Mutation - TCGA Type Chromosome Start Position End Position Strand Variant Classification Variant Type Reference Allele Tumor_seq Allele 1 Tumor_seq Allele 2 Tumor Sample Barcode Matched Norm Sample Barcode Genome Change cDNA Change Codon Change Protein Change ACC 9 32487537 32487537 + Missense_Mutation SNP G G T TCGA-OR-A5JP-01A-11D-A29I-10 TCGA-OR-A5JP-10A-01D-A29L-10 g.chr9:32487537G>T c.1307C>A c.(1306-1308)gCg>gAg p.A436E BLCA 9 32457121 32457121 + Nonstop_Mutation SNP C C G TCGA-XF-AAN3-01A-11D-A42E-08 TCGA-XF-AAN3-10A-01D-A42H-08 g.chr9:32457121C>G c.2777G>C c.(2776-2778)tGa>tCa p.*926S BLCA 9 32466325 32466325 + Missense_Mutation SNP C C T TCGA-BT-A3PK-01A-21D-A21Z-08 TCGA-BT-A3PK-10A-01D-A21Z-08 g.chr9:32466325C>T c.2300G>A c.(2299-2301)cGc>cAc p.R767H BLCA 9 32485206 32485206 + Missense_Mutation SNP C C G TCGA-LT-A5Z6-01A-11D-A289-08 TCGA-LT-A5Z6-10A-01D-A289-08 g.chr9:32485206C>G c.1447G>C c.(1447-1449)Gag>Cag p.E483Q BLCA 9 32487490 32487493 + Frame_Shift_Del DEL CTTG CTTG - TCGA-G2-A3IE-01A-11D-A20D-08 TCGA-G2-A3IE-10A-01D-A20D-08 g.chr9:32487490_32487493delCTTG c.1351_1354delCAAG c.(1351-1356)caagttfs p.QV451fs BLCA 9 32488167 32488167 + Missense_Mutation SNP C C G TCGA-XF-A9T8-01A-11D-A391-08 TCGA-XF-A9T8-10A-01D-A394-08 g.chr9:32488167C>G c.988G>C c.(988-990)Gag>Cag p.E330Q BLCA 9 32489410 32489410 + Missense_Mutation SNP C C T TCGA-G2-AA3C-01A-21D-A391-08 TCGA-G2-AA3C-10A-01D-A394-08 g.chr9:32489410C>T c.731G>A c.(730-732)aGa>aAa p.R244K BLCA 9 32492516 32492516 + Missense_Mutation SNP C C T TCGA-DK-AA6L-01A-11D-A391-08 TCGA-DK-AA6L-10A-01D-A394-08 g.chr9:32492516C>T c.444G>A c.(442-444)atG>atA p.M148I BLCA 9 32500809 32500809 + Missense_Mutation SNP G G A TCGA-GD-A3OP-01A-21D-A21Z-08 TCGA-GD-A3OP-10A-01D-A21Z-08 g.chr9:32500809G>A c.235C>T c.(235-237)Cat>Tat p.H79Y BRCA 9 32459494 32459494 + Missense_Mutation SNP G G A TCGA-A2-A25D-01A-12D-A16D-09 TCGA-A2-A25D-10A-01D-A16D-09 g.chr9:32459494G>A c.2356C>T c.(2356-2358)Cat>Tat p.H786Y BRCA 9 32466374 32466374 + Missense_Mutation SNP C C T TCGA-AC-A2QI-01A-12D-A19Y-09 TCGA-AC-A2QI-10A-01D-A19Y-09 g.chr9:32466374C>T c.2251G>A c.(2251-2253)Gaa>Aaa p.E751K BRCA 9 32481365 32481365 + Silent SNP G G C TCGA-AN-A0FT-01A-11W-A050-09 TCGA-AN-A0FT-10A-01W-A055-09 g.chr9:32481365G>C c.1611C>G c.(1609-1611)gcC>gcG p.A537A BRCA 9 32481395 32481395 + Silent SNP G G A TCGA-AN-A0FT-01A-11W-A050-09 TCGA-AN-A0FT-10A-01W-A055-09 g.chr9:32481395G>A c.1581C>T c.(1579-1581)gaC>gaT p.D527D BRCA 9 32487531 32487531 + Missense_Mutation SNP A A G TCGA-D8-A1XK-01A-21D-A14K-09 TCGA-D8-A1XK-10A-01D-A14K-09 g.chr9:32487531A>G c.1313T>C c.(1312-1314)gTg>gCg p.V438A BRCA 9 32491384 32491384 + Silent SNP A A G TCGA-C8-A12P-01A-11D-A10Y-09 TCGA-C8-A12P-10A-01D-A110-09 g.chr9:32491384A>G c.606T>C c.(604-606)gaT>gaC p.D202D BRCA 9 32492507 32492507 + Silent SNP A A C TCGA-A8-A0A6-01A-12W-A071-09 TCGA-A8-A0A6-10A-01W-A071-09 g.chr9:32492507A>C c.453T>G c.(451-453)ggT>ggG p.G151G CESC 9 32485206 32485206 + Missense_Mutation SNP C C T TCGA-JW-A5VJ-01A-11D-A28B-09 TCGA-JW-A5VJ-10A-01D-A28E-09 g.chr9:32485206C>T c.1447G>A c.(1447-1449)Gag>Aag p.E483K COAD 9 32457200 32457200 + Missense_Mutation SNP C C T TCGA-D5-5539-01A-01D-1650-10 TCGA-D5-5539-10A-01D-1650-10 g.chr9:32457200C>T c.2698G>A c.(2698-2700)Gga>Aga p.G900R COAD 9 32457301 32457301 + Missense_Mutation SNP C C T TCGA-AA-A01P-01A-21W-A096-10 TCGA-AA-A01P-11A-11W-A096-10 g.chr9:32457301C>T c.2597G>A c.(2596-2598)cGa>cAa p.R866Q COAD 9 32459462 32459462 + Frame_Shift_Del DEL T T - TCGA-A6-3809-01A-01W-0995-10 TCGA-A6-3809-11A-01W-0995-10 g.chr9:32459462delT c.2388delA c.(2386-2388)aaafs p.K796fs COAD 9 32466436 32466436 + Missense_Mutation SNP C C G TCGA-AZ-6605-01A-11D-1835-10 TCGA-AZ-6605-11A-01D-1835-10 g.chr9:32466436C>G c.2189G>C c.(2188-2190)aGa>aCa p.R730T COAD 9 32480254 32480254 + Silent SNP G G A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr9:32480254G>A c.1737C>T c.(1735-1737)ttC>ttT p.F579F COAD 9 32480268 32480268 + Nonsense_Mutation SNP G G A TCGA-AA-3952-01A-01W-0995-10 TCGA-AA-3952-10A-01W-0995-10 g.chr9:32480268G>A c.1723C>T c.(1723-1725)Cga>Tga p.R575* COAD 9 32481340 32481340 + Missense_Mutation SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr9:32481340G>A c.1636C>T c.(1636-1638)Cgg>Tgg p.R546W COAD 9 32485255 32485255 + Silent SNP C C A TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chr9:32485255C>A c.1398G>T c.(1396-1398)cgG>cgT p.R466R COAD 9 32487983 32487983 + Missense_Mutation SNP A A T TCGA-D5-6540-01A-11D-1719-10 TCGA-D5-6540-10A-01D-1719-10 g.chr9:32487983A>T c.1172T>A c.(1171-1173)cTa>cAa p.L391Q COAD 9 32488079 32488079 + Missense_Mutation SNP G G A TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr9:32488079G>A c.1076C>T c.(1075-1077)aCg>aTg p.T359M COAD 9 32488833 32488833 + Frame_Shift_Del DEL T T - TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chr9:32488833delT c.852delA c.(850-852)aaafs p.K284fs COAD 9 32489410 32489410 + Missense_Mutation SNP C C A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr9:32489410C>A c.731G>T c.(730-732)aGa>aTa p.R244I COAD 9 32491320 32491320 + Missense_Mutation SNP C C T TCGA-AA-3982-01A-02W-0995-10 TCGA-AA-3982-10A-01W-0999-10 g.chr9:32491320C>T c.670G>A c.(670-672)Gag>Aag p.E224K COAD 9 32493893 32493893 + Frame_Shift_Del DEL T T - TCGA-CK-5913-01A-11D-1650-10 TCGA-CK-5913-10A-01D-1650-10 g.chr9:32493893delT c.289delA c.(289-291)attfs p.I97fs COAD 9 32526077 32526077 + Missense_Mutation SNP C C T TCGA-AA-3525-01A-02W-0833-10 TCGA-AA-3525-10A-01W-0833-10 g.chr9:32526077C>T c.88G>A c.(88-90)Gcc>Acc p.A30T COADREAD 9 32457200 32457200 + Missense_Mutation SNP C C T TCGA-D5-5539-01A-01D-1650-10 TCGA-D5-5539-10A-01D-1650-10 g.chr9:32457200C>T c.2698G>A c.(2698-2700)Gga>Aga p.G900R COADREAD 9 32457301 32457301 + Missense_Mutation SNP C C T TCGA-AA-A01P-01A-21W-A096-10 TCGA-AA-A01P-11A-11W-A096-10 g.chr9:32457301C>T c.2597G>A c.(2596-2598)cGa>cAa p.R866Q COADREAD 9 32457312 32457312 + Missense_Mutation SNP T T C TCGA-AG-3593-01A-01W-0831-10 TCGA-AG-3593-10A-01W-0831-10 g.chr9:32457312T>C c.2586A>G c.(2584-2586)atA>atG p.I862M COADREAD 9 32459462 32459462 + Frame_Shift_Del DEL T T - TCGA-A6-3809-01A-01W-0995-10 TCGA-A6-3809-11A-01W-0995-10 g.chr9:32459462delT c.2388delA c.(2386-2388)aaafs p.K796fs COADREAD 9 32466353 32466353 + Nonsense_Mutation SNP C C A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr9:32466353C>A c.2272G>T c.(2272-2274)Gaa>Taa p.E758* COADREAD 9 32466436 32466436 + Missense_Mutation SNP C C G TCGA-AZ-6605-01A-11D-1835-10 TCGA-AZ-6605-11A-01D-1835-10 g.chr9:32466436C>G c.2189G>C c.(2188-2190)aGa>aCa p.R730T COADREAD 9 32480254 32480254 + Silent SNP G G A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr9:32480254G>A c.1737C>T c.(1735-1737)ttC>ttT p.F579F COADREAD 9 32480268 32480268 + Nonsense_Mutation SNP G G A TCGA-AA-3952-01A-01W-0995-10 TCGA-AA-3952-10A-01W-0995-10 g.chr9:32480268G>A c.1723C>T c.(1723-1725)Cga>Tga p.R575* COADREAD 9 32481340 32481340 + Missense_Mutation SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr9:32481340G>A c.1636C>T c.(1636-1638)Cgg>Tgg p.R546W COADREAD 9 32485255 32485255 + Silent SNP C C A TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chr9:32485255C>A c.1398G>T c.(1396-1398)cgG>cgT p.R466R COADREAD 9 32487983 32487983 + Missense_Mutation SNP A A T TCGA-D5-6540-01A-11D-1719-10 TCGA-D5-6540-10A-01D-1719-10 g.chr9:32487983A>T c.1172T>A c.(1171-1173)cTa>cAa p.L391Q COADREAD 9 32488079 32488079 + Missense_Mutation SNP G G A TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr9:32488079G>A c.1076C>T c.(1075-1077)aCg>aTg p.T359M COADREAD 9 32488833 32488833 + Frame_Shift_Del DEL T T - TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chr9:32488833delT c.852delA c.(850-852)aaafs p.K284fs COADREAD 9 32489410 32489410 + Missense_Mutation SNP C C A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr9:32489410C>A c.731G>T c.(730-732)aGa>aTa p.R244I COADREAD 9 32491320 32491320 + Missense_Mutation SNP C C T TCGA-AA-3982-01A-02W-0995-10 TCGA-AA-3982-10A-01W-0999-10 g.chr9:32491320C>T c.670G>A c.(670-672)Gag>Aag p.E224K COADREAD 9 32493818 32493818 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr9:32493818C>T c.364G>A c.(364-366)Gat>Aat p.D122N COADREAD 9 32493893 32493893 + Frame_Shift_Del DEL T T - TCGA-CK-5913-01A-11D-1650-10 TCGA-CK-5913-10A-01D-1650-10 g.chr9:32493893delT c.289delA c.(289-291)attfs p.I97fs COADREAD 9 32493914 32493914 + Missense_Mutation SNP C C T TCGA-CI-6622-01A-11D-1826-10 TCGA-CI-6622-10A-01D-1826-10 g.chr9:32493914C>T c.268G>A c.(268-270)Gaa>Aaa p.E90K COADREAD 9 32526077 32526077 + Missense_Mutation SNP C C T TCGA-AA-3525-01A-02W-0833-10 TCGA-AA-3525-10A-01W-0833-10 g.chr9:32526077C>T c.88G>A c.(88-90)Gcc>Acc p.A30T DLBC 9 32457307 32457308 + Frame_Shift_Ins INS - - AGAA TCGA-G8-6914-01A-11D-2210-10 TCGA-G8-6914-14A-01D-2210-10 g.chr9:32457307_32457308insAGAA c.2590_2591insTTCT c.(2590-2592)tgtfs p.C864fs DLBC 9 32481339 32481339 + Splice_Site SNP C C T TCGA-G8-6914-01A-11D-2210-10 TCGA-G8-6914-14A-01D-2210-10 g.chr9:32481339C>T c.1637G>A c.(1636-1638)cGg>cAg p.R546Q DLBC 9 32492529 32492529 + Missense_Mutation SNP G G A TCGA-G8-6324-01A-11D-2210-10 TCGA-G8-6324-10A-01D-2210-10 g.chr9:32492529G>A c.431C>T c.(430-432)tCt>tTt p.S144F ESCA 9 32457349 32457349 + Missense_Mutation SNP G G T TCGA-R6-A8W5-01B-11D-A37C-09 TCGA-R6-A8W5-10A-01D-A37F-09 g.chr9:32457349G>T c.2549C>A c.(2548-2550)cCa>cAa p.P850Q ESCA 9 32459470 32459470 + Nonsense_Mutation SNP G G A TCGA-S8-A6BW-01A-11D-A31U-09 TCGA-S8-A6BW-10A-01D-A31U-09 g.chr9:32459470G>A c.2380C>T c.(2380-2382)Caa>Taa p.Q794* ESCA 9 32467918 32467918 + Missense_Mutation SNP G G T TCGA-L5-A4OH-01A-11D-A27G-09 TCGA-L5-A4OH-11A-11D-A27G-09 g.chr9:32467918G>T c.2027C>A c.(2026-2028)cCg>cAg p.P676Q HNSC 9 32472994 32472994 + Missense_Mutation SNP C C T TCGA-CV-A45O-01A-21D-A24D-08 TCGA-CV-A45O-10A-01D-A24F-08 g.chr9:32472994C>T c.1993G>A c.(1993-1995)Ggc>Agc p.G665S HNSC 9 32488812 32488812 + Silent SNP C C T TCGA-D6-6517-01A-11D-1870-08 TCGA-D6-6517-10A-01D-1870-08 g.chr9:32488812C>T c.873G>A c.(871-873)ggG>ggA p.G291G HNSC 9 32493813 32493813 + Silent SNP G G A TCGA-CR-7365-01A-11D-2012-08 TCGA-CR-7365-10A-01D-2013-08 g.chr9:32493813G>A c.369C>T c.(367-369)atC>atT p.I123I HNSC 9 32493895 32493895 + Missense_Mutation SNP T T G TCGA-CV-7245-01A-11D-2012-08 TCGA-CV-7245-10A-01D-2013-08 g.chr9:32493895T>G c.287A>C c.(286-288)aAa>aCa p.K96T HNSC 9 32500912 32500912 + Missense_Mutation SNP C C A TCGA-CN-4723-01A-01D-1434-08 TCGA-CN-4723-10A-01D-1434-08 g.chr9:32500912C>A c.132G>T c.(130-132)gaG>gaT p.E44D KIPAN 9 32459420 32459420 + Nonsense_Mutation SNP G G T TCGA-GL-A59R-01A-11D-A26P-10 TCGA-GL-A59R-10A-01D-A26P-10 g.chr9:32459420G>T c.2430C>A c.(2428-2430)tgC>tgA p.C810* KIPAN 9 32466289 32466289 + Splice_Site DEL T T - TCGA-2Z-A9J3-01A-12D-A382-10 TCGA-2Z-A9J3-10A-01D-A385-10 g.chr9:32466289delT c.2336delA c.(2335-2337)aag>ag p.K779fs KIPAN 9 32467853 32467868 + Frame_Shift_Del DEL AGGTGGCAATCAGAAT AGGTGGCAATCAGAAT - TCGA-A4-8517-01A-11D-2396-08 TCGA-A4-8517-10A-01D-2396-08 g.chr9:32467853_32467868delAGGTGGCAATCAGAAT c.2077_2092delATTCTGATTGCCACCT c.(2077-2094)attctgattgccacctcafs p.ILIATS693fs KIPAN 9 32467857 32467857 + Silent SNP G G A TCGA-5P-A9JY-01A-11D-A42J-10 TCGA-5P-A9JY-10A-01D-A42M-10 g.chr9:32467857G>A c.2088C>T c.(2086-2088)gcC>gcT p.A696A KIPAN 9 32480246 32480246 + Missense_Mutation SNP A A T TCGA-B8-5164-01A-01D-1421-08 TCGA-B8-5164-10A-01D-1421-08 g.chr9:32480246A>T c.1745T>A c.(1744-1746)aTt>aAt p.I582N KIPAN 9 32488009 32488009 + Silent SNP C C T TCGA-BP-5185-01A-01D-1429-08 TCGA-BP-5185-11A-01D-1429-08 g.chr9:32488009C>T c.1146G>A c.(1144-1146)ccG>ccA p.P382P KIRC 9 32480246 32480246 + Missense_Mutation SNP A A T TCGA-B8-5164-01A-01D-1421-08 TCGA-B8-5164-10A-01D-1421-08 g.chr9:32480246A>T c.1745T>A c.(1744-1746)aTt>aAt p.I582N KIRC 9 32488009 32488009 + Silent SNP C C T TCGA-BP-5185-01A-01D-1429-08 TCGA-BP-5185-11A-01D-1429-08 g.chr9:32488009C>T c.1146G>A c.(1144-1146)ccG>ccA p.P382P KIRP 9 32459420 32459420 + Nonsense_Mutation SNP G G T TCGA-GL-A59R-01A-11D-A26P-10 TCGA-GL-A59R-10A-01D-A26P-10 g.chr9:32459420G>T c.2430C>A c.(2428-2430)tgC>tgA p.C810* KIRP 9 32466289 32466289 + Splice_Site DEL T T - TCGA-2Z-A9J3-01A-12D-A382-10 TCGA-2Z-A9J3-10A-01D-A385-10 g.chr9:32466289delT c.2336delA c.(2335-2337)aag>ag p.K779fs KIRP 9 32467853 32467868 + Frame_Shift_Del DEL AGGTGGCAATCAGAAT AGGTGGCAATCAGAAT - TCGA-A4-8517-01A-11D-2396-08 TCGA-A4-8517-10A-01D-2396-08 g.chr9:32467853_32467868delAGGTGGCAATCAGAAT c.2077_2092delATTCTGATTGCCACCT c.(2077-2094)attctgattgccacctcafs p.ILIATS693fs KIRP 9 32467857 32467857 + Silent SNP G G A TCGA-5P-A9JY-01A-11D-A42J-10 TCGA-5P-A9JY-10A-01D-A42M-10 g.chr9:32467857G>A c.2088C>T c.(2086-2088)gcC>gcT p.A696A LIHC 9 32457126 32457126 + Silent SNP G G T TCGA-DD-AACH-01A-11D-A40R-10 TCGA-DD-AACH-10A-01D-A40U-10 g.chr9:32457126G>T c.2772C>A c.(2770-2772)tcC>tcA p.S924S LIHC 9 32457172 32457178 + Frame_Shift_Del DEL TTCCACT TTCCACT - TCGA-CC-5258-01A-01D-A12Z-10 TCGA-CC-5258-10A-01D-A12Z-10 g.chr9:32457172_32457178delTTCCACT c.2720_2726delAGTGGAA c.(2719-2727)aagtggaagfs p.KWK907fs LIHC 9 32466317 32466317 + Missense_Mutation SNP T T C TCGA-DD-A3A1-01A-11D-A20W-10 TCGA-DD-A3A1-11A-11D-A20W-10 g.chr9:32466317T>C c.2308A>G c.(2308-2310)Aca>Gca p.T770A LIHC 9 32488833 32488833 + Frame_Shift_Del DEL T T - TCGA-DD-A1EG-01A-11D-A20W-10 TCGA-DD-A1EG-10A-01D-A20W-10 g.chr9:32488833delT c.852delA c.(850-852)aaafs p.K284fs LIHC 9 32489378 32489378 + Missense_Mutation SNP T T C TCGA-ED-A7XO-01A-11D-A34Z-10 TCGA-ED-A7XO-10A-01D-A34Z-10 g.chr9:32489378T>C c.763A>G c.(763-765)Atg>Gtg p.M255V LUAD 9 32457215 32457215 + Missense_Mutation SNP C C T TCGA-86-8278-01A-11D-2284-08 TCGA-86-8278-10A-01D-2284-08 g.chr9:32457215C>T c.2683G>A c.(2683-2685)Gag>Aag p.E895K LUAD 9 32466353 32466353 + Missense_Mutation SNP C C G TCGA-44-7661-01A-11D-2063-08 TCGA-44-7661-10A-01D-2063-08 g.chr9:32466353C>G c.2272G>C c.(2272-2274)Gaa>Caa p.E758Q LUAD 9 32480281 32480281 + Silent SNP G G A TCGA-69-7980-01A-11D-2184-08 TCGA-69-7980-10A-01D-2184-08 g.chr9:32480281G>A c.1710C>T c.(1708-1710)ttC>ttT p.F570F LUAD 9 32481382 32481382 + Missense_Mutation SNP T T A TCGA-17-Z031-01A-01W-0746-08 TCGA-17-Z031-11A-01W-0746-08 g.chr9:32481382T>A c.1594A>T c.(1594-1596)Agc>Tgc p.S532C LUAD 9 32487951 32487951 + Silent SNP G G A TCGA-44-4112-01A-01D-1105-08 TCGA-44-4112-10A-01D-1458-08 g.chr9:32487951G>A c.1204C>T c.(1204-1206)Ctg>Ttg p.L402L LUAD 9 32488878 32488878 + Silent SNP T T A TCGA-17-Z028-01A-01W-0746-08 TCGA-17-Z028-11A-01W-0746-08 g.chr9:32488878T>A c.807A>T c.(805-807)ggA>ggT p.G269G LUAD 9 32492480 32492480 + Silent SNP G G A TCGA-75-5126-01A-01D-1753-08 TCGA-75-5126-10A-01D-1753-08 g.chr9:32492480G>A c.480C>T c.(478-480)ctC>ctT p.L160L LUAD 9 32500900 32500900 + Missense_Mutation SNP C C A TCGA-64-5779-01A-01D-1625-08 TCGA-64-5779-10A-01D-1625-08 g.chr9:32500900C>A c.144G>T c.(142-144)aaG>aaT p.K48N LUAD 9 32500928 32500928 + Missense_Mutation SNP T T A TCGA-53-7626-01A-12D-2063-08 TCGA-53-7626-10A-01D-2063-08 g.chr9:32500928T>A c.116A>T c.(115-117)cAg>cTg p.Q39L LUSC 9 32488093 32488093 + Missense_Mutation SNP G G T TCGA-60-2725-01A-01D-1267-08 TCGA-60-2725-11A-01D-1267-08 g.chr9:32488093G>T c.1062C>A c.(1060-1062)aaC>aaA p.N354K LUSC 9 32526089 32526089 + Missense_Mutation SNP G G T TCGA-21-1077-01A-01D-1521-08 TCGA-21-1077-11A-01D-1521-08 g.chr9:32526089G>T c.76C>A c.(76-78)Ctg>Atg p.L26M OV 9 32485257 32485257 + Missense_Mutation SNP G G A TCGA-24-2030-01A-01W-0722-08 TCGA-24-2030-10A-01W-0722-08 g.chr9:32485257G>A c.1396C>T c.(1396-1398)Cgg>Tgg p.R466W OV 9 32487984 32487984 + Missense_Mutation SNP G G C TCGA-23-1110-01A-01D-0428-08 TCGA-23-1110-10A-01D-0428-08 g.chr9:32487984G>C c.1171C>G c.(1171-1173)Cta>Gta p.L391V OV 9 32493809 32493809 + Missense_Mutation SNP A A G TCGA-29-1781-01A-01W-0633-09 TCGA-29-1781-10A-01W-0634-09 g.chr9:32493809A>G c.373T>C c.(373-375)Tct>Cct p.S125P PAAD 9 32485248 32485248 + Missense_Mutation SNP C C A TCGA-YB-A89D-01A-12D-A36O-08 TCGA-YB-A89D-10A-01D-A367-08 g.chr9:32485248C>A c.1405G>T c.(1405-1407)Gac>Tac p.D469Y PAAD 9 32488121 32488121 + Missense_Mutation SNP A A G TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr9:32488121A>G c.1034T>C c.(1033-1035)aTt>aCt p.I345T PRAD 9 32457353 32457353 + Missense_Mutation SNP T T C TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr9:32457353T>C c.2545A>G c.(2545-2547)Aag>Gag p.K849E PRAD 9 32457378 32457378 + Silent SNP T T C TCGA-V1-A9OH-01A-11D-A41K-08 TCGA-V1-A9OH-10A-01D-A41N-08 g.chr9:32457378T>C c.2520A>G c.(2518-2520)gaA>gaG p.E840E PRAD 9 32466305 32466305 + Missense_Mutation SNP C C A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr9:32466305C>A c.2320G>T c.(2320-2322)Gca>Tca p.A774S PRAD 9 32488832 32488833 + Frame_Shift_Ins INS - - T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr9:32488832_32488833insT c.852_853insA c.(850-855)aaattcfs p.F285fs PRAD 9 32491392 32491392 + Missense_Mutation SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr9:32491392G>A c.598C>T c.(598-600)Ctt>Ttt p.L200F READ 9 32457312 32457312 + Missense_Mutation SNP T T C TCGA-AG-3593-01A-01W-0831-10 TCGA-AG-3593-10A-01W-0831-10 g.chr9:32457312T>C c.2586A>G c.(2584-2586)atA>atG p.I862M READ 9 32466353 32466353 + Nonsense_Mutation SNP C C A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr9:32466353C>A c.2272G>T c.(2272-2274)Gaa>Taa p.E758* READ 9 32493818 32493818 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr9:32493818C>T c.364G>A c.(364-366)Gat>Aat p.D122N READ 9 32493914 32493914 + Missense_Mutation SNP C C T TCGA-CI-6622-01A-11D-1826-10 TCGA-CI-6622-10A-01D-1826-10 g.chr9:32493914C>T c.268G>A c.(268-270)Gaa>Aaa p.E90K SARC 9 32500870 32500870 + Silent SNP G G A TCGA-QQ-A5V9-01A-11D-A32I-09 TCGA-QQ-A5V9-11A-31D-A32I-09 g.chr9:32500870G>A c.174C>T c.(172-174)ctC>ctT p.L58L SKCM 9 32477025 32477025 + Missense_Mutation SNP C C T TCGA-GN-A266-06A-11D-A197-08 TCGA-GN-A266-10A-01D-A199-08 g.chr9:32477025C>T c.1879G>A c.(1879-1881)Gag>Aag p.E627K SKCM 9 32487516 32487516 + Missense_Mutation SNP T T C TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr9:32487516T>C c.1328A>G c.(1327-1329)aAa>aGa p.K443R SKCM 9 32493803 32493803 + Silent SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr9:32493803G>A c.379C>T c.(379-381)Ctg>Ttg p.L127L SKCM 9 32500834 32500834 + Silent SNP G G A TCGA-D3-A2JP-06A-11D-A19A-08 TCGA-D3-A2JP-10A-01D-A19A-08 g.chr9:32500834G>A c.210C>T c.(208-210)ttC>ttT p.F70F SKCM 9 32500834 32500834 + Silent SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr9:32500834G>A c.210C>T c.(208-210)ttC>ttT p.F70F SKCM 9 32500845 32500845 + Missense_Mutation SNP C C T TCGA-EE-A2GJ-06A-11D-A196-08 TCGA-EE-A2GJ-10A-01D-A198-08 g.chr9:32500845C>T c.199G>A c.(199-201)Gaa>Aaa p.E67K

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BLCA-CN 9 32467874 32467874 single base substitution G A missense_variant H488Y 1462C>T BLCA-CN 9 32467874 32467874 single base substitution G A missense_variant H620Y 1858C>T BLCA-CN 9 32467874 32467874 single base substitution G A missense_variant H646Y 1936C>T BLCA-CN 9 32467874 32467874 single base substitution G A missense_variant H691Y 2071C>T BLCA-CN 9 32485192 32485192 single base substitution C G missense_variant K284N 852G>C BLCA-CN 9 32485192 32485192 single base substitution C G missense_variant K416N 1248G>C BLCA-CN 9 32485192 32485192 single base substitution C G missense_variant K442N 1326G>C BLCA-CN 9 32485192 32485192 single base substitution C G missense_variant K487N 1461G>C BLCA-CN 9 32485206 32485206 single base substitution C A stop_gained E280* 838G>T BLCA-CN 9 32485206 32485206 single base substitution C A stop_gained E412* 1234G>T BLCA-CN 9 32485206 32485206 single base substitution C A stop_gained E438* 1312G>T BLCA-CN 9 32485206 32485206 single base substitution C A stop_gained E483* 1447G>T BLCA-US 9 32487490 32487493 deletion of <=200bp CTTG - frameshift_variant QV248 BLCA-US 9 32487490 32487493 deletion of <=200bp CTTG - frameshift_variant QV380 BLCA-US 9 32487490 32487493 deletion of <=200bp CTTG - frameshift_variant QV406 BLCA-US 9 32487490 32487493 deletion of <=200bp CTTG - frameshift_variant QV451 BLCA-US 9 32500809 32500809 single base substitution G A 5_prime_UTR_variant BLCA-US 9 32500809 32500809 single base substitution G A intron_variant BLCA-US 9 32500809 32500809 single base substitution G A missense_variant H79Y 235C>T BRCA-EU 9 32450490 32450490 single base substitution C A downstream_gene_variant BRCA-EU 9 32450805 32450805 single base substitution G C downstream_gene_variant BRCA-EU 9 32455311 32455311 single base substitution G A 3_prime_UTR_variant BRCA-EU 9 32455311 32455311 single base substitution G A downstream_gene_variant BRCA-EU 9 32455744 32455744 single base substitution A G 3_prime_UTR_variant BRCA-EU 9 32455744 32455744 single base substitution A G downstream_gene_variant BRCA-EU 9 32456172 32456172 single base substitution G A 3_prime_UTR_variant BRCA-EU 9 32456172 32456172 single base substitution G A downstream_gene_variant BRCA-EU 9 32459532 32459532 single base substitution C T intron_variant BRCA-EU 9 32459978 32459978 single base substitution G C intron_variant BRCA-EU 9 32460464 32460464 single base substitution G A intron_variant BRCA-EU 9 32460484 32460484 insertion of <=200bp - A intron_variant BRCA-EU 9 32460610 32460610 single base substitution A G intron_variant BRCA-EU 9 32461432 32461432 single base substitution G A downstream_gene_variant BRCA-EU 9 32461432 32461432 single base substitution G A intron_variant BRCA-EU 9 32464515 32464515 single base substitution G A downstream_gene_variant BRCA-EU 9 32464515 32464515 single base substitution G A intron_variant BRCA-EU 9 32465142 32465142 single base substitution A C downstream_gene_variant BRCA-EU 9 32465142 32465142 single base substitution A C intron_variant BRCA-EU 9 32466716 32466716 deletion of <=200bp G - intron_variant BRCA-EU 9 32467890 32467890 single base substitution G C missense_variant F482L 1446C>G BRCA-EU 9 32467890 32467890 single base substitution G C missense_variant F614L 1842C>G BRCA-EU 9 32467890 32467890 single base substitution G C missense_variant F640L 1920C>G BRCA-EU 9 32467890 32467890 single base substitution G C missense_variant F685L 2055C>G BRCA-EU 9 32467902 32467902 single base substitution T C missense_variant I478M 1434A>G BRCA-EU 9 32467902 32467902 single base substitution T C missense_variant I610M 1830A>G BRCA-EU 9 32467902 32467902 single base substitution T C missense_variant I636M 1908A>G BRCA-EU 9 32467902 32467902 single base substitution T C missense_variant I681M 2043A>G BRCA-EU 9 32468536 32468536 single base substitution C T intron_variant BRCA-EU 9 32469301 32469301 single base substitution G A intron_variant BRCA-EU 9 32470423 32470423 single base substitution G C intron_variant BRCA-EU 9 32471214 32471214 single base substitution C T intron_variant BRCA-EU 9 32475809 32475809 single base substitution T G intron_variant BRCA-EU 9 32476166 32476166 single base substitution G A intron_variant BRCA-EU 9 32476428 32476428 single base substitution G A intron_variant BRCA-EU 9 32476513 32476513 deletion of <=200bp A - intron_variant BRCA-EU 9 32478419 32478419 single base substitution G A intron_variant BRCA-EU 9 32478686 32478686 single base substitution G C intron_variant BRCA-EU 9 32478788 32478788 single base substitution G A intron_variant BRCA-EU 9 32480671 32480671 single base substitution C A intron_variant BRCA-EU 9 32482317 32482317 single base substitution T C intron_variant BRCA-EU 9 32485816 32485816 single base substitution C T intron_variant BRCA-EU 9 32487629 32487629 single base substitution G T splice_region_variant BRCA-EU 9 32487866 32487866 single base substitution T A intron_variant BRCA-EU 9 32487936 32487936 single base substitution G A splice_region_variant BRCA-EU 9 32488015 32488015 single base substitution T C synonymous_variant Q177Q 531A>G BRCA-EU 9 32488015 32488015 single base substitution T C synonymous_variant Q309Q 927A>G BRCA-EU 9 32488015 32488015 single base substitution T C synonymous_variant Q335Q 1005A>G BRCA-EU 9 32488015 32488015 single base substitution T C synonymous_variant Q380Q 1140A>G BRCA-EU 9 32489806 32489806 single base substitution T A intron_variant BRCA-EU 9 32490356 32490356 single base substitution G A intron_variant BRCA-EU 9 32490894 32490894 single base substitution A G intron_variant BRCA-EU 9 32491075 32491075 deletion of <=200bp A - intron_variant BRCA-EU 9 32491093 32491093 single base substitution G C intron_variant BRCA-EU 9 32492057 32492057 single base substitution G A intron_variant BRCA-EU 9 32492367 32492367 single base substitution T C intron_variant BRCA-EU 9 32493866 32493866 single base substitution G C 5_prime_UTR_variant BRCA-EU 9 32493866 32493866 single base substitution G C missense_variant L106V 316C>G BRCA-EU 9 32493866 32493866 single base substitution G C missense_variant L35V 103C>G BRCA-EU 9 32493866 32493866 single base substitution G C missense_variant L61V 181C>G BRCA-EU 9 32494011 32494011 single base substitution G A intron_variant BRCA-EU 9 32494436 32494436 single base substitution G T intron_variant BRCA-EU 9 32494637 32494637 single base substitution C G intron_variant BRCA-EU 9 32494794 32494794 single base substitution T C intron_variant BRCA-EU 9 32495122 32495122 single base substitution C G intron_variant BRCA-EU 9 32495236 32495236 single base substitution G A intron_variant BRCA-EU 9 32496278 32496278 single base substitution A G intron_variant BRCA-EU 9 32498599 32498599 single base substitution G C intron_variant BRCA-EU 9 32500656 32500656 single base substitution C G intron_variant BRCA-EU 9 32501667 32501667 single base substitution G C intron_variant BRCA-EU 9 32504641 32504641 single base substitution C A intron_variant BRCA-EU 9 32504641 32504641 single base substitution C A upstream_gene_variant BRCA-EU 9 32505365 32505365 single base substitution C G intron_variant BRCA-EU 9 32505365 32505365 single base substitution C G upstream_gene_variant BRCA-EU 9 32507162 32507162 single base substitution C T intron_variant BRCA-EU 9 32507162 32507162 single base substitution C T upstream_gene_variant BRCA-EU 9 32507443 32507443 single base substitution G C intron_variant BRCA-EU 9 32507443 32507443 single base substitution G C upstream_gene_variant BRCA-EU 9 32507884 32507884 single base substitution G A intron_variant BRCA-EU 9 32508149 32508149 single base substitution G A intron_variant BRCA-EU 9 32509920 32509920 single base substitution C G intron_variant BRCA-EU 9 32510375 32510375 single base substitution A C intron_variant BRCA-EU 9 32511591 32511591 single base substitution G C intron_variant BRCA-EU 9 32513937 32513937 single base substitution G T intron_variant BRCA-EU 9 32514510 32514510 single base substitution G A intron_variant BRCA-EU 9 32514512 32514512 single base substitution G A intron_variant BRCA-EU 9 32514845 32514845 insertion of <=200bp - T intron_variant BRCA-EU 9 32516067 32516067 single base substitution C T intron_variant BRCA-EU 9 32516763 32516763 single base substitution C T intron_variant BRCA-EU 9 32518834 32518834 single base substitution A T intron_variant BRCA-EU 9 32520500 32520500 single base substitution G C intron_variant BRCA-EU 9 32520965 32520965 single base substitution G A intron_variant BRCA-EU 9 32521856 32521856 single base substitution T A intron_variant BRCA-EU 9 32524234 32524234 single base substitution C T intron_variant BRCA-EU 9 32529945 32529945 single base substitution G T upstream_gene_variant BRCA-EU 9 32530028 32530028 single base substitution G C upstream_gene_variant BRCA-EU 9 32530236 32530236 single base substitution A C upstream_gene_variant BRCA-EU 9 32530569 32530570 deletion of <=200bp GT - upstream_gene_variant BRCA-FR 9 32455095 32455095 single base substitution G A downstream_gene_variant BRCA-FR 9 32469301 32469301 single base substitution G A intron_variant BRCA-FR 9 32470513 32470513 single base substitution T C intron_variant BRCA-FR 9 32475809 32475809 single base substitution T G intron_variant BRCA-FR 9 32478419 32478419 single base substitution G A intron_variant BRCA-FR 9 32478686 32478686 single base substitution G C intron_variant BRCA-FR 9 32487187 32487187 single base substitution T C intron_variant BRCA-FR 9 32507443 32507443 single base substitution G C intron_variant BRCA-FR 9 32507443 32507443 single base substitution G C upstream_gene_variant BRCA-FR 9 32514510 32514510 single base substitution G A intron_variant BRCA-UK 9 32476428 32476428 single base substitution G A intron_variant BRCA-UK 9 32495122 32495122 single base substitution C G intron_variant BRCA-UK 9 32520500 32520500 single base substitution G C intron_variant BRCA-UK 9 32529137 32529137 single base substitution C T upstream_gene_variant BRCA-US 9 32459494 32459494 single base substitution G A missense_variant H583Y 1747C>T BRCA-US 9 32459494 32459494 single base substitution G A missense_variant H715Y 2143C>T BRCA-US 9 32459494 32459494 single base substitution G A missense_variant H741Y 2221C>T BRCA-US 9 32459494 32459494 single base substitution G A missense_variant H786Y 2356C>T BRCA-US 9 32466374 32466374 single base substitution C T downstream_gene_variant BRCA-US 9 32466374 32466374 single base substitution C T missense_variant E548K 1642G>A BRCA-US 9 32466374 32466374 single base substitution C T missense_variant E680K 2038G>A BRCA-US 9 32466374 32466374 single base substitution C T missense_variant E706K 2116G>A BRCA-US 9 32466374 32466374 single base substitution C T missense_variant E751K 2251G>A BRCA-US 9 32481365 32481365 single base substitution G C synonymous_variant A334A 1002C>G BRCA-US 9 32481365 32481365 single base substitution G C synonymous_variant A466A 1398C>G BRCA-US 9 32481365 32481365 single base substitution G C synonymous_variant A492A 1476C>G BRCA-US 9 32481365 32481365 single base substitution G C synonymous_variant A537A 1611C>G BRCA-US 9 32481395 32481395 single base substitution G A synonymous_variant D324D 972C>T BRCA-US 9 32481395 32481395 single base substitution G A synonymous_variant D456D 1368C>T BRCA-US 9 32481395 32481395 single base substitution G A synonymous_variant D482D 1446C>T BRCA-US 9 32481395 32481395 single base substitution G A synonymous_variant D527D 1581C>T BRCA-US 9 32487531 32487531 single base substitution A G missense_variant V235A 704T>C BRCA-US 9 32487531 32487531 single base substitution A G missense_variant V367A 1100T>C BRCA-US 9 32487531 32487531 single base substitution A G missense_variant V393A 1178T>C BRCA-US 9 32487531 32487531 single base substitution A G missense_variant V438A 1313T>C BRCA-US 9 32491384 32491384 single base substitution A G 5_prime_UTR_variant BRCA-US 9 32491384 32491384 single base substitution A G synonymous_variant D131D 393T>C BRCA-US 9 32491384 32491384 single base substitution A G synonymous_variant D157D 471T>C BRCA-US 9 32491384 32491384 single base substitution A G synonymous_variant D202D 606T>C BRCA-US 9 32492507 32492507 single base substitution A C intron_variant BRCA-US 9 32492507 32492507 single base substitution A C synonymous_variant G106G 318T>G BRCA-US 9 32492507 32492507 single base substitution A C synonymous_variant G151G 453T>G BRCA-US 9 32492507 32492507 single base substitution A C synonymous_variant G80G 240T>G BTCA-JP 9 32459234 32459234 single base substitution A G intron_variant BTCA-JP 9 32485256 32485256 single base substitution C T missense_variant R263Q 788G>A BTCA-JP 9 32485256 32485256 single base substitution C T missense_variant R395Q 1184G>A BTCA-JP 9 32485256 32485256 single base substitution C T missense_variant R421Q 1262G>A BTCA-JP 9 32485256 32485256 single base substitution C T missense_variant R466Q 1397G>A BTCA-JP 9 32492348 32492348 single base substitution C T intron_variant CESC-US 9 32485206 32485206 single base substitution C T missense_variant E280K 838G>A CESC-US 9 32485206 32485206 single base substitution C T missense_variant E412K 1234G>A CESC-US 9 32485206 32485206 single base substitution C T missense_variant E438K 1312G>A CESC-US 9 32485206 32485206 single base substitution C T missense_variant E483K 1447G>A CLLE-ES 9 32460505 32460505 single base substitution T A intron_variant CLLE-ES 9 32466089 32466089 single base substitution T A downstream_gene_variant CLLE-ES 9 32466089 32466089 single base substitution T A intron_variant CLLE-ES 9 32466353 32466353 single base substitution C T downstream_gene_variant CLLE-ES 9 32466353 32466353 single base substitution C T missense_variant E555K 1663G>A CLLE-ES 9 32466353 32466353 single base substitution C T missense_variant E687K 2059G>A CLLE-ES 9 32466353 32466353 single base substitution C T missense_variant E713K 2137G>A CLLE-ES 9 32466353 32466353 single base substitution C T missense_variant E758K 2272G>A CLLE-ES 9 32506921 32506921 single base substitution T C intron_variant CLLE-ES 9 32506921 32506921 single base substitution T C upstream_gene_variant CLLE-ES 9 32517388 32517388 single base substitution G A intron_variant CLLE-ES 9 32518509 32518509 single base substitution T C intron_variant CLLE-ES 9 32530957 32530957 insertion of <=200bp - TTT upstream_gene_variant COAD-US 9 32457200 32457200 single base substitution C T missense_variant G697R 2089G>A COAD-US 9 32457200 32457200 single base substitution C T missense_variant G829R 2485G>A COAD-US 9 32457200 32457200 single base substitution C T missense_variant G855R 2563G>A COAD-US 9 32457200 32457200 single base substitution C T missense_variant G900R 2698G>A COAD-US 9 32459450 32459450 single base substitution T G synonymous_variant V597V 1791A>C COAD-US 9 32459450 32459450 single base substitution T G synonymous_variant V729V 2187A>C COAD-US 9 32459450 32459450 single base substitution T G synonymous_variant V755V 2265A>C COAD-US 9 32459450 32459450 single base substitution T G synonymous_variant V800V 2400A>C COAD-US 9 32466436 32466436 single base substitution C G missense_variant R527T 1580G>C COAD-US 9 32466436 32466436 single base substitution C G missense_variant R659T 1976G>C COAD-US 9 32466436 32466436 single base substitution C G missense_variant R685T 2054G>C COAD-US 9 32466436 32466436 single base substitution C G missense_variant R730T 2189G>C COAD-US 9 32466436 32466436 single base substitution C G splice_acceptor_variant COAD-US 9 32480251 32480251 single base substitution A T missense_variant D377E 1131T>A COAD-US 9 32480251 32480251 single base substitution A T missense_variant D509E 1527T>A COAD-US 9 32480251 32480251 single base substitution A T missense_variant D535E 1605T>A COAD-US 9 32480251 32480251 single base substitution A T missense_variant D580E 1740T>A COAD-US 9 32480254 32480254 single base substitution G A synonymous_variant F376F 1128C>T COAD-US 9 32480254 32480254 single base substitution G A synonymous_variant F508F 1524C>T COAD-US 9 32480254 32480254 single base substitution G A synonymous_variant F534F 1602C>T COAD-US 9 32480254 32480254 single base substitution G A synonymous_variant F579F 1737C>T COAD-US 9 32488079 32488079 single base substitution G A missense_variant T156M 467C>T COAD-US 9 32488079 32488079 single base substitution G A missense_variant T288M 863C>T COAD-US 9 32488079 32488079 single base substitution G A missense_variant T314M 941C>T COAD-US 9 32488079 32488079 single base substitution G A missense_variant T359M 1076C>T COAD-US 9 32488833 32488833 deletion of <=200bp T - frameshift_variant K213 COAD-US 9 32488833 32488833 deletion of <=200bp T - frameshift_variant K239 COAD-US 9 32488833 32488833 deletion of <=200bp T - frameshift_variant K284 COAD-US 9 32488833 32488833 deletion of <=200bp T - frameshift_variant K81 COAD-US 9 32489410 32489410 single base substitution C A missense_variant R173I 518G>T COAD-US 9 32489410 32489410 single base substitution C A missense_variant R199I 596G>T COAD-US 9 32489410 32489410 single base substitution C A missense_variant R244I 731G>T COAD-US 9 32489410 32489410 single base substitution C A missense_variant R41I 122G>T COAD-US 9 32526146 32526146 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant COAD-US 9 32526146 32526146 single base substitution G A missense_variant R7C 19C>T COCA-CN 9 32458940 32458940 single base substitution C T intron_variant COCA-CN 9 32459456 32459456 single base substitution T A missense_variant K595N 1785A>T COCA-CN 9 32459456 32459456 single base substitution T A missense_variant K727N 2181A>T COCA-CN 9 32459456 32459456 single base substitution T A missense_variant K753N 2259A>T COCA-CN 9 32459456 32459456 single base substitution T A missense_variant K798N 2394A>T COCA-CN 9 32467916 32467916 single base substitution C T missense_variant A474T 1420G>A COCA-CN 9 32467916 32467916 single base substitution C T missense_variant A606T 1816G>A COCA-CN 9 32467916 32467916 single base substitution C T missense_variant A632T 1894G>A COCA-CN 9 32467916 32467916 single base substitution C T missense_variant A677T 2029G>A COCA-CN 9 32474377 32474377 single base substitution C T intron_variant COCA-CN 9 32476996 32476996 single base substitution G A synonymous_variant T433T 1299C>T COCA-CN 9 32476996 32476996 single base substitution G A synonymous_variant T565T 1695C>T COCA-CN 9 32476996 32476996 single base substitution G A synonymous_variant T591T 1773C>T COCA-CN 9 32476996 32476996 single base substitution G A synonymous_variant T636T 1908C>T COCA-CN 9 32480435 32480435 single base substitution G A intron_variant COCA-CN 9 32481314 32481314 single base substitution C T intron_variant COCA-CN 9 32485139 32485139 single base substitution G A intron_variant COCA-CN 9 32485190 32485190 single base substitution C A missense_variant R285I 854G>T COCA-CN 9 32485190 32485190 single base substitution C A missense_variant R417I 1250G>T COCA-CN 9 32485190 32485190 single base substitution C A missense_variant R443I 1328G>T COCA-CN 9 32485190 32485190 single base substitution C A missense_variant R488I 1463G>T COCA-CN 9 32486534 32486534 single base substitution G T intron_variant COCA-CN 9 32491309 32491309 single base substitution A G synonymous_variant C156C 468T>C COCA-CN 9 32491309 32491309 single base substitution A G synonymous_variant C182C 546T>C COCA-CN 9 32491309 32491309 single base substitution A G synonymous_variant C227C 681T>C COCA-CN 9 32491309 32491309 single base substitution A G synonymous_variant C24C 72T>C COCA-CN 9 32493366 32493366 single base substitution G A intron_variant COCA-CN 9 32493690 32493690 single base substitution T C intron_variant COCA-CN 9 32497471 32497471 single base substitution C T intron_variant COCA-CN 9 32500860 32500860 single base substitution A T 5_prime_UTR_premature_start_codon_gain_variant COCA-CN 9 32500860 32500860 single base substitution A T intron_variant COCA-CN 9 32500860 32500860 single base substitution A T missense_variant L62M 184T>A COCA-CN 9 32501444 32501444 single base substitution C T intron_variant COCA-CN 9 32508257 32508257 single base substitution A T intron_variant COCA-CN 9 32520589 32520589 single base substitution C G intron_variant COCA-CN 9 32522129 32522129 single base substitution A G intron_variant EOPC-DE 9 32452680 32452680 single base substitution C T downstream_gene_variant ESAD-UK 9 32450777 32450777 single base substitution G A downstream_gene_variant ESAD-UK 9 32450938 32450938 single base substitution A T downstream_gene_variant ESAD-UK 9 32452388 32452388 single base substitution G T downstream_gene_variant ESAD-UK 9 32452595 32452595 single base substitution A G downstream_gene_variant ESAD-UK 9 32453944 32453944 single base substitution A G downstream_gene_variant ESAD-UK 9 32455895 32455895 single base substitution G C 3_prime_UTR_variant ESAD-UK 9 32455895 32455895 single base substitution G C downstream_gene_variant ESAD-UK 9 32457559 32457559 single base substitution A G intron_variant ESAD-UK 9 32457877 32457877 single base substitution T G intron_variant ESAD-UK 9 32464066 32464066 single base substitution C T downstream_gene_variant ESAD-UK 9 32464066 32464066 single base substitution C T intron_variant ESAD-UK 9 32466951 32466951 single base substitution T C intron_variant ESAD-UK 9 32468899 32468899 single base substitution T A intron_variant ESAD-UK 9 32469081 32469081 single base substitution C T intron_variant ESAD-UK 9 32470992 32470992 single base substitution C T intron_variant ESAD-UK 9 32474328 32474328 single base substitution A C intron_variant ESAD-UK 9 32474670 32474670 single base substitution C T intron_variant ESAD-UK 9 32474950 32474950 single base substitution A T intron_variant ESAD-UK 9 32475178 32475178 single base substitution G A intron_variant ESAD-UK 9 32475344 32475344 single base substitution A T intron_variant ESAD-UK 9 32482127 32482127 single base substitution C T intron_variant ESAD-UK 9 32482382 32482382 single base substitution G A intron_variant ESAD-UK 9 32482714 32482714 deletion of <=200bp G - intron_variant ESAD-UK 9 32482722 32482732 deletion of <=200bp TGGCACGCACC - intron_variant ESAD-UK 9 32486176 32486176 single base substitution G T intron_variant ESAD-UK 9 32487412 32487412 single base substitution A C intron_variant ESAD-UK 9 32487495 32487495 single base substitution T C missense_variant E247G 740A>G ESAD-UK 9 32487495 32487495 single base substitution T C missense_variant E379G 1136A>G ESAD-UK 9 32487495 32487495 single base substitution T C missense_variant E405G 1214A>G ESAD-UK 9 32487495 32487495 single base substitution T C missense_variant E450G 1349A>G ESAD-UK 9 32489499 32489499 single base substitution T A intron_variant ESAD-UK 9 32493905 32493905 single base substitution C G 5_prime_UTR_variant ESAD-UK 9 32493905 32493905 single base substitution C G missense_variant D22H 64G>C ESAD-UK 9 32493905 32493905 single base substitution C G missense_variant D48H 142G>C ESAD-UK 9 32493905 32493905 single base substitution C G missense_variant D93H 277G>C ESAD-UK 9 32494051 32494051 single base substitution A T intron_variant ESAD-UK 9 32494479 32494479 single base substitution A C intron_variant ESAD-UK 9 32494559 32494559 single base substitution C A intron_variant ESAD-UK 9 32496809 32496809 single base substitution A C intron_variant ESAD-UK 9 32498498 32498498 single base substitution A C 5_prime_UTR_premature_start_codon_gain_variant ESAD-UK 9 32498498 32498498 single base substitution A C intron_variant ESAD-UK 9 32499242 32499242 single base substitution T A intron_variant ESAD-UK 9 32499812 32499812 single base substitution G A intron_variant ESAD-UK 9 32500108 32500108 single base substitution G A intron_variant ESAD-UK 9 32502511 32502511 single base substitution T C intron_variant ESAD-UK 9 32504235 32504235 single base substitution C T intron_variant ESAD-UK 9 32504235 32504235 single base substitution C T upstream_gene_variant ESAD-UK 9 32504425 32504425 single base substitution C G intron_variant ESAD-UK 9 32504425 32504425 single base substitution C G upstream_gene_variant ESAD-UK 9 32505823 32505823 single base substitution C T intron_variant ESAD-UK 9 32505823 32505823 single base substitution C T upstream_gene_variant ESAD-UK 9 32506135 32506136 deletion of <=200bp AA - intron_variant ESAD-UK 9 32506135 32506136 deletion of <=200bp AA - upstream_gene_variant ESAD-UK 9 32506680 32506680 single base substitution C T intron_variant ESAD-UK 9 32506680 32506680 single base substitution C T upstream_gene_variant ESAD-UK 9 32507645 32507645 single base substitution A G intron_variant ESAD-UK 9 32507645 32507645 single base substitution A G upstream_gene_variant ESAD-UK 9 32509220 32509220 single base substitution G C intron_variant ESAD-UK 9 32513637 32513637 single base substitution A C intron_variant ESAD-UK 9 32513863 32513863 single base substitution C G intron_variant ESAD-UK 9 32514817 32514817 single base substitution C T intron_variant ESAD-UK 9 32515415 32515415 single base substitution C T intron_variant ESAD-UK 9 32518046 32518046 single base substitution T C intron_variant ESAD-UK 9 32518666 32518666 single base substitution C G intron_variant ESAD-UK 9 32519824 32519824 deletion of <=200bp T - intron_variant ESAD-UK 9 32522647 32522647 single base substitution G A intron_variant ESAD-UK 9 32527238 32527238 single base substitution T C upstream_gene_variant ESAD-UK 9 32530977 32530977 single base substitution T G upstream_gene_variant ESCA-CN 9 32466184 32466184 single base substitution G A downstream_gene_variant ESCA-CN 9 32466184 32466184 single base substitution G A intron_variant ESCA-CN 9 32488237 32488237 single base substitution G C intron_variant KIRC-US 9 32480246 32480246 single base substitution A T missense_variant I379N 1136T>A KIRC-US 9 32480246 32480246 single base substitution A T missense_variant I511N 1532T>A KIRC-US 9 32480246 32480246 single base substitution A T missense_variant I537N 1610T>A KIRC-US 9 32480246 32480246 single base substitution A T missense_variant I582N 1745T>A KIRC-US 9 32488009 32488009 single base substitution C T synonymous_variant P179P 537G>A KIRC-US 9 32488009 32488009 single base substitution C T synonymous_variant P311P 933G>A KIRC-US 9 32488009 32488009 single base substitution C T synonymous_variant P337P 1011G>A KIRC-US 9 32488009 32488009 single base substitution C T synonymous_variant P382P 1146G>A KIRP-US 9 32459420 32459420 single base substitution G T stop_gained C607* 1821C>A KIRP-US 9 32459420 32459420 single base substitution G T stop_gained C739* 2217C>A KIRP-US 9 32459420 32459420 single base substitution G T stop_gained C765* 2295C>A KIRP-US 9 32459420 32459420 single base substitution G T stop_gained C810* 2430C>A KIRP-US 9 32467853 32467868 deletion of <=200bp AGGTGGCAATCAGAAT - frameshift_variant ILIATS490 KIRP-US 9 32467853 32467868 deletion of <=200bp AGGTGGCAATCAGAAT - frameshift_variant ILIATS622 KIRP-US 9 32467853 32467868 deletion of <=200bp AGGTGGCAATCAGAAT - frameshift_variant ILIATS648 KIRP-US 9 32467853 32467868 deletion of <=200bp AGGTGGCAATCAGAAT - frameshift_variant ILIATS693 LAML-KR 9 32495676 32495676 single base substitution G T intron_variant LICA-FR 9 32457323 32457323 single base substitution T C missense_variant R656G 1966A>G LICA-FR 9 32457323 32457323 single base substitution T C missense_variant R788G 2362A>G LICA-FR 9 32457323 32457323 single base substitution T C missense_variant R814G 2440A>G LICA-FR 9 32457323 32457323 single base substitution T C missense_variant R859G 2575A>G LICA-FR 9 32473285 32473285 insertion of <=200bp - T intron_variant LICA-FR 9 32494157 32494157 single base substitution A G intron_variant LICA-FR 9 32495658 32495658 insertion of <=200bp - T intron_variant LIHC-US 9 32457157 32457157 single base substitution T C missense_variant E711G 2132A>G LIHC-US 9 32457157 32457157 single base substitution T C missense_variant E843G 2528A>G LIHC-US 9 32457157 32457157 single base substitution T C missense_variant E869G 2606A>G LIHC-US 9 32457157 32457157 single base substitution T C missense_variant E914G 2741A>G LIHC-US 9 32457172 32457178 deletion of <=200bp TTCCACT - frameshift_variant KWK704 LIHC-US 9 32457172 32457178 deletion of <=200bp TTCCACT - frameshift_variant KWK836 LIHC-US 9 32457172 32457178 deletion of <=200bp TTCCACT - frameshift_variant KWK862 LIHC-US 9 32457172 32457178 deletion of <=200bp TTCCACT - frameshift_variant KWK907 LIHC-US 9 32489378 32489378 single base substitution T C missense_variant M184V 550A>G LIHC-US 9 32489378 32489378 single base substitution T C missense_variant M210V 628A>G LIHC-US 9 32489378 32489378 single base substitution T C missense_variant M255V 763A>G LIHC-US 9 32489378 32489378 single base substitution T C missense_variant M52V 154A>G LINC-JP 9 32457132 32457132 single base substitution T A missense_variant E719D 2157A>T LINC-JP 9 32457132 32457132 single base substitution T A missense_variant E851D 2553A>T LINC-JP 9 32457132 32457132 single base substitution T A missense_variant E877D 2631A>T LINC-JP 9 32457132 32457132 single base substitution T A missense_variant E922D 2766A>T LINC-JP 9 32466035 32466035 single base substitution T C downstream_gene_variant LINC-JP 9 32466035 32466035 single base substitution T C intron_variant LINC-JP 9 32480151 32480151 single base substitution G T intron_variant LINC-JP 9 32485196 32485196 single base substitution G A missense_variant A283V 848C>T LINC-JP 9 32485196 32485196 single base substitution G A missense_variant A415V 1244C>T LINC-JP 9 32485196 32485196 single base substitution G A missense_variant A441V 1322C>T LINC-JP 9 32485196 32485196 single base substitution G A missense_variant A486V 1457C>T LINC-JP 9 32485231 32485231 single base substitution G A synonymous_variant I271I 813C>T LINC-JP 9 32485231 32485231 single base substitution G A synonymous_variant I403I 1209C>T LINC-JP 9 32485231 32485231 single base substitution G A synonymous_variant I429I 1287C>T LINC-JP 9 32485231 32485231 single base substitution G A synonymous_variant I474I 1422C>T LINC-JP 9 32486053 32486053 single base substitution T C intron_variant LINC-JP 9 32505147 32505147 single base substitution G T intron_variant LINC-JP 9 32505147 32505147 single base substitution G T upstream_gene_variant LINC-JP 9 32518613 32518613 single base substitution G T intron_variant LINC-JP 9 32528389 32528389 single base substitution T A upstream_gene_variant LIRI-JP 9 32455180 32455180 single base substitution A G downstream_gene_variant LIRI-JP 9 32455204 32455204 single base substitution A C downstream_gene_variant LIRI-JP 9 32456412 32456412 single base substitution G T 3_prime_UTR_variant LIRI-JP 9 32456412 32456412 single base substitution G T downstream_gene_variant LIRI-JP 9 32465826 32465826 single base substitution T C downstream_gene_variant LIRI-JP 9 32465826 32465826 single base substitution T C intron_variant LIRI-JP 9 32465826 32465826 single base substitution T G downstream_gene_variant LIRI-JP 9 32465826 32465826 single base substitution T G intron_variant LIRI-JP 9 32466355 32466355 single base substitution T G downstream_gene_variant LIRI-JP 9 32466355 32466355 single base substitution T G missense_variant K554T 1661A>C LIRI-JP 9 32466355 32466355 single base substitution T G missense_variant K686T 2057A>C LIRI-JP 9 32466355 32466355 single base substitution T G missense_variant K712T 2135A>C LIRI-JP 9 32466355 32466355 single base substitution T G missense_variant K757T 2270A>C LIRI-JP 9 32468883 32468883 single base substitution A G intron_variant LIRI-JP 9 32469802 32469802 single base substitution C T intron_variant LIRI-JP 9 32471412 32471412 single base substitution T G intron_variant LIRI-JP 9 32473058 32473058 single base substitution T A missense_variant L440F 1320A>T LIRI-JP 9 32473058 32473058 single base substitution T A missense_variant L572F 1716A>T LIRI-JP 9 32473058 32473058 single base substitution T A missense_variant L598F 1794A>T LIRI-JP 9 32473058 32473058 single base substitution T A missense_variant L643F 1929A>T LIRI-JP 9 32473945 32473945 single base substitution G A intron_variant LIRI-JP 9 32477432 32477432 single base substitution A C intron_variant LIRI-JP 9 32480288 32480288 single base substitution T G missense_variant K365T 1094A>C LIRI-JP 9 32480288 32480288 single base substitution T G missense_variant K497T 1490A>C LIRI-JP 9 32480288 32480288 single base substitution T G missense_variant K523T 1568A>C LIRI-JP 9 32480288 32480288 single base substitution T G missense_variant K568T 1703A>C LIRI-JP 9 32480639 32480639 single base substitution A T intron_variant LIRI-JP 9 32483906 32483906 single base substitution T A intron_variant LIRI-JP 9 32485644 32485644 single base substitution T G intron_variant LIRI-JP 9 32485799 32485799 single base substitution A G intron_variant LIRI-JP 9 32486555 32486555 single base substitution C T intron_variant LIRI-JP 9 32488864 32488864 single base substitution G C stop_gained S203* 608C>G LIRI-JP 9 32488864 32488864 single base substitution G C stop_gained S229* 686C>G LIRI-JP 9 32488864 32488864 single base substitution G C stop_gained S274* 821C>G LIRI-JP 9 32488864 32488864 single base substitution G C stop_gained S71* 212C>G LIRI-JP 9 32490372 32490372 single base substitution A G intron_variant LIRI-JP 9 32491905 32491905 single base substitution T A intron_variant LIRI-JP 9 32493588 32493588 single base substitution T C intron_variant LIRI-JP 9 32494924 32494924 single base substitution G A intron_variant LIRI-JP 9 32495445 32495445 single base substitution C T intron_variant LIRI-JP 9 32496610 32496610 single base substitution A T intron_variant LIRI-JP 9 32497218 32497218 single base substitution T C intron_variant LIRI-JP 9 32500017 32500017 single base substitution T C intron_variant LIRI-JP 9 32507032 32507032 single base substitution T G intron_variant LIRI-JP 9 32507032 32507032 single base substitution T G upstream_gene_variant LIRI-JP 9 32508122 32508122 single base substitution T A intron_variant LIRI-JP 9 32509104 32509104 single base substitution G A intron_variant LIRI-JP 9 32514712 32514712 single base substitution T G intron_variant LIRI-JP 9 32521481 32521481 single base substitution A G intron_variant LIRI-JP 9 32526553 32526553 single base substitution T G upstream_gene_variant LIRI-JP 9 32528344 32528344 single base substitution T C upstream_gene_variant LIRI-JP 9 32530604 32530604 single base substitution T G upstream_gene_variant LIRI-JP 9 32530667 32530667 single base substitution T A upstream_gene_variant LIRI-JP 9 32530684 32530684 single base substitution T C upstream_gene_variant LIRI-JP 9 32530935 32530935 single base substitution C G upstream_gene_variant LUSC-KR 9 32451845 32451845 single base substitution G A downstream_gene_variant LUSC-KR 9 32459605 32459605 single base substitution C T intron_variant LUSC-KR 9 32468380 32468380 single base substitution C A intron_variant LUSC-KR 9 32469453 32469453 single base substitution G A intron_variant LUSC-KR 9 32472252 32472252 single base substitution C G intron_variant LUSC-KR 9 32475106 32475106 single base substitution C T intron_variant LUSC-KR 9 32475827 32475827 single base substitution C T intron_variant LUSC-KR 9 32491738 32491738 single base substitution T A intron_variant LUSC-KR 9 32492798 32492798 single base substitution C A intron_variant LUSC-KR 9 32495676 32495676 single base substitution G T intron_variant LUSC-KR 9 32499347 32499347 single base substitution A T intron_variant LUSC-KR 9 32503707 32503707 single base substitution C G intron_variant LUSC-KR 9 32503707 32503707 single base substitution C G upstream_gene_variant LUSC-KR 9 32508448 32508448 single base substitution G A intron_variant LUSC-KR 9 32511262 32511262 single base substitution C A intron_variant LUSC-KR 9 32511441 32511441 single base substitution C T intron_variant LUSC-KR 9 32520144 32520144 single base substitution G C intron_variant LUSC-KR 9 32520773 32520773 single base substitution T C intron_variant LUSC-KR 9 32522378 32522378 single base substitution T C intron_variant LUSC-KR 9 32528126 32528126 single base substitution C A upstream_gene_variant LUSC-KR 9 32528128 32528128 single base substitution C A upstream_gene_variant LUSC-KR 9 32529706 32529706 single base substitution T A upstream_gene_variant LUSC-US 9 32488093 32488093 single base substitution G T missense_variant N151K 453C>A LUSC-US 9 32488093 32488093 single base substitution G T missense_variant N283K 849C>A LUSC-US 9 32488093 32488093 single base substitution G T missense_variant N309K 927C>A LUSC-US 9 32488093 32488093 single base substitution G T missense_variant N354K 1062C>A LUSC-US 9 32526089 32526089 single base substitution G T 5_prime_UTR_premature_start_codon_gain_variant LUSC-US 9 32526089 32526089 single base substitution G T missense_variant L26M 76C>A MALY-DE 9 32454389 32454389 single base substitution T G downstream_gene_variant MALY-DE 9 32468975 32468975 single base substitution G A intron_variant MALY-DE 9 32473161 32473161 single base substitution A G intron_variant MALY-DE 9 32479460 32479460 single base substitution T C intron_variant MALY-DE 9 32479700 32479700 single base substitution T C intron_variant MALY-DE 9 32482186 32482187 deletion of <=200bp TG - intron_variant MALY-DE 9 32489222 32489222 single base substitution T G intron_variant MALY-DE 9 32499162 32499162 single base substitution G A intron_variant MALY-DE 9 32504037 32504038 deletion of <=200bp AC - intron_variant MALY-DE 9 32504037 32504038 deletion of <=200bp AC - upstream_gene_variant MALY-DE 9 32507204 32507211 deletion of <=200bp CAGTATCA - intron_variant MALY-DE 9 32507204 32507211 deletion of <=200bp CAGTATCA - upstream_gene_variant MALY-DE 9 32507512 32507512 single base substitution A G intron_variant MALY-DE 9 32507512 32507512 single base substitution A G upstream_gene_variant MALY-DE 9 32508646 32508646 single base substitution T A intron_variant MALY-DE 9 32518383 32518383 deletion of <=200bp A - intron_variant MALY-DE 9 32520185 32520185 single base substitution T A intron_variant MALY-DE 9 32527602 32527602 single base substitution A C upstream_gene_variant MALY-DE 9 32529869 32529885 deletion of <=200bp TTTTTTTTTTTTTTTTT - upstream_gene_variant MALY-DE 9 32530967 32530967 insertion of <=200bp - T upstream_gene_variant MELA-AU 9 32450983 32450983 single base substitution G A downstream_gene_variant MELA-AU 9 32451271 32451271 single base substitution C T downstream_gene_variant MELA-AU 9 32455549 32455549 single base substitution C T 3_prime_UTR_variant MELA-AU 9 32455549 32455549 single base substitution C T downstream_gene_variant MELA-AU 9 32457272 32457272 single base substitution G A missense_variant H673Y 2017C>T MELA-AU 9 32457272 32457272 single base substitution G A missense_variant H805Y 2413C>T MELA-AU 9 32457272 32457272 single base substitution G A missense_variant H831Y 2491C>T MELA-AU 9 32457272 32457272 single base substitution G A missense_variant H876Y 2626C>T MELA-AU 9 32458204 32458204 single base substitution G A intron_variant MELA-AU 9 32458212 32458212 single base substitution T C intron_variant MELA-AU 9 32460134 32460134 single base substitution C T intron_variant MELA-AU 9 32460839 32460839 single base substitution C T intron_variant MELA-AU 9 32461425 32461425 single base substitution T C downstream_gene_variant MELA-AU 9 32461425 32461425 single base substitution T C intron_variant MELA-AU 9 32462458 32462458 single base substitution A T downstream_gene_variant MELA-AU 9 32462458 32462458 single base substitution A T intron_variant MELA-AU 9 32463123 32463123 single base substitution A G downstream_gene_variant MELA-AU 9 32463123 32463123 single base substitution A G intron_variant MELA-AU 9 32463976 32463976 single base substitution G A downstream_gene_variant MELA-AU 9 32463976 32463976 single base substitution G A intron_variant MELA-AU 9 32464411 32464411 single base substitution G A downstream_gene_variant MELA-AU 9 32464411 32464411 single base substitution G A intron_variant MELA-AU 9 32465179 32465179 single base substitution G A downstream_gene_variant MELA-AU 9 32465179 32465179 single base substitution G A intron_variant MELA-AU 9 32467404 32467404 single base substitution G A intron_variant MELA-AU 9 32468109 32468109 single base substitution G A intron_variant MELA-AU 9 32468439 32468439 single base substitution G A intron_variant MELA-AU 9 32469341 32469341 single base substitution G A intron_variant MELA-AU 9 32469430 32469431 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 9 32469690 32469690 single base substitution G A intron_variant MELA-AU 9 32470014 32470014 single base substitution G A intron_variant MELA-AU 9 32470045 32470045 single base substitution G A intron_variant MELA-AU 9 32470594 32470594 single base substitution C T intron_variant MELA-AU 9 32470681 32470681 single base substitution G A intron_variant MELA-AU 9 32471581 32471581 single base substitution G A intron_variant MELA-AU 9 32472150 32472150 single base substitution A G intron_variant MELA-AU 9 32472403 32472403 single base substitution T C intron_variant MELA-AU 9 32472489 32472489 single base substitution C T intron_variant MELA-AU 9 32472546 32472546 single base substitution C T intron_variant MELA-AU 9 32473156 32473156 single base substitution A G intron_variant MELA-AU 9 32473195 32473195 single base substitution G A intron_variant MELA-AU 9 32474107 32474107 single base substitution G A intron_variant MELA-AU 9 32476197 32476197 single base substitution C T intron_variant MELA-AU 9 32476495 32476495 single base substitution C T intron_variant MELA-AU 9 32477094 32477094 single base substitution G A missense_variant P401S 1201C>T MELA-AU 9 32477094 32477094 single base substitution G A missense_variant P533S 1597C>T MELA-AU 9 32477094 32477094 single base substitution G A missense_variant P559S 1675C>T MELA-AU 9 32477094 32477094 single base substitution G A missense_variant P604S 1810C>T MELA-AU 9 32477698 32477698 single base substitution G A intron_variant MELA-AU 9 32477931 32477932 multiple base substitution (>=2bp and <=200bp) GG AT intron_variant MELA-AU 9 32478804 32478804 single base substitution C T intron_variant MELA-AU 9 32479265 32479265 single base substitution C T intron_variant MELA-AU 9 32479370 32479370 single base substitution G A intron_variant MELA-AU 9 32479453 32479453 single base substitution G A intron_variant MELA-AU 9 32479622 32479622 single base substitution G A intron_variant MELA-AU 9 32479654 32479654 single base substitution G A intron_variant MELA-AU 9 32480265 32480265 single base substitution C T missense_variant A373T 1117G>A MELA-AU 9 32480265 32480265 single base substitution C T missense_variant A505T 1513G>A MELA-AU 9 32480265 32480265 single base substitution C T missense_variant A531T 1591G>A MELA-AU 9 32480265 32480265 single base substitution C T missense_variant A576T 1726G>A MELA-AU 9 32480670 32480670 single base substitution C T intron_variant MELA-AU 9 32481203 32481203 single base substitution C T intron_variant MELA-AU 9 32481249 32481249 single base substitution G A intron_variant MELA-AU 9 32482185 32482185 single base substitution T G intron_variant MELA-AU 9 32482915 32482915 single base substitution G A intron_variant MELA-AU 9 32483245 32483245 single base substitution C T intron_variant MELA-AU 9 32483403 32483403 single base substitution G A intron_variant MELA-AU 9 32483803 32483804 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 9 32484297 32484297 single base substitution G A intron_variant MELA-AU 9 32484729 32484729 single base substitution G A intron_variant MELA-AU 9 32484887 32484887 single base substitution G A intron_variant MELA-AU 9 32484986 32484986 single base substitution G A intron_variant MELA-AU 9 32486377 32486377 single base substitution G A intron_variant MELA-AU 9 32486459 32486459 single base substitution A T intron_variant MELA-AU 9 32486753 32486753 single base substitution C T intron_variant MELA-AU 9 32489999 32489999 single base substitution A T intron_variant MELA-AU 9 32490077 32490077 single base substitution G A intron_variant MELA-AU 9 32490724 32490724 single base substitution G A intron_variant MELA-AU 9 32491274 32491274 single base substitution G A intron_variant MELA-AU 9 32491698 32491698 single base substitution G A intron_variant MELA-AU 9 32491889 32491889 single base substitution T G intron_variant MELA-AU 9 32491969 32491969 single base substitution G A intron_variant MELA-AU 9 32492051 32492051 single base substitution G A intron_variant MELA-AU 9 32492189 32492189 single base substitution C T intron_variant MELA-AU 9 32492304 32492304 single base substitution G A intron_variant MELA-AU 9 32493317 32493317 single base substitution C T intron_variant MELA-AU 9 32493504 32493504 single base substitution C T intron_variant MELA-AU 9 32494038 32494038 single base substitution G A intron_variant MELA-AU 9 32494963 32494963 single base substitution G A intron_variant MELA-AU 9 32495334 32495334 single base substitution G A intron_variant MELA-AU 9 32495812 32495812 single base substitution C T intron_variant MELA-AU 9 32497377 32497377 single base substitution G A intron_variant MELA-AU 9 32497779 32497779 single base substitution T A intron_variant MELA-AU 9 32498899 32498899 single base substitution C T intron_variant MELA-AU 9 32499846 32499846 single base substitution G A intron_variant MELA-AU 9 32499919 32499919 single base substitution G A intron_variant MELA-AU 9 32500569 32500569 single base substitution A G intron_variant MELA-AU 9 32501186 32501186 single base substitution G A intron_variant MELA-AU 9 32501247 32501247 single base substitution G A intron_variant MELA-AU 9 32501411 32501411 single base substitution G A intron_variant MELA-AU 9 32501947 32501947 single base substitution A G intron_variant MELA-AU 9 32502571 32502571 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant MELA-AU 9 32502571 32502571 single base substitution G A intron_variant MELA-AU 9 32503150 32503151 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 9 32503150 32503151 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 9 32504236 32504236 single base substitution G A intron_variant MELA-AU 9 32504236 32504236 single base substitution G A upstream_gene_variant MELA-AU 9 32505485 32505485 single base substitution G A intron_variant MELA-AU 9 32505485 32505485 single base substitution G A upstream_gene_variant MELA-AU 9 32505528 32505528 single base substitution G A intron_variant MELA-AU 9 32505528 32505528 single base substitution G A upstream_gene_variant MELA-AU 9 32505623 32505623 single base substitution C T intron_variant MELA-AU 9 32505623 32505623 single base substitution C T upstream_gene_variant MELA-AU 9 32505875 32505875 single base substitution G A intron_variant MELA-AU 9 32505875 32505875 single base substitution G A upstream_gene_variant MELA-AU 9 32506590 32506590 single base substitution G A intron_variant MELA-AU 9 32506590 32506590 single base substitution G A upstream_gene_variant MELA-AU 9 32507024 32507024 single base substitution G A intron_variant MELA-AU 9 32507024 32507024 single base substitution G A upstream_gene_variant MELA-AU 9 32507252 32507252 single base substitution G A intron_variant MELA-AU 9 32507252 32507252 single base substitution G A upstream_gene_variant MELA-AU 9 32508395 32508395 single base substitution C A intron_variant MELA-AU 9 32508522 32508522 single base substitution G A intron_variant MELA-AU 9 32509396 32509396 single base substitution G A intron_variant MELA-AU 9 32509686 32509686 single base substitution G A intron_variant MELA-AU 9 32510288 32510288 single base substitution G A intron_variant MELA-AU 9 32511182 32511182 single base substitution G A intron_variant MELA-AU 9 32511846 32511846 single base substitution G A intron_variant MELA-AU 9 32512660 32512660 single base substitution G A intron_variant MELA-AU 9 32513873 32513873 single base substitution T A intron_variant MELA-AU 9 32514528 32514528 single base substitution A G intron_variant MELA-AU 9 32514547 32514547 single base substitution G A intron_variant MELA-AU 9 32514762 32514762 single base substitution G A intron_variant MELA-AU 9 32514990 32514990 single base substitution G A intron_variant MELA-AU 9 32515776 32515776 single base substitution G A intron_variant MELA-AU 9 32516977 32516977 single base substitution G A intron_variant MELA-AU 9 32518086 32518086 single base substitution G A intron_variant MELA-AU 9 32518356 32518356 single base substitution T A intron_variant MELA-AU 9 32518603 32518603 single base substitution C T intron_variant MELA-AU 9 32518825 32518825 single base substitution C T intron_variant MELA-AU 9 32520091 32520091 single base substitution G A intron_variant MELA-AU 9 32520714 32520715 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 9 32521275 32521275 single base substitution C T intron_variant MELA-AU 9 32522006 32522006 single base substitution G T intron_variant MELA-AU 9 32522896 32522896 single base substitution A G intron_variant MELA-AU 9 32523799 32523799 single base substitution C T intron_variant MELA-AU 9 32523899 32523899 single base substitution T C intron_variant MELA-AU 9 32524575 32524575 single base substitution G A intron_variant MELA-AU 9 32527859 32527859 single base substitution G A upstream_gene_variant MELA-AU 9 32527933 32527933 single base substitution G A upstream_gene_variant MELA-AU 9 32528284 32528284 single base substitution G A upstream_gene_variant MELA-AU 9 32528370 32528370 single base substitution G A upstream_gene_variant MELA-AU 9 32528696 32528696 single base substitution G A upstream_gene_variant MELA-AU 9 32530159 32530159 single base substitution G A upstream_gene_variant ORCA-IN 9 32453422 32453422 single base substitution G T downstream_gene_variant OV-AU 9 32461803 32461803 single base substitution C T downstream_gene_variant OV-AU 9 32461803 32461803 single base substitution C T intron_variant OV-AU 9 32464618 32464618 single base substitution A C downstream_gene_variant OV-AU 9 32464618 32464618 single base substitution A C intron_variant OV-AU 9 32466504 32466504 single base substitution G C intron_variant OV-AU 9 32475754 32475754 single base substitution C A intron_variant OV-AU 9 32476800 32476800 single base substitution T C intron_variant OV-AU 9 32479824 32479824 single base substitution G C intron_variant OV-AU 9 32492562 32492562 single base substitution G T intron_variant OV-AU 9 32493124 32493124 single base substitution A T intron_variant OV-AU 9 32493489 32493489 single base substitution G T intron_variant OV-AU 9 32493880 32493880 single base substitution T G 5_prime_UTR_variant OV-AU 9 32493880 32493880 single base substitution T G missense_variant E101A 302A>C OV-AU 9 32493880 32493880 single base substitution T G missense_variant E30A 89A>C OV-AU 9 32493880 32493880 single base substitution T G missense_variant E56A 167A>C OV-AU 9 32496989 32496989 single base substitution T C intron_variant OV-AU 9 32499004 32499004 single base substitution G C intron_variant OV-AU 9 32505443 32505443 single base substitution T C intron_variant OV-AU 9 32505443 32505443 single base substitution T C upstream_gene_variant OV-AU 9 32505631 32505631 single base substitution C G intron_variant OV-AU 9 32505631 32505631 single base substitution C G upstream_gene_variant OV-AU 9 32506324 32506324 single base substitution G A intron_variant OV-AU 9 32506324 32506324 single base substitution G A upstream_gene_variant OV-AU 9 32506680 32506680 single base substitution C T intron_variant OV-AU 9 32506680 32506680 single base substitution C T upstream_gene_variant OV-AU 9 32508538 32508538 single base substitution G C intron_variant OV-AU 9 32517748 32517748 single base substitution C G intron_variant OV-AU 9 32519741 32519741 single base substitution A C intron_variant OV-AU 9 32526363 32526363 single base substitution G C upstream_gene_variant OV-AU 9 32526889 32526889 single base substitution G C upstream_gene_variant PACA-AU 9 32451676 32451678 deletion of <=200bp CTT - downstream_gene_variant PACA-AU 9 32457559 32457559 single base substitution A G intron_variant PACA-AU 9 32468941 32468941 single base substitution C T intron_variant PACA-AU 9 32469510 32469510 single base substitution G C intron_variant PACA-AU 9 32475443 32475443 single base substitution G T intron_variant PACA-AU 9 32476607 32476607 single base substitution A T intron_variant PACA-AU 9 32476850 32476850 single base substitution C T intron_variant PACA-AU 9 32476994 32476994 single base substitution C T missense_variant R434K 1301G>A PACA-AU 9 32476994 32476994 single base substitution C T missense_variant R566K 1697G>A PACA-AU 9 32476994 32476994 single base substitution C T missense_variant R592K 1775G>A PACA-AU 9 32476994 32476994 single base substitution C T missense_variant R637K 1910G>A PACA-AU 9 32479391 32479391 deletion of <=200bp A - intron_variant PACA-AU 9 32484895 32484895 single base substitution G A intron_variant PACA-AU 9 32486271 32486271 single base substitution G A intron_variant PACA-AU 9 32489377 32489377 single base substitution A G missense_variant M184T 551T>C PACA-AU 9 32489377 32489377 single base substitution A G missense_variant M210T 629T>C PACA-AU 9 32489377 32489377 single base substitution A G missense_variant M255T 764T>C PACA-AU 9 32489377 32489377 single base substitution A G missense_variant M52T 155T>C PACA-AU 9 32493070 32493070 single base substitution G T intron_variant PACA-AU 9 32498456 32498456 single base substitution C A 5_prime_UTR_variant PACA-AU 9 32498456 32498456 single base substitution C A intron_variant PACA-AU 9 32501098 32501098 single base substitution G T intron_variant PACA-AU 9 32504442 32504442 deletion of <=200bp A - intron_variant PACA-AU 9 32504442 32504442 deletion of <=200bp A - upstream_gene_variant PACA-AU 9 32508330 32508330 single base substitution C T intron_variant PACA-AU 9 32514051 32514051 single base substitution A G intron_variant PACA-AU 9 32514738 32514738 single base substitution T C intron_variant PACA-AU 9 32518605 32518605 single base substitution T C intron_variant PACA-AU 9 32530965 32530966 deletion of <=200bp TG - upstream_gene_variant PACA-CA 9 32453182 32453182 single base substitution C T downstream_gene_variant PACA-CA 9 32455629 32455629 insertion of <=200bp - A 3_prime_UTR_variant PACA-CA 9 32455629 32455629 insertion of <=200bp - A downstream_gene_variant PACA-CA 9 32458109 32458109 single base substitution G T intron_variant PACA-CA 9 32459236 32459236 insertion of <=200bp - T intron_variant PACA-CA 9 32467279 32467279 single base substitution C G intron_variant PACA-CA 9 32470596 32470596 single base substitution C T intron_variant PACA-CA 9 32476843 32476843 single base substitution C A intron_variant PACA-CA 9 32476967 32476967 insertion of <=200bp - A intron_variant PACA-CA 9 32480370 32480370 single base substitution T C intron_variant PACA-CA 9 32483276 32483276 single base substitution C T intron_variant PACA-CA 9 32489593 32489593 single base substitution A C intron_variant PACA-CA 9 32489887 32489901 deletion of <=200bp TTCTCAAATGATATT - intron_variant PACA-CA 9 32490022 32490022 single base substitution A C intron_variant PACA-CA 9 32491093 32491110 deletion of <=200bp GAAGAAAAAAAGATAGTG - intron_variant PACA-CA 9 32492375 32492375 single base substitution G A intron_variant PACA-CA 9 32493779 32493779 single base substitution C A 5_prime_UTR_variant PACA-CA 9 32493779 32493779 single base substitution C A stop_gained E135* 403G>T PACA-CA 9 32493779 32493779 single base substitution C A stop_gained E64* 190G>T PACA-CA 9 32493779 32493779 single base substitution C A stop_gained E90* 268G>T PACA-CA 9 32496103 32496103 single base substitution T C intron_variant PACA-CA 9 32498321 32498321 single base substitution C T intron_variant PACA-CA 9 32498321 32498321 single base substitution C T missense_variant C6Y 17G>A PACA-CA 9 32499242 32499242 single base substitution T A intron_variant PACA-CA 9 32500918 32500918 single base substitution C A 5_prime_UTR_premature_start_codon_gain_variant PACA-CA 9 32500918 32500918 single base substitution C A intron_variant PACA-CA 9 32500918 32500918 single base substitution C A missense_variant Q42H 126G>T PACA-CA 9 32502503 32502503 single base substitution C A intron_variant PACA-CA 9 32505529 32505529 single base substitution G A intron_variant PACA-CA 9 32505529 32505529 single base substitution G A upstream_gene_variant PACA-CA 9 32505580 32505580 single base substitution G A intron_variant PACA-CA 9 32505580 32505580 single base substitution G A upstream_gene_variant PACA-CA 9 32505701 32505701 single base substitution G T intron_variant PACA-CA 9 32505701 32505701 single base substitution G T upstream_gene_variant PACA-CA 9 32510229 32510229 single base substitution A G intron_variant PACA-CA 9 32514893 32514893 single base substitution C T intron_variant PACA-CA 9 32516766 32516766 single base substitution G A intron_variant PACA-CA 9 32517494 32517494 single base substitution T A intron_variant PACA-CA 9 32518114 32518114 single base substitution C A intron_variant PACA-CA 9 32518640 32518640 single base substitution A C intron_variant PACA-CA 9 32521328 32521328 single base substitution G A intron_variant PACA-CA 9 32524496 32524496 single base substitution C T intron_variant PACA-CA 9 32526224 32526224 single base substitution G T 5_prime_UTR_variant PACA-CA 9 32526224 32526224 single base substitution G T upstream_gene_variant PACA-CA 9 32530044 32530044 single base substitution C T upstream_gene_variant PACA-CA 9 32530569 32530570 deletion of <=200bp GT - upstream_gene_variant PAEN-AU 9 32509712 32509712 insertion of <=200bp - AACAA intron_variant PAEN-IT 9 32451202 32451202 single base substitution G A downstream_gene_variant PAEN-IT 9 32478233 32478233 single base substitution G C intron_variant PBCA-DE 9 32460484 32460484 insertion of <=200bp - A intron_variant PBCA-DE 9 32470564 32470564 single base substitution C A intron_variant PBCA-DE 9 32473152 32473152 single base substitution T A intron_variant PBCA-DE 9 32478770 32478770 single base substitution C T intron_variant PBCA-DE 9 32481339 32481339 single base substitution C T missense_variant R343Q 1028G>A PBCA-DE 9 32481339 32481339 single base substitution C T missense_variant R475Q 1424G>A PBCA-DE 9 32481339 32481339 single base substitution C T missense_variant R501Q 1502G>A PBCA-DE 9 32481339 32481339 single base substitution C T missense_variant R546Q 1637G>A PBCA-DE 9 32482640 32482640 single base substitution C T intron_variant PBCA-DE 9 32489191 32489191 insertion of <=200bp - A intron_variant PBCA-DE 9 32493953 32493953 insertion of <=200bp - A intron_variant PBCA-DE 9 32509637 32509637 single base substitution C T intron_variant PBCA-DE 9 32515174 32515174 single base substitution C T intron_variant PBCA-DE 9 32525009 32525009 single base substitution G A intron_variant PRAD-CA 9 32485886 32485886 single base substitution G A intron_variant PRAD-CA 9 32503090 32503090 single base substitution C T intron_variant PRAD-CA 9 32503090 32503090 single base substitution C T upstream_gene_variant PRAD-UK 9 32465302 32465302 single base substitution G C downstream_gene_variant PRAD-UK 9 32465302 32465302 single base substitution G C intron_variant PRAD-UK 9 32483112 32483112 single base substitution C T intron_variant PRAD-UK 9 32485669 32485669 single base substitution G C intron_variant PRAD-UK 9 32489471 32489471 single base substitution A T intron_variant PRAD-UK 9 32489472 32489472 single base substitution T G intron_variant PRAD-UK 9 32489919 32489919 single base substitution G A intron_variant PRAD-UK 9 32490876 32490876 single base substitution G A intron_variant PRAD-UK 9 32491034 32491034 single base substitution C A intron_variant PRAD-UK 9 32491966 32491966 single base substitution G A intron_variant PRAD-UK 9 32494749 32494749 single base substitution C T intron_variant PRAD-UK 9 32505822 32505822 single base substitution G A intron_variant PRAD-UK 9 32505822 32505822 single base substitution G A upstream_gene_variant PRAD-UK 9 32520839 32520857 deletion of <=200bp CTCAGGCCGGGGCTGGTGA - intron_variant PRAD-UK 9 32521051 32521051 single base substitution G T intron_variant PRAD-UK 9 32524511 32524511 insertion of <=200bp - A intron_variant PRAD-UK 9 32525415 32525415 single base substitution T C intron_variant PRAD-UK 9 32528847 32528847 single base substitution C A upstream_gene_variant READ-US 9 32493914 32493914 single base substitution C T 5_prime_UTR_variant READ-US 9 32493914 32493914 single base substitution C T missense_variant E19K 55G>A READ-US 9 32493914 32493914 single base substitution C T missense_variant E45K 133G>A READ-US 9 32493914 32493914 single base substitution C T missense_variant E90K 268G>A RECA-EU 9 32450503 32450503 single base substitution C G downstream_gene_variant RECA-EU 9 32469164 32469164 single base substitution C G intron_variant RECA-EU 9 32482961 32482961 single base substitution A G intron_variant RECA-EU 9 32493947 32493947 single base substitution A T splice_region_variant RECA-EU 9 32500739 32500739 single base substitution T G intron_variant RECA-EU 9 32504067 32504067 single base substitution C A intron_variant RECA-EU 9 32504067 32504067 single base substitution C A upstream_gene_variant RECA-EU 9 32505580 32505580 single base substitution G A intron_variant RECA-EU 9 32505580 32505580 single base substitution G A upstream_gene_variant RECA-EU 9 32512415 32512415 single base substitution T C intron_variant RECA-EU 9 32526570 32526570 single base substitution T G upstream_gene_variant SKCA-BR 9 32452958 32452958 single base substitution A C downstream_gene_variant SKCA-BR 9 32461009 32461009 single base substitution G A intron_variant SKCA-BR 9 32461316 32461316 single base substitution G A intron_variant SKCA-BR 9 32466030 32466030 single base substitution C T downstream_gene_variant SKCA-BR 9 32466030 32466030 single base substitution C T intron_variant SKCA-BR 9 32466715 32466716 deletion of <=200bp AG - intron_variant SKCA-BR 9 32466716 32466716 single base substitution G A intron_variant SKCA-BR 9 32468409 32468409 single base substitution G A intron_variant SKCA-BR 9 32471484 32471484 single base substitution G A intron_variant SKCA-BR 9 32476511 32476511 single base substitution G A intron_variant SKCA-BR 9 32476665 32476665 single base substitution C A intron_variant SKCA-BR 9 32478905 32478905 single base substitution A T intron_variant SKCA-BR 9 32480654 32480654 single base substitution G A intron_variant SKCA-BR 9 32485693 32485693 single base substitution C T intron_variant SKCA-BR 9 32490378 32490378 insertion of <=200bp - TAAC intron_variant SKCA-BR 9 32491990 32491990 single base substitution C T intron_variant SKCA-BR 9 32494118 32494118 single base substitution A G intron_variant SKCA-BR 9 32499310 32499310 single base substitution A T intron_variant SKCA-BR 9 32499447 32499447 single base substitution A T intron_variant SKCA-BR 9 32500311 32500311 single base substitution G A intron_variant SKCA-BR 9 32501323 32501323 insertion of <=200bp - CA intron_variant SKCA-BR 9 32501342 32501345 deletion of <=200bp AAAT - intron_variant SKCA-BR 9 32501345 32501345 single base substitution T A intron_variant SKCA-BR 9 32502697 32502697 single base substitution C T 5_prime_UTR_variant SKCA-BR 9 32502697 32502697 single base substitution C T intron_variant SKCA-BR 9 32504666 32504666 single base substitution G A intron_variant SKCA-BR 9 32504666 32504666 single base substitution G A upstream_gene_variant SKCA-BR 9 32504865 32504865 single base substitution A T intron_variant SKCA-BR 9 32504865 32504865 single base substitution A T upstream_gene_variant SKCA-BR 9 32510046 32510046 single base substitution G A intron_variant SKCA-BR 9 32510413 32510413 single base substitution G T intron_variant SKCA-BR 9 32515315 32515315 single base substitution C A intron_variant SKCA-BR 9 32515953 32515953 single base substitution G A intron_variant SKCA-BR 9 32520813 32520851 deletion of <=200bp GTGGTGGCTCAGGCTGGGCGTGGTGGCTCAGGCCGGGGC - intron_variant SKCA-BR 9 32523444 32523444 single base substitution A C intron_variant SKCA-BR 9 32524597 32524597 insertion of <=200bp - TC intron_variant SKCA-BR 9 32524598 32524598 single base substitution T C intron_variant SKCA-BR 9 32526360 32526360 single base substitution T G upstream_gene_variant SKCA-BR 9 32527492 32527493 deletion of <=200bp CT - upstream_gene_variant SKCA-BR 9 32530960 32530960 insertion of <=200bp - GT upstream_gene_variant SKCM-US 9 32477025 32477025 single base substitution C T missense_variant E424K 1270G>A SKCM-US 9 32477025 32477025 single base substitution C T missense_variant E556K 1666G>A SKCM-US 9 32477025 32477025 single base substitution C T missense_variant E582K 1744G>A SKCM-US 9 32477025 32477025 single base substitution C T missense_variant E627K 1879G>A SKCM-US 9 32487516 32487516 single base substitution T C missense_variant K240R 719A>G SKCM-US 9 32487516 32487516 single base substitution T C missense_variant K372R 1115A>G SKCM-US 9 32487516 32487516 single base substitution T C missense_variant K398R 1193A>G SKCM-US 9 32487516 32487516 single base substitution T C missense_variant K443R 1328A>G SKCM-US 9 32493803 32493803 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant SKCM-US 9 32493803 32493803 single base substitution G A synonymous_variant L127L 379C>T SKCM-US 9 32493803 32493803 single base substitution G A synonymous_variant L56L 166C>T SKCM-US 9 32493803 32493803 single base substitution G A synonymous_variant L82L 244C>T SKCM-US 9 32500834 32500834 single base substitution G A 5_prime_UTR_variant SKCM-US 9 32500834 32500834 single base substitution G A intron_variant SKCM-US 9 32500834 32500834 single base substitution G A synonymous_variant F70F 210C>T SKCM-US 9 32500845 32500845 single base substitution C T 5_prime_UTR_variant SKCM-US 9 32500845 32500845 single base substitution C T intron_variant SKCM-US 9 32500845 32500845 single base substitution C T missense_variant E67K 199G>A STAD-US 9 32457294 32457294 single base substitution G C missense_variant N665K 1995C>G STAD-US 9 32457294 32457294 single base substitution G C missense_variant N797K 2391C>G STAD-US 9 32457294 32457294 single base substitution G C missense_variant N823K 2469C>G STAD-US 9 32457294 32457294 single base substitution G C missense_variant N868K 2604C>G STAD-US 9 32459462 32459462 deletion of <=200bp T - frameshift_variant K593 STAD-US 9 32459462 32459462 deletion of <=200bp T - frameshift_variant K725 STAD-US 9 32459462 32459462 deletion of <=200bp T - frameshift_variant K751 STAD-US 9 32459462 32459462 deletion of <=200bp T - frameshift_variant K796 STAD-US 9 32466435 32466435 single base substitution T C missense_variant E526G 1577A>G STAD-US 9 32466435 32466435 single base substitution T C synonymous_variant R527R 1581A>G STAD-US 9 32466435 32466435 single base substitution T C synonymous_variant R659R 1977A>G STAD-US 9 32466435 32466435 single base substitution T C synonymous_variant R685R 2055A>G STAD-US 9 32466435 32466435 single base substitution T C synonymous_variant R730R 2190A>G STAD-US 9 32481357 32481357 deletion of <=200bp A - frameshift_variant L337 STAD-US 9 32481357 32481357 deletion of <=200bp A - frameshift_variant L469 STAD-US 9 32481357 32481357 deletion of <=200bp A - frameshift_variant L495 STAD-US 9 32481357 32481357 deletion of <=200bp A - frameshift_variant L540 STAD-US 9 32481366 32481366 single base substitution G A missense_variant A334V 1001C>T STAD-US 9 32481366 32481366 single base substitution G A missense_variant A466V 1397C>T STAD-US 9 32481366 32481366 single base substitution G A missense_variant A492V 1475C>T STAD-US 9 32481366 32481366 single base substitution G A missense_variant A537V 1610C>T STAD-US 9 32485235 32485235 single base substitution T C missense_variant Y270C 809A>G STAD-US 9 32485235 32485235 single base substitution T C missense_variant Y402C 1205A>G STAD-US 9 32485235 32485235 single base substitution T C missense_variant Y428C 1283A>G STAD-US 9 32485235 32485235 single base substitution T C missense_variant Y473C 1418A>G STAD-US 9 32487537 32487537 single base substitution G A missense_variant A233V 698C>T STAD-US 9 32487537 32487537 single base substitution G A missense_variant A365V 1094C>T STAD-US 9 32487537 32487537 single base substitution G A missense_variant A391V 1172C>T STAD-US 9 32487537 32487537 single base substitution G A missense_variant A436V 1307C>T STAD-US 9 32487588 32487588 deletion of <=200bp T - frameshift_variant N216 STAD-US 9 32487588 32487588 deletion of <=200bp T - frameshift_variant N348 STAD-US 9 32487588 32487588 deletion of <=200bp T - frameshift_variant N374 STAD-US 9 32487588 32487588 deletion of <=200bp T - frameshift_variant N419 STAD-US 9 32488855 32488855 single base substitution A C missense_variant I206R 617T>G STAD-US 9 32488855 32488855 single base substitution A C missense_variant I232R 695T>G STAD-US 9 32488855 32488855 single base substitution A C missense_variant I277R 830T>G STAD-US 9 32488855 32488855 single base substitution A C missense_variant I74R 221T>G STAD-US 9 32492458 32492458 single base substitution G A intron_variant STAD-US 9 32492458 32492458 single base substitution G A missense_variant P123S 367C>T STAD-US 9 32492458 32492458 single base substitution G A missense_variant P168S 502C>T STAD-US 9 32492458 32492458 single base substitution G A missense_variant P97S 289C>T STAD-US 9 32500831 32500831 single base substitution A G 5_prime_UTR_variant STAD-US 9 32500831 32500831 single base substitution A G intron_variant STAD-US 9 32500831 32500831 single base substitution A G synonymous_variant R71R 213T>C STAD-US 9 32526164 32526164 single base substitution T C 5_prime_UTR_variant STAD-US 9 32526164 32526164 single base substitution T C start_lost M1V 1A>G THCA-US 9 32457322 32457322 single base substitution C T missense_variant R656K 1967G>A THCA-US 9 32457322 32457322 single base substitution C T missense_variant R788K 2363G>A THCA-US 9 32457322 32457322 single base substitution C T missense_variant R814K 2441G>A THCA-US 9 32457322 32457322 single base substitution C T missense_variant R859K 2576G>A UCEC-US 9 32459383 32459383 single base substitution C T missense_variant V620I 1858G>A UCEC-US 9 32459383 32459383 single base substitution C T missense_variant V752I 2254G>A UCEC-US 9 32459383 32459383 single base substitution C T missense_variant V778I 2332G>A UCEC-US 9 32459383 32459383 single base substitution C T missense_variant V823I 2467G>A UCEC-US 9 32459487 32459487 single base substitution T G missense_variant K585T 1754A>C UCEC-US 9 32459487 32459487 single base substitution T G missense_variant K717T 2150A>C UCEC-US 9 32459487 32459487 single base substitution T G missense_variant K743T 2228A>C UCEC-US 9 32459487 32459487 single base substitution T G missense_variant K788T 2363A>C UCEC-US 9 32466345 32466345 single base substitution C A downstream_gene_variant UCEC-US 9 32466345 32466345 single base substitution C A missense_variant M557I 1671G>T UCEC-US 9 32466345 32466345 single base substitution C A missense_variant M689I 2067G>T UCEC-US 9 32466345 32466345 single base substitution C A missense_variant M715I 2145G>T UCEC-US 9 32466345 32466345 single base substitution C A missense_variant M760I 2280G>T UCEC-US 9 32467809 32467809 single base substitution G T synonymous_variant V509V 1527C>A UCEC-US 9 32467809 32467809 single base substitution G T synonymous_variant V641V 1923C>A UCEC-US 9 32467809 32467809 single base substitution G T synonymous_variant V667V 2001C>A UCEC-US 9 32467809 32467809 single base substitution G T synonymous_variant V712V 2136C>A UCEC-US 9 32477073 32477073 single base substitution G T missense_variant L408I 1222C>A UCEC-US 9 32477073 32477073 single base substitution G T missense_variant L540I 1618C>A UCEC-US 9 32477073 32477073 single base substitution G T missense_variant L566I 1696C>A UCEC-US 9 32477073 32477073 single base substitution G T missense_variant L611I 1831C>A UCEC-US 9 32477110 32477110 single base substitution T G missense_variant E395D 1185A>C UCEC-US 9 32477110 32477110 single base substitution T G missense_variant E527D 1581A>C UCEC-US 9 32477110 32477110 single base substitution T G missense_variant E553D 1659A>C UCEC-US 9 32477110 32477110 single base substitution T G missense_variant E598D 1794A>C UCEC-US 9 32480217 32480217 single base substitution C T missense_variant E389K 1165G>A UCEC-US 9 32480217 32480217 single base substitution C T missense_variant E521K 1561G>A UCEC-US 9 32480217 32480217 single base substitution C T missense_variant E547K 1639G>A UCEC-US 9 32480217 32480217 single base substitution C T missense_variant E592K 1774G>A UCEC-US 9 32488074 32488074 single base substitution G A missense_variant P158S 472C>T UCEC-US 9 32488074 32488074 single base substitution G A missense_variant P290S 868C>T UCEC-US 9 32488074 32488074 single base substitution G A missense_variant P316S 946C>T UCEC-US 9 32488074 32488074 single base substitution G A missense_variant P361S 1081C>T UCEC-US 9 32488794 32488794 single base substitution C T synonymous_variant A226A 678G>A UCEC-US 9 32488794 32488794 single base substitution C T synonymous_variant A252A 756G>A UCEC-US 9 32488794 32488794 single base substitution C T synonymous_variant A297A 891G>A UCEC-US 9 32488794 32488794 single base substitution C T synonymous_variant A94A 282G>A UCEC-US 9 32488887 32488887 single base substitution T G splice_acceptor_variant UCEC-US 9 32489410 32489410 single base substitution C A missense_variant R173I 518G>T UCEC-US 9 32489410 32489410 single base substitution C A missense_variant R199I 596G>T UCEC-US 9 32489410 32489410 single base substitution C A missense_variant R244I 731G>T UCEC-US 9 32489410 32489410 single base substitution C A missense_variant R41I 122G>T UCEC-US 9 32491325 32491325 single base substitution A C missense_variant L151R 452T>G UCEC-US 9 32491325 32491325 single base substitution A C missense_variant L177R 530T>G UCEC-US 9 32491325 32491325 single base substitution A C missense_variant L19R 56T>G UCEC-US 9 32491325 32491325 single base substitution A C missense_variant L222R 665T>G UCEC-US 9 32491420 32491420 single base substitution T G splice_acceptor_variant UCEC-US 9 32493801 32493801 single base substitution C T 5_prime_UTR_variant UCEC-US 9 32493801 32493801 single base substitution C T synonymous_variant L127L 381G>A UCEC-US 9 32493801 32493801 single base substitution C T synonymous_variant L56L 168G>A UCEC-US 9 32493801 32493801 single base substitution C T synonymous_variant L82L 246G>A UCEC-US 9 32493845 32493845 single base substitution C A 5_prime_UTR_variant UCEC-US 9 32493845 32493845 single base substitution C A stop_gained E113* 337G>T UCEC-US 9 32493845 32493845 single base substitution C A stop_gained E42* 124G>T UCEC-US 9 32493845 32493845 single base substitution C A stop_gained E68* 202G>T UCEC-US 9 32493856 32493856 single base substitution C T 5_prime_UTR_variant UCEC-US 9 32493856 32493856 single base substitution C T missense_variant R109H 326G>A UCEC-US 9 32493856 32493856 single base substitution C T missense_variant R38H 113G>A UCEC-US 9 32493856 32493856 single base substitution C T missense_variant R64H 191G>A

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand SNUH_G45_S1 COSM3982816 c.1376-3T>C p.? Unknown 9:32485282-32485282 - PT35 COSM5912903 c.2291C>T p.S764F Substitution - Missense 9:32466336-32466336 - HCC26T COSM3664301 c.1422C>T p.I474I Substitution - coding silent 9:32485233-32485233 - T2664 COSM4676887 c.948A>C p.R316S Substitution - Missense 9:32488739-32488739 - 8066479 COSM3780734 c.1910G>A p.R637K Substitution - Missense 9:32476996-32476996 - B86 COSM1756119 c.1461G>C p.K487N Substitution - Missense 9:32485194-32485194 - TCGA-FW-A3R5-06 COSM3656818 c.210C>T p.F70F Substitution - coding silent 9:32500836-32500836 - 06-P036 COSM4588766 c.9C>T p.T3T Substitution - coding silent 9:32526158-32526158 - M14 COSM1674448 c.2665A>C p.I889L Substitution - Missense 9:32457235-32457235 - 091-01-6TD COSM145307 c.2272G>A p.E758K Substitution - Missense 9:32466355-32466355 - 08-P8005 COSM4588761 c.2102A>C p.D701A Substitution - Missense 9:32467845-32467845 - TCGA-EE-A2GJ-06 COSM3656819 c.199G>A p.E67K Substitution - Missense 9:32500847-32500847 - HCC59T COSM3664300 c.2766A>T p.E922D Substitution - Missense 9:32457134-32457134 - TCGA-BR-8372-01 COSM3906810 c.1610C>T p.A537V Substitution - Missense 9:32481368-32481368 - RMS105_ COSM3763882 c.19C>T p.R7C Substitution - Missense 9:32526148-32526148 - TCGA-AP-A059-01 COSM1108179 c.337G>T p.E113* Substitution - Nonsense 9:32493847-32493847 - 587376 COSM1203280 c.1523A>G p.K508R Substitution - Missense 9:32481455-32481455 - TCGA-AN-A0FT-01 COSM455819 c.1581C>T p.D527D Substitution - coding silent 9:32481397-32481397 - CAL33 COSM2772039 c.2749C>T p.P917S Substitution - Missense 9:32457151-32457151 - SS6003121 COSM3849415 c.1349A>G p.E450G Substitution - Missense 9:32487497-32487497 - sysucc-1163T COSM5459437 c.681T>C p.C227C Substitution - coding silent 9:32491311-32491311 - B86-Tumor COSM1756119 c.1461G>C p.K487N Substitution - Missense 9:32485194-32485194 - TCGA-BR-4362-01 COSM3906806 c.2190A>G p.R730R Substitution - coding silent 9:32466437-32466437 - CH-56-T2 COSM5651132 c.592G>A p.E198K Substitution - Missense 9:32491400-32491400 - TCGA-23-1110-01 COSM70424 c.1171C>G p.L391V Substitution - Missense 9:32487986-32487986 - T1154 COSM4676889 c.289_290insA p.I97fs*2 Insertion - Frameshift 9:32493894-32493895 - TCGA-AP-A056-01 COSM1108163 c.2280G>T p.M760I Substitution - Missense 9:32466347-32466347 - TCGA-BR-7707-01 COSM3906817 c.502C>T p.P168S Substitution - Missense 9:32492460-32492460 - CHC1044T COSM4791025 c.2575A>G p.R859G Substitution - Missense 9:32457325-32457325 - TCGA-AZ-6605-01 COSM1461971 c.2189G>C p.R730T Substitution - Missense 9:32466438-32466438 - TCGA-HU-A4GU-01 COSM3906816 c.830T>G p.I277R Substitution - Missense 9:32488857-32488857 - HCC2998 COSM1108161 c.2467G>A p.V823I Substitution - Missense 9:32459385-32459385 - T578 COSM1108161 c.2467G>A p.V823I Substitution - Missense 9:32459385-32459385 - ESO-1154 COSM1249921 c.1371G>A p.Q457Q Substitution - coding silent 9:32487475-32487475 - TCGA-B5-A11H-01 COSM1108180 c.326G>A p.R109H Substitution - Missense 9:32493858-32493858 - sysucc-274T COSM5476875 c.2394A>T p.K798N Substitution - Missense 9:32459458-32459458 - KM12 COSM1674449 c.1232C>T p.S411L Substitution - Missense 9:32487614-32487614 - CRC-02T COSM5455777 c.1908C>T p.T636T Substitution - coding silent 9:32476998-32476998 - TCGA-AA-A010-01 COSM280344 c.1636C>T p.R546W Substitution - Missense 9:32481342-32481342 - 2521243 COSM5886615 c.412G>A p.E138K Substitution - Missense 9:32493772-32493772 - KM12 COSM1674449 c.1232C>T p.S411L Substitution - Missense 9:32487614-32487614 - BN50T COSM1624902 c.1457C>T p.A486V Substitution - Missense 9:32485198-32485198 - B88 COSM1756118 c.2071C>T p.H691Y Substitution - Missense 9:32467876-32467876 - AOCS-117-3-3 COSM4152244 c.302A>C p.E101A Substitution - Missense 9:32493882-32493882 - EV001-M1 COSM1161926 c.1335T>A p.N445K Substitution - Missense 9:32487511-32487511 - ESO-409 COSM1249922 c.241+1G>A p.? Unknown 9:32500804-32500804 - 091 COSM145307 c.2272G>A p.E758K Substitution - Missense 9:32466355-32466355 - WA13 COSM237285 c.106+4A>G p.? Unknown 9:32526057-32526057 - TCGA-GL-A59R-01 COSM3996508 c.2430C>A p.C810* Substitution - Nonsense 9:32459422-32459422 - CHC1044T COSM4791025 c.2575A>G p.R859G Substitution - Missense 9:32457325-32457325 - 8064157 COSM3395781 c.764T>C p.M255T Substitution - Missense 9:32489379-32489379 - PD24304a COSM5787452 c.1140A>G p.Q380Q Substitution - coding silent 9:32488017-32488017 - PDA_074 COSM3763882 c.19C>T p.R7C Substitution - Missense 9:32526148-32526148 - TCGA-D5-5539-01 COSM1461969 c.2698G>A p.G900R Substitution - Missense 9:32457202-32457202 - ESO-580 COSM1249923 c.2129A>T p.N710I Substitution - Missense 9:32467818-32467818 - TCGA-AN-A0FT-01 COSM455818 c.1611C>G p.A537A Substitution - coding silent 9:32481367-32481367 - PD22361a COSM5798765 c.1212+7C>T p.? Unknown 9:32487938-32487938 - TCGA-AC-A2QI-01 COSM3848319 c.2251G>A p.E751K Substitution - Missense 9:32466376-32466376 - T2950 COSM4676890 c.22A>G p.S8G Substitution - Missense 9:32526145-32526145 - N742T COSM236405 c.797C>A p.T266K Substitution - Missense 9:32489346-32489346 - TCGA-D1-A17Q-01 COSM1108176 c.665T>G p.L222R Substitution - Missense 9:32491327-32491327 - PD4952a COSM5787967 c.2055C>G p.F685L Substitution - Missense 9:32467892-32467892 - HCC59 COSM3664300 c.2766A>T p.E922D Substitution - Missense 9:32457134-32457134 - RK003_C COSM53415 c.1929A>T p.L643F Substitution - Missense 9:32473060-32473060 - 2318491 COSM4776707 c.17G>A p.R6Q Substitution - Missense 9:32526150-32526150 - PT21_2 COSM5901591 c.493G>A p.E165K Substitution - Missense 9:32492469-32492469 - PD4952a COSM5787956 c.2043A>G p.I681M Substitution - Missense 9:32467904-32467904 - TCGA-AA-3982-01 COSM297800 c.670G>A p.E224K Substitution - Missense 9:32491322-32491322 - TCGA-AM-5821-01 COSM3763882 c.19C>T p.R7C Substitution - Missense 9:32526148-32526148 - Pa21C COSM85160 c.1924G>C p.A642P Substitution - Missense 9:32473065-32473065 - 12924 COSM5616118 c.1095C>G p.I365M Substitution - Missense 9:32488062-32488062 - TCGA-CC-5258-01 COSM4933355 c.2741A>G p.E914G Substitution - Missense 9:32457159-32457159 - MDA-N COSM1674448 c.2665A>C p.I889L Substitution - Missense 9:32457235-32457235 - TCGA-AM-5821-01 COSM3763881 c.1740T>A p.D580E Substitution - Missense 9:32480253-32480253 - LUAD-NYU201 COSM371500 c.797C>T p.T266I Substitution - Missense 9:32489346-32489346 - TCGA-C8-A12P-01 COSM455820 c.606T>C p.D202D Substitution - coding silent 9:32491386-32491386 - TCGA-L6-A4EU-01 COSM3375225 c.2576G>A p.R859K Substitution - Missense 9:32457324-32457324 - T3499 COSM4676885 c.1747G>T p.E583* Substitution - Nonsense 9:32480246-32480246 - TCGA-B5-A0K9-01 COSM1108178 c.381G>A p.L127L Substitution - coding silent 9:32493803-32493803 - EV001-M2a COSM1161926 c.1335T>A p.N445K Substitution - Missense 9:32487511-32487511 - TCGA-CM-6171-01 COSM1461977 c.1076C>T p.T359M Substitution - Missense 9:32488081-32488081 - TCGA-AM-5821-01 COSM3763879 c.2400A>C p.V800V Substitution - coding silent 9:32459452-32459452 - 30374 COSM5043983 c.2007G>C p.Q669H Substitution - Missense 9:32472982-32472982 - TCGA-AP-A059-01 COSM1108177 c.572-2A>C p.? Unknown 9:32491422-32491422 - TCGA-D9-A6EC-06 COSM4403488 c.1328A>G p.K443R Substitution - Missense 9:32487518-32487518 - RMS111_ COSM3763882 c.19C>T p.R7C Substitution - Missense 9:32526148-32526148 - 61 COSM5738568 c.888_889insT p.A297fs*8 Insertion - Frameshift 9:32488798-32488799 - TCGA-BS-A0UV-01 COSM1108172 c.1081C>T p.P361S Substitution - Missense 9:32488076-32488076 - T3021 COSM1461979 c.289delA p.I97fs*11 Deletion - Frameshift 9:32493895-32493895 - S0080 COSM5884845 c.1459A>C p.K487Q Substitution - Missense 9:32485196-32485196 - TCGA-GN-A266-06 COSM3656814 c.1879G>A p.E627K Substitution - Missense 9:32477027-32477027 - TCGA-JW-A5VJ-01 COSM4818578 c.1447G>A p.E483K Substitution - Missense 9:32485208-32485208 - ESCC_127 COSM5641579 c.1155G>A p.M385I Substitution - Missense 9:32488002-32488002 - TCGA-29-1781-01 COSM1331585 c.373T>C p.S125P Substitution - Missense 9:32493811-32493811 - D7 COSM5007649 c.2068G>T p.D690Y Substitution - Missense 9:32467879-32467879 - T30 COSM3763881 c.1740T>A p.D580E Substitution - Missense 9:32480253-32480253 - TCGA-D1-A103-01 COSM1108164 c.2136C>A p.V712V Substitution - coding silent 9:32467811-32467811 - TCGA-AP-A056-01 COSM1108162 c.2363A>C p.K788T Substitution - Missense 9:32459489-32459489 - TCGA-ED-A7XO-01 COSM4929147 c.763A>G p.M255V Substitution - Missense 9:32489380-32489380 - TCGA-BS-A0UF-01 COSM1108169 c.1774G>A p.E592K Substitution - Missense 9:32480219-32480219 - I2L-P19Ta-Tumor-Organoid COSM5367760 c.242-4_242-3insT p.? Unknown 9:32493945-32493946 - 426 COSM4432966 c.954G>A p.G318G Substitution - coding silent 9:32488203-32488203 - RW2982 COSM4649808 c.1907C>G p.T636S Substitution - Missense 9:32476999-32476999 - YUZINO COSM1701027 c.182T>G p.L61R Substitution - Missense 9:32500864-32500864 - TCGA-AX-A0J0-01 COSM1108166 c.1794A>C p.E598D Substitution - Missense 9:32477112-32477112 - HT115 COSM2772046 c.2300G>A p.R767H Substitution - Missense 9:32466327-32466327 - CHLA-258 COSM4588765 c.1059C>T p.N353N Substitution - coding silent 9:32488098-32488098 - NB06C COSM1236352 c.1471A>C p.K491Q Substitution - Missense 9:32485184-32485184 - MDA-MB-435 COSM1674448 c.2665A>C p.I889L Substitution - Missense 9:32457235-32457235 - RMS112_ COSM3763882 c.19C>T p.R7C Substitution - Missense 9:32526148-32526148 - LUAD-NYU847 COSM376953 c.241G>T p.G81C Substitution - Missense 9:32500805-32500805 - TCGA-CI-6622-01 COSM1569301 c.268G>A p.E90K Substitution - Missense 9:32493916-32493916 - TCGA-D1-A17Q-01 COSM1108175 c.731G>T p.R244I Substitution - Missense 9:32489412-32489412 - LUAD-S01357 COSM392523 c.1880_1900del21 p.E627_F633delETITILF Deletion - In frame SKNEP1 COSM2772065 c.1440G>C p.R480S Substitution - Missense 9:32485215-32485215 - CRC-03T COSM5451974 c.184T>A p.L62M Substitution - Missense 9:32500862-32500862 - RKO COSM4649328 c.1395A>G p.S465S Substitution - coding silent 9:32485260-32485260 - TCGA-D8-A1XK-01 COSM3848320 c.1313T>C p.V438A Substitution - Missense 9:32487533-32487533 - B88-Tumor COSM1756118 c.2071C>T p.H691Y Substitution - Missense 9:32467876-32467876 - TCGA-G9-6342-01 COSM3675320 c.2154G>T p.V718V Substitution - coding silent 9:32467793-32467793 - EV001-M2b COSM1161926 c.1335T>A p.N445K Substitution - Missense 9:32487511-32487511 - TCGA-60-2725-01 COSM753663 c.1062C>A p.N354K Substitution - Missense 9:32488095-32488095 - LUAD-B02077 COSM335291 c.1581C>A p.D527E Substitution - Missense 9:32481397-32481397 - HCC2998 COSM1108161 c.2467G>A p.V823I Substitution - Missense 9:32459385-32459385 - TCGA-A2-A25D-01 COSM1489931 c.2356C>T p.H786Y Substitution - Missense 9:32459496-32459496 - B86-Tumor COSM1756120 c.1447G>T p.E483* Substitution - Nonsense 9:32485208-32485208 - B86 COSM1756120 c.1447G>T p.E483* Substitution - Nonsense 9:32485208-32485208 - pfg016T COSM1643807 c.2297delT p.L766fs*58 Deletion - Frameshift 9:32466330-32466330 - PDA_027 COSM3763882 c.19C>T p.R7C Substitution - Missense 9:32526148-32526148 - TCGA-CG-5721-01 COSM3906814 c.1418A>G p.Y473C Substitution - Missense 9:32485237-32485237 - SNUH_G45_S1 COSM3982817 c.1323A>G p.T441T Substitution - coding silent 9:32487523-32487523 - TCGA-BR-8381-01 COSM3906805 c.2604C>G p.N868K Substitution - Missense 9:32457296-32457296 - TCGA-CA-6717-01 COSM1461972 c.1737C>T p.F579F Substitution - coding silent 9:32480256-32480256 - Pat_30_B COSM5876097 c.2186-4_2186-2delATA p.? Unknown 9:32466443-32466445 - HCC26 COSM3664301 c.1422C>T p.I474I Substitution - coding silent 9:32485233-32485233 - BD134T COSM5494441 c.1397G>A p.R466Q Substitution - Missense 9:32485258-32485258 - TCGA-BS-A0UF-01 COSM1108165 c.1831C>A p.L611I Substitution - Missense 9:32477075-32477075 - TCGA-BR-7703-01 COSM3906819 c.1A>G p.M1V Substitution - Missense 9:32526166-32526166 - DLD1 COSM4626424 c.1167T>G p.N389K Substitution - Missense 9:32487990-32487990 - ATL027 COSM5711290 c.635T>A p.F212Y Substitution - Missense 9:32491357-32491357 - TCGA-GD-A3OP-01 COSM1314749 c.235C>T p.H79Y Substitution - Missense 9:32500811-32500811 - TCGA-CA-6717-01 COSM1108175 c.731G>T p.R244I Substitution - Missense 9:32489412-32489412 - BN50 COSM1624902 c.1457C>T p.A486V Substitution - Missense 9:32485198-32485198 - TCGA-FW-A3R5-06 COSM3926680 c.379C>T p.L127L Substitution - coding silent 9:32493805-32493805 - CSCC-18-T COSM4537935 c.2481G>A p.E827E Substitution - coding silent 9:32459371-32459371 - RMS10_ COSM3763882 c.19C>T p.R7C Substitution - Missense 9:32526148-32526148 - T3174 COSM4676886 c.1738G>A p.D580N Substitution - Missense 9:32480255-32480255 - TCGA-D3-A2JP-06 COSM3656818 c.210C>T p.F70F Substitution - coding silent 9:32500836-32500836 - HCT8 COSM4635730 c.1806G>T p.R602S Substitution - Missense 9:32477100-32477100 - D3 COSM5006728 c.736T>C p.Y246H Substitution - Missense 9:32489407-32489407 - TCGA-BR-6452-01 COSM3906818 c.213T>C p.R71R Substitution - coding silent 9:32500833-32500833 - YUHOIN COSM1701026 c.2614G>A p.D872N Substitution - Missense 9:32457286-32457286 - HT55 COSM2772041 c.2602A>C p.N868H Substitution - Missense 9:32457298-32457298 - TCGA-21-1077-01 COSM753662 c.76C>A p.L26M Substitution - Missense 9:32526091-32526091 - YUHOIN COSM1701025 c.2686G>C p.D896H Substitution - Missense 9:32457214-32457214 - 169 COSM1461979 c.289delA p.I97fs*11 Deletion - Frameshift 9:32493895-32493895 - TCGA-BR-A4QL-01 COSM3906815 c.1307C>T p.A436V Substitution - Missense 9:32487539-32487539 - PT19_2 COSM5943406 c.1481-6delT p.? Unknown 9:32481503-32481503 - TCGA-AY-6197-01 COSM1461978 c.852delA p.K284fs*63 Deletion - Frameshift 9:32488835-32488835 - ESO-0129 COSM1249920 c.2719A>T p.K907* Substitution - Nonsense 9:32457181-32457181 - TCGA-AP-A051-01 COSM1108161 c.2467G>A p.V823I Substitution - Missense 9:32459385-32459385 - LIM2405 COSM4643340 c.1922A>G p.D641G Substitution - Missense 9:32476984-32476984 - TCGA-BP-5185-01 COSM487361 c.1146G>A p.P382P Substitution - coding silent 9:32488011-32488011 - CHC433T COSM4406872 c.2709A>G p.T903T Substitution - coding silent 9:32457191-32457191 - NPC41F COSM4997059 c.2101G>A p.D701N Substitution - Missense 9:32467846-32467846 - T19 COSM5617991 c.930C>G p.F310L Substitution - Missense 9:32488757-32488757 - RK091_C01 COSM1636152 c.821C>G p.S274* Substitution - Nonsense 9:32488866-32488866 - EV001-R4 COSM1161926 c.1335T>A p.N445K Substitution - Missense 9:32487511-32487511 - 2492729 COSM5726300 c.1051C>T p.L351F Substitution - Missense 9:32488106-32488106 - SNU-C2B COSM4615379 c.2421_2422insA p.L808fs*15 Insertion - Frameshift 9:32459430-32459431 - TCGA-B8-5164-01 COSM487360 c.1745T>A p.I582N Substitution - Missense 9:32480248-32480248 - TCGA-BS-A0UF-01 COSM1108173 c.891G>A p.A297A Substitution - coding silent 9:32488796-32488796 - PCSI_0057_Pa_X COSM3382376 c.126G>T p.Q42H Substitution - Missense 9:32500920-32500920 - TCGA-D1-A16X-01 COSM1108174 c.800-2A>C p.? Unknown 9:32488889-32488889 - T3603 COSM4676888 c.369C>A p.I123I Substitution - coding silent 9:32493815-32493815 - 001 COSM1161926 c.1335T>A p.N445K Substitution - Missense 9:32487511-32487511 - TCGA-B5-A0JY-01 COSM1108179 c.337G>T p.E113* Substitution - Nonsense 9:32493847-32493847 - Gp5D COSM2772071 c.878T>C p.V293A Substitution - Missense 9:32488809-32488809 - TCGA-24-2030-01 COSM70423 c.1396C>T p.R466W Substitution - Missense 9:32485259-32485259 - RMS106_ COSM3763882 c.19C>T p.R7C Substitution - Missense 9:32526148-32526148 - TCGA-A8-A0A6-01 COSM3848321 c.453T>G p.G151G Substitution - coding silent 9:32492509-32492509 - ccRCC-94 COSM1661426 c.64C>A p.P22T Substitution - Missense 9:32526103-32526103 - C0097T COSM4422571 c.242-7T>A p.? Unknown 9:32493949-32493949 - SJHGG011_D COSM4969124 c.57C>A p.T19T Substitution - coding silent 9:32526110-32526110 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.190621;Hs.190622 9p12 609631

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A - Frameshift p.L766Yfs*58 c.2297delT 9 32466328 STAD AGACTC - IntronicDeletion . c.2186-281_2186-276delGAGTCT 9 32466715 CLL A G IntronicSNV . c.1481-18T>C 9 32481513 STAD A G Synonymous p.D202D c.606T>C 9 32491384 BRCA A - IntronicDeletion . c.242-13delT 9 32493953 STAD - A IntronicInsertion . c.799+52dupT 9 32489290 ESCA A T Missense p.I582N c.1745T>A 9 32480246 RCCC A T Missense p.L711H c.2132T>A 9 32467813 COREAD C A Missense p.K48N c.144G>T 9 32500900 LUAD C T IntronicSNV . c.1924-1628G>A 9 32474691 PIA C T Missense p.E224K c.670G>A 9 32491320 COREAD C T Missense p.E67K c.199G>A 9 32500845 CM C T Missense p.E758K c.2272G>A 9 32466353 CLL C T Missense p.R109H c.326G>A 9 32493856 UCEC C T Missense p.R767H c.2300G>A 9 32466325 BLCA C T SpliceDonorSNV . c.241+1G>A 9 32500802 ESCA C T Synonymous p.E66E c.198G>A 9 32500846 CM C T Synonymous p.G291G c.873G>A 9 32488812 HNSC C T Synonymous p.L127L c.381G>A 9 32493801 UCEC C T Synonymous p.P382P c.1146G>A 9 32488009 RCCC C T Synonymous p.Q457Q c.1371G>A 9 32487473 ESCA CTTG - Frameshift p.Q451Lfs*24 c.1351_1354delCAAG 9 32487490 BLCA G A Missense p.H786Y c.2356C>T 9 32459494 BRCA G A Missense p.H79Y c.235C>T 9 32500809 BLCA G A Missense p.R466W c.1396C>T 9 32485257 OV G A Nonsense p.R575* c.1723C>T 9 32480268 COREAD G A Synonymous p.D527D c.1581C>T 9 32481395 BRCA G A Synonymous p.F70F c.210C>T 9 32500834 CM G A Synonymous p.I123I c.369C>T 9 32493813 HNSC G A Synonymous p.L160L c.480C>T 9 32492480 LUAD G A Synonymous p.L402L c.1204C>T 9 32487951 LUAD G C Missense p.A642P c.1924G>C 9 32473063 PAAD G C Missense p.I365M c.1095C>G 9 32488060 NSCLC G C Missense p.L391V c.1171C>G 9 32487984 OV G C Synonymous p.A537A c.1611C>G 9 32481365 BRCA G T 3-UTRSNV . c.2775+711C>A 9 32456412 HC G T Missense p.L26M c.76C>A 9 32526089 LUSC G T Missense p.L552I c.1654C>A 9 32480337 LUAD G T Missense p.N354K c.1062C>A 9 32488093 LUSC T A Missense p.L643F c.1929A>T 9 32473058 HC T A Missense p.N710I c.2129A>T 9 32467816 ESCA T A Nonsense p.K907* c.2719A>T 9 32457179 ESCA T A Synonymous p.G269G c.807A>T 9 32488878 LUAD T C IntronicSNV . c.106+7550A>G 9 32518509 CLL T C Missense p.I862M c.2586A>G 9 32457312 COREAD T G Missense p.K491Q c.1471A>C 9 32485182 NB T G Missense p.K96T c.287A>C 9 32493895 HNSC