Mutation - TCGA Type Chromosome Start Position End Position Strand Variant Classification Variant Type Reference Allele Tumor_seq Allele 1 Tumor_seq Allele 2 Tumor Sample Barcode Matched Norm Sample Barcode Genome Change cDNA Change Codon Change Protein Change BLCA 9 135042359 135042359 + Frame_Shift_Del DEL G G - TCGA-K4-A83P-01A-11D-A34U-08 TCGA-K4-A83P-10A-01D-A34X-08 g.chr9:135042359delG c.141delG c.(139-141)aagfs p.K47fs BLCA 9 135102364 135102364 + Missense_Mutation SNP G G A TCGA-E5-A4TZ-01A-11D-A31L-08 TCGA-E5-A4TZ-10B-01D-A31J-08 g.chr9:135102364G>A c.986G>A c.(985-987)cGg>cAg p.R329Q BLCA 9 135116296 135116296 + Splice_Site SNP G G A TCGA-XF-AAN0-01A-11D-A42E-08 TCGA-XF-AAN0-10A-01D-A42H-08 g.chr9:135116296G>A c.e7-1 BLCA 9 135116329 135116329 + Missense_Mutation SNP G G A TCGA-E5-A4U1-01A-11D-A31L-08 TCGA-E5-A4U1-10B-01D-A31J-08 g.chr9:135116329G>A c.1255G>A c.(1255-1257)Gac>Aac p.D419N BRCA 9 135073544 135073544 + Silent SNP C C T TCGA-AR-A2LK-01A-11D-A17W-09 TCGA-AR-A2LK-10A-01D-A17W-09 g.chr9:135073544C>T c.405C>T c.(403-405)gaC>gaT p.D135D BRCA 9 135073714 135073714 + Missense_Mutation SNP G G A TCGA-C8-A138-01A-11D-A10Y-09 TCGA-C8-A138-10A-01D-A110-09 g.chr9:135073714G>A c.575G>A c.(574-576)cGc>cAc p.R192H BRCA 9 135073814 135073814 + Silent SNP C C T TCGA-C8-A12M-01A-11D-A135-09 TCGA-C8-A12M-10A-01D-A110-09 g.chr9:135073814C>T c.675C>T c.(673-675)ccC>ccT p.P225P BRCA 9 135102255 135102255 + Missense_Mutation SNP G G A TCGA-D8-A1XQ-01A-11D-A14K-09 TCGA-D8-A1XQ-10A-01D-A14K-09 g.chr9:135102255G>A c.877G>A c.(877-879)Gcc>Acc p.A293T CESC 9 135042303 135042303 + Missense_Mutation SNP G G C TCGA-C5-A1MH-01A-11D-A14W-08 TCGA-C5-A1MH-10A-01D-A14W-08 g.chr9:135042303G>C c.85G>C c.(85-87)Gat>Cat p.D29H CESC 9 135042422 135042422 + Missense_Mutation SNP C C G TCGA-FU-A23L-01A-11D-A16O-08 TCGA-FU-A23L-10A-01D-A16O-08 g.chr9:135042422C>G c.204C>G c.(202-204)ttC>ttG p.F68L CESC 9 135073615 135073615 + Missense_Mutation SNP G G A TCGA-C5-A1MJ-01A-11D-A14W-08 TCGA-C5-A1MJ-10A-01D-A14W-08 g.chr9:135073615G>A c.476G>A c.(475-477)cGc>cAc p.R159H CESC 9 135073664 135073664 + Silent SNP C C T TCGA-EK-A2PM-01A-11D-A18J-09 TCGA-EK-A2PM-10A-01D-A18J-09 g.chr9:135073664C>T c.525C>T c.(523-525)ttC>ttT p.F175F CESC 9 135102404 135102404 + Silent SNP C C T TCGA-UC-A7PD-01A-11D-A351-09 TCGA-UC-A7PD-11A-12D-A351-09 g.chr9:135102404C>T c.1026C>T c.(1024-1026)aaC>aaT p.N342N COAD 9 135042236 135042236 + Silent SNP G G A TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr9:135042236G>A c.18G>A c.(16-18)gcG>gcA p.A6A COAD 9 135042390 135042390 + Missense_Mutation SNP G G T TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr9:135042390G>T c.172G>T c.(172-174)Ggc>Tgc p.G58C COAD 9 135042407 135042407 + Frame_Shift_Del DEL C C - TCGA-AD-6895-01A-11D-1924-10 TCGA-AD-6895-10A-01D-1924-10 g.chr9:135042407delC c.189delC c.(187-189)gacfs p.D63fs COAD 9 135073412 135073412 + Silent SNP G G A TCGA-A6-6653-01A-11D-1771-10 TCGA-A6-6653-10A-01D-1771-10 g.chr9:135073412G>A c.273G>A c.(271-273)ccG>ccA p.P91P COAD 9 135073568 135073568 + Silent SNP C C T TCGA-AA-3872-01A-01W-0995-10 TCGA-AA-3872-10A-01W-0995-10 g.chr9:135073568C>T c.429C>T c.(427-429)taC>taT p.Y143Y COAD 9 135073621 135073621 + Nonsense_Mutation SNP G G A TCGA-D5-6535-01A-11D-1719-10 TCGA-D5-6535-10A-01D-1719-10 g.chr9:135073621G>A c.482G>A c.(481-483)tGg>tAg p.W161* COAD 9 135073715 135073715 + Silent SNP C C T TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr9:135073715C>T c.576C>T c.(574-576)cgC>cgT p.R192R COAD 9 135073815 135073815 + Missense_Mutation SNP G G A TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr9:135073815G>A c.676G>A c.(676-678)Gac>Aac p.D226N COAD 9 135073821 135073821 + Missense_Mutation SNP C C T TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr9:135073821C>T c.682C>T c.(682-684)Cgc>Tgc p.R228C COAD 9 135073825 135073825 + Missense_Mutation SNP A A C TCGA-AA-3966-01A-01W-1073-09 TCGA-AA-3966-10A-01W-1073-09 g.chr9:135073825A>C c.686A>C c.(685-687)aAc>aCc p.N229T COAD 9 135073941 135073941 + Missense_Mutation SNP C C T TCGA-CK-5913-01A-11D-1650-10 TCGA-CK-5913-10A-01D-1650-10 g.chr9:135073941C>T c.802C>T c.(802-804)Cgg>Tgg p.R268W COAD 9 135102260 135102260 + Missense_Mutation SNP C C A TCGA-AD-6965-01A-11D-1924-10 TCGA-AD-6965-10A-01D-1924-10 g.chr9:135102260C>A c.882C>A c.(880-882)aaC>aaA p.N294K COAD 9 135102320 135102320 + Silent SNP C C T TCGA-AA-3976-01A-01W-0995-10 TCGA-AA-3976-10A-01W-0999-10 g.chr9:135102320C>T c.942C>T c.(940-942)ccC>ccT p.P314P COAD 9 135114575 135114575 + Missense_Mutation SNP C C T TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr9:135114575C>T c.1139C>T c.(1138-1140)aCg>aTg p.T380M COAD 9 135117321 135117321 + Silent SNP C C T TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr9:135117321C>T c.1416C>T c.(1414-1416)aaC>aaT p.N472N COADREAD 9 135042236 135042236 + Silent SNP G G A TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr9:135042236G>A c.18G>A c.(16-18)gcG>gcA p.A6A COADREAD 9 135042390 135042390 + Missense_Mutation SNP G G T TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr9:135042390G>T c.172G>T c.(172-174)Ggc>Tgc p.G58C COADREAD 9 135042407 135042407 + Frame_Shift_Del DEL C C - TCGA-AD-6895-01A-11D-1924-10 TCGA-AD-6895-10A-01D-1924-10 g.chr9:135042407delC c.189delC c.(187-189)gacfs p.D63fs COADREAD 9 135073412 135073412 + Silent SNP G G A TCGA-A6-6653-01A-11D-1771-10 TCGA-A6-6653-10A-01D-1771-10 g.chr9:135073412G>A c.273G>A c.(271-273)ccG>ccA p.P91P COADREAD 9 135073568 135073568 + Silent SNP C C T TCGA-AA-3872-01A-01W-0995-10 TCGA-AA-3872-10A-01W-0995-10 g.chr9:135073568C>T c.429C>T c.(427-429)taC>taT p.Y143Y COADREAD 9 135073621 135073621 + Nonsense_Mutation SNP G G A TCGA-D5-6535-01A-11D-1719-10 TCGA-D5-6535-10A-01D-1719-10 g.chr9:135073621G>A c.482G>A c.(481-483)tGg>tAg p.W161* COADREAD 9 135073643 135073643 + Silent SNP C C T TCGA-AG-3999-01A-01W-1073-09 TCGA-AG-3999-10A-01W-1073-09 g.chr9:135073643C>T c.504C>T c.(502-504)gcC>gcT p.A168A COADREAD 9 135073715 135073715 + Silent SNP C C T TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr9:135073715C>T c.576C>T c.(574-576)cgC>cgT p.R192R COADREAD 9 135073815 135073815 + Missense_Mutation SNP G G A TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr9:135073815G>A c.676G>A c.(676-678)Gac>Aac p.D226N COADREAD 9 135073821 135073821 + Missense_Mutation SNP C C T TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr9:135073821C>T c.682C>T c.(682-684)Cgc>Tgc p.R228C COADREAD 9 135073825 135073825 + Missense_Mutation SNP A A C TCGA-AA-3966-01A-01W-1073-09 TCGA-AA-3966-10A-01W-1073-09 g.chr9:135073825A>C c.686A>C c.(685-687)aAc>aCc p.N229T COADREAD 9 135073918 135073918 + Missense_Mutation SNP C C T TCGA-AG-3898-01A-01W-1073-09 TCGA-AG-3898-10A-01W-1073-09 g.chr9:135073918C>T c.779C>T c.(778-780)gCg>gTg p.A260V COADREAD 9 135073941 135073941 + Missense_Mutation SNP C C T TCGA-CK-5913-01A-11D-1650-10 TCGA-CK-5913-10A-01D-1650-10 g.chr9:135073941C>T c.802C>T c.(802-804)Cgg>Tgg p.R268W COADREAD 9 135102260 135102260 + Missense_Mutation SNP C C A TCGA-AD-6965-01A-11D-1924-10 TCGA-AD-6965-10A-01D-1924-10 g.chr9:135102260C>A c.882C>A c.(880-882)aaC>aaA p.N294K COADREAD 9 135102320 135102320 + Silent SNP C C T TCGA-AA-3976-01A-01W-0995-10 TCGA-AA-3976-10A-01W-0999-10 g.chr9:135102320C>T c.942C>T c.(940-942)ccC>ccT p.P314P COADREAD 9 135114575 135114575 + Missense_Mutation SNP C C T TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr9:135114575C>T c.1139C>T c.(1138-1140)aCg>aTg p.T380M COADREAD 9 135117321 135117321 + Silent SNP C C T TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr9:135117321C>T c.1416C>T c.(1414-1416)aaC>aaT p.N472N ESCA 9 135073473 135073473 + Missense_Mutation SNP T T C TCGA-IG-A5B8-01A-11D-A28B-09 TCGA-IG-A5B8-10A-01D-A28E-09 g.chr9:135073473T>C c.334T>C c.(334-336)Tgg>Cgg p.W112R ESCA 9 135102326 135102326 + Silent SNP C C T TCGA-R6-A8WG-01A-11D-A37C-09 TCGA-R6-A8WG-10A-01D-A37F-09 g.chr9:135102326C>T c.948C>T c.(946-948)tgC>tgT p.C316C GBM 9 135042315 135042315 + Missense_Mutation SNP A A C TCGA-76-6656-01A-11D-1845-08 TCGA-76-6656-10A-01D-1845-08 g.chr9:135042315A>C c.97A>C c.(97-99)Acc>Ccc p.T33P GBM 9 135073844 135073844 + Silent SNP G G A TCGA-06-5858-01A-01D-1696-08 TCGA-06-5858-10A-01D-1696-08 g.chr9:135073844G>A c.705G>A c.(703-705)acG>acA p.T235T GBMLGG 9 135042315 135042315 + Missense_Mutation SNP A A C TCGA-76-6656-01A-11D-1845-08 TCGA-76-6656-10A-01D-1845-08 g.chr9:135042315A>C c.97A>C c.(97-99)Acc>Ccc p.T33P GBMLGG 9 135073844 135073844 + Silent SNP G G A TCGA-06-5858-01A-01D-1696-08 TCGA-06-5858-10A-01D-1696-08 g.chr9:135073844G>A c.705G>A c.(703-705)acG>acA p.T235T GBMLGG 9 135073845 135073845 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr9:135073845C>T c.706C>T c.(706-708)Cgg>Tgg p.R236W HNSC 9 135073644 135073644 + Missense_Mutation SNP G G A TCGA-CR-6481-01A-11D-1870-08 TCGA-CR-6481-10A-01D-1870-08 g.chr9:135073644G>A c.505G>A c.(505-507)Gag>Aag p.E169K HNSC 9 135073814 135073814 + Silent SNP C C T TCGA-MT-A67D-01A-31D-A30E-08 TCGA-MT-A67D-10A-01D-A30H-08 g.chr9:135073814C>T c.675C>T c.(673-675)ccC>ccT p.P225P HNSC 9 135102294 135102294 + Missense_Mutation SNP G G A TCGA-CN-A63Y-01A-11D-A30E-08 TCGA-CN-A63Y-10A-01D-A30H-08 g.chr9:135102294G>A c.916G>A c.(916-918)Gag>Aag p.E306K KICH 9 135073709 135073709 + Silent SNP G G A TCGA-KN-8428-01A-11D-2310-10 TCGA-KN-8428-11A-01D-2311-10 g.chr9:135073709G>A c.570G>A c.(568-570)gcG>gcA p.A190A KIPAN 9 135073709 135073709 + Silent SNP G G A TCGA-KN-8428-01A-11D-2310-10 TCGA-KN-8428-11A-01D-2311-10 g.chr9:135073709G>A c.570G>A c.(568-570)gcG>gcA p.A190A KIPAN 9 135102354 135102354 + Silent SNP C C A TCGA-CW-6090-01A-11D-1669-08 TCGA-CW-6090-11A-01D-1669-08 g.chr9:135102354C>A c.976C>A c.(976-978)Cgg>Agg p.R326R KIRC 9 135102354 135102354 + Silent SNP C C A TCGA-CW-6090-01A-11D-1669-08 TCGA-CW-6090-11A-01D-1669-08 g.chr9:135102354C>A c.976C>A c.(976-978)Cgg>Agg p.R326R LGG 9 135073845 135073845 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr9:135073845C>T c.706C>T c.(706-708)Cgg>Tgg p.R236W LIHC 9 135042407 135042407 + Frame_Shift_Del DEL C C - TCGA-DD-A1EG-01A-11D-A20W-10 TCGA-DD-A1EG-10A-01D-A20W-10 g.chr9:135042407delC c.189delC c.(187-189)gacfs p.D63fs LIHC 9 135116364 135116364 + Silent SNP C C A TCGA-ED-A7PZ-01A-11D-A33Q-10 TCGA-ED-A7PZ-10A-01D-A33Q-10 g.chr9:135116364C>A c.1290C>A c.(1288-1290)cgC>cgA p.R430R LIHC 9 135117276 135117276 + Missense_Mutation SNP C C A TCGA-CC-A5UE-01A-11D-A28X-10 TCGA-CC-A5UE-10A-01D-A28X-10 g.chr9:135117276C>A c.1371C>A c.(1369-1371)gaC>gaA p.D457E LUAD 9 135042385 135042385 + Missense_Mutation SNP C C T TCGA-44-7669-01A-21D-2063-08 TCGA-44-7669-10A-01D-2063-08 g.chr9:135042385C>T c.167C>T c.(166-168)cCc>cTc p.P56L LUAD 9 135073412 135073412 + Silent SNP G G A TCGA-97-8175-01A-11D-2284-08 TCGA-97-8175-10A-01D-2284-08 g.chr9:135073412G>A c.273G>A c.(271-273)ccG>ccA p.P91P LUAD 9 135073437 135073437 + Nonsense_Mutation SNP G G T TCGA-05-4427-01A-21D-1855-08 TCGA-05-4427-10A-01D-1855-08 g.chr9:135073437G>T c.298G>T c.(298-300)Gag>Tag p.E100* LUAD 9 135073442 135073442 + Silent SNP G G A TCGA-69-7979-01A-11D-2184-08 TCGA-69-7979-10A-01D-2184-08 g.chr9:135073442G>A c.303G>A c.(301-303)gaG>gaA p.E101E LUAD 9 135073529 135073529 + Silent SNP C C A TCGA-64-1677-01A-01W-0928-08 TCGA-64-1677-10A-01W-0928-08 g.chr9:135073529C>A c.390C>A c.(388-390)acC>acA p.T130T LUAD 9 135073530 135073530 + Missense_Mutation SNP G G A TCGA-64-1677-01A-01W-0928-08 TCGA-64-1677-10A-01W-0928-08 g.chr9:135073530G>A c.391G>A c.(391-393)Gtg>Atg p.V131M LUAD 9 135073628 135073628 + Silent SNP C C A TCGA-78-7155-01A-11D-2036-08 TCGA-78-7155-10A-01D-2036-08 g.chr9:135073628C>A c.489C>A c.(487-489)ccC>ccA p.P163P LUAD 9 135073778 135073778 + Silent SNP C C T TCGA-55-7726-01A-11D-2167-08 TCGA-55-7726-10A-01D-2167-08 g.chr9:135073778C>T c.639C>T c.(637-639)ttC>ttT p.F213F LUAD 9 135073796 135073796 + Missense_Mutation SNP C C A TCGA-17-Z016-01A-01W-0746-08 TCGA-17-Z016-11A-01W-0746-08 g.chr9:135073796C>A c.657C>A c.(655-657)ttC>ttA p.F219L LUAD 9 135073902 135073902 + Silent SNP C C A TCGA-55-A4DG-01A-11D-A24D-08 TCGA-55-A4DG-10A-01D-A24F-08 g.chr9:135073902C>A c.763C>A c.(763-765)Cgg>Agg p.R255R LUAD 9 135102294 135102294 + Missense_Mutation SNP G G C TCGA-05-4382-01A-01D-1931-08 TCGA-05-4382-10A-01D-1265-08 g.chr9:135102294G>C c.916G>C c.(916-918)Gag>Cag p.E306Q LUAD 9 135102355 135102355 + Missense_Mutation SNP G G T TCGA-44-7670-01A-11D-2063-08 TCGA-44-7670-10A-01D-2063-08 g.chr9:135102355G>T c.977G>T c.(976-978)cGg>cTg p.R326L LUAD 9 135102363 135102363 + Silent SNP C C A TCGA-50-6594-01A-11D-1753-08 TCGA-50-6594-11A-01D-1753-08 g.chr9:135102363C>A c.985C>A c.(985-987)Cgg>Agg p.R329R LUAD 9 135102405 135102405 + Missense_Mutation SNP G G A TCGA-99-8025-01A-11D-2238-08 TCGA-99-8025-10A-01D-2238-08 g.chr9:135102405G>A c.1027G>A c.(1027-1029)Gcc>Acc p.A343T LUAD 9 135114645 135114645 + Missense_Mutation SNP G G T TCGA-55-5899-01A-11D-1625-08 TCGA-55-5899-10A-01D-1625-08 g.chr9:135114645G>T c.1209G>T c.(1207-1209)gaG>gaT p.E403D LUAD 9 135114648 135114648 + Silent SNP C C T TCGA-69-7980-01A-11D-2184-08 TCGA-69-7980-10A-01D-2184-08 g.chr9:135114648C>T c.1212C>T c.(1210-1212)aaC>aaT p.N404N LUAD 9 135116406 135116406 + Silent SNP G G A TCGA-MP-A4TH-01A-31D-A25L-08 TCGA-MP-A4TH-10A-01D-A25L-08 g.chr9:135116406G>A c.1332G>A c.(1330-1332)acG>acA p.T444T LUAD 9 135116431 135116431 + Splice_Site SNP C C A TCGA-55-7576-01A-11D-2063-08 TCGA-55-7576-10A-01D-2063-08 g.chr9:135116431C>A c.1357C>A c.(1357-1359)Ccc>Acc p.P453T LUSC 9 135073791 135073791 + Missense_Mutation SNP C C A TCGA-22-5472-01A-01D-1632-08 TCGA-22-5472-11A-11D-1632-08 g.chr9:135073791C>A c.652C>A c.(652-654)Cgc>Agc p.R218S LUSC 9 135073852 135073852 + Missense_Mutation SNP A A G TCGA-66-2773-01A-01D-1267-08 TCGA-66-2773-11A-01D-1267-08 g.chr9:135073852A>G c.713A>G c.(712-714)gAg>gGg p.E238G LUSC 9 135114558 135114558 + Silent SNP C C T TCGA-33-4583-01A-01D-1441-08 TCGA-33-4583-11A-01D-1441-08 g.chr9:135114558C>T c.1122C>T c.(1120-1122)gtC>gtT p.V374V PAAD 9 135073361 135073361 + Silent SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr9:135073361C>T c.222C>T c.(220-222)ccC>ccT p.P74P PAAD 9 135073579 135073579 + Missense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr9:135073579C>T c.440C>T c.(439-441)aCg>aTg p.T147M PAAD 9 135073735 135073735 + Missense_Mutation SNP A A G TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr9:135073735A>G c.596A>G c.(595-597)tAc>tGc p.Y199C PAAD 9 135073905 135073905 + Silent SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr9:135073905C>T c.766C>T c.(766-768)Ctg>Ttg p.L256L PAAD 9 135073991 135073991 + Silent SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr9:135073991C>T c.852C>T c.(850-852)atC>atT p.I284I PAAD 9 135102349 135102349 + Missense_Mutation SNP G G A TCGA-HZ-A9TJ-01A-11D-A40W-08 TCGA-HZ-A9TJ-10A-01D-A40W-08 g.chr9:135102349G>A c.971G>A c.(970-972)cGc>cAc p.R324H PAAD 9 135102389 135102389 + Silent SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr9:135102389C>T c.1011C>T c.(1009-1011)ccC>ccT p.P337P PAAD 9 135105980 135105980 + Missense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr9:135105980G>A c.1052G>A c.(1051-1053)gGc>gAc p.G351D PAAD 9 135114495 135114495 + Silent SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr9:135114495C>T c.1059C>T c.(1057-1059)tgC>tgT p.C353C PAAD 9 135114577 135114577 + Nonsense_Mutation SNP C C T TCGA-2J-AAB6-01A-11D-A40W-08 TCGA-2J-AAB6-10A-01D-A40W-08 g.chr9:135114577C>T c.1141C>T c.(1141-1143)Cga>Tga p.R381* PAAD 9 135117335 135117335 + Missense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr9:135117335G>A c.1430G>A c.(1429-1431)tGc>tAc p.C477Y PRAD 9 135073364 135073364 + Silent SNP C C T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr9:135073364C>T c.225C>T c.(223-225)taC>taT p.Y75Y PRAD 9 135073796 135073796 + Silent SNP C C T TCGA-KK-A59V-01A-11D-A29Q-08 TCGA-KK-A59V-11A-11D-A29Q-08 g.chr9:135073796C>T c.657C>T c.(655-657)ttC>ttT p.F219F PRAD 9 135073943 135073943 + Silent SNP G G T TCGA-J9-A8CM-01A-11D-A34U-08 TCGA-J9-A8CM-10A-01D-A34X-08 g.chr9:135073943G>T c.804G>T c.(802-804)cgG>cgT p.R268R PRAD 9 135102298 135102298 + Missense_Mutation SNP G G T TCGA-M7-A725-01A-12D-A32B-08 TCGA-M7-A725-10A-01D-A329-08 g.chr9:135102298G>T c.920G>T c.(919-921)tGc>tTc p.C307F READ 9 135073643 135073643 + Silent SNP C C T TCGA-AG-3999-01A-01W-1073-09 TCGA-AG-3999-10A-01W-1073-09 g.chr9:135073643C>T c.504C>T c.(502-504)gcC>gcT p.A168A READ 9 135073918 135073918 + Missense_Mutation SNP C C T TCGA-AG-3898-01A-01W-1073-09 TCGA-AG-3898-10A-01W-1073-09 g.chr9:135073918C>T c.779C>T c.(778-780)gCg>gTg p.A260V SARC 9 135116314 135116314 + Missense_Mutation SNP A A G TCGA-DX-AB30-01A-11D-A38Z-09 TCGA-DX-AB30-10A-01D-A38Z-09 g.chr9:135116314A>G c.1240A>G c.(1240-1242)Ata>Gta p.I414V SKCM 9 135042273 135042273 + Missense_Mutation SNP T T A TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr9:135042273T>A c.55T>A c.(55-57)Tat>Aat p.Y19N SKCM 9 135042402 135042402 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr9:135042402G>A c.184G>A c.(184-186)Gga>Aga p.G62R SKCM 9 135073590 135073590 + Silent SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr9:135073590C>T c.451C>T c.(451-453)Ctg>Ttg p.L151L SKCM 9 135073874 135073874 + Silent SNP G G A TCGA-FW-A3TV-06A-11D-A23B-08 TCGA-FW-A3TV-10A-01D-A23B-08 g.chr9:135073874G>A c.735G>A c.(733-735)gaG>gaA p.E245E SKCM 9 135073983 135073983 + Missense_Mutation SNP G G A TCGA-FS-A1ZZ-06A-11D-A197-08 TCGA-FS-A1ZZ-10A-01D-A199-08 g.chr9:135073983G>A c.844G>A c.(844-846)Gag>Aag p.E282K SKCM 9 135102365 135102365 + Silent SNP G G A TCGA-EE-A29H-06A-12D-A197-08 TCGA-EE-A29H-10A-01D-A199-08 g.chr9:135102365G>A c.987G>A c.(985-987)cgG>cgA p.R329R

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BLCA-CN 9 135073824 135073824 single base substitution A T missense_variant N229Y 685A>T BOCA-FR 9 135048537 135048537 single base substitution G T intron_variant BRCA-EU 9 135033156 135033156 single base substitution G A upstream_gene_variant BRCA-EU 9 135033374 135033374 single base substitution A G upstream_gene_variant BRCA-EU 9 135036148 135036148 single base substitution G C upstream_gene_variant BRCA-EU 9 135036354 135036354 single base substitution G T upstream_gene_variant BRCA-EU 9 135036416 135036416 single base substitution G A upstream_gene_variant BRCA-EU 9 135037518 135037518 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant BRCA-EU 9 135038599 135038599 single base substitution C T intron_variant BRCA-EU 9 135038889 135038889 single base substitution G T intron_variant BRCA-EU 9 135040869 135040869 single base substitution T C intron_variant BRCA-EU 9 135041960 135041960 single base substitution G T 5_prime_UTR_premature_start_codon_gain_variant BRCA-EU 9 135044900 135044900 single base substitution C A intron_variant BRCA-EU 9 135045136 135045136 single base substitution G A intron_variant BRCA-EU 9 135045993 135045993 single base substitution G A intron_variant BRCA-EU 9 135046077 135046077 deletion of <=200bp G - intron_variant BRCA-EU 9 135047340 135047340 single base substitution G C intron_variant BRCA-EU 9 135047719 135047719 single base substitution C T intron_variant BRCA-EU 9 135047939 135047939 single base substitution C A intron_variant BRCA-EU 9 135048233 135048233 single base substitution C T intron_variant BRCA-EU 9 135051548 135051548 single base substitution C T intron_variant BRCA-EU 9 135054976 135054976 single base substitution C T intron_variant BRCA-EU 9 135056699 135056699 single base substitution G A intron_variant BRCA-EU 9 135057115 135057115 single base substitution T A intron_variant BRCA-EU 9 135057150 135057150 single base substitution C A intron_variant BRCA-EU 9 135057443 135057443 single base substitution A T intron_variant BRCA-EU 9 135057788 135057788 single base substitution C A intron_variant BRCA-EU 9 135058834 135058834 single base substitution A G intron_variant BRCA-EU 9 135058937 135058937 single base substitution G A intron_variant BRCA-EU 9 135060995 135060995 insertion of <=200bp - C intron_variant BRCA-EU 9 135062569 135062569 single base substitution C T intron_variant BRCA-EU 9 135064217 135064217 single base substitution G A intron_variant BRCA-EU 9 135064977 135064977 single base substitution G C intron_variant BRCA-EU 9 135065242 135065242 single base substitution G T intron_variant BRCA-EU 9 135066130 135066130 single base substitution G A intron_variant BRCA-EU 9 135066144 135066144 single base substitution G C intron_variant BRCA-EU 9 135066360 135066360 single base substitution G T intron_variant BRCA-EU 9 135068002 135068002 single base substitution G A intron_variant BRCA-EU 9 135068144 135068144 single base substitution G C intron_variant BRCA-EU 9 135068258 135068258 single base substitution C T intron_variant BRCA-EU 9 135069292 135069292 single base substitution C T intron_variant BRCA-EU 9 135070279 135070279 single base substitution C T intron_variant BRCA-EU 9 135070357 135070357 single base substitution G C intron_variant BRCA-EU 9 135070425 135070425 single base substitution A G intron_variant BRCA-EU 9 135070639 135070639 single base substitution C G intron_variant BRCA-EU 9 135072244 135072244 single base substitution G A intron_variant BRCA-EU 9 135072632 135072632 single base substitution C T intron_variant BRCA-EU 9 135072731 135072731 single base substitution G A intron_variant BRCA-EU 9 135072879 135072879 single base substitution G A intron_variant BRCA-EU 9 135073480 135073480 single base substitution G A missense_variant R114H 341G>A BRCA-EU 9 135073988 135073988 single base substitution C A synonymous_variant V283V 849C>A BRCA-EU 9 135074134 135074134 single base substitution C T intron_variant BRCA-EU 9 135074156 135074156 single base substitution C T intron_variant BRCA-EU 9 135074564 135074564 single base substitution G T intron_variant BRCA-EU 9 135075616 135075616 single base substitution G T intron_variant BRCA-EU 9 135076336 135076336 single base substitution C A intron_variant BRCA-EU 9 135078363 135078363 single base substitution T C intron_variant BRCA-EU 9 135080317 135080347 deletion of <=200bp GAGGTACCCATGAGGATGGCTATTATTGGAA - intron_variant BRCA-EU 9 135080995 135080995 single base substitution C T intron_variant BRCA-EU 9 135085048 135085048 single base substitution G C intron_variant BRCA-EU 9 135085494 135085494 single base substitution G C intron_variant BRCA-EU 9 135086098 135086098 single base substitution T A intron_variant BRCA-EU 9 135086375 135086375 single base substitution C T intron_variant BRCA-EU 9 135087995 135087995 single base substitution C T intron_variant BRCA-EU 9 135088026 135088026 single base substitution G A intron_variant BRCA-EU 9 135090261 135090261 single base substitution A T intron_variant BRCA-EU 9 135090824 135090824 single base substitution G A intron_variant BRCA-EU 9 135092761 135092761 single base substitution G C intron_variant BRCA-EU 9 135093632 135093632 single base substitution C T intron_variant BRCA-EU 9 135093841 135093841 single base substitution T A intron_variant BRCA-EU 9 135094056 135094056 single base substitution G A intron_variant BRCA-EU 9 135094363 135094363 single base substitution G A intron_variant BRCA-EU 9 135094656 135094656 single base substitution T A intron_variant BRCA-EU 9 135096515 135096515 single base substitution G T intron_variant BRCA-EU 9 135096525 135096525 single base substitution A G intron_variant BRCA-EU 9 135096530 135096530 single base substitution T C intron_variant BRCA-EU 9 135096895 135096895 single base substitution C T intron_variant BRCA-EU 9 135097442 135097442 single base substitution C T intron_variant BRCA-EU 9 135098293 135098293 single base substitution T C intron_variant BRCA-EU 9 135098700 135098700 single base substitution G A intron_variant BRCA-EU 9 135099767 135099767 single base substitution G C intron_variant BRCA-EU 9 135101541 135101541 single base substitution C G intron_variant BRCA-EU 9 135101671 135101671 single base substitution G A intron_variant BRCA-EU 9 135102127 135102127 single base substitution C A intron_variant BRCA-EU 9 135102299 135102299 single base substitution C T synonymous_variant C307C 921C>T BRCA-EU 9 135103295 135103295 single base substitution A G intron_variant BRCA-EU 9 135103508 135103508 single base substitution C G intron_variant BRCA-EU 9 135103902 135103902 single base substitution C T intron_variant BRCA-EU 9 135104120 135104120 insertion of <=200bp - T intron_variant BRCA-EU 9 135104198 135104198 single base substitution G A intron_variant BRCA-EU 9 135104409 135104409 single base substitution G T intron_variant BRCA-EU 9 135105946 135105946 single base substitution C A intron_variant BRCA-EU 9 135106021 135106021 single base substitution T A intron_variant BRCA-EU 9 135106248 135106248 single base substitution C A intron_variant BRCA-EU 9 135106345 135106345 single base substitution G A intron_variant BRCA-EU 9 135107165 135107165 single base substitution C T downstream_gene_variant BRCA-EU 9 135107165 135107165 single base substitution C T intron_variant BRCA-EU 9 135107518 135107518 single base substitution G A downstream_gene_variant BRCA-EU 9 135107518 135107518 single base substitution G A intron_variant BRCA-EU 9 135107834 135107834 single base substitution G A downstream_gene_variant BRCA-EU 9 135107834 135107834 single base substitution G A intron_variant BRCA-EU 9 135109733 135109733 single base substitution G C downstream_gene_variant BRCA-EU 9 135109733 135109733 single base substitution G C intron_variant BRCA-EU 9 135110225 135110225 single base substitution C G downstream_gene_variant BRCA-EU 9 135110225 135110225 single base substitution C G intron_variant BRCA-EU 9 135111199 135111199 single base substitution G A downstream_gene_variant BRCA-EU 9 135111199 135111199 single base substitution G A intron_variant BRCA-EU 9 135111199 135111199 single base substitution G A upstream_gene_variant BRCA-EU 9 135111940 135111940 single base substitution T G intron_variant BRCA-EU 9 135111940 135111940 single base substitution T G upstream_gene_variant BRCA-EU 9 135111970 135111970 single base substitution G A intron_variant BRCA-EU 9 135111970 135111970 single base substitution G A upstream_gene_variant BRCA-EU 9 135113478 135113478 single base substitution C T intron_variant BRCA-EU 9 135113478 135113478 single base substitution C T upstream_gene_variant BRCA-EU 9 135114245 135114245 single base substitution C A intron_variant BRCA-EU 9 135114245 135114245 single base substitution C A upstream_gene_variant BRCA-EU 9 135114578 135114578 single base substitution G A missense_variant R373Q 1118G>A BRCA-EU 9 135114578 135114578 single base substitution G A missense_variant R381Q 1142G>A BRCA-EU 9 135114578 135114578 single base substitution G A missense_variant R387Q 1160G>A BRCA-EU 9 135114578 135114578 single base substitution G A upstream_gene_variant BRCA-EU 9 135115556 135115556 single base substitution A T intron_variant BRCA-EU 9 135115556 135115556 single base substitution A T upstream_gene_variant BRCA-EU 9 135115813 135115813 single base substitution G C intron_variant BRCA-EU 9 135115813 135115813 single base substitution G C upstream_gene_variant BRCA-EU 9 135116685 135116685 single base substitution G A intron_variant BRCA-EU 9 135116685 135116685 single base substitution G A upstream_gene_variant BRCA-EU 9 135117505 135117505 deletion of <=200bp C - 3_prime_UTR_variant BRCA-EU 9 135117505 135117505 deletion of <=200bp C - exon_variant BRCA-EU 9 135117639 135117639 single base substitution G A 3_prime_UTR_variant BRCA-EU 9 135117639 135117639 single base substitution G A downstream_gene_variant BRCA-EU 9 135118876 135118876 single base substitution C G 3_prime_UTR_variant BRCA-EU 9 135118876 135118876 single base substitution C G downstream_gene_variant BRCA-EU 9 135118923 135118923 single base substitution C A 3_prime_UTR_variant BRCA-EU 9 135118923 135118923 single base substitution C A downstream_gene_variant BRCA-EU 9 135119217 135119217 single base substitution G A 3_prime_UTR_variant BRCA-EU 9 135119217 135119217 single base substitution G A downstream_gene_variant BRCA-EU 9 135121565 135121565 single base substitution C G downstream_gene_variant BRCA-EU 9 135122560 135122560 single base substitution G T downstream_gene_variant BRCA-EU 9 135124055 135124055 single base substitution C T downstream_gene_variant BRCA-FR 9 135032474 135032474 single base substitution G A upstream_gene_variant BRCA-FR 9 135036148 135036148 single base substitution G C upstream_gene_variant BRCA-FR 9 135050994 135050994 single base substitution A T intron_variant BRCA-FR 9 135058937 135058937 single base substitution G A intron_variant BRCA-FR 9 135063644 135063644 single base substitution G T intron_variant BRCA-FR 9 135068144 135068144 single base substitution G C intron_variant BRCA-FR 9 135071108 135071108 single base substitution C T intron_variant BRCA-FR 9 135075616 135075616 single base substitution G T intron_variant BRCA-FR 9 135078416 135078416 single base substitution G T intron_variant BRCA-FR 9 135082448 135082448 single base substitution G C intron_variant BRCA-FR 9 135085048 135085048 single base substitution G C intron_variant BRCA-FR 9 135088105 135088105 single base substitution G A intron_variant BRCA-FR 9 135093633 135093633 single base substitution G A intron_variant BRCA-FR 9 135097442 135097442 single base substitution C T intron_variant BRCA-FR 9 135103902 135103902 single base substitution C T intron_variant BRCA-FR 9 135111295 135111295 single base substitution G A downstream_gene_variant BRCA-FR 9 135111295 135111295 single base substitution G A intron_variant BRCA-FR 9 135111295 135111295 single base substitution G A upstream_gene_variant BRCA-FR 9 135111970 135111970 single base substitution G A intron_variant BRCA-FR 9 135111970 135111970 single base substitution G A upstream_gene_variant BRCA-FR 9 135113826 135113826 single base substitution G A intron_variant BRCA-FR 9 135113826 135113826 single base substitution G A upstream_gene_variant BRCA-FR 9 135122687 135122687 single base substitution C T downstream_gene_variant BRCA-UK 9 135057893 135057893 single base substitution C T intron_variant BRCA-UK 9 135069117 135069117 single base substitution G A intron_variant BRCA-UK 9 135076580 135076580 single base substitution G C intron_variant BRCA-UK 9 135112069 135112069 single base substitution G A intron_variant BRCA-UK 9 135112069 135112069 single base substitution G A upstream_gene_variant BRCA-UK 9 135114245 135114245 single base substitution C A intron_variant BRCA-UK 9 135114245 135114245 single base substitution C A upstream_gene_variant BRCA-US 9 135073544 135073544 single base substitution C T synonymous_variant D135D 405C>T BRCA-US 9 135073714 135073714 single base substitution G A missense_variant R192H 575G>A BRCA-US 9 135073814 135073814 single base substitution C T synonymous_variant P225P 675C>T BRCA-US 9 135102255 135102255 single base substitution G A missense_variant A293T 877G>A BRCA-US 9 135106788 135106788 single base substitution G A intron_variant BRCA-US 9 135106788 135106788 single base substitution G A synonymous_variant E387E 1161G>A BRCA-US 9 135116302 135116302 deletion of <=200bp A - exon_variant BRCA-US 9 135116302 135116302 deletion of <=200bp A - frameshift_variant N402 BRCA-US 9 135116302 135116302 deletion of <=200bp A - frameshift_variant N410 BRCA-US 9 135116302 135116302 deletion of <=200bp A - frameshift_variant N416 BRCA-US 9 135116302 135116302 deletion of <=200bp A - upstream_gene_variant BRCA-US 9 135116406 135116406 single base substitution G A exon_variant BRCA-US 9 135116406 135116406 single base substitution G A synonymous_variant T436T 1308G>A BRCA-US 9 135116406 135116406 single base substitution G A synonymous_variant T444T 1332G>A BRCA-US 9 135116406 135116406 single base substitution G A synonymous_variant T450T 1350G>A BRCA-US 9 135116406 135116406 single base substitution G A upstream_gene_variant BTCA-JP 9 135073568 135073568 single base substitution C T synonymous_variant Y143Y 429C>T BTCA-JP 9 135073640 135073640 single base substitution C T synonymous_variant Y167Y 501C>T BTCA-JP 9 135073770 135073770 single base substitution G A missense_variant V211M 631G>A BTCA-JP 9 135073831 135073831 single base substitution A G missense_variant D231G 692A>G BTCA-JP 9 135114363 135114363 single base substitution C T intron_variant BTCA-JP 9 135114363 135114363 single base substitution C T missense_variant S348F 1043C>T BTCA-JP 9 135114363 135114363 single base substitution C T upstream_gene_variant CESC-US 9 135042303 135042303 single base substitution G C missense_variant D29H 85G>C CESC-US 9 135042422 135042422 single base substitution C G missense_variant F68L 204C>G CESC-US 9 135073615 135073615 single base substitution G A missense_variant R159H 476G>A CESC-US 9 135073664 135073664 single base substitution C T synonymous_variant F175F 525C>T CESC-US 9 135102404 135102404 single base substitution C T synonymous_variant N342N 1026C>T CLLE-ES 9 135049704 135049704 insertion of <=200bp - CGGG intron_variant CLLE-ES 9 135057725 135057725 single base substitution C A intron_variant CLLE-ES 9 135080232 135080232 single base substitution G A intron_variant CLLE-ES 9 135090371 135090371 single base substitution C T intron_variant CLLE-ES 9 135104447 135104447 single base substitution G A intron_variant CLLE-ES 9 135118879 135118879 single base substitution T A 3_prime_UTR_variant CLLE-ES 9 135118879 135118879 single base substitution T A downstream_gene_variant COAD-US 9 135042390 135042390 single base substitution G T missense_variant G58C 172G>T COAD-US 9 135042407 135042407 deletion of <=200bp C - frameshift_variant D63 COAD-US 9 135073412 135073412 single base substitution G A synonymous_variant P91P 273G>A COAD-US 9 135073621 135073621 single base substitution G A stop_gained W161* 482G>A COAD-US 9 135073715 135073715 single base substitution C T synonymous_variant R192R 576C>T COAD-US 9 135073815 135073815 single base substitution G A missense_variant D226N 676G>A COAD-US 9 135073821 135073821 single base substitution C T missense_variant R228C 682C>T COAD-US 9 135073877 135073877 single base substitution C T synonymous_variant F246F 738C>T COAD-US 9 135073941 135073941 single base substitution C T missense_variant R268W 802C>T COAD-US 9 135102254 135102254 single base substitution C T synonymous_variant H292H 876C>T COAD-US 9 135102260 135102260 single base substitution C A missense_variant N294K 882C>A COAD-US 9 135102363 135102363 single base substitution C T missense_variant R329W 985C>T COAD-US 9 135114575 135114575 single base substitution C T missense_variant T372M 1115C>T COAD-US 9 135114575 135114575 single base substitution C T missense_variant T380M 1139C>T COAD-US 9 135114575 135114575 single base substitution C T missense_variant T386M 1157C>T COAD-US 9 135114575 135114575 single base substitution C T upstream_gene_variant COCA-CN 9 135037953 135037953 single base substitution C G intron_variant COCA-CN 9 135042365 135042365 single base substitution C T synonymous_variant Y49Y 147C>T COCA-CN 9 135042580 135042580 single base substitution G A intron_variant COCA-CN 9 135049637 135049637 single base substitution T C intron_variant COCA-CN 9 135060219 135060219 single base substitution G T intron_variant COCA-CN 9 135071191 135071191 single base substitution T A intron_variant COCA-CN 9 135073480 135073480 single base substitution G A missense_variant R114H 341G>A COCA-CN 9 135073493 135073493 single base substitution G A synonymous_variant P118P 354G>A COCA-CN 9 135073516 135073516 single base substitution C T missense_variant S126L 377C>T COCA-CN 9 135073610 135073610 single base substitution C T synonymous_variant N157N 471C>T COCA-CN 9 135073714 135073714 single base substitution G A missense_variant R192H 575G>A COCA-CN 9 135073773 135073773 single base substitution C T missense_variant R212C 634C>T COCA-CN 9 135073821 135073821 single base substitution C T missense_variant R228C 682C>T COCA-CN 9 135073856 135073856 single base substitution C T synonymous_variant S239S 717C>T COCA-CN 9 135073918 135073918 single base substitution C T missense_variant A260V 779C>T COCA-CN 9 135083124 135083124 single base substitution C T intron_variant COCA-CN 9 135087425 135087425 single base substitution C T intron_variant COCA-CN 9 135087950 135087950 single base substitution G A intron_variant COCA-CN 9 135088988 135088988 single base substitution C G intron_variant COCA-CN 9 135090262 135090262 single base substitution T A intron_variant COCA-CN 9 135091819 135091819 single base substitution G A intron_variant COCA-CN 9 135100616 135100616 single base substitution C T intron_variant COCA-CN 9 135101315 135101315 single base substitution G A intron_variant COCA-CN 9 135102255 135102255 single base substitution G A missense_variant A293T 877G>A COCA-CN 9 135102294 135102294 single base substitution G A missense_variant E306K 916G>A COCA-CN 9 135102463 135102463 single base substitution G A intron_variant COCA-CN 9 135105855 135105855 single base substitution G A intron_variant COCA-CN 9 135106691 135106691 single base substitution C A intron_variant COCA-CN 9 135106691 135106691 single base substitution C A missense_variant T355N 1064C>A COCA-CN 9 135114180 135114180 single base substitution G A intron_variant COCA-CN 9 135114180 135114180 single base substitution G A upstream_gene_variant EOPC-DE 9 135049520 135049520 single base substitution T C intron_variant EOPC-DE 9 135077951 135077951 single base substitution A T intron_variant EOPC-DE 9 135100200 135100200 single base substitution T A intron_variant EOPC-DE 9 135100380 135100380 single base substitution C T intron_variant EOPC-DE 9 135119827 135119827 single base substitution G A 3_prime_UTR_variant EOPC-DE 9 135119827 135119827 single base substitution G A downstream_gene_variant EOPC-DE 9 135122866 135122866 single base substitution T A downstream_gene_variant ESAD-UK 9 135033382 135033382 single base substitution G A upstream_gene_variant ESAD-UK 9 135033442 135033442 single base substitution C T upstream_gene_variant ESAD-UK 9 135033896 135033896 single base substitution T C upstream_gene_variant ESAD-UK 9 135034906 135034906 single base substitution T C upstream_gene_variant ESAD-UK 9 135035350 135035350 single base substitution G C upstream_gene_variant ESAD-UK 9 135036810 135036810 single base substitution G A upstream_gene_variant ESAD-UK 9 135036926 135036926 single base substitution C T upstream_gene_variant ESAD-UK 9 135037814 135037814 single base substitution G A intron_variant ESAD-UK 9 135038105 135038105 single base substitution G C intron_variant ESAD-UK 9 135039431 135039431 single base substitution G A intron_variant ESAD-UK 9 135039938 135039938 single base substitution C T intron_variant ESAD-UK 9 135040560 135040560 single base substitution C G intron_variant ESAD-UK 9 135041151 135041151 single base substitution G A intron_variant ESAD-UK 9 135041309 135041309 single base substitution G A intron_variant ESAD-UK 9 135042779 135042779 single base substitution G C intron_variant ESAD-UK 9 135045136 135045136 single base substitution G A intron_variant ESAD-UK 9 135048781 135048781 single base substitution G A intron_variant ESAD-UK 9 135049104 135049104 single base substitution G A intron_variant ESAD-UK 9 135049692 135049692 single base substitution G A intron_variant ESAD-UK 9 135051612 135051612 single base substitution T G intron_variant ESAD-UK 9 135054466 135054466 single base substitution T G intron_variant ESAD-UK 9 135054966 135054966 single base substitution G T intron_variant ESAD-UK 9 135055423 135055423 single base substitution G A intron_variant ESAD-UK 9 135059663 135059663 single base substitution G A intron_variant ESAD-UK 9 135061488 135061488 single base substitution G A intron_variant ESAD-UK 9 135061994 135061994 single base substitution G A intron_variant ESAD-UK 9 135062782 135062782 single base substitution G A intron_variant ESAD-UK 9 135063465 135063465 single base substitution C T intron_variant ESAD-UK 9 135063749 135063749 single base substitution G A intron_variant ESAD-UK 9 135064798 135064798 insertion of <=200bp - A intron_variant ESAD-UK 9 135066261 135066261 single base substitution C G intron_variant ESAD-UK 9 135066516 135066516 single base substitution G A intron_variant ESAD-UK 9 135067434 135067434 single base substitution C G intron_variant ESAD-UK 9 135067577 135067577 single base substitution A G intron_variant ESAD-UK 9 135068202 135068202 single base substitution G A intron_variant ESAD-UK 9 135068770 135068770 single base substitution G T intron_variant ESAD-UK 9 135069657 135069657 single base substitution T C intron_variant ESAD-UK 9 135070030 135070030 single base substitution C T intron_variant ESAD-UK 9 135070544 135070544 single base substitution A C intron_variant ESAD-UK 9 135070681 135070681 deletion of <=200bp T - intron_variant ESAD-UK 9 135070735 135070735 single base substitution G A intron_variant ESAD-UK 9 135070808 135070808 single base substitution G T intron_variant ESAD-UK 9 135071187 135071187 single base substitution T A intron_variant ESAD-UK 9 135072167 135072167 single base substitution G A intron_variant ESAD-UK 9 135072893 135072893 single base substitution G A intron_variant ESAD-UK 9 135073687 135073687 single base substitution G A missense_variant R183H 548G>A ESAD-UK 9 135073806 135073806 single base substitution G T missense_variant A223S 667G>T ESAD-UK 9 135074388 135074388 single base substitution G T intron_variant ESAD-UK 9 135074457 135074457 single base substitution A G intron_variant ESAD-UK 9 135074922 135074922 single base substitution G A intron_variant ESAD-UK 9 135074982 135074982 single base substitution C T intron_variant ESAD-UK 9 135075029 135075029 single base substitution T G intron_variant ESAD-UK 9 135075532 135075532 single base substitution C T intron_variant ESAD-UK 9 135077096 135077096 single base substitution T C intron_variant ESAD-UK 9 135077753 135077753 single base substitution G C intron_variant ESAD-UK 9 135077795 135077795 single base substitution C A intron_variant ESAD-UK 9 135078708 135078708 single base substitution C A intron_variant ESAD-UK 9 135079224 135079224 single base substitution A T intron_variant ESAD-UK 9 135079724 135079724 single base substitution C G intron_variant ESAD-UK 9 135079844 135079844 single base substitution G A intron_variant ESAD-UK 9 135081287 135081287 single base substitution A C intron_variant ESAD-UK 9 135081429 135081429 single base substitution C A intron_variant ESAD-UK 9 135082049 135082049 single base substitution G A intron_variant ESAD-UK 9 135082747 135082747 single base substitution G A intron_variant ESAD-UK 9 135083580 135083580 single base substitution T A intron_variant ESAD-UK 9 135084506 135084506 single base substitution A T intron_variant ESAD-UK 9 135084821 135084821 single base substitution G T intron_variant ESAD-UK 9 135085027 135085027 single base substitution C T intron_variant ESAD-UK 9 135085042 135085042 single base substitution G T intron_variant ESAD-UK 9 135085553 135085553 single base substitution G T intron_variant ESAD-UK 9 135085554 135085554 single base substitution C T intron_variant ESAD-UK 9 135086636 135086636 single base substitution C T intron_variant ESAD-UK 9 135087359 135087359 single base substitution T G intron_variant ESAD-UK 9 135087896 135087896 single base substitution C T intron_variant ESAD-UK 9 135087904 135087904 single base substitution G A intron_variant ESAD-UK 9 135087949 135087949 single base substitution C T intron_variant ESAD-UK 9 135089992 135089992 single base substitution G T intron_variant ESAD-UK 9 135090264 135090264 single base substitution T A intron_variant ESAD-UK 9 135090466 135090466 single base substitution G T intron_variant ESAD-UK 9 135092938 135092938 single base substitution C G intron_variant ESAD-UK 9 135096120 135096120 single base substitution C A intron_variant ESAD-UK 9 135096591 135096591 single base substitution T G intron_variant ESAD-UK 9 135096850 135096850 single base substitution G A intron_variant ESAD-UK 9 135097972 135097972 single base substitution T C intron_variant ESAD-UK 9 135100125 135100125 single base substitution C G intron_variant ESAD-UK 9 135100654 135100654 single base substitution T A intron_variant ESAD-UK 9 135100735 135100735 single base substitution A G intron_variant ESAD-UK 9 135101070 135101070 single base substitution T A intron_variant ESAD-UK 9 135102355 135102355 single base substitution G A missense_variant R326Q 977G>A ESAD-UK 9 135103063 135103063 single base substitution C A intron_variant ESAD-UK 9 135103301 135103301 single base substitution C T intron_variant ESAD-UK 9 135103535 135103535 single base substitution G A intron_variant ESAD-UK 9 135105501 135105501 single base substitution G A intron_variant ESAD-UK 9 135105727 135105727 single base substitution C T intron_variant ESAD-UK 9 135107056 135107056 single base substitution G A downstream_gene_variant ESAD-UK 9 135107056 135107056 single base substitution G A intron_variant ESAD-UK 9 135108431 135108431 single base substitution G T downstream_gene_variant ESAD-UK 9 135108431 135108431 single base substitution G T intron_variant ESAD-UK 9 135110529 135110529 single base substitution G A downstream_gene_variant ESAD-UK 9 135110529 135110529 single base substitution G A intron_variant ESAD-UK 9 135111579 135111579 single base substitution G T downstream_gene_variant ESAD-UK 9 135111579 135111579 single base substitution G T intron_variant ESAD-UK 9 135111579 135111579 single base substitution G T upstream_gene_variant ESAD-UK 9 135112365 135112365 single base substitution T G intron_variant ESAD-UK 9 135112365 135112365 single base substitution T G upstream_gene_variant ESAD-UK 9 135112807 135112807 single base substitution G C intron_variant ESAD-UK 9 135112807 135112807 single base substitution G C upstream_gene_variant ESAD-UK 9 135113890 135113890 single base substitution A T intron_variant ESAD-UK 9 135113890 135113890 single base substitution A T upstream_gene_variant ESAD-UK 9 135113982 135113982 single base substitution G C intron_variant ESAD-UK 9 135113982 135113982 single base substitution G C upstream_gene_variant ESAD-UK 9 135114744 135114744 single base substitution G A intron_variant ESAD-UK 9 135114744 135114744 single base substitution G A upstream_gene_variant ESAD-UK 9 135115027 135115027 single base substitution T G intron_variant ESAD-UK 9 135115027 135115027 single base substitution T G upstream_gene_variant ESAD-UK 9 135115544 135115544 single base substitution G C intron_variant ESAD-UK 9 135115544 135115544 single base substitution G C upstream_gene_variant ESAD-UK 9 135115900 135115900 single base substitution C T intron_variant ESAD-UK 9 135115900 135115900 single base substitution C T upstream_gene_variant ESAD-UK 9 135116424 135116424 single base substitution C T exon_variant ESAD-UK 9 135116424 135116424 single base substitution C T synonymous_variant G442G 1326C>T ESAD-UK 9 135116424 135116424 single base substitution C T synonymous_variant G450G 1350C>T ESAD-UK 9 135116424 135116424 single base substitution C T synonymous_variant G456G 1368C>T ESAD-UK 9 135116424 135116424 single base substitution C T upstream_gene_variant ESAD-UK 9 135116948 135116948 single base substitution A G intron_variant ESAD-UK 9 135117765 135117768 deletion of <=200bp TCTC - 3_prime_UTR_variant ESAD-UK 9 135117765 135117768 deletion of <=200bp TCTC - downstream_gene_variant ESAD-UK 9 135121498 135121498 single base substitution A G downstream_gene_variant ESAD-UK 9 135122656 135122656 single base substitution C A downstream_gene_variant ESAD-UK 9 135122925 135122925 insertion of <=200bp - T downstream_gene_variant ESCA-CN 9 135116338 135116347 deletion of <=200bp AACGAGACCG - exon_variant ESCA-CN 9 135116338 135116347 deletion of <=200bp AACGAGACCG - frameshift_variant NETG414 ESCA-CN 9 135116338 135116347 deletion of <=200bp AACGAGACCG - frameshift_variant NETG422 ESCA-CN 9 135116338 135116347 deletion of <=200bp AACGAGACCG - frameshift_variant NETG428 ESCA-CN 9 135116338 135116347 deletion of <=200bp AACGAGACCG - upstream_gene_variant GACA-CN 9 135114496 135114496 single base substitution G T stop_gained E346* 1036G>T GACA-CN 9 135114496 135114496 single base substitution G T stop_gained E354* 1060G>T GACA-CN 9 135114496 135114496 single base substitution G T stop_gained E360* 1078G>T GACA-CN 9 135114496 135114496 single base substitution G T upstream_gene_variant GBM-US 9 135042315 135042315 single base substitution A C missense_variant T33P 97A>C GBM-US 9 135073844 135073844 single base substitution G A synonymous_variant T235T 705G>A GBM-US 9 135073896 135073896 single base substitution C T missense_variant R253C 757C>T KIRC-US 9 135102354 135102354 single base substitution C A synonymous_variant R326R 976C>A LAML-KR 9 135049243 135049243 single base substitution T C intron_variant LAML-KR 9 135049509 135049509 single base substitution A G intron_variant LAML-KR 9 135056726 135056726 single base substitution G T intron_variant LAML-KR 9 135061226 135061226 single base substitution T G intron_variant LAML-KR 9 135070896 135070896 single base substitution A T intron_variant LAML-KR 9 135094853 135094853 single base substitution A G intron_variant LAML-KR 9 135094855 135094855 single base substitution C G intron_variant LAML-KR 9 135103976 135103976 single base substitution A C intron_variant LAML-KR 9 135116594 135116594 single base substitution A G intron_variant LAML-KR 9 135116594 135116594 single base substitution A G upstream_gene_variant LICA-CN 9 135073493 135073493 single base substitution G T synonymous_variant P118P 354G>T LICA-CN 9 135116336 135116336 single base substitution G T exon_variant LICA-CN 9 135116336 135116336 single base substitution G T missense_variant C413F 1238G>T LICA-CN 9 135116336 135116336 single base substitution G T missense_variant C421F 1262G>T LICA-CN 9 135116336 135116336 single base substitution G T missense_variant C427F 1280G>T LICA-CN 9 135116336 135116336 single base substitution G T upstream_gene_variant LICA-CN 9 135116365 135116365 single base substitution G T exon_variant LICA-CN 9 135116365 135116365 single base substitution G T stop_gained E423* 1267G>T LICA-CN 9 135116365 135116365 single base substitution G T stop_gained E431* 1291G>T LICA-CN 9 135116365 135116365 single base substitution G T stop_gained E437* 1309G>T LICA-CN 9 135116365 135116365 single base substitution G T upstream_gene_variant LICA-CN 9 135116377 135116377 single base substitution G T exon_variant LICA-CN 9 135116377 135116377 single base substitution G T missense_variant G427C 1279G>T LICA-CN 9 135116377 135116377 single base substitution G T missense_variant G435C 1303G>T LICA-CN 9 135116377 135116377 single base substitution G T missense_variant G441C 1321G>T LICA-CN 9 135116377 135116377 single base substitution G T upstream_gene_variant LICA-FR 9 135034081 135034081 single base substitution T A upstream_gene_variant LICA-FR 9 135075189 135075189 single base substitution T G intron_variant LICA-FR 9 135102022 135102022 single base substitution C T intron_variant LICA-FR 9 135122450 135122450 single base substitution G A downstream_gene_variant LIHC-US 9 135116364 135116364 single base substitution C A exon_variant LIHC-US 9 135116364 135116364 single base substitution C A synonymous_variant R422R 1266C>A LIHC-US 9 135116364 135116364 single base substitution C A synonymous_variant R430R 1290C>A LIHC-US 9 135116364 135116364 single base substitution C A synonymous_variant R436R 1308C>A LIHC-US 9 135116364 135116364 single base substitution C A upstream_gene_variant LIHC-US 9 135117276 135117276 single base substitution C A exon_variant LIHC-US 9 135117276 135117276 single base substitution C A missense_variant D449E 1347C>A LIHC-US 9 135117276 135117276 single base substitution C A missense_variant D457E 1371C>A LIHC-US 9 135117276 135117276 single base substitution C A missense_variant D463E 1389C>A LINC-JP 9 135042211 135042211 single base substitution G A 5_prime_UTR_variant LINC-JP 9 135050335 135050335 single base substitution T C intron_variant LINC-JP 9 135064455 135064455 single base substitution C T intron_variant LINC-JP 9 135073263 135073263 single base substitution T C intron_variant LINC-JP 9 135079221 135079221 single base substitution G A intron_variant LINC-JP 9 135086979 135086979 single base substitution C G intron_variant LINC-JP 9 135093536 135093536 single base substitution A G intron_variant LINC-JP 9 135114689 135114689 single base substitution T G intron_variant LINC-JP 9 135114689 135114689 single base substitution T G upstream_gene_variant LINC-JP 9 135114728 135114728 single base substitution G T intron_variant LINC-JP 9 135114728 135114728 single base substitution G T upstream_gene_variant LIRI-JP 9 135033892 135033892 single base substitution A G upstream_gene_variant LIRI-JP 9 135034070 135034070 single base substitution C G upstream_gene_variant LIRI-JP 9 135035062 135035062 single base substitution A G upstream_gene_variant LIRI-JP 9 135036022 135036022 single base substitution A T upstream_gene_variant LIRI-JP 9 135036556 135036556 single base substitution C G upstream_gene_variant LIRI-JP 9 135039420 135039420 single base substitution C A intron_variant LIRI-JP 9 135040249 135040249 single base substitution G A intron_variant LIRI-JP 9 135041951 135041951 single base substitution G T 5_prime_UTR_premature_start_codon_gain_variant LIRI-JP 9 135042765 135042765 single base substitution T C intron_variant LIRI-JP 9 135042939 135042939 single base substitution C T intron_variant LIRI-JP 9 135043760 135043760 single base substitution T C intron_variant LIRI-JP 9 135043841 135043841 single base substitution G A intron_variant LIRI-JP 9 135045539 135045539 single base substitution C T intron_variant LIRI-JP 9 135046543 135046543 single base substitution G T intron_variant LIRI-JP 9 135047811 135047811 single base substitution C T intron_variant LIRI-JP 9 135048661 135048661 single base substitution C T intron_variant LIRI-JP 9 135050411 135050411 single base substitution G A intron_variant LIRI-JP 9 135051912 135051912 single base substitution T C intron_variant LIRI-JP 9 135053009 135053009 single base substitution A G intron_variant LIRI-JP 9 135055707 135055707 single base substitution C A intron_variant LIRI-JP 9 135058881 135058881 single base substitution C A intron_variant LIRI-JP 9 135061049 135061049 single base substitution T C intron_variant LIRI-JP 9 135061625 135061625 single base substitution G A intron_variant LIRI-JP 9 135062636 135062636 single base substitution G C intron_variant LIRI-JP 9 135064306 135064306 single base substitution G A intron_variant LIRI-JP 9 135064995 135064995 single base substitution G T intron_variant LIRI-JP 9 135066418 135066418 single base substitution G T intron_variant LIRI-JP 9 135068822 135068822 single base substitution A G intron_variant LIRI-JP 9 135072148 135072148 single base substitution A G intron_variant LIRI-JP 9 135072424 135072424 single base substitution G A intron_variant LIRI-JP 9 135077697 135077697 single base substitution C G intron_variant LIRI-JP 9 135079042 135079042 single base substitution G A intron_variant LIRI-JP 9 135079785 135079785 single base substitution G A intron_variant LIRI-JP 9 135080601 135080601 single base substitution T C intron_variant LIRI-JP 9 135080706 135080706 single base substitution A G intron_variant LIRI-JP 9 135080810 135080810 single base substitution A G intron_variant LIRI-JP 9 135083131 135083131 single base substitution G A intron_variant LIRI-JP 9 135084091 135084091 single base substitution T G intron_variant LIRI-JP 9 135084469 135084469 single base substitution C T intron_variant LIRI-JP 9 135085617 135085617 single base substitution C T intron_variant LIRI-JP 9 135087416 135087416 single base substitution G T intron_variant LIRI-JP 9 135089688 135089688 single base substitution G T intron_variant LIRI-JP 9 135089822 135089822 single base substitution G C intron_variant LIRI-JP 9 135090057 135090057 single base substitution G A intron_variant LIRI-JP 9 135091161 135091161 single base substitution C A intron_variant LIRI-JP 9 135091710 135091710 single base substitution C T intron_variant LIRI-JP 9 135093240 135093240 single base substitution G T intron_variant LIRI-JP 9 135095731 135095731 single base substitution T G intron_variant LIRI-JP 9 135099816 135099816 single base substitution C T intron_variant LIRI-JP 9 135099949 135099949 single base substitution T C intron_variant LIRI-JP 9 135100689 135100689 single base substitution G A intron_variant LIRI-JP 9 135101401 135101401 single base substitution G T intron_variant LIRI-JP 9 135101845 135101845 single base substitution C T intron_variant LIRI-JP 9 135102163 135102163 single base substitution C A intron_variant LIRI-JP 9 135102299 135102299 single base substitution C T synonymous_variant C307C 921C>T LIRI-JP 9 135102355 135102355 single base substitution G T missense_variant R326L 977G>T LIRI-JP 9 135102622 135102622 single base substitution A G intron_variant LIRI-JP 9 135110337 135110337 single base substitution T A downstream_gene_variant LIRI-JP 9 135110337 135110337 single base substitution T A intron_variant LIRI-JP 9 135111492 135111492 single base substitution G T downstream_gene_variant LIRI-JP 9 135111492 135111492 single base substitution G T intron_variant LIRI-JP 9 135111492 135111492 single base substitution G T upstream_gene_variant LIRI-JP 9 135111953 135111953 single base substitution T C intron_variant LIRI-JP 9 135111953 135111953 single base substitution T C upstream_gene_variant LIRI-JP 9 135112183 135112183 single base substitution G A intron_variant LIRI-JP 9 135112183 135112183 single base substitution G A upstream_gene_variant LIRI-JP 9 135114605 135114605 single base substitution T G missense_variant L382R 1145T>G LIRI-JP 9 135114605 135114605 single base substitution T G missense_variant L390R 1169T>G LIRI-JP 9 135114605 135114605 single base substitution T G missense_variant L396R 1187T>G LIRI-JP 9 135114605 135114605 single base substitution T G upstream_gene_variant LIRI-JP 9 135115081 135115081 single base substitution C A intron_variant LIRI-JP 9 135115081 135115081 single base substitution C A upstream_gene_variant LIRI-JP 9 135115685 135115685 single base substitution T C intron_variant LIRI-JP 9 135115685 135115685 single base substitution T C upstream_gene_variant LIRI-JP 9 135118011 135118011 single base substitution G T 3_prime_UTR_variant LIRI-JP 9 135118011 135118011 single base substitution G T downstream_gene_variant LIRI-JP 9 135121230 135121230 single base substitution G A downstream_gene_variant LIRI-JP 9 135123360 135123360 single base substitution A C downstream_gene_variant LIRI-JP 9 135124387 135124387 single base substitution G A downstream_gene_variant LUSC-KR 9 135041860 135041860 single base substitution G A 5_prime_UTR_variant LUSC-KR 9 135043419 135043419 single base substitution G A intron_variant LUSC-KR 9 135046176 135046176 single base substitution C T intron_variant LUSC-KR 9 135046284 135046284 single base substitution G T intron_variant LUSC-KR 9 135048744 135048744 single base substitution G T intron_variant LUSC-KR 9 135049466 135049466 single base substitution C T intron_variant LUSC-KR 9 135050647 135050647 single base substitution G A intron_variant LUSC-KR 9 135056726 135056726 single base substitution G T intron_variant LUSC-KR 9 135060049 135060049 single base substitution G C intron_variant LUSC-KR 9 135060467 135060467 single base substitution G A intron_variant LUSC-KR 9 135061244 135061244 single base substitution T G intron_variant LUSC-KR 9 135061282 135061282 single base substitution A G intron_variant LUSC-KR 9 135064320 135064320 single base substitution C T intron_variant LUSC-KR 9 135073611 135073611 single base substitution G T missense_variant G158W 472G>T LUSC-KR 9 135080768 135080768 single base substitution C T intron_variant LUSC-KR 9 135081895 135081895 single base substitution G C intron_variant LUSC-KR 9 135081915 135081915 single base substitution G T intron_variant LUSC-KR 9 135083131 135083131 single base substitution G T intron_variant LUSC-KR 9 135083747 135083747 single base substitution C T intron_variant LUSC-KR 9 135084194 135084194 single base substitution G T intron_variant LUSC-KR 9 135084807 135084807 single base substitution C A intron_variant LUSC-KR 9 135086525 135086525 single base substitution G A intron_variant LUSC-KR 9 135088427 135088427 single base substitution C T intron_variant LUSC-KR 9 135091616 135091616 single base substitution C G intron_variant LUSC-KR 9 135092604 135092604 single base substitution G T intron_variant LUSC-KR 9 135093186 135093186 single base substitution G A intron_variant LUSC-KR 9 135093239 135093239 single base substitution G T intron_variant LUSC-KR 9 135103481 135103481 single base substitution C G intron_variant LUSC-KR 9 135103931 135103931 single base substitution A C intron_variant LUSC-KR 9 135111915 135111915 single base substitution C A intron_variant LUSC-KR 9 135111915 135111915 single base substitution C A upstream_gene_variant LUSC-KR 9 135113285 135113285 single base substitution C A intron_variant LUSC-KR 9 135113285 135113285 single base substitution C A upstream_gene_variant LUSC-KR 9 135117399 135117399 single base substitution C A exon_variant LUSC-KR 9 135117399 135117399 single base substitution C A synonymous_variant G490G 1470C>A LUSC-KR 9 135117399 135117399 single base substitution C A synonymous_variant G498G 1494C>A LUSC-KR 9 135117399 135117399 single base substitution C A synonymous_variant G504G 1512C>A LUSC-KR 9 135121811 135121811 single base substitution T G downstream_gene_variant LUSC-KR 9 135123409 135123409 single base substitution G T downstream_gene_variant LUSC-US 9 135073791 135073791 single base substitution C A missense_variant R218S 652C>A LUSC-US 9 135073852 135073852 single base substitution A G missense_variant E238G 713A>G LUSC-US 9 135114558 135114558 single base substitution C T synonymous_variant V366V 1098C>T LUSC-US 9 135114558 135114558 single base substitution C T synonymous_variant V374V 1122C>T LUSC-US 9 135114558 135114558 single base substitution C T synonymous_variant V380V 1140C>T LUSC-US 9 135114558 135114558 single base substitution C T upstream_gene_variant MALY-DE 9 135032643 135032643 single base substitution G A upstream_gene_variant MALY-DE 9 135033082 135033082 single base substitution T C upstream_gene_variant MALY-DE 9 135043975 135043975 single base substitution G A intron_variant MALY-DE 9 135046098 135046099 deletion of <=200bp GA - intron_variant MALY-DE 9 135049098 135049098 single base substitution C T intron_variant MALY-DE 9 135052542 135052542 single base substitution T A intron_variant MALY-DE 9 135056291 135056292 deletion of <=200bp CA - intron_variant MALY-DE 9 135057348 135057349 deletion of <=200bp TG - intron_variant MALY-DE 9 135057501 135057501 single base substitution A G intron_variant MALY-DE 9 135058809 135058809 single base substitution T A intron_variant MALY-DE 9 135070681 135070681 insertion of <=200bp - T intron_variant MALY-DE 9 135071548 135071548 deletion of <=200bp T - intron_variant MALY-DE 9 135074392 135074392 single base substitution C T intron_variant MALY-DE 9 135075326 135075326 single base substitution A T intron_variant MALY-DE 9 135077104 135077104 single base substitution G A intron_variant MALY-DE 9 135080389 135080389 single base substitution G A intron_variant MALY-DE 9 135094376 135094376 single base substitution G A intron_variant MALY-DE 9 135096603 135096603 single base substitution G T intron_variant MALY-DE 9 135096845 135096845 single base substitution T A intron_variant MALY-DE 9 135102676 135102676 single base substitution C T intron_variant MALY-DE 9 135103175 135103175 single base substitution C T intron_variant MALY-DE 9 135119119 135119119 single base substitution C T 3_prime_UTR_variant MALY-DE 9 135119119 135119119 single base substitution C T downstream_gene_variant MALY-DE 9 135121498 135121498 single base substitution A G downstream_gene_variant MELA-AU 9 135032415 135032415 single base substitution G A upstream_gene_variant MELA-AU 9 135032678 135032678 single base substitution C T upstream_gene_variant MELA-AU 9 135032717 135032718 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 9 135032742 135032742 single base substitution G A upstream_gene_variant MELA-AU 9 135033052 135033052 single base substitution G A upstream_gene_variant MELA-AU 9 135033596 135033596 single base substitution T A upstream_gene_variant MELA-AU 9 135033751 135033751 single base substitution G A upstream_gene_variant MELA-AU 9 135033839 135033840 multiple base substitution (>=2bp and <=200bp) TT CC upstream_gene_variant MELA-AU 9 135033913 135033913 single base substitution C T upstream_gene_variant MELA-AU 9 135033930 135033930 single base substitution G A upstream_gene_variant MELA-AU 9 135033943 135033943 single base substitution G A upstream_gene_variant MELA-AU 9 135034118 135034118 single base substitution G A upstream_gene_variant MELA-AU 9 135034147 135034147 single base substitution C T upstream_gene_variant MELA-AU 9 135034234 135034234 single base substitution C A upstream_gene_variant MELA-AU 9 135034542 135034542 single base substitution G A upstream_gene_variant MELA-AU 9 135034957 135034957 single base substitution G A upstream_gene_variant MELA-AU 9 135035103 135035103 single base substitution T C upstream_gene_variant MELA-AU 9 135035173 135035173 single base substitution G A upstream_gene_variant MELA-AU 9 135035420 135035420 single base substitution G A upstream_gene_variant MELA-AU 9 135035582 135035582 single base substitution G A upstream_gene_variant MELA-AU 9 135035700 135035700 single base substitution C T upstream_gene_variant MELA-AU 9 135035708 135035708 single base substitution C T upstream_gene_variant MELA-AU 9 135036407 135036407 single base substitution G A upstream_gene_variant MELA-AU 9 135036754 135036755 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 9 135036776 135036776 single base substitution G A upstream_gene_variant MELA-AU 9 135037100 135037100 single base substitution G A upstream_gene_variant MELA-AU 9 135038296 135038296 single base substitution G A intron_variant MELA-AU 9 135039027 135039027 single base substitution C T intron_variant MELA-AU 9 135039032 135039032 single base substitution G A intron_variant MELA-AU 9 135039514 135039514 single base substitution C T intron_variant MELA-AU 9 135039722 135039722 single base substitution C T intron_variant MELA-AU 9 135039866 135039866 single base substitution C T intron_variant MELA-AU 9 135040164 135040164 single base substitution G A intron_variant MELA-AU 9 135040361 135040361 single base substitution G A intron_variant MELA-AU 9 135040754 135040754 single base substitution C T intron_variant MELA-AU 9 135041365 135041366 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 9 135041859 135041859 single base substitution G A 5_prime_UTR_variant MELA-AU 9 135042135 135042135 single base substitution C T 5_prime_UTR_variant MELA-AU 9 135042139 135042139 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant MELA-AU 9 135042153 135042153 single base substitution C T 5_prime_UTR_variant MELA-AU 9 135042154 135042154 single base substitution C T 5_prime_UTR_variant MELA-AU 9 135042493 135042493 single base substitution C T intron_variant MELA-AU 9 135042525 135042525 single base substitution A C intron_variant MELA-AU 9 135042902 135042902 single base substitution C T intron_variant MELA-AU 9 135043064 135043064 single base substitution G A intron_variant MELA-AU 9 135043119 135043119 single base substitution C T intron_variant MELA-AU 9 135043733 135043734 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 9 135044023 135044023 single base substitution G A intron_variant MELA-AU 9 135044846 135044846 single base substitution C T intron_variant MELA-AU 9 135045015 135045015 single base substitution C G intron_variant MELA-AU 9 135045560 135045560 single base substitution G A intron_variant MELA-AU 9 135045590 135045590 single base substitution C T intron_variant MELA-AU 9 135045645 135045645 single base substitution G A intron_variant MELA-AU 9 135045650 135045650 single base substitution G A intron_variant MELA-AU 9 135045803 135045803 single base substitution C T intron_variant MELA-AU 9 135045810 135045810 single base substitution C T intron_variant MELA-AU 9 135045822 135045822 single base substitution C T intron_variant MELA-AU 9 135045835 135045835 single base substitution C T intron_variant MELA-AU 9 135045872 135045872 single base substitution C T intron_variant MELA-AU 9 135046084 135046084 single base substitution G A intron_variant MELA-AU 9 135046156 135046157 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 9 135046733 135046733 single base substitution G A intron_variant MELA-AU 9 135046919 135046919 single base substitution G A intron_variant MELA-AU 9 135047181 135047181 single base substitution G A intron_variant MELA-AU 9 135047219 135047219 single base substitution G A intron_variant MELA-AU 9 135047494 135047494 single base substitution C T intron_variant MELA-AU 9 135048032 135048032 single base substitution C T intron_variant MELA-AU 9 135048147 135048147 single base substitution C T intron_variant MELA-AU 9 135048208 135048208 single base substitution C T intron_variant MELA-AU 9 135048357 135048357 single base substitution C T intron_variant MELA-AU 9 135048613 135048613 single base substitution G C intron_variant MELA-AU 9 135048725 135048725 single base substitution G A intron_variant MELA-AU 9 135048955 135048955 single base substitution C T intron_variant MELA-AU 9 135049060 135049060 single base substitution C T intron_variant MELA-AU 9 135049227 135049227 single base substitution G A intron_variant MELA-AU 9 135049380 135049380 single base substitution G A intron_variant MELA-AU 9 135049606 135049606 single base substitution G A intron_variant MELA-AU 9 135049676 135049676 single base substitution G A intron_variant MELA-AU 9 135049880 135049880 single base substitution C T intron_variant MELA-AU 9 135049895 135049895 single base substitution C T intron_variant MELA-AU 9 135049898 135049898 single base substitution G A intron_variant MELA-AU 9 135050130 135050130 single base substitution G A intron_variant MELA-AU 9 135050413 135050413 single base substitution C T intron_variant MELA-AU 9 135050903 135050903 single base substitution G T intron_variant MELA-AU 9 135051195 135051195 single base substitution G A intron_variant MELA-AU 9 135051539 135051539 single base substitution C T intron_variant MELA-AU 9 135051697 135051697 single base substitution C T intron_variant MELA-AU 9 135051745 135051745 single base substitution C T intron_variant MELA-AU 9 135052019 135052019 single base substitution G A intron_variant MELA-AU 9 135052084 135052084 single base substitution G A intron_variant MELA-AU 9 135052156 135052156 single base substitution C T intron_variant MELA-AU 9 135052319 135052319 single base substitution C T intron_variant MELA-AU 9 135052425 135052425 single base substitution G A intron_variant MELA-AU 9 135052577 135052577 single base substitution T C intron_variant MELA-AU 9 135052843 135052843 insertion of <=200bp - T intron_variant MELA-AU 9 135053546 135053546 single base substitution G C intron_variant MELA-AU 9 135053694 135053695 multiple base substitution (>=2bp and <=200bp) CC TA intron_variant MELA-AU 9 135053889 135053889 single base substitution C T intron_variant MELA-AU 9 135054087 135054087 single base substitution G A intron_variant MELA-AU 9 135055321 135055321 single base substitution C T intron_variant MELA-AU 9 135055405 135055405 single base substitution C T intron_variant MELA-AU 9 135055913 135055914 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 9 135055977 135055977 single base substitution C T intron_variant MELA-AU 9 135055997 135055997 single base substitution T C intron_variant MELA-AU 9 135055998 135055998 single base substitution C T intron_variant MELA-AU 9 135056343 135056343 single base substitution C T intron_variant MELA-AU 9 135056516 135056516 single base substitution G A intron_variant MELA-AU 9 135056876 135056876 single base substitution T A intron_variant MELA-AU 9 135056906 135056906 single base substitution C T intron_variant MELA-AU 9 135057181 135057181 single base substitution A G intron_variant MELA-AU 9 135057627 135057627 single base substitution G A intron_variant MELA-AU 9 135057628 135057628 single base substitution G C intron_variant MELA-AU 9 135058005 135058005 single base substitution C T intron_variant MELA-AU 9 135058202 135058202 single base substitution C G intron_variant MELA-AU 9 135058992 135058992 single base substitution T G intron_variant MELA-AU 9 135059033 135059033 single base substitution G A intron_variant MELA-AU 9 135059152 135059152 single base substitution C T intron_variant MELA-AU 9 135059157 135059157 single base substitution G A intron_variant MELA-AU 9 135059310 135059310 single base substitution G A intron_variant MELA-AU 9 135059354 135059354 single base substitution C T intron_variant MELA-AU 9 135059572 135059572 single base substitution C T intron_variant MELA-AU 9 135059735 135059735 single base substitution G A intron_variant MELA-AU 9 135059768 135059768 single base substitution C T intron_variant MELA-AU 9 135060195 135060195 single base substitution G A intron_variant MELA-AU 9 135060620 135060620 single base substitution C T intron_variant MELA-AU 9 135060725 135060725 single base substitution G A intron_variant MELA-AU 9 135060834 135060834 single base substitution C T intron_variant MELA-AU 9 135061089 135061089 single base substitution C T intron_variant MELA-AU 9 135061281 135061281 single base substitution G A intron_variant MELA-AU 9 135061803 135061803 single base substitution C T intron_variant MELA-AU 9 135062042 135062042 single base substitution G T intron_variant MELA-AU 9 135062280 135062280 single base substitution G A intron_variant MELA-AU 9 135062284 135062284 single base substitution G C intron_variant MELA-AU 9 135062545 135062546 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 9 135063191 135063191 single base substitution G A intron_variant MELA-AU 9 135063235 135063235 single base substitution G A intron_variant MELA-AU 9 135063269 135063269 single base substitution G A intron_variant MELA-AU 9 135063401 135063401 single base substitution C T intron_variant MELA-AU 9 135063544 135063544 single base substitution C T intron_variant MELA-AU 9 135063617 135063617 single base substitution C T intron_variant MELA-AU 9 135063817 135063817 single base substitution G A intron_variant MELA-AU 9 135064028 135064028 single base substitution G A intron_variant MELA-AU 9 135064442 135064442 single base substitution G A intron_variant MELA-AU 9 135064635 135064635 single base substitution C T intron_variant MELA-AU 9 135064649 135064649 single base substitution G A intron_variant MELA-AU 9 135064990 135064990 single base substitution C T intron_variant MELA-AU 9 135065129 135065129 single base substitution T C intron_variant MELA-AU 9 135065728 135065728 single base substitution G A intron_variant MELA-AU 9 135065820 135065820 single base substitution C T intron_variant MELA-AU 9 135065823 135065824 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 9 135066038 135066038 single base substitution G A intron_variant MELA-AU 9 135066259 135066259 single base substitution C T intron_variant MELA-AU 9 135066394 135066395 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 9 135066746 135066746 single base substitution C T intron_variant MELA-AU 9 135066755 135066755 single base substitution G A intron_variant MELA-AU 9 135066793 135066793 single base substitution C T intron_variant MELA-AU 9 135067313 135067313 single base substitution G A intron_variant MELA-AU 9 135067434 135067434 single base substitution C T intron_variant MELA-AU 9 135067520 135067520 single base substitution G A intron_variant MELA-AU 9 135067676 135067676 single base substitution C T intron_variant MELA-AU 9 135067736 135067736 single base substitution G A intron_variant MELA-AU 9 135067799 135067799 single base substitution G A intron_variant MELA-AU 9 135068338 135068338 single base substitution C T intron_variant MELA-AU 9 135068487 135068487 single base substitution C T intron_variant MELA-AU 9 135068727 135068727 single base substitution G T intron_variant MELA-AU 9 135068895 135068895 single base substitution G A intron_variant MELA-AU 9 135068930 135068930 single base substitution G A intron_variant MELA-AU 9 135069083 135069083 single base substitution C T intron_variant MELA-AU 9 135069636 135069636 single base substitution C T intron_variant MELA-AU 9 135069743 135069743 single base substitution G A intron_variant MELA-AU 9 135069825 135069825 single base substitution G A intron_variant MELA-AU 9 135069843 135069844 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 9 135069920 135069920 single base substitution C T intron_variant MELA-AU 9 135070589 135070589 single base substitution C T intron_variant MELA-AU 9 135071048 135071048 single base substitution C T intron_variant MELA-AU 9 135071308 135071308 single base substitution C T intron_variant MELA-AU 9 135071641 135071641 single base substitution G A intron_variant MELA-AU 9 135071800 135071800 single base substitution G A intron_variant MELA-AU 9 135071821 135071821 single base substitution C T intron_variant MELA-AU 9 135072043 135072043 single base substitution C T intron_variant MELA-AU 9 135072597 135072597 single base substitution G A intron_variant MELA-AU 9 135072603 135072603 single base substitution C T intron_variant MELA-AU 9 135072639 135072639 single base substitution G A intron_variant MELA-AU 9 135072690 135072690 single base substitution C T intron_variant MELA-AU 9 135072695 135072695 single base substitution G A intron_variant MELA-AU 9 135072963 135072963 single base substitution C T intron_variant MELA-AU 9 135072970 135072970 single base substitution G A intron_variant MELA-AU 9 135073162 135073162 single base substitution G A intron_variant MELA-AU 9 135073415 135073415 single base substitution C A synonymous_variant P92P 276C>A MELA-AU 9 135073580 135073580 single base substitution G A synonymous_variant T147T 441G>A MELA-AU 9 135073600 135073600 single base substitution C T missense_variant S154F 461C>T MELA-AU 9 135073664 135073664 single base substitution C T synonymous_variant F175F 525C>T MELA-AU 9 135073760 135073760 single base substitution G A synonymous_variant K207K 621G>A MELA-AU 9 135073769 135073769 single base substitution C T synonymous_variant H210H 630C>T MELA-AU 9 135073882 135073882 single base substitution C T missense_variant T248I 743C>T MELA-AU 9 135073952 135073952 single base substitution C T synonymous_variant L271L 813C>T MELA-AU 9 135074066 135074066 single base substitution G A intron_variant MELA-AU 9 135074168 135074168 single base substitution C T intron_variant MELA-AU 9 135074216 135074216 single base substitution G A intron_variant MELA-AU 9 135074786 135074786 single base substitution A T intron_variant MELA-AU 9 135075007 135075007 single base substitution C T intron_variant MELA-AU 9 135075781 135075781 single base substitution G A intron_variant MELA-AU 9 135075891 135075891 single base substitution C T intron_variant MELA-AU 9 135075902 135075902 single base substitution A G intron_variant MELA-AU 9 135076083 135076083 single base substitution G A intron_variant MELA-AU 9 135076090 135076090 single base substitution G A intron_variant MELA-AU 9 135076480 135076480 single base substitution A G intron_variant MELA-AU 9 135076536 135076536 single base substitution G A intron_variant MELA-AU 9 135076590 135076590 single base substitution G A intron_variant MELA-AU 9 135076660 135076660 single base substitution G A intron_variant MELA-AU 9 135076686 135076686 single base substitution C T intron_variant MELA-AU 9 135076872 135076872 single base substitution G A intron_variant MELA-AU 9 135076964 135076964 single base substitution C T intron_variant MELA-AU 9 135076986 135076986 single base substitution G A intron_variant MELA-AU 9 135077676 135077676 single base substitution G A intron_variant MELA-AU 9 135077917 135077917 single base substitution G A intron_variant MELA-AU 9 135078599 135078599 single base substitution C A intron_variant MELA-AU 9 135078822 135078822 single base substitution G A intron_variant MELA-AU 9 135079295 135079295 single base substitution G A intron_variant MELA-AU 9 135079322 135079322 single base substitution G A intron_variant MELA-AU 9 135079375 135079375 single base substitution C T intron_variant MELA-AU 9 135079477 135079477 single base substitution G A intron_variant MELA-AU 9 135079698 135079698 single base substitution C T intron_variant MELA-AU 9 135079707 135079707 single base substitution C T intron_variant MELA-AU 9 135079713 135079713 single base substitution C T intron_variant MELA-AU 9 135079719 135079719 single base substitution C T intron_variant MELA-AU 9 135079905 135079905 single base substitution C T intron_variant MELA-AU 9 135079955 135079955 single base substitution G A intron_variant MELA-AU 9 135080005 135080005 single base substitution G A intron_variant MELA-AU 9 135080198 135080198 single base substitution C T intron_variant MELA-AU 9 135080266 135080266 single base substitution C T intron_variant MELA-AU 9 135080397 135080397 single base substitution C T intron_variant MELA-AU 9 135080618 135080618 single base substitution A G intron_variant MELA-AU 9 135080801 135080801 single base substitution C T intron_variant MELA-AU 9 135081047 135081047 single base substitution C T intron_variant MELA-AU 9 135081239 135081239 single base substitution G A intron_variant MELA-AU 9 135081251 135081251 single base substitution G A intron_variant MELA-AU 9 135081414 135081414 single base substitution A G intron_variant MELA-AU 9 135081721 135081721 single base substitution C T intron_variant MELA-AU 9 135082066 135082066 single base substitution A G intron_variant MELA-AU 9 135082217 135082217 single base substitution C T intron_variant MELA-AU 9 135082282 135082282 single base substitution G A intron_variant MELA-AU 9 135082294 135082294 single base substitution C T intron_variant MELA-AU 9 135082367 135082368 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 9 135082470 135082470 single base substitution C T intron_variant MELA-AU 9 135082507 135082507 single base substitution C T intron_variant MELA-AU 9 135082727 135082727 single base substitution G T intron_variant MELA-AU 9 135082880 135082880 single base substitution C T intron_variant MELA-AU 9 135083056 135083056 single base substitution C A intron_variant MELA-AU 9 135083068 135083068 single base substitution C T intron_variant MELA-AU 9 135083401 135083401 single base substitution G A intron_variant MELA-AU 9 135083418 135083418 single base substitution G A intron_variant MELA-AU 9 135083568 135083568 single base substitution G A intron_variant MELA-AU 9 135083986 135083986 single base substitution G A intron_variant MELA-AU 9 135084052 135084052 single base substitution G A intron_variant MELA-AU 9 135084268 135084268 single base substitution G A intron_variant MELA-AU 9 135084319 135084319 single base substitution C T intron_variant MELA-AU 9 135084347 135084347 single base substitution C T intron_variant MELA-AU 9 135084707 135084707 single base substitution T C intron_variant MELA-AU 9 135084847 135084847 single base substitution G A intron_variant MELA-AU 9 135084928 135084928 single base substitution C T intron_variant MELA-AU 9 135084970 135084970 single base substitution C T intron_variant MELA-AU 9 135085120 135085120 single base substitution G A intron_variant MELA-AU 9 135085166 135085166 single base substitution G A intron_variant MELA-AU 9 135085805 135085805 single base substitution G A intron_variant MELA-AU 9 135085978 135085978 single base substitution C T intron_variant MELA-AU 9 135086019 135086019 single base substitution C T intron_variant MELA-AU 9 135086233 135086233 single base substitution C T intron_variant MELA-AU 9 135086542 135086542 single base substitution C T intron_variant MELA-AU 9 135086633 135086633 single base substitution C T intron_variant MELA-AU 9 135087045 135087045 single base substitution G A intron_variant MELA-AU 9 135087110 135087111 multiple base substitution (>=2bp and <=200bp) GG AC intron_variant MELA-AU 9 135087267 135087267 single base substitution C T intron_variant MELA-AU 9 135087387 135087387 single base substitution G A intron_variant MELA-AU 9 135087493 135087493 single base substitution C T intron_variant MELA-AU 9 135087511 135087511 single base substitution C T intron_variant MELA-AU 9 135087524 135087524 single base substitution C T intron_variant MELA-AU 9 135087574 135087574 single base substitution C T intron_variant MELA-AU 9 135087898 135087898 single base substitution G A intron_variant MELA-AU 9 135087996 135087997 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 9 135088048 135088048 single base substitution C T intron_variant MELA-AU 9 135088098 135088098 single base substitution C T intron_variant MELA-AU 9 135088326 135088326 single base substitution A T intron_variant MELA-AU 9 135088494 135088494 single base substitution C T intron_variant MELA-AU 9 135088511 135088511 single base substitution A G intron_variant MELA-AU 9 135088889 135088889 single base substitution C T intron_variant MELA-AU 9 135088891 135088891 single base substitution T A intron_variant MELA-AU 9 135088912 135088912 single base substitution C T intron_variant MELA-AU 9 135089031 135089031 single base substitution G A intron_variant MELA-AU 9 135089067 135089067 single base substitution G A intron_variant MELA-AU 9 135089147 135089147 single base substitution G A intron_variant MELA-AU 9 135089250 135089250 single base substitution G A intron_variant MELA-AU 9 135089417 135089417 single base substitution C T intron_variant MELA-AU 9 135089466 135089466 single base substitution C T intron_variant MELA-AU 9 135089502 135089502 single base substitution C T intron_variant MELA-AU 9 135089537 135089537 single base substitution G A intron_variant MELA-AU 9 135089585 135089585 single base substitution C T intron_variant MELA-AU 9 135089634 135089634 single base substitution C T intron_variant MELA-AU 9 135090120 135090120 single base substitution G A intron_variant MELA-AU 9 135090498 135090498 single base substitution G A intron_variant MELA-AU 9 135090795 135090795 single base substitution C T intron_variant MELA-AU 9 135090922 135090922 single base substitution G A intron_variant MELA-AU 9 135091072 135091072 single base substitution A T intron_variant MELA-AU 9 135091096 135091097 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 9 135091165 135091165 single base substitution C T intron_variant MELA-AU 9 135091239 135091239 single base substitution C T intron_variant MELA-AU 9 135091609 135091610 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 9 135091801 135091801 single base substitution C G intron_variant MELA-AU 9 135091930 135091930 single base substitution G A intron_variant MELA-AU 9 135092093 135092093 single base substitution G T intron_variant MELA-AU 9 135092163 135092163 single base substitution G A intron_variant MELA-AU 9 135092972 135092972 single base substitution T G intron_variant MELA-AU 9 135092993 135092993 single base substitution G A intron_variant MELA-AU 9 135093698 135093698 single base substitution C T intron_variant MELA-AU 9 135094083 135094083 single base substitution C T intron_variant MELA-AU 9 135094774 135094774 single base substitution A G intron_variant MELA-AU 9 135094959 135094959 single base substitution C T intron_variant MELA-AU 9 135095165 135095165 single base substitution C T intron_variant MELA-AU 9 135095315 135095315 single base substitution A T intron_variant MELA-AU 9 135095396 135095396 single base substitution C T intron_variant MELA-AU 9 135095509 135095509 single base substitution C T intron_variant MELA-AU 9 135095510 135095510 single base substitution C A intron_variant MELA-AU 9 135095548 135095548 single base substitution C T intron_variant MELA-AU 9 135096101 135096101 single base substitution C T intron_variant MELA-AU 9 135096572 135096572 single base substitution C G intron_variant MELA-AU 9 135096624 135096638 deletion of <=200bp CATTCCAGGCAGAGG - intron_variant MELA-AU 9 135096731 135096731 single base substitution G A intron_variant MELA-AU 9 135096790 135096790 single base substitution C T intron_variant MELA-AU 9 135096970 135096970 single base substitution A G intron_variant MELA-AU 9 135097237 135097237 single base substitution G A intron_variant MELA-AU 9 135097241 135097241 single base substitution C T intron_variant MELA-AU 9 135097360 135097360 single base substitution G A intron_variant MELA-AU 9 135097361 135097361 single base substitution G A intron_variant MELA-AU 9 135097512 135097512 single base substitution C T intron_variant MELA-AU 9 135097662 135097662 single base substitution G C intron_variant MELA-AU 9 135097730 135097730 single base substitution C T intron_variant MELA-AU 9 135097844 135097844 single base substitution C T intron_variant MELA-AU 9 135097857 135097857 single base substitution C T intron_variant MELA-AU 9 135098036 135098036 single base substitution T C intron_variant MELA-AU 9 135098093 135098093 single base substitution G A intron_variant MELA-AU 9 135098102 135098102 single base substitution G A intron_variant MELA-AU 9 135098113 135098113 single base substitution C T intron_variant MELA-AU 9 135098303 135098303 single base substitution G A intron_variant MELA-AU 9 135098530 135098530 single base substitution T A intron_variant MELA-AU 9 135098542 135098542 single base substitution C T intron_variant MELA-AU 9 135098712 135098712 single base substitution G A intron_variant MELA-AU 9 135099155 135099155 single base substitution C T intron_variant MELA-AU 9 135099416 135099416 single base substitution C T intron_variant MELA-AU 9 135099616 135099616 single base substitution C T intron_variant MELA-AU 9 135099828 135099828 single base substitution C T intron_variant MELA-AU 9 135099958 135099958 single base substitution T A intron_variant MELA-AU 9 135099961 135099961 single base substitution C T intron_variant MELA-AU 9 135100556 135100556 single base substitution G A intron_variant MELA-AU 9 135100749 135100749 single base substitution C T intron_variant MELA-AU 9 135101949 135101949 single base substitution A C intron_variant MELA-AU 9 135102121 135102121 single base substitution C T intron_variant MELA-AU 9 135102310 135102310 single base substitution C T missense_variant T311I 932C>T MELA-AU 9 135102353 135102353 single base substitution C T synonymous_variant T325T 975C>T MELA-AU 9 135102708 135102708 single base substitution T G intron_variant MELA-AU 9 135102745 135102746 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 9 135102762 135102762 single base substitution G A intron_variant MELA-AU 9 135102880 135102880 single base substitution G A intron_variant MELA-AU 9 135103004 135103004 single base substitution C T intron_variant MELA-AU 9 135103011 135103011 single base substitution C T intron_variant MELA-AU 9 135103379 135103379 single base substitution C T intron_variant MELA-AU 9 135103504 135103504 single base substitution G A intron_variant MELA-AU 9 135103564 135103564 single base substitution C T intron_variant MELA-AU 9 135103712 135103712 single base substitution C T intron_variant MELA-AU 9 135104116 135104116 single base substitution C T intron_variant MELA-AU 9 135104534 135104534 single base substitution C T intron_variant MELA-AU 9 135104657 135104657 single base substitution C T intron_variant MELA-AU 9 135104750 135104750 single base substitution C T intron_variant MELA-AU 9 135104777 135104777 single base substitution C T intron_variant MELA-AU 9 135104867 135104867 single base substitution C T intron_variant MELA-AU 9 135105246 135105246 single base substitution G A intron_variant MELA-AU 9 135105370 135105370 single base substitution C T intron_variant MELA-AU 9 135105471 135105471 single base substitution C T intron_variant MELA-AU 9 135105504 135105504 single base substitution G A intron_variant MELA-AU 9 135105975 135105975 single base substitution C T intron_variant MELA-AU 9 135105975 135105975 single base substitution C T synonymous_variant S349S 1047C>T MELA-AU 9 135106274 135106274 single base substitution G A intron_variant MELA-AU 9 135106429 135106429 single base substitution C T intron_variant MELA-AU 9 135106457 135106457 single base substitution C A intron_variant MELA-AU 9 135106535 135106535 single base substitution G A intron_variant MELA-AU 9 135106697 135106697 single base substitution C T intron_variant MELA-AU 9 135106697 135106697 single base substitution C T missense_variant P357L 1070C>T MELA-AU 9 135106852 135106852 single base substitution T G intron_variant MELA-AU 9 135106852 135106852 single base substitution T G missense_variant L409V 1225T>G MELA-AU 9 135106955 135106955 single base substitution C T downstream_gene_variant MELA-AU 9 135106955 135106955 single base substitution C T intron_variant MELA-AU 9 135107142 135107142 single base substitution G A downstream_gene_variant MELA-AU 9 135107142 135107142 single base substitution G A intron_variant MELA-AU 9 135107233 135107234 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 9 135107233 135107234 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 9 135107427 135107427 single base substitution C T downstream_gene_variant MELA-AU 9 135107427 135107427 single base substitution C T intron_variant MELA-AU 9 135107461 135107461 single base substitution C T downstream_gene_variant MELA-AU 9 135107461 135107461 single base substitution C T intron_variant MELA-AU 9 135107584 135107584 single base substitution C T downstream_gene_variant MELA-AU 9 135107584 135107584 single base substitution C T intron_variant MELA-AU 9 135107760 135107760 single base substitution G A downstream_gene_variant MELA-AU 9 135107760 135107760 single base substitution G A intron_variant MELA-AU 9 135107912 135107912 single base substitution G A downstream_gene_variant MELA-AU 9 135107912 135107912 single base substitution G A intron_variant MELA-AU 9 135107957 135107957 single base substitution C T downstream_gene_variant MELA-AU 9 135107957 135107957 single base substitution C T intron_variant MELA-AU 9 135107995 135107995 single base substitution C T downstream_gene_variant MELA-AU 9 135107995 135107995 single base substitution C T intron_variant MELA-AU 9 135108130 135108130 single base substitution C T downstream_gene_variant MELA-AU 9 135108130 135108130 single base substitution C T intron_variant MELA-AU 9 135108161 135108161 single base substitution C T downstream_gene_variant MELA-AU 9 135108161 135108161 single base substitution C T intron_variant MELA-AU 9 135108189 135108189 single base substitution C T downstream_gene_variant MELA-AU 9 135108189 135108189 single base substitution C T intron_variant MELA-AU 9 135108193 135108193 single base substitution C T downstream_gene_variant MELA-AU 9 135108193 135108193 single base substitution C T intron_variant MELA-AU 9 135108342 135108342 single base substitution C T downstream_gene_variant MELA-AU 9 135108342 135108342 single base substitution C T intron_variant MELA-AU 9 135108595 135108595 single base substitution G A downstream_gene_variant MELA-AU 9 135108595 135108595 single base substitution G A intron_variant MELA-AU 9 135108740 135108740 single base substitution G A downstream_gene_variant MELA-AU 9 135108740 135108740 single base substitution G A intron_variant MELA-AU 9 135108848 135108848 single base substitution G A downstream_gene_variant MELA-AU 9 135108848 135108848 single base substitution G A intron_variant MELA-AU 9 135109113 135109113 single base substitution G A downstream_gene_variant MELA-AU 9 135109113 135109113 single base substitution G A intron_variant MELA-AU 9 135109114 135109114 single base substitution G A downstream_gene_variant MELA-AU 9 135109114 135109114 single base substitution G A intron_variant MELA-AU 9 135109136 135109136 single base substitution C T downstream_gene_variant MELA-AU 9 135109136 135109136 single base substitution C T intron_variant MELA-AU 9 135109402 135109402 single base substitution G A downstream_gene_variant MELA-AU 9 135109402 135109402 single base substitution G A intron_variant MELA-AU 9 135109915 135109915 single base substitution G A downstream_gene_variant MELA-AU 9 135109915 135109915 single base substitution G A intron_variant MELA-AU 9 135110221 135110221 single base substitution A G downstream_gene_variant MELA-AU 9 135110221 135110221 single base substitution A G intron_variant MELA-AU 9 135110274 135110274 single base substitution C T downstream_gene_variant MELA-AU 9 135110274 135110274 single base substitution C T intron_variant MELA-AU 9 135110364 135110364 single base substitution G A downstream_gene_variant MELA-AU 9 135110364 135110364 single base substitution G A intron_variant MELA-AU 9 135110494 135110494 single base substitution C T downstream_gene_variant MELA-AU 9 135110494 135110494 single base substitution C T intron_variant MELA-AU 9 135110556 135110556 single base substitution C T downstream_gene_variant MELA-AU 9 135110556 135110556 single base substitution C T intron_variant MELA-AU 9 135110662 135110662 single base substitution G A downstream_gene_variant MELA-AU 9 135110662 135110662 single base substitution G A intron_variant MELA-AU 9 135110947 135110947 single base substitution G A downstream_gene_variant MELA-AU 9 135110947 135110947 single base substitution G A intron_variant MELA-AU 9 135111088 135111088 single base substitution G A downstream_gene_variant MELA-AU 9 135111088 135111088 single base substitution G A intron_variant MELA-AU 9 135111088 135111088 single base substitution G A upstream_gene_variant MELA-AU 9 135111181 135111181 single base substitution C T downstream_gene_variant MELA-AU 9 135111181 135111181 single base substitution C T intron_variant MELA-AU 9 135111181 135111181 single base substitution C T upstream_gene_variant MELA-AU 9 135111405 135111405 single base substitution C T downstream_gene_variant MELA-AU 9 135111405 135111405 single base substitution C T intron_variant MELA-AU 9 135111405 135111405 single base substitution C T upstream_gene_variant MELA-AU 9 135111464 135111464 single base substitution C T downstream_gene_variant MELA-AU 9 135111464 135111464 single base substitution C T intron_variant MELA-AU 9 135111464 135111464 single base substitution C T upstream_gene_variant MELA-AU 9 135111637 135111637 single base substitution A T downstream_gene_variant MELA-AU 9 135111637 135111637 single base substitution A T intron_variant MELA-AU 9 135111637 135111637 single base substitution A T upstream_gene_variant MELA-AU 9 135111852 135111852 single base substitution G A downstream_gene_variant MELA-AU 9 135111852 135111852 single base substitution G A intron_variant MELA-AU 9 135111852 135111852 single base substitution G A upstream_gene_variant MELA-AU 9 135111962 135111962 single base substitution G A intron_variant MELA-AU 9 135111962 135111962 single base substitution G A upstream_gene_variant MELA-AU 9 135112240 135112240 single base substitution A G intron_variant MELA-AU 9 135112240 135112240 single base substitution A G upstream_gene_variant MELA-AU 9 135112607 135112607 single base substitution G A intron_variant MELA-AU 9 135112607 135112607 single base substitution G A upstream_gene_variant MELA-AU 9 135112630 135112630 single base substitution C T intron_variant MELA-AU 9 135112630 135112630 single base substitution C T upstream_gene_variant MELA-AU 9 135112804 135112804 single base substitution C T intron_variant MELA-AU 9 135112804 135112804 single base substitution C T upstream_gene_variant MELA-AU 9 135113498 135113498 single base substitution G A intron_variant MELA-AU 9 135113498 135113498 single base substitution G A upstream_gene_variant MELA-AU 9 135113595 135113595 single base substitution G A intron_variant MELA-AU 9 135113595 135113595 single base substitution G A upstream_gene_variant MELA-AU 9 135113619 135113619 single base substitution C T intron_variant MELA-AU 9 135113619 135113619 single base substitution C T upstream_gene_variant MELA-AU 9 135113774 135113774 single base substitution G A intron_variant MELA-AU 9 135113774 135113774 single base substitution G A upstream_gene_variant MELA-AU 9 135114077 135114077 single base substitution C T intron_variant MELA-AU 9 135114077 135114077 single base substitution C T upstream_gene_variant MELA-AU 9 135114239 135114239 single base substitution C T intron_variant MELA-AU 9 135114239 135114239 single base substitution C T upstream_gene_variant MELA-AU 9 135114337 135114337 single base substitution G A intron_variant MELA-AU 9 135114337 135114337 single base substitution G A upstream_gene_variant MELA-AU 9 135114338 135114338 insertion of <=200bp - A intron_variant MELA-AU 9 135114338 135114338 insertion of <=200bp - A upstream_gene_variant MELA-AU 9 135114351 135114351 single base substitution C G intron_variant MELA-AU 9 135114351 135114351 single base substitution C G splice_region_variant MELA-AU 9 135114351 135114351 single base substitution C G upstream_gene_variant MELA-AU 9 135114359 135114359 single base substitution C T intron_variant MELA-AU 9 135114359 135114359 single base substitution C T missense_variant P347S 1039C>T MELA-AU 9 135114359 135114359 single base substitution C T upstream_gene_variant MELA-AU 9 135114929 135114929 single base substitution G A intron_variant MELA-AU 9 135114929 135114929 single base substitution G A upstream_gene_variant MELA-AU 9 135115500 135115500 single base substitution C T intron_variant MELA-AU 9 135115500 135115500 single base substitution C T upstream_gene_variant MELA-AU 9 135117155 135117155 single base substitution C T intron_variant MELA-AU 9 135118094 135118094 single base substitution C T 3_prime_UTR_variant MELA-AU 9 135118094 135118094 single base substitution C T downstream_gene_variant MELA-AU 9 135118760 135118760 single base substitution C T 3_prime_UTR_variant MELA-AU 9 135118760 135118760 single base substitution C T downstream_gene_variant MELA-AU 9 135118903 135118903 single base substitution C G 3_prime_UTR_variant MELA-AU 9 135118903 135118903 single base substitution C G downstream_gene_variant MELA-AU 9 135119152 135119152 single base substitution G A 3_prime_UTR_variant MELA-AU 9 135119152 135119152 single base substitution G A downstream_gene_variant MELA-AU 9 135119174 135119174 single base substitution G A 3_prime_UTR_variant MELA-AU 9 135119174 135119174 single base substitution G A downstream_gene_variant MELA-AU 9 135119575 135119575 single base substitution C T 3_prime_UTR_variant MELA-AU 9 135119575 135119575 single base substitution C T downstream_gene_variant MELA-AU 9 135119662 135119662 single base substitution G A 3_prime_UTR_variant MELA-AU 9 135119662 135119662 single base substitution G A downstream_gene_variant MELA-AU 9 135120052 135120052 single base substitution G A downstream_gene_variant MELA-AU 9 135121004 135121004 single base substitution G A downstream_gene_variant MELA-AU 9 135121194 135121194 single base substitution C T downstream_gene_variant MELA-AU 9 135121542 135121542 single base substitution G A downstream_gene_variant MELA-AU 9 135121791 135121791 single base substitution G A downstream_gene_variant MELA-AU 9 135121972 135121972 single base substitution C T downstream_gene_variant MELA-AU 9 135122184 135122184 single base substitution A C downstream_gene_variant MELA-AU 9 135122741 135122741 single base substitution C T downstream_gene_variant MELA-AU 9 135122932 135122932 single base substitution G A downstream_gene_variant MELA-AU 9 135123130 135123130 single base substitution G A downstream_gene_variant MELA-AU 9 135123503 135123503 single base substitution C T downstream_gene_variant MELA-AU 9 135123581 135123581 single base substitution G A downstream_gene_variant MELA-AU 9 135123727 135123727 single base substitution C T downstream_gene_variant MELA-AU 9 135124524 135124524 single base substitution C T downstream_gene_variant MELA-AU 9 135124606 135124606 single base substitution G A downstream_gene_variant MELA-AU 9 135124764 135124764 single base substitution G A downstream_gene_variant MELA-AU 9 135124884 135124884 single base substitution G A downstream_gene_variant MELA-AU 9 135124910 135124910 single base substitution C T downstream_gene_variant ORCA-IN 9 135043293 135043293 single base substitution G T intron_variant ORCA-IN 9 135067765 135067765 single base substitution G T intron_variant ORCA-IN 9 135083222 135083222 single base substitution G A intron_variant ORCA-IN 9 135086703 135086703 single base substitution G A intron_variant OV-AU 9 135046275 135046275 single base substitution G C intron_variant OV-AU 9 135047387 135047387 single base substitution A C intron_variant OV-AU 9 135047477 135047477 single base substitution G A intron_variant OV-AU 9 135048868 135048868 single base substitution A G intron_variant OV-AU 9 135050720 135050720 single base substitution C T intron_variant OV-AU 9 135052164 135052164 single base substitution T C intron_variant OV-AU 9 135057557 135057557 single base substitution G A intron_variant OV-AU 9 135057712 135057712 single base substitution A C intron_variant OV-AU 9 135064864 135064864 single base substitution C T intron_variant OV-AU 9 135071006 135071006 single base substitution G A intron_variant OV-AU 9 135074030 135074030 single base substitution A C intron_variant OV-AU 9 135076260 135076260 single base substitution T G intron_variant OV-AU 9 135076400 135076400 single base substitution C G intron_variant OV-AU 9 135078609 135078609 single base substitution C G intron_variant OV-AU 9 135085581 135085581 single base substitution C T intron_variant OV-AU 9 135090126 135090126 single base substitution C T intron_variant OV-AU 9 135094314 135094314 single base substitution G A intron_variant OV-AU 9 135095704 135095704 single base substitution C A intron_variant OV-AU 9 135096000 135096000 single base substitution C T intron_variant OV-AU 9 135099089 135099089 single base substitution G T intron_variant OV-AU 9 135099174 135099174 single base substitution C A intron_variant OV-AU 9 135099304 135099304 single base substitution C T intron_variant OV-AU 9 135099305 135099305 single base substitution C G intron_variant OV-AU 9 135101548 135101548 single base substitution T A intron_variant OV-AU 9 135103633 135103633 single base substitution C A intron_variant OV-AU 9 135103852 135103852 single base substitution C G intron_variant OV-AU 9 135106139 135106139 single base substitution A C intron_variant OV-AU 9 135121477 135121477 single base substitution C T downstream_gene_variant PACA-AU 9 135034972 135034972 single base substitution C G upstream_gene_variant PACA-AU 9 135037261 135037261 single base substitution G A upstream_gene_variant PACA-AU 9 135041988 135041991 deletion of <=200bp TCTG - 5_prime_UTR_variant PACA-AU 9 135043241 135043241 single base substitution C A intron_variant PACA-AU 9 135043694 135043694 single base substitution C A intron_variant PACA-AU 9 135046472 135046472 single base substitution G A intron_variant PACA-AU 9 135047762 135047762 single base substitution G A intron_variant PACA-AU 9 135047820 135047820 single base substitution A C intron_variant PACA-AU 9 135048048 135048048 single base substitution C T intron_variant PACA-AU 9 135049189 135049189 single base substitution C A intron_variant PACA-AU 9 135049314 135049314 single base substitution A G intron_variant PACA-AU 9 135054275 135054275 single base substitution G A intron_variant PACA-AU 9 135055024 135055024 single base substitution C T intron_variant PACA-AU 9 135059804 135059804 single base substitution T C intron_variant PACA-AU 9 135065860 135065860 single base substitution G T intron_variant PACA-AU 9 135066484 135066484 single base substitution C T intron_variant PACA-AU 9 135070411 135070411 single base substitution A C intron_variant PACA-AU 9 135072324 135072324 single base substitution G A intron_variant PACA-AU 9 135073222 135073222 single base substitution A T intron_variant PACA-AU 9 135073739 135073739 single base substitution G A synonymous_variant S200S 600G>A PACA-AU 9 135079271 135079271 single base substitution C T intron_variant PACA-AU 9 135081582 135081582 single base substitution G A intron_variant PACA-AU 9 135082546 135082546 single base substitution A G intron_variant PACA-AU 9 135082793 135082793 single base substitution G T intron_variant PACA-AU 9 135084155 135084155 single base substitution G T intron_variant PACA-AU 9 135085166 135085166 single base substitution G A intron_variant PACA-AU 9 135087314 135087314 single base substitution T G intron_variant PACA-AU 9 135093200 135093200 single base substitution G A intron_variant PACA-AU 9 135093439 135093439 single base substitution G A intron_variant PACA-AU 9 135093459 135093459 single base substitution G A intron_variant PACA-AU 9 135093709 135093709 single base substitution C T intron_variant PACA-AU 9 135094028 135094028 single base substitution C T intron_variant PACA-AU 9 135094785 135094785 single base substitution C A intron_variant PACA-AU 9 135099817 135099817 single base substitution G A intron_variant PACA-AU 9 135112941 135112941 single base substitution C T intron_variant PACA-AU 9 135112941 135112941 single base substitution C T upstream_gene_variant PACA-AU 9 135114847 135114847 single base substitution C A intron_variant PACA-AU 9 135114847 135114847 single base substitution C A upstream_gene_variant PACA-AU 9 135117966 135117966 single base substitution T G 3_prime_UTR_variant PACA-AU 9 135117966 135117966 single base substitution T G downstream_gene_variant PACA-AU 9 135118920 135118920 single base substitution C T 3_prime_UTR_variant PACA-AU 9 135118920 135118920 single base substitution C T downstream_gene_variant PACA-AU 9 135121428 135121428 deletion of <=200bp C - downstream_gene_variant PACA-AU 9 135122680 135122680 single base substitution G A downstream_gene_variant PACA-CA 9 135035865 135035865 single base substitution C T upstream_gene_variant PACA-CA 9 135039107 135039107 single base substitution C T intron_variant PACA-CA 9 135045101 135045101 single base substitution C T intron_variant PACA-CA 9 135046471 135046471 single base substitution C T intron_variant PACA-CA 9 135048365 135048365 single base substitution C T intron_variant PACA-CA 9 135048892 135048892 single base substitution C T intron_variant PACA-CA 9 135049181 135049181 single base substitution G A intron_variant PACA-CA 9 135049193 135049193 single base substitution C T intron_variant PACA-CA 9 135052451 135052451 single base substitution A C intron_variant PACA-CA 9 135053529 135053529 single base substitution C A intron_variant PACA-CA 9 135055505 135055505 single base substitution C T intron_variant PACA-CA 9 135056098 135056098 single base substitution C T intron_variant PACA-CA 9 135056290 135056290 insertion of <=200bp - CA intron_variant PACA-CA 9 135057085 135057085 single base substitution C T intron_variant PACA-CA 9 135057554 135057554 single base substitution C T intron_variant PACA-CA 9 135060264 135060264 single base substitution G A intron_variant PACA-CA 9 135063153 135063153 single base substitution G T intron_variant PACA-CA 9 135063827 135063827 single base substitution C A intron_variant PACA-CA 9 135064000 135064000 single base substitution G A intron_variant PACA-CA 9 135064779 135064779 single base substitution G A intron_variant PACA-CA 9 135065201 135065201 deletion of <=200bp T - intron_variant PACA-CA 9 135065545 135065545 single base substitution G A intron_variant PACA-CA 9 135067247 135067247 single base substitution C T intron_variant PACA-CA 9 135067753 135067753 single base substitution G A intron_variant PACA-CA 9 135073889 135073889 single base substitution C T synonymous_variant T250T 750C>T PACA-CA 9 135077950 135077950 single base substitution C G intron_variant PACA-CA 9 135082061 135082061 single base substitution T A intron_variant PACA-CA 9 135082622 135082622 deletion of <=200bp T - intron_variant PACA-CA 9 135083741 135083741 single base substitution C A intron_variant PACA-CA 9 135084844 135084844 single base substitution G A intron_variant PACA-CA 9 135084987 135084987 single base substitution C T intron_variant PACA-CA 9 135085791 135085791 single base substitution G A intron_variant PACA-CA 9 135088133 135088133 single base substitution G C intron_variant PACA-CA 9 135088225 135088225 single base substitution C A intron_variant PACA-CA 9 135091054 135091054 single base substitution G A intron_variant PACA-CA 9 135091129 135091129 single base substitution G T intron_variant PACA-CA 9 135092286 135092286 single base substitution G T intron_variant PACA-CA 9 135092413 135092413 single base substitution G A intron_variant PACA-CA 9 135092818 135092818 single base substitution C T intron_variant PACA-CA 9 135093327 135093327 single base substitution C A intron_variant PACA-CA 9 135097153 135097153 single base substitution G A intron_variant PACA-CA 9 135098081 135098081 single base substitution C T intron_variant PACA-CA 9 135098747 135098747 single base substitution G A intron_variant PACA-CA 9 135098812 135098812 single base substitution G A intron_variant PACA-CA 9 135099537 135099537 single base substitution C T intron_variant PACA-CA 9 135100783 135100783 insertion of <=200bp - T intron_variant PACA-CA 9 135102542 135102542 single base substitution G A intron_variant PACA-CA 9 135104461 135104461 single base substitution C T intron_variant PACA-CA 9 135111111 135111111 deletion of <=200bp G - downstream_gene_variant PACA-CA 9 135111111 135111111 deletion of <=200bp G - intron_variant PACA-CA 9 135111111 135111111 deletion of <=200bp G - upstream_gene_variant PACA-CA 9 135112253 135112253 single base substitution G C intron_variant PACA-CA 9 135112253 135112253 single base substitution G C upstream_gene_variant PACA-CA 9 135112801 135112801 single base substitution C T intron_variant PACA-CA 9 135112801 135112801 single base substitution C T upstream_gene_variant PACA-CA 9 135115028 135115028 deletion of <=200bp G - intron_variant PACA-CA 9 135115028 135115028 deletion of <=200bp G - upstream_gene_variant PACA-CA 9 135115127 135115127 single base substitution G A intron_variant PACA-CA 9 135115127 135115127 single base substitution G A upstream_gene_variant PACA-CA 9 135115210 135115210 single base substitution T G intron_variant PACA-CA 9 135115210 135115210 single base substitution T G upstream_gene_variant PACA-CA 9 135120557 135120557 single base substitution G A downstream_gene_variant PACA-CA 9 135122159 135122159 single base substitution G A downstream_gene_variant PACA-CA 9 135124161 135124161 single base substitution A T downstream_gene_variant PACA-CA 9 135124226 135124226 deletion of <=200bp C - downstream_gene_variant PAEN-AU 9 135037924 135037924 single base substitution T A intron_variant PAEN-AU 9 135042978 135042978 single base substitution G A intron_variant PAEN-AU 9 135050389 135050389 single base substitution C T intron_variant PAEN-AU 9 135068720 135068720 single base substitution C G intron_variant PAEN-AU 9 135090072 135090072 single base substitution G T intron_variant PAEN-AU 9 135094620 135094620 single base substitution G A intron_variant PAEN-AU 9 135112236 135112236 single base substitution C A intron_variant PAEN-AU 9 135112236 135112236 single base substitution C A upstream_gene_variant PBCA-DE 9 135032508 135032508 single base substitution G A upstream_gene_variant PBCA-DE 9 135044868 135044868 single base substitution A G intron_variant PBCA-DE 9 135049194 135049194 insertion of <=200bp - GGAT intron_variant PBCA-DE 9 135057429 135057429 single base substitution C G intron_variant PBCA-DE 9 135066015 135066015 insertion of <=200bp - T intron_variant PBCA-DE 9 135079391 135079391 single base substitution G T intron_variant PBCA-DE 9 135082036 135082036 deletion of <=200bp A - intron_variant PBCA-DE 9 135091682 135091682 single base substitution A G intron_variant PBCA-DE 9 135099829 135099829 single base substitution C T intron_variant PBCA-DE 9 135113496 135113496 deletion of <=200bp C - intron_variant PBCA-DE 9 135113496 135113496 deletion of <=200bp C - upstream_gene_variant PBCA-DE 9 135118759 135118759 single base substitution C G 3_prime_UTR_variant PBCA-DE 9 135118759 135118759 single base substitution C G downstream_gene_variant PBCA-DE 9 135124145 135124145 insertion of <=200bp - AAT downstream_gene_variant PRAD-CA 9 135053063 135053063 single base substitution G T intron_variant PRAD-CA 9 135060619 135060619 single base substitution C T intron_variant PRAD-CA 9 135061982 135061982 single base substitution T A intron_variant PRAD-CA 9 135063715 135063715 single base substitution G A intron_variant PRAD-CA 9 135073479 135073479 single base substitution C T missense_variant R114C 340C>T PRAD-CA 9 135103176 135103176 single base substitution G A intron_variant PRAD-CA 9 135120193 135120193 single base substitution G A downstream_gene_variant PRAD-CA 9 135124345 135124345 single base substitution C G downstream_gene_variant PRAD-UK 9 135041677 135041677 single base substitution G T intron_variant PRAD-UK 9 135041678 135041678 single base substitution G T intron_variant PRAD-UK 9 135062033 135062033 single base substitution C A intron_variant PRAD-UK 9 135089454 135089454 single base substitution G A intron_variant PRAD-UK 9 135100889 135100889 single base substitution T G intron_variant PRAD-UK 9 135103232 135103232 single base substitution C A intron_variant PRAD-UK 9 135104324 135104324 single base substitution C A intron_variant PRAD-UK 9 135110250 135110250 single base substitution C T downstream_gene_variant PRAD-UK 9 135110250 135110250 single base substitution C T intron_variant PRAD-UK 9 135111308 135111308 single base substitution G A downstream_gene_variant PRAD-UK 9 135111308 135111308 single base substitution G A intron_variant PRAD-UK 9 135111308 135111308 single base substitution G A upstream_gene_variant PRAD-UK 9 135122450 135122450 single base substitution G A downstream_gene_variant PRAD-UK 9 135124799 135124799 single base substitution C G downstream_gene_variant PRAD-US 9 135073796 135073796 single base substitution C T synonymous_variant F219F 657C>T READ-US 9 135073913 135073913 single base substitution C T synonymous_variant R258R 774C>T RECA-EU 9 135032863 135032863 single base substitution A T upstream_gene_variant RECA-EU 9 135032866 135032866 single base substitution A G upstream_gene_variant RECA-EU 9 135040289 135040289 single base substitution A C intron_variant RECA-EU 9 135045081 135045081 single base substitution T A intron_variant RECA-EU 9 135047438 135047438 single base substitution G T intron_variant RECA-EU 9 135053871 135053871 single base substitution C A intron_variant RECA-EU 9 135063968 135063968 single base substitution G A intron_variant RECA-EU 9 135072295 135072295 single base substitution A T intron_variant RECA-EU 9 135087693 135087693 single base substitution C T intron_variant RECA-EU 9 135091730 135091730 single base substitution G C intron_variant RECA-EU 9 135104691 135104691 single base substitution A G intron_variant RECA-EU 9 135111671 135111671 single base substitution G C downstream_gene_variant RECA-EU 9 135111671 135111671 single base substitution G C intron_variant RECA-EU 9 135111671 135111671 single base substitution G C upstream_gene_variant SKCA-BR 9 135035238 135035238 single base substitution G A upstream_gene_variant SKCA-BR 9 135036884 135036884 single base substitution A C upstream_gene_variant SKCA-BR 9 135037377 135037377 single base substitution T C 5_prime_UTR_variant SKCA-BR 9 135041727 135041727 single base substitution A C intron_variant SKCA-BR 9 135041966 135041966 single base substitution G A 5_prime_UTR_variant SKCA-BR 9 135043455 135043455 single base substitution T C intron_variant SKCA-BR 9 135045563 135045563 single base substitution T G intron_variant SKCA-BR 9 135046146 135046146 single base substitution T C intron_variant SKCA-BR 9 135047635 135047635 single base substitution T G intron_variant SKCA-BR 9 135048592 135048592 single base substitution A C intron_variant SKCA-BR 9 135054140 135054140 single base substitution T G intron_variant SKCA-BR 9 135054348 135054349 deletion of <=200bp CA - intron_variant SKCA-BR 9 135054386 135054389 deletion of <=200bp TCCC - intron_variant SKCA-BR 9 135054444 135054444 single base substitution C T intron_variant SKCA-BR 9 135055884 135055884 single base substitution T C intron_variant SKCA-BR 9 135058266 135058266 single base substitution T C intron_variant SKCA-BR 9 135058473 135058473 single base substitution A G intron_variant SKCA-BR 9 135062506 135062506 single base substitution C T intron_variant SKCA-BR 9 135062928 135062928 insertion of <=200bp - AAC intron_variant SKCA-BR 9 135063547 135063547 single base substitution C T intron_variant SKCA-BR 9 135064450 135064450 single base substitution C G intron_variant SKCA-BR 9 135064455 135064455 single base substitution C T intron_variant SKCA-BR 9 135064805 135064806 deletion of <=200bp AG - intron_variant SKCA-BR 9 135064906 135064906 single base substitution C T intron_variant SKCA-BR 9 135065037 135065037 single base substitution T A intron_variant SKCA-BR 9 135065279 135065279 single base substitution G A intron_variant SKCA-BR 9 135067198 135067198 single base substitution T C intron_variant SKCA-BR 9 135067579 135067579 single base substitution C T intron_variant SKCA-BR 9 135067629 135067629 single base substitution G A intron_variant SKCA-BR 9 135069137 135069137 single base substitution C T intron_variant SKCA-BR 9 135071263 135071263 single base substitution C T intron_variant SKCA-BR 9 135071372 135071372 single base substitution G A intron_variant SKCA-BR 9 135073941 135073941 single base substitution C T missense_variant R268W 802C>T SKCA-BR 9 135073998 135073998 single base substitution T G splice_donor_variant SKCA-BR 9 135074010 135074010 single base substitution A G intron_variant SKCA-BR 9 135074112 135074112 single base substitution G A intron_variant SKCA-BR 9 135074216 135074216 single base substitution G A intron_variant SKCA-BR 9 135075628 135075628 single base substitution T G intron_variant SKCA-BR 9 135076866 135076866 single base substitution C T intron_variant SKCA-BR 9 135077016 135077016 single base substitution C T intron_variant SKCA-BR 9 135077146 135077146 single base substitution G T intron_variant SKCA-BR 9 135078399 135078399 single base substitution C T intron_variant SKCA-BR 9 135082037 135082037 single base substitution G A intron_variant SKCA-BR 9 135083691 135083691 single base substitution T G intron_variant SKCA-BR 9 135085997 135085997 single base substitution T C intron_variant SKCA-BR 9 135086287 135086287 insertion of <=200bp - TCA intron_variant SKCA-BR 9 135087294 135087294 single base substitution G T intron_variant SKCA-BR 9 135087892 135087892 single base substitution G A intron_variant SKCA-BR 9 135087997 135087997 single base substitution G A intron_variant SKCA-BR 9 135088768 135088768 single base substitution C T intron_variant SKCA-BR 9 135088831 135088831 single base substitution G A intron_variant SKCA-BR 9 135090262 135090262 single base substitution T A intron_variant SKCA-BR 9 135090263 135090263 single base substitution T A intron_variant SKCA-BR 9 135091024 135091024 single base substitution G A intron_variant SKCA-BR 9 135091041 135091041 single base substitution C T intron_variant SKCA-BR 9 135091801 135091817 deletion of <=200bp CTGTGTGTGTGTGTATG - intron_variant SKCA-BR 9 135091803 135091803 single base substitution G C intron_variant SKCA-BR 9 135091805 135091805 single base substitution G C intron_variant SKCA-BR 9 135091811 135091815 deletion of <=200bp GTGTA - intron_variant SKCA-BR 9 135091819 135091819 single base substitution G C intron_variant SKCA-BR 9 135091821 135091821 single base substitution G C intron_variant SKCA-BR 9 135092619 135092619 single base substitution T A intron_variant SKCA-BR 9 135092720 135092720 single base substitution G A intron_variant SKCA-BR 9 135094127 135094127 single base substitution A C intron_variant SKCA-BR 9 135094708 135094708 single base substitution C T intron_variant SKCA-BR 9 135094959 135094959 insertion of <=200bp - CA intron_variant SKCA-BR 9 135094976 135094976 single base substitution G A intron_variant SKCA-BR 9 135095016 135095016 single base substitution C T intron_variant SKCA-BR 9 135095848 135095849 deletion of <=200bp CT - intron_variant SKCA-BR 9 135096731 135096731 single base substitution G A intron_variant SKCA-BR 9 135096861 135096861 single base substitution C T intron_variant SKCA-BR 9 135097925 135097925 single base substitution C T intron_variant SKCA-BR 9 135098490 135098490 single base substitution G A intron_variant SKCA-BR 9 135102694 135102694 single base substitution C T intron_variant SKCA-BR 9 135103021 135103021 single base substitution G A intron_variant SKCA-BR 9 135103280 135103280 single base substitution A C intron_variant SKCA-BR 9 135103945 135103945 insertion of <=200bp - CT intron_variant SKCA-BR 9 135104490 135104490 single base substitution G A intron_variant SKCA-BR 9 135106339 135106339 single base substitution A C intron_variant SKCA-BR 9 135106782 135106782 single base substitution C T intron_variant SKCA-BR 9 135106782 135106782 single base substitution C T synonymous_variant I385I 1155C>T SKCA-BR 9 135107987 135107987 single base substitution G A downstream_gene_variant SKCA-BR 9 135107987 135107987 single base substitution G A intron_variant SKCA-BR 9 135109499 135109499 single base substitution C T downstream_gene_variant SKCA-BR 9 135109499 135109499 single base substitution C T intron_variant SKCA-BR 9 135112493 135112493 single base substitution T G intron_variant SKCA-BR 9 135112493 135112493 single base substitution T G upstream_gene_variant SKCA-BR 9 135112816 135112816 single base substitution A C intron_variant SKCA-BR 9 135112816 135112816 single base substitution A C upstream_gene_variant SKCA-BR 9 135117046 135117046 single base substitution A G intron_variant SKCA-BR 9 135119060 135119060 single base substitution C T 3_prime_UTR_variant SKCA-BR 9 135119060 135119060 single base substitution C T downstream_gene_variant SKCA-BR 9 135120908 135120908 single base substitution G A downstream_gene_variant SKCA-BR 9 135121525 135121525 single base substitution C T downstream_gene_variant SKCA-BR 9 135122917 135122917 insertion of <=200bp - TC downstream_gene_variant SKCA-BR 9 135123341 135123341 insertion of <=200bp - CA downstream_gene_variant SKCA-BR 9 135124790 135124790 single base substitution C T downstream_gene_variant SKCM-US 9 135042273 135042273 single base substitution T A missense_variant Y19N 55T>A SKCM-US 9 135042377 135042377 single base substitution G A synonymous_variant K53K 159G>A SKCM-US 9 135042402 135042402 single base substitution G A missense_variant G62R 184G>A SKCM-US 9 135073590 135073590 single base substitution C T synonymous_variant L151L 451C>T SKCM-US 9 135073874 135073874 single base substitution G A synonymous_variant E245E 735G>A SKCM-US 9 135073983 135073983 single base substitution G A missense_variant E282K 844G>A SKCM-US 9 135102341 135102341 single base substitution G A synonymous_variant K321K 963G>A SKCM-US 9 135102365 135102365 single base substitution G A synonymous_variant R329R 987G>A STAD-US 9 135042324 135042324 single base substitution T C missense_variant F36L 106T>C STAD-US 9 135073374 135073374 single base substitution A G missense_variant N79D 235A>G STAD-US 9 135073412 135073412 single base substitution G A synonymous_variant P91P 273G>A STAD-US 9 135073517 135073517 single base substitution G A synonymous_variant S126S 378G>A STAD-US 9 135073569 135073569 single base substitution G A missense_variant G144S 430G>A STAD-US 9 135073571 135073571 single base substitution C T synonymous_variant G144G 432C>T STAD-US 9 135073611 135073611 single base substitution G A missense_variant G158R 472G>A STAD-US 9 135073695 135073695 single base substitution T C missense_variant S186P 556T>C STAD-US 9 135073809 135073809 single base substitution G A missense_variant G224S 670G>A STAD-US 9 135073834 135073834 single base substitution A G missense_variant N232S 695A>G STAD-US 9 135073887 135073887 single base substitution A G missense_variant T250A 748A>G STAD-US 9 135102276 135102276 single base substitution G A missense_variant E300K 898G>A STAD-US 9 135102326 135102326 single base substitution C T synonymous_variant C316C 948C>T STAD-US 9 135102359 135102359 single base substitution C A synonymous_variant S327S 981C>A STAD-US 9 135114555 135114555 single base substitution C T synonymous_variant C365C 1095C>T STAD-US 9 135114555 135114555 single base substitution C T synonymous_variant C373C 1119C>T STAD-US 9 135114555 135114555 single base substitution C T synonymous_variant C379C 1137C>T STAD-US 9 135114555 135114555 single base substitution C T upstream_gene_variant STAD-US 9 135114577 135114577 single base substitution C T stop_gained R373* 1117C>T STAD-US 9 135114577 135114577 single base substitution C T stop_gained R381* 1141C>T STAD-US 9 135114577 135114577 single base substitution C T stop_gained R387* 1159C>T STAD-US 9 135114577 135114577 single base substitution C T upstream_gene_variant STAD-US 9 135114621 135114621 single base substitution C T synonymous_variant N387N 1161C>T STAD-US 9 135114621 135114621 single base substitution C T synonymous_variant N395N 1185C>T STAD-US 9 135114621 135114621 single base substitution C T synonymous_variant N401N 1203C>T STAD-US 9 135114621 135114621 single base substitution C T upstream_gene_variant STAD-US 9 135116378 135116378 single base substitution G T exon_variant STAD-US 9 135116378 135116378 single base substitution G T missense_variant G427V 1280G>T STAD-US 9 135116378 135116378 single base substitution G T missense_variant G435V 1304G>T STAD-US 9 135116378 135116378 single base substitution G T missense_variant G441V 1322G>T STAD-US 9 135116378 135116378 single base substitution G T upstream_gene_variant STAD-US 9 135116397 135116397 single base substitution C T exon_variant STAD-US 9 135116397 135116397 single base substitution C T synonymous_variant C433C 1299C>T STAD-US 9 135116397 135116397 single base substitution C T synonymous_variant C441C 1323C>T STAD-US 9 135116397 135116397 single base substitution C T synonymous_variant C447C 1341C>T STAD-US 9 135116397 135116397 single base substitution C T upstream_gene_variant THCA-SA 9 135073863 135073863 single base substitution G A missense_variant G242S 724G>A THCA-SA 9 135073877 135073877 single base substitution C T synonymous_variant F246F 738C>T THCA-SA 9 135102320 135102320 single base substitution C T synonymous_variant P314P 942C>T THCA-US 9 135073480 135073480 single base substitution G T missense_variant R114L 341G>T UCEC-US 9 135073579 135073579 single base substitution C T missense_variant T147M 440C>T UCEC-US 9 135114519 135114519 single base substitution C T synonymous_variant R353R 1059C>T UCEC-US 9 135114519 135114519 single base substitution C T synonymous_variant R361R 1083C>T UCEC-US 9 135114519 135114519 single base substitution C T synonymous_variant R367R 1101C>T UCEC-US 9 135114519 135114519 single base substitution C T upstream_gene_variant

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand TCGA-06-5858-01 COSM3413400 c.705G>A p.T235T Substitution - coding silent 9:132198457-132198457 + ML_108_T_01 COSM5038021 c.802C>T p.R268W Substitution - Missense 9:132198554-132198554 + HCC055T COSM5823946 c.1291G>T p.E431* Substitution - Nonsense 9:132240978-132240978 + C135 COSM4618835 c.589G>A p.E197K Substitution - Missense 9:132198341-132198341 + TCGA-EE-A3J5-06 COSM3926330 c.963G>A p.K321K Substitution - coding silent 9:132226954-132226954 + PCSI_0090_Pa_X COSM1643766 c.750C>T p.T250T Substitution - coding silent 9:132198502-132198502 + I2L-P19Ta-Tumor-Organoid COSM3905024 c.670G>A p.G224S Substitution - Missense 9:132198422-132198422 + YUMOBER COSM5410579 c.21C>T p.L7L Substitution - coding silent 9:132166852-132166852 + TCGA-D5-6928-01 COSM4371493 c.576C>T p.R192R Substitution - coding silent 9:132198328-132198328 + TCGA-D5-6535-01 COSM5163635 c.482G>A p.W161* Substitution - Nonsense 9:132198234-132198234 + T3090 COSM4708494 c.429C>T p.Y143Y Substitution - coding silent 9:132198181-132198181 + TCGA-CC-A5UE-01 COSM4934006 c.1371C>A p.D457E Substitution - Missense 9:132241889-132241889 + CPCG0078-F1 COSM4880905 c.340C>T p.R114C Substitution - Missense 9:132198092-132198092 + 1N34-VS-1T34 COSM4974817 c.949G>A p.G317S Substitution - Missense 9:132226940-132226940 + TCGA-AG-3999-01 COSM289222 c.504C>T p.A168A Substitution - coding silent 9:132198256-132198256 + TCGA-CW-6090-01 COSM487157 c.976C>A p.R326R Substitution - coding silent 9:132226967-132226967 + TCGA-CG-5726-01 COSM3905006 c.273G>A p.P91P Substitution - coding silent 9:132198025-132198025 + 2292385 COSM4610536 c.634C>T p.R212C Substitution - Missense 9:132198386-132198386 + 46M COSM4371511 c.969C>T p.F323F Substitution - coding silent 9:132226960-132226960 + PD9597a COSM5799788 c.341G>A p.R114H Substitution - Missense 9:132198093-132198093 + Pat_76_A COSM5875750 c.94C>T p.P32S Substitution - Missense 9:132166925-132166925 + B23-Tumor COSM1756006 c.685A>T p.N229Y Substitution - Missense 9:132198437-132198437 + CRC-9 COSM304601 c.652C>T p.R218C Substitution - Missense 9:132198404-132198404 + TCGA-CM-6680-01 COSM3699491 c.985C>T p.R329W Substitution - Missense 9:132226976-132226976 + 61 COSM5738769 c.433C>T p.R145W Substitution - Missense 9:132198185-132198185 + CRC-13T COSM5479399 c.377C>T p.S126L Substitution - Missense 9:132198129-132198129 + sysucc-1317T COSM4610534 c.634C>T p.R212C Substitution - Missense 9:132198386-132198386 + ESO-0019 COSM1259638 c.288C>T p.F96F Substitution - coding silent 9:132198040-132198040 + CSCC-31-T COSM4530810 c.172G>A p.G58S Substitution - Missense 9:132167003-132167003 + TCGA-F1-6177-01 COSM3905015 c.432C>T p.G144G Substitution - coding silent 9:132198184-132198184 + 134398 COSM325981 c.1392G>T p.Q464H Substitution - Missense 9:132241910-132241910 + TCGA-33-4583-01 COSM753348 c.1122C>T p.V374V Substitution - coding silent 9:132239171-132239171 + T2932 COSM4708495 c.487C>T p.P163S Substitution - Missense 9:132198239-132198239 + TCGA-76-6656-01 COSM3748405 c.97A>C p.T33P Substitution - Missense 9:132166928-132166928 + TCGA-06-0190-02 COSM3413403 c.757C>T p.R253C Substitution - Missense 9:132198509-132198509 + ESO-0009 COSM1259637 c.780G>A p.A260A Substitution - coding silent 9:132198532-132198532 + sysucc-1317T COSM1239646 c.877G>A p.A293T Substitution - Missense 9:132226868-132226868 + TCGA-BR-8487-01 COSM3905019 c.556T>C p.S186P Substitution - Missense 9:132198308-132198308 + TCGA-FW-A3R5-06 COSM3926324 c.184G>A p.G62R Substitution - Missense 9:132167015-132167015 + TCGA-IP-7968-01 COSM3905018 c.472G>A p.G158R Substitution - Missense 9:132198224-132198224 + TCGA-CD-A4MG-01 COSM3905027 c.695A>G p.N232S Substitution - Missense 9:132198447-132198447 + TCGA-AM-5820-01 COSM3763691 c.876C>T p.H292H Substitution - coding silent 9:132226867-132226867 + S02351 COSM5695240 c.751G>T p.D251Y Substitution - Missense 9:132198503-132198503 + TCGA-FW-A3R5-06 COSM3926329 c.451C>T p.L151L Substitution - coding silent 9:132198203-132198203 + sysucc-704T COSM5766532 c.147C>T p.Y49Y Substitution - coding silent 9:132166978-132166978 + 23_tFL COSM4171863 c.32G>A p.C11Y Substitution - Missense 9:132166863-132166863 + T3340 COSM4708500 c.550G>A p.D184N Substitution - Missense 9:132198302-132198302 + TCGA-AM-5820-01 COSM455512 c.738C>T p.F246F Substitution - coding silent 9:132198490-132198490 + T2197 COSM4708504 c.1035C>T p.A345A Substitution - coding silent 9:132230576-132230576 + I2L-P7-Tumor-Organoid COSM5359144 c.857+9delG p.? Unknown 9:132198618-132198618 + TCGA-AM-5820-01 COSM3763693 c.876C>T p.H292H Substitution - coding silent 9:132226867-132226867 + TCGA-CK-5913-01 COSM5038021 c.802C>T p.R268W Substitution - Missense 9:132198554-132198554 + T41 COSM5345724 c.786C>T p.G262G Substitution - coding silent 9:132198538-132198538 + sysucc-912T COSM5764957 c.1064C>A p.T355N Substitution - Missense 9:132231304-132231304 + T41 COSM5345722 c.786C>T p.G262G Substitution - coding silent 9:132198538-132198538 + TCGA-AA-3976-01 COSM297521 c.942C>T p.P314P Substitution - coding silent 9:132226933-132226933 + BD46T COSM5520336 c.692A>G p.D231G Substitution - Missense 9:132198444-132198444 + TCGA-CM-4743-01 COSM1460670 c.682C>T p.R228C Substitution - Missense 9:132198434-132198434 + S02351 COSM5695238 c.751G>T p.D251Y Substitution - Missense 9:132198503-132198503 + TCGA-CG-5723-01 COSM3905033 c.898G>A p.E300K Substitution - Missense 9:132226889-132226889 + TCGA-C5-A1MJ-01 COSM4842815 c.476G>A p.R159H Substitution - Missense 9:132198228-132198228 + CSCC-44-T COSM4555278 c.648G>A p.R216R Substitution - coding silent 9:132198400-132198400 + BD231T COSM5496883 c.631G>A p.V211M Substitution - Missense 9:132198383-132198383 + T16 COSM5618896 c.828C>T p.Y276Y Substitution - coding silent 9:132198580-132198580 + HCC080T COSM5810548 c.354G>T p.P118P Substitution - coding silent 9:132198106-132198106 + RK187_C01 COSM1554225 c.977G>T p.R326L Substitution - Missense 9:132226968-132226968 + TCGA-HC-7079-01 COSM3675265 c.352C>A p.P118T Substitution - Missense 9:132198104-132198104 + sysucc-704T COSM5766530 c.147C>T p.Y49Y Substitution - coding silent 9:132166978-132166978 + PD23567a COSM5777678 c.849C>A p.V283V Substitution - coding silent 9:132198601-132198601 + sysucc-1317T COSM3847908 c.877G>A p.A293T Substitution - Missense 9:132226868-132226868 + HCC136T COSM5817131 c.1262G>T p.C421F Substitution - Missense 9:132240949-132240949 + PTC-10C COSM3763693 c.876C>T p.H292H Substitution - coding silent 9:132226867-132226867 + TCGA-FW-A3TV-06 COSM3655069 c.735G>A p.E245E Substitution - coding silent 9:132198487-132198487 + 59 COSM5735120 c.539G>A p.R180H Substitution - Missense 9:132198291-132198291 + TCGA-HU-A4GQ-01 COSM3905046 c.1304G>T p.G435V Substitution - Missense 9:132240991-132240991 + ML_108_T_01 COSM1460671 c.802C>T p.R268W Substitution - Missense 9:132198554-132198554 + PCSI_0090_Pa_X COSM5419907 c.750C>T p.T250T Substitution - coding silent 9:132198502-132198502 + T2932 COSM4708497 c.487C>T p.P163S Substitution - Missense 9:132198239-132198239 + TCGA-CG-5721-01 COSM3905001 c.106T>C p.F36L Substitution - Missense 9:132166937-132166937 + TCGA-AD-6965-01 COSM1460672 c.882C>A p.N294K Substitution - Missense 9:132226873-132226873 + T3724 COSM4708503 c.646C>T p.R216W Substitution - Missense 9:132198398-132198398 + pfg068T COSM4761699 c.568G>A p.A190T Substitution - Missense 9:132198320-132198320 + sysucc-1370T COSM5472697 c.354G>A p.P118P Substitution - coding silent 9:132198106-132198106 + TCGA-CG-5726-01 COSM3905022 c.670G>A p.G224S Substitution - Missense 9:132198422-132198422 + TCGA-C5-A1MH-01 COSM4820962 c.85G>C p.D29H Substitution - Missense 9:132166916-132166916 + I2L-P19Ta-Tumor-Biopsy COSM3905024 c.670G>A p.G224S Substitution - Missense 9:132198422-132198422 + TCGA-C5-A1MH-01 COSM4820960 c.85G>C p.D29H Substitution - Missense 9:132166916-132166916 + Au4 COSM5604281 c.975C>T p.T325T Substitution - coding silent 9:132226966-132226966 + BL4 COSM4408488 c.857+2T>G p.? Unknown 9:132198611-132198611 + PTC-28C COSM3763691 c.876C>T p.H292H Substitution - coding silent 9:132226867-132226867 + TCGA-BR-8680-01 COSM3905004 c.235A>G p.N79D Substitution - Missense 9:132197987-132197987 + BL4 COSM4408490 c.857+2T>G p.? Unknown 9:132198611-132198611 + CSCC-6-T COSM4502498 c.614C>T p.S205F Substitution - Missense 9:132198366-132198366 + SC_9020 COSM5551157 c.1126T>A p.C376S Substitution - Missense 9:132239175-132239175 + TCGA-BR-6852-01 COSM3905010 c.430G>A p.G144S Substitution - Missense 9:132198182-132198182 + pfg068T COSM4761697 c.568G>A p.A190T Substitution - Missense 9:132198320-132198320 + TCGA-BR-4292-01 COSM3905009 c.378G>A p.S126S Substitution - coding silent 9:132198130-132198130 + SC_9081 COSM4371497 c.635G>A p.R212H Substitution - Missense 9:132198387-132198387 + PD23567a COSM5777680 c.849C>A p.V283V Substitution - coding silent 9:132198601-132198601 + HCT15 COSM4611674 c.188_189insC p.E66fs*1 Insertion - Frameshift 9:132167019-132167020 + PTC_288 COSM5958082 c.724G>A p.G242S Substitution - Missense 9:132198476-132198476 + Sample_1 COSM4408488 c.857+2T>G p.? Unknown 9:132198611-132198611 + PD9597a COSM5799790 c.341G>A p.R114H Substitution - Missense 9:132198093-132198093 + TCGA-G9-6499-01 COSM3675262 c.272C>A p.P91Q Substitution - Missense 9:132198024-132198024 + TCGA-AC-A2QH-01 COSM5835652 c.1228delA p.N410fs*5 Deletion - Frameshift 9:132240915-132240915 + Pat_76_B COSM5875750 c.94C>T p.P32S Substitution - Missense 9:132166925-132166925 + LUAD-FH5PJ COSM403981 c.1475A>C p.D492A Substitution - Missense 9:132241993-132241993 + TCGA-AA-3966-01 COSM273031 c.686A>C p.N229T Substitution - Missense 9:132198438-132198438 + S02284 COSM5684267 c.763C>A p.R255R Substitution - coding silent 9:132198515-132198515 + TCGA-29-2427-01 COSM119850 c.313A>C p.T105P Substitution - Missense 9:132198065-132198065 + CHC320T COSM4408490 c.857+2T>G p.? Unknown 9:132198611-132198611 + DLD1 COSM4611674 c.188_189insC p.E66fs*1 Insertion - Frameshift 9:132167019-132167020 + TCGA-EB-A44O-01 COSM3655066 c.159G>A p.K53K Substitution - coding silent 9:132166990-132166990 + TCGA-KK-A59V-01 COSM4504138 c.657C>T p.F219F Substitution - coding silent 9:132198409-132198409 + CSCC-6-T COSM4502500 c.614C>T p.S205F Substitution - Missense 9:132198366-132198366 + CSCC-44-T COSM4561776 c.898G>C p.E300Q Substitution - Missense 9:132226889-132226889 + PTC-7C COSM3763691 c.876C>T p.H292H Substitution - coding silent 9:132226867-132226867 + CSCC-49-T COSM4541199 c.295G>A p.E99K Substitution - Missense 9:132198047-132198047 + sysucc-1370T COSM5472695 c.354G>A p.P118P Substitution - coding silent 9:132198106-132198106 + TCGA-D7-A4YV-01 COSM3905044 c.1185C>T p.N395N Substitution - coding silent 9:132239234-132239234 + TCGA-AA-3492-01 COSM1460665 c.172G>T p.G58C Substitution - Missense 9:132167003-132167003 + TCGA-AZ-6601-01 COSM1460673 c.1139C>T p.T380M Substitution - Missense 9:132239188-132239188 + TCGA-AD-6895-01 COSM1460666 c.189delC p.P65fs*69 Deletion - Frameshift 9:132167020-132167020 + TCGA-A7-A26E-01 COSM3847910 c.1332G>A p.T444T Substitution - coding silent 9:132241019-132241019 + TCGA-HU-A4GQ-01 COSM3905036 c.948C>T p.C316C Substitution - coding silent 9:132226939-132226939 + DLD1 COSM4626367 c.520G>A p.A174T Substitution - Missense 9:132198272-132198272 + CSCC-55-T COSM4544463 c.357G>A p.L119L Substitution - coding silent 9:132198109-132198109 + sysucc-1135T COSM5480030 c.916G>A p.E306K Substitution - Missense 9:132226907-132226907 + TCGA-C8-A138-01 COSM455510 c.575G>A p.R192H Substitution - Missense 9:132198327-132198327 + TCGA-HU-A4GQ-01 COSM3905039 c.981C>A p.S327S Substitution - coding silent 9:132226972-132226972 + T3306 COSM3212338 c.501C>T p.Y167Y Substitution - coding silent 9:132198253-132198253 + TCGA-C8-A12M-01 COSM5835651 c.675C>T p.P225P Substitution - coding silent 9:132198427-132198427 + TCGA-D5-6535-01 COSM1460667 c.482G>A p.W161* Substitution - Nonsense 9:132198234-132198234 + sysucc-809T COSM5156537 c.682C>T p.R228C Substitution - Missense 9:132198434-132198434 + SNUH_G76_S1 COSM3763690 c.738C>T p.F246F Substitution - coding silent 9:132198490-132198490 + TCGA-AD-6895-01 COSM5130049 c.189delC p.P65fs*69 Deletion - Frameshift 9:132167020-132167020 + 59 COSM5735122 c.539G>A p.R180H Substitution - Missense 9:132198291-132198291 + TCGA-EB-A44O-01 COSM3655064 c.159G>A p.K53K Substitution - coding silent 9:132166990-132166990 + Pat_76_A COSM5875748 c.94C>T p.P32S Substitution - Missense 9:132166925-132166925 + pfg043T COSM4761705 c.926A>G p.H309R Substitution - Missense 9:132226917-132226917 + DLD1 COSM4626365 c.520G>A p.A174T Substitution - Missense 9:132198272-132198272 + 61 COSM5738767 c.433C>T p.R145W Substitution - Missense 9:132198185-132198185 + Au4 COSM5604280 c.441G>A p.T147T Substitution - coding silent 9:132198193-132198193 + LUAD_E00565 COSM389720 c.1120G>T p.V374F Substitution - Missense 9:132239169-132239169 + TCGA-D5-6928-01 COSM1460669 c.676G>A p.D226N Substitution - Missense 9:132198428-132198428 + TCGA-CG-5726-01 COSM305439 c.273G>A p.P91P Substitution - coding silent 9:132198025-132198025 + BD46T COSM5520334 c.692A>G p.D231G Substitution - Missense 9:132198444-132198444 + PR-02-2480 COSM246125 c.1357+2T>A p.? Unknown 9:132241046-132241046 + TCGA-CG-5726-01 COSM3905024 c.670G>A p.G224S Substitution - Missense 9:132198422-132198422 + TCGA-CG-5723-01 COSM3905031 c.898G>A p.E300K Substitution - Missense 9:132226889-132226889 + CSCC-11-T COSM4478097 c.220C>T p.P74S Substitution - Missense 9:132197972-132197972 + TCGA-A6-6653-01 COSM3905006 c.273G>A p.P91P Substitution - coding silent 9:132198025-132198025 + TCGA-CG-5721-01 COSM3904999 c.106T>C p.F36L Substitution - Missense 9:132166937-132166937 + MD-284 COSM302780 c.484C>A p.Q162K Substitution - Missense 9:132198236-132198236 + TCGA-ED-A7PZ-01 COSM4916893 c.1290C>A p.R430R Substitution - coding silent 9:132240977-132240977 + TCGA-CM-4743-01 COSM5156537 c.682C>T p.R228C Substitution - Missense 9:132198434-132198434 + SC_9008 COSM1554223 c.1212C>T p.N404N Substitution - coding silent 9:132239261-132239261 + PTC-7C COSM3763693 c.876C>T p.H292H Substitution - coding silent 9:132226867-132226867 + sysucc-1317T COSM5069651 c.779C>T p.A260V Substitution - Missense 9:132198531-132198531 + TCGA-BH-A0B6-01 COSM3847909 c.1161G>A p.E387E Substitution - coding silent 9:132231401-132231401 + 19M COSM5579144 c.305G>A p.G102D Substitution - Missense 9:132198057-132198057 + TCGA-D5-6928-01 COSM1460668 c.576C>T p.R192R Substitution - coding silent 9:132198328-132198328 + LUAD-E00443 COSM364138 c.985C>T p.R329W Substitution - Missense 9:132226976-132226976 + I2L-P7-Tumor-Organoid COSM5359142 c.857+9delG p.? Unknown 9:132198618-132198618 + sysucc-1317T COSM4610536 c.634C>T p.R212C Substitution - Missense 9:132198386-132198386 + ESO-1488 COSM1259639 c.88G>T p.E30* Substitution - Nonsense 9:132166919-132166919 + DLD1 COSM4611672 c.188_189insC p.E66fs*1 Insertion - Frameshift 9:132167019-132167020 + TCGA-AM-5820-01 COSM3763690 c.738C>T p.F246F Substitution - coding silent 9:132198490-132198490 + TCGA-BR-6452-01 COSM3905048 c.1323C>T p.C441C Substitution - coding silent 9:132241010-132241010 + CSCC-44-T COSM4555276 c.648G>A p.R216R Substitution - coding silent 9:132198400-132198400 + HCC080T COSM5810546 c.354G>T p.P118P Substitution - coding silent 9:132198106-132198106 + LUAD-YINHD COSM351858 c.464T>A p.L155Q Substitution - Missense 9:132198216-132198216 + TCGA-AG-3898-01 COSM288969 c.779C>T p.A260V Substitution - Missense 9:132198531-132198531 + TCGA-D8-A1XQ-01 COSM1239646 c.877G>A p.A293T Substitution - Missense 9:132226868-132226868 + TCGA-DJ-A3VM-01 COSM3375146 c.341G>T p.R114L Substitution - Missense 9:132198093-132198093 + CSCC-44-T COSM4499385 c.540C>T p.R180R Substitution - coding silent 9:132198292-132198292 + CSCC-44-T COSM4499387 c.540C>T p.R180R Substitution - coding silent 9:132198292-132198292 + CSCC-31-T COSM4554498 c.622G>A p.E208K Substitution - Missense 9:132198374-132198374 + S01023 COSM5666826 c.786C>A p.G262G Substitution - coding silent 9:132198538-132198538 + B23-Tumor COSM4007079 c.685A>T p.N229Y Substitution - Missense 9:132198437-132198437 + PTC_288 COSM5958084 c.724G>A p.G242S Substitution - Missense 9:132198476-132198476 + TCGA-CK-5913-01 COSM1460671 c.802C>T p.R268W Substitution - Missense 9:132198554-132198554 + B23 COSM1756006 c.685A>T p.N229Y Substitution - Missense 9:132198437-132198437 + 1604875 COSM141280 c.221C>T p.P74L Substitution - Missense 9:132197973-132197973 + 2334199 COSM322123 c.911A>G p.Q304R Substitution - Missense 9:132226902-132226902 + TCGA-CD-A4MG-01 COSM3905028 c.748A>G p.T250A Substitution - Missense 9:132198500-132198500 + T2197 COSM4708505 c.1035C>T p.A345A Substitution - coding silent 9:132230576-132230576 + Au4 COSM5604283 c.975C>T p.T325T Substitution - coding silent 9:132226966-132226966 + CSCC-44-T COSM4561778 c.898G>C p.E300Q Substitution - Missense 9:132226889-132226889 + TCGA-EE-A2MR-06 COSM3655063 c.55T>A p.Y19N Substitution - Missense 9:132166886-132166886 + T3152 COSM4708506 c.1157A>G p.Q386R Substitution - Missense 9:132239206-132239206 + TCGA-FU-A23L-01 COSM462432 c.204C>G p.F68L Substitution - Missense 9:132167035-132167035 + HCC061T COSM5805579 c.1303G>T p.G435C Substitution - Missense 9:132240990-132240990 + UACC-62 COSM1674915 c.251C>T p.S84F Substitution - Missense 9:132198003-132198003 + TCGA-AR-A2LK-01 COSM3847906 c.405C>T p.D135D Substitution - coding silent 9:132198157-132198157 + TCGA-06-0190-02 COSM3413405 c.757C>T p.R253C Substitution - Missense 9:132198509-132198509 + TCGA-G9-6499-01 COSM3675264 c.272C>A p.P91Q Substitution - Missense 9:132198024-132198024 + TCGA-D5-6928-01 COSM5165951 c.676G>A p.D226N Substitution - Missense 9:132198428-132198428 + J80_T COSM3952415 c.472G>T p.G158W Substitution - Missense 9:132198224-132198224 + BD184T COSM296370 c.429C>T p.Y143Y Substitution - coding silent 9:132198181-132198181 + HCT15 COSM4611672 c.188_189insC p.E66fs*1 Insertion - Frameshift 9:132167019-132167020 + TCGA-FW-A3TV-06 COSM3655067 c.735G>A p.E245E Substitution - coding silent 9:132198487-132198487 + TCGA-FS-A1ZZ-06 COSM3655070 c.844G>A p.E282K Substitution - Missense 9:132198596-132198596 + 2292385 COSM4610534 c.634C>T p.R212C Substitution - Missense 9:132198386-132198386 + TCGA-D8-A1XQ-01 COSM3847908 c.877G>A p.A293T Substitution - Missense 9:132226868-132226868 + S02284 COSM5684269 c.763C>A p.R255R Substitution - coding silent 9:132198515-132198515 + TCGA-A5-A0GP-01 COSM1106208 c.1083C>T p.R361R Substitution - coding silent 9:132239132-132239132 + SC_9081 COSM3212344 c.635G>A p.R212H Substitution - Missense 9:132198387-132198387 + CRC-04T COSM5468471 c.471C>T p.N157N Substitution - coding silent 9:132198223-132198223 + TCGA-HU-A4GQ-01 COSM3905034 c.948C>T p.C316C Substitution - coding silent 9:132226939-132226939 + TCGA-EE-A2MR-06 COSM3655061 c.55T>A p.Y19N Substitution - Missense 9:132166886-132166886 + TCGA-EI-6882-01 COSM3432942 c.774C>T p.R258R Substitution - coding silent 9:132198526-132198526 + pfg016T COSM1643766 c.750C>T p.T250T Substitution - coding silent 9:132198502-132198502 + T1764 COSM3212338 c.501C>T p.Y167Y Substitution - coding silent 9:132198253-132198253 + XHDG38 COSM3763691 c.876C>T p.H292H Substitution - coding silent 9:132226867-132226867 + T3306 COSM4371478 c.501C>T p.Y167Y Substitution - coding silent 9:132198253-132198253 + LUAD-F00121 COSM365921 c.938G>T p.G313V Substitution - Missense 9:132226929-132226929 + S02285 COSM5685032 c.1540A>C p.T514P Substitution - Missense 9:132242058-132242058 + TCGA-IP-7968-01 COSM3905016 c.472G>A p.G158R Substitution - Missense 9:132198224-132198224 + I2L-P19Ta-Tumor-Organoid COSM3905022 c.670G>A p.G224S Substitution - Missense 9:132198422-132198422 + CSCC-31-T COSM4554500 c.622G>A p.E208K Substitution - Missense 9:132198374-132198374 + CSCC-31-T COSM4504136 c.657C>T p.F219F Substitution - coding silent 9:132198409-132198409 + T16 COSM455513 c.828C>T p.Y276Y Substitution - coding silent 9:132198580-132198580 + SNUH_G76_S1 COSM455512 c.738C>T p.F246F Substitution - coding silent 9:132198490-132198490 + TCGA-AD-6965-01 COSM5131989 c.882C>A p.N294K Substitution - Missense 9:132226873-132226873 + sysucc-1944T COSM455510 c.575G>A p.R192H Substitution - Missense 9:132198327-132198327 + sysucc-1135T COSM5480032 c.916G>A p.E306K Substitution - Missense 9:132226907-132226907 + 23_tFL COSM4171865 c.32G>A p.C11Y Substitution - Missense 9:132166863-132166863 + CHC320T COSM4408488 c.857+2T>G p.? Unknown 9:132198611-132198611 + T3340 COSM4708498 c.550G>A p.D184N Substitution - Missense 9:132198302-132198302 + cSCCP7 COSM139807 c.295G>A p.E99K Substitution - Missense 9:132198047-132198047 + J80_T COSM3952417 c.472G>T p.G158W Substitution - Missense 9:132198224-132198224 + TCGA-F1-6177-01 COSM3905013 c.432C>T p.G144G Substitution - coding silent 9:132198184-132198184 + TCGA-AR-A2LK-01 COSM3847904 c.405C>T p.D135D Substitution - coding silent 9:132198157-132198157 + 40M COSM5585988 c.663C>T p.I221I Substitution - coding silent 9:132198415-132198415 + TCGA-EE-A29H-06 COSM3655073 c.987G>A p.R329R Substitution - coding silent 9:132226978-132226978 + TCGA-EE-A29H-06 COSM3655075 c.987G>A p.R329R Substitution - coding silent 9:132226978-132226978 + CSCC-31-T COSM4530812 c.172G>A p.G58S Substitution - Missense 9:132167003-132167003 + CSCC-35-T COSM4495322 c.450C>T p.V150V Substitution - coding silent 9:132198202-132198202 + PTC-28C COSM3763693 c.876C>T p.H292H Substitution - coding silent 9:132226867-132226867 + TCGA-BR-4370-01 COSM3905042 c.1141C>T p.R381* Substitution - Nonsense 9:132239190-132239190 + TCGA-FW-A3R5-06 COSM3926327 c.451C>T p.L151L Substitution - coding silent 9:132198203-132198203 + 6115250 COSM5558077 c.1309A>C p.K437Q Substitution - Missense 9:132240996-132240996 + GC9_T COSM146368 c.1060G>T p.E354* Substitution - Nonsense 9:132239109-132239109 + TCGA-66-2773-01 COSM753349 c.713A>G p.E238G Substitution - Missense 9:132198465-132198465 + CPCG0078-F1 COSM4880907 c.340C>T p.R114C Substitution - Missense 9:132198092-132198092 + 19M COSM5579146 c.305G>A p.G102D Substitution - Missense 9:132198057-132198057 + I2L-P19Ta-Tumor-Biopsy COSM3905022 c.670G>A p.G224S Substitution - Missense 9:132198422-132198422 + TCGA-CD-A4MG-01 COSM3905030 c.748A>G p.T250A Substitution - Missense 9:132198500-132198500 + T3724 COSM4708501 c.646C>T p.R216W Substitution - Missense 9:132198398-132198398 + 250T COSM4382383 c.704C>T p.T235M Substitution - Missense 9:132198456-132198456 + TCGA-EI-6882-01 COSM3432944 c.774C>T p.R258R Substitution - coding silent 9:132198526-132198526 + 46M COSM3212351 c.969C>T p.F323F Substitution - coding silent 9:132226960-132226960 + N-Thy009 COSM5069651 c.779C>T p.A260V Substitution - Missense 9:132198531-132198531 + RK187_C01 COSM3745867 c.977G>T p.R326L Substitution - Missense 9:132226968-132226968 + S02322 COSM5691626 c.405C>A p.D135E Substitution - Missense 9:132198157-132198157 + TCGA-BT-A2LA-01 COSM1314580 c.711G>A p.L237L Substitution - coding silent 9:132198463-132198463 + T3090 COSM296370 c.429C>T p.Y143Y Substitution - coding silent 9:132198181-132198181 + TCGA-BR-8487-01 COSM3905021 c.556T>C p.S186P Substitution - Missense 9:132198308-132198308 + ESO-859 COSM1239646 c.877G>A p.A293T Substitution - Missense 9:132226868-132226868 + TCGA-FS-A1ZZ-06 COSM3655072 c.844G>A p.E282K Substitution - Missense 9:132198596-132198596 + 8067926 COSM4389335 c.600G>A p.S200S Substitution - coding silent 9:132198352-132198352 + HN_62854 COSM121354 c.78G>A p.V26V Substitution - coding silent 9:132166909-132166909 + TCGA-EK-A2PM-01 COSM4831651 c.525C>T p.F175F Substitution - coding silent 9:132198277-132198277 + TCGA-CM-6680-01 COSM364138 c.985C>T p.R329W Substitution - Missense 9:132226976-132226976 + sysucc-1944T COSM4371491 c.575G>A p.R192H Substitution - Missense 9:132198327-132198327 + CRC-13T COSM5479397 c.377C>T p.S126L Substitution - Missense 9:132198129-132198129 + TCGA-KK-A59V-01 COSM4504136 c.657C>T p.F219F Substitution - coding silent 9:132198409-132198409 + TCGA-FW-A3R5-06 COSM3926326 c.184G>A p.G62R Substitution - Missense 9:132167015-132167015 + Pat_76_B COSM5875748 c.94C>T p.P32S Substitution - Missense 9:132166925-132166925 + 08-237 COSM305439 c.273G>A p.P91P Substitution - coding silent 9:132198025-132198025 + TCGA-DJ-A3VM-01 COSM3375144 c.341G>T p.R114L Substitution - Missense 9:132198093-132198093 + TCGA-C8-A138-01 COSM4371491 c.575G>A p.R192H Substitution - Missense 9:132198327-132198327 + pfg039T COSM4761700 c.602G>A p.R201H Substitution - Missense 9:132198354-132198354 + 587376 COSM1217988 c.17C>T p.A6V Substitution - Missense 9:132166848-132166848 + T1764 COSM4371478 c.501C>T p.Y167Y Substitution - coding silent 9:132198253-132198253 + cSCCP8 COSM143719 c.436_437CC>AT p.P146I Substitution - Missense 9:132198188-132198189 + sysucc-1317T COSM288969 c.779C>T p.A260V Substitution - Missense 9:132198531-132198531 + 40M COSM5585990 c.663C>T p.I221I Substitution - coding silent 9:132198415-132198415 + sysucc-809T COSM1460670 c.682C>T p.R228C Substitution - Missense 9:132198434-132198434 + Sample_1 COSM4408490 c.857+2T>G p.? Unknown 9:132198611-132198611 + CSCC-31-T COSM4504138 c.657C>T p.F219F Substitution - coding silent 9:132198409-132198409 + TCGA-76-6656-01 COSM3748407 c.97A>C p.T33P Substitution - Missense 9:132166928-132166928 + TCGA-AA-3492-01 COSM5097713 c.172G>T p.G58C Substitution - Missense 9:132167003-132167003 + TCGA-C8-A12M-01 COSM455511 c.675C>T p.P225P Substitution - coding silent 9:132198427-132198427 + LUAD-CHTN-3090346 COSM357124 c.783G>T p.L261L Substitution - coding silent 9:132198535-132198535 + BD231T COSM5496881 c.631G>A p.V211M Substitution - Missense 9:132198383-132198383 + 389 COSM4427766 c.676G>T p.D226Y Substitution - Missense 9:132198428-132198428 + TCGA-C5-A1MJ-01 COSM4842817 c.476G>A p.R159H Substitution - Missense 9:132198228-132198228 + PD13619a COSM5783599 c.1142G>A p.R381Q Substitution - Missense 9:132239191-132239191 + TCGA-AK-3447-01 COSM1497037 c.549C>T p.R183R Substitution - coding silent 9:132198301-132198301 + TCGA-BR-8680-01 COSM3905002 c.235A>G p.N79D Substitution - Missense 9:132197987-132197987 + S02322 COSM5691624 c.405C>A p.D135E Substitution - Missense 9:132198157-132198157 + N-Thy009 COSM288969 c.779C>T p.A260V Substitution - Missense 9:132198531-132198531 + TCGA-EE-A3J5-06 COSM3926332 c.963G>A p.K321K Substitution - coding silent 9:132226954-132226954 + PTC-10C COSM3763691 c.876C>T p.H292H Substitution - coding silent 9:132226867-132226867 + TCGA-BR-6852-01 COSM3905012 c.430G>A p.G144S Substitution - Missense 9:132198182-132198182 + TCGA-06-5858-01 COSM3413402 c.705G>A p.T235T Substitution - coding silent 9:132198457-132198457 + TCGA-BR-4184-01 COSM3905040 c.1119C>T p.C373C Substitution - coding silent 9:132239168-132239168 + TCGA-HC-7079-01 COSM3675267 c.352C>A p.P118T Substitution - Missense 9:132198104-132198104 + TCGA-CD-A4MG-01 COSM3905025 c.695A>G p.N232S Substitution - Missense 9:132198447-132198447 + CSCC-11-T COSM4478095 c.220C>T p.P74S Substitution - Missense 9:132197972-132197972 + YUMOBER COSM5410581 c.21C>T p.L7L Substitution - coding silent 9:132166852-132166852 + TCGA-AA-3872-01 COSM296370 c.429C>T p.Y143Y Substitution - coding silent 9:132198181-132198181 + TCGA-HU-A4GQ-01 COSM3905037 c.981C>A p.S327S Substitution - coding silent 9:132226972-132226972 + XHDG38 COSM3763693 c.876C>T p.H292H Substitution - coding silent 9:132226867-132226867 + 8067926 COSM4389333 c.600G>A p.S200S Substitution - coding silent 9:132198352-132198352 + S01023 COSM5666824 c.786C>A p.G262G Substitution - coding silent 9:132198538-132198538 + TCGA-EK-A2PM-01 COSM4831653 c.525C>T p.F175F Substitution - coding silent 9:132198277-132198277 + C135 COSM4618833 c.589G>A p.E197K Substitution - Missense 9:132198341-132198341 + pfg043T COSM4761703 c.926A>G p.H309R Substitution - Missense 9:132226917-132226917 + CSCC-35-T COSM4495324 c.450C>T p.V150V Substitution - coding silent 9:132198202-132198202 + 250T COSM4382381 c.704C>T p.T235M Substitution - Missense 9:132198456-132198456 + TCGA-A6-6653-01 COSM305439 c.273G>A p.P91P Substitution - coding silent 9:132198025-132198025 + CSCC-49-T COSM139807 c.295G>A p.E99K Substitution - Missense 9:132198047-132198047 + 389 COSM4427764 c.676G>T p.D226Y Substitution - Missense 9:132198428-132198428 + CSCC-55-T COSM4544465 c.357G>A p.L119L Substitution - coding silent 9:132198109-132198109 + pfg039T COSM4761702 c.602G>A p.R201H Substitution - Missense 9:132198354-132198354 + CRC-04T COSM5468473 c.471C>T p.N157N Substitution - coding silent 9:132198223-132198223 + TCGA-D1-A176-01 COSM1106207 c.440C>T p.T147M Substitution - Missense 9:132198192-132198192 + TCGA-22-5472-01 COSM752489 c.652C>A p.R218S Substitution - Missense 9:132198404-132198404 + BD184T COSM4708494 c.429C>T p.Y143Y Substitution - coding silent 9:132198181-132198181 + Au4 COSM5604278 c.441G>A p.T147T Substitution - coding silent 9:132198193-132198193 + 1N34-VS-1T34 COSM4974819 c.949G>A p.G317S Substitution - Missense 9:132226940-132226940 + TCGA-BR-4292-01 COSM3905007 c.378G>A p.S126S Substitution - coding silent 9:132198130-132198130 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.163642 9q34

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer - AC IntronicInsertion . c.1054+2738_1054+2739insAC 9 135108720 CM A C Missense p.T105P c.313A>C 9 135073452 OV A C Missense p.T33P c.97A>C 9 135042315 GBM A G Missense p.E238G c.713A>G 9 135073852 LUSC A G Missense p.Q304R c.911A>G 9 135102289 SCLC C A Missense p.F219L c.657C>A 9 135073796 LUAD C A Missense p.P118T c.352C>A 9 135073491 PRAD C A Missense p.P91Q c.272C>A 9 135073411 PRAD C A Missense p.R218S c.652C>A 9 135073791 LUSC C A Synonymous p.R326R c.976C>A 9 135102354 RCCC C A Synonymous p.R329R c.985C>A 9 135102363 LUAD CG AA Missense p.V131M c.390_391delinsAA 9 135073529 LUAD C G IntronicSNV . c.213+9795C>G 9 135052226 PIA C T IntronicSNV . c.858-11865C>T 9 135090371 CLL C T Missense p.A260V c.779C>T 9 135073918 COREAD C T Missense p.R253C c.757C>T 9 135073896 GBM C T Missense p.T147M c.440C>T 9 135073579 UCEC C T Nonsense p.R381* c.1141C>T 9 135114577 STAD C T Synonymous p.A168A c.504C>T 9 135073643 COREAD C T Synonymous p.F213F c.639C>T 9 135073778 BRCA C T Synonymous p.F96F c.288C>T 9 135073427 ESCA C T Synonymous p.G144G c.432C>T 9 135073571 STAD C T Synonymous p.P225P c.675C>T 9 135073814 BRCA C T Synonymous p.P225P c.675C>T 9 135073814 STAD C T Synonymous p.P314P c.942C>T 9 135102320 COREAD C T Synonymous p.R361R c.1083C>T 9 135114519 UCEC C T Synonymous p.T250T c.750C>T 9 135073889 STAD C T Synonymous p.V374V c.1122C>T 9 135114558 LUSC C T Synonymous p.Y143Y c.429C>T 9 135073568 COREAD G A IntronicSNV . c.857+6236G>A 9 135080232 CLL G A Missense p.A293T c.877G>A 9 135102255 ESCA G A Missense p.D136N c.406G>A 9 135073545 CM G A Missense p.E169K c.505G>A 9 135073644 HNSC G A Missense p.E282K c.844G>A 9 135073983 CM G A Missense p.G144S c.430G>A 9 135073569 STAD G A Missense p.G224S c.670G>A 9 135073809 STAD G A Missense p.G331S c.991G>A 9 135102369 MM G A Missense p.R192H c.575G>A 9 135073714 BRCA G A Synonymous p.K321K c.963G>A 9 135102341 CM G A Synonymous p.K53K c.159G>A 9 135042377 CM G A Synonymous p.L237L c.711G>A 9 135073850 BLCA G A Synonymous p.P91P c.273G>A 9 135073412 STAD G A Synonymous p.R236R c.708G>A 9 135073847 HNSC G A Synonymous p.R329R c.987G>A 9 135102365 CM G A Synonymous p.S126S c.378G>A 9 135073517 STAD G A Synonymous p.T235T c.705G>A 9 135073844 STAD G A Synonymous p.V26V c.78G>A 9 135042296 HNSC G T Missense p.E403D c.1209G>T 9 135114645 LUAD G T Missense p.M1I c.3G>T 9 135042221 LUAD G T Missense p.Q464H c.1392G>T 9 135117297 SCLC G T Nonsense p.E100* c.298G>T 9 135073437 LUAD G T Nonsense p.E30* c.88G>T 9 135042306 ESCA T G Missense p.L291R c.872T>G 9 135102250 CM