA-IQ-A61L-01A-11D-A30E-08 TCGA-IQ-A61L-10A-01D-A30H-08 g.chr9:32543994G>A c.529C>T c.(529-531)Cga>Tga p.R177* KIPAN 9 32541815 32541815 + Missense_Mutation SNP C C G TCGA-DZ-6133-01A-11D-1961-08 TCGA-DZ-6133-10A-01D-1962-08 g.chr9:32541815C>G c.2708G>C c.(2707-2709)cGt>cCt p.R903P KIPAN 9 32541932 32541932 + Missense_Mutation SNP C C T TCGA-PJ-A5Z9-01A-11D-A28G-10 TCGA-PJ-A5Z9-10A-01D-A28G-10 g.chr9:32541932C>T c.2591G>A c.(2590-2592)aGc>aAc p.S864N KIPAN 9 32542179 32542179 + Missense_Mutation SNP T T C TCGA-UZ-A9PN-01A-11D-A382-10 TCGA-UZ-A9PN-10A-01D-A385-10 g.chr9:32542179T>C c.2344A>G c.(2344-2346)Acc>Gcc p.T782A KIPAN 9 32543270 32543270 + Missense_Mutation SNP T T C TCGA-DZ-6135-01A-11D-1961-08 TCGA-DZ-6135-10A-01D-1962-08 g.chr9:32543270T>C c.1253A>G c.(1252-1254)gAt>gGt p.D418G KIPAN 9 32543675 32543675 + Missense_Mutation SNP G G A TCGA-B0-4818-01A-01D-1501-10 TCGA-B0-4818-11A-01D-1501-10 g.chr9:32543675G>A c.848C>T c.(847-849)gCt>gTt p.A283V KIRC 9 32543675 32543675 + Missense_Mutation SNP G G A TCGA-B0-4818-01A-01D-1501-10 TCGA-B0-4818-11A-01D-1501-10 g.chr9:32543675G>A c.848C>T c.(847-849)gCt>gTt p.A283V KIRP 9 32541815 32541815 + Missense_Mutation SNP C C G TCGA-DZ-6133-01A-11D-1961-08 TCGA-DZ-6133-10A-01D-1962-08 g.chr9:32541815C>G c.2708G>C c.(2707-2709)cGt>cCt p.R903P KIRP 9 32541932 32541932 + Missense_Mutation SNP C C T TCGA-PJ-A5Z9-01A-11D-A28G-10 TCGA-PJ-A5Z9-10A-01D-A28G-10 g.chr9:32541932C>T c.2591G>A c.(2590-2592)aGc>aAc p.S864N KIRP 9 32542179 32542179 + Missense_Mutation SNP T T C TCGA-UZ-A9PN-01A-11D-A382-10 TCGA-UZ-A9PN-10A-01D-A385-10 g.chr9:32542179T>C c.2344A>G c.(2344-2346)Acc>Gcc p.T782A KIRP 9 32543270 32543270 + Missense_Mutation SNP T T C TCGA-DZ-6135-01A-11D-1961-08 TCGA-DZ-6135-10A-01D-1962-08 g.chr9:32543270T>C c.1253A>G c.(1252-1254)gAt>gGt p.D418G LGG 9 32541485 32541485 + Missense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr9:32541485C>A c.3038G>T c.(3037-3039)aGt>aTt p.S1013I LGG 9 32542146 32542146 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr9:32542146C>T c.2377G>A c.(2377-2379)Gga>Aga p.G793R LIHC 9 32541494 32541494 + Missense_Mutation SNP T T C TCGA-ES-A2HT-01A-12D-A183-10 TCGA-ES-A2HT-11A-11D-A183-10 g.chr9:32541494T>C c.3029A>G c.(3028-3030)aAc>aGc p.N1010S LIHC 9 32543499 32543499 + Missense_Mutation SNP G G A TCGA-WQ-AB4B-01A-11D-A40P-10 TCGA-WQ-AB4B-10A-01D-A40P-10 g.chr9:32543499G>A c.1024C>T c.(1024-1026)Cca>Tca p.P342S LIHC 9 32543636 32543636 + Missense_Mutation SNP A A G TCGA-MI-A75C-01A-11D-A32G-10 TCGA-MI-A75C-10A-01D-A32G-10 g.chr9:32543636A>G c.887T>C c.(886-888)tTa>tCa p.L296S LIHC 9 32543942 32543942 + Nonsense_Mutation SNP G G C TCGA-DD-A73C-01A-12D-A33K-10 TCGA-DD-A73C-10A-01D-A33K-10 g.chr9:32543942G>C c.581C>G c.(580-582)tCa>tGa p.S194* LIHC 9 32544180 32544180 + Missense_Mutation SNP A A G TCGA-WQ-A9G7-01A-11D-A36X-10 TCGA-WQ-A9G7-10A-01D-A370-10 g.chr9:32544180A>G c.343T>C c.(343-345)Tac>Cac p.Y115H LIHC 9 32550784 32550784 + Silent SNP C C T TCGA-UB-A7MF-01A-11D-A33K-10 TCGA-UB-A7MF-10A-01D-A33K-10 g.chr9:32550784C>T c.186G>A c.(184-186)ccG>ccA p.P62P LUAD 9 32541401 32541401 + Missense_Mutation SNP T T C TCGA-97-7938-01A-11D-2167-08 TCGA-97-7938-10A-01D-2167-08 g.chr9:32541401T>C c.3122A>G c.(3121-3123)gAc>gGc p.D1041G LUAD 9 32541434 32541434 + Missense_Mutation SNP C C A TCGA-44-7659-01A-11D-2063-08 TCGA-44-7659-10A-01D-2063-08 g.chr9:32541434C>A c.3089G>T c.(3088-3090)cGg>cTg p.R1030L LUAD 9 32541658 32541658 + Missense_Mutation SNP T T C TCGA-44-3398-01A-01D-1105-08 TCGA-44-3398-10A-01D-1105-08 g.chr9:32541658T>C c.2865A>G c.(2863-2865)atA>atG p.I955M LUAD 9 32542019 32542019 + Missense_Mutation SNP T T C TCGA-95-7567-01A-11D-2063-08 TCGA-95-7567-10A-01D-2063-08 g.chr9:32542019T>C c.2504A>G c.(2503-2505)aAc>aGc p.N835S LUAD 9 32542380 32542380 + Missense_Mutation SNP C C A TCGA-17-Z045-01A-01W-0746-08 TCGA-17-Z045-11A-01W-0747-08 g.chr9:32542380C>A c.2143G>T c.(2143-2145)Ggg>Tgg p.G715W LUAD 9 32542600 32542600 + Missense_Mutation SNP T T A TCGA-86-7954-01A-11D-2184-08 TCGA-86-7954-10A-01D-2184-08 g.chr9:32542600T>A c.1923A>T c.(1921-1923)agA>agT p.R641S LUAD 9 32542697 32542697 + Missense_Mutation SNP C C A TCGA-55-6979-01A-11D-1945-08 TCGA-55-6979-11A-01D-1945-08 g.chr9:32542697C>A c.1826G>T c.(1825-1827)gGg>gTg p.G609V LUAD 9 32543115 32543115 + Missense_Mutation SNP C C G TCGA-49-4486-01A-01D-1265-08 TCGA-49-4486-11A-01D-1265-08 g.chr9:32543115C>G c.1408G>C c.(1408-1410)Gac>Cac p.D470H LUAD 9 32543811 32543811 + Missense_Mutation SNP T T A TCGA-38-4626-01A-01D-1553-08 TCGA-38-4626-11A-01D-1553-08 g.chr9:32543811T>A c.712A>T c.(712-714)Agg>Tgg p.R238W LUAD 9 32544225 32544225 + Missense_Mutation SNP C C T TCGA-78-8640-01A-11D-2393-08 TCGA-78-8640-11A-01D-2393-08 g.chr9:32544225C>T c.298G>A c.(298-300)Gat>Aat p.D100N LUAD 9 32544246 32544246 + Missense_Mutation SNP C C G TCGA-44-2656-01A-02D-0969-08 TCGA-44-2656-10A-01D-0969-08 g.chr9:32544246C>G c.277G>C c.(277-279)Gta>Cta p.V93L LUAD 9 32544314 32544314 + Missense_Mutation SNP G G A TCGA-NJ-A4YI-01A-11D-A25L-08 TCGA-NJ-A4YI-10A-01D-A25L-08 g.chr9:32544314G>A c.209C>T c.(208-210)tCa>tTa p.S70L LUAD 9 32550857 32550857 + Frame_Shift_Del DEL C C - TCGA-NJ-A4YF-01A-12D-A25L-08 TCGA-NJ-A4YF-10A-01D-A25L-08 g.chr9:32550857delC c.113delG c.(112-114)ggafs p.G38fs LUSC 9 32541488 32541488 + Missense_Mutation SNP G G A TCGA-37-4141-01A-02D-1352-08 TCGA-37-4141-10A-01D-1352-08 g.chr9:32541488G>A c.3035C>T c.(3034-3036)cCc>cTc p.P1012L LUSC 9 32541551 32541551 + Missense_Mutation SNP G G A TCGA-22-1012-01A-01D-1521-08 TCGA-22-1012-11A-01D-1521-08 g.chr9:32541551G>A c.2972C>T c.(2971-2973)tCa>tTa p.S991L LUSC 9 32541567 32541567 + Missense_Mutation SNP G G A TCGA-66-2795-01A-02D-0983-08 TCGA-66-2795-11A-01D-0983-08 g.chr9:32541567G>A c.2956C>T c.(2956-2958)Cca>Tca p.P986S LUSC 9 32542506 32542506 + Missense_Mutation SNP G G T TCGA-18-3406-01A-01D-0983-08 TCGA-18-3406-11A-01D-0983-08 g.chr9:32542506G>T c.2017C>A c.(2017-2019)Cgt>Agt p.R673S LUSC 9 32542684 32542684 + Missense_Mutation SNP C C A TCGA-39-5030-01A-01D-1441-08 TCGA-39-5030-11A-01D-1441-08 g.chr9:32542684C>A c.1839G>T c.(1837-1839)aaG>aaT p.K613N LUSC 9 32543158 32543158 + Silent SNP C C A TCGA-39-5031-01A-01D-1441-08 TCGA-39-5031-11A-01D-1441-08 g.chr9:32543158C>A c.1365G>T c.(1363-1365)acG>acT p.T455T LUSC 9 32543189 32543189 + Missense_Mutation SNP G G A TCGA-34-5928-01A-11D-1817-08 TCGA-34-5928-10A-01D-1817-08 g.chr9:32543189G>A c.1334C>T c.(1333-1335)tCa>tTa p.S445L LUSC 9 32543732 32543732 + Missense_Mutation SNP C C A TCGA-66-2793-01A-01D-1267-08 TCGA-66-2793-11A-01D-1267-08 g.chr9:32543732C>A c.791G>T c.(790-792)cGt>cTt p.R264L OV 9 32542101 32542101 + Nonsense_Mutation SNP C C A TCGA-25-1321-01A-01W-0492-08 TCGA-25-1321-10A-01W-0492-08 g.chr9:32542101C>A c.2422G>T c.(2422-2424)Gaa>Taa p.E808* OV 9 32543969 32543969 + Missense_Mutation SNP G G T TCGA-61-2008-01A-02W-0722-08 TCGA-61-2008-11A-01W-0722-08 g.chr9:32543969G>T c.554C>A c.(553-555)aCa>aAa p.T185K OV 9 32544141 32544141 + Missense_Mutation SNP C C T TCGA-13-0755-01A-01W-0372-09 TCGA-13-0755-10A-01W-0372-09 g.chr9:32544141C>T c.382G>A c.(382-384)Gta>Ata p.V128I PAAD 9 32541482 32541482 + Missense_Mutation SNP T T G TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr9:32541482T>G c.3041A>C c.(3040-3042)aAc>aCc p.N1014T PAAD 9 32542262 32542262 + Frame_Shift_Del DEL T T - TCGA-2L-AAQA-01A-21D-A38G-08 TCGA-2L-AAQA-11A-11D-A38J-08 g.chr9:32542262delT c.2261delA c.(2260-2262)aatfs p.N755fs PAAD 9 32542262 32542262 + Frame_Shift_Del DEL T T - TCGA-XN-A8T3-01A-11D-A36O-08 TCGA-XN-A8T3-10A-01D-A367-08 g.chr9:32542262delT c.2261delA c.(2260-2262)aatfs p.N755fs PAAD 9 32542990 32542990 + Silent SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr9:32542990C>T c.1533G>A c.(1531-1533)gaG>gaA p.E511E PAAD 9 32543588 32543588 + Missense_Mutation SNP C C A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr9:32543588C>A c.935G>T c.(934-936)gGa>gTa p.G312V PAAD 9 32544209 32544209 + Missense_Mutation SNP A A G TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr9:32544209A>G c.314T>C c.(313-315)aTa>aCa p.I105T PRAD 9 32541790 32541790 + Silent SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr9:32541790G>A c.2733C>T c.(2731-2733)gaC>gaT p.D911D PRAD 9 32541842 32541842 + Missense_Mutation SNP T T C TCGA-V1-A8MG-01A-11D-A364-08 TCGA-V1-A8MG-10A-01D-A362-08 g.chr9:32541842T>C c.2681A>G c.(2680-2682)aAg>aGg p.K894R PRAD 9 32542457 32542457 + Missense_Mutation SNP C C T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr9:32542457C>T c.2066G>A c.(2065-2067)cGt>cAt p.R689H PRAD 9 32543368 32543368 + Silent SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr9:32543368G>A c.1155C>T c.(1153-1155)agC>agT p.S385S PRAD 9 32543932 32543932 + Silent SNP A A C TCGA-EJ-7317-01A-31D-2114-08 TCGA-EJ-7317-10A-01D-2114-08 g.chr9:32543932A>C c.591T>G c.(589-591)ggT>ggG p.G197G PRAD 9 32544153 32544154 + Frame_Shift_Del DEL AG AG - TCGA-G9-6343-01A-21D-1961-08 TCGA-G9-6343-10A-01D-1961-08 g.chr9:32544153_32544154delAG c.369_370delCT c.(367-372)ttctgtfs p.FC123fs READ 9 32541757 32541757 + Silent SNP C C T TCGA-DY-A1H8-01A-21D-A152-10 TCGA-DY-A1H8-10A-01D-A152-10 g.chr9:32541757C>T c.2766G>A c.(2764-2766)gaG>gaA p.E922E READ 9 32541758 32541758 + Missense_Mutation SNP T T C TCGA-DC-5869-01A-01D-1657-10 TCGA-DC-5869-10A-01D-1657-10 g.chr9:32541758T>C c.2765A>G c.(2764-2766)gAg>gGg p.E922G READ 9 32542101 32542101 + Missense_Mutation SNP C C T TCGA-AF-6655-01A-11D-1826-10 TCGA-AF-6655-10A-01D-1826-10 g.chr9:32542101C>T c.2422G>A c.(2422-2424)Gaa>Aaa p.E808K READ 9 32542526 32542526 + Missense_Mutation SNP C C T TCGA-AG-3892-01A-01W-1073-09 TCGA-AG-3892-10A-01W-1073-09 g.chr9:32542526C>T c.1997G>A c.(1996-1998)aGc>aAc p.S666N READ 9 32542594 32542594 + Missense_Mutation SNP T T G TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr9:32542594T>G c.1929A>C c.(1927-1929)aaA>aaC p.K643N READ 9 32543404 32543404 + Missense_Mutation SNP A A C TCGA-AG-A014-01A-02W-A00K-09 TCGA-AG-A014-10A-01W-A00K-09 g.chr9:32543404A>C c.1119T>G c.(1117-1119)aaT>aaG p.N373K READ 9 32543427 32543427 + Missense_Mutation SNP C C A TCGA-EI-6507-01A-11D-1733-10 TCGA-EI-6507-10A-01D-1733-10 g.chr9:32543427C>A c.1096G>T c.(1096-1098)Gca>Tca p.A366S READ 9 32543970 32543970 + Missense_Mutation SNP T T C TCGA-AG-3732-01A-11D-1657-10 TCGA-AG-3732-11A-01D-1657-10 g.chr9:32543970T>C c.553A>G c.(553-555)Aca>Gca p.T185A READ 9 32543970 32543970 + Missense_Mutation SNP T T C TCGA-G5-6235-01A-11D-1733-10 TCGA-G5-6235-10A-01D-1733-10 g.chr9:32543970T>C c.553A>G c.(553-555)Aca>Gca p.T185A SKCM 9 32541428 32541428 + Missense_Mutation SNP G G A TCGA-GN-A266-06A-11D-A197-08 TCGA-GN-A266-10A-01D-A199-08 g.chr9:32541428G>A c.3095C>T c.(3094-3096)tCa>tTa p.S1032L SKCM 9 32541581 32541581 + Missense_Mutation SNP G G A TCGA-DA-A1IA-06A-11D-A196-08 TCGA-DA-A1IA-10A-01D-A198-08 g.chr9:32541581G>A c.2942C>T c.(2941-2943)aCt>aTt p.T981I SKCM 9 32542037 32542037 + Missense_Mutation SNP G G A TCGA-EE-A3JB-06A-11D-A21A-08 TCGA-EE-A3JB-10A-01D-A21A-08 g.chr9:32542037G>A c.2486C>T c.(2485-2487)tCa>tTa p.S829L SKCM 9 32543175 32543175 + Missense_Mutation SNP C C T TCGA-D3-A2JF-06A-11D-A196-08 TCGA-D3-A2JF-10A-01D-A198-08 g.chr9:32543175C>T c.1348G>A c.(1348-1350)Gtc>Atc p.V450I SKCM 9 32543665 32543665 + Silent SNP G G A TCGA-GN-A266-06A-11D-A197-08 TCGA-GN-A266-10A-01D-A199-08 g.chr9:32543665G>A c.858C>T c.(856-858)ttC>ttT p.F286F SKCM 9 32544245 32544245 + Missense_Mutation SNP A A T TCGA-EE-A2GM-06B-11D-A196-08 TCGA-EE-A2GM-10A-01D-A198-08 g.chr9:32544245A>T c.278T>A c.(277-279)gTa>gAa p.V93E

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation AML-US 9 32542498 32542498 single base substitution A T missense_variant S610R 1830T>A AML-US 9 32542498 32542498 single base substitution A T missense_variant S675R 2025T>A BLCA-CN 9 32541987 32541987 single base substitution T A missense_variant S781C 2341A>T BLCA-CN 9 32541987 32541987 single base substitution T A missense_variant S846C 2536A>T BLCA-US 9 32541498 32541498 single base substitution C T missense_variant E1009K 3025G>A BLCA-US 9 32541498 32541498 single base substitution C T missense_variant E944K 2830G>A BLCA-US 9 32543021 32543021 single base substitution G A missense_variant S436F 1307C>T BLCA-US 9 32543021 32543021 single base substitution G A missense_variant S501F 1502C>T BLCA-US 9 32543241 32543241 single base substitution A C missense_variant S363A 1087T>G BLCA-US 9 32543241 32543241 single base substitution A C missense_variant S428A 1282T>G BLCA-US 9 32544000 32544000 single base substitution C T missense_variant D110N 328G>A BLCA-US 9 32544000 32544000 single base substitution C T missense_variant D175N 523G>A BLCA-US 9 32544067 32544067 single base substitution C T synonymous_variant V152V 456G>A BLCA-US 9 32544067 32544067 single base substitution C T synonymous_variant V87V 261G>A BLCA-US 9 32544192 32544192 single base substitution C G missense_variant D111H 331G>C BLCA-US 9 32544192 32544192 single base substitution C G missense_variant D46H 136G>C BLCA-US 9 32544237 32544237 single base substitution C T missense_variant D31N 91G>A BLCA-US 9 32544237 32544237 single base substitution C T missense_variant D96N 286G>A BLCA-US 9 32544239 32544239 single base substitution G A missense_variant A30V 89C>T BLCA-US 9 32544239 32544239 single base substitution G A missense_variant A95V 284C>T BLCA-US 9 32553939 32553939 single base substitution C T upstream_gene_variant BOCA-FR 9 32550359 32550359 single base substitution A G intron_variant BRCA-EU 9 32537320 32537320 single base substitution C T downstream_gene_variant BRCA-EU 9 32537930 32537930 single base substitution G A downstream_gene_variant BRCA-EU 9 32538247 32538247 single base substitution G A downstream_gene_variant BRCA-EU 9 32540246 32540246 single base substitution C A downstream_gene_variant BRCA-EU 9 32543078 32543078 single base substitution C A missense_variant G417V 1250G>T BRCA-EU 9 32543078 32543078 single base substitution C A missense_variant G482V 1445G>T BRCA-EU 9 32543645 32543645 single base substitution A C missense_variant L228R 683T>G BRCA-EU 9 32543645 32543645 single base substitution A C missense_variant L293R 878T>G BRCA-EU 9 32543694 32543694 single base substitution G T missense_variant R212S 634C>A BRCA-EU 9 32543694 32543694 single base substitution G T missense_variant R277S 829C>A BRCA-EU 9 32545196 32545196 insertion of <=200bp - A intron_variant BRCA-EU 9 32546270 32546270 deletion of <=200bp T - intron_variant BRCA-EU 9 32547104 32547104 single base substitution C G intron_variant BRCA-EU 9 32547959 32547959 single base substitution A T intron_variant BRCA-EU 9 32549145 32549145 single base substitution A C intron_variant BRCA-EU 9 32549305 32549305 deletion of <=200bp A - intron_variant BRCA-EU 9 32549316 32549316 single base substitution A G intron_variant BRCA-EU 9 32550185 32550185 deletion of <=200bp C - intron_variant BRCA-EU 9 32551290 32551291 deletion of <=200bp CT - intron_variant BRCA-EU 9 32552559 32552559 deletion of <=200bp G - upstream_gene_variant BRCA-EU 9 32553073 32553073 single base substitution T C upstream_gene_variant BRCA-EU 9 32554827 32554827 single base substitution T C upstream_gene_variant BRCA-FR 9 32554076 32554076 single base substitution G C upstream_gene_variant BRCA-UK 9 32541070 32541070 single base substitution C T 3_prime_UTR_variant BRCA-UK 9 32551700 32551700 single base substitution G A intron_variant BRCA-US 9 32541997 32541997 single base substitution G T synonymous_variant T777T 2331C>A BRCA-US 9 32541997 32541997 single base substitution G T synonymous_variant T842T 2526C>A BRCA-US 9 32542676 32542676 single base substitution C T missense_variant R551K 1652G>A BRCA-US 9 32542676 32542676 single base substitution C T missense_variant R616K 1847G>A BRCA-US 9 32543678 32543678 single base substitution G A missense_variant S217L 650C>T BRCA-US 9 32543678 32543678 single base substitution G A missense_variant S282L 845C>T BRCA-US 9 32544087 32544087 single base substitution C G missense_variant D146H 436G>C BRCA-US 9 32544087 32544087 single base substitution C G missense_variant D81H 241G>C BTCA-JP 9 32544122 32544122 deletion of <=200bp T - frameshift_variant N134 BTCA-JP 9 32544122 32544122 deletion of <=200bp T - frameshift_variant N69 BTCA-JP 9 32550702 32550702 single base substitution C A intron_variant BTCA-JP 9 32551777 32551777 single base substitution C T intron_variant BTCA-JP 9 32551852 32551852 single base substitution A G intron_variant CESC-US 9 32542047 32542047 single base substitution G A stop_gained Q761* 2281C>T CESC-US 9 32542047 32542047 single base substitution G A stop_gained Q826* 2476C>T CESC-US 9 32542367 32542367 single base substitution G A missense_variant S654F 1961C>T CESC-US 9 32542367 32542367 single base substitution G A missense_variant S719F 2156C>T CESC-US 9 32542823 32542823 single base substitution G C stop_gained S502* 1505C>G CESC-US 9 32542823 32542823 single base substitution G C stop_gained S567* 1700C>G CESC-US 9 32551295 32551295 single base substitution C A intron_variant COAD-US 9 32542034 32542034 single base substitution G A missense_variant S765L 2294C>T COAD-US 9 32542034 32542034 single base substitution G A missense_variant S830L 2489C>T COAD-US 9 32542995 32542995 single base substitution T C missense_variant M445V 1333A>G COAD-US 9 32542995 32542995 single base substitution T C missense_variant M510V 1528A>G COAD-US 9 32543901 32543901 single base substitution C T missense_variant D143N 427G>A COAD-US 9 32543901 32543901 single base substitution C T missense_variant D208N 622G>A COAD-US 9 32543902 32543902 single base substitution C T synonymous_variant P142P 426G>A COAD-US 9 32543902 32543902 single base substitution C T synonymous_variant P207P 621G>A COAD-US 9 32544122 32544122 deletion of <=200bp T - frameshift_variant N134 COAD-US 9 32544122 32544122 deletion of <=200bp T - frameshift_variant N69 COAD-US 9 32550896 32550896 single base substitution G C intron_variant COAD-US 9 32550896 32550896 single base substitution G C missense_variant S25W 74C>G COCA-CN 9 32543202 32543202 single base substitution T C missense_variant T376A 1126A>G COCA-CN 9 32543202 32543202 single base substitution T C missense_variant T441A 1321A>G COCA-CN 9 32543379 32543379 single base substitution C T missense_variant E317K 949G>A COCA-CN 9 32543379 32543379 single base substitution C T missense_variant E382K 1144G>A COCA-CN 9 32543445 32543445 single base substitution G A stop_gained R295* 883C>T COCA-CN 9 32543445 32543445 single base substitution G A stop_gained R360* 1078C>T COCA-CN 9 32550822 32550822 single base substitution G A intron_variant COCA-CN 9 32550822 32550822 single base substitution G A missense_variant R50W 148C>T COCA-CN 9 32552803 32552803 single base substitution T C upstream_gene_variant ESAD-UK 9 32535970 32535970 single base substitution G T downstream_gene_variant ESAD-UK 9 32536836 32536836 single base substitution C T downstream_gene_variant ESAD-UK 9 32538213 32538213 single base substitution T C downstream_gene_variant ESAD-UK 9 32539881 32539881 single base substitution T C downstream_gene_variant ESAD-UK 9 32540140 32540140 single base substitution C T downstream_gene_variant ESAD-UK 9 32541226 32541226 single base substitution G A 3_prime_UTR_variant ESAD-UK 9 32541733 32541733 single base substitution A G synonymous_variant G865G 2595T>C ESAD-UK 9 32541733 32541733 single base substitution A G synonymous_variant G930G 2790T>C ESAD-UK 9 32543599 32543599 deletion of <=200bp A - frameshift_variant F243 ESAD-UK 9 32543599 32543599 deletion of <=200bp A - frameshift_variant F308 ESAD-UK 9 32543733 32543733 single base substitution G A missense_variant R199C 595C>T ESAD-UK 9 32543733 32543733 single base substitution G A missense_variant R264C 790C>T ESAD-UK 9 32543909 32543911 deletion of <=200bp GTT - disruptive_inframe_deletion TT139T ESAD-UK 9 32543909 32543911 deletion of <=200bp GTT - disruptive_inframe_deletion TT204T ESAD-UK 9 32544096 32544096 single base substitution G A stop_gained Q143* 427C>T ESAD-UK 9 32544096 32544096 single base substitution G A stop_gained Q78* 232C>T ESAD-UK 9 32545284 32545284 single base substitution C T intron_variant ESAD-UK 9 32546142 32546142 single base substitution A C intron_variant ESAD-UK 9 32546331 32546331 single base substitution A G intron_variant ESAD-UK 9 32547623 32547623 single base substitution C A intron_variant ESAD-UK 9 32547841 32547841 deletion of <=200bp T - intron_variant ESAD-UK 9 32549701 32549701 single base substitution A G intron_variant ESAD-UK 9 32550212 32550212 single base substitution C A intron_variant ESAD-UK 9 32550397 32550397 single base substitution T C intron_variant ESAD-UK 9 32551039 32551039 single base substitution C T intron_variant ESAD-UK 9 32552294 32552294 single base substitution A G intron_variant ESAD-UK 9 32554328 32554328 single base substitution G A upstream_gene_variant ESAD-UK 9 32554466 32554466 single base substitution G A upstream_gene_variant ESCA-CN 9 32543173 32543173 single base substitution G C synonymous_variant V385V 1155C>G ESCA-CN 9 32543173 32543173 single base substitution G C synonymous_variant V450V 1350C>G GBM-US 9 32543467 32543467 single base substitution T C missense_variant I287M 861A>G GBM-US 9 32543467 32543467 single base substitution T C missense_variant I352M 1056A>G KIRC-US 9 32543675 32543675 single base substitution G A missense_variant A218V 653C>T KIRC-US 9 32543675 32543675 single base substitution G A missense_variant A283V 848C>T KIRP-US 9 32541815 32541815 single base substitution C G missense_variant R838P 2513G>C KIRP-US 9 32541815 32541815 single base substitution C G missense_variant R903P 2708G>C KIRP-US 9 32541932 32541932 single base substitution C T missense_variant S799N 2396G>A KIRP-US 9 32541932 32541932 single base substitution C T missense_variant S864N 2591G>A KIRP-US 9 32543270 32543270 single base substitution T C missense_variant D353G 1058A>G KIRP-US 9 32543270 32543270 single base substitution T C missense_variant D418G 1253A>G LAML-KR 9 32541535 32541535 single base substitution G A synonymous_variant L931L 2793C>T LAML-KR 9 32541535 32541535 single base substitution G A synonymous_variant L996L 2988C>T LICA-CN 9 32541534 32541534 single base substitution C T missense_variant D932N 2794G>A LICA-CN 9 32541534 32541534 single base substitution C T missense_variant D997N 2989G>A LICA-CN 9 32550959 32550959 single base substitution T A intron_variant LICA-CN 9 32550959 32550959 single base substitution T A missense_variant Q4L 11A>T LICA-FR 9 32542384 32542384 single base substitution C T synonymous_variant R648R 1944G>A LICA-FR 9 32542384 32542384 single base substitution C T synonymous_variant R713R 2139G>A LICA-FR 9 32543297 32543297 single base substitution G A missense_variant A344V 1031C>T LICA-FR 9 32543297 32543297 single base substitution G A missense_variant A409V 1226C>T LICA-FR 9 32544286 32544286 single base substitution G T missense_variant N14K 42C>A LICA-FR 9 32544286 32544286 single base substitution G T missense_variant N79K 237C>A LIHC-US 9 32543636 32543636 single base substitution A G missense_variant L231S 692T>C LIHC-US 9 32543636 32543636 single base substitution A G missense_variant L296S 887T>C LIHC-US 9 32543942 32543942 single base substitution G C stop_gained S129* 386C>G LIHC-US 9 32543942 32543942 single base substitution G C stop_gained S194* 581C>G LIHC-US 9 32544214 32544214 single base substitution A G synonymous_variant C103C 309T>C LIHC-US 9 32544214 32544214 single base substitution A G synonymous_variant C38C 114T>C LIHC-US 9 32550784 32550784 single base substitution C T intron_variant LIHC-US 9 32550784 32550784 single base substitution C T synonymous_variant P62P 186G>A LINC-JP 9 32541246 32541246 insertion of <=200bp - A 3_prime_UTR_variant LINC-JP 9 32544382 32544382 single base substitution C G intron_variant LINC-JP 9 32552409 32552415 deletion of <=200bp GCGGACT - intron_variant LIRI-JP 9 32536385 32536385 single base substitution C T downstream_gene_variant LIRI-JP 9 32537384 32537384 single base substitution G A downstream_gene_variant LIRI-JP 9 32537429 32537429 single base substitution T C downstream_gene_variant LIRI-JP 9 32537777 32537777 single base substitution C T downstream_gene_variant LIRI-JP 9 32538425 32538425 single base substitution A T downstream_gene_variant LIRI-JP 9 32539185 32539185 single base substitution G C downstream_gene_variant LIRI-JP 9 32542927 32542927 single base substitution G A synonymous_variant C467C 1401C>T LIRI-JP 9 32542927 32542927 single base substitution G A synonymous_variant C532C 1596C>T LIRI-JP 9 32544081 32544081 single base substitution T C missense_variant I148V 442A>G LIRI-JP 9 32544081 32544081 single base substitution T C missense_variant I83V 247A>G LIRI-JP 9 32544827 32544827 deletion of <=200bp A - intron_variant LIRI-JP 9 32546384 32546384 single base substitution G C intron_variant LIRI-JP 9 32546914 32546914 single base substitution T C intron_variant LIRI-JP 9 32549046 32549046 single base substitution G T intron_variant LIRI-JP 9 32549718 32549718 single base substitution T C intron_variant LIRI-JP 9 32550467 32550467 single base substitution G C intron_variant LIRI-JP 9 32552407 32552407 single base substitution C A intron_variant LIRI-JP 9 32552582 32552582 single base substitution A G upstream_gene_variant LIRI-JP 9 32554305 32554305 single base substitution C T upstream_gene_variant LIRI-JP 9 32554356 32554356 single base substitution A C upstream_gene_variant LIRI-JP 9 32554528 32554528 single base substitution G A upstream_gene_variant LUSC-KR 9 32541535 32541535 single base substitution G A synonymous_variant L931L 2793C>T LUSC-KR 9 32541535 32541535 single base substitution G A synonymous_variant L996L 2988C>T LUSC-KR 9 32545230 32545230 single base substitution T C intron_variant LUSC-KR 9 32546244 32546244 single base substitution C G intron_variant LUSC-KR 9 32551370 32551370 single base substitution T A intron_variant LUSC-KR 9 32552246 32552246 single base substitution C T intron_variant LUSC-US 9 32541488 32541488 single base substitution G A missense_variant P1012L 3035C>T LUSC-US 9 32541488 32541488 single base substitution G A missense_variant P947L 2840C>T LUSC-US 9 32541551 32541551 single base substitution G A missense_variant S926L 2777C>T LUSC-US 9 32541551 32541551 single base substitution G A missense_variant S991L 2972C>T LUSC-US 9 32541567 32541567 single base substitution G A missense_variant P921S 2761C>T LUSC-US 9 32541567 32541567 single base substitution G A missense_variant P986S 2956C>T LUSC-US 9 32542506 32542506 single base substitution G T missense_variant R608S 1822C>A LUSC-US 9 32542506 32542506 single base substitution G T missense_variant R673S 2017C>A LUSC-US 9 32542684 32542684 single base substitution C A missense_variant K548N 1644G>T LUSC-US 9 32542684 32542684 single base substitution C A missense_variant K613N 1839G>T LUSC-US 9 32543158 32543158 single base substitution C A synonymous_variant T390T 1170G>T LUSC-US 9 32543158 32543158 single base substitution C A synonymous_variant T455T 1365G>T LUSC-US 9 32543189 32543189 single base substitution G A missense_variant S380L 1139C>T LUSC-US 9 32543189 32543189 single base substitution G A missense_variant S445L 1334C>T LUSC-US 9 32543732 32543732 single base substitution C A missense_variant R199L 596G>T LUSC-US 9 32543732 32543732 single base substitution C A missense_variant R264L 791G>T MALY-DE 9 32547367 32547367 single base substitution C T intron_variant MELA-AU 9 32536004 32536004 single base substitution C G downstream_gene_variant MELA-AU 9 32537058 32537058 single base substitution C T downstream_gene_variant MELA-AU 9 32537311 32537311 single base substitution C T downstream_gene_variant MELA-AU 9 32538783 32538783 single base substitution G A downstream_gene_variant MELA-AU 9 32538974 32538974 single base substitution G A downstream_gene_variant MELA-AU 9 32538976 32538976 single base substitution G A downstream_gene_variant MELA-AU 9 32539088 32539088 single base substitution G A downstream_gene_variant MELA-AU 9 32541030 32541030 single base substitution A C 3_prime_UTR_variant MELA-AU 9 32541452 32541452 single base substitution C T missense_variant R1024K 3071G>A MELA-AU 9 32541452 32541452 single base substitution C T missense_variant R959K 2876G>A MELA-AU 9 32542433 32542433 single base substitution C T missense_variant G632E 1895G>A MELA-AU 9 32542433 32542433 single base substitution C T missense_variant G697E 2090G>A MELA-AU 9 32542767 32542767 single base substitution G A missense_variant P521S 1561C>T MELA-AU 9 32542767 32542767 single base substitution G A missense_variant P586S 1756C>T MELA-AU 9 32543439 32543439 single base substitution G A missense_variant P297S 889C>T MELA-AU 9 32543439 32543439 single base substitution G A missense_variant P362S 1084C>T MELA-AU 9 32543988 32543988 single base substitution G A missense_variant R114C 340C>T MELA-AU 9 32543988 32543988 single base substitution G A missense_variant R179C 535C>T MELA-AU 9 32544686 32544686 single base substitution C T intron_variant MELA-AU 9 32545073 32545073 single base substitution G A intron_variant MELA-AU 9 32545550 32545550 single base substitution G A intron_variant MELA-AU 9 32547003 32547003 single base substitution T C intron_variant MELA-AU 9 32547218 32547218 single base substitution A T intron_variant MELA-AU 9 32547879 32547879 single base substitution G A intron_variant MELA-AU 9 32548240 32548240 single base substitution G A intron_variant MELA-AU 9 32548936 32548936 single base substitution G C intron_variant MELA-AU 9 32549215 32549215 single base substitution G A intron_variant MELA-AU 9 32549943 32549943 single base substitution A G intron_variant MELA-AU 9 32550687 32550687 single base substitution G A intron_variant MELA-AU 9 32551471 32551471 single base substitution G A intron_variant MELA-AU 9 32552279 32552279 single base substitution G A intron_variant MELA-AU 9 32552332 32552332 single base substitution G A intron_variant MELA-AU 9 32553415 32553415 single base substitution C T upstream_gene_variant MELA-AU 9 32554896 32554896 single base substitution G A upstream_gene_variant MELA-AU 9 32556920 32556920 single base substitution G T upstream_gene_variant MELA-AU 9 32557520 32557520 single base substitution G A upstream_gene_variant ORCA-IN 9 32540913 32540913 single base substitution T C 3_prime_UTR_variant ORCA-IN 9 32544314 32544314 single base substitution G A missense_variant S5L 14C>T ORCA-IN 9 32544314 32544314 single base substitution G A missense_variant S70L 209C>T ORCA-IN 9 32548306 32548306 single base substitution G C intron_variant OV-AU 9 32539503 32539503 single base substitution T C downstream_gene_variant OV-AU 9 32541004 32541004 single base substitution C T 3_prime_UTR_variant OV-AU 9 32541468 32541468 single base substitution G A stop_gained Q1019* 3055C>T OV-AU 9 32541468 32541468 single base substitution G A stop_gained Q954* 2860C>T OV-AU 9 32546892 32546892 single base substitution C A intron_variant OV-AU 9 32548217 32548217 single base substitution A T intron_variant OV-AU 9 32548829 32548829 single base substitution G T intron_variant OV-AU 9 32550577 32550577 single base substitution A C intron_variant OV-AU 9 32552460 32552460 single base substitution G C 5_prime_UTR_variant OV-AU 9 32555550 32555550 single base substitution A G upstream_gene_variant OV-US 9 32544141 32544141 single base substitution C T missense_variant V128I 382G>A OV-US 9 32544141 32544141 single base substitution C T missense_variant V63I 187G>A PACA-AU 9 32538786 32538786 deletion of <=200bp T - downstream_gene_variant PACA-AU 9 32543842 32543842 deletion of <=200bp A - frameshift_variant I162 PACA-AU 9 32543842 32543842 deletion of <=200bp A - frameshift_variant I227 PACA-AU 9 32545524 32545524 single base substitution C A intron_variant PACA-AU 9 32556486 32556486 single base substitution G A upstream_gene_variant PACA-CA 9 32540305 32540305 insertion of <=200bp - C downstream_gene_variant PACA-CA 9 32542471 32542476 deletion of <=200bp GCTCCG - inframe_deletion RS618 PACA-CA 9 32542471 32542476 deletion of <=200bp GCTCCG - inframe_deletion RS683 PACA-CA 9 32544904 32544904 single base substitution G A intron_variant PACA-CA 9 32549410 32549410 single base substitution C T intron_variant PAEN-AU 9 32555939 32555939 single base substitution T C upstream_gene_variant PAEN-IT 9 32541258 32541258 single base substitution A T 3_prime_UTR_variant PBCA-DE 9 32549222 32549222 single base substitution G A intron_variant PBCA-DE 9 32557029 32557034 deletion of <=200bp TATTAA - upstream_gene_variant PRAD-CA 9 32535847 32535847 single base substitution C T downstream_gene_variant PRAD-CA 9 32545458 32545458 single base substitution G C intron_variant PRAD-UK 9 32544575 32544575 single base substitution T G intron_variant PRAD-UK 9 32552093 32552093 single base substitution G T intron_variant PRAD-US 9 32543932 32543932 single base substitution A C synonymous_variant G132G 396T>G PRAD-US 9 32543932 32543932 single base substitution A C synonymous_variant G197G 591T>G PRAD-US 9 32544153 32544154 deletion of <=200bp AG - frameshift_variant FC123 PRAD-US 9 32544153 32544154 deletion of <=200bp AG - frameshift_variant FC58 READ-US 9 32543427 32543427 single base substitution C A missense_variant A301S 901G>T READ-US 9 32543427 32543427 single base substitution C A missense_variant A366S 1096G>T RECA-EU 9 32538357 32538357 single base substitution C T downstream_gene_variant RECA-EU 9 32547976 32547976 single base substitution G A intron_variant RECA-EU 9 32548509 32548509 single base substitution A T intron_variant RECA-EU 9 32552466 32552466 single base substitution A G 5_prime_UTR_variant RECA-EU 9 32554167 32554167 single base substitution A G upstream_gene_variant RECA-EU 9 32557447 32557447 single base substitution A T upstream_gene_variant SKCA-BR 9 32540131 32540131 single base substitution T A downstream_gene_variant SKCA-BR 9 32545515 32545515 single base substitution T A intron_variant SKCA-BR 9 32549284 32549284 single base substitution G A intron_variant SKCA-BR 9 32551139 32551139 single base substitution T C intron_variant SKCA-BR 9 32552164 32552164 insertion of <=200bp - TCTC intron_variant SKCA-BR 9 32552282 32552282 single base substitution G A intron_variant SKCA-BR 9 32555238 32555238 single base substitution G A upstream_gene_variant SKCA-BR 9 32555536 32555536 single base substitution C A upstream_gene_variant SKCM-US 9 32541428 32541428 single base substitution G A missense_variant S1032L 3095C>T SKCM-US 9 32541428 32541428 single base substitution G A missense_variant S967L 2900C>T SKCM-US 9 32541581 32541581 single base substitution G A missense_variant T916I 2747C>T SKCM-US 9 32541581 32541581 single base substitution G A missense_variant T981I 2942C>T SKCM-US 9 32541774 32541774 single base substitution C T missense_variant D852N 2554G>A SKCM-US 9 32541774 32541774 single base substitution C T missense_variant D917N 2749G>A SKCM-US 9 32542037 32542037 single base substitution G A missense_variant S764L 2291C>T SKCM-US 9 32542037 32542037 single base substitution G A missense_variant S829L 2486C>T SKCM-US 9 32543175 32543175 single base substitution C T missense_variant V385I 1153G>A SKCM-US 9 32543175 32543175 single base substitution C T missense_variant V450I 1348G>A SKCM-US 9 32543665 32543665 single base substitution G A synonymous_variant F221F 663C>T SKCM-US 9 32543665 32543665 single base substitution G A synonymous_variant F286F 858C>T SKCM-US 9 32544245 32544245 single base substitution A T missense_variant V28E 83T>A SKCM-US 9 32544245 32544245 single base substitution A T missense_variant V93E 278T>A STAD-US 9 32541411 32541411 single base substitution G C missense_variant L1038V 3112C>G STAD-US 9 32541411 32541411 single base substitution G C missense_variant L973V 2917C>G STAD-US 9 32541935 32541935 single base substitution C T missense_variant R798Q 2393G>A STAD-US 9 32541935 32541935 single base substitution C T missense_variant R863Q 2588G>A STAD-US 9 32542036 32542036 single base substitution T C synonymous_variant S764S 2292A>G STAD-US 9 32542036 32542036 single base substitution T C synonymous_variant S829S 2487A>G STAD-US 9 32542476 32542476 single base substitution G A missense_variant R618W 1852C>T STAD-US 9 32542476 32542476 single base substitution G A missense_variant R683W 2047C>T STAD-US 9 32542941 32542941 single base substitution C T missense_variant D463N 1387G>A STAD-US 9 32542941 32542941 single base substitution C T missense_variant D528N 1582G>A STAD-US 9 32543727 32543727 single base substitution C G missense_variant G201R 601G>C STAD-US 9 32543727 32543727 single base substitution C G missense_variant G266R 796G>C STAD-US 9 32543953 32543953 single base substitution A G synonymous_variant A125A 375T>C STAD-US 9 32543953 32543953 single base substitution A G synonymous_variant A190A 570T>C STAD-US 9 32544006 32544006 single base substitution T C missense_variant T108A 322A>G STAD-US 9 32544006 32544006 single base substitution T C missense_variant T173A 517A>G STAD-US 9 32544122 32544122 deletion of <=200bp T - frameshift_variant N134 STAD-US 9 32544122 32544122 deletion of <=200bp T - frameshift_variant N69 STAD-US 9 32550787 32550787 single base substitution C T intron_variant STAD-US 9 32550787 32550787 single base substitution C T synonymous_variant A61A 183G>A THCA-US 9 32541435 32541435 single base substitution G A missense_variant R1030W 3088C>T THCA-US 9 32541435 32541435 single base substitution G A missense_variant R965W 2893C>T UCEC-US 9 32541534 32541534 single base substitution C T missense_variant D932N 2794G>A UCEC-US 9 32541534 32541534 single base substitution C T missense_variant D997N 2989G>A UCEC-US 9 32541770 32541770 single base substitution G T missense_variant S853Y 2558C>A UCEC-US 9 32541770 32541770 single base substitution G T missense_variant S918Y 2753C>A UCEC-US 9 32541988 32541988 single base substitution G A synonymous_variant D780D 2340C>T UCEC-US 9 32541988 32541988 single base substitution G A synonymous_variant D845D 2535C>T UCEC-US 9 32542291 32542291 single base substitution A G synonymous_variant F679F 2037T>C UCEC-US 9 32542291 32542291 single base substitution A G synonymous_variant F744F 2232T>C UCEC-US 9 32542508 32542508 single base substitution G T missense_variant S607Y 1820C>A UCEC-US 9 32542508 32542508 single base substitution G T missense_variant S672Y 2015C>A UCEC-US 9 32542651 32542651 single base substitution C A missense_variant M559I 1677G>T UCEC-US 9 32542651 32542651 single base substitution C A missense_variant M624I 1872G>T UCEC-US 9 32542663 32542663 single base substitution C T synonymous_variant G555G 1665G>A UCEC-US 9 32542663 32542663 single base substitution C T synonymous_variant G620G 1860G>A UCEC-US 9 32542715 32542715 single base substitution C T missense_variant R538H 1613G>A UCEC-US 9 32542715 32542715 single base substitution C T missense_variant R603H 1808G>A UCEC-US 9 32542873 32542873 single base substitution A G synonymous_variant C485C 1455T>C UCEC-US 9 32542873 32542873 single base substitution A G synonymous_variant C550C 1650T>C UCEC-US 9 32543046 32543046 single base substitution C A stop_gained E428* 1282G>T UCEC-US 9 32543046 32543046 single base substitution C A stop_gained E493* 1477G>T UCEC-US 9 32543128 32543128 single base substitution G A synonymous_variant D400D 1200C>T UCEC-US 9 32543128 32543128 single base substitution G A synonymous_variant D465D 1395C>T UCEC-US 9 32543323 32543323 single base substitution C A missense_variant E335D 1005G>T UCEC-US 9 32543323 32543323 single base substitution C A missense_variant E400D 1200G>T UCEC-US 9 32543483 32543483 single base substitution C T missense_variant R282Q 845G>A UCEC-US 9 32543483 32543483 single base substitution C T missense_variant R347Q 1040G>A UCEC-US 9 32543511 32543511 single base substitution A G missense_variant S273P 817T>C UCEC-US 9 32543511 32543511 single base substitution A G missense_variant S338P 1012T>C UCEC-US 9 32543588 32543588 single base substitution C T missense_variant G247E 740G>A UCEC-US 9 32543588 32543588 single base substitution C T missense_variant G312E 935G>A UCEC-US 9 32543853 32543853 single base substitution C A missense_variant D159Y 475G>T UCEC-US 9 32543853 32543853 single base substitution C A missense_variant D224Y 670G>T UCEC-US 9 32543907 32543907 single base substitution G A missense_variant P141S 421C>T UCEC-US 9 32543907 32543907 single base substitution G A missense_variant P206S 616C>T UCEC-US 9 32543930 32543930 single base substitution G T missense_variant P133H 398C>A UCEC-US 9 32543930 32543930 single base substitution G T missense_variant P198H 593C>A UCEC-US 9 32544158 32544158 single base substitution T G missense_variant K122T 365A>C UCEC-US 9 32544158 32544158 single base substitution T G missense_variant K57T 170A>C UCEC-US 9 32544292 32544292 single base substitution C A missense_variant M12I 36G>T UCEC-US 9 32544292 32544292 single base substitution C A missense_variant M77I 231G>T

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand TCGA-AK-3465-01 COSM1497079 c.2646T>A p.H882Q Substitution - Missense 9:32541879-32541879 - C135 COSM1569300 c.2422G>A p.E808K Substitution - Missense 9:32542103-32542103 - TCGA-EK-A2RC-01 COSM4848662 c.2476C>T p.Q826* Substitution - Nonsense 9:32542049-32542049 - TCGA-66-2795-01 COSM753659 c.2956C>T p.P986S Substitution - Missense 9:32541569-32541569 - LAU63 COSM233630 c.2209C>T p.P737S Substitution - Missense 9:32542316-32542316 - TCGA-AY-5543-01 COSM1461983 c.1528A>G p.M510V Substitution - Missense 9:32542997-32542997 - TCGA-26-6174-01 COSM3413589 c.1056A>G p.I352M Substitution - Missense 9:32543469-32543469 - B23 COSM1756123 c.2536A>T p.S846C Substitution - Missense 9:32541989-32541989 - TCGA-AA-3864-01 COSM5115538 c.2346C>T p.T782T Substitution - coding silent 9:32542179-32542179 - TCGA-FD-A3B3-01 COSM1314751 c.523G>A p.D175N Substitution - Missense 9:32544002-32544002 - CHOL48 COSM1744593 c.1828C>T p.H610Y Substitution - Missense 9:32542697-32542697 - TCGA-AK-3447-01 COSM1497078 c.2637T>A p.T879T Substitution - coding silent 9:32541888-32541888 - Detroit_562 COSM4595112 c.254G>A p.G85D Substitution - Missense 9:32544271-32544271 - LUAD-S01315 COSM346118 c.2006G>C p.R669T Substitution - Missense 9:32542519-32542519 - TCGA-D1-A174-01 COSM1108198 c.593C>A p.P198H Substitution - Missense 9:32543932-32543932 - RMS230 COSM5881231 c.2347G>A p.G783R Substitution - Missense 9:32542178-32542178 - TCGA-BS-A0UV-01 COSM1108193 c.1040G>A p.R347Q Substitution - Missense 9:32543485-32543485 - YUKLAB COSM1701030 c.1024_1025CC>TT p.P342L Substitution - Missense 9:32543500-32543501 - 2557_CLM COSM5757362 c.59C>T p.P20L Substitution - Missense 9:32550913-32550913 - YUFERY COSM5410982 c.802C>T p.R268* Substitution - Nonsense 9:32543723-32543723 - TCGA-D1-A17F-01 COSM1108187 c.1860G>A p.G620G Substitution - coding silent 9:32542665-32542665 - TCGA-13-0755-01 COSM76787 c.382G>A p.V128I Substitution - Missense 9:32544143-32544143 - CSCC-56-T COSM4484565 c.2825C>T p.P942L Substitution - Missense 9:32541700-32541700 - TCGA-AP-A0LT-01 COSM1108191 c.1395C>T p.D465D Substitution - coding silent 9:32543130-32543130 - TCGA-AA-3815-01 COSM1461984 c.1115C>T p.A372V Substitution - Missense 9:32543410-32543410 - TCGA-B5-A0JY-01 COSM1108182 c.2753C>A p.S918Y Substitution - Missense 9:32541772-32541772 - CSCC-31-T COSM4476390 c.2065C>T p.R689C Substitution - Missense 9:32542460-32542460 - AOCS-149-1-7 COSM4152245 c.3055C>T p.Q1019* Substitution - Nonsense 9:32541470-32541470 - LUAD-E00897 COSM364827 c.1965A>T p.R655S Substitution - Missense 9:32542560-32542560 - PT33 COSM5908959 c.2440C>T p.R814C Substitution - Missense 9:32542085-32542085 - TARGET-20-PASMYS-04A-02D COSM5487436 c.2025T>A p.S675R Substitution - Missense 9:32542500-32542500 - ESCC_140 COSM5643458 c.76G>A p.E26K Substitution - Missense 9:32550896-32550896 - TCGA-AN-A046-01 COSM3848322 c.1847G>A p.R616K Substitution - Missense 9:32542678-32542678 - TCGA-G9-6333-01 COSM3675322 c.541C>A p.R181S Substitution - Missense 9:32543984-32543984 - TCGA-AY-4071-01 COSM287689 c.2488T>C p.S830P Substitution - Missense 9:32542037-32542037 - TCGA-EI-6507-01 COSM1569299 c.1096G>T p.A366S Substitution - Missense 9:32543429-32543429 - T2957 COSM4735354 c.1730C>T p.S577F Substitution - Missense 9:32542795-32542795 - I2L-P26-Tumor-Organoid COSM5359489 c.1686G>C p.E562D Substitution - Missense 9:32542839-32542839 - PD9572a COSM2772112 c.1445G>T p.G482V Substitution - Missense 9:32543080-32543080 - pfg116T COSM4752301 c.2583G>C p.K861N Substitution - Missense 9:32541942-32541942 - TCGA-CA-6717-01 COSM3699301 c.622G>A p.D208N Substitution - Missense 9:32543903-32543903 - SWE-48 COSM1180174 c.2808A>C p.Q936H Substitution - Missense 9:32541717-32541717 - T2269 COSM4735351 c.2863A>C p.I955L Substitution - Missense 9:32541662-32541662 - 325 COSM98046 c.875G>A p.C292Y Substitution - Missense 9:32543650-32543650 - TCGA-CG-4438-01 COSM3906820 c.3112C>G p.L1038V Substitution - Missense 9:32541413-32541413 - CN-AML-08-T COSM5425629 c.2988C>T p.L996L Substitution - coding silent 9:32541537-32541537 - STC291 COSM1674451 c.779G>A p.R260Q Substitution - Missense 9:32543746-32543746 - TCGA-39-5031-01 COSM753656 c.1365G>T p.T455T Substitution - coding silent 9:32543160-32543160 - TCGA-A3-3346-01 COSM1497078 c.2637T>A p.T879T Substitution - coding silent 9:32541888-32541888 - TCGA-CD-8536-01 COSM3906822 c.2487A>G p.S829S Substitution - coding silent 9:32542038-32542038 - YUDAB COSM1701029 c.1087T>C p.F363L Substitution - Missense 9:32543438-32543438 - 587256 COSM1230084 c.562C>T p.R188* Substitution - Nonsense 9:32543963-32543963 - TCGA-AX-A0J0-01 COSM1108200 c.231G>T p.M77I Substitution - Missense 9:32544294-32544294 - SNU-175 COSM2772091 c.2587C>T p.R863W Substitution - Missense 9:32541938-32541938 - sysucc-1317T COSM5450575 c.148C>T p.R50W Substitution - Missense 9:32550824-32550824 - TCGA-EE-A3JB-06 COSM4898715 c.2486C>T p.S829L Substitution - Missense 9:32542039-32542039 - YUPAER COSM5410981 c.1615C>T p.L539F Substitution - Missense 9:32542910-32542910 - MDA-N COSM1674450 c.3037A>G p.S1013G Substitution - Missense 9:32541488-32541488 - ESCC_BICR_054T COSM5444349 c.1350C>G p.V450V Substitution - coding silent 9:32543175-32543175 - TCGA-BG-A0M4-01 COSM1108181 c.2989G>A p.D997N Substitution - Missense 9:32541536-32541536 - PT37 COSM4476390 c.2065C>T p.R689C Substitution - Missense 9:32542460-32542460 - PT14_1 COSM5896971 c.431C>T p.P144L Substitution - Missense 9:32544094-32544094 - T263 COSM4735350 c.2904T>C p.I968I Substitution - coding silent 9:32541621-32541621 - TCGA-GN-A266-06 COSM3656820 c.3095C>T p.S1032L Substitution - Missense 9:32541430-32541430 - LS174T COSM2772093 c.2564A>G p.H855R Substitution - Missense 9:32541961-32541961 - TCGA-BR-A4QL-01 COSM3906821 c.2588G>A p.R863Q Substitution - Missense 9:32541937-32541937 - 90827 COSM330555 c.1102T>C p.F368L Substitution - Missense 9:32543423-32543423 - CCK81 COSM2772140 c.329T>C p.F110S Substitution - Missense 9:32544196-32544196 - TCGA-A8-A06Q-01 COSM455823 c.845C>T p.S282L Substitution - Missense 9:32543680-32543680 - TCGA-EI-6882-01 COSM4614375 c.2261delA p.N754fs*34 Deletion - Frameshift 9:32542264-32542264 - TCGA-D1-A17M-01 COSM1108183 c.2535C>T p.D845D Substitution - coding silent 9:32541990-32541990 - 325 COSM3723929 c.875G>A p.C292Y Substitution - Missense 9:32543650-32543650 - 587238 COSM1230080 c.1079G>A p.R360Q Substitution - Missense 9:32543446-32543446 - TCGA-EJ-5495-01 COSM1132514 c.2991T>C p.D997D Substitution - coding silent 9:32541534-32541534 - 587228 COSM1230081 c.541C>T p.R181C Substitution - Missense 9:32543984-32543984 - TCGA-EJ-7125-01 COSM3675321 c.2048G>T p.R683L Substitution - Missense 9:32542477-32542477 - TCGA-BS-A0UJ-01 COSM1108184 c.2232T>C p.F744F Substitution - coding silent 9:32542293-32542293 - TCGA-BT-A20J-01 COSM422388 c.331G>C p.D111H Substitution - Missense 9:32544194-32544194 - LS180 COSM2772092 c.2584A>T p.T862S Substitution - Missense 9:32541941-32541941 - TCGA-DZ-6133-01 COSM3996509 c.2708G>C p.R903P Substitution - Missense 9:32541817-32541817 - T2269 COSM4735352 c.2442T>C p.R814R Substitution - coding silent 9:32542083-32542083 - LS180 COSM2772093 c.2564A>G p.H855R Substitution - Missense 9:32541961-32541961 - TCGA-BH-A0EB-01 COSM455821 c.2526C>A p.T842T Substitution - coding silent 9:32541999-32541999 - T3011 COSM4735357 c.723G>A p.T241T Substitution - coding silent 9:32543802-32543802 - STC252 COSM2772091 c.2587C>T p.R863W Substitution - Missense 9:32541938-32541938 - BK0029 COSM4186762 c.2359G>T p.V787L Substitution - Missense 9:32542166-32542166 - TCGA-B5-A11E-01 COSM1108192 c.1200G>T p.E400D Substitution - Missense 9:32543325-32543325 - GC_356T-GC_356N COSM4774606 c.235A>C p.N79H Substitution - Missense 9:32544290-32544290 - HCC2998 COSM1674451 c.779G>A p.R260Q Substitution - Missense 9:32543746-32543746 - ESO-859 COSM1240489 c.2441G>A p.R814H Substitution - Missense 9:32542084-32542084 - TCGA-CC-5260-01 COSM4937423 c.309T>C p.C103C Substitution - coding silent 9:32544216-32544216 - MDA-MB-435 COSM1674450 c.3037A>G p.S1013G Substitution - Missense 9:32541488-32541488 - LS174T COSM4614375 c.2261delA p.N754fs*34 Deletion - Frameshift 9:32542264-32542264 - CSCC-6-T COSM4539924 c.2758G>C p.V920L Substitution - Missense 9:32541767-32541767 - MN-47 COSM1578598 c.1149A>T p.E383D Substitution - Missense 9:32543376-32543376 - EGC15 COSM5063883 c.2819delT p.L940fs*13 Deletion - Frameshift 9:32541706-32541706 - TCGA-34-5928-01 COSM753655 c.1334C>T p.S445L Substitution - Missense 9:32543191-32543191 - TCGA-25-1321-01 COSM79079 c.2422G>T p.E808* Substitution - Nonsense 9:32542103-32542103 - TCGA-AA-3966-01 COSM273371 c.1364C>T p.T455M Substitution - Missense 9:32543161-32543161 - TCGA-D3-A2JF-06 COSM3656822 c.1348G>A p.V450I Substitution - Missense 9:32543177-32543177 - PT35 COSM5912974 c.640G>T p.E214* Substitution - Nonsense 9:32543885-32543885 - TCGA-EL-A3ZH-01 COSM3375226 c.3088C>T p.R1030W Substitution - Missense 9:32541437-32541437 - TCGA-A3-3346-01 COSM1497079 c.2646T>A p.H882Q Substitution - Missense 9:32541879-32541879 - LS180 COSM4614375 c.2261delA p.N754fs*34 Deletion - Frameshift 9:32542264-32542264 - TCGA-AP-A0LM-01 COSM1108194 c.1012T>C p.S338P Substitution - Missense 9:32543513-32543513 - TCGA-Q1-A73O-01 COSM4834579 c.2156C>T p.S719F Substitution - Missense 9:32542369-32542369 - BZ28 COSM5758815 c.3019G>A p.D1007N Substitution - Missense 9:32541506-32541506 - 587222 COSM1230082 c.1469G>T p.R490M Substitution - Missense 9:32543056-32543056 - RK050_C01 COSM1636153 c.1596C>T p.C532C Substitution - coding silent 9:32542929-32542929 - B23-Tumor COSM1756123 c.2536A>T p.S846C Substitution - Missense 9:32541989-32541989 - ESO-161 COSM1268317 c.2871T>G p.A957A Substitution - coding silent 9:32541654-32541654 - TCGA-CK-5916-01 COSM3699651 c.621G>A p.P207P Substitution - coding silent 9:32543904-32543904 - GC_315T-GC_315N COSM4773821 c.751C>G p.Q251E Substitution - Missense 9:32543774-32543774 - TCGA-GN-A266-06 COSM3656823 c.858C>T p.F286F Substitution - coding silent 9:32543667-32543667 - TCGA-EJ-7317-01 COSM1472152 c.591T>G p.G197G Substitution - coding silent 9:32543934-32543934 - 01-P034 COSM4588767 c.2810A>G p.N937S Substitution - Missense 9:32541715-32541715 - TCGA-B5-A0JY-01 COSM1108185 c.2015C>A p.S672Y Substitution - Missense 9:32542510-32542510 - TCGA-66-2793-01 COSM753654 c.791G>T p.R264L Substitution - Missense 9:32543734-32543734 - TCGA-AA-3977-01 COSM5120107 c.509C>A p.S170Y Substitution - Missense 9:32544016-32544016 - CHC1751T COSM4802326 c.237C>A p.N79K Substitution - Missense 9:32544288-32544288 - CCK81 COSM2772095 c.2281T>C p.Y761H Substitution - Missense 9:32542244-32542244 - S02273 COSM5682284 c.29C>T p.P10L Substitution - Missense 9:32550943-32550943 - TCGA-18-3406-01 COSM753658 c.2017C>A p.R673S Substitution - Missense 9:32542508-32542508 - LC_C21 COSM1187697 c.3061G>T p.E1021* Substitution - Nonsense 9:32541464-32541464 - T3262 COSM4735355 c.1502C>A p.S501Y Substitution - Missense 9:32543023-32543023 - TCGA-AA-A010-01 COSM285870 c.2148C>T p.Y716Y Substitution - coding silent 9:32542377-32542377 - CSCC-40-T COSM4499164 c.535C>T p.R179C Substitution - Missense 9:32543990-32543990 - TCGA-BS-A0UF-01 COSM1108199 c.365A>C p.K122T Substitution - Missense 9:32544160-32544160 - CSCC-56-T COSM4531797 c.1826G>A p.G609E Substitution - Missense 9:32542699-32542699 - LUAD-S01409 COSM346954 c.1806A>T p.S602S Substitution - coding silent 9:32542719-32542719 - HCC152T COSM1108181 c.2989G>A p.D997N Substitution - Missense 9:32541536-32541536 - YUKRIN COSM1701028 c.2942C>T p.T981I Substitution - Missense 9:32541583-32541583 - CSCC-56-T COSM4569824 c.2075T>C p.L692S Substitution - Missense 9:32542450-32542450 - HCC003T COSM5819607 c.11A>T p.Q4L Substitution - Missense 9:32550961-32550961 - TCGA-61-2008-01 COSM73046 c.554C>A p.T185K Substitution - Missense 9:32543971-32543971 - TCGA-CG-4306-01 COSM3906823 c.2047C>T p.R683W Substitution - Missense 9:32542478-32542478 - TCGA-NH-A5IV-01 COSM5184457 c.2386C>T p.R796* Substitution - Nonsense 9:32542139-32542139 - TCGA-AA-3662-01 COSM3763883 c.74C>G p.S25W Substitution - Missense 9:32550898-32550898 - 12M COSM5577811 c.892C>T p.P298S Substitution - Missense 9:32543633-32543633 - TCGA-BR-4362-01 COSM3906826 c.570T>C p.A190A Substitution - coding silent 9:32543955-32543955 - HCT8 COSM2772089 c.2784T>C p.N928N Substitution - coding silent 9:32541741-32541741 - TCGA-B5-A0JY-01 COSM1108190 c.1477G>T p.E493* Substitution - Nonsense 9:32543048-32543048 - TCGA-BS-A0UV-01 COSM1108186 c.1872G>T p.M624I Substitution - Missense 9:32542653-32542653 - TCGA-AG-3892-01 COSM258231 c.1997G>A p.S666N Substitution - Missense 9:32542528-32542528 - TCGA-DD-A73C-01 COSM4916734 c.581C>G p.S194* Substitution - Nonsense 9:32543944-32543944 - ccRCC-5 COSM1664635 c.687G>C p.Q229H Substitution - Missense 9:32543838-32543838 - TCGA-39-5030-01 COSM753657 c.1839G>T p.K613N Substitution - Missense 9:32542686-32542686 - TCGA-AD-A5EJ-01 COSM5134057 c.380G>A p.C127Y Substitution - Missense 9:32544145-32544145 - YUFIT COSM5410980 c.2229C>T p.S743S Substitution - coding silent 9:32542296-32542296 - CHC892T COSM4960865 c.1226C>T p.A409V Substitution - Missense 9:32543299-32543299 - LUAD-D01603 COSM338109 c.2589G>T p.R863R Substitution - coding silent 9:32541936-32541936 - TCGA-37-4141-01 COSM753661 c.3035C>T p.P1012L Substitution - Missense 9:32541490-32541490 - H650 COSM1194379 c.2757A>T p.E919D Substitution - Missense 9:32541768-32541768 - TCGA-GV-A3QI-01 COSM1314752 c.456G>A p.V152V Substitution - coding silent 9:32544069-32544069 - CN-AML-NR-08-Dx COSM5425629 c.2988C>T p.L996L Substitution - coding silent 9:32541537-32541537 - 2293784 COSM4609594 c.1676A>G p.K559R Substitution - Missense 9:32542849-32542849 - TCGA-HU-A4GN-01 COSM3906827 c.517A>G p.T173A Substitution - Missense 9:32544008-32544008 - CHC892T COSM4796149 c.2139G>A p.R713R Substitution - coding silent 9:32542386-32542386 - sysucc-311T COSM5467675 c.1321A>G p.T441A Substitution - Missense 9:32543204-32543204 - RK167_C01 COSM1636154 c.442A>G p.I148V Substitution - Missense 9:32544083-32544083 - 2521243 COSM5886648 c.352C>T p.R118C Substitution - Missense 9:32544173-32544173 - TCGA-AF-A56L-01 COSM5066340 c.1396G>A p.D466N Substitution - Missense 9:32543129-32543129 - TCGA-AA-3672-01 COSM1461987 c.401delA p.N134fs*19 Deletion - Frameshift 9:32544124-32544124 - TCGA-13-0755-01 COSM1461990 c.382G>A p.V128I Substitution - Missense 9:32544143-32544143 - TCGA-EE-A2GM-06 COSM3656824 c.278T>A p.V93E Substitution - Missense 9:32544247-32544247 - SNU-175 COSM2772119 c.1047G>A p.E349E Substitution - coding silent 9:32543478-32543478 - pfg143T COSM4752302 c.904C>T p.R302C Substitution - Missense 9:32543621-32543621 - TCGA-AY-6197-01 COSM1461987 c.401delA p.N134fs*19 Deletion - Frameshift 9:32544124-32544124 - TCGA-UB-A7MF-01 COSM4918904 c.186G>A p.P62P Substitution - coding silent 9:32550786-32550786 - I2L-P7-Tumor-Organoid COSM1230080 c.1079G>A p.R360Q Substitution - Missense 9:32543446-32543446 - pfg019T COSM1643808 c.1952G>T p.S651I Substitution - Missense 9:32542573-32542573 - TCGA-BT-A20J-01 COSM422389 c.1502C>T p.S501F Substitution - Missense 9:32543023-32543023 - TCGA-D1-A17Q-01 COSM1108188 c.1808G>A p.R603H Substitution - Missense 9:32542717-32542717 - RK050_C COSM1636153 c.1596C>T p.C532C Substitution - coding silent 9:32542929-32542929 - TCGA-CJ-4644-01 COSM1137988 c.2048G>A p.R683Q Substitution - Missense 9:32542477-32542477 - TCGA-A3-3320-01 COSM1497078 c.2637T>A p.T879T Substitution - coding silent 9:32541888-32541888 - LUAD-RT-S01813 COSM383591 c.2996G>T p.R999I Substitution - Missense 9:32541529-32541529 - 587222 COSM1230083 c.563G>A p.R188Q Substitution - Missense 9:32543962-32543962 - LS174T COSM2772092 c.2584A>T p.T862S Substitution - Missense 9:32541941-32541941 - TCGA-AG-A014-01 COSM265303 c.1119T>G p.N373K Substitution - Missense 9:32543406-32543406 - TCGA-BL-A0C8-01 COSM422387 c.286G>A p.D96N Substitution - Missense 9:32544239-32544239 - TCGA-AN-A0AJ-01 COSM455824 c.436G>C p.D146H Substitution - Missense 9:32544089-32544089 - ESCC_41 COSM5629627 c.1325C>A p.S442Y Substitution - Missense 9:32543200-32543200 - HCT15 COSM2772089 c.2784T>C p.N928N Substitution - coding silent 9:32541741-32541741 - TCGA-GD-A3OQ-01 COSM1314750 c.1282T>G p.S428A Substitution - Missense 9:32543243-32543243 - T368 COSM1288575 c.377G>A p.R126H Substitution - Missense 9:32544148-32544148 - WA28 COSM238338 c.2463G>A p.K821K Substitution - coding silent 9:32542062-32542062 - HCC2998 COSM1674451 c.779G>A p.R260Q Substitution - Missense 9:32543746-32543746 - cSCCP6 COSM136707 c.1039C>T p.R347* Substitution - Nonsense 9:32543486-32543486 - TCGA-B0-5701-01 COSM487363 c.2103A>G p.K701K Substitution - coding silent 9:32542422-32542422 - CHC1751T COSM4802326 c.237C>A p.N79K Substitution - Missense 9:32544288-32544288 - TCGA-BR-8058-01 COSM3906825 c.796G>C p.G266R Substitution - Missense 9:32543729-32543729 - TCGA-MI-A75C-01 COSM4923130 c.887T>C p.L296S Substitution - Missense 9:32543638-32543638 - PT25 COSM5904917 c.1123G>A p.D375N Substitution - Missense 9:32543402-32543402 - SNUH_G76_S1 COSM4416861 c.1171G>A p.V391I Substitution - Missense 9:32543354-32543354 - S01861 COSM5671474 c.2883G>C p.V961V Substitution - coding silent 9:32541642-32541642 - CHC892T COSM4960865 c.1226C>T p.A409V Substitution - Missense 9:32543299-32543299 - TCGA-B0-4818-01 COSM487364 c.848C>T p.A283V Substitution - Missense 9:32543677-32543677 - TCGA-AP-A051-01 COSM1108195 c.935G>A p.G312E Substitution - Missense 9:32543590-32543590 - STC252 COSM1108188 c.1808G>A p.R603H Substitution - Missense 9:32542717-32542717 - Gp2D COSM4628871 c.2356C>G p.R786G Substitution - Missense 9:32542169-32542169 - TCGA-EB-A44P-01 COSM3656821 c.2749G>A p.D917N Substitution - Missense 9:32541776-32541776 - TCGA-AA-A00N-01 COSM277764 c.2060G>T p.R687I Substitution - Missense 9:32542465-32542465 - CHC892T COSM4796149 c.2139G>A p.R713R Substitution - coding silent 9:32542386-32542386 - TCGA-AD-A5EJ-01 COSM5134058 c.282A>G p.P94P Substitution - coding silent 9:32544243-32544243 - TCGA-DZ-6135-01 COSM3996511 c.1253A>G p.D418G Substitution - Missense 9:32543272-32543272 - TCGA-AA-A024-01 COSM287393 c.1039C>T p.R347* Substitution - Nonsense 9:32543486-32543486 - TCGA-22-1012-01 COSM753660 c.2972C>T p.S991L Substitution - Missense 9:32541553-32541553 - TCGA-AB-2813-03 COSM1319611 c.177G>T p.R59S Substitution - Missense 9:32550795-32550795 - TCGA-DM-A28F-01 COSM1461982 c.2489C>T p.S830L Substitution - Missense 9:32542036-32542036 - TCGA-B0-4810-01 COSM487362 c.2504A>G p.N835S Substitution - Missense 9:32542021-32542021 - TCGA-AP-A051-01 COSM1108197 c.616C>T p.P206S Substitution - Missense 9:32543909-32543909 - TCGA-DK-A2I4-01 COSM3779940 c.3025G>A p.E1009K Substitution - Missense 9:32541500-32541500 - SNU-175 COSM2772084 c.3121G>T p.D1041Y Substitution - Missense 9:32541404-32541404 - TCGA-D1-A103-01 COSM1108196 c.670G>T p.D224Y Substitution - Missense 9:32543855-32543855 - TCGA-DA-A1IA-06 COSM1701028 c.2942C>T p.T981I Substitution - Missense 9:32541583-32541583 - ESO-0459 COSM1268316 c.2410G>C p.E804Q Substitution - Missense 9:32542115-32542115 - TCGA-A3-3316-01 COSM1497078 c.2637T>A p.T879T Substitution - coding silent 9:32541888-32541888 - TCGA-BR-6852-01 COSM3906828 c.183G>A p.A61A Substitution - coding silent 9:32550789-32550789 - DLD1 COSM2772089 c.2784T>C p.N928N Substitution - coding silent 9:32541741-32541741 - T3091 COSM4735356 c.1297G>A p.V433I Substitution - Missense 9:32543228-32543228 - TARGET-30-PATDXC COSM1288575 c.377G>A p.R126H Substitution - Missense 9:32544148-32544148 - T263 COSM4735353 c.1944T>C p.T648T Substitution - coding silent 9:32542581-32542581 - TCGA-PJ-A5Z9-01 COSM3996510 c.2591G>A p.S864N Substitution - Missense 9:32541934-32541934 - PD18037a COSM5773855 c.878T>G p.L293R Substitution - Missense 9:32543647-32543647 - MZ7-mel COSM25350 c.2766G>A p.E922E Substitution - coding silent 9:32541759-32541759 - BD223T COSM1461987 c.401delA p.N134fs*19 Deletion - Frameshift 9:32544124-32544124 - TCGA-EK-A2RK-01 COSM4829001 c.1700C>G p.S567* Substitution - Nonsense 9:32542825-32542825 - TCGA-CD-A48A-01 COSM3906824 c.1582G>A p.D528N Substitution - Missense 9:32542943-32542943 - TCGA-AP-A059-01 COSM1108189 c.1650T>C p.C550C Substitution - coding silent 9:32542875-32542875 - TCGA-BL-A0C8-01 COSM422386 c.284C>T p.A95V Substitution - Missense 9:32544241-32544241 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.589962 9p21 609507

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C Missense p.N373K c.1119T>G 9 32543404 COREAD A C Missense p.S428A c.1282T>G 9 32543241 BLCA A C Synonymous p.A957A c.2871T>G 9 32541652 ESCA A C Synonymous p.G197G c.591T>G 9 32543932 PRAD AG - Frameshift p.F123Lfs*14 c.369_370delCT 9 32544153 PRAD A G Missense p.S830P c.2488T>C 9 32542035 COREAD A T Missense p.V93E c.278T>A 9 32544245 CM C A Missense p.G715W c.2143G>T 9 32542380 LUAD C A Missense p.K613N c.1839G>T 9 32542684 LUSC C A Missense p.R264L c.791G>T 9 32543732 LUSC C A Missense p.S651I c.1952G>T 9 32542571 STAD C A Nonsense p.E808* c.2422G>T 9 32542101 OV C A Synonymous p.T455T c.1365G>T 9 32543158 LUSC C G Missense p.D111H c.331G>C 9 32544192 BLCA C G Missense p.D146H c.436G>C 9 32544087 BRCA C G Missense p.D470H c.1408G>C 9 32543115 LUAD C G Missense p.E804Q c.2410G>C 9 32542113 ESCA C G Missense p.V93L c.277G>C 9 32544246 LUAD C T Missense p.D175N c.523G>A 9 32544000 BLCA C T Missense p.D96N c.286G>A 9 32544237 BLCA C T Missense p.D997N c.2989G>A 9 32541534 UCEC C T Missense p.E1009K c.3025G>A 9 32541498 BLCA C T Missense p.R126H c.377G>A 9 32544146 NB C T Missense p.R640K c.1919G>A 9 32542604 HNSC C T Missense p.R801Q c.2402G>A 9 32542121 STAD C T Missense p.R814H c.2441G>A 9 32542082 ESCA C T Missense p.V128I c.382G>A 9 32544141 OV C T Missense p.V450I c.1348G>A 9 32543175 CM C T Synonymous p.A61A c.183G>A 9 32550787 STAD C T Synonymous p.G620G c.1860G>A 9 32542663 UCEC C T Synonymous p.V152V c.456G>A 9 32544067 BLCA G A Missense p.A283V c.848C>T 9 32543675 RCCC G A Missense p.A95V c.284C>T 9 32544239 BLCA G A Missense p.H729Y c.2185C>T 9 32542338 HNSC G A Missense p.P1012L c.3035C>T 9 32541488 LUSC G A Missense p.P986S c.2956C>T 9 32541567 LUSC G A Missense p.R683W c.2047C>T 9 32542476 STAD G A Missense p.S282L c.845C>T 9 32543678 BRCA G A Missense p.S445L c.1334C>T 9 32543189 LUSC G A Missense p.S501F c.1502C>T 9 32543021 BLCA G A Missense p.S829L c.2486C>T 9 32542037 CM G A Missense p.S918F c.2753C>T 9 32541770 HNSC G A Missense p.S991L c.2972C>T 9 32541551 LUSC G A Missense p.T981I c.2942C>T 9 32541581 CM G A Nonsense p.R347* c.1039C>T 9 32543484 COREAD G A Synonymous p.C532C c.1596C>T 9 32542927 HC G A Synonymous p.D465D c.1395C>T 9 32543128 UCEC G A Synonymous p.D845D c.2535C>T 9 32541988 UCEC G A Synonymous p.I322I c.966C>T 9 32543557 CM G A Synonymous p.S743S c.2229C>T 9 32542294 CM G C Missense p.L1038V c.3112C>G 9 32541411 STAD G T Missense p.P198H c.593C>A 9 32543930 UCEC G T Missense p.R181S c.541C>A 9 32543982 PRAD G T Missense p.R673S c.2017C>A 9 32542506 LUSC G T Missense p.T185K c.554C>A 9 32543969 OV G T Synonymous p.T842T c.2526C>A 9 32541997 BRCA T A Missense p.K964M c.2891A>T 9 32541632 HNSC T A Missense p.R238W c.712A>T 9 32543811 LUAD T C Missense p.I352M c.1056A>G 9 32543467 GBM T C Missense p.I955M c.2865A>G 9 32541658 LUAD