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 8 88885067 88885067 + Missense_Mutation SNP G G T TCGA-OR-A5KB-01A-11D-A30A-10 TCGA-OR-A5KB-11A-11D-A30A-10 g.chr8:88885067G>T c.1133C>A c.(1132-1134)gCa>gAa p.A378E ACC 8 88885852 88885852 + Silent SNP C C T TCGA-PK-A5HB-01A-11D-A29I-10 TCGA-PK-A5HB-11A-11D-A29L-10 g.chr8:88885852C>T c.348G>A c.(346-348)ccG>ccA p.P116P BLCA 8 88885024 88885024 + Missense_Mutation SNP G G T TCGA-DK-A6AW-01A-11D-A30E-08 TCGA-DK-A6AW-10A-01D-A30H-08 g.chr8:88885024G>T c.1176C>A c.(1174-1176)ttC>ttA p.F392L BLCA 8 88885074 88885074 + Nonsense_Mutation SNP G G A TCGA-XF-A9T5-01A-11D-A42E-08 TCGA-XF-A9T5-10A-01D-A42H-08 g.chr8:88885074G>A c.1126C>T c.(1126-1128)Cga>Tga p.R376* BLCA 8 88885180 88885180 + Silent SNP G G A TCGA-H4-A2HQ-01A-11D-A17V-08 TCGA-H4-A2HQ-10A-01D-A17V-08 g.chr8:88885180G>A c.1020C>T c.(1018-1020)atC>atT p.I340I BLCA 8 88885212 88885212 + Missense_Mutation SNP C C A TCGA-CU-A0YN-01A-21D-A10S-08 TCGA-CU-A0YN-11A-11D-A10S-08 g.chr8:88885212C>A c.988G>T c.(988-990)Gcg>Tcg p.A330S BLCA 8 88885230 88885230 + Nonsense_Mutation SNP C C A TCGA-DK-A3IU-01A-11D-A20D-08 TCGA-DK-A3IU-10A-01D-A20D-08 g.chr8:88885230C>A c.970G>T c.(970-972)Gaa>Taa p.E324* BLCA 8 88885245 88885245 + Missense_Mutation SNP G G A TCGA-FD-A3N6-01A-11D-A21A-08 TCGA-FD-A3N6-10A-01D-A21A-08 g.chr8:88885245G>A c.955C>T c.(955-957)Ccc>Tcc p.P319S BLCA 8 88885315 88885315 + Missense_Mutation SNP C C G TCGA-DK-A1AC-01A-11D-A13W-08 TCGA-DK-A1AC-10A-01D-A13W-08 g.chr8:88885315C>G c.885G>C c.(883-885)aaG>aaC p.K295N BLCA 8 88885545 88885545 + Missense_Mutation SNP G G T TCGA-UY-A78O-01A-12D-A339-08 TCGA-UY-A78O-10A-01D-A339-08 g.chr8:88885545G>T c.655C>A c.(655-657)Cag>Aag p.Q219K BLCA 8 88885584 88885584 + Nonsense_Mutation SNP G G A TCGA-FD-A6TC-01A-21D-A339-08 TCGA-FD-A6TC-10A-21D-A339-08 g.chr8:88885584G>A c.616C>T c.(616-618)Cag>Tag p.Q206* BLCA 8 88885587 88885587 + Missense_Mutation SNP A A G TCGA-K4-A6FZ-01A-11D-A31L-08 TCGA-K4-A6FZ-10A-01D-A31J-08 g.chr8:88885587A>G c.613T>C c.(613-615)Tct>Cct p.S205P BLCA 8 88885613 88885613 + Missense_Mutation SNP G G A TCGA-FD-A3SS-01A-12D-A22Z-08 TCGA-FD-A3SS-10A-01D-A22Z-08 g.chr8:88885613G>A c.587C>T c.(586-588)gCg>gTg p.A196V BLCA 8 88886082 88886082 + Missense_Mutation SNP C C T TCGA-2F-A9KP-01A-11D-A38G-08 TCGA-2F-A9KP-10A-01D-A38J-08 g.chr8:88886082C>T c.118G>A c.(118-120)Gcc>Acc p.A40T BLCA 8 88886086 88886086 + Missense_Mutation SNP T T A TCGA-CU-A3QU-01A-11D-A22Z-08 TCGA-CU-A3QU-10B-01D-A22Z-08 g.chr8:88886086T>A c.114A>T c.(112-114)agA>agT p.R38S BRCA 8 88885140 88885140 + Missense_Mutation SNP A A G TCGA-A2-A0T5-01A-21D-A099-09 TCGA-A2-A0T5-10A-01D-A099-09 g.chr8:88885140A>G c.1060T>C c.(1060-1062)Tcc>Ccc p.S354P BRCA 8 88885215 88885215 + Missense_Mutation SNP C C T TCGA-A2-A0D1-01A-11W-A050-09 TCGA-A2-A0D1-10A-01W-A055-09 g.chr8:88885215C>T c.985G>A c.(985-987)Gtg>Atg p.V329M BRCA 8 88885220 88885220 + Missense_Mutation SNP C C T TCGA-A2-A0YK-01A-22D-A117-09 TCGA-A2-A0YK-10A-01D-A117-09 g.chr8:88885220C>T c.980G>A c.(979-981)gGa>gAa p.G327E BRCA 8 88885242 88885242 + Missense_Mutation SNP C C T TCGA-A8-A09N-01A-11W-A019-09 TCGA-A8-A09N-10A-01W-A021-09 g.chr8:88885242C>T c.958G>A c.(958-960)Gtg>Atg p.V320M BRCA 8 88885440 88885440 + Missense_Mutation SNP G G A TCGA-BH-A0HA-01A-11D-A12Q-09 TCGA-BH-A0HA-11A-31D-A12Q-09 g.chr8:88885440G>A c.760C>T c.(760-762)Cgc>Tgc p.R254C BRCA 8 88885659 88885659 + Missense_Mutation SNP G G T TCGA-C8-A131-01A-11D-A10Y-09 TCGA-C8-A131-10A-01D-A110-09 g.chr8:88885659G>T c.541C>A c.(541-543)Cag>Aag p.Q181K BRCA 8 88885903 88885903 + Silent SNP G G A TCGA-BH-A18G-01A-11D-A12B-09 TCGA-BH-A18G-10A-01D-A12B-09 g.chr8:88885903G>A c.297C>T c.(295-297)taC>taT p.Y99Y BRCA 8 88885923 88885923 + Nonsense_Mutation SNP C C A TCGA-A2-A3XY-01A-11D-A23C-09 TCGA-A2-A3XY-10A-01D-A23C-09 g.chr8:88885923C>A c.277G>T c.(277-279)Gaa>Taa p.E93* BRCA 8 88886087 88886087 + Missense_Mutation SNP C C T TCGA-E2-A10C-01A-21D-A10M-09 TCGA-E2-A10C-10A-01D-A10M-09 g.chr8:88886087C>T c.113G>A c.(112-114)aGa>aAa p.R38K CESC 8 88885044 88885044 + Missense_Mutation SNP G G A TCGA-EK-A2RD-01A-12D-A20U-09 TCGA-EK-A2RD-10A-01D-A20U-09 g.chr8:88885044G>A c.1156C>T c.(1156-1158)Cgg>Tgg p.R386W CESC 8 88885075 88885075 + Silent SNP G G A TCGA-UC-A7PF-01A-11D-A351-09 TCGA-UC-A7PF-11A-31D-A351-09 g.chr8:88885075G>A c.1125C>T c.(1123-1125)ttC>ttT p.F375F CESC 8 88885439 88885439 + Missense_Mutation SNP C C T TCGA-EK-A2RA-01A-11D-A18J-09 TCGA-EK-A2RA-10A-01D-A18J-09 g.chr8:88885439C>T c.761G>A c.(760-762)cGc>cAc p.R254H CESC 8 88885653 88885653 + Missense_Mutation SNP G G A TCGA-EK-A2RB-01A-11D-A18J-09 TCGA-EK-A2RB-10A-01D-A18J-09 g.chr8:88885653G>A c.547C>T c.(547-549)Cct>Tct p.P183S CHOL 8 88886183 88886183 + Missense_Mutation SNP G G A TCGA-W5-AA2I-01A-32D-A417-09 TCGA-W5-AA2I-10A-01D-A41A-09 g.chr8:88886183G>A c.17C>T c.(16-18)cCg>cTg p.P6L COAD 8 88885043 88885043 + Missense_Mutation SNP C C T TCGA-AA-3548-01A-01W-0831-10 TCGA-AA-3548-10A-01W-0831-10 g.chr8:88885043C>T c.1157G>A c.(1156-1158)cGg>cAg p.R386Q COAD 8 88885043 88885043 + Missense_Mutation SNP C C T TCGA-AD-6964-01A-11D-1924-10 TCGA-AD-6964-10A-01D-1924-10 g.chr8:88885043C>T c.1157G>A c.(1156-1158)cGg>cAg p.R386Q COAD 8 88885084 88885084 + Silent SNP G G A TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr8:88885084G>A c.1116C>T c.(1114-1116)ctC>ctT p.L372L COAD 8 88885117 88885117 + Silent SNP G G A TCGA-AA-3866-01A-01W-0995-10 TCGA-AA-3866-10A-01W-0995-10 g.chr8:88885117G>A c.1083C>T c.(1081-1083)aaC>aaT p.N361N COAD 8 88885187 88885187 + Missense_Mutation SNP G G A TCGA-AA-3845-01A-01W-0995-10 TCGA-AA-3845-10A-01W-0995-10 g.chr8:88885187G>A c.1013C>T c.(1012-1014)aCg>aTg p.T338M COAD 8 88885201 88885201 + Silent SNP G G A TCGA-D5-6930-01A-11D-1924-10 TCGA-D5-6930-10A-01D-1924-10 g.chr8:88885201G>A c.999C>T c.(997-999)ggC>ggT p.G333G COAD 8 88885206 88885206 + Missense_Mutation SNP C C T TCGA-AA-A02W-01A-01W-A00E-09 TCGA-AA-A02W-10A-01W-A00E-09 g.chr8:88885206C>T c.994G>A c.(994-996)Gtg>Atg p.V332M COAD 8 88885354 88885354 + Silent SNP G G T TCGA-AA-A02O-01A-21W-A096-10 TCGA-AA-A02O-11A-11W-A096-10 g.chr8:88885354G>T c.846C>A c.(844-846)ggC>ggA p.G282G COAD 8 88885382 88885382 + Missense_Mutation SNP A A G TCGA-AA-A01R-01A-21W-A096-10 TCGA-AA-A01R-11A-12W-A096-10 g.chr8:88885382A>G c.818T>C c.(817-819)gTg>gCg p.V273A COAD 8 88885420 88885420 + Missense_Mutation SNP G G C TCGA-D5-6898-01A-11D-1924-10 TCGA-D5-6898-10A-01D-1924-10 g.chr8:88885420G>C c.780C>G c.(778-780)agC>agG p.S260R COAD 8 88885439 88885439 + Missense_Mutation SNP C C T TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr8:88885439C>T c.761G>A c.(760-762)cGc>cAc p.R254H COAD 8 88885440 88885440 + Missense_Mutation SNP G G A TCGA-AA-A022-01A-21W-A096-10 TCGA-AA-A022-11A-11W-A096-10 g.chr8:88885440G>A c.760C>T c.(760-762)Cgc>Tgc p.R254C COAD 8 88885440 88885440 + Missense_Mutation SNP G G A TCGA-AD-5900-01A-11D-1650-10 TCGA-AD-5900-10A-01D-1650-10 g.chr8:88885440G>A c.760C>T c.(760-762)Cgc>Tgc p.R254C COAD 8 88885491 88885491 + Missense_Mutation SNP G G A TCGA-F4-6570-01A-11D-1771-10 TCGA-F4-6570-10A-01D-1771-10 g.chr8:88885491G>A c.709C>T c.(709-711)Cct>Tct p.P237S COAD 8 88885654 88885654 + Silent SNP G G T TCGA-F4-6806-01A-11D-1835-10 TCGA-F4-6806-10A-01D-1835-10 g.chr8:88885654G>T c.546C>A c.(544-546)atC>atA p.I182I COAD 8 88885682 88885682 + Missense_Mutation SNP C C T TCGA-AA-3994-01A-01W-1073-09 TCGA-AA-3994-10A-01W-1073-09 g.chr8:88885682C>T c.518G>A c.(517-519)cGg>cAg p.R173Q COAD 8 88885685 88885685 + Missense_Mutation SNP C C T TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr8:88885685C>T c.515G>A c.(514-516)cGt>cAt p.R172H COAD 8 88885686 88885686 + Missense_Mutation SNP G G A TCGA-AA-3821-01A-01W-0995-10 TCGA-AA-3821-10A-01W-0995-10 g.chr8:88885686G>A c.514C>T c.(514-516)Cgt>Tgt p.R172C COAD 8 88885686 88885686 + Missense_Mutation SNP G G A TCGA-F4-6856-01A-11D-1924-10 TCGA-F4-6856-10A-01D-1924-10 g.chr8:88885686G>A c.514C>T c.(514-516)Cgt>Tgt p.R172C COAD 8 88885717 88885717 + Silent SNP C C T TCGA-AA-A02O-01A-21W-A096-10 TCGA-AA-A02O-11A-11W-A096-10 g.chr8:88885717C>T c.483G>A c.(481-483)gcG>gcA p.A161A COAD 8 88885719 88885719 + Missense_Mutation SNP C C G TCGA-F4-6460-01A-11D-1771-10 TCGA-F4-6460-10B-01D-1771-10 g.chr8:88885719C>G c.481G>C c.(481-483)Gcg>Ccg p.A161P COAD 8 88885751 88885751 + Missense_Mutation SNP G G A TCGA-CM-5348-01A-21D-1719-10 TCGA-CM-5348-10A-01D-1719-10 g.chr8:88885751G>A c.449C>T c.(448-450)gCa>gTa p.A150V COAD 8 88885814 88885814 + Missense_Mutation SNP G G T TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr8:88885814G>T c.386C>A c.(385-387)tCt>tAt p.S129Y COAD 8 88885863 88885863 + Missense_Mutation SNP G G A TCGA-AA-3534-01A-01W-0831-10 TCGA-AA-3534-10A-01W-0831-10 g.chr8:88885863G>A c.337C>T c.(337-339)Cgg>Tgg p.R113W COAD 8 88885907 88885907 + Missense_Mutation SNP T T C TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr8:88885907T>C c.293A>G c.(292-294)aAg>aGg p.K98R COAD 8 88885963 88885963 + Silent SNP C C T TCGA-D5-6931-01A-11D-1924-10 TCGA-D5-6931-10A-01D-1924-10 g.chr8:88885963C>T c.237G>A c.(235-237)gcG>gcA p.A79A COAD 8 88885974 88885974 + Missense_Mutation SNP G G A TCGA-AA-3950-01A-02W-0995-10 TCGA-AA-3950-10A-01W-0995-10 g.chr8:88885974G>A c.226C>T c.(226-228)Cgc>Tgc p.R76C COAD 8 88885982 88885982 + Missense_Mutation SNP C C T TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr8:88885982C>T c.218G>A c.(217-219)cGa>cAa p.R73Q COAD 8 88886022 88886022 + Nonsense_Mutation SNP G G A TCGA-AA-3842-01A-01W-0995-10 TCGA-AA-3842-10A-01W-0995-10 g.chr8:88886022G>A c.178C>T c.(178-180)Cag>Tag p.Q60* COAD 8 88886052 88886052 + Missense_Mutation SNP G G A TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chr8:88886052G>A c.148C>T c.(148-150)Cgt>Tgt p.R50C COAD 8 88886074 88886074 + Nonsense_Mutation SNP A A T TCGA-CK-6746-01A-11D-1835-10 TCGA-CK-6746-10A-01D-1835-10 g.chr8:88886074A>T c.126T>A c.(124-126)taT>taA p.Y42* COAD 8 88886083 88886083 + Silent SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr8:88886083G>A c.117C>T c.(115-117)ttC>ttT p.F39F COADREAD 8 88885043 88885043 + Missense_Mutation SNP C C T TCGA-AA-3548-01A-01W-0831-10 TCGA-AA-3548-10A-01W-0831-10 g.chr8:88885043C>T c.1157G>A c.(1156-1158)cGg>cAg p.R386Q COADREAD 8 88885043 88885043 + Missense_Mutation SNP C C T TCGA-AD-6964-01A-11D-1924-10 TCGA-AD-6964-10A-01D-1924-10 g.chr8:88885043C>T c.1157G>A c.(1156-1158)cGg>cAg p.R386Q COADREAD 8 88885084 88885084 + Silent SNP G G A TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr8:88885084G>A c.1116C>T c.(1114-1116)ctC>ctT p.L372L COADREAD 8 88885117 88885117 + Silent SNP G G A TCGA-AA-3866-01A-01W-0995-10 TCGA-AA-3866-10A-01W-0995-10 g.chr8:88885117G>A c.1083C>T c.(1081-1083)aaC>aaT p.N361N COADREAD 8 88885187 88885187 + Missense_Mutation SNP G G A TCGA-AA-3845-01A-01W-0995-10 TCGA-AA-3845-10A-01W-0995-10 g.chr8:88885187G>A c.1013C>T c.(1012-1014)aCg>aTg p.T338M COADREAD 8 88885187 88885187 + Missense_Mutation SNP G G A TCGA-DY-A0XA-01A-11D-A152-10 TCGA-DY-A0XA-10A-01D-A152-10 g.chr8:88885187G>A c.1013C>T c.(1012-1014)aCg>aTg p.T338M COADREAD 8 88885201 88885201 + Silent SNP G G A TCGA-D5-6930-01A-11D-1924-10 TCGA-D5-6930-10A-01D-1924-10 g.chr8:88885201G>A c.999C>T c.(997-999)ggC>ggT p.G333G COADREAD 8 88885206 88885206 + Missense_Mutation SNP C C T TCGA-AA-A02W-01A-01W-A00E-09 TCGA-AA-A02W-10A-01W-A00E-09 g.chr8:88885206C>T c.994G>A c.(994-996)Gtg>Atg p.V332M COADREAD 8 88885308 88885308 + Missense_Mutation SNP C C A TCGA-CI-6622-01A-11D-1826-10 TCGA-CI-6622-10A-01D-1826-10 g.chr8:88885308C>A c.892G>T c.(892-894)Gac>Tac p.D298Y COADREAD 8 88885354 88885354 + Silent SNP G G T TCGA-AA-A02O-01A-21W-A096-10 TCGA-AA-A02O-11A-11W-A096-10 g.chr8:88885354G>T c.846C>A c.(844-846)ggC>ggA p.G282G COADREAD 8 88885382 88885382 + Missense_Mutation SNP A A G TCGA-AA-A01R-01A-21W-A096-10 TCGA-AA-A01R-11A-12W-A096-10 g.chr8:88885382A>G c.818T>C c.(817-819)gTg>gCg p.V273A COADREAD 8 88885420 88885420 + Missense_Mutation SNP G G C TCGA-D5-6898-01A-11D-1924-10 TCGA-D5-6898-10A-01D-1924-10 g.chr8:88885420G>C c.780C>G c.(778-780)agC>agG p.S260R COADREAD 8 88885439 88885439 + Missense_Mutation SNP C C T TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr8:88885439C>T c.761G>A c.(760-762)cGc>cAc p.R254H COADREAD 8 88885440 88885440 + Missense_Mutation SNP G G A TCGA-AA-A022-01A-21W-A096-10 TCGA-AA-A022-11A-11W-A096-10 g.chr8:88885440G>A c.760C>T c.(760-762)Cgc>Tgc p.R254C COADREAD 8 88885440 88885440 + Missense_Mutation SNP G G A TCGA-AD-5900-01A-11D-1650-10 TCGA-AD-5900-10A-01D-1650-10 g.chr8:88885440G>A c.760C>T c.(760-762)Cgc>Tgc p.R254C COADREAD 8 88885451 88885451 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr8:88885451C>T c.749G>A c.(748-750)gGc>gAc p.G250D COADREAD 8 88885491 88885491 + Missense_Mutation SNP G G A TCGA-F4-6570-01A-11D-1771-10 TCGA-F4-6570-10A-01D-1771-10 g.chr8:88885491G>A c.709C>T c.(709-711)Cct>Tct p.P237S COADREAD 8 88885654 88885654 + Silent SNP G G T TCGA-F4-6806-01A-11D-1835-10 TCGA-F4-6806-10A-01D-1835-10 g.chr8:88885654G>T c.546C>A c.(544-546)atC>atA p.I182I COADREAD 8 88885682 88885682 + Missense_Mutation SNP C C T TCGA-AA-3994-01A-01W-1073-09 TCGA-AA-3994-10A-01W-1073-09 g.chr8:88885682C>T c.518G>A c.(517-519)cGg>cAg p.R173Q COADREAD 8 88885685 88885685 + Missense_Mutation SNP C C T TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr8:88885685C>T c.515G>A c.(514-516)cGt>cAt p.R172H COADREAD 8 88885686 88885686 + Missense_Mutation SNP G G A TCGA-AA-3821-01A-01W-0995-10 TCGA-AA-3821-10A-01W-0995-10 g.chr8:88885686G>A c.514C>T c.(514-516)Cgt>Tgt p.R172C COADREAD 8 88885686 88885686 + Missense_Mutation SNP G G A TCGA-F4-6856-01A-11D-1924-10 TCGA-F4-6856-10A-01D-1924-10 g.chr8:88885686G>A c.514C>T c.(514-516)Cgt>Tgt p.R172C COADREAD 8 88885717 88885717 + Silent SNP C C T TCGA-AA-A02O-01A-21W-A096-10 TCGA-AA-A02O-11A-11W-A096-10 g.chr8:88885717C>T c.483G>A c.(481-483)gcG>gcA p.A161A COADREAD 8 88885717 88885717 + Silent SNP C C T TCGA-AF-2687-01A-02D-1733-10 TCGA-AF-2687-10A-01D-1733-10 g.chr8:88885717C>T c.483G>A c.(481-483)gcG>gcA p.A161A COADREAD 8 88885719 88885719 + Missense_Mutation SNP C C G TCGA-F4-6460-01A-11D-1771-10 TCGA-F4-6460-10B-01D-1771-10 g.chr8:88885719C>G c.481G>C c.(481-483)Gcg>Ccg p.A161P COADREAD 8 88885751 88885751 + Missense_Mutation SNP G G A TCGA-AF-2687-01A-02D-1733-10 TCGA-AF-2687-10A-01D-1733-10 g.chr8:88885751G>A c.449C>T c.(448-450)gCa>gTa p.A150V COADREAD 8 88885751 88885751 + Missense_Mutation SNP G G A TCGA-CM-5348-01A-21D-1719-10 TCGA-CM-5348-10A-01D-1719-10 g.chr8:88885751G>A c.449C>T c.(448-450)gCa>gTa p.A150V COADREAD 8 88885807 88885807 + Nonsense_Mutation SNP G G T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr8:88885807G>T c.393C>A c.(391-393)tgC>tgA p.C131* COADREAD 8 88885814 88885814 + Missense_Mutation SNP G G T TCGA-AG-3892-01A-01W-1073-09 TCGA-AG-3892-10A-01W-1073-09 g.chr8:88885814G>T c.386C>A c.(385-387)tCt>tAt p.S129Y COADREAD 8 88885814 88885814 + Missense_Mutation SNP G G T TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr8:88885814G>T c.386C>A c.(385-387)tCt>tAt p.S129Y COADREAD 8 88885863 88885863 + Missense_Mutation SNP G G A TCGA-AA-3534-01A-01W-0831-10 TCGA-AA-3534-10A-01W-0831-10 g.chr8:88885863G>A c.337C>T c.(337-339)Cgg>Tgg p.R113W COADREAD 8 88885907 88885907 + Missense_Mutation SNP T T C TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr8:88885907T>C c.293A>G c.(292-294)aAg>aGg p.K98R COADREAD 8 88885963 88885963 + Silent SNP C C T TCGA-D5-6931-01A-11D-1924-10 TCGA-D5-6931-10A-01D-1924-10 g.chr8:88885963C>T c.237G>A c.(235-237)gcG>gcA p.A79A COADREAD 8 88885974 88885974 + Missense_Mutation SNP G G A TCGA-AA-3950-01A-02W-0995-10 TCGA-AA-3950-10A-01W-0995-10 g.chr8:88885974G>A c.226C>T c.(226-228)Cgc>Tgc p.R76C COADREAD 8 88885982 88885982 + Missense_Mutation SNP C C T TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr8:88885982C>T c.218G>A c.(217-219)cGa>cAa p.R73Q COADREAD 8 88886022 88886022 + Nonsense_Mutation SNP G G A TCGA-AA-3842-01A-01W-0995-10 TCGA-AA-3842-10A-01W-0995-10 g.chr8:88886022G>A c.178C>T c.(178-180)Cag>Tag p.Q60* COADREAD 8 88886052 88886052 + Missense_Mutation SNP G G A TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chr8:88886052G>A c.148C>T c.(148-150)Cgt>Tgt p.R50C COADREAD 8 88886074 88886074 + Nonsense_Mutation SNP A A T TCGA-CK-6746-01A-11D-1835-10 TCGA-CK-6746-10A-01D-1835-10 g.chr8:88886074A>T c.126T>A c.(124-126)taT>taA p.Y42* COADREAD 8 88886083 88886083 + Silent SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr8:88886083G>A c.117C>T c.(115-117)ttC>ttT p.F39F COADREAD 8 88886083 88886083 + Silent SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr8:88886083G>A c.117C>T c.(115-117)ttC>ttT p.F39F DLBC 8 88885256 88885256 + Missense_Mutation SNP G G A TCGA-G8-6324-01A-11D-2210-10 TCGA-G8-6324-10A-01D-2210-10 g.chr8:88885256G>A c.944C>T c.(943-945)tCc>tTc p.S315F ESCA 8 88885726 88885726 + Silent SNP C C G TCGA-IG-A3QL-01A-11D-A247-09 TCGA-IG-A3QL-10A-01D-A247-09 g.chr8:88885726C>G c.474G>C c.(472-474)ctG>ctC p.L158L ESCA 8 88885764 88885764 + Missense_Mutation SNP A A G TCGA-2H-A9GI-01A-11D-A37C-09 TCGA-2H-A9GI-11A-11D-A37F-09 g.chr8:88885764A>G c.436T>C c.(436-438)Ttc>Ctc p.F146L ESCA 8 88885799 88885799 + Nonsense_Mutation SNP G G T TCGA-VR-A8EO-01A-11D-A36J-09 TCGA-VR-A8EO-10A-01D-A36M-09 g.chr8:88885799G>T c.401C>A c.(400-402)tCa>tAa p.S134* ESCA 8 88886083 88886083 + Silent SNP G G A TCGA-LN-A49M-01A-21D-A27G-09 TCGA-LN-A49M-10A-01D-A27G-09 g.chr8:88886083G>A c.117C>T c.(115-117)ttC>ttT p.F39F GBM 8 88886046 88886046 + Missense_Mutation SNP T T A TCGA-76-4934-01A-01D-1486-08 TCGA-76-4934-10A-01D-1486-08 g.chr8:88886046T>A c.154A>T c.(154-156)Agc>Tgc p.S52C GBM 8 88886131 88886131 + Silent SNP G G C TCGA-76-6282-01A-11D-1696-08 TCGA-76-6282-10A-01D-1696-08 g.chr8:88886131G>C c.69C>G c.(67-69)ctC>ctG p.L23L GBMLGG 8 88885128 88885128 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr8:88885128C>T c.1072G>A c.(1072-1074)Gcc>Acc p.A358T GBMLGG 8 88885200 88885200 + Missense_Mutation SNP G G C TCGA-DU-5852-01A-11D-1705-08 TCGA-DU-5852-10A-01D-1705-08 g.chr8:88885200G>C c.1000C>G c.(1000-1002)Cag>Gag p.Q334E GBMLGG 8 88885738 88885738 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr8:88885738G>T c.462C>A c.(460-462)agC>agA p.S154R GBMLGG 8 88886046 88886046 + Missense_Mutation SNP T T A TCGA-76-4934-01A-01D-1486-08 TCGA-76-4934-10A-01D-1486-08 g.chr8:88886046T>A c.154A>T c.(154-156)Agc>Tgc p.S52C GBMLGG 8 88886131 88886131 + Silent SNP G G C TCGA-76-6282-01A-11D-1696-08 TCGA-76-6282-10A-01D-1696-08 g.chr8:88886131G>C c.69C>G c.(67-69)ctC>ctG p.L23L HNSC 8 88885018 88885018 + Silent SNP G G A TCGA-DQ-7592-01A-11D-2078-08 TCGA-DQ-7592-10A-01D-2078-08 g.chr8:88885018G>A c.1182C>T c.(1180-1182)taC>taT p.Y394Y HNSC 8 88885084 88885084 + Silent SNP G G A TCGA-D6-6516-01A-11D-1870-08 TCGA-D6-6516-10A-01D-1870-08 g.chr8:88885084G>A c.1116C>T c.(1114-1116)ctC>ctT p.L372L HNSC 8 88885093 88885093 + Silent SNP A A C TCGA-P3-A5Q5-01A-11D-A28R-08 TCGA-P3-A5Q5-10A-01D-A28U-08 g.chr8:88885093A>C c.1107T>G c.(1105-1107)tcT>tcG p.S369S HNSC 8 88885104 88885104 + Missense_Mutation SNP C C T TCGA-CN-4737-01A-01D-1434-08 TCGA-CN-4737-10A-01D-1434-08 g.chr8:88885104C>T c.1096G>A c.(1096-1098)Gtg>Atg p.V366M HNSC 8 88885106 88885106 + Missense_Mutation SNP C C A TCGA-CV-A461-01A-41D-A25Y-08 TCGA-CV-A461-10A-01D-A25Y-08 g.chr8:88885106C>A c.1094G>T c.(1093-1095)aGt>aTt p.S365I HNSC 8 88885295 88885295 + Missense_Mutation SNP G G A TCGA-CV-7261-01A-11D-2012-08 TCGA-CV-7261-10A-01D-2013-08 g.chr8:88885295G>A c.905C>T c.(904-906)aCt>aTt p.T302I HNSC 8 88885472 88885472 + Missense_Mutation SNP C C T TCGA-UF-A71E-01A-31D-A34J-08 TCGA-UF-A71E-10B-01D-A34M-08 g.chr8:88885472C>T c.728G>A c.(727-729)tGt>tAt p.C243Y HNSC 8 88885612 88885612 + Silent SNP C C T TCGA-CN-4730-01A-01D-1434-08 TCGA-CN-4730-10A-01D-1434-08 g.chr8:88885612C>T c.588G>A c.(586-588)gcG>gcA p.A196A HNSC 8 88885685 88885685 + Missense_Mutation SNP C C T TCGA-BA-A6DF-01A-11D-A30E-08 TCGA-BA-A6DF-10A-01D-A30H-08 g.chr8:88885685C>T c.515G>A c.(514-516)cGt>cAt p.R172H HNSC 8 88885717 88885717 + Silent SNP C C T TCGA-CR-6484-01A-11D-1870-08 TCGA-CR-6484-10A-01D-1870-08 g.chr8:88885717C>T c.483G>A c.(481-483)gcG>gcA p.A161A HNSC 8 88885723 88885723 + Silent SNP G G T TCGA-CR-7402-01A-11D-2012-08 TCGA-CR-7402-10A-01D-2013-08 g.chr8:88885723G>T c.477C>A c.(475-477)ctC>ctA p.L159L HNSC 8 88886016 88886016 + Missense_Mutation SNP G G A TCGA-CR-7398-01A-11D-2012-08 TCGA-CR-7398-10A-01D-2013-08 g.chr8:88886016G>A c.184C>T c.(184-186)Cat>Tat p.H62Y HNSC 8 88886033 88886033 + Missense_Mutation SNP C C A TCGA-CN-5373-01A-01D-1434-08 TCGA-CN-5373-10A-01D-1434-08 g.chr8:88886033C>A c.167G>T c.(166-168)aGg>aTg p.R56M HNSC 8 88886052 88886052 + Missense_Mutation SNP G G T TCGA-CV-6945-01A-11D-1912-08 TCGA-CV-6945-10A-01D-1912-08 g.chr8:88886052G>T c.148C>A c.(148-150)Cgt>Agt p.R50S HNSC 8 88886082 88886082 + Missense_Mutation SNP C C A TCGA-CN-6021-01A-11D-1683-08 TCGA-CN-6021-10A-01D-1683-08 g.chr8:88886082C>A c.118G>T c.(118-120)Gcc>Tcc p.A40S HNSC 8 88886149 88886149 + Missense_Mutation SNP C C A TCGA-CR-7369-01A-11D-2129-08 TCGA-CR-7369-10A-01D-2129-08 g.chr8:88886149C>A c.51G>T c.(49-51)aaG>aaT p.K17N HNSC 8 88886175 88886175 + Missense_Mutation SNP G G T TCGA-D6-A74Q-01A-11D-A34J-08 TCGA-D6-A74Q-10A-02D-A34M-08 g.chr8:88886175G>T c.25C>A c.(25-27)Ctc>Atc p.L9I HNSC 8 88886180 88886180 + Missense_Mutation SNP C C G TCGA-CV-7440-01A-11D-2129-08 TCGA-CV-7440-10A-01D-2129-08 g.chr8:88886180C>G c.20G>C c.(19-21)cGa>cCa p.R7P KIPAN 8 88885732 88885732 + Silent SNP G G A TCGA-BP-4988-01A-01D-1462-08 TCGA-BP-4988-11A-01D-1462-08 g.chr8:88885732G>A c.468C>T c.(466-468)gcC>gcT p.A156A KIPAN 8 88885869 88885869 + Missense_Mutation SNP C C G TCGA-B1-A654-01A-11D-A31X-10 TCGA-B1-A654-10A-01D-A31X-10 g.chr8:88885869C>G c.331G>C c.(331-333)Gag>Cag p.E111Q KIRC 8 88885732 88885732 + Silent SNP G G A TCGA-BP-4988-01A-01D-1462-08 TCGA-BP-4988-11A-01D-1462-08 g.chr8:88885732G>A c.468C>T c.(466-468)gcC>gcT p.A156A KIRP 8 88885869 88885869 + Missense_Mutation SNP C C G TCGA-B1-A654-01A-11D-A31X-10 TCGA-B1-A654-10A-01D-A31X-10 g.chr8:88885869C>G c.331G>C c.(331-333)Gag>Cag p.E111Q LGG 8 88885128 88885128 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr8:88885128C>T c.1072G>A c.(1072-1074)Gcc>Acc p.A358T LGG 8 88885200 88885200 + Missense_Mutation SNP G G C TCGA-DU-5852-01A-11D-1705-08 TCGA-DU-5852-10A-01D-1705-08 g.chr8:88885200G>C c.1000C>G c.(1000-1002)Cag>Gag p.Q334E LGG 8 88885738 88885738 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr8:88885738G>T c.462C>A c.(460-462)agC>agA p.S154R LIHC 8 88885079 88885079 + Frame_Shift_Del DEL C C - TCGA-DD-A3A1-01A-11D-A20W-10 TCGA-DD-A3A1-11A-11D-A20W-10 g.chr8:88885079delC c.1121delG c.(1120-1122)ggcfs p.G374fs LIHC 8 88885237 88885246 + Frame_Shift_Del DEL ATGCACGGGT ATGCACGGGT - TCGA-BC-A10U-01A-11D-A12Z-10 TCGA-BC-A10U-11A-11D-A12Z-10 g.chr8:88885237_88885246delATGCACGGGT c.954_963delACCCGTGCAT c.(952-963)ctacccgtgcatfs p.LPVH318fs LIHC 8 88885240 88885242 + In_Frame_Del DEL CAC CAC - TCGA-BC-A10U-01A-11D-A12Z-10 TCGA-BC-A10U-11A-11D-A12Z-10 g.chr8:88885240_88885242delCAC c.958_960delGTG c.(958-960)gtgdel p.V320del LIHC 8 88885245 88885246 + Frame_Shift_Del DEL GT GT - TCGA-BC-A10U-01A-11D-A12Z-10 TCGA-BC-A10U-11A-11D-A12Z-10 g.chr8:88885245_88885246delGT c.954_955delAC c.(952-957)ctacccfs p.P319fs LIHC 8 88885313 88885313 + Missense_Mutation SNP A A G TCGA-DD-A1EK-01A-11D-A20W-10 TCGA-DD-A1EK-10A-01D-A20W-10 g.chr8:88885313A>G c.887T>C c.(886-888)cTg>cCg p.L296P LIHC 8 88885352 88885352 + Missense_Mutation SNP T T A TCGA-2Y-A9H9-01A-21D-A38X-10 TCGA-2Y-A9H9-10A-01D-A38X-10 g.chr8:88885352T>A c.848A>T c.(847-849)cAa>cTa p.Q283L LIHC 8 88885852 88885852 + Silent SNP C C A TCGA-DD-AADC-01A-11D-A40R-10 TCGA-DD-AADC-10A-01D-A40U-10 g.chr8:88885852C>A c.348G>T c.(346-348)ccG>ccT p.P116P LIHC 8 88886016 88886016 + Missense_Mutation SNP G G A TCGA-CC-5264-01A-01D-A12Z-10 TCGA-CC-5264-10A-01D-A12Z-10 g.chr8:88886016G>A c.184C>T c.(184-186)Cat>Tat p.H62Y LUAD 8 88885054 88885054 + Silent SNP G G T TCGA-NJ-A4YQ-01A-11D-A25L-08 TCGA-NJ-A4YQ-10A-01D-A25L-08 g.chr8:88885054G>T c.1146C>A c.(1144-1146)ctC>ctA p.L382L LUAD 8 88885068 88885068 + Missense_Mutation SNP C C A TCGA-86-8358-01A-11D-2323-08 TCGA-86-8358-10A-01D-2323-08 g.chr8:88885068C>A c.1132G>T c.(1132-1134)Gca>Tca p.A378S LUAD 8 88885084 88885084 + Silent SNP G G C TCGA-55-8507-01A-11D-2393-08 TCGA-55-8507-10A-01D-2393-08 g.chr8:88885084G>C c.1116C>G c.(1114-1116)ctC>ctG p.L372L LUAD 8 88885086 88885086 + Missense_Mutation SNP G G T TCGA-95-7039-01A-11D-1945-08 TCGA-95-7039-10A-01D-1946-08 g.chr8:88885086G>T c.1114C>A c.(1114-1116)Ctc>Atc p.L372I LUAD 8 88885094 88885094 + Missense_Mutation SNP G G T TCGA-86-6851-01A-11D-1945-08 TCGA-86-6851-10A-01D-1946-08 g.chr8:88885094G>T c.1106C>A c.(1105-1107)tCt>tAt p.S369Y LUAD 8 88885101 88885101 + Frame_Shift_Del DEL C C - TCGA-44-7671-01A-11D-2063-08 TCGA-44-7671-10A-01D-2063-08 g.chr8:88885101delC c.1099delG c.(1099-1101)gccfs p.A367fs LUAD 8 88885102 88885102 + Silent SNP C C A TCGA-69-A59K-01A-11D-A25L-08 TCGA-69-A59K-10A-01D-A25L-08 g.chr8:88885102C>A c.1098G>T c.(1096-1098)gtG>gtT p.V366V LUAD 8 88885129 88885129 + Silent SNP G G A TCGA-78-7149-01A-11D-2036-08 TCGA-78-7149-10A-01D-2036-08 g.chr8:88885129G>A c.1071C>T c.(1069-1071)ccC>ccT p.P357P LUAD 8 88885129 88885129 + Silent SNP G G C TCGA-17-Z053-01A-01W-0747-08 TCGA-17-Z053-11A-01W-0747-08 g.chr8:88885129G>C c.1071C>G c.(1069-1071)ccC>ccG p.P357P LUAD 8 88885169 88885169 + Missense_Mutation SNP C C A TCGA-17-Z009-01A-01W-0746-08 TCGA-17-Z009-11A-01W-0746-08 g.chr8:88885169C>A c.1031G>T c.(1030-1032)cGt>cTt p.R344L LUAD 8 88885169 88885169 + Missense_Mutation SNP C C A TCGA-44-8117-01A-11D-2238-08 TCGA-44-8117-10A-01D-2238-08 g.chr8:88885169C>A c.1031G>T c.(1030-1032)cGt>cTt p.R344L LUAD 8 88885200 88885200 + Missense_Mutation SNP G G T TCGA-17-Z015-01A-01W-0746-08 TCGA-17-Z015-11A-01W-0746-08 g.chr8:88885200G>T c.1000C>A c.(1000-1002)Cag>Aag p.Q334K LUAD 8 88885201 88885201 + Silent SNP G G T TCGA-95-A4VP-01A-21D-A25L-08 TCGA-95-A4VP-10A-01D-A25L-08 g.chr8:88885201G>T c.999C>A c.(997-999)ggC>ggA p.G333G LUAD 8 88885206 88885206 + Missense_Mutation SNP C C A TCGA-75-6214-01A-41D-1945-08 TCGA-75-6214-10A-01D-1946-08 g.chr8:88885206C>A c.994G>T c.(994-996)Gtg>Ttg p.V332L LUAD 8 88885242 88885242 + Missense_Mutation SNP C C A TCGA-99-8028-01A-11D-2238-08 TCGA-99-8028-10A-01D-2238-08 g.chr8:88885242C>A c.958G>T c.(958-960)Gtg>Ttg p.V320L LUAD 8 88885284 88885284 + Missense_Mutation SNP T T G TCGA-44-8120-01A-11D-2238-08 TCGA-44-8120-10A-01D-2238-08 g.chr8:88885284T>G c.916A>C c.(916-918)Aca>Cca p.T306P LUAD 8 88885345 88885345 + Silent SNP C C G TCGA-97-8179-01A-11D-2284-08 TCGA-97-8179-10A-01D-2284-08 g.chr8:88885345C>G c.855G>C c.(853-855)ctG>ctC p.L285L LUAD 8 88885345 88885345 + Silent SNP C C G TCGA-99-8028-01A-11D-2238-08 TCGA-99-8028-10A-01D-2238-08 g.chr8:88885345C>G c.855G>C c.(853-855)ctG>ctC p.L285L LUAD 8 88885347 88885347 + Frame_Shift_Del DEL G G - TCGA-95-7947-01A-11D-2184-08 TCGA-95-7947-10A-01D-2184-08 g.chr8:88885347delG c.853delC c.(853-855)ctgfs p.L285fs LUAD 8 88885415 88885415 + Nonsense_Mutation SNP C C T TCGA-86-8674-01A-21D-2393-08 TCGA-86-8674-10A-01D-2393-08 g.chr8:88885415C>T c.785G>A c.(784-786)tGg>tAg p.W262* LUAD 8 88885420 88885420 + Missense_Mutation SNP G G C TCGA-55-8203-01A-11D-2238-08 TCGA-55-8203-10A-01D-2238-08 g.chr8:88885420G>C c.780C>G c.(778-780)agC>agG p.S260R LUAD 8 88885425 88885425 + Missense_Mutation SNP C C A TCGA-49-4494-01A-01D-1265-08 TCGA-49-4494-11A-01D-1265-08 g.chr8:88885425C>A c.775G>T c.(775-777)Ggc>Tgc p.G259C LUAD 8 88885435 88885435 + Nonsense_Mutation SNP A A T TCGA-38-4632-01A-01D-1753-08 TCGA-38-4632-11A-01D-1753-08 g.chr8:88885435A>T c.765T>A c.(763-765)tgT>tgA p.C255* LUAD 8 88885437 88885437 + Missense_Mutation SNP A A T TCGA-38-4632-01A-01D-1753-08 TCGA-38-4632-11A-01D-1753-08 g.chr8:88885437A>T c.763T>A c.(763-765)Tgt>Agt p.C255S LUAD 8 88885446 88885446 + Missense_Mutation SNP C C T TCGA-53-7813-01A-11D-2167-08 TCGA-53-7813-10A-01D-2167-08 g.chr8:88885446C>T c.754G>A c.(754-756)Gat>Aat p.D252N LUAD 8 88885456 88885456 + Frame_Shift_Del DEL G G - TCGA-64-5779-01A-01D-1625-08 TCGA-64-5779-10A-01D-1625-08 g.chr8:88885456delG c.744delC c.(742-744)atcfs p.I248fs LUAD 8 88885535 88885536 + Frame_Shift_Ins INS - - A TCGA-44-5644-01A-21D-2036-08 TCGA-44-5644-10A-01D-2036-08 g.chr8:88885535_88885536insA c.664_665insT c.(664-666)gggfs p.G222fs LUAD 8 88885535 88885536 + Frame_Shift_Ins INS - - A TCGA-55-7574-01A-11D-2036-08 TCGA-55-7574-10A-01D-2036-08 g.chr8:88885535_88885536insA c.664_665insT c.(664-666)gggfs p.G222fs LUAD 8 88885536 88885536 + Missense_Mutation SNP C C A TCGA-55-8506-01A-11D-2393-08 TCGA-55-8506-10A-01D-2393-08 g.chr8:88885536C>A c.664G>T c.(664-666)Ggg>Tgg p.G222W LUAD 8 88885555 88885555 + Silent SNP C C A TCGA-55-7727-01A-11D-2167-08 TCGA-55-7727-10A-01D-2167-08 g.chr8:88885555C>A c.645G>T c.(643-645)acG>acT p.T215T LUAD 8 88885555 88885555 + Silent SNP C C T TCGA-78-7220-01A-11D-2036-08 TCGA-78-7220-10A-01D-2036-08 g.chr8:88885555C>T c.645G>A c.(643-645)acG>acA p.T215T LUAD 8 88885612 88885612 + Silent SNP C C A TCGA-97-A4M7-01A-11D-A24P-08 TCGA-97-A4M7-10A-01D-A24P-08 g.chr8:88885612C>A c.588G>T c.(586-588)gcG>gcT p.A196A LUAD 8 88885612 88885612 + Silent SNP C C T TCGA-86-8358-01A-11D-2323-08 TCGA-86-8358-10A-01D-2323-08 g.chr8:88885612C>T c.588G>A c.(586-588)gcG>gcA p.A196A LUAD 8 88885613 88885613 + Missense_Mutation SNP G G A TCGA-J2-A4AD-01A-11D-A24D-08 TCGA-J2-A4AD-10A-01D-A24F-08 g.chr8:88885613G>A c.587C>T c.(586-588)gCg>gTg p.A196V LUAD 8 88885615 88885615 + Missense_Mutation SNP G G T TCGA-75-5122-01A-01D-1753-08 TCGA-75-5122-10A-01D-1753-08 g.chr8:88885615G>T c.585C>A c.(583-585)caC>caA p.H195Q LUAD 8 88885654 88885654 + Silent SNP G G A TCGA-17-Z031-01A-01W-0746-08 TCGA-17-Z031-11A-01W-0746-08 g.chr8:88885654G>A c.546C>T c.(544-546)atC>atT p.I182I LUAD 8 88885671 88885671 + Missense_Mutation SNP G G T TCGA-44-6777-01A-11D-1855-08 TCGA-44-6777-10A-01D-1855-08 g.chr8:88885671G>T c.529C>A c.(529-531)Ctt>Att p.L177I LUAD 8 88885672 88885672 + Missense_Mutation SNP C C G TCGA-17-Z045-01A-01W-0746-08 TCGA-17-Z045-11A-01W-0747-08 g.chr8:88885672C>G c.528G>C c.(526-528)atG>atC p.M176I LUAD 8 88885699 88885699 + Missense_Mutation SNP G G T TCGA-NJ-A4YI-01A-11D-A25L-08 TCGA-NJ-A4YI-10A-01D-A25L-08 g.chr8:88885699G>T c.501C>A c.(499-501)agC>agA p.S167R LUAD 8 88885714 88885714 + Silent SNP C C A TCGA-55-7994-01A-11D-2184-08 TCGA-55-7994-10A-01D-2184-08 g.chr8:88885714C>A c.486G>T c.(484-486)tcG>tcT p.S162S LUAD 8 88885731 88885731 + Missense_Mutation SNP C C T TCGA-38-4627-01A-01D-1553-08 TCGA-38-4627-11A-01D-1553-08 g.chr8:88885731C>T c.469G>A c.(469-471)Gtg>Atg p.V157M LUAD 8 88885745 88885745 + Missense_Mutation SNP G G T TCGA-44-7669-01A-21D-2063-08 TCGA-44-7669-10A-01D-2063-08 g.chr8:88885745G>T c.455C>A c.(454-456)aCt>aAt p.T152N LUAD 8 88885757 88885757 + Frame_Shift_Del DEL C C - TCGA-95-7043-01A-11D-1945-08 TCGA-95-7043-10A-01D-1946-08 g.chr8:88885757delC c.443delG c.(442-444)ggafs p.G148fs LUAD 8 88885761 88885761 + Missense_Mutation SNP C C A TCGA-69-7980-01A-11D-2184-08 TCGA-69-7980-10A-01D-2184-08 g.chr8:88885761C>A c.439G>T c.(439-441)Gtg>Ttg p.V147L LUAD 8 88885768 88885768 + Silent SNP C C G TCGA-05-4397-01A-01D-1265-08 TCGA-05-4397-10A-01D-1265-08 g.chr8:88885768C>G c.432G>C c.(430-432)ctG>ctC p.L144L LUAD 8 88885795 88885795 + Silent SNP C C A TCGA-L4-A4E5-01A-11D-A24P-08 TCGA-L4-A4E5-10A-01D-A24P-08 g.chr8:88885795C>A c.405G>T c.(403-405)ctG>ctT p.L135L LUAD 8 88885795 88885795 + Silent SNP C C A TCGA-MP-A4TF-01A-11D-A25L-08 TCGA-MP-A4TF-10A-01D-A25L-08 g.chr8:88885795C>A c.405G>T c.(403-405)ctG>ctT p.L135L LUAD 8 88885796 88885796 + Missense_Mutation SNP A A G TCGA-L4-A4E5-01A-11D-A24P-08 TCGA-L4-A4E5-10A-01D-A24P-08 g.chr8:88885796A>G c.404T>C c.(403-405)cTg>cCg p.L135P LUAD 8 88885797 88885797 + Missense_Mutation SNP G G T TCGA-91-6836-01A-21D-1855-08 TCGA-91-6836-11A-01D-1855-08 g.chr8:88885797G>T c.403C>A c.(403-405)Ctg>Atg p.L135M LUAD 8 88885799 88885799 + Nonsense_Mutation SNP G G T TCGA-05-5425-01A-02D-1625-08 TCGA-05-5425-10A-01D-1625-08 g.chr8:88885799G>T c.401C>A c.(400-402)tCa>tAa p.S134* LUAD 8 88885822 88885822 + Silent SNP C C T TCGA-86-6851-01A-11D-1945-08 TCGA-86-6851-10A-01D-1946-08 g.chr8:88885822C>T c.378G>A c.(376-378)aaG>aaA p.K126K LUAD 8 88885827 88885827 + Missense_Mutation SNP G G A TCGA-69-7979-01A-11D-2184-08 TCGA-69-7979-10A-01D-2184-08 g.chr8:88885827G>A c.373C>T c.(373-375)Cgg>Tgg p.R125W LUAD 8 88885833 88885833 + Missense_Mutation SNP G G T TCGA-55-8616-01A-11D-2393-08 TCGA-55-8616-10A-01D-2393-08 g.chr8:88885833G>T c.367C>A c.(367-369)Cct>Act p.P123T LUAD 8 88885853 88885853 + Missense_Mutation SNP G G T TCGA-97-7937-01A-11D-2167-08 TCGA-97-7937-10A-01D-2167-08 g.chr8:88885853G>T c.347C>A c.(346-348)cCg>cAg p.P116Q LUAD 8 88885853 88885853 + Missense_Mutation SNP G G T TCGA-O1-A52J-01A-11D-A25L-08 TCGA-O1-A52J-10A-01D-A25L-08 g.chr8:88885853G>T c.347C>A c.(346-348)cCg>cAg p.P116Q LUAD 8 88885855 88885855 + Nonsense_Mutation SNP G G T TCGA-64-1676-01A-01D-0969-08 TCGA-64-1676-10A-01D-0969-08 g.chr8:88885855G>T c.345C>A c.(343-345)taC>taA p.Y115* LUAD 8 88885873 88885873 + Silent SNP G G C TCGA-55-8094-01A-11D-2238-08 TCGA-55-8094-10A-01D-2238-08 g.chr8:88885873G>C c.327C>G c.(325-327)acC>acG p.T109T LUAD 8 88885885 88885885 + Silent SNP T T A TCGA-55-8204-01A-11D-2238-08 TCGA-55-8204-10A-01D-2238-08 g.chr8:88885885T>A c.315A>T c.(313-315)cgA>cgT p.R105R LUAD 8 88885887 88885887 + Silent SNP G G T TCGA-69-7979-01A-11D-2184-08 TCGA-69-7979-10A-01D-2184-08 g.chr8:88885887G>T c.313C>A c.(313-315)Cga>Aga p.R105R LUAD 8 88885892 88885892 + Missense_Mutation SNP G G T TCGA-55-7283-01A-11D-2036-08 TCGA-55-7283-11A-01D-2036-08 g.chr8:88885892G>T c.308C>A c.(307-309)aCc>aAc p.T103N LUAD 8 88885901 88885901 + Missense_Mutation SNP C C A TCGA-MP-A4T4-01A-11D-A25L-08 TCGA-MP-A4T4-10A-01D-A25L-08 g.chr8:88885901C>A c.299G>T c.(298-300)gGc>gTc p.G100V LUAD 8 88885901 88885901 + Missense_Mutation SNP C C T TCGA-44-7669-01A-21D-2063-08 TCGA-44-7669-10A-01D-2063-08 g.chr8:88885901C>T c.299G>A c.(298-300)gGc>gAc p.G100D LUAD 8 88885913 88885913 + Missense_Mutation SNP C C A TCGA-55-8614-01A-11D-2393-08 TCGA-55-8614-10A-01D-2393-08 g.chr8:88885913C>A c.287G>T c.(286-288)gGc>gTc p.G96V LUAD 8 88885952 88885952 + Missense_Mutation SNP G G A TCGA-55-8506-01A-11D-2393-08 TCGA-55-8506-10A-01D-2393-08 g.chr8:88885952G>A c.248C>T c.(247-249)aCt>aTt p.T83I LUAD 8 88885956 88885956 + Missense_Mutation SNP T T A TCGA-55-8096-01A-11D-2238-08 TCGA-55-8096-10A-01D-2238-08 g.chr8:88885956T>A c.244A>T c.(244-246)Aac>Tac p.N82Y LUAD 8 88885963 88885963 + Silent SNP C C A TCGA-55-8506-01A-11D-2393-08 TCGA-55-8506-10A-01D-2393-08 g.chr8:88885963C>A c.237G>T c.(235-237)gcG>gcT p.A79A LUAD 8 88885966 88885966 + Silent SNP C C A TCGA-50-6590-01A-12D-1855-08 TCGA-50-6590-11A-01D-1855-08 g.chr8:88885966C>A c.234G>T c.(232-234)ctG>ctT p.L78L LUAD 8 88885973 88885973 + Missense_Mutation SNP C C A TCGA-50-5930-01A-11D-1753-08 TCGA-50-5930-11A-01D-1753-08 g.chr8:88885973C>A c.227G>T c.(226-228)cGc>cTc p.R76L LUAD 8 88885984 88885984 + Missense_Mutation SNP G G T TCGA-MP-A4SV-01A-11D-A24P-08 TCGA-MP-A4SV-10A-01D-A24P-08 g.chr8:88885984G>T c.216C>A c.(214-216)gaC>gaA p.D72E LUAD 8 88886032 88886032 + Missense_Mutation SNP C C G TCGA-05-4389-01A-01D-1265-08 TCGA-05-4389-10A-01D-1265-08 g.chr8:88886032C>G c.168G>C c.(166-168)agG>agC p.R56S LUAD 8 88886052 88886052 + Missense_Mutation SNP G G A TCGA-17-Z042-01A-01W-0746-08 TCGA-17-Z042-11A-01W-0746-08 g.chr8:88886052G>A c.148C>T c.(148-150)Cgt>Tgt p.R50C LUAD 8 88886059 88886059 + Silent SNP G G T TCGA-78-7155-01A-11D-2036-08 TCGA-78-7155-10A-01D-2036-08 g.chr8:88886059G>T c.141C>A c.(139-141)cgC>cgA p.R47R LUAD 8 88886072 88886072 + Missense_Mutation SNP C C A TCGA-55-7815-01A-11D-2167-08 TCGA-55-7815-10A-01D-2167-08 g.chr8:88886072C>A c.128G>T c.(127-129)tGc>tTc p.C43F LUAD 8 88886136 88886136 + Nonsense_Mutation SNP C C A TCGA-NJ-A4YQ-01A-11D-A25L-08 TCGA-NJ-A4YQ-10A-01D-A25L-08 g.chr8:88886136C>A c.64G>T c.(64-66)Gga>Tga p.G22* LUAD 8 88886137 88886137 + Silent SNP C C A TCGA-86-6851-01A-11D-1945-08 TCGA-86-6851-10A-01D-1946-08 g.chr8:88886137C>A c.63G>T c.(61-63)gtG>gtT p.V21V LUAD 8 88886189 88886189 + Missense_Mutation SNP T T C TCGA-17-Z023-01A-01W-0746-08 TCGA-17-Z023-11A-01W-0746-08 g.chr8:88886189T>C c.11A>G c.(10-12)aAa>aGa p.K4R LUAD 8 88886192 88886192 + Missense_Mutation SNP C C A TCGA-55-A491-01A-11D-A24D-08 TCGA-55-A491-10A-01D-A24F-08 g.chr8:88886192C>A c.8G>T c.(7-9)aGc>aTc p.S3I LUSC 8 88885116 88885116 + Missense_Mutation SNP C C A TCGA-60-2719-01A-01D-1522-08 TCGA-60-2719-11A-01D-1522-08 g.chr8:88885116C>A c.1084G>T c.(1084-1086)Gac>Tac p.D362Y LUSC 8 88885208 88885208 + Missense_Mutation SNP G G A TCGA-37-5819-01A-01D-1632-08 TCGA-37-5819-10A-01D-1632-08 g.chr8:88885208G>A c.992C>T c.(991-993)gCc>gTc p.A331V LUSC 8 88885348 88885348 + Silent SNP G G A TCGA-18-3409-01A-01D-0983-08 TCGA-18-3409-11A-01D-0983-08 g.chr8:88885348G>A c.852C>T c.(850-852)ttC>ttT p.F284F LUSC 8 88885462 88885462 + Silent SNP C C A TCGA-34-5239-01A-21D-1817-08 TCGA-34-5239-10A-01D-1817-08 g.chr8:88885462C>A c.738G>T c.(736-738)ggG>ggT p.G246G LUSC 8 88885511 88885511 + Missense_Mutation SNP T T C TCGA-66-2766-01A-01D-1522-08 TCGA-66-2766-11A-01D-1522-08 g.chr8:88885511T>C c.689A>G c.(688-690)cAg>cGg p.Q230R LUSC 8 88885555 88885555 + Silent SNP C C G TCGA-33-4586-01A-01D-1441-08 TCGA-33-4586-11A-01D-1441-08 g.chr8:88885555C>G c.645G>C c.(643-645)acG>acC p.T215T LUSC 8 88885614 88885614 + Missense_Mutation SNP C C A TCGA-66-2767-01A-01D-1522-08 TCGA-66-2767-11A-01D-1522-08 g.chr8:88885614C>A c.586G>T c.(586-588)Gcg>Tcg p.A196S LUSC 8 88885715 88885715 + Nonsense_Mutation SNP G G T TCGA-43-6143-01A-11D-1817-08 TCGA-43-6143-11A-01D-1817-08 g.chr8:88885715G>T c.485C>A c.(484-486)tCg>tAg p.S162* LUSC 8 88885742 88885742 + Missense_Mutation SNP G G T TCGA-34-5240-01A-01D-1441-08 TCGA-34-5240-10A-01D-1441-08 g.chr8:88885742G>T c.458C>A c.(457-459)cCa>cAa p.P153Q LUSC 8 88885761 88885761 + Missense_Mutation SNP C C A TCGA-18-3414-01A-01D-0983-08 TCGA-18-3414-11A-01D-0983-08 g.chr8:88885761C>A c.439G>T c.(439-441)Gtg>Ttg p.V147L LUSC 8 88885771 88885771 + Silent SNP C C A TCGA-18-4083-01A-01D-1352-08 TCGA-18-4083-11A-01D-1352-08 g.chr8:88885771C>A c.429G>T c.(427-429)ctG>ctT p.L143L LUSC 8 88885776 88885776 + Missense_Mutation SNP G G A TCGA-66-2787-01A-01D-0983-08 TCGA-66-2787-11A-01D-0983-08 g.chr8:88885776G>A c.424C>T c.(424-426)Ctt>Ttt p.L142F LUSC 8 88885863 88885863 + Missense_Mutation SNP G G A TCGA-66-2744-01A-01D-0983-08 TCGA-66-2744-11A-01D-0983-08 g.chr8:88885863G>A c.337C>T c.(337-339)Cgg>Tgg p.R113W LUSC 8 88885963 88885963 + Silent SNP C C A TCGA-22-1016-01A-01D-1521-08 TCGA-22-1016-11A-01D-1521-08 g.chr8:88885963C>A c.237G>T c.(235-237)gcG>gcT p.A79A LUSC 8 88885967 88885967 + Missense_Mutation SNP A A G TCGA-18-3414-01A-01D-0983-08 TCGA-18-3414-11A-01D-0983-08 g.chr8:88885967A>G c.233T>C c.(232-234)cTg>cCg p.L78P LUSC 8 88886097 88886097 + Missense_Mutation SNP C C A TCGA-22-5482-01A-01D-1632-08 TCGA-22-5482-11A-01D-1632-08 g.chr8:88886097C>A c.103G>T c.(103-105)Ggt>Tgt p.G35C OV 8 88885117 88885117 + Silent SNP G G A TCGA-24-1845-01A-01W-0639-09 TCGA-24-1845-10A-01W-0639-09 g.chr8:88885117G>A c.1083C>T c.(1081-1083)aaC>aaT p.N361N OV 8 88885717 88885717 + Silent SNP C C T TCGA-42-2590-01A-01D-1526-09 TCGA-42-2590-10A-01D-1526-09 g.chr8:88885717C>T c.483G>A c.(481-483)gcG>gcA p.A161A OV 8 88885752 88885752 + Missense_Mutation SNP C C G TCGA-13-1504-01A-01W-0545-08 TCGA-13-1504-10A-01W-0546-08 g.chr8:88885752C>G c.448G>C c.(448-450)Gca>Cca p.A150P OV 8 88886089 88886089 + Silent SNP G G A TCGA-29-1702-01A-01W-0633-09 TCGA-29-1702-10A-01W-0633-09 g.chr8:88886089G>A c.111C>T c.(109-111)ctC>ctT p.L37L OV 8 88886141 88886141 + Missense_Mutation SNP C C T TCGA-29-1775-01A-01W-0639-09 TCGA-29-1775-10A-01W-0639-09 g.chr8:88886141C>T c.59G>A c.(58-60)aGa>aAa p.R20K OV 8 88886199 88886204 + Start_Codon_Del DEL TTTCGT TTTCGT - TCGA-13-0913-01A-01W-0420-08 TCGA-13-0913-10A-01D-0399-08 g.chr8:88886199_88886204delTTTCGT PAAD 8 88885063 88885063 + Silent SNP T T C TCGA-IB-A5SQ-01A-11D-A32N-08 TCGA-IB-A5SQ-10A-01D-A32N-08 g.chr8:88885063T>C c.1137A>G c.(1135-1137)ccA>ccG p.P379P PAAD 8 88885210 88885210 + Silent SNP C C A TCGA-LB-A7SX-01A-11D-A33T-08 TCGA-LB-A7SX-10A-01D-A33W-08 g.chr8:88885210C>A c.990G>T c.(988-990)gcG>gcT p.A330A PAAD 8 88885634 88885634 + Missense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr8:88885634G>A c.566C>T c.(565-567)gCc>gTc p.A189V PAAD 8 88885789 88885789 + Missense_Mutation SNP G G T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr8:88885789G>T c.411C>A c.(409-411)caC>caA p.H137Q PCPG 8 88886083 88886083 + Silent SNP G G A TCGA-QR-A700-01A-11D-A35D-08 TCGA-QR-A700-10A-01D-A35B-08 g.chr8:88886083G>A c.117C>T c.(115-117)ttC>ttT p.F39F PRAD 8 88885073 88885073 + Missense_Mutation SNP C C T TCGA-EJ-5530-01A-01D-1576-08 TCGA-EJ-5530-10A-01D-1577-08 g.chr8:88885073C>T c.1127G>A c.(1126-1128)cGa>cAa p.R376Q PRAD 8 88885088 88885088 + Missense_Mutation SNP C C T TCGA-EJ-7797-01A-11D-2260-08 TCGA-EJ-7797-10A-01D-2260-08 g.chr8:88885088C>T c.1112G>A c.(1111-1113)cGc>cAc p.R371H PRAD 8 88885128 88885128 + Missense_Mutation SNP C C T TCGA-HC-7077-01A-11D-1961-08 TCGA-HC-7077-10A-01D-1961-08 g.chr8:88885128C>T c.1072G>A c.(1072-1074)Gcc>Acc p.A358T PRAD 8 88885613 88885613 + Missense_Mutation SNP G G A TCGA-EJ-A6RC-01A-11D-A32B-08 TCGA-EJ-A6RC-10A-01D-A329-08 g.chr8:88885613G>A c.587C>T c.(586-588)gCg>gTg p.A196V PRAD 8 88885836 88885836 + Missense_Mutation SNP C C T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr8:88885836C>T c.364G>A c.(364-366)Gtc>Atc p.V122I PRAD 8 88886040 88886040 + Missense_Mutation SNP T T C TCGA-FC-A6HD-01A-11D-A31L-08 TCGA-FC-A6HD-10A-01D-A31J-08 g.chr8:88886040T>C c.160A>G c.(160-162)Atg>Gtg p.M54V READ 8 88885187 88885187 + Missense_Mutation SNP G G A TCGA-DY-A0XA-01A-11D-A152-10 TCGA-DY-A0XA-10A-01D-A152-10 g.chr8:88885187G>A c.1013C>T c.(1012-1014)aCg>aTg p.T338M READ 8 88885308 88885308 + Missense_Mutation SNP C C A TCGA-CI-6622-01A-11D-1826-10 TCGA-CI-6622-10A-01D-1826-10 g.chr8:88885308C>A c.892G>T c.(892-894)Gac>Tac p.D298Y READ 8 88885451 88885451 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr8:88885451C>T c.749G>A c.(748-750)gGc>gAc p.G250D READ 8 88885717 88885717 + Silent SNP C C T TCGA-AF-2687-01A-02D-1733-10 TCGA-AF-2687-10A-01D-1733-10 g.chr8:88885717C>T c.483G>A c.(481-483)gcG>gcA p.A161A READ 8 88885751 88885751 + Missense_Mutation SNP G G A TCGA-AF-2687-01A-02D-1733-10 TCGA-AF-2687-10A-01D-1733-10 g.chr8:88885751G>A c.449C>T c.(448-450)gCa>gTa p.A150V READ 8 88885807 88885807 + Nonsense_Mutation SNP G G T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr8:88885807G>T c.393C>A c.(391-393)tgC>tgA p.C131* READ 8 88885814 88885814 + Missense_Mutation SNP G G T TCGA-AG-3892-01A-01W-1073-09 TCGA-AG-3892-10A-01W-1073-09 g.chr8:88885814G>T c.386C>A c.(385-387)tCt>tAt p.S129Y READ 8 88886083 88886083 + Silent SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr8:88886083G>A c.117C>T c.(115-117)ttC>ttT p.F39F SARC 8 88885852 88885852 + Silent SNP C C T TCGA-WK-A8XO-01A-11D-A37C-09 TCGA-WK-A8XO-10A-01D-A37F-09 g.chr8:88885852C>T c.348G>A c.(346-348)ccG>ccA p.P116P SARC 8 88885861 88885861 + Silent SNP C C T TCGA-DX-AB2E-01A-11D-A38Z-09 TCGA-DX-AB2E-10A-01D-A38Z-09 g.chr8:88885861C>T c.339G>A c.(337-339)cgG>cgA p.R113R SARC 8 88885986 88885986 + Missense_Mutation SNP C C T TCGA-QC-A6FX-01A-11D-A32I-09 TCGA-QC-A6FX-10B-01D-A32I-09 g.chr8:88885986C>T c.214G>A c.(214-216)Gac>Aac p.D72N SKCM 8 88885042 88885042 + Silent SNP C C T TCGA-EE-A29E-06A-11D-A197-08 TCGA-EE-A29E-10A-01D-A199-08 g.chr8:88885042C>T c.1158G>A c.(1156-1158)cgG>cgA p.R386R SKCM 8 88885042 88885042 + Silent SNP C C T TCGA-EE-A29M-06A-11D-A196-08 TCGA-EE-A29M-10A-01D-A198-08 g.chr8:88885042C>T c.1158G>A c.(1156-1158)cgG>cgA p.R386R SKCM 8 88885043 88885043 + Missense_Mutation SNP C C T TCGA-EE-A29E-06A-11D-A197-08 TCGA-EE-A29E-10A-01D-A199-08 g.chr8:88885043C>T c.1157G>A c.(1156-1158)cGg>cAg p.R386Q SKCM 8 88885043 88885043 + Missense_Mutation SNP C C T TCGA-EE-A29M-06A-11D-A196-08 TCGA-EE-A29M-10A-01D-A198-08 g.chr8:88885043C>T c.1157G>A c.(1156-1158)cGg>cAg p.R386Q SKCM 8 88885075 88885075 + Silent SNP G G A TCGA-EE-A29M-06A-11D-A196-08 TCGA-EE-A29M-10A-01D-A198-08 g.chr8:88885075G>A c.1125C>T c.(1123-1125)ttC>ttT p.F375F SKCM 8 88885086 88885086 + Missense_Mutation SNP G G A TCGA-D3-A2JH-06A-11D-A196-08 TCGA-D3-A2JH-10A-01D-A198-08 g.chr8:88885086G>A c.1114C>T c.(1114-1116)Ctc>Ttc p.L372F SKCM 8 88885087 88885087 + Silent SNP G G A TCGA-D3-A2JH-06A-11D-A196-08 TCGA-D3-A2JH-10A-01D-A198-08 g.chr8:88885087G>A c.1113C>T c.(1111-1113)cgC>cgT p.R371R SKCM 8 88885109 88885109 + Missense_Mutation SNP G G A TCGA-FS-A1Z3-06A-11D-A197-08 TCGA-FS-A1Z3-10A-01D-A199-08 g.chr8:88885109G>A c.1091C>T c.(1090-1092)cCc>cTc p.P364L SKCM 8 88885116 88885116 + Missense_Mutation SNP C C T TCGA-FS-A1ZB-06A-12D-A197-08 TCGA-FS-A1ZB-10A-01D-A199-08 g.chr8:88885116C>T c.1084G>A c.(1084-1086)Gac>Aac p.D362N SKCM 8 88885171 88885171 + Silent SNP G G A TCGA-ER-A19H-06A-12D-A196-08 TCGA-ER-A19H-10A-01D-A198-08 g.chr8:88885171G>A c.1029C>T c.(1027-1029)ctC>ctT p.L343L SKCM 8 88885185 88885185 + Missense_Mutation SNP T T C TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr8:88885185T>C c.1015A>G c.(1015-1017)Aga>Gga p.R339G SKCM 8 88885216 88885216 + Silent SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr8:88885216G>A c.984C>T c.(982-984)gtC>gtT p.V328V SKCM 8 88885234 88885234 + Silent SNP C C G TCGA-EE-A3JI-06A-11D-A21A-08 TCGA-EE-A3JI-10A-01D-A21A-08 g.chr8:88885234C>G c.966G>C c.(964-966)gtG>gtC p.V322V SKCM 8 88885264 88885264 + Silent SNP C C T TCGA-EE-A3AE-06A-11D-A196-08 TCGA-EE-A3AE-10A-01D-A198-08 g.chr8:88885264C>T c.936G>A c.(934-936)gtG>gtA p.V312V SKCM 8 88885275 88885275 + Missense_Mutation SNP C C T TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr8:88885275C>T c.925G>A c.(925-927)Gaa>Aaa p.E309K SKCM 8 88885275 88885275 + Missense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr8:88885275C>T c.925G>A c.(925-927)Gaa>Aaa p.E309K SKCM 8 88885275 88885275 + Missense_Mutation SNP C C T TCGA-GN-A266-06A-11D-A197-08 TCGA-GN-A266-10A-01D-A199-08 g.chr8:88885275C>T c.925G>A c.(925-927)Gaa>Aaa p.E309K SKCM 8 88885348 88885348 + Silent SNP G G A TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr8:88885348G>A c.852C>T c.(850-852)ttC>ttT p.F284F SKCM 8 88885780 88885780 + Silent SNP G G A TCGA-EE-A2GR-06A-11D-A197-08 TCGA-EE-A2GR-10A-01D-A199-08 g.chr8:88885780G>A c.420C>T c.(418-420)tcC>tcT p.S140S SKCM 8 88885781 88885781 + Missense_Mutation SNP G G A TCGA-FS-A4F0-06A-11D-A24R-08 TCGA-FS-A4F0-10A-01D-A24R-08 g.chr8:88885781G>A c.419C>T c.(418-420)tCc>tTc p.S140F SKCM 8 88885791 88885791 + Missense_Mutation SNP G G A TCGA-EE-A3J8-06A-11D-A20D-08 TCGA-EE-A3J8-10A-01D-A20D-08 g.chr8:88885791G>A c.409C>T c.(409-411)Cac>Tac p.H137Y SKCM 8 88885802 88885802 + Missense_Mutation SNP G G A TCGA-D3-A51R-06A-11D-A25O-08 TCGA-D3-A51R-10A-01D-A25O-08 g.chr8:88885802G>A c.398C>T c.(397-399)gCc>gTc p.A133V SKCM 8 88885802 88885802 + Missense_Mutation SNP G G A TCGA-FR-A3YN-06A-11D-A23B-08 TCGA-FR-A3YN-10A-01D-A23B-08 g.chr8:88885802G>A c.398C>T c.(397-399)gCc>gTc p.A133V SKCM 8 88885814 88885814 + Missense_Mutation SNP G G A TCGA-ER-A195-06A-11D-A196-08 TCGA-ER-A195-10A-01D-A198-08 g.chr8:88885814G>A c.386C>T c.(385-387)tCt>tTt p.S129F SKCM 8 88885815 88885815 + Missense_Mutation SNP A A T TCGA-EE-A29E-06A-11D-A197-08 TCGA-EE-A29E-10A-01D-A199-08 g.chr8:88885815A>T c.385T>A c.(385-387)Tct>Act p.S129T SKCM 8 88885825 88885825 + Silent SNP C C T TCGA-EE-A3JD-06A-11D-A20D-08 TCGA-EE-A3JD-10A-01D-A20D-08 g.chr8:88885825C>T c.375G>A c.(373-375)cgG>cgA p.R125R SKCM 8 88885827 88885827 + Missense_Mutation SNP G G A TCGA-EE-A29M-06A-11D-A196-08 TCGA-EE-A29M-10A-01D-A198-08 g.chr8:88885827G>A c.373C>T c.(373-375)Cgg>Tgg p.R125W SKCM 8 88885871 88885871 + Missense_Mutation SNP G G A TCGA-EE-A2A1-06A-11D-A197-08 TCGA-EE-A2A1-10A-01D-A199-08 g.chr8:88885871G>A c.329C>T c.(328-330)cCt>cTt p.P110L SKCM 8 88885876 88885876 + Silent SNP C C T TCGA-EE-A29D-06A-11D-A197-08 TCGA-EE-A29D-10A-01D-A199-08 g.chr8:88885876C>T c.324G>A c.(322-324)acG>acA p.T108T SKCM 8 88885999 88885999 + Silent SNP G G A TCGA-EE-A29V-06A-12D-A197-08 TCGA-EE-A29V-10A-01D-A199-08 g.chr8:88885999G>A c.201C>T c.(199-201)tcC>tcT p.S67S SKCM 8 88886007 88886007 + Missense_Mutation SNP C C T TCGA-D3-A5GO-06A-12D-A27K-08 TCGA-D3-A5GO-10A-01D-A27N-08 g.chr8:88886007C>T c.193G>A c.(193-195)Gat>Aat p.D65N SKCM 8 88886022 88886022 + Nonsense_Mutation SNP G G A TCGA-ER-A19F-06A-11D-A196-08 TCGA-ER-A19F-10A-01D-A198-08 g.chr8:88886022G>A c.178C>T c.(178-180)Cag>Tag p.Q60* SKCM 8 88886023 88886023 + Silent SNP G G A TCGA-ER-A19F-06A-11D-A196-08 TCGA-ER-A19F-10A-01D-A198-08 g.chr8:88886023G>A c.177C>T c.(175-177)gtC>gtT p.V59V SKCM 8 88886032 88886032 + Silent SNP C C T TCGA-EE-A29L-06A-12D-A196-08 TCGA-EE-A29L-10A-01D-A198-08 g.chr8:88886032C>T c.168G>A c.(166-168)agG>agA p.R56R SKCM 8 88886058 88886058 + Missense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr8:88886058C>T c.142G>A c.(142-144)Gag>Aag p.E48K SKCM 8 88886083 88886083 + Silent SNP G G A TCGA-ER-A42L-06A-11D-A24R-08 TCGA-ER-A42L-10A-01D-A24R-08 g.chr8:88886083G>A c.117C>T c.(115-117)ttC>ttT p.F39F SKCM 8 88886163 88886163 + Missense_Mutation SNP C C T TCGA-FS-A1Z3-06A-11D-A197-08 TCGA-FS-A1Z3-10A-01D-A199-08 g.chr8:88886163C>T c.37G>A c.(37-39)Gac>Aac p.D13N

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BLCA-US 8 88885180 88885180 single base substitution G A synonymous_variant I340I 1020C>T BLCA-US 8 88885212 88885212 single base substitution C A missense_variant A330S 988G>T BLCA-US 8 88885230 88885230 single base substitution C A stop_gained E324* 970G>T BLCA-US 8 88885315 88885315 single base substitution C G missense_variant K295N 885G>C BLCA-US 8 88885613 88885613 single base substitution G A missense_variant A196V 587C>T BLCA-US 8 88886086 88886086 single base substitution T A missense_variant R38S 114A>T BRCA-EU 8 88878152 88878152 single base substitution C G downstream_gene_variant BRCA-EU 8 88878184 88878184 single base substitution G A downstream_gene_variant BRCA-EU 8 88878366 88878366 single base substitution G T downstream_gene_variant BRCA-EU 8 88879448 88879448 single base substitution G A downstream_gene_variant BRCA-EU 8 88880070 88880070 single base substitution G T downstream_gene_variant BRCA-EU 8 88881384 88881384 single base substitution A C downstream_gene_variant BRCA-EU 8 88881472 88881472 single base substitution C T downstream_gene_variant BRCA-EU 8 88881951 88881951 single base substitution G C downstream_gene_variant BRCA-EU 8 88882565 88882565 single base substitution A G downstream_gene_variant BRCA-EU 8 88882723 88882723 single base substitution T C downstream_gene_variant BRCA-EU 8 88882754 88882754 single base substitution C G downstream_gene_variant BRCA-EU 8 88884893 88884893 single base substitution G A 3_prime_UTR_variant BRCA-EU 8 88885042 88885042 single base substitution C A synonymous_variant R386R 1158G>T BRCA-EU 8 88885333 88885333 single base substitution G T missense_variant D289E 867C>A BRCA-EU 8 88885983 88885983 single base substitution G A stop_gained R73* 217C>T BRCA-EU 8 88886157 88886157 single base substitution G A stop_gained Q15* 43C>T BRCA-EU 8 88886353 88886353 single base substitution G A upstream_gene_variant BRCA-EU 8 88886401 88886401 single base substitution G A upstream_gene_variant BRCA-EU 8 88886786 88886786 single base substitution C G upstream_gene_variant BRCA-EU 8 88887227 88887227 single base substitution T C upstream_gene_variant BRCA-EU 8 88887932 88887946 deletion of <=200bp GTAAGTTTTTATCCA - upstream_gene_variant BRCA-EU 8 88887967 88887967 single base substitution G C upstream_gene_variant BRCA-EU 8 88888586 88888586 single base substitution A C upstream_gene_variant BRCA-EU 8 88888790 88888790 single base substitution C T upstream_gene_variant BRCA-EU 8 88888835 88888835 single base substitution C T upstream_gene_variant BRCA-EU 8 88890247 88890247 deletion of <=200bp A - upstream_gene_variant BRCA-EU 8 88890728 88890728 single base substitution G C upstream_gene_variant BRCA-EU 8 88891109 88891109 single base substitution G T upstream_gene_variant BRCA-FR 8 88881472 88881472 single base substitution C T downstream_gene_variant BRCA-FR 8 88881951 88881951 single base substitution G C downstream_gene_variant BRCA-FR 8 88884009 88884009 single base substitution T A 3_prime_UTR_variant BRCA-FR 8 88884893 88884893 single base substitution G A 3_prime_UTR_variant BRCA-UK 8 88878781 88878781 single base substitution G C downstream_gene_variant BRCA-UK 8 88885718 88885718 single base substitution G A missense_variant A161V 482C>T BRCA-UK 8 88888586 88888586 single base substitution A C upstream_gene_variant BRCA-US 8 88885140 88885140 single base substitution A G missense_variant S354P 1060T>C BRCA-US 8 88885215 88885215 single base substitution C T missense_variant V329M 985G>A BRCA-US 8 88885220 88885220 single base substitution C T missense_variant G327E 980G>A BRCA-US 8 88885242 88885242 single base substitution C T missense_variant V320M 958G>A BRCA-US 8 88885440 88885440 single base substitution G A missense_variant R254C 760C>T BRCA-US 8 88885659 88885659 single base substitution G T missense_variant Q181K 541C>A BRCA-US 8 88885903 88885903 single base substitution G A synonymous_variant Y99Y 297C>T BRCA-US 8 88885923 88885923 single base substitution C A stop_gained E93* 277G>T BRCA-US 8 88886087 88886087 single base substitution C T missense_variant R38K 113G>A BTCA-JP 8 88884986 88884986 single base substitution G A 3_prime_UTR_variant BTCA-JP 8 88885139 88885139 single base substitution G A missense_variant S354F 1061C>T BTCA-JP 8 88885242 88885242 single base substitution C T missense_variant V320M 958G>A BTCA-JP 8 88885577 88885577 single base substitution A G missense_variant V208A 623T>C BTCA-JP 8 88885826 88885826 single base substitution C T missense_variant R125Q 374G>A BTCA-JP 8 88885837 88885837 single base substitution G A synonymous_variant Y121Y 363C>T BTCA-JP 8 88886184 88886184 single base substitution G A missense_variant P6S 16C>T CESC-US 8 88885044 88885044 single base substitution G A missense_variant R386W 1156C>T CESC-US 8 88885075 88885075 single base substitution G A synonymous_variant F375F 1125C>T CESC-US 8 88885439 88885439 single base substitution C T missense_variant R254H 761G>A CESC-US 8 88885653 88885653 single base substitution G A missense_variant P183S 547C>T CLLE-ES 8 88885563 88885563 single base substitution C T missense_variant V213M 637G>A CLLE-ES 8 88890399 88890399 single base substitution A T upstream_gene_variant COAD-US 8 88885043 88885043 single base substitution C T missense_variant R386Q 1157G>A COAD-US 8 88885084 88885084 single base substitution G A synonymous_variant L372L 1116C>T COAD-US 8 88885201 88885201 single base substitution G A synonymous_variant G333G 999C>T COAD-US 8 88885420 88885420 single base substitution G C missense_variant S260R 780C>G COAD-US 8 88885439 88885439 single base substitution C T missense_variant R254H 761G>A COAD-US 8 88885440 88885440 single base substitution G A missense_variant R254C 760C>T COAD-US 8 88885491 88885491 single base substitution G A missense_variant P237S 709C>T COAD-US 8 88885685 88885685 single base substitution C T missense_variant R172H 515G>A COAD-US 8 88885686 88885686 single base substitution G A missense_variant R172C 514C>T COAD-US 8 88885695 88885695 single base substitution G A missense_variant P169S 505C>T COAD-US 8 88885719 88885719 single base substitution C G missense_variant A161P 481G>C COAD-US 8 88885814 88885814 single base substitution G T missense_variant S129Y 386C>A COAD-US 8 88885872 88885872 single base substitution G T missense_variant P110T 328C>A COAD-US 8 88885963 88885963 single base substitution C T synonymous_variant A79A 237G>A COAD-US 8 88886052 88886052 single base substitution G A missense_variant R50C 148C>T COAD-US 8 88886057 88886057 single base substitution T C missense_variant E48G 143A>G COCA-CN 8 88885184 88885184 single base substitution C A missense_variant R339I 1016G>T COCA-CN 8 88885194 88885194 single base substitution A G missense_variant C336R 1006T>C COCA-CN 8 88885211 88885211 single base substitution G A missense_variant A330V 989C>T COCA-CN 8 88885242 88885242 single base substitution C T missense_variant V320M 958G>A COCA-CN 8 88885450 88885450 single base substitution G A synonymous_variant G250G 750C>T COCA-CN 8 88885462 88885462 single base substitution C A synonymous_variant G246G 738G>T COCA-CN 8 88885674 88885674 single base substitution T C missense_variant M176V 526A>G COCA-CN 8 88885716 88885716 single base substitution A G missense_variant S162P 484T>C COCA-CN 8 88885827 88885827 single base substitution G A missense_variant R125W 373C>T COCA-CN 8 88885862 88885862 single base substitution C T missense_variant R113Q 338G>A COCA-CN 8 88886186 88886186 single base substitution C A missense_variant R5I 14G>T COCA-CN 8 88886210 88886210 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant COCA-CN 8 88886350 88886350 single base substitution G A upstream_gene_variant COCA-CN 8 88886700 88886700 single base substitution G A upstream_gene_variant COCA-CN 8 88887132 88887132 single base substitution G A upstream_gene_variant COCA-CN 8 88887237 88887237 single base substitution A G upstream_gene_variant COCA-CN 8 88887885 88887885 single base substitution A G upstream_gene_variant EOPC-DE 8 88884147 88884147 single base substitution T A 3_prime_UTR_variant ESAD-UK 8 88878004 88878004 single base substitution A C downstream_gene_variant ESAD-UK 8 88878078 88878078 single base substitution T C downstream_gene_variant ESAD-UK 8 88878080 88878080 deletion of <=200bp C - downstream_gene_variant ESAD-UK 8 88878711 88878711 single base substitution T C downstream_gene_variant ESAD-UK 8 88878722 88878722 single base substitution C T downstream_gene_variant ESAD-UK 8 88879104 88879104 single base substitution T G downstream_gene_variant ESAD-UK 8 88879282 88879282 single base substitution A G downstream_gene_variant ESAD-UK 8 88879426 88879426 single base substitution A G downstream_gene_variant ESAD-UK 8 88879548 88879548 single base substitution A C downstream_gene_variant ESAD-UK 8 88879797 88879797 single base substitution A G downstream_gene_variant ESAD-UK 8 88880081 88880081 single base substitution A C downstream_gene_variant ESAD-UK 8 88880282 88880282 single base substitution A C downstream_gene_variant ESAD-UK 8 88880958 88880958 single base substitution A C downstream_gene_variant ESAD-UK 8 88880958 88880958 single base substitution A G downstream_gene_variant ESAD-UK 8 88880960 88880960 single base substitution T G downstream_gene_variant ESAD-UK 8 88881105 88881105 single base substitution A G downstream_gene_variant ESAD-UK 8 88881106 88881106 single base substitution A C downstream_gene_variant ESAD-UK 8 88881624 88881624 single base substitution A G downstream_gene_variant ESAD-UK 8 88881916 88881916 single base substitution C T downstream_gene_variant ESAD-UK 8 88882401 88882401 single base substitution T G downstream_gene_variant ESAD-UK 8 88882502 88882502 single base substitution G T downstream_gene_variant ESAD-UK 8 88882903 88882903 single base substitution C T downstream_gene_variant ESAD-UK 8 88882942 88882942 single base substitution G C downstream_gene_variant ESAD-UK 8 88883082 88883082 single base substitution A T 3_prime_UTR_variant ESAD-UK 8 88883446 88883446 single base substitution T G 3_prime_UTR_variant ESAD-UK 8 88883567 88883567 single base substitution A C 3_prime_UTR_variant ESAD-UK 8 88883807 88883807 deletion of <=200bp C - 3_prime_UTR_variant ESAD-UK 8 88883881 88883881 single base substitution A C 3_prime_UTR_variant ESAD-UK 8 88884398 88884398 single base substitution T C 3_prime_UTR_variant ESAD-UK 8 88884608 88884608 single base substitution C A 3_prime_UTR_variant ESAD-UK 8 88884761 88884761 single base substitution C A 3_prime_UTR_variant ESAD-UK 8 88884934 88884934 single base substitution C T 3_prime_UTR_variant ESAD-UK 8 88884979 88884979 single base substitution A C 3_prime_UTR_variant ESAD-UK 8 88885004 88885004 single base substitution C A 3_prime_UTR_variant ESAD-UK 8 88885014 88885014 single base substitution A T stop_lost *396K 1186T>A ESAD-UK 8 88885064 88885064 single base substitution G A missense_variant P379L 1136C>T ESAD-UK 8 88885187 88885187 single base substitution G A missense_variant T338M 1013C>T ESAD-UK 8 88885614 88885614 single base substitution C T missense_variant A196T 586G>A ESAD-UK 8 88885754 88885754 single base substitution A G missense_variant L149P 446T>C ESAD-UK 8 88885978 88885978 single base substitution A G synonymous_variant F74F 222T>C ESAD-UK 8 88886203 88886203 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant ESAD-UK 8 88886686 88886686 single base substitution G A upstream_gene_variant ESAD-UK 8 88887749 88887749 insertion of <=200bp - T upstream_gene_variant ESAD-UK 8 88887935 88887935 single base substitution A C upstream_gene_variant ESAD-UK 8 88888245 88888245 single base substitution T G upstream_gene_variant ESAD-UK 8 88888422 88888422 single base substitution A C upstream_gene_variant ESAD-UK 8 88888522 88888522 single base substitution T G upstream_gene_variant ESAD-UK 8 88888744 88888744 single base substitution T C upstream_gene_variant ESAD-UK 8 88889025 88889025 single base substitution T A upstream_gene_variant ESAD-UK 8 88889259 88889259 single base substitution G C upstream_gene_variant ESAD-UK 8 88889457 88889457 insertion of <=200bp - C upstream_gene_variant ESAD-UK 8 88890241 88890241 single base substitution G T upstream_gene_variant ESAD-UK 8 88890457 88890457 single base substitution A C upstream_gene_variant ESAD-UK 8 88891234 88891234 single base substitution T C upstream_gene_variant ESAD-UK 8 88891247 88891247 single base substitution T G upstream_gene_variant ESCA-CN 8 88885044 88885044 single base substitution G A missense_variant R386W 1156C>T ESCA-CN 8 88885446 88885446 single base substitution C A missense_variant D252Y 754G>T ESCA-CN 8 88885502 88885502 single base substitution G T missense_variant A233E 698C>A ESCA-CN 8 88885519 88885519 single base substitution G C synonymous_variant V227V 681C>G ESCA-CN 8 88885886 88885886 single base substitution C T missense_variant R105Q 314G>A ESCA-CN 8 88885929 88885929 single base substitution G A stop_gained Q91* 271C>T ESCA-CN 8 88886141 88886141 single base substitution C G missense_variant R20T 59G>C GBM-US 8 88886046 88886046 single base substitution T A missense_variant S52C 154A>T GBM-US 8 88886131 88886131 single base substitution G C synonymous_variant L23L 69C>G KIRC-US 8 88885732 88885732 single base substitution G A synonymous_variant A156A 468C>T KIRP-US 8 88885869 88885869 single base substitution C G missense_variant E111Q 331G>C LGG-US 8 88885200 88885200 single base substitution G C missense_variant Q334E 1000C>G LICA-CN 8 88885356 88885356 single base substitution C A missense_variant G282C 844G>T LICA-CN 8 88885873 88885873 single base substitution G T synonymous_variant T109T 327C>A LICA-FR 8 88885672 88885672 single base substitution C A missense_variant M176I 528G>T LICA-FR 8 88885884 88885884 single base substitution C A missense_variant G106C 316G>T LICA-FR 8 88885952 88885952 single base substitution G T missense_variant T83N 248C>A LICA-FR 8 88886169 88886169 single base substitution C A stop_gained E11* 31G>T LICA-FR 8 88889355 88889355 single base substitution C G upstream_gene_variant LIHC-US 8 88885240 88885242 deletion of <=200bp CAC - inframe_deletion V320 LIHC-US 8 88885245 88885246 deletion of <=200bp GT - frameshift_variant LP318 LIHC-US 8 88885313 88885313 single base substitution A G missense_variant L296P 887T>C LIHC-US 8 88886016 88886016 single base substitution G A missense_variant H62Y 184C>T LINC-JP 8 88879161 88879161 single base substitution T C downstream_gene_variant LINC-JP 8 88879330 88879330 single base substitution G T downstream_gene_variant LINC-JP 8 88879774 88879774 single base substitution A G downstream_gene_variant LINC-JP 8 88882194 88882194 single base substitution T C downstream_gene_variant LINC-JP 8 88884094 88884094 single base substitution A G 3_prime_UTR_variant LINC-JP 8 88884947 88884947 single base substitution G T 3_prime_UTR_variant LINC-JP 8 88885275 88885275 single base substitution C T missense_variant E309K 925G>A LINC-JP 8 88885740 88885740 single base substitution T C missense_variant S154G 460A>G LINC-JP 8 88886039 88886039 single base substitution A G missense_variant M54T 161T>C LINC-JP 8 88886089 88886089 single base substitution G A synonymous_variant L37L 111C>T LIRI-JP 8 88878133 88878133 single base substitution G A downstream_gene_variant LIRI-JP 8 88878752 88878752 single base substitution A G downstream_gene_variant LIRI-JP 8 88878884 88878884 single base substitution C G downstream_gene_variant LIRI-JP 8 88879916 88879916 single base substitution A G downstream_gene_variant LIRI-JP 8 88881184 88881184 single base substitution T C downstream_gene_variant LIRI-JP 8 88882705 88882705 single base substitution T C downstream_gene_variant LIRI-JP 8 88883590 88883590 single base substitution A T 3_prime_UTR_variant LIRI-JP 8 88883627 88883627 single base substitution T A 3_prime_UTR_variant LIRI-JP 8 88883916 88883916 single base substitution A G 3_prime_UTR_variant LIRI-JP 8 88883919 88883919 single base substitution A G 3_prime_UTR_variant LIRI-JP 8 88883930 88883930 single base substitution C T 3_prime_UTR_variant LIRI-JP 8 88884109 88884109 single base substitution C T 3_prime_UTR_variant LIRI-JP 8 88884273 88884273 single base substitution C T 3_prime_UTR_variant LIRI-JP 8 88884297 88884297 single base substitution T C 3_prime_UTR_variant LIRI-JP 8 88884511 88884511 single base substitution A T 3_prime_UTR_variant LIRI-JP 8 88885174 88885174 single base substitution G A synonymous_variant S342S 1026C>T LIRI-JP 8 88886025 88886025 single base substitution C A missense_variant V59F 175G>T LIRI-JP 8 88886279 88886279 single base substitution G T 5_prime_UTR_variant LIRI-JP 8 88886545 88886545 single base substitution A T upstream_gene_variant LIRI-JP 8 88886788 88886788 single base substitution C A upstream_gene_variant LIRI-JP 8 88886823 88886823 single base substitution C T upstream_gene_variant LIRI-JP 8 88887391 88887391 single base substitution T G upstream_gene_variant LIRI-JP 8 88887789 88887789 single base substitution T A upstream_gene_variant LIRI-JP 8 88888810 88888810 single base substitution C A upstream_gene_variant LIRI-JP 8 88889045 88889045 single base substitution A G upstream_gene_variant LIRI-JP 8 88889210 88889210 single base substitution G A upstream_gene_variant LIRI-JP 8 88890173 88890173 single base substitution A G upstream_gene_variant LIRI-JP 8 88890371 88890371 single base substitution C A upstream_gene_variant LIRI-JP 8 88890917 88890917 single base substitution A G upstream_gene_variant LIRI-JP 8 88891255 88891255 single base substitution A T upstream_gene_variant LUSC-KR 8 88878479 88878479 single base substitution A T downstream_gene_variant LUSC-KR 8 88878787 88878787 single base substitution T C downstream_gene_variant LUSC-KR 8 88879373 88879373 single base substitution G T downstream_gene_variant LUSC-KR 8 88879891 88879891 single base substitution C A downstream_gene_variant LUSC-KR 8 88880886 88880886 single base substitution C A downstream_gene_variant LUSC-KR 8 88881042 88881042 single base substitution A T downstream_gene_variant LUSC-KR 8 88881203 88881203 single base substitution C A downstream_gene_variant LUSC-KR 8 88881380 88881380 single base substitution A G downstream_gene_variant LUSC-KR 8 88881507 88881507 single base substitution G A downstream_gene_variant LUSC-KR 8 88881596 88881596 single base substitution G C downstream_gene_variant LUSC-KR 8 88881915 88881915 single base substitution G T downstream_gene_variant LUSC-KR 8 88882089 88882089 single base substitution A T downstream_gene_variant LUSC-KR 8 88882119 88882119 single base substitution G T downstream_gene_variant LUSC-KR 8 88882637 88882637 single base substitution G T downstream_gene_variant LUSC-KR 8 88883101 88883101 single base substitution G C 3_prime_UTR_variant LUSC-KR 8 88883728 88883728 single base substitution A G 3_prime_UTR_variant LUSC-KR 8 88884625 88884625 single base substitution C A 3_prime_UTR_variant LUSC-KR 8 88885271 88885271 single base substitution C A missense_variant G310V 929G>T LUSC-KR 8 88885561 88885561 single base substitution C A synonymous_variant V213V 639G>T LUSC-KR 8 88886279 88886279 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant LUSC-KR 8 88886335 88886335 single base substitution C A upstream_gene_variant LUSC-KR 8 88887397 88887397 single base substitution C T upstream_gene_variant LUSC-KR 8 88887764 88887764 single base substitution G C upstream_gene_variant LUSC-KR 8 88888283 88888283 single base substitution C A upstream_gene_variant LUSC-KR 8 88888660 88888660 single base substitution C A upstream_gene_variant LUSC-KR 8 88888905 88888905 single base substitution A T upstream_gene_variant LUSC-KR 8 88889273 88889273 single base substitution T A upstream_gene_variant LUSC-KR 8 88889739 88889739 single base substitution C A upstream_gene_variant LUSC-KR 8 88890896 88890896 single base substitution T C upstream_gene_variant LUSC-KR 8 88890974 88890974 single base substitution T A upstream_gene_variant LUSC-KR 8 88891159 88891159 single base substitution G A upstream_gene_variant LUSC-KR 8 88891160 88891160 single base substitution T A upstream_gene_variant LUSC-US 8 88885116 88885116 single base substitution C A missense_variant D362Y 1084G>T LUSC-US 8 88885208 88885208 single base substitution G A missense_variant A331V 992C>T LUSC-US 8 88885348 88885348 single base substitution G A synonymous_variant F284F 852C>T LUSC-US 8 88885462 88885462 single base substitution C A synonymous_variant G246G 738G>T LUSC-US 8 88885511 88885511 single base substitution T C missense_variant Q230R 689A>G LUSC-US 8 88885555 88885555 single base substitution C G synonymous_variant T215T 645G>C LUSC-US 8 88885614 88885614 single base substitution C A missense_variant A196S 586G>T LUSC-US 8 88885715 88885715 single base substitution G T stop_gained S162* 485C>A LUSC-US 8 88885742 88885742 single base substitution G T missense_variant P153Q 458C>A LUSC-US 8 88885761 88885761 single base substitution C A missense_variant V147L 439G>T LUSC-US 8 88885771 88885771 single base substitution C A synonymous_variant L143L 429G>T LUSC-US 8 88885776 88885776 single base substitution G A missense_variant L142F 424C>T LUSC-US 8 88885863 88885863 single base substitution G A missense_variant R113W 337C>T LUSC-US 8 88885963 88885963 single base substitution C A synonymous_variant A79A 237G>T LUSC-US 8 88885967 88885967 single base substitution A G missense_variant L78P 233T>C LUSC-US 8 88886097 88886097 single base substitution C A missense_variant G35C 103G>T MALY-DE 8 88878045 88878045 single base substitution T G downstream_gene_variant MALY-DE 8 88880126 88880126 single base substitution A C downstream_gene_variant MALY-DE 8 88880654 88880654 single base substitution C T downstream_gene_variant MALY-DE 8 88880833 88880833 single base substitution A T downstream_gene_variant MALY-DE 8 88881983 88881983 single base substitution A G downstream_gene_variant MALY-DE 8 88883256 88883256 deletion of <=200bp A - 3_prime_UTR_variant MALY-DE 8 88883562 88883562 single base substitution C T 3_prime_UTR_variant MALY-DE 8 88885246 88885246 single base substitution T G synonymous_variant L318L 954A>C MALY-DE 8 88885585 88885585 single base substitution A T synonymous_variant S205S 615T>A MALY-DE 8 88885715 88885715 single base substitution G A missense_variant S162L 485C>T MALY-DE 8 88885886 88885886 single base substitution C T missense_variant R105Q 314G>A MALY-DE 8 88887394 88887394 single base substitution G A upstream_gene_variant MALY-DE 8 88889991 88889991 single base substitution A T upstream_gene_variant MALY-DE 8 88890236 88890236 single base substitution A G upstream_gene_variant MALY-DE 8 88890265 88890265 single base substitution T C upstream_gene_variant MELA-AU 8 88878006 88878006 single base substitution G A downstream_gene_variant MELA-AU 8 88878027 88878027 single base substitution C T downstream_gene_variant MELA-AU 8 88878071 88878071 single base substitution T A downstream_gene_variant MELA-AU 8 88878078 88878078 single base substitution T C downstream_gene_variant MELA-AU 8 88878149 88878149 single base substitution C T downstream_gene_variant MELA-AU 8 88878157 88878157 single base substitution G A downstream_gene_variant MELA-AU 8 88878165 88878165 single base substitution C T downstream_gene_variant MELA-AU 8 88878200 88878200 single base substitution G A downstream_gene_variant MELA-AU 8 88878211 88878211 single base substitution G A downstream_gene_variant MELA-AU 8 88878391 88878391 single base substitution A C downstream_gene_variant MELA-AU 8 88878486 88878486 single base substitution G A downstream_gene_variant MELA-AU 8 88878617 88878617 single base substitution C T downstream_gene_variant MELA-AU 8 88878720 88878720 single base substitution C T downstream_gene_variant MELA-AU 8 88878852 88878852 single base substitution G A downstream_gene_variant MELA-AU 8 88878857 88878857 single base substitution T A downstream_gene_variant MELA-AU 8 88878947 88878947 single base substitution G A downstream_gene_variant MELA-AU 8 88879033 88879033 single base substitution C T downstream_gene_variant MELA-AU 8 88879134 88879134 single base substitution G A downstream_gene_variant MELA-AU 8 88879167 88879167 single base substitution G A downstream_gene_variant MELA-AU 8 88879278 88879278 single base substitution G A downstream_gene_variant MELA-AU 8 88879317 88879317 single base substitution G A downstream_gene_variant MELA-AU 8 88879370 88879370 single base substitution G A downstream_gene_variant MELA-AU 8 88879462 88879462 single base substitution G A downstream_gene_variant MELA-AU 8 88879572 88879572 single base substitution G C downstream_gene_variant MELA-AU 8 88879602 88879602 single base substitution T G downstream_gene_variant MELA-AU 8 88879693 88879694 multiple base substitution (>=2bp and <=200bp) CA GT downstream_gene_variant MELA-AU 8 88879886 88879886 single base substitution G A downstream_gene_variant MELA-AU 8 88879964 88879964 single base substitution G A downstream_gene_variant MELA-AU 8 88880297 88880297 single base substitution G A downstream_gene_variant MELA-AU 8 88880338 88880338 single base substitution T C downstream_gene_variant MELA-AU 8 88880360 88880360 single base substitution A G downstream_gene_variant MELA-AU 8 88880382 88880382 single base substitution G A downstream_gene_variant MELA-AU 8 88880467 88880467 single base substitution C T downstream_gene_variant MELA-AU 8 88880563 88880563 single base substitution G C downstream_gene_variant MELA-AU 8 88880597 88880597 single base substitution G A downstream_gene_variant MELA-AU 8 88880662 88880662 single base substitution G A downstream_gene_variant MELA-AU 8 88880690 88880690 single base substitution G A downstream_gene_variant MELA-AU 8 88881104 88881104 single base substitution G A downstream_gene_variant MELA-AU 8 88881203 88881203 single base substitution C T downstream_gene_variant MELA-AU 8 88881205 88881205 single base substitution C T downstream_gene_variant MELA-AU 8 88881306 88881306 single base substitution G A downstream_gene_variant MELA-AU 8 88881573 88881573 single base substitution G A downstream_gene_variant MELA-AU 8 88881612 88881612 single base substitution C T downstream_gene_variant MELA-AU 8 88881814 88881814 single base substitution C T downstream_gene_variant MELA-AU 8 88881855 88881855 single base substitution G A downstream_gene_variant MELA-AU 8 88882081 88882081 single base substitution A G downstream_gene_variant MELA-AU 8 88882298 88882298 single base substitution A T downstream_gene_variant MELA-AU 8 88882553 88882553 single base substitution C T downstream_gene_variant MELA-AU 8 88882630 88882630 single base substitution C T downstream_gene_variant MELA-AU 8 88882649 88882649 single base substitution G A downstream_gene_variant MELA-AU 8 88882828 88882828 single base substitution C T downstream_gene_variant MELA-AU 8 88882831 88882831 single base substitution C T downstream_gene_variant MELA-AU 8 88882869 88882869 single base substitution T A downstream_gene_variant MELA-AU 8 88883376 88883376 single base substitution C T 3_prime_UTR_variant MELA-AU 8 88883626 88883626 single base substitution T A 3_prime_UTR_variant MELA-AU 8 88883808 88883808 single base substitution C T 3_prime_UTR_variant MELA-AU 8 88883873 88883873 single base substitution C T 3_prime_UTR_variant MELA-AU 8 88883952 88883952 single base substitution C A 3_prime_UTR_variant MELA-AU 8 88884012 88884012 single base substitution C T 3_prime_UTR_variant MELA-AU 8 88884109 88884109 single base substitution C T 3_prime_UTR_variant MELA-AU 8 88884150 88884150 single base substitution A C 3_prime_UTR_variant MELA-AU 8 88884441 88884441 single base substitution G A 3_prime_UTR_variant MELA-AU 8 88884592 88884592 single base substitution G A 3_prime_UTR_variant MELA-AU 8 88884627 88884627 single base substitution A G 3_prime_UTR_variant MELA-AU 8 88884806 88884806 single base substitution G A 3_prime_UTR_variant MELA-AU 8 88884925 88884925 single base substitution C T 3_prime_UTR_variant MELA-AU 8 88884989 88884989 single base substitution C T 3_prime_UTR_variant MELA-AU 8 88885033 88885033 single base substitution A G synonymous_variant L389L 1167T>C MELA-AU 8 88885116 88885116 single base substitution C T missense_variant D362N 1084G>A MELA-AU 8 88885314 88885314 single base substitution G A synonymous_variant L296L 886C>T MELA-AU 8 88885348 88885348 single base substitution G A synonymous_variant F284F 852C>T MELA-AU 8 88885654 88885654 single base substitution G A synonymous_variant I182I 546C>T MELA-AU 8 88885758 88885758 single base substitution C T missense_variant G148R 442G>A MELA-AU 8 88885762 88885762 single base substitution G A synonymous_variant F146F 438C>T MELA-AU 8 88885876 88885876 single base substitution C T synonymous_variant T108T 324G>A MELA-AU 8 88886004 88886004 single base substitution G A missense_variant P66S 196C>T MELA-AU 8 88886032 88886032 single base substitution C T synonymous_variant R56R 168G>A MELA-AU 8 88886155 88886155 single base substitution C T synonymous_variant Q15Q 45G>A MELA-AU 8 88886202 88886202 single base substitution C T 5_prime_UTR_variant MELA-AU 8 88886219 88886219 single base substitution C T 5_prime_UTR_variant MELA-AU 8 88886409 88886409 single base substitution C T upstream_gene_variant MELA-AU 8 88886445 88886445 single base substitution G A upstream_gene_variant MELA-AU 8 88886613 88886613 single base substitution G A upstream_gene_variant MELA-AU 8 88886656 88886656 single base substitution C T upstream_gene_variant MELA-AU 8 88886713 88886713 single base substitution C T upstream_gene_variant MELA-AU 8 88886822 88886822 single base substitution C T upstream_gene_variant MELA-AU 8 88887073 88887073 single base substitution T A upstream_gene_variant MELA-AU 8 88887183 88887183 single base substitution A G upstream_gene_variant MELA-AU 8 88887212 88887212 single base substitution C T upstream_gene_variant MELA-AU 8 88887217 88887217 single base substitution C T upstream_gene_variant MELA-AU 8 88887259 88887259 single base substitution T G upstream_gene_variant MELA-AU 8 88887406 88887409 deletion of <=200bp TTTA - upstream_gene_variant MELA-AU 8 88887531 88887531 single base substitution C T upstream_gene_variant MELA-AU 8 88887550 88887550 single base substitution C G upstream_gene_variant MELA-AU 8 88887597 88887597 single base substitution G T upstream_gene_variant MELA-AU 8 88887635 88887635 single base substitution T C upstream_gene_variant MELA-AU 8 88887698 88887698 single base substitution C T upstream_gene_variant MELA-AU 8 88887769 88887769 single base substitution C T upstream_gene_variant MELA-AU 8 88888178 88888178 single base substitution T A upstream_gene_variant MELA-AU 8 88888190 88888190 single base substitution C T upstream_gene_variant MELA-AU 8 88888226 88888226 single base substitution G A upstream_gene_variant MELA-AU 8 88888298 88888298 single base substitution C T upstream_gene_variant MELA-AU 8 88888440 88888440 insertion of <=200bp - CCAT upstream_gene_variant MELA-AU 8 88888555 88888555 single base substitution C T upstream_gene_variant MELA-AU 8 88888575 88888575 single base substitution C T upstream_gene_variant MELA-AU 8 88888584 88888584 single base substitution G A upstream_gene_variant MELA-AU 8 88888643 88888643 single base substitution G A upstream_gene_variant MELA-AU 8 88888670 88888670 single base substitution G A upstream_gene_variant MELA-AU 8 88888922 88888922 single base substitution T A upstream_gene_variant MELA-AU 8 88888947 88888947 single base substitution G A upstream_gene_variant MELA-AU 8 88889014 88889014 single base substitution G A upstream_gene_variant MELA-AU 8 88889101 88889101 single base substitution T A upstream_gene_variant MELA-AU 8 88889243 88889243 single base substitution G A upstream_gene_variant MELA-AU 8 88889251 88889251 single base substitution G A upstream_gene_variant MELA-AU 8 88889355 88889355 single base substitution C T upstream_gene_variant MELA-AU 8 88889557 88889557 single base substitution A C upstream_gene_variant MELA-AU 8 88889650 88889650 single base substitution G A upstream_gene_variant MELA-AU 8 88889671 88889671 single base substitution C T upstream_gene_variant MELA-AU 8 88890077 88890077 single base substitution C T upstream_gene_variant MELA-AU 8 88890096 88890096 single base substitution C T upstream_gene_variant MELA-AU 8 88890246 88890246 single base substitution G A upstream_gene_variant MELA-AU 8 88890325 88890325 single base substitution G A upstream_gene_variant MELA-AU 8 88890406 88890406 single base substitution A G upstream_gene_variant MELA-AU 8 88890655 88890655 single base substitution T A upstream_gene_variant MELA-AU 8 88890725 88890725 single base substitution G A upstream_gene_variant MELA-AU 8 88890818 88890818 single base substitution G A upstream_gene_variant MELA-AU 8 88890928 88890928 single base substitution C T upstream_gene_variant MELA-AU 8 88890994 88890994 single base substitution G A upstream_gene_variant MELA-AU 8 88891004 88891004 single base substitution G T upstream_gene_variant MELA-AU 8 88891014 88891014 single base substitution A C upstream_gene_variant MELA-AU 8 88891044 88891044 single base substitution C T upstream_gene_variant ORCA-IN 8 88879202 88879202 single base substitution G T downstream_gene_variant ORCA-IN 8 88879917 88879917 single base substitution G C downstream_gene_variant ORCA-IN 8 88887288 88887288 single base substitution G C upstream_gene_variant OV-AU 8 88879163 88879163 single base substitution G A downstream_gene_variant OV-AU 8 88879241 88879241 single base substitution A T downstream_gene_variant OV-AU 8 88881469 88881469 single base substitution G A downstream_gene_variant OV-AU 8 88884179 88884179 single base substitution T G 3_prime_UTR_variant OV-AU 8 88884181 88884181 single base substitution G T 3_prime_UTR_variant OV-AU 8 88885898 88885898 single base substitution A T missense_variant I101N 302T>A OV-AU 8 88886082 88886082 single base substitution C T missense_variant A40T 118G>A OV-AU 8 88886278 88886278 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant OV-AU 8 88886683 88886683 single base substitution G A upstream_gene_variant OV-AU 8 88886841 88886841 single base substitution T A upstream_gene_variant OV-AU 8 88888229 88888229 single base substitution C G upstream_gene_variant OV-AU 8 88888530 88888530 single base substitution C G upstream_gene_variant OV-AU 8 88888719 88888719 single base substitution C G upstream_gene_variant OV-AU 8 88889196 88889196 single base substitution T C upstream_gene_variant OV-AU 8 88889843 88889843 single base substitution A T upstream_gene_variant PACA-AU 8 88878087 88878090 deletion of <=200bp TCTT - downstream_gene_variant PACA-AU 8 88878607 88878607 single base substitution G A downstream_gene_variant PACA-AU 8 88880592 88880592 single base substitution G T downstream_gene_variant PACA-AU 8 88881712 88881712 single base substitution G A downstream_gene_variant PACA-AU 8 88881917 88881917 single base substitution G A downstream_gene_variant PACA-AU 8 88883090 88883090 single base substitution T A 3_prime_UTR_variant PACA-AU 8 88883102 88883102 single base substitution C A 3_prime_UTR_variant PACA-AU 8 88884746 88884746 single base substitution G T 3_prime_UTR_variant PACA-AU 8 88885469 88885469 single base substitution C T missense_variant R244H 731G>A PACA-AU 8 88885678 88885678 single base substitution A T synonymous_variant P174P 522T>A PACA-AU 8 88885852 88885852 single base substitution C T synonymous_variant P116P 348G>A PACA-AU 8 88886016 88886016 single base substitution G A missense_variant H62Y 184C>T PACA-AU 8 88886060 88886060 single base substitution C T missense_variant R47H 140G>A PACA-AU 8 88886064 88886064 single base substitution C A missense_variant A46S 136G>T PACA-AU 8 88886070 88886070 single base substitution G A missense_variant R44C 130C>T PACA-AU 8 88887248 88887248 single base substitution G A upstream_gene_variant PACA-AU 8 88887279 88887279 deletion of <=200bp T - upstream_gene_variant PACA-AU 8 88887716 88887716 single base substitution A C upstream_gene_variant PACA-AU 8 88887991 88887991 single base substitution A G upstream_gene_variant PACA-AU 8 88888171 88888171 single base substitution C T upstream_gene_variant PACA-AU 8 88889234 88889234 single base substitution T G upstream_gene_variant PACA-CA 8 88878035 88878035 single base substitution T A downstream_gene_variant PACA-CA 8 88878186 88878186 single base substitution G A downstream_gene_variant PACA-CA 8 88878899 88878899 single base substitution A T downstream_gene_variant PACA-CA 8 88879297 88879297 single base substitution A G downstream_gene_variant PACA-CA 8 88879862 88879862 single base substitution G T downstream_gene_variant PACA-CA 8 88879937 88879937 single base substitution C T downstream_gene_variant PACA-CA 8 88880436 88880436 single base substitution A T downstream_gene_variant PACA-CA 8 88881669 88881669 single base substitution C A downstream_gene_variant PACA-CA 8 88881688 88881688 single base substitution C T downstream_gene_variant PACA-CA 8 88881832 88881832 single base substitution G A downstream_gene_variant PACA-CA 8 88881964 88881964 single base substitution G A downstream_gene_variant PACA-CA 8 88882170 88882170 single base substitution C A downstream_gene_variant PACA-CA 8 88882389 88882389 single base substitution C T downstream_gene_variant PACA-CA 8 88882544 88882544 single base substitution G A downstream_gene_variant PACA-CA 8 88882879 88882879 single base substitution A C downstream_gene_variant PACA-CA 8 88883105 88883105 single base substitution G C 3_prime_UTR_variant PACA-CA 8 88883810 88883810 single base substitution C T 3_prime_UTR_variant PACA-CA 8 88883884 88883884 single base substitution G A 3_prime_UTR_variant PACA-CA 8 88884172 88884172 insertion of <=200bp - T 3_prime_UTR_variant PACA-CA 8 88884196 88884196 single base substitution T C 3_prime_UTR_variant PACA-CA 8 88884225 88884225 single base substitution G C 3_prime_UTR_variant PACA-CA 8 88884744 88884744 single base substitution A G 3_prime_UTR_variant PACA-CA 8 88884993 88884993 single base substitution C T 3_prime_UTR_variant PACA-CA 8 88885042 88885042 single base substitution C T synonymous_variant R386R 1158G>A PACA-CA 8 88885084 88885084 single base substitution G A synonymous_variant L372L 1116C>T PACA-CA 8 88885288 88885288 single base substitution A T stop_gained C304* 912T>A PACA-CA 8 88885357 88885357 single base substitution A G synonymous_variant D281D 843T>C PACA-CA 8 88885599 88885599 single base substitution T G missense_variant S201R 601A>C PACA-CA 8 88886039 88886039 single base substitution A G missense_variant M54T 161T>C PACA-CA 8 88887133 88887133 single base substitution C T upstream_gene_variant PACA-CA 8 88887548 88887548 single base substitution C T upstream_gene_variant PACA-CA 8 88887761 88887761 single base substitution T G upstream_gene_variant PACA-CA 8 88889688 88889688 single base substitution A C upstream_gene_variant PACA-CA 8 88891098 88891098 single base substitution G A upstream_gene_variant PAEN-AU 8 88879102 88879102 single base substitution A C downstream_gene_variant PBCA-DE 8 88880358 88880358 single base substitution C T downstream_gene_variant PBCA-DE 8 88884332 88884332 single base substitution C T 3_prime_UTR_variant PBCA-DE 8 88886051 88886051 single base substitution C T missense_variant R50H 149G>A PRAD-CA 8 88878607 88878607 single base substitution G A downstream_gene_variant PRAD-CA 8 88878904 88878904 single base substitution C T downstream_gene_variant PRAD-CA 8 88881775 88881775 single base substitution G A downstream_gene_variant PRAD-CA 8 88884888 88884888 single base substitution C A 3_prime_UTR_variant PRAD-CA 8 88886317 88886317 single base substitution G T upstream_gene_variant PRAD-CA 8 88887724 88887724 single base substitution G A upstream_gene_variant PRAD-CA 8 88887945 88887945 single base substitution C A upstream_gene_variant PRAD-UK 8 88878786 88878786 single base substitution G A downstream_gene_variant PRAD-UK 8 88881081 88881081 single base substitution T A downstream_gene_variant PRAD-UK 8 88881827 88881827 single base substitution C T downstream_gene_variant PRAD-UK 8 88882731 88882731 single base substitution T C downstream_gene_variant PRAD-UK 8 88883299 88883299 single base substitution C G 3_prime_UTR_variant PRAD-UK 8 88883337 88883337 single base substitution A T 3_prime_UTR_variant PRAD-UK 8 88884045 88884045 insertion of <=200bp - T 3_prime_UTR_variant PRAD-UK 8 88884048 88884048 insertion of <=200bp - T 3_prime_UTR_variant PRAD-UK 8 88886020 88886020 single base substitution C G missense_variant Q60H 180G>C PRAD-UK 8 88887318 88887318 single base substitution G T upstream_gene_variant PRAD-US 8 88885073 88885073 single base substitution C T missense_variant R376Q 1127G>A PRAD-US 8 88885088 88885088 single base substitution C T missense_variant R371H 1112G>A PRAD-US 8 88885128 88885128 single base substitution C T missense_variant A358T 1072G>A PRAD-US 8 88886040 88886040 single base substitution T C missense_variant M54V 160A>G READ-US 8 88885187 88885187 single base substitution G A missense_variant T338M 1013C>T READ-US 8 88885308 88885308 single base substitution C A missense_variant D298Y 892G>T READ-US 8 88885469 88885469 single base substitution C T missense_variant R244H 731G>A READ-US 8 88885556 88885556 single base substitution G A missense_variant T215M 644C>T RECA-EU 8 88878802 88878802 single base substitution A T downstream_gene_variant RECA-EU 8 88879077 88879077 single base substitution G T downstream_gene_variant SKCA-BR 8 88878080 88878080 single base substitution C T downstream_gene_variant SKCA-BR 8 88878781 88878781 single base substitution G A downstream_gene_variant SKCA-BR 8 88878989 88878989 single base substitution T C downstream_gene_variant SKCA-BR 8 88879736 88879736 single base substitution C T downstream_gene_variant SKCA-BR 8 88881659 88881659 single base substitution C T downstream_gene_variant SKCA-BR 8 88883235 88883235 single base substitution C T 3_prime_UTR_variant SKCA-BR 8 88885140 88885140 single base substitution A G missense_variant S354P 1060T>C SKCA-BR 8 88885144 88885144 single base substitution T G synonymous_variant I352I 1056A>C SKCA-BR 8 88885536 88885536 single base substitution C T missense_variant G222R 664G>A SKCA-BR 8 88886595 88886595 single base substitution C T upstream_gene_variant SKCA-BR 8 88886613 88886613 single base substitution G A upstream_gene_variant SKCA-BR 8 88887133 88887133 single base substitution C T upstream_gene_variant SKCA-BR 8 88888552 88888552 single base substitution C T upstream_gene_variant SKCM-US 8 88885075 88885075 single base substitution G A synonymous_variant F375F 1125C>T SKCM-US 8 88885081 88885081 single base substitution C T synonymous_variant G373G 1119G>A SKCM-US 8 88885109 88885109 single base substitution G A missense_variant P364L 1091C>T SKCM-US 8 88885116 88885116 single base substitution C T missense_variant D362N 1084G>A SKCM-US 8 88885139 88885139 single base substitution G A missense_variant S354F 1061C>T SKCM-US 8 88885163 88885163 single base substitution C T missense_variant G346D 1037G>A SKCM-US 8 88885171 88885171 single base substitution G A synonymous_variant L343L 1029C>T SKCM-US 8 88885185 88885185 single base substitution T C missense_variant R339G 1015A>G SKCM-US 8 88885216 88885216 single base substitution G A synonymous_variant V328V 984C>T SKCM-US 8 88885234 88885234 single base substitution C G synonymous_variant V322V 966G>C SKCM-US 8 88885264 88885264 single base substitution C T synonymous_variant V312V 936G>A SKCM-US 8 88885275 88885275 single base substitution C T missense_variant E309K 925G>A SKCM-US 8 88885348 88885348 single base substitution G A synonymous_variant F284F 852C>T SKCM-US 8 88885780 88885780 single base substitution G A synonymous_variant S140S 420C>T SKCM-US 8 88885781 88885781 single base substitution G A missense_variant S140F 419C>T SKCM-US 8 88885791 88885791 single base substitution G A missense_variant H137Y 409C>T SKCM-US 8 88885802 88885802 single base substitution G A missense_variant A133V 398C>T SKCM-US 8 88885814 88885814 single base substitution G A missense_variant S129F 386C>T SKCM-US 8 88885815 88885815 single base substitution A T missense_variant S129T 385T>A SKCM-US 8 88885825 88885825 single base substitution C T synonymous_variant R125R 375G>A SKCM-US 8 88885827 88885827 single base substitution G A missense_variant R125W 373C>T SKCM-US 8 88885871 88885871 single base substitution G A missense_variant P110L 329C>T SKCM-US 8 88885876 88885876 single base substitution C T synonymous_variant T108T 324G>A SKCM-US 8 88885999 88885999 single base substitution G A synonymous_variant S67S 201C>T SKCM-US 8 88886004 88886004 single base substitution G A missense_variant P66S 196C>T SKCM-US 8 88886007 88886007 single base substitution C T missense_variant D65N 193G>A SKCM-US 8 88886032 88886032 single base substitution C T synonymous_variant R56R 168G>A SKCM-US 8 88886058 88886058 single base substitution C T missense_variant E48K 142G>A SKCM-US 8 88886136 88886136 single base substitution C T missense_variant G22R 64G>A SKCM-US 8 88886163 88886163 single base substitution C T missense_variant D13N 37G>A SKCM-US 8 88886169 88886169 single base substitution C T missense_variant E11K 31G>A STAD-US 8 88885021 88885021 single base substitution G T synonymous_variant S393S 1179C>A STAD-US 8 88885231 88885231 single base substitution G A synonymous_variant N323N 969C>T STAD-US 8 88885305 88885305 single base substitution A C missense_variant L299V 895T>G STAD-US 8 88885339 88885339 single base substitution T C synonymous_variant S287S 861A>G STAD-US 8 88885496 88885496 single base substitution A G missense_variant M235T 704T>C STAD-US 8 88885724 88885724 single base substitution A G missense_variant L159P 476T>C STAD-US 8 88885868 88885868 single base substitution T C missense_variant E111G 332A>G STAD-US 8 88885901 88885901 single base substitution C T missense_variant G100D 299G>A STAD-US 8 88885905 88885905 single base substitution A G missense_variant Y99H 295T>C STAD-US 8 88885921 88885921 single base substitution T G missense_variant E93D 279A>C STAD-US 8 88886059 88886059 single base substitution G A synonymous_variant R47R 141C>T STAD-US 8 88886149 88886149 single base substitution C A missense_variant K17N 51G>T UCEC-US 8 88885088 88885088 single base substitution C T missense_variant R371H 1112G>A UCEC-US 8 88885123 88885123 single base substitution C T synonymous_variant S359S 1077G>A UCEC-US 8 88885184 88885184 single base substitution C A missense_variant R339I 1016G>T UCEC-US 8 88885215 88885215 single base substitution C T missense_variant V329M 985G>A UCEC-US 8 88885279 88885279 single base substitution C T synonymous_variant Q307Q 921G>A UCEC-US 8 88885325 88885325 single base substitution C A missense_variant G292V 875G>T UCEC-US 8 88885469 88885469 single base substitution C T missense_variant R244H 731G>A UCEC-US 8 88885505 88885505 single base substitution A G missense_variant F232S 695T>C UCEC-US 8 88885529 88885529 single base substitution C A missense_variant S224I 671G>T UCEC-US 8 88885544 88885544 single base substitution T C missense_variant Q219R 656A>G UCEC-US 8 88885717 88885717 single base substitution C T synonymous_variant A161A 483G>A UCEC-US 8 88885797 88885797 single base substitution G A synonymous_variant L135L 403C>T UCEC-US 8 88885892 88885892 single base substitution G T missense_variant T103N 308C>A UCEC-US 8 88885963 88885963 single base substitution C T synonymous_variant A79A 237G>A UCEC-US 8 88885964 88885964 single base substitution G A missense_variant A79V 236C>T UCEC-US 8 88885973 88885973 single base substitution C T missense_variant R76H 227G>A UCEC-US 8 88886060 88886060 single base substitution C T missense_variant R47H 140G>A

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand ESO-1059 COSM1249741 c.96C>A p.N32K Substitution - Missense 8:87873876-87873876 - TCGA-FS-A4F0-06 COSM3651600 c.419C>T p.S140F Substitution - Missense 8:87873553-87873553 - LUAD-NYU1096 COSM369197 c.1031G>A p.R344H Substitution - Missense 8:87872941-87872941 - YUCROFT COSM1700322 c.1058C>T p.P353L Substitution - Missense 8:87872914-87872914 - S02403 COSM5700591 c.547C>A p.P183T Substitution - Missense 8:87873425-87873425 - CSCC-31-T COSM1102275 c.237G>A p.A79A Substitution - coding silent 8:87873735-87873735 - 8070208 COSM4388449 c.184C>T p.H62Y Substitution - Missense 8:87873788-87873788 - LUAD-S01357 COSM387910 c.907A>T p.K303* Substitution - Nonsense 8:87873065-87873065 - YUNEXUS COSM5409936 c.996G>A p.V332V Substitution - coding silent 8:87872976-87872976 - CSCC-11-T COSM4463606 c.129C>T p.C43C Substitution - coding silent 8:87873843-87873843 - CHC1035T COSM250775 c.31G>T p.E11* Substitution - Nonsense 8:87873941-87873941 - LS180 COSM2790013 c.703A>G p.M235V Substitution - Missense 8:87873269-87873269 - CSCC-27-T COSM4460755 c.1178C>T p.S393F Substitution - Missense 8:87872794-87872794 - CSCC-44-T COSM4504230 c.659C>T p.S220L Substitution - Missense 8:87873313-87873313 - TCGA-AD-5900-01 COSM197945 c.760C>T p.R254C Substitution - Missense 8:87873212-87873212 - PCSI_0069_Pa_X COSM3382331 c.601A>C p.S201R Substitution - Missense 8:87873371-87873371 - LUAD-U6SJ7 COSM400308 c.299G>T p.G100V Substitution - Missense 8:87873673-87873673 - tumor_4128852 COSM5948310 c.615T>A p.S205S Substitution - coding silent 8:87873357-87873357 - TCGA-FW-A3R5-06 COSM3925685 c.142G>A p.E48K Substitution - Missense 8:87873830-87873830 - S00943 COSM316513 c.402A>G p.S134S Substitution - coding silent 8:87873570-87873570 - TCGA-AD-6964-01 COSM197942 c.1157G>A p.R386Q Substitution - Missense 8:87872815-87872815 - XHDG20 COSM4768840 c.710C>A p.P237H Substitution - Missense 8:87873262-87873262 - HCC3T COSM1624245 c.925G>A p.E309K Substitution - Missense 8:87873047-87873047 - P09-1580 COSM243965 c.379G>A p.V127M Substitution - Missense 8:87873593-87873593 - 35M COSM5580778 c.276C>T p.V92V Substitution - coding silent 8:87873696-87873696 - TCGA-13-1504-01 COSM70400 c.448G>C p.A150P Substitution - Missense 8:87873524-87873524 - Pat_36_B COSM4676371 c.347C>T p.P116L Substitution - Missense 8:87873625-87873625 - T3038 COSM4676372 c.265G>A p.V89M Substitution - Missense 8:87873707-87873707 - HCT8 COSM1102278 c.140G>A p.R47H Substitution - Missense 8:87873832-87873832 - ESCC_78 COSM5635521 c.960G>A p.V320V Substitution - coding silent 8:87873012-87873012 - TCGA-A5-A0GP-01 COSM1102275 c.237G>A p.A79A Substitution - coding silent 8:87873735-87873735 - LUAD-CHTN-MAD06-00668 COSM360452 c.1028T>C p.L343P Substitution - Missense 8:87872944-87872944 - TCGA-AA-A02W-01 COSM287576 c.994G>A p.V332M Substitution - Missense 8:87872978-87872978 - sysucc-311T COSM5467511 c.484T>C p.S162P Substitution - Missense 8:87873488-87873488 - S00946 COSM316514 c.1094G>A p.S365N Substitution - Missense 8:87872878-87872878 - 226 COSM4425921 c.945C>T p.S315S Substitution - coding silent 8:87873027-87873027 - TCGA-GN-A266-06 COSM1624245 c.925G>A p.E309K Substitution - Missense 8:87873047-87873047 - ESOCB11T COSM369197 c.1031G>A p.R344H Substitution - Missense 8:87872941-87872941 - 1255_T COSM3952019 c.411C>A p.H137Q Substitution - Missense 8:87873561-87873561 - TCGA-FW-A3R5-06 COSM1624245 c.925G>A p.E309K Substitution - Missense 8:87873047-87873047 - ESO-0459 COSM1249740 c.1085A>G p.D362G Substitution - Missense 8:87872887-87872887 - cSCCP6 COSM136668 c.1045C>T p.L349F Substitution - Missense 8:87872927-87872927 - HT115 COSM1458521 c.148C>T p.R50C Substitution - Missense 8:87873824-87873824 - TCGA-34-5240-01 COSM751517 c.458C>A p.P153Q Substitution - Missense 8:87873514-87873514 - PCSI_0125_Pa_P COSM3382329 c.912T>A p.C304* Substitution - Nonsense 8:87873060-87873060 - TCGA-B5-A0JY-01 COSM1102266 c.1016G>T p.R339I Substitution - Missense 8:87872956-87872956 - Gp5D COSM2790044 c.21A>G p.R7R Substitution - coding silent 8:87873951-87873951 - Pat_66_A COSM5875081 c.323C>T p.T108M Substitution - Missense 8:87873649-87873649 - ESCC_160 COSM5647470 c.1135C>T p.P379S Substitution - Missense 8:87872837-87872837 - TCGA-ER-A19H-06 COSM3651597 c.1029C>T p.L343L Substitution - coding silent 8:87872943-87872943 - TCGA-AA-A02O-01 COSM300863 c.846C>A p.G282G Substitution - coding silent 8:87873126-87873126 - TCGA-EE-A29L-06 COSM3651609 c.168G>A p.R56R Substitution - coding silent 8:87873804-87873804 - TCGA-F1-6177-01 COSM3901921 c.295T>C p.Y99H Substitution - Missense 8:87873677-87873677 - TCGA-34-5239-01 COSM751522 c.738G>T p.G246G Substitution - coding silent 8:87873234-87873234 - TCGA-BF-A1PU-01 COSM751523 c.852C>T p.F284F Substitution - coding silent 8:87873120-87873120 - TCGA-HU-A4H6-01 COSM3901923 c.141C>T p.R47R Substitution - coding silent 8:87873831-87873831 - TCGA-66-2787-01 COSM751515 c.424C>T p.L142F Substitution - Missense 8:87873548-87873548 - TCGA-EE-A29M-06 COSM3651591 c.1125C>T p.F375F Substitution - coding silent 8:87872847-87872847 - TCGA-A2-A0T5-01 COSM3835096 c.1060T>C p.S354P Substitution - Missense 8:87872912-87872912 - PT48 COSM3651594 c.1084G>A p.D362N Substitution - Missense 8:87872888-87872888 - TCGA-FD-A3SS-01 COSM3779403 c.587C>T p.A196V Substitution - Missense 8:87873385-87873385 - TCGA-DU-5852-01 COSM3929658 c.1000C>G p.Q334E Substitution - Missense 8:87872972-87872972 - ESCC_125 COSM2790027 c.348G>A p.P116P Substitution - coding silent 8:87873624-87873624 - TCGA-ER-A195-06 COSM1700324 c.386C>T p.S129F Substitution - Missense 8:87873586-87873586 - TCGA-33-4586-01 COSM751520 c.645G>C p.T215T Substitution - coding silent 8:87873327-87873327 - BD124T COSM5492401 c.363C>T p.Y121Y Substitution - coding silent 8:87873609-87873609 - TCGA-AX-A0J0-01 COSM1102278 c.140G>A p.R47H Substitution - Missense 8:87873832-87873832 - TCGA-F4-6856-01 COSM294295 c.514C>T p.R172C Substitution - Missense 8:87873458-87873458 - PT35 COSM3651601 c.409C>T p.H137Y Substitution - Missense 8:87873563-87873563 - TCGA-H4-A2HQ-01 COSM1314249 c.1020C>T p.I340I Substitution - coding silent 8:87872952-87872952 - 40M COSM5409936 c.996G>A p.V332V Substitution - coding silent 8:87872976-87872976 - TCGA-AY-6197-01 COSM1458521 c.148C>T p.R50C Substitution - Missense 8:87873824-87873824 - 35M COSM5580777 c.167G>A p.R56K Substitution - Missense 8:87873805-87873805 - 7285 COSM5616026 c.878C>G p.T293S Substitution - Missense 8:87873094-87873094 - TCGA-13-0913-01 COSM1330883 c.1delA p.? Unknown TCGA-FS-A1ZB-06 COSM3651594 c.1084G>A p.D362N Substitution - Missense 8:87872888-87872888 - TCGA-A5-A0GH-01 COSM1102265 c.1077G>A p.S359S Substitution - coding silent 8:87872895-87872895 - HCT15 COSM1673997 c.979G>A p.G327R Substitution - Missense 8:87872993-87872993 - TCGA-AP-A0LM-01 COSM1102276 c.236C>T p.A79V Substitution - Missense 8:87873736-87873736 - sysucc-1397T COSM5475201 c.526A>G p.M176V Substitution - Missense 8:87873446-87873446 - SJRHB056 COSM3737771 c.736G>T p.G246W Substitution - Missense 8:87873236-87873236 - Au9 COSM176945 c.117C>T p.F39F Substitution - coding silent 8:87873855-87873855 - TCGA-FS-A1Z3-06 COSM3651610 c.37G>A p.D13N Substitution - Missense 8:87873935-87873935 - ESCC-F20 COSM5047319 c.434G>A p.C145Y Substitution - Missense 8:87873538-87873538 - CHOL53 COSM1743146 c.919C>A p.Q307K Substitution - Missense 8:87873053-87873053 - TCGA-18-3414-01 COSM316516 c.439G>T p.V147L Substitution - Missense 8:87873533-87873533 - 61 COSM5738381 c.899G>T p.R300M Substitution - Missense 8:87873073-87873073 - PDA_063 COSM197946 c.337C>T p.R113W Substitution - Missense 8:87873635-87873635 - 194 COSM145300 c.637G>A p.V213M Substitution - Missense 8:87873335-87873335 - ICGC_MB69 COSM3765413 c.149G>A p.R50H Substitution - Missense 8:87873823-87873823 - PT37 COSM4820372 c.1156C>T p.R386W Substitution - Missense 8:87872816-87872816 - CHC302T COSM250774 c.316G>T p.G106C Substitution - Missense 8:87873656-87873656 - TCGA-DD-A1EK-01 COSM4934417 c.887T>C p.L296P Substitution - Missense 8:87873085-87873085 - T2197 COSM3835097 c.297C>T p.Y99Y Substitution - coding silent 8:87873675-87873675 - CSCC-35-T COSM4425921 c.945C>T p.S315S Substitution - coding silent 8:87873027-87873027 - YUSMI COSM4509373 c.804C>T p.S268S Substitution - coding silent 8:87873168-87873168 - cSCCP1 COSM134252 c.970G>A p.E324K Substitution - Missense 8:87873002-87873002 - Pat_15_A COSM5875082 c.175G>A p.V59I Substitution - Missense 8:87873797-87873797 - YUROC COSM3925685 c.142G>A p.E48K Substitution - Missense 8:87873830-87873830 - TCGA-EE-A2GR-06 COSM3651599 c.420C>T p.S140S Substitution - coding silent 8:87873552-87873552 - TCGA-D9-A6EC-06 COSM4400551 c.1015A>G p.R339G Substitution - Missense 8:87872957-87872957 - S01366 COSM316515 c.329C>A p.P110H Substitution - Missense 8:87873643-87873643 - LP6005500-DNA_C03 COSM5033248 c.1186T>A p.*396K Nonstop extension 8:87872786-87872786 - LUAD-S01482 COSM347512 c.501C>A p.S167R Substitution - Missense 8:87873471-87873471 - TCGA-AA-A00N-01 COSM274739 c.293A>G p.K98R Substitution - Missense 8:87873679-87873679 - ESCC-128T COSM3942805 c.314G>A p.R105Q Substitution - Missense 8:87873658-87873658 - TCGA-D5-6930-01 COSM1458513 c.999C>T p.G333G Substitution - coding silent 8:87872973-87872973 - CSCC-20-T COSM4368789 c.197C>T p.P66L Substitution - Missense 8:87873775-87873775 - S01022 COSM5666210 c.177C>T p.V59V Substitution - coding silent 8:87873795-87873795 - TCGA-ER-A194-01 COSM3651607 c.196C>T p.P66S Substitution - Missense 8:87873776-87873776 - ESO-043 COSM1132682 c.1127G>A p.R376Q Substitution - Missense 8:87872845-87872845 - TCGA-D1-A16F-01 COSM1102273 c.403C>T p.L135L Substitution - coding silent 8:87873569-87873569 - PDA_049 COSM5000634 c.1057C>A p.P353T Substitution - Missense 8:87872915-87872915 - TCGA-37-5819-01 COSM751525 c.992C>T p.A331V Substitution - Missense 8:87872980-87872980 - 587360 COSM1203066 c.1072G>A p.A358T Substitution - Missense 8:87872900-87872900 - LUAD-U6SJ7 COSM400309 c.17C>A p.P6Q Substitution - Missense 8:87873955-87873955 - TCGA-EK-A2RA-01 COSM1458515 c.761G>A p.R254H Substitution - Missense 8:87873211-87873211 - ESCC_BICR_045T COSM5441798 c.698C>A p.A233E Substitution - Missense 8:87873274-87873274 - SJDES001-R COSM4588240 c.718T>C p.F240L Substitution - Missense 8:87873254-87873254 - S02350 COSM5694901 c.102delA p.G35fs*11 Deletion - Frameshift 8:87873870-87873870 - CSCC-27-T COSM4496559 c.477C>T p.L159L Substitution - coding silent 8:87873495-87873495 - TCGA-BR-6802-01 COSM3901916 c.861A>G p.S287S Substitution - coding silent 8:87873111-87873111 - CSCC-5-T COSM176945 c.117C>T p.F39F Substitution - coding silent 8:87873855-87873855 - TCGA-24-1845-01 COSM296085 c.1083C>T p.N361N Substitution - coding silent 8:87872889-87872889 - SM-4AX84 COSM4412610 c.446T>C p.L149P Substitution - Missense 8:87873526-87873526 - TCGA-D3-A5GO-06 COSM3651608 c.193G>A p.D65N Substitution - Missense 8:87873779-87873779 - ESCC-178T COSM3942806 c.271C>T p.Q91* Substitution - Nonsense 8:87873701-87873701 - TCGA-66-2767-01 COSM751519 c.586G>T p.A196S Substitution - Missense 8:87873386-87873386 - TCGA-G4-6302-01 COSM3699199 c.328C>A p.P110T Substitution - Missense 8:87873644-87873644 - 8057473 COSM2790027 c.348G>A p.P116P Substitution - coding silent 8:87873624-87873624 - TCGA-HC-7077-01 COSM1203066 c.1072G>A p.A358T Substitution - Missense 8:87872900-87872900 - LUAD-LC15C COSM342044 c.39C>A p.D13E Substitution - Missense 8:87873933-87873933 - PCSI_0083_Pa_P COSM3382330 c.843T>C p.D281D Substitution - coding silent 8:87873129-87873129 - H1672 COSM316512 c.1026C>A p.S342R Substitution - Missense 8:87872946-87872946 - 454 COSM606564 c.414G>T p.L138F Substitution - Missense 8:87873558-87873558 - TCGA-66-2744-01 COSM197946 c.337C>T p.R113W Substitution - Missense 8:87873635-87873635 - 951_T COSM3952020 c.193G>T p.D65Y Substitution - Missense 8:87873779-87873779 - TCGA-F4-6460-01 COSM1458519 c.481G>C p.A161P Substitution - Missense 8:87873491-87873491 - TCGA-42-2590-01 COSM300864 c.483G>A p.A161A Substitution - coding silent 8:87873489-87873489 - TCGA-CI-6622-01 COSM1569520 c.892G>T p.D298Y Substitution - Missense 8:87873080-87873080 - AOCS-134-3-9 COSM4151923 c.302T>A p.I101N Substitution - Missense 8:87873670-87873670 - TCGA-29-1775-01 COSM1330884 c.59G>A p.R20K Substitution - Missense 8:87873913-87873913 - SJDOSTEOS010 COSM1102277 c.227G>A p.R76H Substitution - Missense 8:87873745-87873745 - T3024 COSM4676368 c.888G>A p.L296L Substitution - coding silent 8:87873084-87873084 - TCGA-D5-6928-01 COSM1458518 c.515G>A p.R172H Substitution - Missense 8:87873457-87873457 - PD4084a COSM160338 c.482C>T p.A161V Substitution - Missense 8:87873490-87873490 - TCGA-CU-A3QU-01 COSM3779404 c.114A>T p.R38S Substitution - Missense 8:87873858-87873858 - PT52 COSM5939802 c.536G>A p.S179N Substitution - Missense 8:87873436-87873436 - PR-01-2554 COSM242510 c.226C>T p.R76C Substitution - Missense 8:87873746-87873746 - TCGA-EJ-7797-01 COSM1102264 c.1112G>A p.R371H Substitution - Missense 8:87872860-87872860 - TCGA-FR-A3YN-06 COSM3651602 c.398C>T p.A133V Substitution - Missense 8:87873574-87873574 - TCGA-AP-A0LD-01 COSM300864 c.483G>A p.A161A Substitution - coding silent 8:87873489-87873489 - CSCC-44-T COSM3651609 c.168G>A p.R56R Substitution - coding silent 8:87873804-87873804 - T3079 COSM197946 c.337C>T p.R113W Substitution - Missense 8:87873635-87873635 - CHC155T COSM3669926 c.248C>A p.T83N Substitution - Missense 8:87873724-87873724 - 8044436 COSM3395442 c.136G>T p.A46S Substitution - Missense 8:87873836-87873836 - BD124T COSM5492400 c.623T>C p.V208A Substitution - Missense 8:87873349-87873349 - Patient2 COSM1166867 c.545T>C p.I182T Substitution - Missense 8:87873427-87873427 - ESCC_28 COSM5627396 c.137C>T p.A46V Substitution - Missense 8:87873835-87873835 - PDA_004 COSM273637 c.518G>A p.R173Q Substitution - Missense 8:87873454-87873454 - CSCC-45-T COSM1458516 c.709C>T p.P237S Substitution - Missense 8:87873263-87873263 - ESCC-002T COSM3942807 c.59G>C p.R20T Substitution - Missense 8:87873913-87873913 - TCGA-AA-A010-01 COSM176945 c.117C>T p.F39F Substitution - coding silent 8:87873855-87873855 - SW837 COSM1624245 c.925G>A p.E309K Substitution - Missense 8:87873047-87873047 - 40M COSM5584975 c.546C>T p.I182I Substitution - coding silent 8:87873426-87873426 - ESO-H01 COSM1102276 c.236C>T p.A79V Substitution - Missense 8:87873736-87873736 - 587376 COSM256736 c.386C>A p.S129Y Substitution - Missense 8:87873586-87873586 - T298 COSM4676369 c.596C>G p.S199C Substitution - Missense 8:87873376-87873376 - TCGA-BR-4361-01 COSM3901918 c.476T>C p.L159P Substitution - Missense 8:87873496-87873496 - TCGA-DK-A1AC-01 COSM1314250 c.885G>C p.K295N Substitution - Missense 8:87873087-87873087 - T2991 COSM4676371 c.347C>T p.P116L Substitution - Missense 8:87873625-87873625 - TCGA-66-2766-01 COSM751521 c.689A>G p.Q230R Substitution - Missense 8:87873283-87873283 - CSCC-2-T COSM4563988 c.99G>T p.Q33H Substitution - Missense 8:87873873-87873873 - ME016T COSM224963 c.376A>T p.K126* Substitution - Nonsense 8:87873596-87873596 - TCGA-EK-A2RB-01 COSM4820034 c.547C>T p.P183S Substitution - Missense 8:87873425-87873425 - TCGA-F4-6461-01 COSM3763439 c.143A>G p.E48G Substitution - Missense 8:87873829-87873829 - TCGA-BH-A18G-01 COSM3835097 c.297C>T p.Y99Y Substitution - coding silent 8:87873675-87873675 - TCGA-AA-3821-01 COSM294295 c.514C>T p.R172C Substitution - Missense 8:87873458-87873458 - KM12 COSM1673998 c.86T>C p.L29P Substitution - Missense 8:87873886-87873886 - CSCC-15-T COSM4521568 c.1118G>A p.G373E Substitution - Missense 8:87872854-87872854 - TCGA-B5-A11N-01 COSM1102271 c.671G>T p.S224I Substitution - Missense 8:87873301-87873301 - CRC-19T COSM5482223 c.1006T>C p.C336R Substitution - Missense 8:87872966-87872966 - TCGA-AG-3892-01 COSM256736 c.386C>A p.S129Y Substitution - Missense 8:87873586-87873586 - LAU149 COSM134252 c.970G>A p.E324K Substitution - Missense 8:87873002-87873002 - T23 COSM5618147 c.101T>A p.L34Q Substitution - Missense 8:87873871-87873871 - 8047913 COSM1102278 c.140G>A p.R47H Substitution - Missense 8:87873832-87873832 - sysucc-704T COSM5766528 c.338G>A p.R113Q Substitution - Missense 8:87873634-87873634 - 8014964 COSM3395441 c.522T>A p.P174P Substitution - coding silent 8:87873450-87873450 - TCGA-DK-A3IU-01 COSM3779402 c.970G>T p.E324* Substitution - Nonsense 8:87873002-87873002 - CSCC-11-T COSM4562500 c.928G>C p.G310R Substitution - Missense 8:87873044-87873044 - TCGA-E2-A10C-01 COSM454928 c.113G>A p.R38K Substitution - Missense 8:87873859-87873859 - sysucc-1237T COSM454926 c.958G>A p.V320M Substitution - Missense 8:87873014-87873014 - TCGA-22-5482-01 COSM751512 c.103G>T p.G35C Substitution - Missense 8:87873869-87873869 - CRC-02T COSM5455692 c.750C>T p.G250G Substitution - coding silent 8:87873222-87873222 - HCT-15 COSM1673997 c.979G>A p.G327R Substitution - Missense 8:87872993-87872993 - PD9579a COSM2789992 c.1158G>T p.R386R Substitution - coding silent 8:87872814-87872814 - CSCC-29-T COSM751523 c.852C>T p.F284F Substitution - coding silent 8:87873120-87873120 - TCGA-EE-A2A1-06 COSM3651604 c.329C>T p.P110L Substitution - Missense 8:87873643-87873643 - CSCC-27-T COSM4548909 c.45G>A p.Q15Q Substitution - coding silent 8:87873927-87873927 - TCGA-D1-A101-01 COSM294295 c.514C>T p.R172C Substitution - Missense 8:87873458-87873458 - ATL015 COSM1203066 c.1072G>A p.A358T Substitution - Missense 8:87872900-87872900 - TCGA-18-3414-01 COSM751513 c.233T>C p.L78P Substitution - Missense 8:87873739-87873739 - CSCC-29-T COSM4568047 c.992_993CC>TT p.A331V Substitution - Missense 8:87872979-87872980 - T2197 COSM294295 c.514C>T p.R172C Substitution - Missense 8:87873458-87873458 - TCGA-EE-A29E-06 COSM3651592 c.1119G>A p.G373G Substitution - coding silent 8:87872853-87872853 - T1154 COSM176945 c.117C>T p.F39F Substitution - coding silent 8:87873855-87873855 - TCGA-AA-3866-01 COSM296085 c.1083C>T p.N361N Substitution - coding silent 8:87872889-87872889 - TCGA-CA-6718-01 COSM256736 c.386C>A p.S129Y Substitution - Missense 8:87873586-87873586 - TCGA-BS-A0UV-01 COSM1102272 c.656A>G p.Q219R Substitution - Missense 8:87873316-87873316 - CHC302T COSM250774 c.316G>T p.G106C Substitution - Missense 8:87873656-87873656 - LUAD-S00488 COSM404093 c.110T>A p.L37H Substitution - Missense 8:87873862-87873862 - TCGA-BP-4988-01 COSM486735 c.468C>T p.A156A Substitution - coding silent 8:87873504-87873504 - CSCC-55-T COSM4522426 c.1162G>A p.D388N Substitution - Missense 8:87872810-87872810 - TCGA-D1-A17B-01 COSM1102264 c.1112G>A p.R371H Substitution - Missense 8:87872860-87872860 - LUAD_E00522 COSM353609 c.378G>A p.K126K Substitution - coding silent 8:87873594-87873594 - CSCC-31-T COSM3651608 c.193G>A p.D65N Substitution - Missense 8:87873779-87873779 - CSCC-4-T COSM134252 c.970G>A p.E324K Substitution - Missense 8:87873002-87873002 - TCGA-BS-A0TC-01 COSM1102269 c.731G>A p.R244H Substitution - Missense 8:87873241-87873241 - ESCC_BICR_008T COSM5428990 c.681C>G p.V227V Substitution - coding silent 8:87873291-87873291 - HCC81 COSM1624246 c.460A>G p.S154G Substitution - Missense 8:87873512-87873512 - 2292383 COSM242510 c.226C>T p.R76C Substitution - Missense 8:87873746-87873746 - CSCC-11-T COSM3925683 c.984C>T p.V328V Substitution - coding silent 8:87872988-87872988 - TCGA-AP-A059-01 COSM1102268 c.875G>T p.G292V Substitution - Missense 8:87873097-87873097 - 0124_CRUK_PC_0124_T1_DNA COSM5420991 c.180G>C p.Q60H Substitution - Missense 8:87873792-87873792 - TCGA-60-2719-01 COSM751526 c.1084G>T p.D362Y Substitution - Missense 8:87872888-87872888 - TCGA-76-4934-01 COSM3413152 c.154A>T p.S52C Substitution - Missense 8:87873818-87873818 - TCGA-EE-A29V-06 COSM3651606 c.201C>T p.S67S Substitution - coding silent 8:87873771-87873771 - Pat_41_B COSM5875080 c.891G>A p.W297* Substitution - Nonsense 8:87873081-87873081 - TCGA-G4-6298-01 COSM3699198 c.505C>T p.P169S Substitution - Missense 8:87873467-87873467 - TCGA-FS-A1Z3-06 COSM3651593 c.1091C>T p.P364L Substitution - Missense 8:87872881-87872881 - TCGA-DY-A0XA-01 COSM197943 c.1013C>T p.T338M Substitution - Missense 8:87872959-87872959 - TCGA-FW-A3R5-06 COSM3925683 c.984C>T p.V328V Substitution - coding silent 8:87872988-87872988 - TCGA-AA-A02O-01 COSM300864 c.483G>A p.A161A Substitution - coding silent 8:87873489-87873489 - Pat_41_B COSM5875079 c.1003G>A p.D335N Substitution - Missense 8:87872969-87872969 - S01366 COSM316515 c.329C>A p.P110H Substitution - Missense 8:87873643-87873643 - SC_9099 COSM5554795 c.524G>A p.G175D Substitution - Missense 8:87873448-87873448 - TCGA-BH-A0HA-01 COSM197945 c.760C>T p.R254C Substitution - Missense 8:87873212-87873212 - HCC059T COSM5809843 c.844G>T p.G282C Substitution - Missense 8:87873128-87873128 - HCC1 COSM1330885 c.111C>T p.L37L Substitution - coding silent 8:87873861-87873861 - S01453 COSM316516 c.439G>T p.V147L Substitution - Missense 8:87873533-87873533 - PD23558a COSM5777615 c.217C>T p.R73* Substitution - Nonsense 8:87873755-87873755 - CHC1035T COSM250775 c.31G>T p.E11* Substitution - Nonsense 8:87873941-87873941 - BD236T COSM3651595 c.1061C>T p.S354F Substitution - Missense 8:87872911-87872911 - TCGA-EE-A29E-06 COSM3651603 c.385T>A p.S129T Substitution - Missense 8:87873587-87873587 - 2334192 COSM316512 c.1026C>A p.S342R Substitution - Missense 8:87872946-87872946 - TCGA-EI-6883-01 COSM1102269 c.731G>A p.R244H Substitution - Missense 8:87873241-87873241 - TCGA-D5-6931-01 COSM1102275 c.237G>A p.A79A Substitution - coding silent 8:87873735-87873735 - CSCC-35-T COSM4458969 c.1106C>T p.S369F Substitution - Missense 8:87872866-87872866 - LUAD-B01811 COSM334880 c.1165C>A p.L389I Substitution - Missense 8:87872807-87872807 - BD72T COSM454926 c.958G>A p.V320M Substitution - Missense 8:87873014-87873014 - TCGA-22-1016-01 COSM751514 c.237G>T p.A79A Substitution - coding silent 8:87873735-87873735 - TCGA-F5-6814-01 COSM3432598 c.644C>T p.T215M Substitution - Missense 8:87873328-87873328 - TCGA-EB-A3Y7-01 COSM3651595 c.1061C>T p.S354F Substitution - Missense 8:87872911-87872911 - AOCS-084-1-X COSM4151924 c.118G>A p.A40T Substitution - Missense 8:87873854-87873854 - TCGA-C8-A131-01 COSM454927 c.541C>A p.Q181K Substitution - Missense 8:87873431-87873431 - TCGA-EB-A431-01 COSM3651611 c.31G>A p.E11K Substitution - Missense 8:87873941-87873941 - YUOMEGA COSM5409937 c.95A>G p.N32S Substitution - Missense 8:87873877-87873877 - TCGA-29-1702-01 COSM1330885 c.111C>T p.L37L Substitution - coding silent 8:87873861-87873861 - T1232 COSM4676370 c.534C>T p.C178C Substitution - coding silent 8:87873438-87873438 - CSCC-19-T COSM4510351 c.834C>T p.I278I Substitution - coding silent 8:87873138-87873138 - HCC4006 COSM1685185 c.101T>C p.L34P Substitution - Missense 8:87873871-87873871 - S01022 COSM5666209 c.451G>T p.D151Y Substitution - Missense 8:87873521-87873521 - Au1 COSM1553490 c.754G>A p.D252N Substitution - Missense 8:87873218-87873218 - 2 COSM1458521 c.148C>T p.R50C Substitution - Missense 8:87873824-87873824 - TCGA-EE-A3JD-06 COSM4395394 c.375G>A p.R125R Substitution - coding silent 8:87873597-87873597 - CPCG0042-F1 COSM3396737 c.139C>T p.R47C Substitution - Missense 8:87873833-87873833 - TCGA-AX-A05Z-01 COSM1102267 c.921G>A p.Q307Q Substitution - coding silent 8:87873051-87873051 - TCGA-EE-A29M-06 COSM141241 c.373C>T p.R125W Substitution - Missense 8:87873599-87873599 - TP_2020 COSM5559162 c.837C>A p.L279L Substitution - coding silent 8:87873135-87873135 - ESO-250 COSM1102276 c.236C>T p.A79V Substitution - Missense 8:87873736-87873736 - ESCC-069T COSM3942804 c.754G>T p.D252Y Substitution - Missense 8:87873218-87873218 - TCGA-D5-6898-01 COSM1458514 c.780C>G p.S260R Substitution - Missense 8:87873192-87873192 - CSCC-30-T COSM4509373 c.804C>T p.S268S Substitution - coding silent 8:87873168-87873168 - TCGA-FC-A6HD-01 COSM3675177 c.160A>G p.M54V Substitution - Missense 8:87873812-87873812 - ESO-007 COSM1249739 c.653A>T p.Q218L Substitution - Missense 8:87873319-87873319 - S02237 COSM5676636 c.218G>C p.R73P Substitution - Missense 8:87873754-87873754 - TCGA-AA-3510-01 COSM1458515 c.761G>A p.R254H Substitution - Missense 8:87873211-87873211 - CSCC-40-T COSM4510973 c.853C>T p.L285L Substitution - coding silent 8:87873119-87873119 - HCC3 COSM1624245 c.925G>A p.E309K Substitution - Missense 8:87873047-87873047 - TCGA-D3-A51R-06 COSM3651602 c.398C>T p.A133V Substitution - Missense 8:87873574-87873574 - TCGA-CU-A0YN-01 COSM422045 c.988G>T p.A330S Substitution - Missense 8:87872984-87872984 - 587220 COSM1203064 c.214G>A p.D72N Substitution - Missense 8:87873758-87873758 - 392 COSM4428349 c.209C>T p.A70V Substitution - Missense 8:87873763-87873763 - TCGA-EB-A3Y6-01 COSM3651596 c.1037G>A p.G346D Substitution - Missense 8:87872935-87872935 - TCGA-BF-A3DM-01 COSM3925686 c.64G>A p.G22R Substitution - Missense 8:87873908-87873908 - TCGA-BG-A0MO-01 COSM1102274 c.308C>A p.T103N Substitution - Missense 8:87873664-87873664 - C135 COSM4618787 c.1071C>A p.P357P Substitution - coding silent 8:87872901-87872901 - CPCG_0042_Pr_P_F0 COSM3396737 c.139C>T p.R47C Substitution - Missense 8:87873833-87873833 - 8031668 COSM1102269 c.731G>A p.R244H Substitution - Missense 8:87873241-87873241 - HCC1T COSM1330885 c.111C>T p.L37L Substitution - coding silent 8:87873861-87873861 - C84 COSM4620258 c.967A>T p.N323Y Substitution - Missense 8:87873005-87873005 - I2L-P8-Tumor-Biopsy COSM5359053 c.373C>A p.R125R Substitution - coding silent 8:87873599-87873599 - C037 COSM1102275 c.237G>A p.A79A Substitution - coding silent 8:87873735-87873735 - TCGA-AA-3492-01 COSM1458512 c.1116C>T p.L372L Substitution - coding silent 8:87872856-87872856 - YUGASP COSM1700323 c.509G>A p.G170E Substitution - Missense 8:87873463-87873463 - 194-01-2TD COSM145300 c.637G>A p.V213M Substitution - Missense 8:87873335-87873335 - PT50 COSM5937340 c.614C>T p.S205F Substitution - Missense 8:87873358-87873358 - CSCC-49-T COSM4438578 c.28G>A p.E10K Substitution - Missense 8:87873944-87873944 - KM12 COSM1673998 c.86T>C p.L29P Substitution - Missense 8:87873886-87873886 - I2L-P8-Tumor-Organoid COSM5359053 c.373C>A p.R125R Substitution - coding silent 8:87873599-87873599 - Pat_37_B COSM3651607 c.196C>T p.P66S Substitution - Missense 8:87873776-87873776 - CH-103-T2 COSM1102275 c.237G>A p.A79A Substitution - coding silent 8:87873735-87873735 - YULAN COSM1203064 c.214G>A p.D72N Substitution - Missense 8:87873758-87873758 - LUAD-FH5PJ COSM394580 c.619C>A p.Q207K Substitution - Missense 8:87873353-87873353 - TCGA-43-6143-01 COSM751518 c.485C>A p.S162* Substitution - Nonsense 8:87873487-87873487 - CSCC-41-T COSM3901920 c.299G>A p.G100D Substitution - Missense 8:87873673-87873673 - BD95T COSM5505604 c.374G>A p.R125Q Substitution - Missense 8:87873598-87873598 - TCGA-F4-6570-01 COSM1458516 c.709C>T p.P237S Substitution - Missense 8:87873263-87873263 - ESO-114 COSM1249742 c.289T>C p.S97P Substitution - Missense 8:87873683-87873683 - LUAD-VUMN6 COSM348140 c.226C>G p.R76G Substitution - Missense 8:87873746-87873746 - ESCC_129 COSM5642000 c.174_175insA p.V59fs*5 Insertion - Frameshift 8:87873797-87873798 - S02255 COSM5680993 c.612G>C p.L204F Substitution - Missense 8:87873360-87873360 - sysucc-1517T COSM454923 c.989C>T p.A330V Substitution - Missense 8:87872983-87872983 - TCGA-D1-A103-01 COSM1102277 c.227G>A p.R76H Substitution - Missense 8:87873745-87873745 - TCGA-18-4083-01 COSM751516 c.429G>T p.L143L Substitution - coding silent 8:87873543-87873543 - 1N44-VS-1T44 COSM4975715 c.51G>A p.K17K Substitution - coding silent 8:87873921-87873921 - TCGA-B5-A0JY-01 COSM1102270 c.695T>C p.F232S Substitution - Missense 8:87873277-87873277 - TCGA-A2-A3XY-01 COSM3835098 c.277G>T p.E93* Substitution - Nonsense 8:87873695-87873695 - 1604875 COSM141241 c.373C>T p.R125W Substitution - Missense 8:87873599-87873599 - CSCC-54-T COSM4455978 c.975A>T p.E325D Substitution - Missense 8:87872997-87872997 - TCGA-76-6282-01 COSM3413153 c.69C>G p.L23L Substitution - coding silent 8:87873903-87873903 - ESCC_BICR_064T COSM4820372 c.1156C>T p.R386W Substitution - Missense 8:87872816-87872816 - SC_9071 COSM3835097 c.297C>T p.Y99Y Substitution - coding silent 8:87873675-87873675 - CHC2103T COSM4952673 c.528G>T p.M176I Substitution - Missense 8:87873444-87873444 - ESCC-D18 COSM4368789 c.197C>T p.P66L Substitution - Missense 8:87873775-87873775 - PT35 COSM5912790 c.89G>A p.R30Q Substitution - Missense 8:87873883-87873883 - TCGA-A2-A0D1-01 COSM454924 c.985G>A p.V329M Substitution - Missense 8:87872987-87872987 - 53M COSM5594486 c.710C>T p.P237L Substitution - Missense 8:87873262-87873262 - ESO-0167 COSM369197 c.1031G>A p.R344H Substitution - Missense 8:87872941-87872941 - PT48 COSM1458516 c.709C>T p.P237S Substitution - Missense 8:87873263-87873263 - 8049749 COSM3395443 c.130C>T p.R44C Substitution - Missense 8:87873842-87873842 - LUAD-F00018 COSM339259 c.425T>G p.L142R Substitution - Missense 8:87873547-87873547 - WSU-HN30 COSM4600559 c.19C>T p.R7* Substitution - Nonsense 8:87873953-87873953 - 587222 COSM1203065 c.1121G>T p.G374V Substitution - Missense 8:87872851-87872851 - TCGA-CD-A4MI-01 COSM3901913 c.1179C>A p.S393S Substitution - coding silent 8:87872793-87872793 - CSCC-37-T COSM4548909 c.45G>A p.Q15Q Substitution - coding silent 8:87873927-87873927 - H442 COSM5044114 c.1036G>A p.G346S Substitution - Missense 8:87872936-87872936 - HX12T COSM1624247 c.161T>C p.M54T Substitution - Missense 8:87873811-87873811 - SC_9007 COSM5569078 c.327C>A p.T109T Substitution - coding silent 8:87873645-87873645 - HCC81T COSM1624246 c.460A>G p.S154G Substitution - Missense 8:87873512-87873512 - TCGA-AA-3994-01 COSM273637 c.518G>A p.R173Q Substitution - Missense 8:87873454-87873454 - TCGA-BS-A0TA-01 COSM141241 c.373C>T p.R125W Substitution - Missense 8:87873599-87873599 - LUAD-E00897 COSM364794 c.406A>T p.N136Y Substitution - Missense 8:87873566-87873566 - TCGA-D7-A4YV-01 COSM3901917 c.704T>C p.M235T Substitution - Missense 8:87873268-87873268 - TCGA-B1-A654-01 COSM4414357 c.331G>C p.E111Q Substitution - Missense 8:87873641-87873641 - Au1 COSM3942805 c.314G>A p.R105Q Substitution - Missense 8:87873658-87873658 - LUAD-B00523 COSM332178 c.1098G>A p.V366V Substitution - coding silent 8:87872874-87872874 - TCGA-DI-A1NN-01 COSM454924 c.985G>A p.V329M Substitution - Missense 8:87872987-87872987 - Pat_15_B COSM5875082 c.175G>A p.V59I Substitution - Missense 8:87873797-87873797 - S01453 COSM316516 c.439G>T p.V147L Substitution - Missense 8:87873533-87873533 - TCGA-EE-A29D-06 COSM3651605 c.324G>A p.T108T Substitution - coding silent 8:87873648-87873648 - TCGA-EE-A3JI-06 COSM3651598 c.966G>C p.V322V Substitution - coding silent 8:87873006-87873006 - RK126_C01 COSM1635898 c.175G>T p.V59F Substitution - Missense 8:87873797-87873797 - TCGA-CG-4465-01 COSM3901915 c.895T>G p.L299V Substitution - Missense 8:87873077-87873077 - TCGA-IN-7806-01 COSM3901914 c.969C>T p.N323N Substitution - coding silent 8:87873003-87873003 - TCGA-BR-A4QL-01 COSM3901924 c.51G>T p.K17N Substitution - Missense 8:87873921-87873921 - PCSI_0473_Pa_P_526 COSM4961541 c.1158G>A p.R386R Substitution - coding silent 8:87872814-87872814 - TCGA-UC-A7PF-01 COSM3651591 c.1125C>T p.F375F Substitution - coding silent 8:87872847-87872847 - S01023 COSM5666817 c.721A>C p.N241H Substitution - Missense 8:87873251-87873251 - CHC2103T COSM4952673 c.528G>T p.M176I Substitution - Missense 8:87873444-87873444 - TCGA-D7-A4Z0-01 COSM3901922 c.279A>C p.E93D Substitution - Missense 8:87873693-87873693 - LUAD-RT-S01699 COSM378534 c.398C>A p.A133D Substitution - Missense 8:87873574-87873574 - LUAD-74TBW COSM355311 c.509G>T p.G170V Substitution - Missense 8:87873463-87873463 - PTC-7C COSM4163109 c.929G>C p.G310A Substitution - Missense 8:87873043-87873043 - PCSI_0083_Pa_X COSM3382330 c.843T>C p.D281D Substitution - coding silent 8:87873129-87873129 - TCGA-EJ-5530-01 COSM1132682 c.1127G>A p.R376Q Substitution - Missense 8:87872845-87872845 - DLD1 COSM1673997 c.979G>A p.G327R Substitution - Missense 8:87872993-87872993 - CSCC-27-T COSM4510028 c.824C>T p.S275F Substitution - Missense 8:87873148-87873148 - TCGA-BR-A4QM-01 COSM3901919 c.332A>G p.E111G Substitution - Missense 8:87873640-87873640 - BD114T COSM5503389 c.16C>T p.P6S Substitution - Missense 8:87873956-87873956 - ESOSCC162T COSM1173431 c.818T>A p.V273E Substitution - Missense 8:87873154-87873154 - 202_T COSM3952018 c.899G>C p.R300T Substitution - Missense 8:87873073-87873073 - CSCC-7-T COSM1203064 c.214G>A p.D72N Substitution - Missense 8:87873758-87873758 - TCGA-A8-A09N-01 COSM454926 c.958G>A p.V320M Substitution - Missense 8:87873014-87873014 - TCGA-A2-A0YK-01 COSM454925 c.980G>A p.G327E Substitution - Missense 8:87872992-87872992 - TCGA-EE-A2MR-06 COSM1624245 c.925G>A p.E309K Substitution - Missense 8:87873047-87873047 - TCGA-EE-A3J8-06 COSM3651601 c.409C>T p.H137Y Substitution - Missense 8:87873563-87873563 - NCI-H460 COSM1673999 c.35C>G p.A12G Substitution - Missense 8:87873937-87873937 - 49M COSM134252 c.970G>A p.E324K Substitution - Missense 8:87873002-87873002 - HCC020T COSM5569078 c.327C>A p.T109T Substitution - coding silent 8:87873645-87873645 - TCGA-EE-A3AE-06 COSM3925684 c.936G>A p.V312V Substitution - coding silent 8:87873036-87873036 - PD24337a COSM5797024 c.867C>A p.D289E Substitution - Missense 8:87873105-87873105 - 2292384 COSM4610277 c.448G>T p.A150S Substitution - Missense 8:87873524-87873524 - RK308_C01 COSM3745679 c.1026C>T p.S342S Substitution - coding silent 8:87872946-87872946 - TCGA-CD-A4MG-01 COSM3901920 c.299G>A p.G100D Substitution - Missense 8:87873673-87873673 - ESCC_127 COSM5641577 c.1122C>A p.G374G Substitution - coding silent 8:87872850-87872850 - CHC155T COSM3669926 c.248C>A p.T83N Substitution - Missense 8:87873724-87873724 - 587284 COSM136668 c.1045C>T p.L349F Substitution - Missense 8:87872927-87872927 - TCGA-EE-A2MR-06 COSM751523 c.852C>T p.F284F Substitution - coding silent 8:87873120-87873120 - TCGA-EK-A2RD-01 COSM4820372 c.1156C>T p.R386W Substitution - Missense 8:87872816-87872816 - YUAKER COSM1700324 c.386C>T p.S129F Substitution - Missense 8:87873586-87873586 - TCGA-18-3409-01 COSM751523 c.852C>T p.F284F Substitution - coding silent 8:87873120-87873120 - 476 COSM4438578 c.28G>A p.E10K Substitution - Missense 8:87873944-87873944 - TCGA-CC-5264-01 COSM4388449 c.184C>T p.H62Y Substitution - Missense 8:87873788-87873788 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.371738 8q21.3

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C Missense p.L299V c.895T>G 8 88885305 STAD A G 3-UTRSNV . c.1185+1096T>C 8 88883919 HC A G Missense p.L78P c.233T>C 8 88885967 LUSC A G Missense p.S97P c.289T>C 8 88885911 ESCA A G Missense p.Y99H c.295T>C 8 88885905 STAD A T Missense p.C255S c.763T>A 8 88885437 LUAD A T Missense p.S268T c.802T>A 8 88885398 STAD A T Nonsense p.C255* c.765T>A 8 88885435 LUAD C A Missense p.A196S c.586G>T 8 88885614 LUSC C A Missense p.A330S c.988G>T 8 88885212 BLCA C A Missense p.A40S c.118G>T 8 88886082 HNSC C A Missense p.D362Y c.1084G>T 8 88885116 LUSC C A Missense p.G259C c.775G>T 8 88885425 LUAD C A Missense p.G35C c.103G>T 8 88886097 LUSC C A Missense p.K17N c.51G>T 8 88886149 HNSC C A Missense p.L138F c.414G>T 8 88885786 LUAD C A Missense p.M1I c.3G>T 8 88886197 LUAD C A Missense p.R344L c.1031G>T 8 88885169 LUAD C A Missense p.R56M c.167G>T 8 88886033 HNSC C A Missense p.V147L c.439G>T 8 88885761 LUSC C A Missense p.V147L c.439G>T 8 88885761 SCLC C A Missense p.V59F c.175G>T 8 88886025 HC C A Nonsense p.E324* c.970G>T 8 88885230 BLCA C A Synonymous p.A79A c.237G>T 8 88885963 LUSC C A Synonymous p.G246G c.738G>T 8 88885462 LUSC C A Synonymous p.L143L c.429G>T 8 88885771 LUSC C A Synonymous p.L78L c.234G>T 8 88885966 LUAD C A Synonymous p.T215T c.645G>T 8 88885555 CM CC TT Missense p.R386Q c.1157_1158delinsAA 8 88885042 CM C G Missense p.A150P c.448G>C 8 88885752 OV C G Missense p.M176I c.528G>C 8 88885672 LUAD C G Missense p.R56S c.168G>C 8 88886032 LUAD C G Missense p.R7P c.20G>C 8 88886180 HNSC C G Synonymous p.L144L c.432G>C 8 88885768 LUAD C G Synonymous p.T215T c.645G>C 8 88885555 LUSC C G Synonymous p.V322V c.966G>C 8 88885234 CM C T 3-UTRSNV . c.1185+26G>A 8 88884989 CM C T Missense p.A358T c.1072G>A 8 88885128 PRAD C T Missense p.D13N c.37G>A 8 88886163 CM C T Missense p.D362N c.1084G>A 8 88885116 CM C T Missense p.G22R c.64G>A 8 88886136 CM C T Missense p.G327E c.980G>A 8 88885220 BRCA C T Missense p.G346S c.1036G>A 8 88885164 STAD C T Missense p.R173Q c.518G>A 8 88885682 COREAD C T Missense p.R244H c.731G>A 8 88885469 UCEC C T Missense p.R344H c.1031G>A 8 88885169 ESCA C T Missense p.R371H c.1112G>A 8 88885088 PRAD C T Missense p.R371H c.1112G>A 8 88885088 UCEC C T Missense p.R376Q c.1127G>A 8 88885073 PRAD C T Missense p.R386Q c.1157G>A 8 88885043 COREAD C T Missense p.R50H c.149G>A 8 88886051 MB C T Missense p.R76H c.227G>A 8 88885973 STAD C T Missense p.S365N c.1094G>A 8 88885106 SCLC C T Missense p.V157M c.469G>A 8 88885731 LUAD C T Missense p.V213M c.637G>A 8 88885563 CLL C T Missense p.V320M c.958G>A 8 88885242 BRCA C T Missense p.V329M c.985G>A 8 88885215 BRCA C T Missense p.V329M c.985G>A 8 88885215 UCEC C T Missense p.V332M c.994G>A 8 88885206 COREAD C T Missense p.V366M c.1096G>A 8 88885104 HNSC C T Synonymous p.A161A c.483G>A 8 88885717 COREAD C T Synonymous p.A161A c.483G>A 8 88885717 HNSC C T Synonymous p.A161A c.483G>A 8 88885717 UCEC C T Synonymous p.A196A c.588G>A 8 88885612 HNSC C T Synonymous p.A79A c.237G>A 8 88885963 UCEC C T Synonymous p.P116P c.348G>A 8 88885852 STAD C T Synonymous p.R125R c.375G>A 8 88885825 CM C T Synonymous p.R56R c.168G>A 8 88886032 CM C T Synonymous p.S359S c.1077G>A 8 88885123 UCEC C T Synonymous p.V312V c.936G>A 8 88885264 CM G A 3-UTRSNV . c.1185+98C>T 8 88884917 CM G A Missense p.A161V c.482C>T 8 88885718 BRCA G A Missense p.A330V c.989C>T 8 88885211 BRCA G A Missense p.A331V c.992C>T 8 88885208 LUSC G A Missense p.H137Y c.409C>T 8 88885791 CM G A Missense p.H269Y c.805C>T 8 88885395 CM G A Missense p.H62Y c.184C>T 8 88886016 HNSC G A Missense p.L142F c.424C>T 8 88885776 LUSC G A Missense p.P110L c.329C>T 8 88885871 CM G A Missense p.P160L c.479C>T 8 88885721 CM G A Missense p.P364L c.1091C>T 8 88885109 CM G A Missense p.P66S c.196C>T 8 88886004 CM G A Missense p.R113W c.337C>T 8 88885863 COREAD G A Missense p.R113W c.337C>T 8 88885863 LUSC G A Missense p.R125W c.373C>T 8 88885827 CM G A Missense p.R50C c.148C>T 8 88886052 LUAD G A Missense p.S129F c.386C>T 8 88885814 CM G A Missense p.T302I c.905C>T 8 88885295 HNSC G A Nonsense p.Q60* c.178C>T 8 88886022 COREAD G A Synonymous p.A156A c.468C>T 8 88885732 RCCC G A Synonymous p.A331A c.993C>T 8 88885207 STAD G A Synonymous p.F284F c.852C>T 8 88885348 CM G A Synonymous p.F36F c.108C>T 8 88886092 CM G A Synonymous p.F375F c.1125C>T 8 88885075 CM G A Synonymous p.I340I c.1020C>T 8 88885180 BLCA G A Synonymous p.L135L c.403C>T 8 88885797 UCEC G A Synonymous p.L343L c.1029C>T 8 88885171 CM G A Synonymous p.N361N c.1083C>T 8 88885117 COREAD G A Synonymous p.S140S c.420C>T 8 88885780 CM G A Synonymous p.S67S c.201C>T 8 88885999 CM G A Synonymous p.Y394Y c.1182C>T 8 88885018 HNSC G C Missense p.Q334E c.1000C>G 8 88885200 LGG G C Missense p.T293S c.878C>G 8 88885322 NSCLC G C Synonymous p.L23L c.69C>G 8 88886131 GBM G C Synonymous p.P357P c.1071C>G 8 88885129 LUAD G - Frameshift p.F249Lfs*25 c.744delC 8 88885456 LUAD GG AA Missense p.L372F c.1113_1114delinsTT 8 88885086 CM GG AA Missense p.Q60* c.177_178delinsTT 8 88886022 CM G T Missense p.H117Q c.351C>A 8 88885849 STAD G T Missense p.H195Q c.585C>A 8 88885615 LUAD G T Missense p.L135M c.403C>A 8 88885797 LUAD G T Missense p.L177I c.529C>A 8 88885671 LUAD G T Missense p.N32K c.96C>A 8 88886104 ESCA G T Missense p.P110H c.329C>A 8 88885871 SCLC G T Missense p.P153Q c.458C>A 8 88885742 LUSC G T Missense p.Q181K c.541C>A 8 88885659 BRCA G T Missense p.Q334K c.1000C>A 8 88885200 LUAD G T Missense p.R50S c.148C>A 8 88886052 HNSC G T Missense p.S342R c.1026C>A 8 88885174 SCLC G T Missense p.S369Y c.1106C>A 8 88885094 HNSC G T Missense p.T103N c.308C>A 8 88885892 UCEC G T Nonsense p.S162* c.485C>A 8 88885715 LUSC G T Nonsense p.Y115* c.345C>A 8 88885855 LUAD G T Synonymous p.G282G c.846C>A 8 88885354 COREAD G T Synonymous p.L159L c.477C>A 8 88885723 LUAD - T 3-UTRInsertion . c.1185+842dupA 8 88884173 HC T A 3-UTRSNV . c.1185+1388A>T 8 88883627 HC T A Missense p.Q218L c.653A>T 8 88885547 ESCA T A Missense p.S52C c.154A>T 8 88886046 GBM T A Nonsense p.K126* c.376A>T 8 88885824 CM T C Missense p.D362G c.1085A>G 8 88885115 ESCA T C Missense p.K4R c.11A>G 8 88886189 LUAD T C Missense p.M54V c.160A>G 8 88886040 PRAD T C Missense p.Q230R c.689A>G 8 88885511 LUSC T C Missense p.T83A c.247A>G 8 88885953 CM T C Synonymous p.S134S c.402A>G 8 88885798 SCLC T C Synonymous p.S287S c.861A>G 8 88885339 STAD