Mutation - TCGA Type Chromosome Start Position End Position Strand Variant Classification Variant Type Reference Allele Tumor_seq Allele 1 Tumor_seq Allele 2 Tumor Sample Barcode Matched Norm Sample Barcode Genome Change cDNA Change Codon Change Protein Change ACC 11 118344186 118344186 + Frame_Shift_Del DEL C C - TCGA-OR-A5LB-01A-11D-A29I-10 TCGA-OR-A5LB-10A-01D-A29L-10 g.chr11:118344186delC c.2312delC c.(2311-2313)accfs p.T771fs ACC 11 118344494 118344495 + Frame_Shift_Del DEL AG AG - TCGA-OR-A5LB-01A-11D-A29I-10 TCGA-OR-A5LB-10A-01D-A29L-10 g.chr11:118344494_118344495delAG c.2620_2621delAG c.(2620-2622)agafs p.R874fs ACC 11 118344503 118344503 + Missense_Mutation SNP G G C TCGA-OR-A5J4-01A-11D-A29I-10 TCGA-OR-A5J4-10A-01D-A29L-10 g.chr11:118344503G>C c.2629G>C c.(2629-2631)Gac>Cac p.D877H ACC 11 118367048 118367048 + Missense_Mutation SNP C C T TCGA-OR-A5LB-01A-11D-A29I-10 TCGA-OR-A5LB-10A-01D-A29L-10 g.chr11:118367048C>T c.5621C>T c.(5620-5622)gCg>gTg p.A1874V ACC 11 118368752 118368752 + Missense_Mutation SNP G G C TCGA-OR-A5JY-01A-31D-A29I-10 TCGA-OR-A5JY-10A-01D-A29L-10 g.chr11:118368752G>C c.5757G>C c.(5755-5757)aaG>aaC p.K1919N BLCA 11 118339535 118339535 + Nonsense_Mutation SNP C C T TCGA-GU-A766-01A-11D-A32B-08 TCGA-GU-A766-10A-01D-A329-08 g.chr11:118339535C>T c.478C>T c.(478-480)Cga>Tga p.R160* BLCA 11 118342391 118342391 + Nonsense_Mutation SNP C C T TCGA-DK-A2I6-01A-12D-A18F-08 TCGA-DK-A2I6-10A-01D-A18F-08 g.chr11:118342391C>T c.517C>T c.(517-519)Cga>Tga p.R173* BLCA 11 118342400 118342400 + Missense_Mutation SNP C C G TCGA-ZF-A9R4-01A-11D-A38G-08 TCGA-ZF-A9R4-10A-01D-A38J-08 g.chr11:118342400C>G c.526C>G c.(526-528)Cgt>Ggt p.R176G BLCA 11 118342446 118342446 + Nonsense_Mutation SNP C C G TCGA-ZF-A9R4-01A-11D-A38G-08 TCGA-ZF-A9R4-10A-01D-A38J-08 g.chr11:118342446C>G c.572C>G c.(571-573)tCa>tGa p.S191* BLCA 11 118342573 118342573 + Missense_Mutation SNP C C G TCGA-GC-A6I1-01A-12D-A31L-08 TCGA-GC-A6I1-10A-01D-A31J-08 g.chr11:118342573C>G c.699C>G c.(697-699)atC>atG p.I233M BLCA 11 118342656 118342656 + Missense_Mutation SNP C C T TCGA-GC-A6I1-01A-12D-A31L-08 TCGA-GC-A6I1-10A-01D-A31J-08 g.chr11:118342656C>T c.782C>T c.(781-783)tCt>tTt p.S261F BLCA 11 118342780 118342780 + Silent SNP G G C TCGA-SY-A9G5-01A-11D-A38G-08 TCGA-SY-A9G5-10A-01D-A38J-08 g.chr11:118342780G>C c.906G>C c.(904-906)cgG>cgC p.R302R BLCA 11 118342797 118342797 + Missense_Mutation SNP C C T TCGA-GU-AATO-01A-11D-A391-08 TCGA-GU-AATO-10A-01D-A394-08 g.chr11:118342797C>T c.923C>T c.(922-924)tCa>tTa p.S308L BLCA 11 118342877 118342877 + Nonsense_Mutation SNP G G T TCGA-SY-A9G5-01A-11D-A38G-08 TCGA-SY-A9G5-10A-01D-A38J-08 g.chr11:118342877G>T c.1003G>T c.(1003-1005)Gaa>Taa p.E335* BLCA 11 118343093 118343093 + Nonsense_Mutation SNP C C T TCGA-K4-A5RH-01A-11D-A30E-08 TCGA-K4-A5RH-10A-01D-A30H-08 g.chr11:118343093C>T c.1219C>T c.(1219-1221)Cga>Tga p.R407* BLCA 11 118343252 118343252 + Missense_Mutation SNP G G A TCGA-SY-A9G5-01A-11D-A38G-08 TCGA-SY-A9G5-10A-01D-A38J-08 g.chr11:118343252G>A c.1378G>A c.(1378-1380)Gaa>Aaa p.E460K BLCA 11 118344057 118344057 + Missense_Mutation SNP C C T TCGA-K4-A4AB-01B-12D-A289-08 TCGA-K4-A4AB-10A-01D-A289-08 g.chr11:118344057C>T c.2183C>T c.(2182-2184)tCt>tTt p.S728F BLCA 11 118344283 118344283 + Silent SNP G G A TCGA-CF-A47X-01A-31D-A23U-08 TCGA-CF-A47X-10A-01D-A23U-08 g.chr11:118344283G>A c.2409G>A c.(2407-2409)ctG>ctA p.L803L BLCA 11 118344287 118344287 + Nonsense_Mutation SNP C C T TCGA-4Z-AA7W-01A-11D-A391-08 TCGA-4Z-AA7W-10A-01D-A394-08 g.chr11:118344287C>T c.2413C>T c.(2413-2415)Cag>Tag p.Q805* BLCA 11 118344314 118344314 + Nonsense_Mutation SNP C C T TCGA-XF-A8HI-01A-11D-A38G-08 TCGA-XF-A8HI-10A-01D-A38J-08 g.chr11:118344314C>T c.2440C>T c.(2440-2442)Cag>Tag p.Q814* BLCA 11 118344511 118344511 + Silent SNP G G A TCGA-DK-A1A3-01A-11D-A13W-08 TCGA-DK-A1A3-10A-01D-A13W-08 g.chr11:118344511G>A c.2637G>A c.(2635-2637)gaG>gaA p.E879E BLCA 11 118344537 118344537 + Missense_Mutation SNP C C T TCGA-K4-A6MB-01A-11D-A31L-08 TCGA-K4-A6MB-10A-01D-A31J-08 g.chr11:118344537C>T c.2663C>T c.(2662-2664)tCa>tTa p.S888L BLCA 11 118344991 118344991 + Missense_Mutation SNP G G C TCGA-E7-A7XN-01A-11D-A34U-08 TCGA-E7-A7XN-10A-01D-A34X-08 g.chr11:118344991G>C c.3117G>C c.(3115-3117)aaG>aaC p.K1039N BLCA 11 118348833 118348833 + Missense_Mutation SNP G G C TCGA-DK-A6B2-01A-11D-A30E-08 TCGA-DK-A6B2-10A-01D-A30H-08 g.chr11:118348833G>C c.3486G>C c.(3484-3486)caG>caC p.Q1162H BLCA 11 118348836 118348836 + Silent SNP G G T TCGA-XF-A9T8-01A-11D-A391-08 TCGA-XF-A9T8-10A-01D-A394-08 g.chr11:118348836G>T c.3489G>T c.(3487-3489)gtG>gtT p.V1163V BLCA 11 118348840 118348840 + Missense_Mutation SNP G G A TCGA-DK-A1AC-01A-11D-A13W-08 TCGA-DK-A1AC-10A-01D-A13W-08 g.chr11:118348840G>A c.3493G>A c.(3493-3495)Gag>Aag p.E1165K BLCA 11 118352585 118352585 + Nonsense_Mutation SNP C C T TCGA-5N-A9KI-01A-31D-A42E-08 TCGA-5N-A9KI-10A-01D-A42H-08 g.chr11:118352585C>T c.3790C>T c.(3790-3792)Cga>Tga p.R1264* BLCA 11 118352808 118352808 + Splice_Site SNP G G A TCGA-FD-A3SJ-01A-12D-A22Z-08 TCGA-FD-A3SJ-10A-01D-A22Z-08 g.chr11:118352808G>A c.e7+1 BLCA 11 118355688 118355688 + Missense_Mutation SNP G G C TCGA-BL-A3JM-01A-12D-A21A-08 TCGA-BL-A3JM-11A-31D-A21A-08 g.chr11:118355688G>C c.4330G>C c.(4330-4332)Gag>Cag p.E1444Q BLCA 11 118359411 118359411 + Frame_Shift_Del DEL A A - TCGA-BT-A2LB-01A-11D-A18F-08 TCGA-BT-A2LB-10A-01D-A18F-08 g.chr11:118359411delA c.4415delA c.(4414-4416)gaafs p.E1472fs BLCA 11 118361911 118361911 + Splice_Site SNP G G A TCGA-BT-A0YX-01A-11D-A10S-08 TCGA-BT-A0YX-10A-01D-A10S-08 g.chr11:118361911G>A c.4697G>A c.(4696-4698)gGa>gAa p.G1566E BLCA 11 118363895 118363895 + Missense_Mutation SNP G G A TCGA-G2-A3VY-01A-11D-A22Z-08 TCGA-G2-A3VY-10A-01D-A22Z-08 g.chr11:118363895G>A c.5119G>A c.(5119-5121)Gat>Aat p.D1707N BLCA 11 118368671 118368671 + Nonsense_Mutation SNP T T G TCGA-FD-A3N5-01A-11D-A21A-08 TCGA-FD-A3N5-10A-01D-A21A-08 g.chr11:118368671T>G c.5676T>G c.(5674-5676)taT>taG p.Y1892* BLCA 11 118369132 118369132 + Silent SNP C C T TCGA-DK-A3X1-01A-12D-A22Z-08 TCGA-DK-A3X1-10A-01D-A22Z-08 g.chr11:118369132C>T c.5841C>T c.(5839-5841)ctC>ctT p.L1947L BLCA 11 118371720 118371720 + Nonsense_Mutation SNP G G A TCGA-XF-A9SM-01A-11D-A42E-08 TCGA-XF-A9SM-10A-01D-A42H-08 g.chr11:118371720G>A c.6168G>A c.(6166-6168)tgG>tgA p.W2056* BLCA 11 118372424 118372425 + Frame_Shift_Del DEL TA TA - TCGA-UY-A78O-01A-12D-A339-08 TCGA-UY-A78O-10A-01D-A339-08 g.chr11:118372424_118372425delTA c.6348_6349delTA c.(6346-6351)attatafs p.II2116fs BLCA 11 118372453 118372453 + Missense_Mutation SNP C C T TCGA-UY-A9PF-01A-11D-A38G-08 TCGA-UY-A9PF-10A-01D-A38J-08 g.chr11:118372453C>T c.6377C>T c.(6376-6378)cCt>cTt p.P2126L BLCA 11 118373371 118373371 + Nonsense_Mutation SNP C C G TCGA-K4-A5RJ-01A-11D-A289-08 TCGA-K4-A5RJ-10A-01D-A289-08 g.chr11:118373371C>G c.6755C>G c.(6754-6756)tCa>tGa p.S2252* BLCA 11 118373660 118373660 + Silent SNP C C T TCGA-DK-AA6S-01A-21D-A391-08 TCGA-DK-AA6S-10A-01D-A394-08 g.chr11:118373660C>T c.7044C>T c.(7042-7044)atC>atT p.I2348I BLCA 11 118373680 118373680 + Missense_Mutation SNP C C T TCGA-ZF-A9RC-01A-11D-A38G-08 TCGA-ZF-A9RC-10A-01D-A38J-08 g.chr11:118373680C>T c.7064C>T c.(7063-7065)tCt>tTt p.S2355F BLCA 11 118373732 118373732 + Missense_Mutation SNP G G C TCGA-MV-A51V-01A-11D-A26M-08 TCGA-MV-A51V-10A-01D-A26K-08 g.chr11:118373732G>C c.7116G>C c.(7114-7116)ttG>ttC p.L2372F BLCA 11 118373897 118373897 + Silent SNP G G A TCGA-FD-A6TB-01A-12D-A339-08 TCGA-FD-A6TB-10A-21D-A339-08 g.chr11:118373897G>A c.7281G>A c.(7279-7281)caG>caA p.Q2427Q BLCA 11 118373957 118373969 + Frame_Shift_Del DEL GGAACCTGGTCAG GGAACCTGGTCAG - TCGA-BT-A20J-01A-11D-A14W-08 TCGA-BT-A20J-11A-11D-A14W-08 g.chr11:118373957_118373969delGGAACCTGGTCAG c.7341_7353delGGAACCTGGTCAG c.(7339-7353)ttggaacctggtcagfs p.LEPGQ2447fs BLCA 11 118374046 118374046 + Missense_Mutation SNP G G A TCGA-MV-A51V-01A-11D-A26M-08 TCGA-MV-A51V-10A-01D-A26K-08 g.chr11:118374046G>A c.7430G>A c.(7429-7431)cGa>cAa p.R2477Q BLCA 11 118374132 118374132 + Missense_Mutation SNP G G A TCGA-BT-A20Q-01A-11D-A14W-08 TCGA-BT-A20Q-11A-11D-A14W-08 g.chr11:118374132G>A c.7516G>A c.(7516-7518)Gaa>Aaa p.E2506K BLCA 11 118374132 118374132 + Missense_Mutation SNP G G C TCGA-CF-A1HR-01A-11D-A13W-08 TCGA-CF-A1HR-10A-01D-A13W-08 g.chr11:118374132G>C c.7516G>C c.(7516-7518)Gaa>Caa p.E2506Q BLCA 11 118374212 118374212 + Missense_Mutation SNP G G T TCGA-K4-A4AC-01A-21D-A26M-08 TCGA-K4-A4AC-10A-01D-A26K-08 g.chr11:118374212G>T c.7596G>T c.(7594-7596)gaG>gaT p.E2532D BLCA 11 118374297 118374298 + Frame_Shift_Ins INS - - CCTC TCGA-FD-A3B6-01A-21D-A20D-08 TCGA-FD-A3B6-10A-01D-A20D-08 g.chr11:118374297_118374298insCCTC c.7681_7682insCCTC c.(7681-7683)gccfs p.-2562fs BLCA 11 118374380 118374380 + Nonsense_Mutation SNP T T A TCGA-GC-A6I3-01A-11D-A31L-08 TCGA-GC-A6I3-10A-01D-A31J-08 g.chr11:118374380T>A c.7764T>A c.(7762-7764)taT>taA p.Y2588* BLCA 11 118374590 118374590 + Missense_Mutation SNP G G C TCGA-BT-A20Q-01A-11D-A14W-08 TCGA-BT-A20Q-11A-11D-A14W-08 g.chr11:118374590G>C c.7974G>C c.(7972-7974)aaG>aaC p.K2658N BLCA 11 118374637 118374637 + Nonsense_Mutation SNP C C G TCGA-GC-A3RC-01A-11D-A22Z-08 TCGA-GC-A3RC-10B-01D-A22Z-08 g.chr11:118374637C>G c.8021C>G c.(8020-8022)tCa>tGa p.S2674* BLCA 11 118374909 118374909 + Missense_Mutation SNP G G C TCGA-BT-A20N-01A-11D-A14W-08 TCGA-BT-A20N-11A-11D-A14W-08 g.chr11:118374909G>C c.8293G>C c.(8293-8295)Gaa>Caa p.E2765Q BLCA 11 118375019 118375019 + Silent SNP C C A TCGA-E5-A4TZ-01A-11D-A31L-08 TCGA-E5-A4TZ-10B-01D-A31J-08 g.chr11:118375019C>A c.8403C>A c.(8401-8403)ctC>ctA p.L2801L BLCA 11 118375024 118375024 + Missense_Mutation SNP C C T TCGA-CU-A0YO-01A-11D-A10S-08 TCGA-CU-A0YO-10A-01D-A10S-08 g.chr11:118375024C>T c.8408C>T c.(8407-8409)tCa>tTa p.S2803L BLCA 11 118375131 118375131 + Missense_Mutation SNP G G A TCGA-BT-A20Q-01A-11D-A14W-08 TCGA-BT-A20Q-11A-11D-A14W-08 g.chr11:118375131G>A c.8515G>A c.(8515-8517)Gat>Aat p.D2839N BLCA 11 118375134 118375134 + Missense_Mutation SNP G G A TCGA-DK-A3X1-01A-12D-A22Z-08 TCGA-DK-A3X1-10A-01D-A22Z-08 g.chr11:118375134G>A c.8518G>A c.(8518-8520)Gac>Aac p.D2840N BLCA 11 118375563 118375563 + Missense_Mutation SNP C C T TCGA-ZF-A9RF-01A-11D-A38G-08 TCGA-ZF-A9RF-10A-01D-A38J-08 g.chr11:118375563C>T c.8947C>T c.(8947-8949)Cca>Tca p.P2983S BLCA 11 118376222 118376222 + Silent SNP C C T TCGA-ZF-AA4V-01A-11D-A38G-08 TCGA-ZF-AA4V-10A-01D-A38J-08 g.chr11:118376222C>T c.9606C>T c.(9604-9606)agC>agT p.S3202S BLCA 11 118376326 118376326 + Missense_Mutation SNP C C G TCGA-XF-A9T8-01A-11D-A391-08 TCGA-XF-A9T8-10A-01D-A394-08 g.chr11:118376326C>G c.9710C>G c.(9709-9711)tCt>tGt p.S3237C BLCA 11 118376446 118376446 + Missense_Mutation SNP C C T TCGA-FD-A6TG-01A-11D-A32B-08 TCGA-FD-A6TG-10A-01D-A329-08 g.chr11:118376446C>T c.9830C>T c.(9829-9831)tCa>tTa p.S3277L BLCA 11 118376454 118376454 + Nonsense_Mutation SNP C C T TCGA-C4-A0F1-01A-11D-A10S-08 TCGA-C4-A0F1-10A-01D-A10S-08 g.chr11:118376454C>T c.9838C>T c.(9838-9840)Cga>Tga p.R3280* BLCA 11 118376908 118376908 + Missense_Mutation SNP C C G TCGA-ZF-A9RF-01A-11D-A38G-08 TCGA-ZF-A9RF-10A-01D-A38J-08 g.chr11:118376908C>G c.10292C>G c.(10291-10293)tCc>tGc p.S3431C BLCA 11 118377246 118377246 + Nonsense_Mutation SNP C C T TCGA-E7-A7XN-01A-11D-A34U-08 TCGA-E7-A7XN-10A-01D-A34X-08 g.chr11:118377246C>T c.10630C>T c.(10630-10632)Cag>Tag p.Q3544* BLCA 11 118378252 118378252 + Missense_Mutation SNP G G A TCGA-UY-A9PD-01A-11D-A38G-08 TCGA-UY-A9PD-10A-01D-A38J-08 g.chr11:118378252G>A c.10754G>A c.(10753-10755)gGa>gAa p.G3585E BLCA 11 118382708 118382708 + Nonsense_Mutation SNP C C G TCGA-GC-A3WC-01A-31D-A22Z-08 TCGA-GC-A3WC-10A-01D-A22Z-08 g.chr11:118382708C>G c.11105C>G c.(11104-11106)tCa>tGa p.S3702* BLCA 11 118390358 118390358 + Silent SNP G G A TCGA-DK-A3X1-01A-12D-A22Z-08 TCGA-DK-A3X1-10A-01D-A22Z-08 g.chr11:118390358G>A c.11163G>A c.(11161-11163)ggG>ggA p.G3721G BLCA 11 118390449 118390449 + Nonsense_Mutation SNP G G T TCGA-DK-A3X1-01A-12D-A22Z-08 TCGA-DK-A3X1-10A-01D-A22Z-08 g.chr11:118390449G>T c.11254G>T c.(11254-11256)Gag>Tag p.E3752* BLCA 11 118390508 118390508 + Splice_Site SNP G G A TCGA-FD-A6TH-01A-11D-A32B-08 TCGA-FD-A6TH-10A-01D-A329-08 g.chr11:118390508G>A c.e32+1 BLCA 11 118392755 118392756 + Frame_Shift_Del DEL TG TG - TCGA-DK-A2I6-01A-12D-A18F-08 TCGA-DK-A2I6-10A-01D-A18F-08 g.chr11:118392755_118392756delTG c.11778_11779delTG c.(11776-11781)attgtcfs p.V3927fs BRCA 11 118343199 118343199 + Missense_Mutation SNP G G A TCGA-E2-A574-01A-11D-A29N-09 TCGA-E2-A574-10A-01D-A29N-09 g.chr11:118343199G>A c.1325G>A c.(1324-1326)cGa>cAa p.R442Q BRCA 11 118343656 118343656 + Silent SNP A A C TCGA-A8-A0A6-01A-12W-A071-09 TCGA-A8-A0A6-10A-01W-A071-09 g.chr11:118343656A>C c.1782A>C c.(1780-1782)tcA>tcC p.S594S BRCA 11 118343828 118343828 + Nonsense_Mutation SNP C C T TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr11:118343828C>T c.1954C>T c.(1954-1956)Cga>Tga p.R652* BRCA 11 118344572 118344572 + Nonsense_Mutation SNP C C T TCGA-AR-A0TX-01A-11D-A099-09 TCGA-AR-A0TX-10A-01D-A099-09 g.chr11:118344572C>T c.2698C>T c.(2698-2700)Cag>Tag p.Q900* BRCA 11 118344574 118344575 + Frame_Shift_Ins INS - - TAAA TCGA-A2-A25E-01A-11D-A167-09 TCGA-A2-A25E-10A-01D-A167-09 g.chr11:118344574_118344575insTAAA c.2700_2701insTAAA c.(2701-2703)agtfs p.S901fs BRCA 11 118344879 118344879 + Missense_Mutation SNP C C G TCGA-C8-A27B-01A-11D-A167-09 TCGA-C8-A27B-10A-01D-A167-09 g.chr11:118344879C>G c.3005C>G c.(3004-3006)tCc>tGc p.S1002C BRCA 11 118350902 118350902 + Nonsense_Mutation SNP C C T TCGA-A8-A07P-01A-11W-A019-09 TCGA-A8-A07P-10A-01W-A021-09 g.chr11:118350902C>T c.3583C>T c.(3583-3585)Cag>Tag p.Q1195* BRCA 11 118352528 118352528 + Missense_Mutation SNP A A C TCGA-A8-A0A6-01A-12W-A071-09 TCGA-A8-A0A6-10A-01W-A071-09 g.chr11:118352528A>C c.3733A>C c.(3733-3735)Acc>Ccc p.T1245P BRCA 11 118354912 118354912 + Silent SNP G G A TCGA-AR-A1AT-01A-11D-A12Q-09 TCGA-AR-A1AT-10A-01D-A12Q-09 g.chr11:118354912G>A c.4101G>A c.(4099-4101)ccG>ccA p.P1367P BRCA 11 118359386 118359386 + Nonsense_Mutation SNP G G T TCGA-E9-A54Y-01A-11D-A25Q-09 TCGA-E9-A54Y-10A-01D-A25Q-09 g.chr11:118359386G>T c.4390G>T c.(4390-4392)Gag>Tag p.E1464* BRCA 11 118363787 118363787 + Missense_Mutation SNP G G C TCGA-AO-A03M-01B-11D-A10M-09 TCGA-AO-A03M-10A-01D-A10M-09 g.chr11:118363787G>C c.5011G>C c.(5011-5013)Gac>Cac p.D1671H BRCA 11 118366575 118366575 + Missense_Mutation SNP A A G TCGA-D8-A1XK-01A-21D-A14K-09 TCGA-D8-A1XK-10A-01D-A14K-09 g.chr11:118366575A>G c.5515A>G c.(5515-5517)Act>Gct p.T1839A BRCA 11 118367017 118367017 + Frame_Shift_Del DEL C C - TCGA-AN-A0FW-01A-11W-A050-09 TCGA-AN-A0FW-10A-01W-A055-09 g.chr11:118367017delC c.5590delC c.(5590-5592)cccfs p.P1865fs BRCA 11 118371701 118371701 + Splice_Site SNP G G A TCGA-BH-A0DE-01A-11D-A10Y-09 TCGA-BH-A0DE-10A-02D-A110-09 g.chr11:118371701G>A c.e25-1 BRCA 11 118372517 118372517 + Silent SNP A A C TCGA-A8-A0A6-01A-12W-A071-09 TCGA-A8-A0A6-10A-01W-A071-09 g.chr11:118372517A>C c.6441A>C c.(6439-6441)acA>acC p.T2147T BRCA 11 118373416 118373416 + Frame_Shift_Del DEL A A - TCGA-A2-A3Y0-01A-11D-A23C-09 TCGA-A2-A3Y0-10A-01D-A23C-09 g.chr11:118373416delA c.6800delA c.(6799-6801)caafs p.Q2267fs BRCA 11 118373824 118373824 + Missense_Mutation SNP A A G TCGA-A2-A3Y0-01A-11D-A23C-09 TCGA-A2-A3Y0-10A-01D-A23C-09 g.chr11:118373824A>G c.7208A>G c.(7207-7209)aAg>aGg p.K2403R BRCA 11 118375222 118375222 + Missense_Mutation SNP C C T TCGA-A2-A0EY-01A-11W-A050-09 TCGA-A2-A0EY-10A-01W-A055-09 g.chr11:118375222C>T c.8606C>T c.(8605-8607)tCa>tTa p.S2869L BRCA 11 118375750 118375750 + Missense_Mutation SNP A A C TCGA-A2-A0YJ-01A-11D-A10G-09 TCGA-A2-A0YJ-10A-01D-A10G-09 g.chr11:118375750A>C c.9134A>C c.(9133-9135)aAg>aCg p.K3045T BRCA 11 118375784 118375784 + Silent SNP G G A TCGA-BH-A18U-01A-21D-A12B-09 TCGA-BH-A18U-11A-23D-A12B-09 g.chr11:118375784G>A c.9168G>A c.(9166-9168)ccG>ccA p.P3056P BRCA 11 118376092 118376092 + Missense_Mutation SNP A A C TCGA-A8-A0A6-01A-12W-A071-09 TCGA-A8-A0A6-10A-01W-A071-09 g.chr11:118376092A>C c.9476A>C c.(9475-9477)cAc>cCc p.H3159P BRCA 11 118376138 118376138 + Silent SNP A A C TCGA-A8-A0A6-01A-12W-A071-09 TCGA-A8-A0A6-10A-01W-A071-09 g.chr11:118376138A>C c.9522A>C c.(9520-9522)ccA>ccC p.P3174P BRCA 11 118376471 118376471 + Silent SNP C C T TCGA-D8-A27G-01A-11D-A16D-09 TCGA-D8-A27G-10A-01D-A16D-09 g.chr11:118376471C>T c.9855C>T c.(9853-9855)atC>atT p.I3285I BRCA 11 118376746 118376746 + Missense_Mutation SNP C C T TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr11:118376746C>T c.10130C>T c.(10129-10131)tCa>tTa p.S3377L BRCA 11 118390417 118390417 + Missense_Mutation SNP G G A TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr11:118390417G>A c.11222G>A c.(11221-11223)cGa>cAa p.R3741Q BRCA 11 118391565 118391565 + Frame_Shift_Del DEL A A - TCGA-D8-A1Y1-01A-21D-A14K-09 TCGA-D8-A1Y1-10A-01D-A14K-09 g.chr11:118391565delA c.11469delA c.(11467-11469)ttafs p.L3823fs BRCA 11 118392845 118392845 + Silent SNP C C G TCGA-AN-A0FD-01A-11W-A050-09 TCGA-AN-A0FD-10A-01W-A055-09 g.chr11:118392845C>G c.11868C>G c.(11866-11868)ccC>ccG p.P3956P CESC 11 118342900 118342900 + Silent SNP A A G TCGA-JW-A852-01A-11D-A351-09 TCGA-JW-A852-10A-01D-A351-09 g.chr11:118342900A>G c.1026A>G c.(1024-1026)aaA>aaG p.K342K CESC 11 118352537 118352537 + Missense_Mutation SNP G G T TCGA-UC-A7PF-01A-11D-A351-09 TCGA-UC-A7PF-11A-31D-A351-09 g.chr11:118352537G>T c.3742G>T c.(3742-3744)Gca>Tca p.A1248S CESC 11 118362470 118362470 + Missense_Mutation SNP G G A TCGA-IR-A3LA-01A-11D-A22X-09 TCGA-IR-A3LA-10A-01D-A22X-09 g.chr11:118362470G>A c.4822G>A c.(4822-4824)Gag>Aag p.E1608K CESC 11 118370615 118370615 + Missense_Mutation SNP C C T TCGA-JW-A5VL-01A-11D-A28B-09 TCGA-JW-A5VL-10A-01D-A28E-09 g.chr11:118370615C>T c.6136C>T c.(6136-6138)Cct>Tct p.P2046S CESC 11 118371806 118371806 + Missense_Mutation SNP G G A TCGA-Q1-A73S-01A-11D-A33O-09 TCGA-Q1-A73S-10B-01D-A33O-09 g.chr11:118371806G>A c.6254G>A c.(6253-6255)aGc>aAc p.S2085N CESC 11 118375513 118375513 + Missense_Mutation SNP C C G TCGA-EA-A3HU-01A-11D-A20U-09 TCGA-EA-A3HU-10B-01D-A20U-09 g.chr11:118375513C>G c.8897C>G c.(8896-8898)tCt>tGt p.S2966C CESC 11 118375583 118375583 + Missense_Mutation SNP G G A TCGA-JW-A5VL-01A-11D-A28B-09 TCGA-JW-A5VL-10A-01D-A28E-09 g.chr11:118375583G>A c.8967G>A c.(8965-8967)atG>atA p.M2989I CESC 11 118376214 118376214 + Missense_Mutation SNP G G C TCGA-EK-A3GK-01A-11D-A20U-09 TCGA-EK-A3GK-10A-01D-A20U-09 g.chr11:118376214G>C c.9598G>C c.(9598-9600)Gaa>Caa p.E3200Q CESC 11 118376933 118376933 + Silent SNP C C T TCGA-JW-A852-01A-11D-A351-09 TCGA-JW-A852-10A-01D-A351-09 g.chr11:118376933C>T c.10317C>T c.(10315-10317)gcC>gcT p.A3439A CESC 11 118377304 118377304 + Missense_Mutation SNP G G T TCGA-Q1-A5R3-01A-11D-A28B-09 TCGA-Q1-A5R3-10B-01D-A28E-09 g.chr11:118377304G>T c.10688G>T c.(10687-10689)aGt>aTt p.S3563I CESC 11 118390460 118390461 + Frame_Shift_Ins INS - - C TCGA-FU-A5XV-01A-11D-A28B-09 TCGA-FU-A5XV-10A-01D-A28E-09 g.chr11:118390460_118390461insC c.11265_11266insC c.(11266-11268)cccfs p.P3756fs CESC 11 118390715 118390715 + Missense_Mutation SNP C C T TCGA-EK-A3GK-01A-11D-A20U-09 TCGA-EK-A3GK-10A-01D-A20U-09 g.chr11:118390715C>T c.11356C>T c.(11356-11358)Cgt>Tgt p.R3786C CHOL 11 118344932 118344932 + Missense_Mutation SNP G G T TCGA-ZH-A8Y5-01A-11D-A417-09 TCGA-ZH-A8Y5-10A-01D-A41A-09 g.chr11:118344932G>T c.3058G>T c.(3058-3060)Gac>Tac p.D1020Y CHOL 11 118365076 118365076 + Missense_Mutation SNP A A T TCGA-W5-AA39-01A-11D-A417-09 TCGA-W5-AA39-10A-01D-A41A-09 g.chr11:118365076A>T c.5243A>T c.(5242-5244)aAa>aTa p.K1748I COAD 11 118307489 118307489 + Missense_Mutation SNP T T C TCGA-G4-6310-01A-11D-1719-10 TCGA-G4-6310-10A-01D-1720-10 g.chr11:118307489T>C c.262T>C c.(262-264)Tcc>Ccc p.S88P COAD 11 118342931 118342931 + Nonsense_Mutation SNP C C T TCGA-CK-4952-01A-01D-1719-10 TCGA-CK-4952-10A-01D-1719-10 g.chr11:118342931C>T c.1057C>T c.(1057-1059)Cga>Tga p.R353* COAD 11 118342933 118342933 + Silent SNP A A G TCGA-CA-6715-01A-21D-1835-10 TCGA-CA-6715-10A-01D-1835-10 g.chr11:118342933A>G c.1059A>G c.(1057-1059)cgA>cgG p.R353R COAD 11 118343017 118343017 + Silent SNP G G A TCGA-AA-3815-01A-01W-0995-10 TCGA-AA-3815-10A-01W-0995-10 g.chr11:118343017G>A c.1143G>A c.(1141-1143)aaG>aaA p.K381K COAD 11 118343236 118343236 + Silent SNP G G A TCGA-AD-6964-01A-11D-1924-10 TCGA-AD-6964-10A-01D-1924-10 g.chr11:118343236G>A c.1362G>A c.(1360-1362)ccG>ccA p.P454P COAD 11 118343316 118343316 + Missense_Mutation SNP G G A TCGA-DM-A1D4-01A-21D-A152-10 TCGA-DM-A1D4-10A-01D-A152-10 g.chr11:118343316G>A c.1442G>A c.(1441-1443)aGc>aAc p.S481N COAD 11 118343475 118343475 + Missense_Mutation SNP C C T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr11:118343475C>T c.1601C>T c.(1600-1602)tCg>tTg p.S534L COAD 11 118343913 118343913 + Missense_Mutation SNP C C T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr11:118343913C>T c.2039C>T c.(2038-2040)tCg>tTg p.S680L COAD 11 118344186 118344186 + Frame_Shift_Del DEL C C - TCGA-A6-5661-01A-01D-1650-10 TCGA-A6-5661-10A-01D-1650-10 g.chr11:118344186delC c.2312delC c.(2311-2313)accfs p.T771fs COAD 11 118344186 118344186 + Frame_Shift_Del DEL C C - TCGA-D5-6930-01A-11D-1924-10 TCGA-D5-6930-10A-01D-1924-10 g.chr11:118344186delC c.2312delC c.(2311-2313)accfs p.T771fs COAD 11 118344458 118344458 + Nonsense_Mutation SNP C C T TCGA-G4-6309-01A-21D-1835-10 TCGA-G4-6309-10A-01D-1835-10 g.chr11:118344458C>T c.2584C>T c.(2584-2586)Cga>Tga p.R862* COAD 11 118347543 118347543 + Missense_Mutation SNP G G T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr11:118347543G>T c.3180G>T c.(3178-3180)gaG>gaT p.E1060D COAD 11 118348807 118348807 + Missense_Mutation SNP C C T TCGA-A6-5666-01A-01D-1650-10 TCGA-A6-5666-10A-01D-1650-10 g.chr11:118348807C>T c.3460C>T c.(3460-3462)Cgg>Tgg p.R1154W COAD 11 118352594 118352594 + Missense_Mutation SNP G G A TCGA-CM-6162-01A-11D-1650-10 TCGA-CM-6162-10A-01D-1650-10 g.chr11:118352594G>A c.3799G>A c.(3799-3801)Gtc>Atc p.V1267I COAD 11 118352614 118352614 + Silent SNP A A G TCGA-AA-3815-01A-01W-0995-10 TCGA-AA-3815-10A-01W-0995-10 g.chr11:118352614A>G c.3819A>G c.(3817-3819)gaA>gaG p.E1273E COAD 11 118352743 118352743 + Frame_Shift_Del DEL A A - TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr11:118352743delA c.3948delA c.(3946-3948)agafs p.R1316fs COAD 11 118359387 118359387 + Missense_Mutation SNP A A G TCGA-F4-6459-01A-11D-1771-10 TCGA-F4-6459-10A-01D-1771-10 g.chr11:118359387A>G c.4391A>G c.(4390-4392)gAg>gGg p.E1464G COAD 11 118359396 118359396 + Missense_Mutation SNP T T C TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr11:118359396T>C c.4400T>C c.(4399-4401)cTg>cCg p.L1467P COAD 11 118360862 118360862 + Missense_Mutation SNP C C T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr11:118360862C>T c.4594C>T c.(4594-4596)Cgc>Tgc p.R1532C COAD 11 118363844 118363844 + Missense_Mutation SNP G G A TCGA-A6-6137-01A-11D-1771-10 TCGA-A6-6137-10A-01D-1806-10 g.chr11:118363844G>A c.5068G>A c.(5068-5070)Gat>Aat p.D1690N COAD 11 118363844 118363844 + Missense_Mutation SNP G G T TCGA-CK-4952-01A-01D-1719-10 TCGA-CK-4952-10A-01D-1719-10 g.chr11:118363844G>T c.5068G>T c.(5068-5070)Gat>Tat p.D1690Y COAD 11 118363845 118363845 + Missense_Mutation SNP A A G TCGA-G4-6306-01A-11D-1771-10 TCGA-G4-6306-10A-01D-1771-10 g.chr11:118363845A>G c.5069A>G c.(5068-5070)gAt>gGt p.D1690G COAD 11 118365419 118365419 + Missense_Mutation SNP G G A TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr11:118365419G>A c.5291G>A c.(5290-5292)cGt>cAt p.R1764H COAD 11 118368705 118368705 + Missense_Mutation SNP G G T TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr11:118368705G>T c.5710G>T c.(5710-5712)Gct>Tct p.A1904S COAD 11 118368707 118368707 + Silent SNP T T C TCGA-AZ-6603-01A-11D-1835-10 TCGA-AZ-6603-11A-02D-1835-10 g.chr11:118368707T>C c.5712T>C c.(5710-5712)gcT>gcC p.A1904A COAD 11 118368731 118368731 + Silent SNP A A G TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr11:118368731A>G c.5736A>G c.(5734-5736)gaA>gaG p.E1912E COAD 11 118369101 118369101 + Frame_Shift_Del DEL A A - TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr11:118369101delA c.5810delA c.(5809-5811)caafs p.Q1937fs COAD 11 118369217 118369217 + Nonsense_Mutation SNP C C T TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr11:118369217C>T c.5926C>T c.(5926-5928)Cga>Tga p.R1976* COAD 11 118369218 118369218 + Missense_Mutation SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr11:118369218G>A c.5927G>A c.(5926-5928)cGa>cAa p.R1976Q COAD 11 118371787 118371787 + Missense_Mutation SNP G G A TCGA-AA-3696-01A-01W-0900-09 TCGA-AA-3696-10A-01W-0900-09 g.chr11:118371787G>A c.6235G>A c.(6235-6237)Gta>Ata p.V2079I COAD 11 118371831 118371831 + Missense_Mutation SNP G G T TCGA-AA-A01G-01A-01W-A005-10 TCGA-AA-A01G-10A-01W-A005-10 g.chr11:118371831G>T c.6279G>T c.(6277-6279)agG>agT p.R2093S COAD 11 118372548 118372548 + Missense_Mutation SNP G G A TCGA-CM-4752-01A-01D-1408-10 TCGA-CM-4752-10A-01D-1408-10 g.chr11:118372548G>A c.6472G>A c.(6472-6474)Ggc>Agc p.G2158S COAD 11 118372554 118372554 + Nonsense_Mutation SNP C C T TCGA-AA-3811-01A-01W-0995-10 TCGA-AA-3811-10A-01W-0995-10 g.chr11:118372554C>T c.6478C>T c.(6478-6480)Cga>Tga p.R2160* COAD 11 118373178 118373178 + Nonsense_Mutation SNP C C T TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr11:118373178C>T c.6562C>T c.(6562-6564)Cga>Tga p.R2188* COAD 11 118373277 118373277 + Missense_Mutation SNP A A G TCGA-CM-5349-01A-21D-1719-10 TCGA-CM-5349-10A-01D-1719-10 g.chr11:118373277A>G c.6661A>G c.(6661-6663)Agg>Ggg p.R2221G COAD 11 118373660 118373660 + Silent SNP C C T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr11:118373660C>T c.7044C>T c.(7042-7044)atC>atT p.I2348I COAD 11 118373666 118373666 + Silent SNP C C A TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr11:118373666C>A c.7050C>A c.(7048-7050)tcC>tcA p.S2350S COAD 11 118373768 118373768 + Missense_Mutation SNP T T A TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr11:118373768T>A c.7152T>A c.(7150-7152)gaT>gaA p.D2384E COAD 11 118374060 118374060 + Missense_Mutation SNP G G A TCGA-A6-6142-01A-11D-1771-10 TCGA-A6-6142-10A-01D-1771-10 g.chr11:118374060G>A c.7444G>A c.(7444-7446)Gtt>Att p.V2482I COAD 11 118374585 118374585 + Missense_Mutation SNP G G T TCGA-A6-2672-01A-01W-0833-10 TCGA-A6-2672-10A-01W-0833-10 g.chr11:118374585G>T c.7969G>T c.(7969-7971)Ggc>Tgc p.G2657C COAD 11 118374605 118374605 + Silent SNP A A G TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr11:118374605A>G c.7989A>G c.(7987-7989)ggA>ggG p.G2663G COAD 11 118374635 118374635 + Silent SNP T T C TCGA-CA-5797-01A-01D-1650-10 TCGA-CA-5797-10A-01D-1650-10 g.chr11:118374635T>C c.8019T>C c.(8017-8019)acT>acC p.T2673T COAD 11 118374635 118374635 + Silent SNP T T C TCGA-CM-5344-01A-21D-1719-10 TCGA-CM-5344-10A-01D-1719-10 g.chr11:118374635T>C c.8019T>C c.(8017-8019)acT>acC p.T2673T COAD 11 118375434 118375434 + Missense_Mutation SNP A A G TCGA-CK-5913-01A-11D-1650-10 TCGA-CK-5913-10A-01D-1650-10 g.chr11:118375434A>G c.8818A>G c.(8818-8820)Act>Gct p.T2940A COAD 11 118375871 118375871 + Missense_Mutation SNP G G A TCGA-F4-6570-01A-11D-1771-10 TCGA-F4-6570-10A-01D-1771-10 g.chr11:118375871G>A c.9255G>A c.(9253-9255)atG>atA p.M3085I COAD 11 118375915 118375915 + Frame_Shift_Del DEL A A - TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr11:118375915delA c.9299delA c.(9298-9300)caafs p.Q3100fs COAD 11 118375917 118375917 + Missense_Mutation SNP A A C TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr11:118375917A>C c.9301A>C c.(9301-9303)Aaa>Caa p.K3101Q COAD 11 118376070 118376070 + Missense_Mutation SNP G G A TCGA-AA-3811-01A-01W-0995-10 TCGA-AA-3811-10A-01W-0995-10 g.chr11:118376070G>A c.9454G>A c.(9454-9456)Gga>Aga p.G3152R COAD 11 118376203 118376203 + Frame_Shift_Del DEL T T - TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr11:118376203delT c.9587delT c.(9586-9588)cttfs p.L3197fs COAD 11 118376479 118376479 + Missense_Mutation SNP G G T TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr11:118376479G>T c.9863G>T c.(9862-9864)aGa>aTa p.R3288I COAD 11 118376683 118376683 + Missense_Mutation SNP C C T TCGA-D5-6529-01A-11D-1771-10 TCGA-D5-6529-10A-01D-1771-10 g.chr11:118376683C>T c.10067C>T c.(10066-10068)gCg>gTg p.A3356V COAD 11 118376816 118376816 + Silent SNP G G A TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr11:118376816G>A c.10200G>A c.(10198-10200)ccG>ccA p.P3400P COAD 11 118376882 118376882 + Silent SNP G G A TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr11:118376882G>A c.10266G>A c.(10264-10266)gcG>gcA p.A3422A COAD 11 118376958 118376958 + Missense_Mutation SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr11:118376958G>A c.10342G>A c.(10342-10344)Gaa>Aaa p.E3448K COAD 11 118377343 118377343 + Missense_Mutation SNP C C T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr11:118377343C>T c.10727C>T c.(10726-10728)tCc>tTc p.S3576F COAD 11 118378315 118378315 + Missense_Mutation SNP A A G TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr11:118378315A>G c.10817A>G c.(10816-10818)cAa>cGa p.Q3606R COAD 11 118382705 118382705 + Missense_Mutation SNP G G A TCGA-F4-6569-01A-11D-1771-10 TCGA-F4-6569-10A-01D-1771-10 g.chr11:118382705G>A c.11102G>A c.(11101-11103)cGa>cAa p.R3701Q COAD 11 118390716 118390716 + Missense_Mutation SNP G G A TCGA-AA-3554-01A-01W-0833-10 TCGA-AA-3554-10A-01W-0833-10 g.chr11:118390716G>A c.11357G>A c.(11356-11358)cGt>cAt p.R3786H COAD 11 118391552 118391552 + Missense_Mutation SNP G G A TCGA-F4-6856-01A-11D-1924-10 TCGA-F4-6856-10A-01D-1924-10 g.chr11:118391552G>A c.11456G>A c.(11455-11457)cGc>cAc p.R3819H COAD 11 118392075 118392075 + Silent SNP C C T TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr11:118392075C>T c.11577C>T c.(11575-11577)gcC>gcT p.A3859A COAD 11 118392088 118392088 + Missense_Mutation SNP C C T TCGA-AA-3525-01A-02W-0833-10 TCGA-AA-3525-10A-01W-0833-10 g.chr11:118392088C>T c.11590C>T c.(11590-11592)Cgc>Tgc p.R3864C COAD 11 118392685 118392685 + Missense_Mutation SNP G G A TCGA-AA-3672-01A-01W-0900-09 TCGA-AA-3672-10A-01W-0900-09 g.chr11:118392685G>A c.11708G>A c.(11707-11709)cGc>cAc p.R3903H COAD 11 118392685 118392685 + Missense_Mutation SNP G G A TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr11:118392685G>A c.11708G>A c.(11707-11709)cGc>cAc p.R3903H COAD 11 118392771 118392771 + Missense_Mutation SNP C C T TCGA-A6-6654-01A-21D-1835-10 TCGA-A6-6654-10A-01D-1835-10 g.chr11:118392771C>T c.11794C>T c.(11794-11796)Cgt>Tgt p.R3932C COADREAD 11 118307489 118307489 + Missense_Mutation SNP T T C TCGA-G4-6310-01A-11D-1719-10 TCGA-G4-6310-10A-01D-1720-10 g.chr11:118307489T>C c.262T>C c.(262-264)Tcc>Ccc p.S88P COADREAD 11 118342931 118342931 + Nonsense_Mutation SNP C C T TCGA-CK-4952-01A-01D-1719-10 TCGA-CK-4952-10A-01D-1719-10 g.chr11:118342931C>T c.1057C>T c.(1057-1059)Cga>Tga p.R353* COADREAD 11 118342933 118342933 + Silent SNP A A G TCGA-CA-6715-01A-21D-1835-10 TCGA-CA-6715-10A-01D-1835-10 g.chr11:118342933A>G c.1059A>G c.(1057-1059)cgA>cgG p.R353R COADREAD 11 118343017 118343017 + Silent SNP G G A TCGA-AA-3815-01A-01W-0995-10 TCGA-AA-3815-10A-01W-0995-10 g.chr11:118343017G>A c.1143G>A c.(1141-1143)aaG>aaA p.K381K COADREAD 11 118343215 118343215 + Silent SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr11:118343215G>A c.1341G>A c.(1339-1341)ccG>ccA p.P447P COADREAD 11 118343236 118343236 + Silent SNP G G A TCGA-AD-6964-01A-11D-1924-10 TCGA-AD-6964-10A-01D-1924-10 g.chr11:118343236G>A c.1362G>A c.(1360-1362)ccG>ccA p.P454P COADREAD 11 118343316 118343316 + Missense_Mutation SNP G G A TCGA-DM-A1D4-01A-21D-A152-10 TCGA-DM-A1D4-10A-01D-A152-10 g.chr11:118343316G>A c.1442G>A c.(1441-1443)aGc>aAc p.S481N COADREAD 11 118343475 118343475 + Missense_Mutation SNP C C T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr11:118343475C>T c.1601C>T c.(1600-1602)tCg>tTg p.S534L COADREAD 11 118343890 118343890 + Silent SNP C C T TCGA-AG-4015-01A-01W-1073-09 TCGA-AG-4015-10A-01W-1073-09 g.chr11:118343890C>T c.2016C>T c.(2014-2016)acC>acT p.T672T COADREAD 11 118343913 118343913 + Missense_Mutation SNP C C T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr11:118343913C>T c.2039C>T c.(2038-2040)tCg>tTg p.S680L COADREAD 11 118344081 118344081 + Missense_Mutation SNP G G T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr11:118344081G>T c.2207G>T c.(2206-2208)aGg>aTg p.R736M COADREAD 11 118344186 118344186 + Frame_Shift_Del DEL C C - TCGA-A6-5661-01A-01D-1650-10 TCGA-A6-5661-10A-01D-1650-10 g.chr11:118344186delC c.2312delC c.(2311-2313)accfs p.T771fs COADREAD 11 118344186 118344186 + Frame_Shift_Del DEL C C - TCGA-D5-6930-01A-11D-1924-10 TCGA-D5-6930-10A-01D-1924-10 g.chr11:118344186delC c.2312delC c.(2311-2313)accfs p.T771fs COADREAD 11 118344186 118344186 + Frame_Shift_Del DEL C C - TCGA-EI-6507-01A-11D-1733-10 TCGA-EI-6507-10A-01D-1733-10 g.chr11:118344186delC c.2312delC c.(2311-2313)accfs p.T771fs COADREAD 11 118344458 118344458 + Nonsense_Mutation SNP C C T TCGA-G4-6309-01A-21D-1835-10 TCGA-G4-6309-10A-01D-1835-10 g.chr11:118344458C>T c.2584C>T c.(2584-2586)Cga>Tga p.R862* COADREAD 11 118347543 118347543 + Missense_Mutation SNP G G T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr11:118347543G>T c.3180G>T c.(3178-3180)gaG>gaT p.E1060D COADREAD 11 118348807 118348807 + Missense_Mutation SNP C C T TCGA-A6-5666-01A-01D-1650-10 TCGA-A6-5666-10A-01D-1650-10 g.chr11:118348807C>T c.3460C>T c.(3460-3462)Cgg>Tgg p.R1154W COADREAD 11 118352594 118352594 + Missense_Mutation SNP G G A TCGA-CM-6162-01A-11D-1650-10 TCGA-CM-6162-10A-01D-1650-10 g.chr11:118352594G>A c.3799G>A c.(3799-3801)Gtc>Atc p.V1267I COADREAD 11 118352614 118352614 + Silent SNP A A G TCGA-AA-3815-01A-01W-0995-10 TCGA-AA-3815-10A-01W-0995-10 g.chr11:118352614A>G c.3819A>G c.(3817-3819)gaA>gaG p.E1273E COADREAD 11 118352743 118352743 + Frame_Shift_Del DEL A A - TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr11:118352743delA c.3948delA c.(3946-3948)agafs p.R1316fs COADREAD 11 118359387 118359387 + Missense_Mutation SNP A A G TCGA-F4-6459-01A-11D-1771-10 TCGA-F4-6459-10A-01D-1771-10 g.chr11:118359387A>G c.4391A>G c.(4390-4392)gAg>gGg p.E1464G COADREAD 11 118359388 118359388 + Silent SNP G G A TCGA-G5-6235-01A-11D-1733-10 TCGA-G5-6235-10A-01D-1733-10 g.chr11:118359388G>A c.4392G>A c.(4390-4392)gaG>gaA p.E1464E COADREAD 11 118359396 118359396 + Missense_Mutation SNP T T C TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr11:118359396T>C c.4400T>C c.(4399-4401)cTg>cCg p.L1467P COADREAD 11 118359410 118359410 + Nonsense_Mutation SNP G G T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr11:118359410G>T c.4414G>T c.(4414-4416)Gaa>Taa p.E1472* COADREAD 11 118360862 118360862 + Missense_Mutation SNP C C T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr11:118360862C>T c.4594C>T c.(4594-4596)Cgc>Tgc p.R1532C COADREAD 11 118362633 118362633 + Missense_Mutation SNP G G A TCGA-AG-3601-01A-01W-0833-10 TCGA-AG-3601-10A-01W-0833-10 g.chr11:118362633G>A c.4985G>A c.(4984-4986)cGc>cAc p.R1662H COADREAD 11 118363844 118363844 + Missense_Mutation SNP G G A TCGA-A6-6137-01A-11D-1771-10 TCGA-A6-6137-10A-01D-1806-10 g.chr11:118363844G>A c.5068G>A c.(5068-5070)Gat>Aat p.D1690N COADREAD 11 118363844 118363844 + Missense_Mutation SNP G G T TCGA-CK-4952-01A-01D-1719-10 TCGA-CK-4952-10A-01D-1719-10 g.chr11:118363844G>T c.5068G>T c.(5068-5070)Gat>Tat p.D1690Y COADREAD 11 118363845 118363845 + Missense_Mutation SNP A A G TCGA-G4-6306-01A-11D-1771-10 TCGA-G4-6306-10A-01D-1771-10 g.chr11:118363845A>G c.5069A>G c.(5068-5070)gAt>gGt p.D1690G COADREAD 11 118365419 118365419 + Missense_Mutation SNP G G A TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr11:118365419G>A c.5291G>A c.(5290-5292)cGt>cAt p.R1764H COADREAD 11 118368705 118368705 + Missense_Mutation SNP G G T TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr11:118368705G>T c.5710G>T c.(5710-5712)Gct>Tct p.A1904S COADREAD 11 118368707 118368707 + Silent SNP T T C TCGA-AZ-6603-01A-11D-1835-10 TCGA-AZ-6603-11A-02D-1835-10 g.chr11:118368707T>C c.5712T>C c.(5710-5712)gcT>gcC p.A1904A COADREAD 11 118368707 118368707 + Silent SNP T T C TCGA-F5-6571-01A-12D-1826-10 TCGA-F5-6571-10A-01D-1826-10 g.chr11:118368707T>C c.5712T>C c.(5710-5712)gcT>gcC p.A1904A COADREAD 11 118368731 118368731 + Silent SNP A A G TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr11:118368731A>G c.5736A>G c.(5734-5736)gaA>gaG p.E1912E COADREAD 11 118369101 118369101 + Frame_Shift_Del DEL A A - TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr11:118369101delA c.5810delA c.(5809-5811)caafs p.Q1937fs COADREAD 11 118369217 118369217 + Nonsense_Mutation SNP C C T TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr11:118369217C>T c.5926C>T c.(5926-5928)Cga>Tga p.R1976* COADREAD 11 118369218 118369218 + Missense_Mutation SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr11:118369218G>A c.5927G>A c.(5926-5928)cGa>cAa p.R1976Q COADREAD 11 118371787 118371787 + Missense_Mutation SNP G G A TCGA-AA-3696-01A-01W-0900-09 TCGA-AA-3696-10A-01W-0900-09 g.chr11:118371787G>A c.6235G>A c.(6235-6237)Gta>Ata p.V2079I COADREAD 11 118371831 118371831 + Missense_Mutation SNP G G T TCGA-AA-A01G-01A-01W-A005-10 TCGA-AA-A01G-10A-01W-A005-10 g.chr11:118371831G>T c.6279G>T c.(6277-6279)agG>agT p.R2093S COADREAD 11 118372548 118372548 + Missense_Mutation SNP G G A TCGA-CM-4752-01A-01D-1408-10 TCGA-CM-4752-10A-01D-1408-10 g.chr11:118372548G>A c.6472G>A c.(6472-6474)Ggc>Agc p.G2158S COADREAD 11 118372554 118372554 + Nonsense_Mutation SNP C C T TCGA-AA-3811-01A-01W-0995-10 TCGA-AA-3811-10A-01W-0995-10 g.chr11:118372554C>T c.6478C>T c.(6478-6480)Cga>Tga p.R2160* COADREAD 11 118373178 118373178 + Nonsense_Mutation SNP C C T TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr11:118373178C>T c.6562C>T c.(6562-6564)Cga>Tga p.R2188* COADREAD 11 118373277 118373277 + Missense_Mutation SNP A A G TCGA-CM-5349-01A-21D-1719-10 TCGA-CM-5349-10A-01D-1719-10 g.chr11:118373277A>G c.6661A>G c.(6661-6663)Agg>Ggg p.R2221G COADREAD 11 118373354 118373354 + Silent SNP C C A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr11:118373354C>A c.6738C>A c.(6736-6738)gtC>gtA p.V2246V COADREAD 11 118373628 118373628 + Missense_Mutation SNP A A T TCGA-DC-6160-01A-11D-1657-10 TCGA-DC-6160-10A-01D-1657-10 g.chr11:118373628A>T c.7012A>T c.(7012-7014)Aca>Tca p.T2338S COADREAD 11 118373660 118373660 + Silent SNP C C T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr11:118373660C>T c.7044C>T c.(7042-7044)atC>atT p.I2348I COADREAD 11 118373666 118373666 + Silent SNP C C A TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr11:118373666C>A c.7050C>A c.(7048-7050)tcC>tcA p.S2350S COADREAD 11 118373690 118373690 + Silent SNP G G A TCGA-AG-A02N-01A-11W-A096-10 TCGA-AG-A02N-11A-11W-A096-10 g.chr11:118373690G>A c.7074G>A c.(7072-7074)tcG>tcA p.S2358S COADREAD 11 118373768 118373768 + Missense_Mutation SNP T T A TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr11:118373768T>A c.7152T>A c.(7150-7152)gaT>gaA p.D2384E COADREAD 11 118374060 118374060 + Missense_Mutation SNP G G A TCGA-A6-6142-01A-11D-1771-10 TCGA-A6-6142-10A-01D-1771-10 g.chr11:118374060G>A c.7444G>A c.(7444-7446)Gtt>Att p.V2482I COADREAD 11 118374585 118374585 + Missense_Mutation SNP G G T TCGA-A6-2672-01A-01W-0833-10 TCGA-A6-2672-10A-01W-0833-10 g.chr11:118374585G>T c.7969G>T c.(7969-7971)Ggc>Tgc p.G2657C COADREAD 11 118374605 118374605 + Silent SNP A A G TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr11:118374605A>G c.7989A>G c.(7987-7989)ggA>ggG p.G2663G COADREAD 11 118374635 118374635 + Silent SNP T T C TCGA-CA-5797-01A-01D-1650-10 TCGA-CA-5797-10A-01D-1650-10 g.chr11:118374635T>C c.8019T>C c.(8017-8019)acT>acC p.T2673T COADREAD 11 118374635 118374635 + Silent SNP T T C TCGA-CM-5344-01A-21D-1719-10 TCGA-CM-5344-10A-01D-1719-10 g.chr11:118374635T>C c.8019T>C c.(8017-8019)acT>acC p.T2673T COADREAD 11 118375434 118375434 + Missense_Mutation SNP A A G TCGA-CK-5913-01A-11D-1650-10 TCGA-CK-5913-10A-01D-1650-10 g.chr11:118375434A>G c.8818A>G c.(8818-8820)Act>Gct p.T2940A COADREAD 11 118375871 118375871 + Missense_Mutation SNP G G A TCGA-F4-6570-01A-11D-1771-10 TCGA-F4-6570-10A-01D-1771-10 g.chr11:118375871G>A c.9255G>A c.(9253-9255)atG>atA p.M3085I COADREAD 11 118375900 118375900 + Missense_Mutation SNP C C A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr11:118375900C>A c.9284C>A c.(9283-9285)cCa>cAa p.P3095Q COADREAD 11 118375915 118375915 + Frame_Shift_Del DEL A A - TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr11:118375915delA c.9299delA c.(9298-9300)caafs p.Q3100fs COADREAD 11 118375917 118375917 + Missense_Mutation SNP A A C TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr11:118375917A>C c.9301A>C c.(9301-9303)Aaa>Caa p.K3101Q COADREAD 11 118376070 118376070 + Missense_Mutation SNP G G A TCGA-AA-3811-01A-01W-0995-10 TCGA-AA-3811-10A-01W-0995-10 g.chr11:118376070G>A c.9454G>A c.(9454-9456)Gga>Aga p.G3152R COADREAD 11 118376203 118376203 + Frame_Shift_Del DEL T T - TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr11:118376203delT c.9587delT c.(9586-9588)cttfs p.L3197fs COADREAD 11 118376479 118376479 + Missense_Mutation SNP G G T TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr11:118376479G>T c.9863G>T c.(9862-9864)aGa>aTa p.R3288I COADREAD 11 118376502 118376502 + Missense_Mutation SNP T T C TCGA-AG-3892-01A-01W-1073-09 TCGA-AG-3892-10A-01W-1073-09 g.chr11:118376502T>C c.9886T>C c.(9886-9888)Ttt>Ctt p.F3296L COADREAD 11 118376683 118376683 + Missense_Mutation SNP C C T TCGA-D5-6529-01A-11D-1771-10 TCGA-D5-6529-10A-01D-1771-10 g.chr11:118376683C>T c.10067C>T c.(10066-10068)gCg>gTg p.A3356V COADREAD 11 118376743 118376743 + Missense_Mutation SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr11:118376743G>A c.10127G>A c.(10126-10128)gGc>gAc p.G3376D COADREAD 11 118376816 118376816 + Silent SNP G G A TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr11:118376816G>A c.10200G>A c.(10198-10200)ccG>ccA p.P3400P COADREAD 11 118376882 118376882 + Silent SNP G G A TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr11:118376882G>A c.10266G>A c.(10264-10266)gcG>gcA p.A3422A COADREAD 11 118376958 118376958 + Missense_Mutation SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr11:118376958G>A c.10342G>A c.(10342-10344)Gaa>Aaa p.E3448K COADREAD 11 118377343 118377343 + Missense_Mutation SNP C C T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr11:118377343C>T c.10727C>T c.(10726-10728)tCc>tTc p.S3576F COADREAD 11 118378315 118378315 + Missense_Mutation SNP A A G TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr11:118378315A>G c.10817A>G c.(10816-10818)cAa>cGa p.Q3606R COADREAD 11 118382705 118382705 + Missense_Mutation SNP G G A TCGA-F4-6569-01A-11D-1771-10 TCGA-F4-6569-10A-01D-1771-10 g.chr11:118382705G>A c.11102G>A c.(11101-11103)cGa>cAa p.R3701Q COADREAD 11 118390716 118390716 + Missense_Mutation SNP G G A TCGA-AA-3554-01A-01W-0833-10 TCGA-AA-3554-10A-01W-0833-10 g.chr11:118390716G>A c.11357G>A c.(11356-11358)cGt>cAt p.R3786H COADREAD 11 118391552 118391552 + Missense_Mutation SNP G G A TCGA-F4-6856-01A-11D-1924-10 TCGA-F4-6856-10A-01D-1924-10 g.chr11:118391552G>A c.11456G>A c.(11455-11457)cGc>cAc p.R3819H COADREAD 11 118392075 118392075 + Silent SNP C C T TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr11:118392075C>T c.11577C>T c.(11575-11577)gcC>gcT p.A3859A COADREAD 11 118392088 118392088 + Missense_Mutation SNP C C T TCGA-AA-3525-01A-02W-0833-10 TCGA-AA-3525-10A-01W-0833-10 g.chr11:118392088C>T c.11590C>T c.(11590-11592)Cgc>Tgc p.R3864C COADREAD 11 118392685 118392685 + Missense_Mutation SNP G G A TCGA-AA-3672-01A-01W-0900-09 TCGA-AA-3672-10A-01W-0900-09 g.chr11:118392685G>A c.11708G>A c.(11707-11709)cGc>cAc p.R3903H COADREAD 11 118392685 118392685 + Missense_Mutation SNP G G A TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr11:118392685G>A c.11708G>A c.(11707-11709)cGc>cAc p.R3903H COADREAD 11 118392771 118392771 + Missense_Mutation SNP C C T TCGA-A6-6654-01A-21D-1835-10 TCGA-A6-6654-10A-01D-1835-10 g.chr11:118392771C>T c.11794C>T c.(11794-11796)Cgt>Tgt p.R3932C DLBC 11 118371761 118371761 + Missense_Mutation SNP A A G TCGA-FF-8047-01A-11D-2210-10 TCGA-FF-8047-10A-01D-2210-10 g.chr11:118371761A>G c.6209A>G c.(6208-6210)aAg>aGg p.K2070R DLBC 11 118372519 118372519 + Missense_Mutation SNP C C T TCGA-FA-A82F-01A-11D-A382-10 TCGA-FA-A82F-10A-01D-A385-10 g.chr11:118372519C>T c.6443C>T c.(6442-6444)cCc>cTc p.P2148L ESCA 11 118343016 118343017 + Frame_Shift_Ins INS - - G TCGA-JY-A93F-01A-21D-A37C-09 TCGA-JY-A93F-10A-01D-A37F-09 g.chr11:118343016_118343017insG c.1142_1143insG c.(1141-1146)aaggggfs p.KG381fs ESCA 11 118343155 118343155 + Silent SNP G G T TCGA-IG-A97H-01A-11D-A387-09 TCGA-IG-A97H-10A-01D-A38A-09 g.chr11:118343155G>T c.1281G>T c.(1279-1281)cgG>cgT p.R427R ESCA 11 118343390 118343390 + Missense_Mutation SNP A A G TCGA-L5-A43J-01A-12D-A247-09 TCGA-L5-A43J-11A-11D-A247-09 g.chr11:118343390A>G c.1516A>G c.(1516-1518)Acc>Gcc p.T506A ESCA 11 118347598 118347598 + Missense_Mutation SNP C C A TCGA-R6-A6Y2-01B-11D-A33E-09 TCGA-R6-A6Y2-10A-01D-A33H-09 g.chr11:118347598C>A c.3235C>A c.(3235-3237)Ctt>Att p.L1079I ESCA 11 118348808 118348808 + Missense_Mutation SNP G G A TCGA-JY-A93F-01A-21D-A37C-09 TCGA-JY-A93F-10A-01D-A37F-09 g.chr11:118348808G>A c.3461G>A c.(3460-3462)cGg>cAg p.R1154Q ESCA 11 118348845 118348845 + Missense_Mutation SNP C C A TCGA-R6-A6Y0-01B-11D-A33E-09 TCGA-R6-A6Y0-10A-01D-A33H-09 g.chr11:118348845C>A c.3498C>A c.(3496-3498)gaC>gaA p.D1166E ESCA 11 118352585 118352585 + Nonsense_Mutation SNP C C T TCGA-L5-A4OP-01A-11D-A27G-09 TCGA-L5-A4OP-11A-11D-A27G-09 g.chr11:118352585C>T c.3790C>T c.(3790-3792)Cga>Tga p.R1264* ESCA 11 118353187 118353187 + Missense_Mutation SNP G G T TCGA-XP-A8T8-01A-11D-A36J-09 TCGA-XP-A8T8-10A-01D-A36M-09 g.chr11:118353187G>T c.4063G>T c.(4063-4065)Gta>Tta p.V1355L ESCA 11 118354912 118354912 + Silent SNP G G T TCGA-L5-A4OH-01A-11D-A27G-09 TCGA-L5-A4OH-11A-11D-A27G-09 g.chr11:118354912G>T c.4101G>T c.(4099-4101)ccG>ccT p.P1367P ESCA 11 118362639 118362639 + Missense_Mutation SNP G G T TCGA-R6-A6Y2-01B-11D-A33E-09 TCGA-R6-A6Y2-10A-01D-A33H-09 g.chr11:118362639G>T c.4991G>T c.(4990-4992)cGg>cTg p.R1664L ESCA 11 118365439 118365439 + Missense_Mutation SNP G G T TCGA-JY-A6FE-01A-11D-A33E-09 TCGA-JY-A6FE-10A-01D-A33H-09 g.chr11:118365439G>T c.5311G>T c.(5311-5313)Gtc>Ttc p.V1771F ESCA 11 118366503 118366503 + Missense_Mutation SNP G G A TCGA-V5-A7RB-01A-11D-A351-09 TCGA-V5-A7RB-10A-01D-A351-09 g.chr11:118366503G>A c.5443G>A c.(5443-5445)Gag>Aag p.E1815K ESCA 11 118374498 118374498 + Frame_Shift_Del DEL T T - TCGA-Q9-A6FU-01A-11D-A31U-09 TCGA-Q9-A6FU-10A-01D-A31U-09 g.chr11:118374498delT c.7882delT c.(7882-7884)tttfs p.F2629fs ESCA 11 118374955 118374955 + Missense_Mutation SNP T T C TCGA-L5-A4OO-01A-11D-A27G-09 TCGA-L5-A4OO-11A-12D-A27G-09 g.chr11:118374955T>C c.8339T>C c.(8338-8340)aTg>aCg p.M2780T ESCA 11 118375063 118375063 + Missense_Mutation SNP C C G TCGA-IG-A3Y9-01A-12D-A247-09 TCGA-IG-A3Y9-10A-01D-A247-09 g.chr11:118375063C>G c.8447C>G c.(8446-8448)tCc>tGc p.S2816C ESCA 11 118375390 118375390 + Missense_Mutation SNP T T A TCGA-LN-A7HV-01A-21D-A351-09 TCGA-LN-A7HV-10A-01D-A351-09 g.chr11:118375390T>A c.8774T>A c.(8773-8775)cTa>cAa p.L2925Q ESCA 11 118376220 118376220 + Missense_Mutation SNP A A G TCGA-2H-A9GK-01A-11D-A37C-09 TCGA-2H-A9GK-11A-11D-A37F-09 g.chr11:118376220A>G c.9604A>G c.(9604-9606)Agc>Ggc p.S3202G ESCA 11 118380790 118380790 + Missense_Mutation SNP T T G TCGA-IG-A51D-01A-11D-A27G-09 TCGA-IG-A51D-10A-01D-A27G-09 g.chr11:118380790T>G c.11019T>G c.(11017-11019)atT>atG p.I3673M ESCA 11 118392772 118392772 + Missense_Mutation SNP G G A TCGA-VR-AA7D-01A-11D-A403-09 TCGA-VR-AA7D-10A-01D-A403-09 g.chr11:118392772G>A c.11795G>A c.(11794-11796)cGt>cAt p.R3932H GBM 11 118359396 118359396 + Missense_Mutation SNP T T C TCGA-41-4097-01A-01D-1353-08 TCGA-41-4097-10A-01D-1353-08 g.chr11:118359396T>C c.4400T>C c.(4399-4401)cTg>cCg p.L1467P GBM 11 118375649 118375649 + Silent SNP A A C TCGA-28-5213-01A-01D-1486-08 TCGA-28-5213-10A-01D-1486-08 g.chr11:118375649A>C c.9033A>C c.(9031-9033)tcA>tcC p.S3011S GBM 11 118376191 118376191 + Missense_Mutation SNP C C T TCGA-06-2565-01A-01D-1494-08 TCGA-06-2565-10A-01D-1494-08 g.chr11:118376191C>T c.9575C>T c.(9574-9576)cCg>cTg p.P3192L GBM 11 118382698 118382698 + Missense_Mutation SNP G G C TCGA-27-2524-01A-01D-1494-08 TCGA-27-2524-10A-01D-1494-08 g.chr11:118382698G>C c.11095G>C c.(11095-11097)Gaa>Caa p.E3699Q GBMLGG 11 118307414 118307416 + In_Frame_Del DEL GCG GCG - TCGA-VM-A8CD-01A-11D-A36O-08 TCGA-VM-A8CD-10A-01D-A367-08 g.chr11:118307414_118307416delGCG c.187_189delGCG c.(187-189)gcgdel p.A67del GBMLGG 11 118342984 118342984 + Silent SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:118342984C>A c.1110C>A c.(1108-1110)acC>acA p.T370T GBMLGG 11 118343733 118343735 + In_Frame_Del DEL CTT CTT - TCGA-DH-A66B-01A-11D-A29Q-08 TCGA-DH-A66B-10A-01D-A29Q-08 g.chr11:118343733_118343735delCTT c.1859_1861delCTT c.(1858-1863)acttct>act p.S621del GBMLGG 11 118344301 118344301 + Silent SNP T T A TCGA-DU-5853-01A-11D-1893-08 TCGA-DU-5853-10A-01D-1893-08 g.chr11:118344301T>A c.2427T>A c.(2425-2427)tcT>tcA p.S809S GBMLGG 11 118344558 118344558 + Missense_Mutation SNP A A G TCGA-S9-A6WL-01A-21D-A33T-08 TCGA-S9-A6WL-10A-01D-A33W-08 g.chr11:118344558A>G c.2684A>G c.(2683-2685)aAg>aGg p.K895R GBMLGG 11 118352537 118352537 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:118352537G>A c.3742G>A c.(3742-3744)Gca>Aca p.A1248T GBMLGG 11 118352683 118352683 + Silent SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:118352683G>A c.3888G>A c.(3886-3888)aaG>aaA p.K1296K GBMLGG 11 118359396 118359396 + Missense_Mutation SNP T T C TCGA-41-4097-01A-01D-1353-08 TCGA-41-4097-10A-01D-1353-08 g.chr11:118359396T>C c.4400T>C c.(4399-4401)cTg>cCg p.L1467P GBMLGG 11 118361992 118361992 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:118361992G>A c.4778G>A c.(4777-4779)cGc>cAc p.R1593H GBMLGG 11 118367049 118367049 + Silent SNP G G A TCGA-HT-7479-01A-11D-2024-08 TCGA-HT-7479-10A-01D-2024-08 g.chr11:118367049G>A c.5622G>A c.(5620-5622)gcG>gcA p.A1874A GBMLGG 11 118373222 118373222 + Silent SNP C C G TCGA-TQ-A7RK-01A-11D-A33T-08 TCGA-TQ-A7RK-10A-01D-A33W-08 g.chr11:118373222C>G c.6606C>G c.(6604-6606)ccC>ccG p.P2202P GBMLGG 11 118373689 118373689 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:118373689C>T c.7073C>T c.(7072-7074)tCg>tTg p.S2358L GBMLGG 11 118374340 118374340 + Missense_Mutation SNP C C T TCGA-HT-7469-01A-11D-2253-08 TCGA-HT-7469-10B-01D-2253-08 g.chr11:118374340C>T c.7724C>T c.(7723-7725)cCc>cTc p.P2575L GBMLGG 11 118374387 118374387 + Missense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:118374387C>A c.7771C>A c.(7771-7773)Ctt>Att p.L2591I GBMLGG 11 118375649 118375649 + Silent SNP A A C TCGA-28-5213-01A-01D-1486-08 TCGA-28-5213-10A-01D-1486-08 g.chr11:118375649A>C c.9033A>C c.(9031-9033)tcA>tcC p.S3011S GBMLGG 11 118376191 118376191 + Missense_Mutation SNP C C T TCGA-06-2565-01A-01D-1494-08 TCGA-06-2565-10A-01D-1494-08 g.chr11:118376191C>T c.9575C>T c.(9574-9576)cCg>cTg p.P3192L GBMLGG 11 118376263 118376263 + Missense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:118376263C>A c.9647C>A c.(9646-9648)tCt>tAt p.S3216Y GBMLGG 11 118380710 118380710 + Missense_Mutation SNP A A G TCGA-CS-5390-01A-02D-1468-08 TCGA-CS-5390-10A-01D-1468-08 g.chr11:118380710A>G c.10939A>G c.(10939-10941)Atg>Gtg p.M3647V GBMLGG 11 118382698 118382698 + Missense_Mutation SNP G G C TCGA-27-2524-01A-01D-1494-08 TCGA-27-2524-10A-01D-1494-08 g.chr11:118382698G>C c.11095G>C c.(11095-11097)Gaa>Caa p.E3699Q GBMLGG 11 118390456 118390456 + Missense_Mutation SNP A A G TCGA-FG-8186-01A-11D-2253-08 TCGA-FG-8186-10A-01D-2253-08 g.chr11:118390456A>G c.11261A>G c.(11260-11262)aAt>aGt p.N3754S GBMLGG 11 118392771 118392771 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:118392771C>T c.11794C>T c.(11794-11796)Cgt>Tgt p.R3932C HNSC 11 118307581 118307581 + Silent SNP C C G TCGA-IQ-A61L-01A-11D-A30E-08 TCGA-IQ-A61L-10A-01D-A30H-08 g.chr11:118307581C>G c.354C>G c.(352-354)gtC>gtG p.V118V HNSC 11 118339526 118339526 + Missense_Mutation SNP G G A TCGA-CR-7365-01A-11D-2012-08 TCGA-CR-7365-10A-01D-2013-08 g.chr11:118339526G>A c.469G>A c.(469-471)Gtc>Atc p.V157I HNSC 11 118342477 118342477 + Silent SNP A A G TCGA-CN-A6V3-01A-12D-A34J-08 TCGA-CN-A6V3-10A-01D-A34M-08 g.chr11:118342477A>G c.603A>G c.(601-603)aaA>aaG p.K201K HNSC 11 118343463 118343463 + Missense_Mutation SNP G G A TCGA-CN-6021-01A-11D-1683-08 TCGA-CN-6021-10A-01D-1683-08 g.chr11:118343463G>A c.1589G>A c.(1588-1590)aGg>aAg p.R530K HNSC 11 118344632 118344632 + Missense_Mutation SNP G G C TCGA-CN-A6V1-01A-12D-A34J-08 TCGA-CN-A6V1-10B-01D-A34M-08 g.chr11:118344632G>C c.2758G>C c.(2758-2760)Gat>Cat p.D920H HNSC 11 118347536 118347536 + Nonsense_Mutation SNP C C A TCGA-CR-7402-01A-11D-2012-08 TCGA-CR-7402-10A-01D-2013-08 g.chr11:118347536C>A c.3173C>A c.(3172-3174)tCa>tAa p.S1058* HNSC 11 118352585 118352585 + Nonsense_Mutation SNP C C T TCGA-CN-5369-01A-01D-1434-08 TCGA-CN-5369-10A-01D-1434-08 g.chr11:118352585C>T c.3790C>T c.(3790-3792)Cga>Tga p.R1264* HNSC 11 118361956 118361956 + Missense_Mutation SNP A A G TCGA-P3-A6T4-01A-11D-A34J-08 TCGA-P3-A6T4-10A-01D-A34M-08 g.chr11:118361956A>G c.4742A>G c.(4741-4743)tAt>tGt p.Y1581C HNSC 11 118361969 118361969 + Missense_Mutation SNP G G A TCGA-CV-7427-01A-11D-2078-08 TCGA-CV-7427-10A-01D-2078-08 g.chr11:118361969G>A c.4755G>A c.(4753-4755)atG>atA p.M1585I HNSC 11 118362545 118362545 + Nonsense_Mutation SNP C C T TCGA-CN-6013-01A-11D-1683-08 TCGA-CN-6013-10A-01D-1683-08 g.chr11:118362545C>T c.4897C>T c.(4897-4899)Cga>Tga p.R1633* HNSC 11 118363941 118363941 + Missense_Mutation SNP C C G TCGA-QK-A6VC-01A-23D-A34J-08 TCGA-QK-A6VC-10B-01D-A34M-08 g.chr11:118363941C>G c.5165C>G c.(5164-5166)tCt>tGt p.S1722C HNSC 11 118368762 118368763 + Frame_Shift_Ins INS - - T TCGA-CV-6952-01A-11D-1912-08 TCGA-CV-6952-10A-01D-1912-08 g.chr11:118368762_118368763insT c.5767_5768insT c.(5767-5769)atgfs p.M1923fs HNSC 11 118369144 118369158 + In_Frame_Del DEL CAGCAACTATCACTT CAGCAACTATCACTT - TCGA-CQ-5333-01A-01D-2394-08 TCGA-CQ-5333-10A-01D-2394-08 g.chr11:118369144_118369158delCAGCAACTATCACTT c.5853_5867delCAGCAACTATCACTT c.(5851-5868)accagcaactatcacttc>acc p.SNYHF1952del HNSC 11 118369199 118369199 + Frame_Shift_Del DEL A A - TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr11:118369199delA c.5908delA c.(5908-5910)aaafs p.K1971fs HNSC 11 118370550 118370550 + Splice_Site SNP G G T TCGA-CV-A6K2-01A-11D-A31L-08 TCGA-CV-A6K2-10A-01D-A31J-08 g.chr11:118370550G>T c.6071G>T c.(6070-6072)gGg>gTg p.G2024V HNSC 11 118370622 118370622 + Missense_Mutation SNP G G T TCGA-T2-A6X2-01A-12D-A34J-08 TCGA-T2-A6X2-10B-01D-A34M-08 g.chr11:118370622G>T c.6143G>T c.(6142-6144)gGa>gTa p.G2048V HNSC 11 118371736 118371736 + Missense_Mutation SNP C C T TCGA-CV-A6JO-01B-11D-A34J-08 TCGA-CV-A6JO-10A-01D-A34M-08 g.chr11:118371736C>T c.6184C>T c.(6184-6186)Cgc>Tgc p.R2062C HNSC 11 118373361 118373361 + Missense_Mutation SNP C C T TCGA-CV-A6JD-01A-11D-A31L-08 TCGA-CV-A6JD-10A-01D-A31J-08 g.chr11:118373361C>T c.6745C>T c.(6745-6747)Cca>Tca p.P2249S HNSC 11 118373938 118373938 + Missense_Mutation SNP A A G TCGA-BB-8601-01A-11D-2394-08 TCGA-BB-8601-10A-01D-2394-08 g.chr11:118373938A>G c.7322A>G c.(7321-7323)cAt>cGt p.H2441R HNSC 11 118374023 118374023 + Missense_Mutation SNP G G C TCGA-CX-7085-01A-21D-2012-08 TCGA-CX-7085-10A-01D-2013-08 g.chr11:118374023G>C c.7407G>C c.(7405-7407)ttG>ttC p.L2469F HNSC 11 118374030 118374030 + Missense_Mutation SNP G G A TCGA-CX-7085-01A-21D-2012-08 TCGA-CX-7085-10A-01D-2013-08 g.chr11:118374030G>A c.7414G>A c.(7414-7416)Gag>Aag p.E2472K HNSC 11 118375349 118375349 + Silent SNP C C A TCGA-CV-6952-01A-11D-1912-08 TCGA-CV-6952-10A-01D-1912-08 g.chr11:118375349C>A c.8733C>A c.(8731-8733)gtC>gtA p.V2911V HNSC 11 118375411 118375411 + Missense_Mutation SNP C C G TCGA-CN-4741-01A-01D-1434-08 TCGA-CN-4741-10A-01D-1434-08 g.chr11:118375411C>G c.8795C>G c.(8794-8796)tCt>tGt p.S2932C HNSC 11 118375875 118375875 + Missense_Mutation SNP C C T TCGA-CV-7238-01A-11D-2012-08 TCGA-CV-7238-10A-01D-2013-08 g.chr11:118375875C>T c.9259C>T c.(9259-9261)Cca>Tca p.P3087S HNSC 11 118376025 118376025 + Missense_Mutation SNP C C G TCGA-CN-4741-01A-01D-1434-08 TCGA-CN-4741-10A-01D-1434-08 g.chr11:118376025C>G c.9409C>G c.(9409-9411)Cca>Gca p.P3137A HNSC 11 118376147 118376147 + Silent SNP C C T TCGA-CN-4741-01A-01D-1434-08 TCGA-CN-4741-10A-01D-1434-08 g.chr11:118376147C>T c.9531C>T c.(9529-9531)atC>atT p.I3177I HNSC 11 118376471 118376471 + Silent SNP C C T TCGA-QK-A8ZA-01A-11D-A391-08 TCGA-QK-A8ZA-10A-01D-A394-08 g.chr11:118376471C>T c.9855C>T c.(9853-9855)atC>atT p.I3285I HNSC 11 118376894 118376894 + Silent SNP C C T TCGA-CQ-A4C9-01A-11D-A25D-08 TCGA-CQ-A4C9-10A-01D-A25E-08 g.chr11:118376894C>T c.10278C>T c.(10276-10278)atC>atT p.I3426I HNSC 11 118377362 118377362 + Splice_Site SNP G G T TCGA-CV-6954-01A-11D-1912-08 TCGA-CV-6954-10A-01D-1912-08 g.chr11:118377362G>T c.e27+1 HNSC 11 118390377 118390377 + Missense_Mutation SNP G G T TCGA-CN-5358-01A-01D-1512-08 TCGA-CN-5358-10A-01D-1512-08 g.chr11:118390377G>T c.11182G>T c.(11182-11184)Gtg>Ttg p.V3728L HNSC 11 118390382 118390382 + Silent SNP C C T TCGA-D6-6516-01A-11D-1870-08 TCGA-D6-6516-10A-01D-1870-08 g.chr11:118390382C>T c.11187C>T c.(11185-11187)ttC>ttT p.F3729F HNSC 11 118392789 118392789 + Missense_Mutation SNP G G A TCGA-CV-7101-01A-11D-2012-08 TCGA-CV-7101-10A-01D-2013-08 g.chr11:118392789G>A c.11812G>A c.(11812-11814)Gag>Aag p.E3938K KIPAN 11 118348895 118348896 + Frame_Shift_Ins INS - - T TCGA-B0-5095-01A-01D-1421-08 TCGA-B0-5095-11A-01D-1421-08 g.chr11:118348895_118348896insT c.3548_3549insT c.(3547-3552)aatatafs p.I1184fs KIPAN 11 118352545 118352545 + Missense_Mutation SNP G G T TCGA-4A-A93X-01A-11D-A36X-10 TCGA-4A-A93X-10A-01D-A370-10 g.chr11:118352545G>T c.3750G>T c.(3748-3750)gaG>gaT p.E1250D KIPAN 11 118352713 118352713 + Silent SNP G G A TCGA-BP-5168-01A-01D-1421-08 TCGA-BP-5168-11A-01D-1421-08 g.chr11:118352713G>A c.3918G>A c.(3916-3918)ccG>ccA p.P1306P KIPAN 11 118366483 118366483 + Missense_Mutation SNP G G A TCGA-SX-A71S-01A-11D-A33Q-10 TCGA-SX-A71S-10A-01D-A33Q-10 g.chr11:118366483G>A c.5423G>A c.(5422-5424)cGa>cAa p.R1808Q KIPAN 11 118370617 118370617 + Silent SNP T T A TCGA-CJ-4912-01A-01D-1429-08 TCGA-CJ-4912-11A-01D-1429-08 g.chr11:118370617T>A c.6138T>A c.(6136-6138)ccT>ccA p.P2046P KIPAN 11 118372561 118372561 + Nonsense_Mutation SNP T T A TCGA-BP-5170-01A-01D-1429-08 TCGA-BP-5170-11A-01D-1429-08 g.chr11:118372561T>A c.6485T>A c.(6484-6486)tTg>tAg p.L2162* KIPAN 11 118373932 118373932 + Missense_Mutation SNP A A C TCGA-Q2-A5QZ-01A-11D-A28G-10 TCGA-Q2-A5QZ-10A-01D-A28G-10 g.chr11:118373932A>C c.7316A>C c.(7315-7317)gAa>gCa p.E2439A KIPAN 11 118375051 118375051 + Missense_Mutation SNP C C A TCGA-CZ-4865-01A-02D-1501-10 TCGA-CZ-4865-11A-01D-1501-10 g.chr11:118375051C>A c.8435C>A c.(8434-8436)aCa>aAa p.T2812K KIPAN 11 118375278 118375278 + Nonsense_Mutation SNP G G T TCGA-BP-5182-01A-01D-1429-08 TCGA-BP-5182-11A-01D-1429-08 g.chr11:118375278G>T c.8662G>T c.(8662-8664)Gaa>Taa p.E2888* KIPAN 11 118377019 118377019 + Frame_Shift_Del DEL C C - TCGA-MH-A857-01A-11D-A34Z-10 TCGA-MH-A857-10A-01D-A34Z-10 g.chr11:118377019delC c.10403delC c.(10402-10404)tccfs p.S3468fs KIPAN 11 118390456 118390456 + Missense_Mutation SNP A A G TCGA-CZ-5465-01A-01D-1806-10 TCGA-CZ-5465-11A-01D-1501-10 g.chr11:118390456A>G c.11261A>G c.(11260-11262)aAt>aGt p.N3754S KIPAN 11 118390700 118390700 + Missense_Mutation SNP C C G TCGA-GL-A9DE-01A-11D-A36X-10 TCGA-GL-A9DE-10A-01D-A370-10 g.chr11:118390700C>G c.11341C>G c.(11341-11343)Ctg>Gtg p.L3781V KIRC 11 118348895 118348896 + Frame_Shift_Ins INS - - T TCGA-B0-5095-01A-01D-1421-08 TCGA-B0-5095-11A-01D-1421-08 g.chr11:118348895_118348896insT c.3548_3549insT c.(3547-3552)aatatafs p.I1184fs KIRC 11 118352713 118352713 + Silent SNP G G A TCGA-BP-5168-01A-01D-1421-08 TCGA-BP-5168-11A-01D-1421-08 g.chr11:118352713G>A c.3918G>A c.(3916-3918)ccG>ccA p.P1306P KIRC 11 118370617 118370617 + Silent SNP T T A TCGA-CJ-4912-01A-01D-1429-08 TCGA-CJ-4912-11A-01D-1429-08 g.chr11:118370617T>A c.6138T>A c.(6136-6138)ccT>ccA p.P2046P KIRC 11 118372561 118372561 + Nonsense_Mutation SNP T T A TCGA-BP-5170-01A-01D-1429-08 TCGA-BP-5170-11A-01D-1429-08 g.chr11:118372561T>A c.6485T>A c.(6484-6486)tTg>tAg p.L2162* KIRC 11 118375051 118375051 + Missense_Mutation SNP C C A TCGA-CZ-4865-01A-02D-1501-10 TCGA-CZ-4865-11A-01D-1501-10 g.chr11:118375051C>A c.8435C>A c.(8434-8436)aCa>aAa p.T2812K KIRC 11 118375278 118375278 + Nonsense_Mutation SNP G G T TCGA-BP-5182-01A-01D-1429-08 TCGA-BP-5182-11A-01D-1429-08 g.chr11:118375278G>T c.8662G>T c.(8662-8664)Gaa>Taa p.E2888* KIRC 11 118390456 118390456 + Missense_Mutation SNP A A G TCGA-CZ-5465-01A-01D-1806-10 TCGA-CZ-5465-11A-01D-1501-10 g.chr11:118390456A>G c.11261A>G c.(11260-11262)aAt>aGt p.N3754S KIRP 11 118352545 118352545 + Missense_Mutation SNP G G T TCGA-4A-A93X-01A-11D-A36X-10 TCGA-4A-A93X-10A-01D-A370-10 g.chr11:118352545G>T c.3750G>T c.(3748-3750)gaG>gaT p.E1250D KIRP 11 118366483 118366483 + Missense_Mutation SNP G G A TCGA-SX-A71S-01A-11D-A33Q-10 TCGA-SX-A71S-10A-01D-A33Q-10 g.chr11:118366483G>A c.5423G>A c.(5422-5424)cGa>cAa p.R1808Q KIRP 11 118373932 118373932 + Missense_Mutation SNP A A C TCGA-Q2-A5QZ-01A-11D-A28G-10 TCGA-Q2-A5QZ-10A-01D-A28G-10 g.chr11:118373932A>C c.7316A>C c.(7315-7317)gAa>gCa p.E2439A KIRP 11 118377019 118377019 + Frame_Shift_Del DEL C C - TCGA-MH-A857-01A-11D-A34Z-10 TCGA-MH-A857-10A-01D-A34Z-10 g.chr11:118377019delC c.10403delC c.(10402-10404)tccfs p.S3468fs KIRP 11 118390700 118390700 + Missense_Mutation SNP C C G TCGA-GL-A9DE-01A-11D-A36X-10 TCGA-GL-A9DE-10A-01D-A370-10 g.chr11:118390700C>G c.11341C>G c.(11341-11343)Ctg>Gtg p.L3781V LGG 11 118307414 118307416 + In_Frame_Del DEL GCG GCG - TCGA-VM-A8CD-01A-11D-A36O-08 TCGA-VM-A8CD-10A-01D-A367-08 g.chr11:118307414_118307416delGCG c.187_189delGCG c.(187-189)gcgdel p.A67del LGG 11 118342984 118342984 + Silent SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:118342984C>A c.1110C>A c.(1108-1110)acC>acA p.T370T LGG 11 118343733 118343735 + In_Frame_Del DEL CTT CTT - TCGA-DH-A66B-01A-11D-A29Q-08 TCGA-DH-A66B-10A-01D-A29Q-08 g.chr11:118343733_118343735delCTT c.1859_1861delCTT c.(1858-1863)acttct>act p.S621del LGG 11 118344301 118344301 + Silent SNP T T A TCGA-DU-5853-01A-11D-1893-08 TCGA-DU-5853-10A-01D-1893-08 g.chr11:118344301T>A c.2427T>A c.(2425-2427)tcT>tcA p.S809S LGG 11 118344558 118344558 + Missense_Mutation SNP A A G TCGA-S9-A6WL-01A-21D-A33T-08 TCGA-S9-A6WL-10A-01D-A33W-08 g.chr11:118344558A>G c.2684A>G c.(2683-2685)aAg>aGg p.K895R LGG 11 118352537 118352537 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:118352537G>A c.3742G>A c.(3742-3744)Gca>Aca p.A1248T LGG 11 118352683 118352683 + Silent SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:118352683G>A c.3888G>A c.(3886-3888)aaG>aaA p.K1296K LGG 11 118361992 118361992 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:118361992G>A c.4778G>A c.(4777-4779)cGc>cAc p.R1593H LGG 11 118367049 118367049 + Silent SNP G G A TCGA-HT-7479-01A-11D-2024-08 TCGA-HT-7479-10A-01D-2024-08 g.chr11:118367049G>A c.5622G>A c.(5620-5622)gcG>gcA p.A1874A LGG 11 118373222 118373222 + Silent SNP C C G TCGA-TQ-A7RK-01A-11D-A33T-08 TCGA-TQ-A7RK-10A-01D-A33W-08 g.chr11:118373222C>G c.6606C>G c.(6604-6606)ccC>ccG p.P2202P LGG 11 118373689 118373689 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:118373689C>T c.7073C>T c.(7072-7074)tCg>tTg p.S2358L LGG 11 118374340 118374340 + Missense_Mutation SNP C C T TCGA-HT-7469-01A-11D-2253-08 TCGA-HT-7469-10B-01D-2253-08 g.chr11:118374340C>T c.7724C>T c.(7723-7725)cCc>cTc p.P2575L LGG 11 118374387 118374387 + Missense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:118374387C>A c.7771C>A c.(7771-7773)Ctt>Att p.L2591I LGG 11 118376263 118376263 + Missense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:118376263C>A c.9647C>A c.(9646-9648)tCt>tAt p.S3216Y LGG 11 118380710 118380710 + Missense_Mutation SNP A A G TCGA-CS-5390-01A-02D-1468-08 TCGA-CS-5390-10A-01D-1468-08 g.chr11:118380710A>G c.10939A>G c.(10939-10941)Atg>Gtg p.M3647V LGG 11 118390456 118390456 + Missense_Mutation SNP A A G TCGA-FG-8186-01A-11D-2253-08 TCGA-FG-8186-10A-01D-2253-08 g.chr11:118390456A>G c.11261A>G c.(11260-11262)aAt>aGt p.N3754S LGG 11 118392771 118392771 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:118392771C>T c.11794C>T c.(11794-11796)Cgt>Tgt p.R3932C LIHC 11 118342966 118342966 + Frame_Shift_Del DEL A A - TCGA-G3-A3CJ-01A-11D-A20W-10 TCGA-G3-A3CJ-10A-01D-A20W-10 g.chr11:118342966delA c.1092delA c.(1090-1092)tcafs p.S364fs LIHC 11 118343010 118343011 + Frame_Shift_Ins INS - - A TCGA-DD-AAW1-01A-11D-A40P-10 TCGA-DD-AAW1-10A-01D-A40P-10 g.chr11:118343010_118343011insA c.1136_1137insA c.(1135-1140)gcaaaafs p.AK379fs LIHC 11 118347552 118347552 + Silent SNP G G A TCGA-DD-AADI-01A-11D-A40R-10 TCGA-DD-AADI-10A-01D-A40U-10 g.chr11:118347552G>A c.3189G>A c.(3187-3189)gtG>gtA p.V1063V LIHC 11 118347664 118347664 + Nonsense_Mutation SNP C C T TCGA-CC-A5UD-01A-11D-A28X-10 TCGA-CC-A5UD-10A-01D-A28X-10 g.chr11:118347664C>T c.3301C>T c.(3301-3303)Cga>Tga p.R1101* LIHC 11 118347674 118347674 + Frame_Shift_Del DEL T T - TCGA-DD-A39Y-01A-11D-A20W-10 TCGA-DD-A39Y-11A-11D-A20W-10 g.chr11:118347674delT c.3311delT c.(3310-3312)attfs p.I1104fs LIHC 11 118359362 118359362 + Missense_Mutation SNP C C T TCGA-DD-AACI-01A-11D-A40R-10 TCGA-DD-AACI-10A-01D-A40U-10 g.chr11:118359362C>T c.4366C>T c.(4366-4368)Cac>Tac p.H1456Y LIHC 11 118362558 118362558 + Frame_Shift_Del DEL A A - TCGA-HP-A5N0-01A-11D-A28X-10 TCGA-HP-A5N0-10A-01D-A28X-10 g.chr11:118362558delA c.4910delA c.(4909-4911)gaafs p.E1637fs LIHC 11 118368716 118368716 + Silent SNP A A G TCGA-FV-A2QR-01A-11D-A20W-10 TCGA-FV-A2QR-11A-11D-A20W-10 g.chr11:118368716A>G c.5721A>G c.(5719-5721)tcA>tcG p.S1907S LIHC 11 118373507 118373507 + Silent SNP G G A TCGA-BC-A10Q-01A-11D-A12Z-10 TCGA-BC-A10Q-11A-11D-A12Z-10 g.chr11:118373507G>A c.6891G>A c.(6889-6891)gtG>gtA p.V2297V LIHC 11 118374231 118374231 + Missense_Mutation SNP C C A TCGA-DD-AACB-01A-11D-A40R-10 TCGA-DD-AACB-10A-01D-A40U-10 g.chr11:118374231C>A c.7615C>A c.(7615-7617)Ctg>Atg p.L2539M LIHC 11 118374237 118374238 + Frame_Shift_Ins INS - - TC TCGA-DD-AACB-01A-11D-A40R-10 TCGA-DD-AACB-10A-01D-A40U-10 g.chr11:118374237_118374238insTC c.7621_7622insTC c.(7621-7623)gaafs p.E2541fs LIHC 11 118374789 118374789 + Missense_Mutation SNP G G A TCGA-DD-A3A9-01A-11D-A25V-10 TCGA-DD-A3A9-11A-11D-A25V-10 g.chr11:118374789G>A c.8173G>A c.(8173-8175)Gag>Aag p.E2725K LIHC 11 118376454 118376454 + Nonsense_Mutation SNP C C T TCGA-CC-A5UE-01A-11D-A28X-10 TCGA-CC-A5UE-10A-01D-A28X-10 g.chr11:118376454C>T c.9838C>T c.(9838-9840)Cga>Tga p.R3280* LIHC 11 118376851 118376851 + Missense_Mutation SNP C C T TCGA-ZP-A9D1-01A-11D-A382-10 TCGA-ZP-A9D1-10B-01D-A385-10 g.chr11:118376851C>T c.10235C>T c.(10234-10236)tCa>tTa p.S3412L LIHC 11 118377090 118377090 + Missense_Mutation SNP A A G TCGA-BC-A3KG-01A-11D-A20W-10 TCGA-BC-A3KG-10A-01D-A20W-10 g.chr11:118377090A>G c.10474A>G c.(10474-10476)Agc>Ggc p.S3492G LIHC 11 118377153 118377153 + Frame_Shift_Del DEL G G - TCGA-G3-A3CJ-01A-11D-A20W-10 TCGA-G3-A3CJ-10A-01D-A20W-10 g.chr11:118377153delG c.10537delG c.(10537-10539)gggfs p.G3514fs LIHC 11 118377321 118377321 + Missense_Mutation SNP A A G TCGA-4R-AA8I-01A-11D-A382-10 TCGA-4R-AA8I-10B-01D-A385-10 g.chr11:118377321A>G c.10705A>G c.(10705-10707)Att>Gtt p.I3569V LIHC 11 118377325 118377325 + Missense_Mutation SNP C C T TCGA-EP-A2KA-01A-11D-A183-10 TCGA-EP-A2KA-10A-01D-A183-10 g.chr11:118377325C>T c.10709C>T c.(10708-10710)cCa>cTa p.P3570L LIHC 11 118392112 118392112 + Missense_Mutation SNP G G A TCGA-ES-A2HS-01A-11D-A183-10 TCGA-ES-A2HS-11A-11D-A183-10 g.chr11:118392112G>A c.11614G>A c.(11614-11616)Gaa>Aaa p.E3872K LUAD 11 118307520 118307520 + Missense_Mutation SNP C C T TCGA-53-7624-01A-11D-2063-08 TCGA-53-7624-10A-01D-2063-08 g.chr11:118307520C>T c.293C>T c.(292-294)tCa>tTa p.S98L LUAD 11 118339515 118339515 + Missense_Mutation SNP C C T TCGA-44-7659-01A-11D-2063-08 TCGA-44-7659-10A-01D-2063-08 g.chr11:118339515C>T c.458C>T c.(457-459)tCa>tTa p.S153L LUAD 11 118342823 118342823 + Missense_Mutation SNP G G T TCGA-62-A46O-01A-11D-A24D-08 TCGA-62-A46O-10A-01D-A24F-08 g.chr11:118342823G>T c.949G>T c.(949-951)Ggt>Tgt p.G317C LUAD 11 118343171 118343171 + Missense_Mutation SNP G G T TCGA-62-A46S-01A-11D-A24D-08 TCGA-62-A46S-10A-01D-A24F-08 g.chr11:118343171G>T c.1297G>T c.(1297-1299)Gat>Tat p.D433Y LUAD 11 118343273 118343273 + Missense_Mutation SNP C C G TCGA-86-8278-01A-11D-2284-08 TCGA-86-8278-10A-01D-2284-08 g.chr11:118343273C>G c.1399C>G c.(1399-1401)Cag>Gag p.Q467E LUAD 11 118344134 118344134 + Missense_Mutation SNP T T C TCGA-55-8089-01A-11D-2238-08 TCGA-55-8089-10A-01D-2238-08 g.chr11:118344134T>C c.2260T>C c.(2260-2262)Tcc>Ccc p.S754P LUAD 11 118344255 118344255 + Missense_Mutation SNP C C T TCGA-55-A491-01A-11D-A24D-08 TCGA-55-A491-10A-01D-A24F-08 g.chr11:118344255C>T c.2381C>T c.(2380-2382)cCa>cTa p.P794L LUAD 11 118344408 118344408 + Missense_Mutation SNP C C T TCGA-55-7994-01A-11D-2184-08 TCGA-55-7994-10A-01D-2184-08 g.chr11:118344408C>T c.2534C>T c.(2533-2535)aCt>aTt p.T845I LUAD 11 118344632 118344632 + Missense_Mutation SNP G G T TCGA-35-4122-01A-01D-1105-08 TCGA-35-4122-10A-01D-1105-08 g.chr11:118344632G>T c.2758G>T c.(2758-2760)Gat>Tat p.D920Y LUAD 11 118352428 118352428 + Splice_Site SNP A A T TCGA-78-8660-01A-11D-2393-08 TCGA-78-8660-10A-01D-2393-08 g.chr11:118352428A>T c.e7-1 LUAD 11 118352634 118352634 + Missense_Mutation SNP G G T TCGA-44-8120-01A-11D-2238-08 TCGA-44-8120-10A-01D-2238-08 g.chr11:118352634G>T c.3839G>T c.(3838-3840)gGg>gTg p.G1280V LUAD 11 118359361 118359361 + Silent SNP C C T TCGA-73-4658-01A-01D-1753-08 TCGA-73-4658-11A-01D-1753-08 g.chr11:118359361C>T c.4365C>T c.(4363-4365)ttC>ttT p.F1455F LUAD 11 118362018 118362018 + Missense_Mutation SNP C C A TCGA-67-3771-01A-01D-1040-01 TCGA-67-3771-10A-01D-1040-01 g.chr11:118362018C>A c.4804C>A c.(4804-4806)Ctt>Att p.L1602I LUAD 11 118362500 118362500 + Missense_Mutation SNP G G T TCGA-69-7978-01A-11D-2184-08 TCGA-69-7978-10A-01D-2184-08 g.chr11:118362500G>T c.4852G>T c.(4852-4854)Gcc>Tcc p.A1618S LUAD 11 118363824 118363824 + Missense_Mutation SNP G G C TCGA-64-5781-01A-01D-1625-08 TCGA-64-5781-10A-01D-1625-08 g.chr11:118363824G>C c.5048G>C c.(5047-5049)cGc>cCc p.R1683P LUAD 11 118363894 118363894 + Frame_Shift_Del DEL A A - TCGA-05-5715-01A-01D-1625-08 TCGA-05-5715-10A-01D-1625-08 g.chr11:118363894delA c.5118delA c.(5116-5118)ttafs p.L1706fs LUAD 11 118366474 118366474 + Missense_Mutation SNP G G T TCGA-55-7994-01A-11D-2184-08 TCGA-55-7994-10A-01D-2184-08 g.chr11:118366474G>T c.5414G>T c.(5413-5415)tGg>tTg p.W1805L LUAD 11 118366490 118366490 + Missense_Mutation SNP A A T TCGA-55-6985-01A-11D-1945-08 TCGA-55-6985-11A-01D-1945-08 g.chr11:118366490A>T c.5430A>T c.(5428-5430)gaA>gaT p.E1810D LUAD 11 118370028 118370028 + Missense_Mutation SNP A A G TCGA-55-8506-01A-11D-2393-08 TCGA-55-8506-10A-01D-2393-08 g.chr11:118370028A>G c.5963A>G c.(5962-5964)gAg>gGg p.E1988G LUAD 11 118370085 118370085 + Missense_Mutation SNP G G A TCGA-62-A46P-01A-11D-A24D-08 TCGA-62-A46P-10A-01D-A24F-08 g.chr11:118370085G>A c.6020G>A c.(6019-6021)aGa>aAa p.R2007K LUAD 11 118370557 118370557 + Missense_Mutation SNP G G C TCGA-NJ-A55A-01A-11D-A25L-08 TCGA-NJ-A55A-10A-01D-A25L-08 g.chr11:118370557G>C c.6078G>C c.(6076-6078)atG>atC p.M2026I LUAD 11 118373179 118373179 + Missense_Mutation SNP G G A TCGA-MP-A4TA-01A-21D-A24P-08 TCGA-MP-A4TA-10A-01D-A24P-08 g.chr11:118373179G>A c.6563G>A c.(6562-6564)cGa>cAa p.R2188Q LUAD 11 118374110 118374110 + Silent SNP C C G TCGA-91-6848-01A-11D-1945-08 TCGA-91-6848-11A-01D-1945-08 g.chr11:118374110C>G c.7494C>G c.(7492-7494)ccC>ccG p.P2498P LUAD 11 118374343 118374343 + Missense_Mutation SNP A A G TCGA-50-5045-01A-01D-1625-08 TCGA-50-5045-10A-01D-1625-08 g.chr11:118374343A>G c.7727A>G c.(7726-7728)aAt>aGt p.N2576S LUAD 11 118374583 118374583 + Missense_Mutation SNP G G C TCGA-J2-A4AD-01A-11D-A24D-08 TCGA-J2-A4AD-10A-01D-A24F-08 g.chr11:118374583G>C c.7967G>C c.(7966-7968)cGa>cCa p.R2656P LUAD 11 118375038 118375038 + Missense_Mutation SNP C C T TCGA-44-A4SS-01A-11D-A24P-08 TCGA-44-A4SS-10A-01D-A24P-08 g.chr11:118375038C>T c.8422C>T c.(8422-8424)Cgc>Tgc p.R2808C LUAD 11 118375125 118375125 + Missense_Mutation SNP A A T TCGA-MP-A4T4-01A-11D-A25L-08 TCGA-MP-A4T4-10A-01D-A25L-08 g.chr11:118375125A>T c.8509A>T c.(8509-8511)Aac>Tac p.N2837Y LUAD 11 118375477 118375477 + Missense_Mutation SNP A A G TCGA-78-7156-01A-11D-2036-08 TCGA-78-7156-10A-01D-2036-08 g.chr11:118375477A>G c.8861A>G c.(8860-8862)gAc>gGc p.D2954G LUAD 11 118375889 118375889 + Silent SNP C C G TCGA-78-8662-01A-11D-2393-08 TCGA-78-8662-10A-01D-2393-08 g.chr11:118375889C>G c.9273C>G c.(9271-9273)ctC>ctG p.L3091L LUAD 11 118376154 118376154 + Missense_Mutation SNP C C A TCGA-17-Z056-01A-01W-0747-08 TCGA-17-Z056-11A-01W-0747-08 g.chr11:118376154C>A c.9538C>A c.(9538-9540)Cct>Act p.P3180T LUAD 11 118376564 118376564 + Silent SNP A A T TCGA-95-7043-01A-11D-1945-08 TCGA-95-7043-10A-01D-1946-08 g.chr11:118376564A>T c.9948A>T c.(9946-9948)acA>acT p.T3316T LUAD 11 118376837 118376837 + Silent SNP A A G TCGA-17-Z055-01A-01W-0747-08 TCGA-17-Z055-11A-01W-0747-08 g.chr11:118376837A>G c.10221A>G c.(10219-10221)ccA>ccG p.P3407P LUAD 11 118376994 118376994 + Missense_Mutation SNP G G C TCGA-38-4625-01A-01D-1553-08 TCGA-38-4625-11A-01D-1553-08 g.chr11:118376994G>C c.10378G>C c.(10378-10380)Gcc>Ccc p.A3460P LUAD 11 118380757 118380758 + Frame_Shift_Ins INS - - A TCGA-91-6828-01A-11D-1855-08 TCGA-91-6828-10A-01D-1855-08 g.chr11:118380757_118380758insA c.10986_10987insA c.(10987-10989)aaafs p.K3663fs LUAD 11 118390389 118390389 + Missense_Mutation SNP G G C TCGA-53-7624-01A-11D-2063-08 TCGA-53-7624-10A-01D-2063-08 g.chr11:118390389G>C c.11194G>C c.(11194-11196)Gag>Cag p.E3732Q LUAD 11 118390412 118390412 + Missense_Mutation SNP C C G TCGA-64-5775-01A-01D-1625-08 TCGA-64-5775-10A-01D-1625-08 g.chr11:118390412C>G c.11217C>G c.(11215-11217)caC>caG p.H3739Q LUAD 11 118390685 118390685 + Missense_Mutation SNP G G C TCGA-53-7624-01A-11D-2063-08 TCGA-53-7624-10A-01D-2063-08 g.chr11:118390685G>C c.11326G>C c.(11326-11328)Gac>Cac p.D3776H LUAD 11 118392124 118392124 + Missense_Mutation SNP G G A TCGA-95-A4VN-01A-11D-A25L-08 TCGA-95-A4VN-10A-01D-A25L-08 g.chr11:118392124G>A c.11626G>A c.(11626-11628)Gac>Aac p.D3876N LUSC 11 118344238 118344238 + Silent SNP C C A TCGA-18-3410-01A-01D-0983-08 TCGA-18-3410-11A-01D-0983-08 g.chr11:118344238C>A c.2364C>A c.(2362-2364)gcC>gcA p.A788A LUSC 11 118352801 118352801 + Nonsense_Mutation SNP G G T TCGA-22-5491-01A-01D-1632-08 TCGA-22-5491-11A-01D-1632-08 g.chr11:118352801G>T c.4006G>T c.(4006-4008)Gaa>Taa p.E1336* LUSC 11 118368740 118368740 + Missense_Mutation SNP C C A TCGA-43-2578-01A-01D-1522-08 TCGA-43-2578-11A-01D-1522-08 g.chr11:118368740C>A c.5745C>A c.(5743-5745)gaC>gaA p.D1915E LUSC 11 118372451 118372451 + Silent SNP T T A TCGA-60-2726-01A-01D-1522-08 TCGA-60-2726-11A-01D-1522-08 g.chr11:118372451T>A c.6375T>A c.(6373-6375)ccT>ccA p.P2125P LUSC 11 118374454 118374454 + Missense_Mutation SNP A A G TCGA-63-6202-01A-11D-1817-08 TCGA-63-6202-10A-01D-1817-08 g.chr11:118374454A>G c.7838A>G c.(7837-7839)aAa>aGa p.K2613R LUSC 11 118374740 118374740 + Silent SNP G G A TCGA-37-3783-01A-01D-1267-08 TCGA-37-3783-10A-01D-1267-08 g.chr11:118374740G>A c.8124G>A c.(8122-8124)caG>caA p.Q2708Q LUSC 11 118376003 118376003 + Silent SNP C C G TCGA-22-5473-01A-01D-1632-08 TCGA-22-5473-11A-11D-1632-08 g.chr11:118376003C>G c.9387C>G c.(9385-9387)ctC>ctG p.L3129L LUSC 11 118376731 118376731 + Missense_Mutation SNP C C G TCGA-66-2786-01A-01D-1522-08 TCGA-66-2786-11A-01D-1522-08 g.chr11:118376731C>G c.10115C>G c.(10114-10116)aCc>aGc p.T3372S LUSC 11 118376855 118376855 + Silent SNP G G A TCGA-18-3409-01A-01D-0983-08 TCGA-18-3409-11A-01D-0983-08 g.chr11:118376855G>A c.10239G>A c.(10237-10239)caG>caA p.Q3413Q LUSC 11 118390362 118390362 + Missense_Mutation SNP C C G TCGA-66-2759-01A-01D-1522-08 TCGA-66-2759-11A-01D-1522-08 g.chr11:118390362C>G c.11167C>G c.(11167-11169)Ctc>Gtc p.L3723V OV 11 118342400 118342400 + Missense_Mutation SNP C C A TCGA-23-1114-01B-01W-0633-09 TCGA-23-1114-10A-01W-0633-09 g.chr11:118342400C>A c.526C>A c.(526-528)Cgt>Agt p.R176S OV 11 118345001 118345001 + Missense_Mutation SNP C C G TCGA-61-1737-01A-01W-0639-09 TCGA-61-1737-11A-01W-0639-09 g.chr11:118345001C>G c.3127C>G c.(3127-3129)Ctt>Gtt p.L1043V OV 11 118350953 118350953 + Splice_Site SNP G G C TCGA-24-1844-01A-01W-0639-09 TCGA-24-1844-10A-01W-0639-09 g.chr11:118350953G>C c.3634G>C c.(3634-3636)Gct>Cct p.A1212P OV 11 118359387 118359387 + Missense_Mutation SNP A A G TCGA-23-1122-01A-01W-0486-08 TCGA-23-1122-10A-01W-0486-08 g.chr11:118359387A>G c.4391A>G c.(4390-4392)gAg>gGg p.E1464G OV 11 118359434 118359434 + Missense_Mutation SNP A A G TCGA-29-1778-01A-01W-0639-09 TCGA-29-1778-10A-01W-0639-09 g.chr11:118359434A>G c.4438A>G c.(4438-4440)Aaa>Gaa p.K1480E OV 11 118363844 118363844 + Missense_Mutation SNP G G C TCGA-13-0885-01A-02W-0421-09 TCGA-13-0885-10A-01W-0421-09 g.chr11:118363844G>C c.5068G>C c.(5068-5070)Gat>Cat p.D1690H OV 11 118373604 118373604 + Missense_Mutation SNP A A G TCGA-13-0912-01A-01W-0421-09 TCGA-13-0912-10A-01W-0421-09 g.chr11:118373604A>G c.6988A>G c.(6988-6990)Aaa>Gaa p.K2330E OV 11 118376575 118376575 + Missense_Mutation SNP G G A TCGA-29-1771-01A-01W-0633-09 TCGA-29-1771-10A-01W-0634-09 g.chr11:118376575G>A c.9959G>A c.(9958-9960)aGc>aAc p.S3320N OV 11 118377264 118377264 + Missense_Mutation SNP G G C TCGA-24-1614-01A-01W-0552-10 TCGA-24-1614-10A-01W-0552-10 g.chr11:118377264G>C c.10648G>C c.(10648-10650)Ggg>Cgg p.G3550R PAAD 11 118343199 118343199 + Missense_Mutation SNP G G A TCGA-US-A77E-01A-11D-A32N-08 TCGA-US-A77E-11A-11D-A32N-08 g.chr11:118343199G>A c.1325G>A c.(1324-1326)cGa>cAa p.R442Q PAAD 11 118344186 118344186 + Frame_Shift_Del DEL C C - TCGA-2J-AABO-01A-21D-A40W-08 TCGA-2J-AABO-10A-01D-A40W-08 g.chr11:118344186delC c.2312delC c.(2311-2313)accfs p.T771fs PAAD 11 118355026 118355026 + Silent SNP T T C TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr11:118355026T>C c.4215T>C c.(4213-4215)ttT>ttC p.F1405F PAAD 11 118373499 118373499 + Missense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr11:118373499G>A c.6883G>A c.(6883-6885)Gac>Aac p.D2295N PAAD 11 118374332 118374332 + Silent SNP A A G TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr11:118374332A>G c.7716A>G c.(7714-7716)caA>caG p.Q2572Q PAAD 11 118375293 118375293 + Missense_Mutation SNP C C A TCGA-3A-A9IZ-01A-12D-A40W-08 TCGA-3A-A9IZ-10A-01D-A40W-08 g.chr11:118375293C>A c.8677C>A c.(8677-8679)Ctt>Att p.L2893I PAAD 11 118375783 118375783 + Missense_Mutation SNP C C T TCGA-HZ-7918-01A-11D-2154-08 TCGA-HZ-7918-10A-01D-2154-08 g.chr11:118375783C>T c.9167C>T c.(9166-9168)cCg>cTg p.P3056L PCPG 11 118372559 118372559 + Silent SNP G G A TCGA-WB-A80O-01A-11D-A35I-08 TCGA-WB-A80O-10A-01D-A35G-08 g.chr11:118372559G>A c.6483G>A c.(6481-6483)ccG>ccA p.P2161P PCPG 11 118376687 118376687 + Silent SNP A A C TCGA-WB-A81S-01A-11D-A35I-08 TCGA-WB-A81S-10A-01D-A35G-08 g.chr11:118376687A>C c.10071A>C c.(10069-10071)tcA>tcC p.S3357S PRAD 11 118307279 118307281 + In_Frame_Del DEL GGC GGC - TCGA-J9-A52C-01A-11D-A26M-08 TCGA-J9-A52C-10A-01D-A26K-08 g.chr11:118307279_118307281delGGC c.52_54delGGC c.(52-54)ggcdel p.G23del PRAD 11 118343036 118343037 + Frame_Shift_Ins INS - - A TCGA-FC-7961-01A-11D-A29Q-08 TCGA-FC-7961-10A-01D-A29Q-08 g.chr11:118343036_118343037insA c.1162_1163insA c.(1162-1164)gaafs p.E388fs PRAD 11 118343381 118343381 + Missense_Mutation SNP C C T TCGA-EJ-7782-01A-11D-2114-08 TCGA-EJ-7782-10A-01D-2114-08 g.chr11:118343381C>T c.1507C>T c.(1507-1509)Cgg>Tgg p.R503W PRAD 11 118343971 118343971 + Silent SNP T T C TCGA-CH-5744-01A-11D-1576-08 TCGA-CH-5744-10A-01D-1576-08 g.chr11:118343971T>C c.2097T>C c.(2095-2097)gcT>gcC p.A699A PRAD 11 118344075 118344076 + Frame_Shift_Ins INS - - A TCGA-V1-A8MU-01A-11D-A377-08 TCGA-V1-A8MU-10A-01D-A37A-08 g.chr11:118344075_118344076insA c.2201_2202insA c.(2200-2205)agaaaafs p.RK734fs PRAD 11 118366536 118366536 + Missense_Mutation SNP G G T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr11:118366536G>T c.5476G>T c.(5476-5478)Gct>Tct p.A1826S PRAD 11 118368689 118368689 + Nonsense_Mutation SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr11:118368689G>A c.5694G>A c.(5692-5694)tgG>tgA p.W1898* PRAD 11 118371737 118371737 + Missense_Mutation SNP G G A TCGA-CH-5769-01A-11D-1576-08 TCGA-CH-5769-11A-01D-1576-08 g.chr11:118371737G>A c.6185G>A c.(6184-6186)cGc>cAc p.R2062H PRAD 11 118374348 118374348 + Frame_Shift_Del DEL A A - TCGA-YL-A8SO-01B-31D-A377-08 TCGA-YL-A8SO-10A-01D-A37A-08 g.chr11:118374348delA c.7732delA c.(7732-7734)accfs p.T2578fs PRAD 11 118376991 118376991 + Missense_Mutation SNP C C T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr11:118376991C>T c.10375C>T c.(10375-10377)Ctt>Ttt p.L3459F PRAD 11 118390416 118390416 + Nonsense_Mutation SNP C C T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr11:118390416C>T c.11221C>T c.(11221-11223)Cga>Tga p.R3741* READ 11 118343215 118343215 + Silent SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr11:118343215G>A c.1341G>A c.(1339-1341)ccG>ccA p.P447P READ 11 118343890 118343890 + Silent SNP C C T TCGA-AG-4015-01A-01W-1073-09 TCGA-AG-4015-10A-01W-1073-09 g.chr11:118343890C>T c.2016C>T c.(2014-2016)acC>acT p.T672T READ 11 118344081 118344081 + Missense_Mutation SNP G G T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr11:118344081G>T c.2207G>T c.(2206-2208)aGg>aTg p.R736M READ 11 118344186 118344186 + Frame_Shift_Del DEL C C - TCGA-EI-6507-01A-11D-1733-10 TCGA-EI-6507-10A-01D-1733-10 g.chr11:118344186delC c.2312delC c.(2311-2313)accfs p.T771fs READ 11 118359388 118359388 + Silent SNP G G A TCGA-G5-6235-01A-11D-1733-10 TCGA-G5-6235-10A-01D-1733-10 g.chr11:118359388G>A c.4392G>A c.(4390-4392)gaG>gaA p.E1464E READ 11 118359410 118359410 + Nonsense_Mutation SNP G G T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr11:118359410G>T c.4414G>T c.(4414-4416)Gaa>Taa p.E1472* READ 11 118362633 118362633 + Missense_Mutation SNP G G A TCGA-AG-3601-01A-01W-0833-10 TCGA-AG-3601-10A-01W-0833-10 g.chr11:118362633G>A c.4985G>A c.(4984-4986)cGc>cAc p.R1662H READ 11 118368707 118368707 + Silent SNP T T C TCGA-F5-6571-01A-12D-1826-10 TCGA-F5-6571-10A-01D-1826-10 g.chr11:118368707T>C c.5712T>C c.(5710-5712)gcT>gcC p.A1904A READ 11 118373354 118373354 + Silent SNP C C A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr11:118373354C>A c.6738C>A c.(6736-6738)gtC>gtA p.V2246V READ 11 118373628 118373628 + Missense_Mutation SNP A A T TCGA-DC-6160-01A-11D-1657-10 TCGA-DC-6160-10A-01D-1657-10 g.chr11:118373628A>T c.7012A>T c.(7012-7014)Aca>Tca p.T2338S READ 11 118373690 118373690 + Silent SNP G G A TCGA-AG-A02N-01A-11W-A096-10 TCGA-AG-A02N-11A-11W-A096-10 g.chr11:118373690G>A c.7074G>A c.(7072-7074)tcG>tcA p.S2358S READ 11 118375900 118375900 + Missense_Mutation SNP C C A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr11:118375900C>A c.9284C>A c.(9283-9285)cCa>cAa p.P3095Q READ 11 118376502 118376502 + Missense_Mutation SNP T T C TCGA-AG-3892-01A-01W-1073-09 TCGA-AG-3892-10A-01W-1073-09 g.chr11:118376502T>C c.9886T>C c.(9886-9888)Ttt>Ctt p.F3296L READ 11 118376743 118376743 + Missense_Mutation SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr11:118376743G>A c.10127G>A c.(10126-10128)gGc>gAc p.G3376D SARC 11 118348798 118348798 + Nonsense_Mutation SNP C C T TCGA-QQ-A8VG-01A-11D-A37C-09 TCGA-QQ-A8VG-10A-01D-A37F-09 g.chr11:118348798C>T c.3451C>T c.(3451-3453)Cga>Tga p.R1151* SARC 11 118352703 118352709 + Frame_Shift_Del DEL TGGTCAT TGGTCAT - TCGA-DX-AB2P-01A-11D-A387-09 TCGA-DX-AB2P-10A-01D-A38A-09 g.chr11:118352703_118352709delTGGTCAT c.3908_3914delTGGTCAT c.(3907-3915)ctggtcatcfs p.LVI1303fs SARC 11 118375819 118375819 + Missense_Mutation SNP C C T TCGA-MJ-A68H-01A-11D-A307-09 TCGA-MJ-A68H-10A-01D-A307-09 g.chr11:118375819C>T c.9203C>T c.(9202-9204)cCa>cTa p.P3068L SARC 11 118376882 118376882 + Silent SNP G G A TCGA-X6-A8C4-01A-11D-A36J-09 TCGA-X6-A8C4-10A-01D-A36M-09 g.chr11:118376882G>A c.10266G>A c.(10264-10266)gcG>gcA p.A3422A SKCM 11 118342713 118342713 + Missense_Mutation SNP C C T TCGA-DA-A1I0-06A-11D-A20D-08 TCGA-DA-A1I0-10B-01D-A20D-08 g.chr11:118342713C>T c.839C>T c.(838-840)cCt>cTt p.P280L SKCM 11 118343024 118343024 + Nonsense_Mutation SNP C C T TCGA-EE-A2GI-06A-11D-A196-08 TCGA-EE-A2GI-10A-01D-A198-08 g.chr11:118343024C>T c.1150C>T c.(1150-1152)Caa>Taa p.Q384* SKCM 11 118343602 118343602 + Silent SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr11:118343602C>T c.1728C>T c.(1726-1728)tcC>tcT p.S576S SKCM 11 118343772 118343772 + Missense_Mutation SNP C C T TCGA-ER-A19S-06A-11D-A196-08 TCGA-ER-A19S-10A-01D-A198-08 g.chr11:118343772C>T c.1898C>T c.(1897-1899)tCc>tTc p.S633F SKCM 11 118343788 118343788 + Silent SNP C C T TCGA-EE-A2GR-06A-11D-A197-08 TCGA-EE-A2GR-10A-01D-A199-08 g.chr11:118343788C>T c.1914C>T c.(1912-1914)gcC>gcT p.A638A SKCM 11 118343920 118343920 + Silent SNP C C T TCGA-D3-A2JO-06A-11D-A196-08 TCGA-D3-A2JO-10A-01D-A198-08 g.chr11:118343920C>T c.2046C>T c.(2044-2046)ctC>ctT p.L682L SKCM 11 118344107 118344107 + Nonsense_Mutation SNP C C T TCGA-FS-A1ZZ-06A-11D-A197-08 TCGA-FS-A1ZZ-10A-01D-A199-08 g.chr11:118344107C>T c.2233C>T c.(2233-2235)Cga>Tga p.R745* SKCM 11 118344279 118344279 + Missense_Mutation SNP C C T TCGA-GF-A6C9-06A-11D-A30X-08 TCGA-GF-A6C9-10A-01D-A30X-08 g.chr11:118344279C>T c.2405C>T c.(2404-2406)tCc>tTc p.S802F SKCM 11 118344383 118344383 + Missense_Mutation SNP C C T TCGA-D3-A51T-06A-11D-A25O-08 TCGA-D3-A51T-10A-01D-A25O-08 g.chr11:118344383C>T c.2509C>T c.(2509-2511)Cct>Tct p.P837S SKCM 11 118344458 118344458 + Nonsense_Mutation SNP C C T TCGA-EE-A2GC-06A-11D-A197-08 TCGA-EE-A2GC-10A-01D-A199-08 g.chr11:118344458C>T c.2584C>T c.(2584-2586)Cga>Tga p.R862* SKCM 11 118344458 118344458 + Nonsense_Mutation SNP C C T TCGA-EE-A3J4-06A-11D-A20D-08 TCGA-EE-A3J4-10A-01D-A20D-08 g.chr11:118344458C>T c.2584C>T c.(2584-2586)Cga>Tga p.R862* SKCM 11 118344497 118344497 + Missense_Mutation SNP G G A TCGA-DA-A1I7-06A-22D-A197-08 TCGA-DA-A1I7-10A-01D-A199-08 g.chr11:118344497G>A c.2623G>A c.(2623-2625)Gag>Aag p.E875K SKCM 11 118344687 118344687 + Missense_Mutation SNP C C T TCGA-D9-A3Z1-06A-11D-A23B-08 TCGA-D9-A3Z1-10A-01D-A23B-08 g.chr11:118344687C>T c.2813C>T c.(2812-2814)tCa>tTa p.S938L SKCM 11 118344862 118344877 + Frame_Shift_Del DEL TAGCACTGTTAAACAT TAGCACTGTTAAACAT - TCGA-FS-A1ZW-06A-12D-A197-08 TCGA-FS-A1ZW-10A-01D-A199-08 g.chr11:118344862_118344877delTAGCACTGTTAAACAT c.2988_3003delTAGCACTGTTAAACAT c.(2986-3003)tctagcactgttaaacatfs p.SSTVKH996fs SKCM 11 118353182 118353182 + Missense_Mutation SNP T T G TCGA-OD-A75X-06A-12D-A32N-08 TCGA-OD-A75X-10A-01D-A32N-08 g.chr11:118353182T>G c.4058T>G c.(4057-4059)aTc>aGc p.I1353S SKCM 11 118353184 118353184 + Missense_Mutation SNP C C T TCGA-EE-A181-06A-11D-A196-08 TCGA-EE-A181-10A-01D-A198-08 g.chr11:118353184C>T c.4060C>T c.(4060-4062)Cct>Tct p.P1354S SKCM 11 118355575 118355575 + Splice_Site SNP A A G TCGA-DA-A1HY-06A-11D-A19A-08 TCGA-DA-A1HY-10A-01D-A19A-08 g.chr11:118355575A>G c.e10-1 SKCM 11 118359392 118359392 + Missense_Mutation SNP C C T TCGA-ER-A193-06A-12D-A197-08 TCGA-ER-A193-10A-01D-A199-08 g.chr11:118359392C>T c.4396C>T c.(4396-4398)Cct>Tct p.P1466S SKCM 11 118359392 118359392 + Missense_Mutation SNP C C T TCGA-FS-A1ZC-06A-11D-A197-08 TCGA-FS-A1ZC-10A-01D-A199-08 g.chr11:118359392C>T c.4396C>T c.(4396-4398)Cct>Tct p.P1466S SKCM 11 118360862 118360862 + Missense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr11:118360862C>T c.4594C>T c.(4594-4596)Cgc>Tgc p.R1532C SKCM 11 118362000 118362000 + Missense_Mutation SNP C C T TCGA-D3-A3C3-06A-12D-A19A-08 TCGA-D3-A3C3-10A-01D-A19A-08 g.chr11:118362000C>T c.4786C>T c.(4786-4788)Cat>Tat p.H1596Y SKCM 11 118362005 118362005 + Silent SNP C C T TCGA-D3-A51T-06A-11D-A25O-08 TCGA-D3-A51T-10A-01D-A25O-08 g.chr11:118362005C>T c.4791C>T c.(4789-4791)tcC>tcT p.S1597S SKCM 11 118362611 118362611 + Missense_Mutation SNP C C T TCGA-EE-A3J8-06A-11D-A20D-08 TCGA-EE-A3J8-10A-01D-A20D-08 g.chr11:118362611C>T c.4963C>T c.(4963-4965)Cgg>Tgg p.R1655W SKCM 11 118363900 118363900 + Silent SNP A A G TCGA-FS-A1ZS-06A-12D-A197-08 TCGA-FS-A1ZS-10A-01D-A199-08 g.chr11:118363900A>G c.5124A>G c.(5122-5124)ctA>ctG p.L1708L SKCM 11 118365428 118365428 + Missense_Mutation SNP C C T TCGA-EE-A3J7-06A-11D-A20D-08 TCGA-EE-A3J7-10A-01D-A20D-08 g.chr11:118365428C>T c.5300C>T c.(5299-5301)cCa>cTa p.P1767L SKCM 11 118365450 118365450 + Silent SNP C C T TCGA-EE-A29L-06A-12D-A196-08 TCGA-EE-A29L-10A-01D-A198-08 g.chr11:118365450C>T c.5322C>T c.(5320-5322)tcC>tcT p.S1774S SKCM 11 118366446 118366446 + Missense_Mutation SNP C C T TCGA-EE-A2GC-06A-11D-A197-08 TCGA-EE-A2GC-10A-01D-A199-08 g.chr11:118366446C>T c.5386C>T c.(5386-5388)Cct>Tct p.P1796S SKCM 11 118366464 118366464 + Missense_Mutation SNP T T A TCGA-ER-A193-06A-12D-A197-08 TCGA-ER-A193-10A-01D-A199-08 g.chr11:118366464T>A c.5404T>A c.(5404-5406)Tat>Aat p.Y1802N SKCM 11 118368764 118368764 + Missense_Mutation SNP G G A TCGA-ER-A2NC-06A-11D-A197-08 TCGA-ER-A2NC-10A-01D-A199-08 g.chr11:118368764G>A c.5769G>A c.(5767-5769)atG>atA p.M1923I SKCM 11 118368765 118368765 + Missense_Mutation SNP G G A TCGA-ER-A2NC-06A-11D-A197-08 TCGA-ER-A2NC-10A-01D-A199-08 g.chr11:118368765G>A c.5770G>A c.(5770-5772)Gct>Act p.A1924T SKCM 11 118372446 118372446 + Nonsense_Mutation SNP C C T TCGA-FS-A1ZS-06A-12D-A197-08 TCGA-FS-A1ZS-10A-01D-A199-08 g.chr11:118372446C>T c.6370C>T c.(6370-6372)Cga>Tga p.R2124* SKCM 11 118372518 118372518 + Missense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr11:118372518C>T c.6442C>T c.(6442-6444)Ccc>Tcc p.P2148S SKCM 11 118373178 118373178 + Nonsense_Mutation SNP C C T TCGA-D3-A3C7-06A-11D-A196-08 TCGA-D3-A3C7-10A-01D-A198-08 g.chr11:118373178C>T c.6562C>T c.(6562-6564)Cga>Tga p.R2188* SKCM 11 118373240 118373240 + Silent SNP G G A TCGA-EE-A3JB-06A-11D-A21A-08 TCGA-EE-A3JB-10A-01D-A21A-08 g.chr11:118373240G>A c.6624G>A c.(6622-6624)cgG>cgA p.R2208R SKCM 11 118373290 118373290 + Missense_Mutation SNP C C T TCGA-EE-A2A2-06A-11D-A196-08 TCGA-EE-A2A2-10A-01D-A198-08 g.chr11:118373290C>T c.6674C>T c.(6673-6675)tCc>tTc p.S2225F SKCM 11 118373290 118373290 + Missense_Mutation SNP C C T TCGA-EE-A3J5-06A-11D-A20D-08 TCGA-EE-A3J5-10A-01D-A20D-08 g.chr11:118373290C>T c.6674C>T c.(6673-6675)tCc>tTc p.S2225F SKCM 11 118373344 118373344 + Missense_Mutation SNP T T C TCGA-FS-A1ZA-06A-11D-A197-08 TCGA-FS-A1ZA-10A-01D-A199-08 g.chr11:118373344T>C c.6728T>C c.(6727-6729)gTt>gCt p.V2243A SKCM 11 118373601 118373601 + Missense_Mutation SNP C C T TCGA-EE-A2GN-06A-11D-A196-08 TCGA-EE-A2GN-10A-01D-A198-08 g.chr11:118373601C>T c.6985C>T c.(6985-6987)Cct>Tct p.P2329S SKCM 11 118373665 118373665 + Missense_Mutation SNP C C T TCGA-EE-A29V-06A-12D-A197-08 TCGA-EE-A29V-10A-01D-A199-08 g.chr11:118373665C>T c.7049C>T c.(7048-7050)tCc>tTc p.S2350F SKCM 11 118373727 118373727 + Missense_Mutation SNP C C T TCGA-DA-A3F8-06A-11D-A20D-08 TCGA-DA-A3F8-10A-01D-A20D-08 g.chr11:118373727C>T c.7111C>T c.(7111-7113)Cat>Tat p.H2371Y SKCM 11 118373881 118373881 + Missense_Mutation SNP C C T TCGA-ER-A3ET-06A-11D-A20D-08 TCGA-ER-A3ET-10A-01D-A20D-08 g.chr11:118373881C>T c.7265C>T c.(7264-7266)tCc>tTc p.S2422F SKCM 11 118374107 118374107 + Silent SNP C C T TCGA-EE-A3AC-06A-11D-A196-08 TCGA-EE-A3AC-10A-01D-A198-08 g.chr11:118374107C>T c.7491C>T c.(7489-7491)gtC>gtT p.V2497V SKCM 11 118374290 118374290 + Silent SNP A A G TCGA-EE-A29X-06A-11D-A196-08 TCGA-EE-A29X-10A-01D-A198-08 g.chr11:118374290A>G c.7674A>G c.(7672-7674)ccA>ccG p.P2558P SKCM 11 118374328 118374328 + Missense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr11:118374328C>T c.7712C>T c.(7711-7713)gCc>gTc p.A2571V SKCM 11 118374553 118374553 + Missense_Mutation SNP C C T TCGA-EE-A3AA-06A-11D-A196-08 TCGA-EE-A3AA-10A-01D-A198-08 g.chr11:118374553C>T c.7937C>T c.(7936-7938)cCa>cTa p.P2646L SKCM 11 118375153 118375153 + Missense_Mutation SNP C C A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr11:118375153C>A c.8537C>A c.(8536-8538)cCt>cAt p.P2846H SKCM 11 118375357 118375357 + Missense_Mutation SNP C C T TCGA-EE-A3JA-06A-11D-A20D-08 TCGA-EE-A3JA-10A-01D-A20D-08 g.chr11:118375357C>T c.8741C>T c.(8740-8742)tCt>tTt p.S2914F SKCM 11 118375399 118375399 + Missense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr11:118375399C>T c.8783C>T c.(8782-8784)cCa>cTa p.P2928L SKCM 11 118375417 118375417 + Nonsense_Mutation SNP T T A TCGA-EE-A3AF-06A-11D-A196-08 TCGA-EE-A3AF-10A-01D-A198-08 g.chr11:118375417T>A c.8801T>A c.(8800-8802)tTg>tAg p.L2934* SKCM 11 118375435 118375435 + Missense_Mutation SNP C C T TCGA-FS-A1Z3-06A-11D-A197-08 TCGA-FS-A1Z3-10A-01D-A199-08 g.chr11:118375435C>T c.8819C>T c.(8818-8820)aCt>aTt p.T2940I SKCM 11 118375900 118375900 + Missense_Mutation SNP C C T TCGA-D3-A3C7-06A-11D-A196-08 TCGA-D3-A3C7-10A-01D-A198-08 g.chr11:118375900C>T c.9284C>T c.(9283-9285)cCa>cTa p.P3095L SKCM 11 118375975 118375975 + Missense_Mutation SNP C C T TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr11:118375975C>T c.9359C>T c.(9358-9360)tCa>tTa p.S3120L SKCM 11 118376065 118376065 + Missense_Mutation SNP G G A TCGA-FS-A1YW-06A-11D-A197-08 TCGA-FS-A1YW-10A-01D-A199-08 g.chr11:118376065G>A c.9449G>A c.(9448-9450)aGc>aAc p.S3150N SKCM 11 118376241 118376241 + Missense_Mutation SNP A A G TCGA-GN-A26D-06A-11D-A19A-08 TCGA-GN-A26D-10A-01D-A19A-08 g.chr11:118376241A>G c.9625A>G c.(9625-9627)Acc>Gcc p.T3209A SKCM 11 118376509 118376509 + Missense_Mutation SNP C C T TCGA-ER-A19A-06A-21D-A197-08 TCGA-ER-A19A-10A-01D-A199-08 g.chr11:118376509C>T c.9893C>T c.(9892-9894)cCg>cTg p.P3298L SKCM 11 118377096 118377096 + Missense_Mutation SNP G G A TCGA-FW-A3TU-06A-11D-A23B-08 TCGA-FW-A3TU-10A-01D-A23B-08 g.chr11:118377096G>A c.10480G>A c.(10480-10482)Gga>Aga p.G3494R SKCM 11 118377097 118377097 + Missense_Mutation SNP G G A TCGA-FW-A3TU-06A-11D-A23B-08 TCGA-FW-A3TU-10A-01D-A23B-08 g.chr11:118377097G>A c.10481G>A c.(10480-10482)gGa>gAa p.G3494E SKCM 11 118390453 118390453 + Missense_Mutation SNP C C T TCGA-DA-A1I5-06A-11D-A197-08 TCGA-DA-A1I5-10A-01D-A199-08 g.chr11:118390453C>T c.11258C>T c.(11257-11259)gCc>gTc p.A3753V

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 11 118359364 118359364 single base substitution C A downstream_gene_variant BLCA-CN 11 118359364 118359364 single base substitution C A missense_variant H1418Q 4254C>A BLCA-CN 11 118359364 118359364 single base substitution C A missense_variant H1456Q 4368C>A BLCA-CN 11 118359364 118359364 single base substitution C A missense_variant H168Q 504C>A BLCA-CN 11 118359433 118359433 single base substitution C G downstream_gene_variant BLCA-CN 11 118359433 118359433 single base substitution C G missense_variant C1441W 4323C>G BLCA-CN 11 118359433 118359433 single base substitution C G missense_variant C1479W 4437C>G BLCA-CN 11 118359433 118359433 single base substitution C G missense_variant C191W 573C>G BLCA-CN 11 118363930 118363930 single base substitution G T downstream_gene_variant BLCA-CN 11 118363930 118363930 single base substitution G T synonymous_variant G1680G 5040G>T BLCA-CN 11 118363930 118363930 single base substitution G T synonymous_variant G1718G 5154G>T BLCA-CN 11 118363930 118363930 single base substitution G T synonymous_variant G1721G 5163G>T BLCA-CN 11 118374172 118374172 single base substitution C T exon_variant BLCA-CN 11 118374172 118374172 single base substitution C T missense_variant T2481I 7442C>T BLCA-CN 11 118374172 118374172 single base substitution C T missense_variant T2519I 7556C>T BLCA-CN 11 118374172 118374172 single base substitution C T missense_variant T2522I 7565C>T BLCA-CN 11 118374172 118374172 single base substitution C T upstream_gene_variant BLCA-CN 11 118375263 118375263 single base substitution C G downstream_gene_variant BLCA-CN 11 118375263 118375263 single base substitution C G missense_variant L2845V 8533C>G BLCA-CN 11 118375263 118375263 single base substitution C G missense_variant L2883V 8647C>G BLCA-CN 11 118375263 118375263 single base substitution C G missense_variant L2886V 8656C>G BLCA-CN 11 118375263 118375263 single base substitution C G upstream_gene_variant BLCA-CN 11 118390707 118390707 single base substitution C G exon_variant BLCA-CN 11 118390707 118390707 single base substitution C G missense_variant S3745C 11234C>G BLCA-CN 11 118390707 118390707 single base substitution C G missense_variant S3783C 11348C>G BLCA-CN 11 118390707 118390707 single base substitution C G missense_variant S3786C 11357C>G BLCA-CN 11 118399399 118399399 single base substitution T C downstream_gene_variant BLCA-US 11 118344511 118344511 single base substitution G A intron_variant BLCA-US 11 118344511 118344511 single base substitution G A synonymous_variant E879E 2637G>A BLCA-US 11 118344511 118344511 single base substitution G A synonymous_variant E912E 2736G>A BLCA-US 11 118369132 118369132 single base substitution C T synonymous_variant L1909L 5727C>T BLCA-US 11 118369132 118369132 single base substitution C T synonymous_variant L1947L 5841C>T BLCA-US 11 118369132 118369132 single base substitution C T synonymous_variant L1950L 5850C>T BLCA-US 11 118369132 118369132 single base substitution C T upstream_gene_variant BLCA-US 11 118390358 118390358 single base substitution G A exon_variant BLCA-US 11 118390358 118390358 single base substitution G A synonymous_variant G3683G 11049G>A BLCA-US 11 118390358 118390358 single base substitution G A synonymous_variant G3721G 11163G>A BLCA-US 11 118390358 118390358 single base substitution G A synonymous_variant G3724G 11172G>A BLCA-US 11 118390358 118390358 single base substitution G A upstream_gene_variant BLCA-US 11 118399332 118399332 single base substitution C G downstream_gene_variant BLCA-US 11 118399370 118399370 single base substitution G C downstream_gene_variant BRCA-EU 11 118303583 118303583 single base substitution C T upstream_gene_variant BRCA-EU 11 118305034 118305034 single base substitution C G upstream_gene_variant BRCA-EU 11 118306032 118306032 single base substitution C A upstream_gene_variant BRCA-EU 11 118309675 118309675 single base substitution G A intron_variant BRCA-EU 11 118311192 118311192 single base substitution T C intron_variant BRCA-EU 11 118312080 118312080 single base substitution G T intron_variant BRCA-EU 11 118312122 118312122 single base substitution T A intron_variant BRCA-EU 11 118315069 118315069 single base substitution C T intron_variant BRCA-EU 11 118315894 118315894 single base substitution C G intron_variant BRCA-EU 11 118316515 118316515 single base substitution C T intron_variant BRCA-EU 11 118317139 118317139 single base substitution C G intron_variant BRCA-EU 11 118317933 118317933 single base substitution G C intron_variant BRCA-EU 11 118319397 118319397 single base substitution G C 3_prime_UTR_variant BRCA-EU 11 118319397 118319397 single base substitution G C intron_variant BRCA-EU 11 118319665 118319665 single base substitution C T 3_prime_UTR_variant BRCA-EU 11 118319665 118319665 single base substitution C T intron_variant BRCA-EU 11 118323966 118323966 single base substitution G T downstream_gene_variant BRCA-EU 11 118323966 118323966 single base substitution G T intron_variant BRCA-EU 11 118323989 118323989 single base substitution C T downstream_gene_variant BRCA-EU 11 118323989 118323989 single base substitution C T intron_variant BRCA-EU 11 118324490 118324490 single base substitution A G downstream_gene_variant BRCA-EU 11 118324490 118324490 single base substitution A G intron_variant BRCA-EU 11 118325892 118325892 single base substitution C T downstream_gene_variant BRCA-EU 11 118325892 118325892 single base substitution C T intron_variant BRCA-EU 11 118326150 118326150 single base substitution C G downstream_gene_variant BRCA-EU 11 118326150 118326150 single base substitution C G intron_variant BRCA-EU 11 118326321 118326321 deletion of <=200bp T - downstream_gene_variant BRCA-EU 11 118326321 118326321 deletion of <=200bp T - intron_variant BRCA-EU 11 118326939 118326965 deletion of <=200bp GCATGGTGGCTAACACCTGTAATCCCA - intron_variant BRCA-EU 11 118326965 118326965 single base substitution A T intron_variant BRCA-EU 11 118326986 118326986 single base substitution G C intron_variant BRCA-EU 11 118327736 118327745 deletion of <=200bp TCTGTCCTTT - intron_variant BRCA-EU 11 118328093 118328093 single base substitution C T intron_variant BRCA-EU 11 118329286 118329286 deletion of <=200bp A - intron_variant BRCA-EU 11 118332688 118332688 single base substitution A G intron_variant BRCA-EU 11 118332721 118332721 single base substitution C T intron_variant BRCA-EU 11 118333729 118333729 single base substitution T G intron_variant BRCA-EU 11 118333850 118333852 deletion of <=200bp TTA - intron_variant BRCA-EU 11 118335075 118335075 single base substitution A C intron_variant BRCA-EU 11 118335530 118335530 single base substitution G C intron_variant BRCA-EU 11 118337506 118337506 single base substitution T C intron_variant BRCA-EU 11 118338704 118338704 single base substitution A C intron_variant BRCA-EU 11 118339630 118339630 single base substitution C G intron_variant BRCA-EU 11 118340164 118340164 single base substitution G C intron_variant BRCA-EU 11 118340773 118340773 single base substitution G A intron_variant BRCA-EU 11 118341476 118341476 single base substitution G A intron_variant BRCA-EU 11 118341484 118341484 single base substitution G C intron_variant BRCA-EU 11 118342802 118342802 single base substitution G A intron_variant BRCA-EU 11 118342802 118342802 single base substitution G A missense_variant E310K 928G>A BRCA-EU 11 118342802 118342802 single base substitution G A missense_variant E343K 1027G>A BRCA-EU 11 118343253 118343253 deletion of <=200bp A - frameshift_variant E460 BRCA-EU 11 118343253 118343253 deletion of <=200bp A - frameshift_variant E493 BRCA-EU 11 118343253 118343253 deletion of <=200bp A - intron_variant BRCA-EU 11 118343606 118343606 single base substitution A G intron_variant BRCA-EU 11 118343606 118343606 single base substitution A G missense_variant I578V 1732A>G BRCA-EU 11 118343606 118343606 single base substitution A G missense_variant I611V 1831A>G BRCA-EU 11 118346580 118346580 single base substitution C T downstream_gene_variant BRCA-EU 11 118346580 118346580 single base substitution C T intron_variant BRCA-EU 11 118346839 118346839 single base substitution C T downstream_gene_variant BRCA-EU 11 118346839 118346839 single base substitution C T intron_variant BRCA-EU 11 118347328 118347328 deletion of <=200bp T - downstream_gene_variant BRCA-EU 11 118347328 118347328 deletion of <=200bp T - intron_variant BRCA-EU 11 118347721 118347721 single base substitution G A downstream_gene_variant BRCA-EU 11 118347721 118347721 single base substitution G A intron_variant BRCA-EU 11 118347721 118347721 single base substitution G A upstream_gene_variant BRCA-EU 11 118348950 118348950 single base substitution C T downstream_gene_variant BRCA-EU 11 118348950 118348950 single base substitution C T intron_variant BRCA-EU 11 118348950 118348950 single base substitution C T upstream_gene_variant BRCA-EU 11 118349361 118349361 single base substitution C G downstream_gene_variant BRCA-EU 11 118349361 118349361 single base substitution C G intron_variant BRCA-EU 11 118349361 118349361 single base substitution C G upstream_gene_variant BRCA-EU 11 118350796 118350821 deletion of <=200bp GATTCACTGATTGTTGCAGACAAAAT - downstream_gene_variant BRCA-EU 11 118350796 118350821 deletion of <=200bp GATTCACTGATTGTTGCAGACAAAAT - intron_variant BRCA-EU 11 118350796 118350821 deletion of <=200bp GATTCACTGATTGTTGCAGACAAAAT - upstream_gene_variant BRCA-EU 11 118351094 118351094 single base substitution G C downstream_gene_variant BRCA-EU 11 118351094 118351094 single base substitution G C intron_variant BRCA-EU 11 118351094 118351094 single base substitution G C upstream_gene_variant BRCA-EU 11 118352178 118352178 single base substitution T G downstream_gene_variant BRCA-EU 11 118352178 118352178 single base substitution T G intron_variant BRCA-EU 11 118352178 118352178 single base substitution T G upstream_gene_variant BRCA-EU 11 118354640 118354641 deletion of <=200bp TT - intron_variant BRCA-EU 11 118354655 118354655 single base substitution A G intron_variant BRCA-EU 11 118354751 118354751 deletion of <=200bp A - intron_variant BRCA-EU 11 118355925 118355925 insertion of <=200bp - A downstream_gene_variant BRCA-EU 11 118355925 118355925 insertion of <=200bp - A intron_variant BRCA-EU 11 118356791 118356791 single base substitution C A downstream_gene_variant BRCA-EU 11 118356791 118356791 single base substitution C A intron_variant BRCA-EU 11 118357309 118357309 single base substitution C T downstream_gene_variant BRCA-EU 11 118357309 118357309 single base substitution C T intron_variant BRCA-EU 11 118357972 118357972 single base substitution C G downstream_gene_variant BRCA-EU 11 118357972 118357972 single base substitution C G intron_variant BRCA-EU 11 118358796 118358796 single base substitution G A downstream_gene_variant BRCA-EU 11 118358796 118358796 single base substitution G A intron_variant BRCA-EU 11 118359362 118359362 single base substitution C G downstream_gene_variant BRCA-EU 11 118359362 118359362 single base substitution C G missense_variant H1418D 4252C>G BRCA-EU 11 118359362 118359362 single base substitution C G missense_variant H1456D 4366C>G BRCA-EU 11 118359362 118359362 single base substitution C G missense_variant H168D 502C>G BRCA-EU 11 118359537 118359537 single base substitution G C downstream_gene_variant BRCA-EU 11 118359537 118359537 single base substitution G C intron_variant BRCA-EU 11 118359770 118359770 single base substitution C G downstream_gene_variant BRCA-EU 11 118359770 118359770 single base substitution C G intron_variant BRCA-EU 11 118360174 118360174 deletion of <=200bp T - intron_variant BRCA-EU 11 118360307 118360307 single base substitution A T intron_variant BRCA-EU 11 118360910 118360910 single base substitution C T stop_gained Q1510* 4528C>T BRCA-EU 11 118360910 118360910 single base substitution C T stop_gained Q1548* 4642C>T BRCA-EU 11 118360910 118360910 single base substitution C T stop_gained Q260* 778C>T BRCA-EU 11 118362557 118362557 single base substitution G A missense_variant E1599K 4795G>A BRCA-EU 11 118362557 118362557 single base substitution G A missense_variant E1637K 4909G>A BRCA-EU 11 118362557 118362557 single base substitution G A missense_variant E1640K 4918G>A BRCA-EU 11 118362557 118362557 single base substitution G A missense_variant E349K 1045G>A BRCA-EU 11 118362787 118362787 single base substitution G C downstream_gene_variant BRCA-EU 11 118362787 118362787 single base substitution G C intron_variant BRCA-EU 11 118363165 118363165 single base substitution C T downstream_gene_variant BRCA-EU 11 118363165 118363165 single base substitution C T intron_variant BRCA-EU 11 118364350 118364350 single base substitution G A downstream_gene_variant BRCA-EU 11 118364350 118364350 single base substitution G A intron_variant BRCA-EU 11 118366957 118366957 single base substitution G C downstream_gene_variant BRCA-EU 11 118366957 118366957 single base substitution G C intron_variant BRCA-EU 11 118366957 118366957 single base substitution G C upstream_gene_variant BRCA-EU 11 118367029 118367029 single base substitution G C downstream_gene_variant BRCA-EU 11 118367029 118367029 single base substitution G C missense_variant E1830Q 5488G>C BRCA-EU 11 118367029 118367029 single base substitution G C missense_variant E1868Q 5602G>C BRCA-EU 11 118367029 118367029 single base substitution G C missense_variant E1871Q 5611G>C BRCA-EU 11 118367029 118367029 single base substitution G C upstream_gene_variant BRCA-EU 11 118367662 118367662 deletion of <=200bp T - intron_variant BRCA-EU 11 118367662 118367662 deletion of <=200bp T - upstream_gene_variant BRCA-EU 11 118367662 118367662 insertion of <=200bp - T intron_variant BRCA-EU 11 118367662 118367662 insertion of <=200bp - T upstream_gene_variant BRCA-EU 11 118368289 118368289 single base substitution T A intron_variant BRCA-EU 11 118368289 118368289 single base substitution T A upstream_gene_variant BRCA-EU 11 118371477 118371477 deletion of <=200bp A - exon_variant BRCA-EU 11 118371477 118371477 deletion of <=200bp A - intron_variant BRCA-EU 11 118371512 118371512 single base substitution G C exon_variant BRCA-EU 11 118371512 118371512 single base substitution G C intron_variant BRCA-EU 11 118372316 118372317 deletion of <=200bp TT - intron_variant BRCA-EU 11 118372316 118372317 deletion of <=200bp TT - upstream_gene_variant BRCA-EU 11 118373654 118373654 single base substitution T C exon_variant BRCA-EU 11 118373654 118373654 single base substitution T C synonymous_variant S2308S 6924T>C BRCA-EU 11 118373654 118373654 single base substitution T C synonymous_variant S2346S 7038T>C BRCA-EU 11 118373654 118373654 single base substitution T C synonymous_variant S2349S 7047T>C BRCA-EU 11 118373654 118373654 single base substitution T C upstream_gene_variant BRCA-EU 11 118375882 118375889 deletion of <=200bp ATGTTCTC - downstream_gene_variant BRCA-EU 11 118375882 118375889 deletion of <=200bp ATGTTCTC - frameshift_variant YVL3051 BRCA-EU 11 118375882 118375889 deletion of <=200bp ATGTTCTC - frameshift_variant YVL3089 BRCA-EU 11 118375882 118375889 deletion of <=200bp ATGTTCTC - frameshift_variant YVL3092 BRCA-EU 11 118375882 118375889 deletion of <=200bp ATGTTCTC - upstream_gene_variant BRCA-EU 11 118376480 118376481 deletion of <=200bp AT - downstream_gene_variant BRCA-EU 11 118376480 118376481 deletion of <=200bp AT - frameshift_variant RS3250 BRCA-EU 11 118376480 118376481 deletion of <=200bp AT - frameshift_variant RS3288 BRCA-EU 11 118376480 118376481 deletion of <=200bp AT - frameshift_variant RS3291 BRCA-EU 11 118376480 118376481 deletion of <=200bp AT - upstream_gene_variant BRCA-EU 11 118377914 118377914 single base substitution G T downstream_gene_variant BRCA-EU 11 118377914 118377914 single base substitution G T intron_variant BRCA-EU 11 118377914 118377914 single base substitution G T upstream_gene_variant BRCA-EU 11 118378667 118378667 single base substitution G C downstream_gene_variant BRCA-EU 11 118378667 118378667 single base substitution G C intron_variant BRCA-EU 11 118378667 118378667 single base substitution G C upstream_gene_variant BRCA-EU 11 118379806 118379806 single base substitution T C downstream_gene_variant BRCA-EU 11 118379806 118379806 single base substitution T C intron_variant BRCA-EU 11 118379806 118379806 single base substitution T C upstream_gene_variant BRCA-EU 11 118380456 118380456 deletion of <=200bp A - downstream_gene_variant BRCA-EU 11 118380456 118380456 deletion of <=200bp A - intron_variant BRCA-EU 11 118380456 118380456 deletion of <=200bp A - upstream_gene_variant BRCA-EU 11 118382028 118382028 single base substitution C G downstream_gene_variant BRCA-EU 11 118382028 118382028 single base substitution C G intron_variant BRCA-EU 11 118382600 118382600 single base substitution C A downstream_gene_variant BRCA-EU 11 118382600 118382600 single base substitution C A intron_variant BRCA-EU 11 118383663 118383663 single base substitution G C downstream_gene_variant BRCA-EU 11 118383663 118383663 single base substitution G C intron_variant BRCA-EU 11 118383858 118383858 single base substitution C T downstream_gene_variant BRCA-EU 11 118383858 118383858 single base substitution C T intron_variant BRCA-EU 11 118383937 118383937 single base substitution C T downstream_gene_variant BRCA-EU 11 118383937 118383937 single base substitution C T intron_variant BRCA-EU 11 118384097 118384097 single base substitution G A downstream_gene_variant BRCA-EU 11 118384097 118384097 single base substitution G A intron_variant BRCA-EU 11 118384892 118384892 single base substitution C T downstream_gene_variant BRCA-EU 11 118384892 118384892 single base substitution C T intron_variant BRCA-EU 11 118386264 118386264 single base substitution G C downstream_gene_variant BRCA-EU 11 118386264 118386264 single base substitution G C intron_variant BRCA-EU 11 118386264 118386264 single base substitution G C upstream_gene_variant BRCA-EU 11 118388315 118388315 single base substitution G A intron_variant BRCA-EU 11 118388315 118388315 single base substitution G A upstream_gene_variant BRCA-EU 11 118389879 118389879 single base substitution C G intron_variant BRCA-EU 11 118389879 118389879 single base substitution C G upstream_gene_variant BRCA-EU 11 118392129 118392129 single base substitution C A exon_variant BRCA-EU 11 118392129 118392129 single base substitution C A missense_variant S3839R 11517C>A BRCA-EU 11 118392129 118392129 single base substitution C A missense_variant S3877R 11631C>A BRCA-EU 11 118392129 118392129 single base substitution C A missense_variant S3880R 11640C>A BRCA-EU 11 118395544 118395564 deletion of <=200bp TAGACCTAGTTACTGCCCTGC - 3_prime_UTR_variant BRCA-EU 11 118395544 118395564 deletion of <=200bp TAGACCTAGTTACTGCCCTGC - downstream_gene_variant BRCA-EU 11 118396954 118396954 single base substitution G A 3_prime_UTR_variant BRCA-EU 11 118396954 118396954 single base substitution G A downstream_gene_variant BRCA-EU 11 118397453 118397453 deletion of <=200bp A - 3_prime_UTR_variant BRCA-EU 11 118397453 118397453 deletion of <=200bp A - downstream_gene_variant BRCA-EU 11 118399604 118399604 single base substitution C T downstream_gene_variant BRCA-EU 11 118399637 118399637 single base substitution G T downstream_gene_variant BRCA-EU 11 118400115 118400115 single base substitution G A downstream_gene_variant BRCA-EU 11 118400118 118400118 single base substitution A T downstream_gene_variant BRCA-EU 11 118400760 118400760 single base substitution A C downstream_gene_variant BRCA-EU 11 118401071 118401071 single base substitution C A downstream_gene_variant BRCA-EU 11 118401414 118401414 single base substitution G A downstream_gene_variant BRCA-EU 11 118401421 118401421 single base substitution C T downstream_gene_variant BRCA-FR 11 118305554 118305554 single base substitution C G upstream_gene_variant BRCA-FR 11 118320479 118320479 single base substitution C G 3_prime_UTR_variant BRCA-FR 11 118320479 118320479 single base substitution C G intron_variant BRCA-FR 11 118346961 118346961 single base substitution A G downstream_gene_variant BRCA-FR 11 118346961 118346961 single base substitution A G intron_variant BRCA-FR 11 118352178 118352178 single base substitution T G downstream_gene_variant BRCA-FR 11 118352178 118352178 single base substitution T G intron_variant BRCA-FR 11 118352178 118352178 single base substitution T G upstream_gene_variant BRCA-FR 11 118354655 118354655 single base substitution A G intron_variant BRCA-FR 11 118386264 118386264 single base substitution G C downstream_gene_variant BRCA-FR 11 118386264 118386264 single base substitution G C intron_variant BRCA-FR 11 118386264 118386264 single base substitution G C upstream_gene_variant BRCA-FR 11 118401071 118401071 single base substitution C A downstream_gene_variant BRCA-FR 11 118401414 118401414 single base substitution G A downstream_gene_variant BRCA-KR 11 118355732 118355732 single base substitution T G downstream_gene_variant BRCA-KR 11 118355732 118355732 single base substitution T G intron_variant BRCA-UK 11 118316515 118316515 single base substitution C T intron_variant BRCA-UK 11 118322127 118322127 single base substitution G C downstream_gene_variant BRCA-UK 11 118322127 118322127 single base substitution G C intron_variant BRCA-UK 11 118326150 118326150 single base substitution C G downstream_gene_variant BRCA-UK 11 118326150 118326150 single base substitution C G intron_variant BRCA-UK 11 118343165 118343165 single base substitution G A intron_variant BRCA-UK 11 118343165 118343165 single base substitution G A missense_variant D431N 1291G>A BRCA-UK 11 118343165 118343165 single base substitution G A missense_variant D464N 1390G>A BRCA-UK 11 118343440 118343440 single base substitution G C intron_variant BRCA-UK 11 118343440 118343440 single base substitution G C missense_variant E522D 1566G>C BRCA-UK 11 118343440 118343440 single base substitution G C missense_variant E555D 1665G>C BRCA-UK 11 118359537 118359537 single base substitution G C downstream_gene_variant BRCA-UK 11 118359537 118359537 single base substitution G C intron_variant BRCA-UK 11 118371512 118371512 single base substitution G C exon_variant BRCA-UK 11 118371512 118371512 single base substitution G C intron_variant BRCA-UK 11 118384572 118384572 single base substitution G A downstream_gene_variant BRCA-UK 11 118384572 118384572 single base substitution G A intron_variant BRCA-US 11 118343199 118343199 single base substitution G A intron_variant BRCA-US 11 118343199 118343199 single base substitution G A missense_variant R442Q 1325G>A BRCA-US 11 118343199 118343199 single base substitution G A missense_variant R475Q 1424G>A BRCA-US 11 118343656 118343656 single base substitution A C intron_variant BRCA-US 11 118343656 118343656 single base substitution A C synonymous_variant S594S 1782A>C BRCA-US 11 118343656 118343656 single base substitution A C synonymous_variant S627S 1881A>C BRCA-US 11 118343828 118343828 single base substitution C T intron_variant BRCA-US 11 118343828 118343828 single base substitution C T stop_gained R652* 1954C>T BRCA-US 11 118343828 118343828 single base substitution C T stop_gained R685* 2053C>T BRCA-US 11 118344572 118344572 single base substitution C T intron_variant BRCA-US 11 118344572 118344572 single base substitution C T stop_gained Q900* 2698C>T BRCA-US 11 118344572 118344572 single base substitution C T stop_gained Q933* 2797C>T BRCA-US 11 118344574 118344574 insertion of <=200bp - TAAA frameshift_variant Q900HK? BRCA-US 11 118344574 118344574 insertion of <=200bp - TAAA frameshift_variant Q933HK? BRCA-US 11 118344574 118344574 insertion of <=200bp - TAAA intron_variant BRCA-US 11 118344879 118344879 single base substitution C G intron_variant BRCA-US 11 118344879 118344879 single base substitution C G missense_variant S1002C 3005C>G BRCA-US 11 118344879 118344879 single base substitution C G missense_variant S1035C 3104C>G BRCA-US 11 118350902 118350902 single base substitution C T downstream_gene_variant BRCA-US 11 118350902 118350902 single base substitution C T stop_gained Q1195* 3583C>T BRCA-US 11 118350902 118350902 single base substitution C T stop_gained Q1228* 3682C>T BRCA-US 11 118350902 118350902 single base substitution C T upstream_gene_variant BRCA-US 11 118352528 118352528 single base substitution A C downstream_gene_variant BRCA-US 11 118352528 118352528 single base substitution A C missense_variant T1245P 3733A>C BRCA-US 11 118352528 118352528 single base substitution A C missense_variant T1278P 3832A>C BRCA-US 11 118352528 118352528 single base substitution A C upstream_gene_variant BRCA-US 11 118354912 118354912 single base substitution G A exon_variant BRCA-US 11 118354912 118354912 single base substitution G A synonymous_variant P117P 351G>A BRCA-US 11 118354912 118354912 single base substitution G A synonymous_variant P1367P 4101G>A BRCA-US 11 118354912 118354912 single base substitution G A synonymous_variant P1400P 4200G>A BRCA-US 11 118359386 118359386 single base substitution G T downstream_gene_variant BRCA-US 11 118359386 118359386 single base substitution G T stop_gained E1426* 4276G>T BRCA-US 11 118359386 118359386 single base substitution G T stop_gained E1464* 4390G>T BRCA-US 11 118359386 118359386 single base substitution G T stop_gained E176* 526G>T BRCA-US 11 118363787 118363787 single base substitution G C downstream_gene_variant BRCA-US 11 118363787 118363787 single base substitution G C missense_variant D1633H 4897G>C BRCA-US 11 118363787 118363787 single base substitution G C missense_variant D1671H 5011G>C BRCA-US 11 118363787 118363787 single base substitution G C missense_variant D1674H 5020G>C BRCA-US 11 118366575 118366575 single base substitution A G downstream_gene_variant BRCA-US 11 118366575 118366575 single base substitution A G missense_variant T1801A 5401A>G BRCA-US 11 118366575 118366575 single base substitution A G missense_variant T1839A 5515A>G BRCA-US 11 118366575 118366575 single base substitution A G missense_variant T1842A 5524A>G BRCA-US 11 118366575 118366575 single base substitution A G upstream_gene_variant BRCA-US 11 118367017 118367017 deletion of <=200bp C - downstream_gene_variant BRCA-US 11 118367017 118367017 deletion of <=200bp C - frameshift_variant P1826 BRCA-US 11 118367017 118367017 deletion of <=200bp C - frameshift_variant P1864 BRCA-US 11 118367017 118367017 deletion of <=200bp C - frameshift_variant P1867 BRCA-US 11 118367017 118367017 deletion of <=200bp C - upstream_gene_variant BRCA-US 11 118371701 118371701 single base substitution G A exon_variant BRCA-US 11 118371701 118371701 single base substitution G A splice_acceptor_variant BRCA-US 11 118372517 118372517 single base substitution A C exon_variant BRCA-US 11 118372517 118372517 single base substitution A C synonymous_variant T2109T 6327A>C BRCA-US 11 118372517 118372517 single base substitution A C synonymous_variant T2147T 6441A>C BRCA-US 11 118372517 118372517 single base substitution A C synonymous_variant T2150T 6450A>C BRCA-US 11 118372517 118372517 single base substitution A C upstream_gene_variant BRCA-US 11 118373416 118373416 deletion of <=200bp A - exon_variant BRCA-US 11 118373416 118373416 deletion of <=200bp A - frameshift_variant Q2229 BRCA-US 11 118373416 118373416 deletion of <=200bp A - frameshift_variant Q2267 BRCA-US 11 118373416 118373416 deletion of <=200bp A - frameshift_variant Q2270 BRCA-US 11 118373416 118373416 deletion of <=200bp A - upstream_gene_variant BRCA-US 11 118373824 118373824 single base substitution A G exon_variant BRCA-US 11 118373824 118373824 single base substitution A G missense_variant K2365R 7094A>G BRCA-US 11 118373824 118373824 single base substitution A G missense_variant K2403R 7208A>G BRCA-US 11 118373824 118373824 single base substitution A G missense_variant K2406R 7217A>G BRCA-US 11 118373824 118373824 single base substitution A G upstream_gene_variant BRCA-US 11 118375222 118375222 single base substitution C T downstream_gene_variant BRCA-US 11 118375222 118375222 single base substitution C T missense_variant S2831L 8492C>T BRCA-US 11 118375222 118375222 single base substitution C T missense_variant S2869L 8606C>T BRCA-US 11 118375222 118375222 single base substitution C T missense_variant S2872L 8615C>T BRCA-US 11 118375222 118375222 single base substitution C T upstream_gene_variant BRCA-US 11 118375750 118375750 single base substitution A C downstream_gene_variant BRCA-US 11 118375750 118375750 single base substitution A C missense_variant K3007T 9020A>C BRCA-US 11 118375750 118375750 single base substitution A C missense_variant K3045T 9134A>C BRCA-US 11 118375750 118375750 single base substitution A C missense_variant K3048T 9143A>C BRCA-US 11 118375750 118375750 single base substitution A C upstream_gene_variant BRCA-US 11 118375784 118375784 single base substitution G A downstream_gene_variant BRCA-US 11 118375784 118375784 single base substitution G A synonymous_variant P3018P 9054G>A BRCA-US 11 118375784 118375784 single base substitution G A synonymous_variant P3056P 9168G>A BRCA-US 11 118375784 118375784 single base substitution G A synonymous_variant P3059P 9177G>A BRCA-US 11 118375784 118375784 single base substitution G A upstream_gene_variant BRCA-US 11 118376092 118376092 single base substitution A C downstream_gene_variant BRCA-US 11 118376092 118376092 single base substitution A C missense_variant H3121P 9362A>C BRCA-US 11 118376092 118376092 single base substitution A C missense_variant H3159P 9476A>C BRCA-US 11 118376092 118376092 single base substitution A C missense_variant H3162P 9485A>C BRCA-US 11 118376092 118376092 single base substitution A C upstream_gene_variant BRCA-US 11 118376138 118376138 single base substitution A C downstream_gene_variant BRCA-US 11 118376138 118376138 single base substitution A C synonymous_variant P3136P 9408A>C BRCA-US 11 118376138 118376138 single base substitution A C synonymous_variant P3174P 9522A>C BRCA-US 11 118376138 118376138 single base substitution A C synonymous_variant P3177P 9531A>C BRCA-US 11 118376138 118376138 single base substitution A C upstream_gene_variant BRCA-US 11 118376471 118376471 single base substitution C T downstream_gene_variant BRCA-US 11 118376471 118376471 single base substitution C T synonymous_variant I3247I 9741C>T BRCA-US 11 118376471 118376471 single base substitution C T synonymous_variant I3285I 9855C>T BRCA-US 11 118376471 118376471 single base substitution C T synonymous_variant I3288I 9864C>T BRCA-US 11 118376471 118376471 single base substitution C T upstream_gene_variant BRCA-US 11 118376746 118376746 single base substitution C T downstream_gene_variant BRCA-US 11 118376746 118376746 single base substitution C T missense_variant S3339L 10016C>T BRCA-US 11 118376746 118376746 single base substitution C T missense_variant S3377L 10130C>T BRCA-US 11 118376746 118376746 single base substitution C T missense_variant S3380L 10139C>T BRCA-US 11 118376746 118376746 single base substitution C T upstream_gene_variant BRCA-US 11 118390417 118390417 single base substitution G A exon_variant BRCA-US 11 118390417 118390417 single base substitution G A missense_variant R3703Q 11108G>A BRCA-US 11 118390417 118390417 single base substitution G A missense_variant R3741Q 11222G>A BRCA-US 11 118390417 118390417 single base substitution G A missense_variant R3744Q 11231G>A BRCA-US 11 118390417 118390417 single base substitution G A upstream_gene_variant BRCA-US 11 118391565 118391565 deletion of <=200bp A - exon_variant BRCA-US 11 118391565 118391565 deletion of <=200bp A - frameshift_variant L3785 BRCA-US 11 118391565 118391565 deletion of <=200bp A - frameshift_variant L3823 BRCA-US 11 118391565 118391565 deletion of <=200bp A - frameshift_variant L3826 BRCA-US 11 118392845 118392845 single base substitution C G exon_variant BRCA-US 11 118392845 118392845 single base substitution C G synonymous_variant P3918P 11754C>G BRCA-US 11 118392845 118392845 single base substitution C G synonymous_variant P3956P 11868C>G BRCA-US 11 118392845 118392845 single base substitution C G synonymous_variant P3959P 11877C>G BTCA-JP 11 118309704 118309704 deletion of <=200bp T - intron_variant BTCA-JP 11 118343011 118343011 deletion of <=200bp A - frameshift_variant A379 BTCA-JP 11 118343011 118343011 deletion of <=200bp A - frameshift_variant A412 BTCA-JP 11 118343011 118343011 deletion of <=200bp A - intron_variant BTCA-JP 11 118343304 118343304 single base substitution C T intron_variant BTCA-JP 11 118343304 118343304 single base substitution C T missense_variant S477F 1430C>T BTCA-JP 11 118343304 118343304 single base substitution C T missense_variant S510F 1529C>T BTCA-JP 11 118344186 118344186 insertion of <=200bp - C frameshift_variant T771T? BTCA-JP 11 118344186 118344186 insertion of <=200bp - C frameshift_variant T804T? BTCA-JP 11 118344186 118344186 insertion of <=200bp - C intron_variant BTCA-JP 11 118344671 118344671 single base substitution C T intron_variant BTCA-JP 11 118344671 118344671 single base substitution C T missense_variant R933W 2797C>T BTCA-JP 11 118344671 118344671 single base substitution C T missense_variant R966W 2896C>T BTCA-JP 11 118347673 118347673 single base substitution A G downstream_gene_variant BTCA-JP 11 118347673 118347673 single base substitution A G missense_variant I1104V 3310A>G BTCA-JP 11 118347673 118347673 single base substitution A G missense_variant I1137V 3409A>G BTCA-JP 11 118347673 118347673 single base substitution A G missense_variant I182V 544A>G BTCA-JP 11 118347673 118347673 single base substitution A G upstream_gene_variant BTCA-JP 11 118353240 118353240 single base substitution C A downstream_gene_variant BTCA-JP 11 118353240 118353240 single base substitution C A intron_variant BTCA-JP 11 118355642 118355642 single base substitution A C downstream_gene_variant BTCA-JP 11 118355642 118355642 single base substitution A C intron_variant BTCA-JP 11 118355642 118355642 single base substitution A C synonymous_variant I1428I 4284A>C BTCA-JP 11 118366529 118366529 single base substitution C A downstream_gene_variant BTCA-JP 11 118366529 118366529 single base substitution C A synonymous_variant I1785I 5355C>A BTCA-JP 11 118366529 118366529 single base substitution C A synonymous_variant I1823I 5469C>A BTCA-JP 11 118366529 118366529 single base substitution C A synonymous_variant I1826I 5478C>A BTCA-JP 11 118366529 118366529 single base substitution C A upstream_gene_variant BTCA-JP 11 118366975 118366975 single base substitution G A downstream_gene_variant BTCA-JP 11 118366975 118366975 single base substitution G A splice_acceptor_variant BTCA-JP 11 118366975 118366975 single base substitution G A upstream_gene_variant BTCA-JP 11 118375427 118375427 single base substitution G T downstream_gene_variant BTCA-JP 11 118375427 118375427 single base substitution G T synonymous_variant R2899R 8697G>T BTCA-JP 11 118375427 118375427 single base substitution G T synonymous_variant R2937R 8811G>T BTCA-JP 11 118375427 118375427 single base substitution G T synonymous_variant R2940R 8820G>T BTCA-JP 11 118375427 118375427 single base substitution G T upstream_gene_variant BTCA-JP 11 118376091 118376091 single base substitution C T downstream_gene_variant BTCA-JP 11 118376091 118376091 single base substitution C T missense_variant H3121Y 9361C>T BTCA-JP 11 118376091 118376091 single base substitution C T missense_variant H3159Y 9475C>T BTCA-JP 11 118376091 118376091 single base substitution C T missense_variant H3162Y 9484C>T BTCA-JP 11 118376091 118376091 single base substitution C T upstream_gene_variant BTCA-JP 11 118376264 118376264 single base substitution T C downstream_gene_variant BTCA-JP 11 118376264 118376264 single base substitution T C synonymous_variant S3178S 9534T>C BTCA-JP 11 118376264 118376264 single base substitution T C synonymous_variant S3216S 9648T>C BTCA-JP 11 118376264 118376264 single base substitution T C synonymous_variant S3219S 9657T>C BTCA-JP 11 118376264 118376264 single base substitution T C upstream_gene_variant BTCA-JP 11 118379822 118379822 single base substitution A T downstream_gene_variant BTCA-JP 11 118379822 118379822 single base substitution A T intron_variant BTCA-JP 11 118379822 118379822 single base substitution A T upstream_gene_variant BTCA-JP 11 118379827 118379827 single base substitution A G downstream_gene_variant BTCA-JP 11 118379827 118379827 single base substitution A G intron_variant BTCA-JP 11 118379827 118379827 single base substitution A G upstream_gene_variant BTCA-JP 11 118390216 118390216 single base substitution A G intron_variant BTCA-JP 11 118390216 118390216 single base substitution A G upstream_gene_variant BTCA-JP 11 118391491 118391491 single base substitution C T exon_variant BTCA-JP 11 118391491 118391491 single base substitution C T intron_variant BTCA-JP 11 118391576 118391576 single base substitution C G exon_variant BTCA-JP 11 118391576 118391576 single base substitution C G missense_variant S3789C 11366C>G BTCA-JP 11 118391576 118391576 single base substitution C G missense_variant S3827C 11480C>G BTCA-JP 11 118391576 118391576 single base substitution C G missense_variant S3830C 11489C>G BTCA-JP 11 118392943 118392943 single base substitution C T 3_prime_UTR_variant BTCA-JP 11 118392943 118392943 single base substitution C T downstream_gene_variant BTCA-JP 11 118392943 118392943 single base substitution C T exon_variant CESC-US 11 118305488 118305488 single base substitution C G upstream_gene_variant CESC-US 11 118342900 118342900 single base substitution A G intron_variant CESC-US 11 118342900 118342900 single base substitution A G synonymous_variant K342K 1026A>G CESC-US 11 118342900 118342900 single base substitution A G synonymous_variant K375K 1125A>G CESC-US 11 118352537 118352537 single base substitution G T downstream_gene_variant CESC-US 11 118352537 118352537 single base substitution G T missense_variant A1248S 3742G>T CESC-US 11 118352537 118352537 single base substitution G T missense_variant A1281S 3841G>T CESC-US 11 118352537 118352537 single base substitution G T upstream_gene_variant CESC-US 11 118362470 118362470 single base substitution G A missense_variant E1570K 4708G>A CESC-US 11 118362470 118362470 single base substitution G A missense_variant E1608K 4822G>A CESC-US 11 118362470 118362470 single base substitution G A missense_variant E1611K 4831G>A CESC-US 11 118362470 118362470 single base substitution G A missense_variant E320K 958G>A CESC-US 11 118370615 118370615 single base substitution C T missense_variant P2008S 6022C>T CESC-US 11 118370615 118370615 single base substitution C T missense_variant P2046S 6136C>T CESC-US 11 118370615 118370615 single base substitution C T missense_variant P2049S 6145C>T CESC-US 11 118370615 118370615 single base substitution C T upstream_gene_variant CESC-US 11 118371806 118371806 single base substitution G A exon_variant CESC-US 11 118371806 118371806 single base substitution G A missense_variant S2047N 6140G>A CESC-US 11 118371806 118371806 single base substitution G A missense_variant S2085N 6254G>A CESC-US 11 118371806 118371806 single base substitution G A missense_variant S2088N 6263G>A CESC-US 11 118375513 118375513 single base substitution C G downstream_gene_variant CESC-US 11 118375513 118375513 single base substitution C G missense_variant S2928C 8783C>G CESC-US 11 118375513 118375513 single base substitution C G missense_variant S2966C 8897C>G CESC-US 11 118375513 118375513 single base substitution C G missense_variant S2969C 8906C>G CESC-US 11 118375513 118375513 single base substitution C G upstream_gene_variant CESC-US 11 118375583 118375583 single base substitution G A downstream_gene_variant CESC-US 11 118375583 118375583 single base substitution G A missense_variant M2951I 8853G>A CESC-US 11 118375583 118375583 single base substitution G A missense_variant M2989I 8967G>A CESC-US 11 118375583 118375583 single base substitution G A missense_variant M2992I 8976G>A CESC-US 11 118375583 118375583 single base substitution G A upstream_gene_variant CESC-US 11 118376214 118376214 single base substitution G C downstream_gene_variant CESC-US 11 118376214 118376214 single base substitution G C missense_variant E3162Q 9484G>C CESC-US 11 118376214 118376214 single base substitution G C missense_variant E3200Q 9598G>C CESC-US 11 118376214 118376214 single base substitution G C missense_variant E3203Q 9607G>C CESC-US 11 118376214 118376214 single base substitution G C upstream_gene_variant CESC-US 11 118376933 118376933 single base substitution C T downstream_gene_variant CESC-US 11 118376933 118376933 single base substitution C T synonymous_variant A3401A 10203C>T CESC-US 11 118376933 118376933 single base substitution C T synonymous_variant A3439A 10317C>T CESC-US 11 118376933 118376933 single base substitution C T synonymous_variant A3442A 10326C>T CESC-US 11 118376933 118376933 single base substitution C T upstream_gene_variant CESC-US 11 118377304 118377304 single base substitution G T downstream_gene_variant CESC-US 11 118377304 118377304 single base substitution G T exon_variant CESC-US 11 118377304 118377304 single base substitution G T missense_variant S3525I 10574G>T CESC-US 11 118377304 118377304 single base substitution G T missense_variant S3563I 10688G>T CESC-US 11 118377304 118377304 single base substitution G T missense_variant S3566I 10697G>T CESC-US 11 118377304 118377304 single base substitution G T upstream_gene_variant CESC-US 11 118390460 118390460 insertion of <=200bp - C exon_variant CESC-US 11 118390460 118390460 insertion of <=200bp - C frameshift_variant E3717D? CESC-US 11 118390460 118390460 insertion of <=200bp - C frameshift_variant E3755D? CESC-US 11 118390460 118390460 insertion of <=200bp - C frameshift_variant E3758D? CESC-US 11 118390460 118390460 insertion of <=200bp - C upstream_gene_variant CESC-US 11 118390715 118390715 single base substitution C T exon_variant CESC-US 11 118390715 118390715 single base substitution C T missense_variant R3748C 11242C>T CESC-US 11 118390715 118390715 single base substitution C T missense_variant R3786C 11356C>T CESC-US 11 118390715 118390715 single base substitution C T missense_variant R3789C 11365C>T CESC-US 11 118399332 118399332 single base substitution C G downstream_gene_variant CLLE-ES 11 118308335 118308335 single base substitution G C intron_variant CLLE-ES 11 118311821 118311821 single base substitution G T intron_variant CLLE-ES 11 118341116 118341116 single base substitution T C intron_variant CLLE-ES 11 118348370 118348370 single base substitution G A downstream_gene_variant CLLE-ES 11 118348370 118348370 single base substitution G A intron_variant CLLE-ES 11 118348370 118348370 single base substitution G A upstream_gene_variant CLLE-ES 11 118382502 118382502 single base substitution G A downstream_gene_variant CLLE-ES 11 118382502 118382502 single base substitution G A intron_variant CLLE-ES 11 118382752 118382752 single base substitution A G downstream_gene_variant CLLE-ES 11 118382752 118382752 single base substitution A G exon_variant CLLE-ES 11 118382752 118382752 single base substitution A G intron_variant CLLE-ES 11 118388951 118388951 single base substitution G T intron_variant CLLE-ES 11 118388951 118388951 single base substitution G T upstream_gene_variant CLLE-ES 11 118394287 118394289 deletion of <=200bp AAT - 3_prime_UTR_variant CLLE-ES 11 118394287 118394289 deletion of <=200bp AAT - downstream_gene_variant COAD-US 11 118343236 118343236 single base substitution G A intron_variant COAD-US 11 118343236 118343236 single base substitution G A synonymous_variant P454P 1362G>A COAD-US 11 118343236 118343236 single base substitution G A synonymous_variant P487P 1461G>A COAD-US 11 118343316 118343316 single base substitution G A intron_variant COAD-US 11 118343316 118343316 single base substitution G A missense_variant S481N 1442G>A COAD-US 11 118343316 118343316 single base substitution G A missense_variant S514N 1541G>A COAD-US 11 118343913 118343913 single base substitution C T intron_variant COAD-US 11 118343913 118343913 single base substitution C T missense_variant S680L 2039C>T COAD-US 11 118343913 118343913 single base substitution C T missense_variant S713L 2138C>T COAD-US 11 118344185 118344185 insertion of <=200bp - C frameshift_variant T771H? COAD-US 11 118344185 118344185 insertion of <=200bp - C frameshift_variant T804H? COAD-US 11 118344185 118344185 insertion of <=200bp - C intron_variant COAD-US 11 118344186 118344186 deletion of <=200bp C - frameshift_variant T771 COAD-US 11 118344186 118344186 deletion of <=200bp C - frameshift_variant T804 COAD-US 11 118344186 118344186 deletion of <=200bp C - intron_variant COAD-US 11 118344458 118344458 single base substitution C T intron_variant COAD-US 11 118344458 118344458 single base substitution C T stop_gained R862* 2584C>T COAD-US 11 118344458 118344458 single base substitution C T stop_gained R895* 2683C>T COAD-US 11 118348807 118348807 single base substitution C T downstream_gene_variant COAD-US 11 118348807 118348807 single base substitution C T missense_variant R1154W 3460C>T COAD-US 11 118348807 118348807 single base substitution C T missense_variant R1187W 3559C>T COAD-US 11 118348807 118348807 single base substitution C T missense_variant R232W 694C>T COAD-US 11 118348807 118348807 single base substitution C T upstream_gene_variant COAD-US 11 118352594 118352594 single base substitution G A downstream_gene_variant COAD-US 11 118352594 118352594 single base substitution G A missense_variant V1267I 3799G>A COAD-US 11 118352594 118352594 single base substitution G A missense_variant V1300I 3898G>A COAD-US 11 118352594 118352594 single base substitution G A missense_variant V17I 49G>A COAD-US 11 118352594 118352594 single base substitution G A upstream_gene_variant COAD-US 11 118352743 118352743 deletion of <=200bp A - downstream_gene_variant COAD-US 11 118352743 118352743 deletion of <=200bp A - exon_variant COAD-US 11 118352743 118352743 deletion of <=200bp A - frameshift_variant R1316 COAD-US 11 118352743 118352743 deletion of <=200bp A - frameshift_variant R1349 COAD-US 11 118352743 118352743 deletion of <=200bp A - frameshift_variant R66 COAD-US 11 118359396 118359396 single base substitution T C downstream_gene_variant COAD-US 11 118359396 118359396 single base substitution T C missense_variant L1429P 4286T>C COAD-US 11 118359396 118359396 single base substitution T C missense_variant L1467P 4400T>C COAD-US 11 118359396 118359396 single base substitution T C missense_variant L179P 536T>C COAD-US 11 118360862 118360862 single base substitution C T missense_variant R1494C 4480C>T COAD-US 11 118360862 118360862 single base substitution C T missense_variant R1532C 4594C>T COAD-US 11 118360862 118360862 single base substitution C T missense_variant R244C 730C>T COAD-US 11 118365419 118365419 single base substitution G A downstream_gene_variant COAD-US 11 118365419 118365419 single base substitution G A missense_variant R1726H 5177G>A COAD-US 11 118365419 118365419 single base substitution G A missense_variant R1764H 5291G>A COAD-US 11 118365419 118365419 single base substitution G A missense_variant R1767H 5300G>A COAD-US 11 118368731 118368731 single base substitution A G synonymous_variant E1874E 5622A>G COAD-US 11 118368731 118368731 single base substitution A G synonymous_variant E1912E 5736A>G COAD-US 11 118368731 118368731 single base substitution A G synonymous_variant E1915E 5745A>G COAD-US 11 118368731 118368731 single base substitution A G upstream_gene_variant COAD-US 11 118369101 118369101 deletion of <=200bp A - frameshift_variant Q1899 COAD-US 11 118369101 118369101 deletion of <=200bp A - frameshift_variant Q1937 COAD-US 11 118369101 118369101 deletion of <=200bp A - frameshift_variant Q1940 COAD-US 11 118369101 118369101 deletion of <=200bp A - upstream_gene_variant COAD-US 11 118373178 118373178 single base substitution C T exon_variant COAD-US 11 118373178 118373178 single base substitution C T stop_gained R2150* 6448C>T COAD-US 11 118373178 118373178 single base substitution C T stop_gained R2188* 6562C>T COAD-US 11 118373178 118373178 single base substitution C T stop_gained R2191* 6571C>T COAD-US 11 118373178 118373178 single base substitution C T upstream_gene_variant COAD-US 11 118373277 118373277 single base substitution A G exon_variant COAD-US 11 118373277 118373277 single base substitution A G missense_variant R2183G 6547A>G COAD-US 11 118373277 118373277 single base substitution A G missense_variant R2221G 6661A>G COAD-US 11 118373277 118373277 single base substitution A G missense_variant R2224G 6670A>G COAD-US 11 118373277 118373277 single base substitution A G upstream_gene_variant COAD-US 11 118374060 118374060 single base substitution G A exon_variant COAD-US 11 118374060 118374060 single base substitution G A missense_variant V2444I 7330G>A COAD-US 11 118374060 118374060 single base substitution G A missense_variant V2482I 7444G>A COAD-US 11 118374060 118374060 single base substitution G A missense_variant V2485I 7453G>A COAD-US 11 118374060 118374060 single base substitution G A upstream_gene_variant COAD-US 11 118375434 118375434 single base substitution A G downstream_gene_variant COAD-US 11 118375434 118375434 single base substitution A G missense_variant T2902A 8704A>G COAD-US 11 118375434 118375434 single base substitution A G missense_variant T2940A 8818A>G COAD-US 11 118375434 118375434 single base substitution A G missense_variant T2943A 8827A>G COAD-US 11 118375434 118375434 single base substitution A G upstream_gene_variant COAD-US 11 118375871 118375871 single base substitution G A downstream_gene_variant COAD-US 11 118375871 118375871 single base substitution G A missense_variant M3047I 9141G>A COAD-US 11 118375871 118375871 single base substitution G A missense_variant M3085I 9255G>A COAD-US 11 118375871 118375871 single base substitution G A missense_variant M3088I 9264G>A COAD-US 11 118375871 118375871 single base substitution G A upstream_gene_variant COAD-US 11 118375915 118375915 deletion of <=200bp A - downstream_gene_variant COAD-US 11 118375915 118375915 deletion of <=200bp A - frameshift_variant Q3062 COAD-US 11 118375915 118375915 deletion of <=200bp A - frameshift_variant Q3100 COAD-US 11 118375915 118375915 deletion of <=200bp A - frameshift_variant Q3103 COAD-US 11 118375915 118375915 deletion of <=200bp A - upstream_gene_variant COAD-US 11 118375917 118375917 single base substitution A C downstream_gene_variant COAD-US 11 118375917 118375917 single base substitution A C missense_variant K3063Q 9187A>C COAD-US 11 118375917 118375917 single base substitution A C missense_variant K3101Q 9301A>C COAD-US 11 118375917 118375917 single base substitution A C missense_variant K3104Q 9310A>C COAD-US 11 118375917 118375917 single base substitution A C upstream_gene_variant COAD-US 11 118376203 118376203 deletion of <=200bp T - downstream_gene_variant COAD-US 11 118376203 118376203 deletion of <=200bp T - frameshift_variant L3158 COAD-US 11 118376203 118376203 deletion of <=200bp T - frameshift_variant L3196 COAD-US 11 118376203 118376203 deletion of <=200bp T - frameshift_variant L3199 COAD-US 11 118376203 118376203 deletion of <=200bp T - upstream_gene_variant COAD-US 11 118376479 118376479 single base substitution G T downstream_gene_variant COAD-US 11 118376479 118376479 single base substitution G T missense_variant R3250I 9749G>T COAD-US 11 118376479 118376479 single base substitution G T missense_variant R3288I 9863G>T COAD-US 11 118376479 118376479 single base substitution G T missense_variant R3291I 9872G>T COAD-US 11 118376479 118376479 single base substitution G T upstream_gene_variant COAD-US 11 118376683 118376683 single base substitution C T downstream_gene_variant COAD-US 11 118376683 118376683 single base substitution C T missense_variant A3318V 9953C>T COAD-US 11 118376683 118376683 single base substitution C T missense_variant A3356V 10067C>T COAD-US 11 118376683 118376683 single base substitution C T missense_variant A3359V 10076C>T COAD-US 11 118376683 118376683 single base substitution C T upstream_gene_variant COAD-US 11 118376816 118376816 single base substitution G A downstream_gene_variant COAD-US 11 118376816 118376816 single base substitution G A synonymous_variant P3362P 10086G>A COAD-US 11 118376816 118376816 single base substitution G A synonymous_variant P3400P 10200G>A COAD-US 11 118376816 118376816 single base substitution G A synonymous_variant P3403P 10209G>A COAD-US 11 118376816 118376816 single base substitution G A upstream_gene_variant COAD-US 11 118376882 118376882 single base substitution G A downstream_gene_variant COAD-US 11 118376882 118376882 single base substitution G A synonymous_variant A3384A 10152G>A COAD-US 11 118376882 118376882 single base substitution G A synonymous_variant A3422A 10266G>A COAD-US 11 118376882 118376882 single base substitution G A synonymous_variant A3425A 10275G>A COAD-US 11 118376882 118376882 single base substitution G A upstream_gene_variant COAD-US 11 118378315 118378315 single base substitution A G downstream_gene_variant COAD-US 11 118378315 118378315 single base substitution A G exon_variant COAD-US 11 118378315 118378315 single base substitution A G missense_variant Q3568R 10703A>G COAD-US 11 118378315 118378315 single base substitution A G missense_variant Q3606R 10817A>G COAD-US 11 118378315 118378315 single base substitution A G missense_variant Q3609R 10826A>G COAD-US 11 118378315 118378315 single base substitution A G upstream_gene_variant COAD-US 11 118382705 118382705 single base substitution G A downstream_gene_variant COAD-US 11 118382705 118382705 single base substitution G A exon_variant COAD-US 11 118382705 118382705 single base substitution G A missense_variant R3663Q 10988G>A COAD-US 11 118382705 118382705 single base substitution G A missense_variant R3701Q 11102G>A COAD-US 11 118382705 118382705 single base substitution G A missense_variant R3704Q 11111G>A COAD-US 11 118391552 118391552 single base substitution G A exon_variant COAD-US 11 118391552 118391552 single base substitution G A missense_variant R3781H 11342G>A COAD-US 11 118391552 118391552 single base substitution G A missense_variant R3819H 11456G>A COAD-US 11 118391552 118391552 single base substitution G A missense_variant R3822H 11465G>A COAD-US 11 118392685 118392685 single base substitution G A exon_variant COAD-US 11 118392685 118392685 single base substitution G A missense_variant R3865H 11594G>A COAD-US 11 118392685 118392685 single base substitution G A missense_variant R3903H 11708G>A COAD-US 11 118392685 118392685 single base substitution G A missense_variant R3906H 11717G>A COAD-US 11 118392771 118392771 single base substitution C T exon_variant COAD-US 11 118392771 118392771 single base substitution C T missense_variant R3894C 11680C>T COAD-US 11 118392771 118392771 single base substitution C T missense_variant R3932C 11794C>T COAD-US 11 118392771 118392771 single base substitution C T missense_variant R3935C 11803C>T COAD-US 11 118392857 118392857 single base substitution C T exon_variant COAD-US 11 118392857 118392857 single base substitution C T synonymous_variant G3922G 11766C>T COAD-US 11 118392857 118392857 single base substitution C T synonymous_variant G3960G 11880C>T COAD-US 11 118392857 118392857 single base substitution C T synonymous_variant G3963G 11889C>T COCA-CN 11 118303854 118303854 single base substitution A T upstream_gene_variant COCA-CN 11 118308120 118308120 single base substitution G C intron_variant COCA-CN 11 118309863 118309863 single base substitution G A intron_variant COCA-CN 11 118309870 118309870 single base substitution C A intron_variant COCA-CN 11 118325830 118325830 single base substitution T G downstream_gene_variant COCA-CN 11 118325830 118325830 single base substitution T G intron_variant COCA-CN 11 118342392 118342392 single base substitution G A intron_variant COCA-CN 11 118342392 118342392 single base substitution G A missense_variant R173Q 518G>A COCA-CN 11 118342392 118342392 single base substitution G A missense_variant R206Q 617G>A COCA-CN 11 118343138 118343138 single base substitution A G intron_variant COCA-CN 11 118343138 118343138 single base substitution A G missense_variant I422V 1264A>G COCA-CN 11 118343138 118343138 single base substitution A G missense_variant I455V 1363A>G COCA-CN 11 118343570 118343570 single base substitution C T intron_variant COCA-CN 11 118343570 118343570 single base substitution C T synonymous_variant L566L 1696C>T COCA-CN 11 118343570 118343570 single base substitution C T synonymous_variant L599L 1795C>T COCA-CN 11 118344107 118344107 single base substitution C T intron_variant COCA-CN 11 118344107 118344107 single base substitution C T stop_gained R745* 2233C>T COCA-CN 11 118344107 118344107 single base substitution C T stop_gained R778* 2332C>T COCA-CN 11 118344108 118344108 single base substitution G A intron_variant COCA-CN 11 118344108 118344108 single base substitution G A missense_variant R745Q 2234G>A COCA-CN 11 118344108 118344108 single base substitution G A missense_variant R778Q 2333G>A COCA-CN 11 118366503 118366503 single base substitution G A downstream_gene_variant COCA-CN 11 118366503 118366503 single base substitution G A missense_variant E1777K 5329G>A COCA-CN 11 118366503 118366503 single base substitution G A missense_variant E1815K 5443G>A COCA-CN 11 118366503 118366503 single base substitution G A missense_variant E1818K 5452G>A COCA-CN 11 118366503 118366503 single base substitution G A upstream_gene_variant COCA-CN 11 118366507 118366507 single base substitution A T downstream_gene_variant COCA-CN 11 118366507 118366507 single base substitution A T missense_variant Q1778L 5333A>T COCA-CN 11 118366507 118366507 single base substitution A T missense_variant Q1816L 5447A>T COCA-CN 11 118366507 118366507 single base substitution A T missense_variant Q1819L 5456A>T COCA-CN 11 118366507 118366507 single base substitution A T upstream_gene_variant COCA-CN 11 118368636 118368636 single base substitution C A intron_variant COCA-CN 11 118368636 118368636 single base substitution C A upstream_gene_variant COCA-CN 11 118369536 118369536 single base substitution A G intron_variant COCA-CN 11 118369536 118369536 single base substitution A G upstream_gene_variant COCA-CN 11 118372443 118372443 single base substitution G A exon_variant COCA-CN 11 118372443 118372443 single base substitution G A missense_variant D2085N 6253G>A COCA-CN 11 118372443 118372443 single base substitution G A missense_variant D2123N 6367G>A COCA-CN 11 118372443 118372443 single base substitution G A missense_variant D2126N 6376G>A COCA-CN 11 118372443 118372443 single base substitution G A upstream_gene_variant COCA-CN 11 118373950 118373950 single base substitution C A exon_variant COCA-CN 11 118373950 118373950 single base substitution C A missense_variant S2407Y 7220C>A COCA-CN 11 118373950 118373950 single base substitution C A missense_variant S2445Y 7334C>A COCA-CN 11 118373950 118373950 single base substitution C A missense_variant S2448Y 7343C>A COCA-CN 11 118373950 118373950 single base substitution C A upstream_gene_variant COCA-CN 11 118376443 118376443 single base substitution C A downstream_gene_variant COCA-CN 11 118376443 118376443 single base substitution C A missense_variant T3238N 9713C>A COCA-CN 11 118376443 118376443 single base substitution C A missense_variant T3276N 9827C>A COCA-CN 11 118376443 118376443 single base substitution C A missense_variant T3279N 9836C>A COCA-CN 11 118376443 118376443 single base substitution C A upstream_gene_variant COCA-CN 11 118376479 118376479 single base substitution G T downstream_gene_variant COCA-CN 11 118376479 118376479 single base substitution G T missense_variant R3250I 9749G>T COCA-CN 11 118376479 118376479 single base substitution G T missense_variant R3288I 9863G>T COCA-CN 11 118376479 118376479 single base substitution G T missense_variant R3291I 9872G>T COCA-CN 11 118376479 118376479 single base substitution G T upstream_gene_variant COCA-CN 11 118377080 118377080 single base substitution C T downstream_gene_variant COCA-CN 11 118377080 118377080 single base substitution C T synonymous_variant D3450D 10350C>T COCA-CN 11 118377080 118377080 single base substitution C T synonymous_variant D3488D 10464C>T COCA-CN 11 118377080 118377080 single base substitution C T synonymous_variant D3491D 10473C>T COCA-CN 11 118377080 118377080 single base substitution C T upstream_gene_variant COCA-CN 11 118391555 118391555 single base substitution T C exon_variant COCA-CN 11 118391555 118391555 single base substitution T C missense_variant F3782S 11345T>C COCA-CN 11 118391555 118391555 single base substitution T C missense_variant F3820S 11459T>C COCA-CN 11 118391555 118391555 single base substitution T C missense_variant F3823S 11468T>C COCA-CN 11 118392976 118392976 single base substitution C T 3_prime_UTR_variant COCA-CN 11 118392976 118392976 single base substitution C T downstream_gene_variant COCA-CN 11 118392976 118392976 single base substitution C T exon_variant COCA-CN 11 118398768 118398768 single base substitution C T downstream_gene_variant COCA-CN 11 118402111 118402111 single base substitution A G downstream_gene_variant COCA-CN 11 118402124 118402124 single base substitution G A downstream_gene_variant EOPC-DE 11 118372562 118372562 single base substitution G C exon_variant EOPC-DE 11 118372562 118372562 single base substitution G C missense_variant L2124F 6372G>C EOPC-DE 11 118372562 118372562 single base substitution G C missense_variant L2162F 6486G>C EOPC-DE 11 118372562 118372562 single base substitution G C missense_variant L2165F 6495G>C EOPC-DE 11 118372562 118372562 single base substitution G C upstream_gene_variant ESAD-UK 11 118302407 118302407 single base substitution T A upstream_gene_variant ESAD-UK 11 118303192 118303192 single base substitution G A upstream_gene_variant ESAD-UK 11 118307601 118307601 single base substitution A G missense_variant N125S 374A>G ESAD-UK 11 118307601 118307601 single base substitution A G missense_variant N42S 125A>G ESAD-UK 11 118307601 118307601 single base substitution A G missense_variant N48S 143A>G ESAD-UK 11 118312397 118312397 single base substitution G T intron_variant ESAD-UK 11 118315616 118315616 single base substitution C T intron_variant ESAD-UK 11 118316978 118316978 single base substitution C T intron_variant ESAD-UK 11 118316988 118316988 single base substitution C T intron_variant ESAD-UK 11 118318259 118318259 single base substitution C G intron_variant ESAD-UK 11 118319343 118319343 single base substitution G T 3_prime_UTR_variant ESAD-UK 11 118319343 118319343 single base substitution G T intron_variant ESAD-UK 11 118319818 118319818 single base substitution T A 3_prime_UTR_variant ESAD-UK 11 118319818 118319818 single base substitution T A intron_variant ESAD-UK 11 118326385 118326385 single base substitution A T downstream_gene_variant ESAD-UK 11 118326385 118326385 single base substitution A T intron_variant ESAD-UK 11 118330500 118330500 single base substitution C G intron_variant ESAD-UK 11 118334014 118334018 deletion of <=200bp TACTT - intron_variant ESAD-UK 11 118336459 118336459 single base substitution G T intron_variant ESAD-UK 11 118336522 118336522 insertion of <=200bp - T intron_variant ESAD-UK 11 118338723 118338723 single base substitution T C intron_variant ESAD-UK 11 118339520 118339522 deletion of <=200bp GAA - inframe_deletion E105 ESAD-UK 11 118339520 118339522 deletion of <=200bp GAA - inframe_deletion E155 ESAD-UK 11 118339520 118339522 deletion of <=200bp GAA - inframe_deletion E188 ESAD-UK 11 118339520 118339522 deletion of <=200bp GAA - inframe_deletion E72 ESAD-UK 11 118343395 118343395 single base substitution T A intron_variant ESAD-UK 11 118343395 118343395 single base substitution T A synonymous_variant P507P 1521T>A ESAD-UK 11 118343395 118343395 single base substitution T A synonymous_variant P540P 1620T>A ESAD-UK 11 118346997 118346997 single base substitution G A downstream_gene_variant ESAD-UK 11 118346997 118346997 single base substitution G A intron_variant ESAD-UK 11 118347729 118347729 single base substitution A G downstream_gene_variant ESAD-UK 11 118347729 118347729 single base substitution A G intron_variant ESAD-UK 11 118347729 118347729 single base substitution A G upstream_gene_variant ESAD-UK 11 118352423 118352423 single base substitution C T downstream_gene_variant ESAD-UK 11 118352423 118352423 single base substitution C T splice_region_variant ESAD-UK 11 118352423 118352423 single base substitution C T upstream_gene_variant ESAD-UK 11 118357419 118357419 single base substitution C A downstream_gene_variant ESAD-UK 11 118357419 118357419 single base substitution C A intron_variant ESAD-UK 11 118357480 118357480 single base substitution C T downstream_gene_variant ESAD-UK 11 118357480 118357480 single base substitution C T intron_variant ESAD-UK 11 118357517 118357517 single base substitution C T downstream_gene_variant ESAD-UK 11 118357517 118357517 single base substitution C T intron_variant ESAD-UK 11 118357638 118357638 single base substitution C T downstream_gene_variant ESAD-UK 11 118357638 118357638 single base substitution C T intron_variant ESAD-UK 11 118357639 118357639 single base substitution C T downstream_gene_variant ESAD-UK 11 118357639 118357639 single base substitution C T intron_variant ESAD-UK 11 118357699 118357699 single base substitution C T downstream_gene_variant ESAD-UK 11 118357699 118357699 single base substitution C T intron_variant ESAD-UK 11 118357813 118357813 single base substitution C T downstream_gene_variant ESAD-UK 11 118357813 118357813 single base substitution C T intron_variant ESAD-UK 11 118358028 118358028 single base substitution A T downstream_gene_variant ESAD-UK 11 118358028 118358028 single base substitution A T intron_variant ESAD-UK 11 118360954 118360954 single base substitution C T synonymous_variant L1524L 4572C>T ESAD-UK 11 118360954 118360954 single base substitution C T synonymous_variant L1562L 4686C>T ESAD-UK 11 118360954 118360954 single base substitution C T synonymous_variant L274L 822C>T ESAD-UK 11 118362013 118362013 single base substitution A G missense_variant E1562G 4685A>G ESAD-UK 11 118362013 118362013 single base substitution A G missense_variant E1600G 4799A>G ESAD-UK 11 118362013 118362013 single base substitution A G missense_variant E312G 935A>G ESAD-UK 11 118368953 118368954 deletion of <=200bp TC - intron_variant ESAD-UK 11 118368953 118368954 deletion of <=200bp TC - upstream_gene_variant ESAD-UK 11 118369003 118369003 single base substitution G T intron_variant ESAD-UK 11 118369003 118369003 single base substitution G T upstream_gene_variant ESAD-UK 11 118369075 118369075 single base substitution G C intron_variant ESAD-UK 11 118369075 118369075 single base substitution G C upstream_gene_variant ESAD-UK 11 118370317 118370317 single base substitution T A intron_variant ESAD-UK 11 118370317 118370317 single base substitution T A upstream_gene_variant ESAD-UK 11 118376322 118376322 single base substitution C T downstream_gene_variant ESAD-UK 11 118376322 118376322 single base substitution C T missense_variant P3198S 9592C>T ESAD-UK 11 118376322 118376322 single base substitution C T missense_variant P3236S 9706C>T ESAD-UK 11 118376322 118376322 single base substitution C T missense_variant P3239S 9715C>T ESAD-UK 11 118376322 118376322 single base substitution C T upstream_gene_variant ESAD-UK 11 118376684 118376684 single base substitution G A downstream_gene_variant ESAD-UK 11 118376684 118376684 single base substitution G A synonymous_variant A3318A 9954G>A ESAD-UK 11 118376684 118376684 single base substitution G A synonymous_variant A3356A 10068G>A ESAD-UK 11 118376684 118376684 single base substitution G A synonymous_variant A3359A 10077G>A ESAD-UK 11 118376684 118376684 single base substitution G A upstream_gene_variant ESAD-UK 11 118378494 118378494 single base substitution G A downstream_gene_variant ESAD-UK 11 118378494 118378494 single base substitution G A intron_variant ESAD-UK 11 118378494 118378494 single base substitution G A upstream_gene_variant ESAD-UK 11 118384524 118384524 single base substitution T C downstream_gene_variant ESAD-UK 11 118384524 118384524 single base substitution T C intron_variant ESAD-UK 11 118387271 118387271 single base substitution G A downstream_gene_variant ESAD-UK 11 118387271 118387271 single base substitution G A intron_variant ESAD-UK 11 118387271 118387271 single base substitution G A upstream_gene_variant ESAD-UK 11 118387833 118387833 single base substitution G A downstream_gene_variant ESAD-UK 11 118387833 118387833 single base substitution G A intron_variant ESAD-UK 11 118387833 118387833 single base substitution G A upstream_gene_variant ESAD-UK 11 118388663 118388663 single base substitution G A intron_variant ESAD-UK 11 118388663 118388663 single base substitution G A upstream_gene_variant ESAD-UK 11 118389349 118389349 single base substitution T A intron_variant ESAD-UK 11 118389349 118389349 single base substitution T A upstream_gene_variant ESAD-UK 11 118389867 118389867 single base substitution G A intron_variant ESAD-UK 11 118389867 118389867 single base substitution G A upstream_gene_variant ESAD-UK 11 118391374 118391374 single base substitution A G exon_variant ESAD-UK 11 118391374 118391374 single base substitution A G intron_variant ESAD-UK 11 118392124 118392124 single base substitution G A exon_variant ESAD-UK 11 118392124 118392124 single base substitution G A missense_variant D3838N 11512G>A ESAD-UK 11 118392124 118392124 single base substitution G A missense_variant D3876N 11626G>A ESAD-UK 11 118392124 118392124 single base substitution G A missense_variant D3879N 11635G>A ESAD-UK 11 118392871 118392871 single base substitution G A exon_variant ESAD-UK 11 118392871 118392871 single base substitution G A missense_variant R3927Q 11780G>A ESAD-UK 11 118392871 118392871 single base substitution G A missense_variant R3965Q 11894G>A ESAD-UK 11 118392871 118392871 single base substitution G A missense_variant R3968Q 11903G>A ESAD-UK 11 118396083 118396096 deletion of <=200bp TGGCGCTGACCCTT - 3_prime_UTR_variant ESAD-UK 11 118396083 118396096 deletion of <=200bp TGGCGCTGACCCTT - downstream_gene_variant ESAD-UK 11 118397453 118397453 deletion of <=200bp A - 3_prime_UTR_variant ESAD-UK 11 118397453 118397453 deletion of <=200bp A - downstream_gene_variant ESAD-UK 11 118397514 118397514 single base substitution T C 3_prime_UTR_variant ESAD-UK 11 118397514 118397514 single base substitution T C downstream_gene_variant ESAD-UK 11 118398154 118398154 single base substitution G A downstream_gene_variant ESAD-UK 11 118399403 118399403 single base substitution C T downstream_gene_variant ESAD-UK 11 118402334 118402334 single base substitution G C downstream_gene_variant ESCA-CN 11 118348809 118348809 single base substitution G T downstream_gene_variant ESCA-CN 11 118348809 118348809 single base substitution G T synonymous_variant R1154R 3462G>T ESCA-CN 11 118348809 118348809 single base substitution G T synonymous_variant R1187R 3561G>T ESCA-CN 11 118348809 118348809 single base substitution G T synonymous_variant R232R 696G>T ESCA-CN 11 118348809 118348809 single base substitution G T upstream_gene_variant ESCA-CN 11 118373197 118373197 single base substitution G A exon_variant ESCA-CN 11 118373197 118373197 single base substitution G A missense_variant R2156H 6467G>A ESCA-CN 11 118373197 118373197 single base substitution G A missense_variant R2194H 6581G>A ESCA-CN 11 118373197 118373197 single base substitution G A missense_variant R2197H 6590G>A ESCA-CN 11 118373197 118373197 single base substitution G A upstream_gene_variant ESCA-CN 11 118395425 118395425 single base substitution G A 3_prime_UTR_variant ESCA-CN 11 118395425 118395425 single base substitution G A downstream_gene_variant GBM-US 11 118359396 118359396 single base substitution T C downstream_gene_variant GBM-US 11 118359396 118359396 single base substitution T C missense_variant L1429P 4286T>C GBM-US 11 118359396 118359396 single base substitution T C missense_variant L1467P 4400T>C GBM-US 11 118359396 118359396 single base substitution T C missense_variant L179P 536T>C GBM-US 11 118375649 118375649 single base substitution A C downstream_gene_variant GBM-US 11 118375649 118375649 single base substitution A C synonymous_variant S2973S 8919A>C GBM-US 11 118375649 118375649 single base substitution A C synonymous_variant S3011S 9033A>C GBM-US 11 118375649 118375649 single base substitution A C synonymous_variant S3014S 9042A>C GBM-US 11 118375649 118375649 single base substitution A C upstream_gene_variant GBM-US 11 118376191 118376191 single base substitution C T downstream_gene_variant GBM-US 11 118376191 118376191 single base substitution C T missense_variant P3154L 9461C>T GBM-US 11 118376191 118376191 single base substitution C T missense_variant P3192L 9575C>T GBM-US 11 118376191 118376191 single base substitution C T missense_variant P3195L 9584C>T GBM-US 11 118376191 118376191 single base substitution C T upstream_gene_variant GBM-US 11 118382698 118382698 single base substitution G C downstream_gene_variant GBM-US 11 118382698 118382698 single base substitution G C exon_variant GBM-US 11 118382698 118382698 single base substitution G C missense_variant E3661Q 10981G>C GBM-US 11 118382698 118382698 single base substitution G C missense_variant E3699Q 11095G>C GBM-US 11 118382698 118382698 single base substitution G C missense_variant E3702Q 11104G>C KIRC-US 11 118348895 118348895 insertion of <=200bp - T downstream_gene_variant KIRC-US 11 118348895 118348895 insertion of <=200bp - T frameshift_variant N1183I? KIRC-US 11 118348895 118348895 insertion of <=200bp - T frameshift_variant N1216I? KIRC-US 11 118348895 118348895 insertion of <=200bp - T frameshift_variant N261I? KIRC-US 11 118348895 118348895 insertion of <=200bp - T upstream_gene_variant KIRC-US 11 118352713 118352713 single base substitution G A downstream_gene_variant KIRC-US 11 118352713 118352713 single base substitution G A exon_variant KIRC-US 11 118352713 118352713 single base substitution G A synonymous_variant P1306P 3918G>A KIRC-US 11 118352713 118352713 single base substitution G A synonymous_variant P1339P 4017G>A KIRC-US 11 118352713 118352713 single base substitution G A synonymous_variant P56P 168G>A KIRC-US 11 118370617 118370617 single base substitution T A synonymous_variant P2008P 6024T>A KIRC-US 11 118370617 118370617 single base substitution T A synonymous_variant P2046P 6138T>A KIRC-US 11 118370617 118370617 single base substitution T A synonymous_variant P2049P 6147T>A KIRC-US 11 118370617 118370617 single base substitution T A upstream_gene_variant KIRC-US 11 118372561 118372561 single base substitution T A exon_variant KIRC-US 11 118372561 118372561 single base substitution T A stop_gained L2124* 6371T>A KIRC-US 11 118372561 118372561 single base substitution T A stop_gained L2162* 6485T>A KIRC-US 11 118372561 118372561 single base substitution T A stop_gained L2165* 6494T>A KIRC-US 11 118372561 118372561 single base substitution T A upstream_gene_variant KIRC-US 11 118375051 118375051 single base substitution C A downstream_gene_variant KIRC-US 11 118375051 118375051 single base substitution C A missense_variant T2774K 8321C>A KIRC-US 11 118375051 118375051 single base substitution C A missense_variant T2812K 8435C>A KIRC-US 11 118375051 118375051 single base substitution C A missense_variant T2815K 8444C>A KIRC-US 11 118375051 118375051 single base substitution C A upstream_gene_variant KIRC-US 11 118375278 118375278 single base substitution G T downstream_gene_variant KIRC-US 11 118375278 118375278 single base substitution G T stop_gained E2850* 8548G>T KIRC-US 11 118375278 118375278 single base substitution G T stop_gained E2888* 8662G>T KIRC-US 11 118375278 118375278 single base substitution G T stop_gained E2891* 8671G>T KIRC-US 11 118375278 118375278 single base substitution G T upstream_gene_variant KIRC-US 11 118390456 118390456 single base substitution A G exon_variant KIRC-US 11 118390456 118390456 single base substitution A G missense_variant N3716S 11147A>G KIRC-US 11 118390456 118390456 single base substitution A G missense_variant N3754S 11261A>G KIRC-US 11 118390456 118390456 single base substitution A G missense_variant N3757S 11270A>G KIRC-US 11 118390456 118390456 single base substitution A G upstream_gene_variant KIRP-US 11 118373932 118373932 single base substitution A C exon_variant KIRP-US 11 118373932 118373932 single base substitution A C missense_variant E2401A 7202A>C KIRP-US 11 118373932 118373932 single base substitution A C missense_variant E2439A 7316A>C KIRP-US 11 118373932 118373932 single base substitution A C missense_variant E2442A 7325A>C KIRP-US 11 118373932 118373932 single base substitution A C upstream_gene_variant LAML-KR 11 118303868 118303868 single base substitution A T upstream_gene_variant LAML-KR 11 118353054 118353054 single base substitution C T downstream_gene_variant LAML-KR 11 118353054 118353054 single base substitution C T intron_variant LAML-KR 11 118354997 118354997 single base substitution G A exon_variant LAML-KR 11 118354997 118354997 single base substitution G A missense_variant D1396N 4186G>A LAML-KR 11 118354997 118354997 single base substitution G A missense_variant D1429N 4285G>A LAML-KR 11 118354997 118354997 single base substitution G A missense_variant D146N 436G>A LAML-KR 11 118369819 118369819 single base substitution G A intron_variant LAML-KR 11 118369819 118369819 single base substitution G A upstream_gene_variant LAML-KR 11 118373677 118373677 single base substitution C G exon_variant LAML-KR 11 118373677 118373677 single base substitution C G missense_variant P2316R 6947C>G LAML-KR 11 118373677 118373677 single base substitution C G missense_variant P2354R 7061C>G LAML-KR 11 118373677 118373677 single base substitution C G missense_variant P2357R 7070C>G LAML-KR 11 118373677 118373677 single base substitution C G upstream_gene_variant LAML-KR 11 118383507 118383507 single base substitution A T downstream_gene_variant LAML-KR 11 118383507 118383507 single base substitution A T intron_variant LGG-US 11 118343733 118343735 deletion of <=200bp CTT - inframe_deletion TS620T LGG-US 11 118343733 118343735 deletion of <=200bp CTT - inframe_deletion TS653T LGG-US 11 118343733 118343735 deletion of <=200bp CTT - intron_variant LGG-US 11 118344301 118344301 single base substitution T A intron_variant LGG-US 11 118344301 118344301 single base substitution T A synonymous_variant S809S 2427T>A LGG-US 11 118344301 118344301 single base substitution T A synonymous_variant S842S 2526T>A LGG-US 11 118374340 118374340 single base substitution C T downstream_gene_variant LGG-US 11 118374340 118374340 single base substitution C T missense_variant P2537L 7610C>T LGG-US 11 118374340 118374340 single base substitution C T missense_variant P2575L 7724C>T LGG-US 11 118374340 118374340 single base substitution C T missense_variant P2578L 7733C>T LGG-US 11 118374340 118374340 single base substitution C T upstream_gene_variant LGG-US 11 118380710 118380710 single base substitution A G downstream_gene_variant LGG-US 11 118380710 118380710 single base substitution A G exon_variant LGG-US 11 118380710 118380710 single base substitution A G missense_variant M3609V 10825A>G LGG-US 11 118380710 118380710 single base substitution A G missense_variant M3647V 10939A>G LGG-US 11 118380710 118380710 single base substitution A G missense_variant M3650V 10948A>G LGG-US 11 118390456 118390456 single base substitution A G exon_variant LGG-US 11 118390456 118390456 single base substitution A G missense_variant N3716S 11147A>G LGG-US 11 118390456 118390456 single base substitution A G missense_variant N3754S 11261A>G LGG-US 11 118390456 118390456 single base substitution A G missense_variant N3757S 11270A>G LGG-US 11 118390456 118390456 single base substitution A G upstream_gene_variant LICA-CN 11 118344245 118344245 single base substitution G T intron_variant LICA-CN 11 118344245 118344245 single base substitution G T missense_variant A791S 2371G>T LICA-CN 11 118344245 118344245 single base substitution G T missense_variant A824S 2470G>T LICA-CN 11 118344817 118344817 single base substitution A T intron_variant LICA-CN 11 118344817 118344817 single base substitution A T synonymous_variant P1014P 3042A>T LICA-CN 11 118344817 118344817 single base substitution A T synonymous_variant P981P 2943A>T LICA-CN 11 118362502 118362502 single base substitution C T synonymous_variant A1580A 4740C>T LICA-CN 11 118362502 118362502 single base substitution C T synonymous_variant A1618A 4854C>T LICA-CN 11 118362502 118362502 single base substitution C T synonymous_variant A1621A 4863C>T LICA-CN 11 118362502 118362502 single base substitution C T synonymous_variant A330A 990C>T LICA-CN 11 118365415 118365415 single base substitution G T downstream_gene_variant LICA-CN 11 118365415 118365415 single base substitution G T stop_gained E1725* 5173G>T LICA-CN 11 118365415 118365415 single base substitution G T stop_gained E1763* 5287G>T LICA-CN 11 118365415 118365415 single base substitution G T stop_gained E1766* 5296G>T LICA-FR 11 118307618 118307618 single base substitution G A missense_variant A131T 391G>A LICA-FR 11 118307618 118307618 single base substitution G A missense_variant A48T 142G>A LICA-FR 11 118307618 118307618 single base substitution G A missense_variant A54T 160G>A LICA-FR 11 118316239 118316239 single base substitution C G intron_variant LICA-FR 11 118316562 118316562 single base substitution A G intron_variant LICA-FR 11 118322372 118322372 deletion of <=200bp T - downstream_gene_variant LICA-FR 11 118322372 118322372 deletion of <=200bp T - intron_variant LICA-FR 11 118323377 118323377 single base substitution C G downstream_gene_variant LICA-FR 11 118323377 118323377 single base substitution C G intron_variant LICA-FR 11 118339203 118339203 single base substitution A G intron_variant LICA-FR 11 118344737 118344737 single base substitution G A intron_variant LICA-FR 11 118344737 118344737 single base substitution G A missense_variant A955T 2863G>A LICA-FR 11 118344737 118344737 single base substitution G A missense_variant A988T 2962G>A LICA-FR 11 118347598 118347598 single base substitution C T downstream_gene_variant LICA-FR 11 118347598 118347598 single base substitution C T missense_variant L1079F 3235C>T LICA-FR 11 118347598 118347598 single base substitution C T missense_variant L1112F 3334C>T LICA-FR 11 118347598 118347598 single base substitution C T missense_variant L157F 469C>T LICA-FR 11 118347598 118347598 single base substitution C T upstream_gene_variant LICA-FR 11 118351853 118351853 single base substitution A G downstream_gene_variant LICA-FR 11 118351853 118351853 single base substitution A G intron_variant LICA-FR 11 118351853 118351853 single base substitution A G upstream_gene_variant LICA-FR 11 118352550 118352550 single base substitution C G downstream_gene_variant LICA-FR 11 118352550 118352550 single base substitution C G missense_variant P1252R 3755C>G LICA-FR 11 118352550 118352550 single base substitution C G missense_variant P1285R 3854C>G LICA-FR 11 118352550 118352550 single base substitution C G missense_variant P2R 5C>G LICA-FR 11 118352550 118352550 single base substitution C G upstream_gene_variant LICA-FR 11 118354922 118354922 single base substitution C T exon_variant LICA-FR 11 118354922 118354922 single base substitution C T stop_gained Q121* 361C>T LICA-FR 11 118354922 118354922 single base substitution C T stop_gained Q1371* 4111C>T LICA-FR 11 118354922 118354922 single base substitution C T stop_gained Q1404* 4210C>T LICA-FR 11 118373951 118373951 single base substitution T A exon_variant LICA-FR 11 118373951 118373951 single base substitution T A synonymous_variant S2407S 7221T>A LICA-FR 11 118373951 118373951 single base substitution T A synonymous_variant S2445S 7335T>A LICA-FR 11 118373951 118373951 single base substitution T A synonymous_variant S2448S 7344T>A LICA-FR 11 118373951 118373951 single base substitution T A upstream_gene_variant LICA-FR 11 118376860 118376860 single base substitution C T downstream_gene_variant LICA-FR 11 118376860 118376860 single base substitution C T missense_variant P3377L 10130C>T LICA-FR 11 118376860 118376860 single base substitution C T missense_variant P3415L 10244C>T LICA-FR 11 118376860 118376860 single base substitution C T missense_variant P3418L 10253C>T LICA-FR 11 118376860 118376860 single base substitution C T upstream_gene_variant LICA-FR 11 118377855 118377855 single base substitution T A downstream_gene_variant LICA-FR 11 118377855 118377855 single base substitution T A intron_variant LICA-FR 11 118377855 118377855 single base substitution T A upstream_gene_variant LIHC-US 11 118342446 118342446 single base substitution C G intron_variant LIHC-US 11 118342446 118342446 single base substitution C G stop_gained S191* 572C>G LIHC-US 11 118342446 118342446 single base substitution C G stop_gained S224* 671C>G LIHC-US 11 118343416 118343416 single base substitution C T intron_variant LIHC-US 11 118343416 118343416 single base substitution C T synonymous_variant P514P 1542C>T LIHC-US 11 118343416 118343416 single base substitution C T synonymous_variant P547P 1641C>T LIHC-US 11 118362558 118362558 deletion of <=200bp A - frameshift_variant E1599 LIHC-US 11 118362558 118362558 deletion of <=200bp A - frameshift_variant E1637 LIHC-US 11 118362558 118362558 deletion of <=200bp A - frameshift_variant E1640 LIHC-US 11 118362558 118362558 deletion of <=200bp A - frameshift_variant E349 LIHC-US 11 118373507 118373507 single base substitution G A exon_variant LIHC-US 11 118373507 118373507 single base substitution G A synonymous_variant V2259V 6777G>A LIHC-US 11 118373507 118373507 single base substitution G A synonymous_variant V2297V 6891G>A LIHC-US 11 118373507 118373507 single base substitution G A synonymous_variant V2300V 6900G>A LIHC-US 11 118373507 118373507 single base substitution G A upstream_gene_variant LIHC-US 11 118374789 118374789 single base substitution G A downstream_gene_variant LIHC-US 11 118374789 118374789 single base substitution G A missense_variant E2687K 8059G>A LIHC-US 11 118374789 118374789 single base substitution G A missense_variant E2725K 8173G>A LIHC-US 11 118374789 118374789 single base substitution G A missense_variant E2728K 8182G>A LIHC-US 11 118374789 118374789 single base substitution G A upstream_gene_variant LIHC-US 11 118376454 118376454 single base substitution C T downstream_gene_variant LIHC-US 11 118376454 118376454 single base substitution C T stop_gained R3242* 9724C>T LIHC-US 11 118376454 118376454 single base substitution C T stop_gained R3280* 9838C>T LIHC-US 11 118376454 118376454 single base substitution C T stop_gained R3283* 9847C>T LIHC-US 11 118376454 118376454 single base substitution C T upstream_gene_variant LIHC-US 11 118377325 118377325 single base substitution C T downstream_gene_variant LIHC-US 11 118377325 118377325 single base substitution C T exon_variant LIHC-US 11 118377325 118377325 single base substitution C T missense_variant P3532L 10595C>T LIHC-US 11 118377325 118377325 single base substitution C T missense_variant P3570L 10709C>T LIHC-US 11 118377325 118377325 single base substitution C T missense_variant P3573L 10718C>T LIHC-US 11 118377325 118377325 single base substitution C T upstream_gene_variant LINC-JP 11 118307732 118307732 single base substitution A G intron_variant LINC-JP 11 118309889 118309889 single base substitution G A intron_variant LINC-JP 11 118314638 118314638 single base substitution G C intron_variant LINC-JP 11 118317476 118317476 single base substitution T C intron_variant LINC-JP 11 118318434 118318434 single base substitution A C 3_prime_UTR_variant LINC-JP 11 118318434 118318434 single base substitution A C intron_variant LINC-JP 11 118337725 118337725 single base substitution A G intron_variant LINC-JP 11 118344186 118344186 deletion of <=200bp C - frameshift_variant T771 LINC-JP 11 118344186 118344186 deletion of <=200bp C - frameshift_variant T804 LINC-JP 11 118344186 118344186 deletion of <=200bp C - intron_variant LINC-JP 11 118347579 118347579 single base substitution C T downstream_gene_variant LINC-JP 11 118347579 118347579 single base substitution C T synonymous_variant C1072C 3216C>T LINC-JP 11 118347579 118347579 single base substitution C T synonymous_variant C1105C 3315C>T LINC-JP 11 118347579 118347579 single base substitution C T synonymous_variant C150C 450C>T LINC-JP 11 118347579 118347579 single base substitution C T upstream_gene_variant LINC-JP 11 118349346 118349346 insertion of <=200bp - T downstream_gene_variant LINC-JP 11 118349346 118349346 insertion of <=200bp - T intron_variant LINC-JP 11 118349346 118349346 insertion of <=200bp - T upstream_gene_variant LINC-JP 11 118351241 118351241 single base substitution A G downstream_gene_variant LINC-JP 11 118351241 118351241 single base substitution A G intron_variant LINC-JP 11 118351241 118351241 single base substitution A G upstream_gene_variant LINC-JP 11 118353054 118353054 deletion of <=200bp C - downstream_gene_variant LINC-JP 11 118353054 118353054 deletion of <=200bp C - intron_variant LINC-JP 11 118354617 118354617 single base substitution T C intron_variant LINC-JP 11 118354942 118354942 single base substitution G A exon_variant LINC-JP 11 118354942 118354942 single base substitution G A synonymous_variant L127L 381G>A LINC-JP 11 118354942 118354942 single base substitution G A synonymous_variant L1377L 4131G>A LINC-JP 11 118354942 118354942 single base substitution G A synonymous_variant L1410L 4230G>A LINC-JP 11 118357103 118357103 single base substitution A T downstream_gene_variant LINC-JP 11 118357103 118357103 single base substitution A T intron_variant LINC-JP 11 118360680 118360680 single base substitution T C intron_variant LINC-JP 11 118361000 118361000 single base substitution G T intron_variant LINC-JP 11 118361079 118361079 single base substitution A G intron_variant LINC-JP 11 118361366 118361366 single base substitution T C intron_variant LINC-JP 11 118361916 118361916 single base substitution T G missense_variant F1530V 4588T>G LINC-JP 11 118361916 118361916 single base substitution T G missense_variant F1568V 4702T>G LINC-JP 11 118361916 118361916 single base substitution T G missense_variant F280V 838T>G LINC-JP 11 118368849 118368849 single base substitution C A intron_variant LINC-JP 11 118368849 118368849 single base substitution C A upstream_gene_variant LINC-JP 11 118373416 118373416 single base substitution A G exon_variant LINC-JP 11 118373416 118373416 single base substitution A G missense_variant Q2229R 6686A>G LINC-JP 11 118373416 118373416 single base substitution A G missense_variant Q2267R 6800A>G LINC-JP 11 118373416 118373416 single base substitution A G missense_variant Q2270R 6809A>G LINC-JP 11 118373416 118373416 single base substitution A G upstream_gene_variant LINC-JP 11 118373709 118373709 single base substitution C G exon_variant LINC-JP 11 118373709 118373709 single base substitution C G missense_variant L2327V 6979C>G LINC-JP 11 118373709 118373709 single base substitution C G missense_variant L2365V 7093C>G LINC-JP 11 118373709 118373709 single base substitution C G missense_variant L2368V 7102C>G LINC-JP 11 118373709 118373709 single base substitution C G upstream_gene_variant LINC-JP 11 118373710 118373710 single base substitution T C exon_variant LINC-JP 11 118373710 118373710 single base substitution T C missense_variant L2327P 6980T>C LINC-JP 11 118373710 118373710 single base substitution T C missense_variant L2365P 7094T>C LINC-JP 11 118373710 118373710 single base substitution T C missense_variant L2368P 7103T>C LINC-JP 11 118373710 118373710 single base substitution T C upstream_gene_variant LINC-JP 11 118374292 118374292 single base substitution T A downstream_gene_variant LINC-JP 11 118374292 118374292 single base substitution T A missense_variant I2521N 7562T>A LINC-JP 11 118374292 118374292 single base substitution T A missense_variant I2559N 7676T>A LINC-JP 11 118374292 118374292 single base substitution T A missense_variant I2562N 7685T>A LINC-JP 11 118374292 118374292 single base substitution T A upstream_gene_variant LINC-JP 11 118375798 118375798 single base substitution A G downstream_gene_variant LINC-JP 11 118375798 118375798 single base substitution A G missense_variant N3023S 9068A>G LINC-JP 11 118375798 118375798 single base substitution A G missense_variant N3061S 9182A>G LINC-JP 11 118375798 118375798 single base substitution A G missense_variant N3064S 9191A>G LINC-JP 11 118375798 118375798 single base substitution A G upstream_gene_variant LINC-JP 11 118377101 118377101 deletion of <=200bp G - downstream_gene_variant LINC-JP 11 118377101 118377101 deletion of <=200bp G - frameshift_variant L3457 LINC-JP 11 118377101 118377101 deletion of <=200bp G - frameshift_variant L3495 LINC-JP 11 118377101 118377101 deletion of <=200bp G - frameshift_variant L3498 LINC-JP 11 118377101 118377101 deletion of <=200bp G - upstream_gene_variant LINC-JP 11 118379970 118379970 single base substitution T C downstream_gene_variant LINC-JP 11 118379970 118379970 single base substitution T C intron_variant LINC-JP 11 118379970 118379970 single base substitution T C upstream_gene_variant LINC-JP 11 118388164 118388164 single base substitution A G intron_variant LINC-JP 11 118388164 118388164 single base substitution A G upstream_gene_variant LINC-JP 11 118390366 118390366 single base substitution A C exon_variant LINC-JP 11 118390366 118390366 single base substitution A C missense_variant H3686P 11057A>C LINC-JP 11 118390366 118390366 single base substitution A C missense_variant H3724P 11171A>C LINC-JP 11 118390366 118390366 single base substitution A C missense_variant H3727P 11180A>C LINC-JP 11 118390366 118390366 single base substitution A C upstream_gene_variant LINC-JP 11 118391537 118391537 single base substitution T C exon_variant LINC-JP 11 118391537 118391537 single base substitution T C missense_variant L3776P 11327T>C LINC-JP 11 118391537 118391537 single base substitution T C missense_variant L3814P 11441T>C LINC-JP 11 118391537 118391537 single base substitution T C missense_variant L3817P 11450T>C LINC-JP 11 118401778 118401778 single base substitution G A downstream_gene_variant LIRI-JP 11 118306683 118306683 single base substitution C T upstream_gene_variant LIRI-JP 11 118307037 118307037 single base substitution C T upstream_gene_variant LIRI-JP 11 118310952 118310952 single base substitution C A intron_variant LIRI-JP 11 118313313 118313313 single base substitution A G intron_variant LIRI-JP 11 118314956 118314956 single base substitution A G intron_variant LIRI-JP 11 118318871 118318871 single base substitution G C 3_prime_UTR_variant LIRI-JP 11 118318871 118318871 single base substitution G C intron_variant LIRI-JP 11 118318928 118318928 single base substitution A G 3_prime_UTR_variant LIRI-JP 11 118318928 118318928 single base substitution A G intron_variant LIRI-JP 11 118319662 118319662 single base substitution A G 3_prime_UTR_variant LIRI-JP 11 118319662 118319662 single base substitution A G intron_variant LIRI-JP 11 118320478 118320478 single base substitution T G 3_prime_UTR_variant LIRI-JP 11 118320478 118320478 single base substitution T G intron_variant LIRI-JP 11 118321881 118321881 single base substitution A G downstream_gene_variant LIRI-JP 11 118321881 118321881 single base substitution A G intron_variant LIRI-JP 11 118322724 118322724 single base substitution A T downstream_gene_variant LIRI-JP 11 118322724 118322724 single base substitution A T intron_variant LIRI-JP 11 118325636 118325636 single base substitution T G downstream_gene_variant LIRI-JP 11 118325636 118325636 single base substitution T G intron_variant LIRI-JP 11 118331812 118331812 single base substitution T C intron_variant LIRI-JP 11 118332064 118332064 single base substitution A G intron_variant LIRI-JP 11 118338072 118338072 single base substitution A C intron_variant LIRI-JP 11 118339382 118339382 single base substitution A G intron_variant LIRI-JP 11 118341633 118341633 single base substitution A T intron_variant LIRI-JP 11 118341746 118341746 single base substitution T C intron_variant LIRI-JP 11 118342410 118342410 single base substitution C G intron_variant LIRI-JP 11 118342410 118342410 single base substitution C G missense_variant P179R 536C>G LIRI-JP 11 118342410 118342410 single base substitution C G missense_variant P212R 635C>G LIRI-JP 11 118344473 118344473 single base substitution A G intron_variant LIRI-JP 11 118344473 118344473 single base substitution A G missense_variant S867G 2599A>G LIRI-JP 11 118344473 118344473 single base substitution A G missense_variant S900G 2698A>G LIRI-JP 11 118347816 118347816 single base substitution G T downstream_gene_variant LIRI-JP 11 118347816 118347816 single base substitution G T intron_variant LIRI-JP 11 118347816 118347816 single base substitution G T upstream_gene_variant LIRI-JP 11 118348998 118348998 single base substitution A G downstream_gene_variant LIRI-JP 11 118348998 118348998 single base substitution A G intron_variant LIRI-JP 11 118348998 118348998 single base substitution A G upstream_gene_variant LIRI-JP 11 118349274 118349274 single base substitution G A downstream_gene_variant LIRI-JP 11 118349274 118349274 single base substitution G A intron_variant LIRI-JP 11 118349274 118349274 single base substitution G A upstream_gene_variant LIRI-JP 11 118349826 118349826 single base substitution C T downstream_gene_variant LIRI-JP 11 118349826 118349826 single base substitution C T intron_variant LIRI-JP 11 118349826 118349826 single base substitution C T upstream_gene_variant LIRI-JP 11 118351023 118351023 single base substitution T C downstream_gene_variant LIRI-JP 11 118351023 118351023 single base substitution T C intron_variant LIRI-JP 11 118351023 118351023 single base substitution T C upstream_gene_variant LIRI-JP 11 118356284 118356284 single base substitution C T downstream_gene_variant LIRI-JP 11 118356284 118356284 single base substitution C T intron_variant LIRI-JP 11 118357294 118357294 single base substitution A G downstream_gene_variant LIRI-JP 11 118357294 118357294 single base substitution A G intron_variant LIRI-JP 11 118357525 118357525 single base substitution C G downstream_gene_variant LIRI-JP 11 118357525 118357525 single base substitution C G intron_variant LIRI-JP 11 118357902 118357902 single base substitution A G downstream_gene_variant LIRI-JP 11 118357902 118357902 single base substitution A G intron_variant LIRI-JP 11 118358526 118358526 single base substitution C A downstream_gene_variant LIRI-JP 11 118358526 118358526 single base substitution C A intron_variant LIRI-JP 11 118360619 118360619 single base substitution A G intron_variant LIRI-JP 11 118360816 118360816 single base substitution C G intron_variant LIRI-JP 11 118363064 118363064 single base substitution G T downstream_gene_variant LIRI-JP 11 118363064 118363064 single base substitution G T intron_variant LIRI-JP 11 118364838 118364838 single base substitution C T downstream_gene_variant LIRI-JP 11 118364838 118364838 single base substitution C T intron_variant LIRI-JP 11 118365807 118365807 single base substitution C A downstream_gene_variant LIRI-JP 11 118365807 118365807 single base substitution C A intron_variant LIRI-JP 11 118368071 118368071 single base substitution T C intron_variant LIRI-JP 11 118368071 118368071 single base substitution T C upstream_gene_variant LIRI-JP 11 118368453 118368453 single base substitution A G intron_variant LIRI-JP 11 118368453 118368453 single base substitution A G upstream_gene_variant LIRI-JP 11 118369542 118369542 single base substitution A G intron_variant LIRI-JP 11 118369542 118369542 single base substitution A G upstream_gene_variant LIRI-JP 11 118370138 118370138 single base substitution A G splice_region_variant LIRI-JP 11 118370138 118370138 single base substitution A G upstream_gene_variant LIRI-JP 11 118370261 118370261 single base substitution G A intron_variant LIRI-JP 11 118370261 118370261 single base substitution G A upstream_gene_variant LIRI-JP 11 118371188 118371188 single base substitution A G intron_variant LIRI-JP 11 118371188 118371188 single base substitution A G upstream_gene_variant LIRI-JP 11 118371227 118371227 single base substitution C T intron_variant LIRI-JP 11 118371227 118371227 single base substitution C T upstream_gene_variant LIRI-JP 11 118373828 118373828 single base substitution A G exon_variant LIRI-JP 11 118373828 118373828 single base substitution A G synonymous_variant L2366L 7098A>G LIRI-JP 11 118373828 118373828 single base substitution A G synonymous_variant L2404L 7212A>G LIRI-JP 11 118373828 118373828 single base substitution A G synonymous_variant L2407L 7221A>G LIRI-JP 11 118373828 118373828 single base substitution A G upstream_gene_variant LIRI-JP 11 118374368 118374368 single base substitution A G downstream_gene_variant LIRI-JP 11 118374368 118374368 single base substitution A G synonymous_variant Q2546Q 7638A>G LIRI-JP 11 118374368 118374368 single base substitution A G synonymous_variant Q2584Q 7752A>G LIRI-JP 11 118374368 118374368 single base substitution A G synonymous_variant Q2587Q 7761A>G LIRI-JP 11 118374368 118374368 single base substitution A G upstream_gene_variant LIRI-JP 11 118375199 118375199 insertion of <=200bp - G downstream_gene_variant LIRI-JP 11 118375199 118375199 insertion of <=200bp - G frameshift_variant Q2823Q? LIRI-JP 11 118375199 118375199 insertion of <=200bp - G frameshift_variant Q2861Q? LIRI-JP 11 118375199 118375199 insertion of <=200bp - G frameshift_variant Q2864Q? LIRI-JP 11 118375199 118375199 insertion of <=200bp - G upstream_gene_variant LIRI-JP 11 118377319 118377328 deletion of <=200bp ACATTCCAGA - downstream_gene_variant LIRI-JP 11 118377319 118377328 deletion of <=200bp ACATTCCAGA - exon_variant LIRI-JP 11 118377319 118377328 deletion of <=200bp ACATTCCAGA - frameshift_variant HIPD3530 LIRI-JP 11 118377319 118377328 deletion of <=200bp ACATTCCAGA - frameshift_variant HIPD3568 LIRI-JP 11 118377319 118377328 deletion of <=200bp ACATTCCAGA - frameshift_variant HIPD3571 LIRI-JP 11 118377319 118377328 deletion of <=200bp ACATTCCAGA - upstream_gene_variant LIRI-JP 11 118377893 118377893 single base substitution G A downstream_gene_variant LIRI-JP 11 118377893 118377893 single base substitution G A intron_variant LIRI-JP 11 118377893 118377893 single base substitution G A upstream_gene_variant LIRI-JP 11 118378214 118378214 single base substitution C A downstream_gene_variant LIRI-JP 11 118378214 118378214 single base substitution C A intron_variant LIRI-JP 11 118378214 118378214 single base substitution C A upstream_gene_variant LIRI-JP 11 118378539 118378539 single base substitution G A downstream_gene_variant LIRI-JP 11 118378539 118378539 single base substitution G A intron_variant LIRI-JP 11 118378539 118378539 single base substitution G A upstream_gene_variant LIRI-JP 11 118382861 118382861 single base substitution A G downstream_gene_variant LIRI-JP 11 118382861 118382861 single base substitution A G exon_variant LIRI-JP 11 118382861 118382861 single base substitution A G intron_variant LIRI-JP 11 118383165 118383165 single base substitution C T downstream_gene_variant LIRI-JP 11 118383165 118383165 single base substitution C T intron_variant LIRI-JP 11 118383442 118383442 single base substitution A G downstream_gene_variant LIRI-JP 11 118383442 118383442 single base substitution A G intron_variant LIRI-JP 11 118387627 118387627 single base substitution A G downstream_gene_variant LIRI-JP 11 118387627 118387627 single base substitution A G intron_variant LIRI-JP 11 118387627 118387627 single base substitution A G upstream_gene_variant LIRI-JP 11 118389132 118389132 single base substitution A G intron_variant LIRI-JP 11 118389132 118389132 single base substitution A G upstream_gene_variant LIRI-JP 11 118391717 118391717 single base substitution A G exon_variant LIRI-JP 11 118391717 118391717 single base substitution A G intron_variant LIRI-JP 11 118392197 118392197 single base substitution C A intron_variant LIRI-JP 11 118394006 118394006 single base substitution C T 3_prime_UTR_variant LIRI-JP 11 118394006 118394006 single base substitution C T downstream_gene_variant LIRI-JP 11 118396832 118396832 single base substitution T G 3_prime_UTR_variant LIRI-JP 11 118396832 118396832 single base substitution T G downstream_gene_variant LIRI-JP 11 118397822 118397822 single base substitution A G downstream_gene_variant LIRI-JP 11 118398788 118398788 single base substitution G T downstream_gene_variant LIRI-JP 11 118400631 118400631 single base substitution G A downstream_gene_variant LUSC-KR 11 118302668 118302668 single base substitution A C upstream_gene_variant LUSC-KR 11 118303882 118303882 single base substitution A G upstream_gene_variant LUSC-KR 11 118308962 118308962 single base substitution G A intron_variant LUSC-KR 11 118309617 118309617 single base substitution A G intron_variant LUSC-KR 11 118313565 118313565 single base substitution C G intron_variant LUSC-KR 11 118313801 118313801 single base substitution C T intron_variant LUSC-KR 11 118320319 118320319 single base substitution G A 3_prime_UTR_variant LUSC-KR 11 118320319 118320319 single base substitution G A intron_variant LUSC-KR 11 118322727 118322727 single base substitution A T downstream_gene_variant LUSC-KR 11 118322727 118322727 single base substitution A T intron_variant LUSC-KR 11 118353054 118353054 single base substitution C T downstream_gene_variant LUSC-KR 11 118353054 118353054 single base substitution C T intron_variant LUSC-KR 11 118353491 118353491 single base substitution G A downstream_gene_variant LUSC-KR 11 118353491 118353491 single base substitution G A intron_variant LUSC-KR 11 118354106 118354106 single base substitution G T intron_variant LUSC-KR 11 118355698 118355698 single base substitution A T downstream_gene_variant LUSC-KR 11 118355698 118355698 single base substitution A T intron_variant LUSC-KR 11 118355698 118355698 single base substitution A T splice_region_variant LUSC-KR 11 118364735 118364735 single base substitution A T downstream_gene_variant LUSC-KR 11 118364735 118364735 single base substitution A T intron_variant LUSC-KR 11 118369582 118369582 single base substitution C G intron_variant LUSC-KR 11 118369582 118369582 single base substitution C G upstream_gene_variant LUSC-KR 11 118370052 118370052 single base substitution G A missense_variant R1958K 5873G>A LUSC-KR 11 118370052 118370052 single base substitution G A missense_variant R1996K 5987G>A LUSC-KR 11 118370052 118370052 single base substitution G A missense_variant R1999K 5996G>A LUSC-KR 11 118370052 118370052 single base substitution G A upstream_gene_variant LUSC-KR 11 118371684 118371684 single base substitution C T exon_variant LUSC-KR 11 118371684 118371684 single base substitution C T intron_variant LUSC-KR 11 118376646 118376646 single base substitution G A downstream_gene_variant LUSC-KR 11 118376646 118376646 single base substitution G A missense_variant V3306I 9916G>A LUSC-KR 11 118376646 118376646 single base substitution G A missense_variant V3344I 10030G>A LUSC-KR 11 118376646 118376646 single base substitution G A missense_variant V3347I 10039G>A LUSC-KR 11 118376646 118376646 single base substitution G A upstream_gene_variant LUSC-KR 11 118382923 118382923 single base substitution A G downstream_gene_variant LUSC-KR 11 118382923 118382923 single base substitution A G exon_variant LUSC-KR 11 118382923 118382923 single base substitution A G intron_variant LUSC-KR 11 118390309 118390309 single base substitution C T exon_variant LUSC-KR 11 118390309 118390309 single base substitution C T intron_variant LUSC-KR 11 118390309 118390309 single base substitution C T upstream_gene_variant LUSC-KR 11 118391297 118391297 single base substitution C T exon_variant LUSC-KR 11 118391297 118391297 single base substitution C T intron_variant LUSC-KR 11 118391375 118391375 single base substitution A G exon_variant LUSC-KR 11 118391375 118391375 single base substitution A G intron_variant LUSC-US 11 118344238 118344238 single base substitution C A intron_variant LUSC-US 11 118344238 118344238 single base substitution C A synonymous_variant A788A 2364C>A LUSC-US 11 118344238 118344238 single base substitution C A synonymous_variant A821A 2463C>A LUSC-US 11 118352801 118352801 single base substitution G T downstream_gene_variant LUSC-US 11 118352801 118352801 single base substitution G T exon_variant LUSC-US 11 118352801 118352801 single base substitution G T stop_gained E1336* 4006G>T LUSC-US 11 118352801 118352801 single base substitution G T stop_gained E1369* 4105G>T LUSC-US 11 118352801 118352801 single base substitution G T stop_gained E86* 256G>T LUSC-US 11 118368740 118368740 single base substitution C A missense_variant D1877E 5631C>A LUSC-US 11 118368740 118368740 single base substitution C A missense_variant D1915E 5745C>A LUSC-US 11 118368740 118368740 single base substitution C A missense_variant D1918E 5754C>A LUSC-US 11 118368740 118368740 single base substitution C A upstream_gene_variant LUSC-US 11 118372451 118372451 single base substitution T A exon_variant LUSC-US 11 118372451 118372451 single base substitution T A synonymous_variant P2087P 6261T>A LUSC-US 11 118372451 118372451 single base substitution T A synonymous_variant P2125P 6375T>A LUSC-US 11 118372451 118372451 single base substitution T A synonymous_variant P2128P 6384T>A LUSC-US 11 118372451 118372451 single base substitution T A upstream_gene_variant LUSC-US 11 118374454 118374454 single base substitution A G downstream_gene_variant LUSC-US 11 118374454 118374454 single base substitution A G missense_variant K2575R 7724A>G LUSC-US 11 118374454 118374454 single base substitution A G missense_variant K2613R 7838A>G LUSC-US 11 118374454 118374454 single base substitution A G missense_variant K2616R 7847A>G LUSC-US 11 118374454 118374454 single base substitution A G upstream_gene_variant LUSC-US 11 118374740 118374740 single base substitution G A downstream_gene_variant LUSC-US 11 118374740 118374740 single base substitution G A synonymous_variant Q2670Q 8010G>A LUSC-US 11 118374740 118374740 single base substitution G A synonymous_variant Q2708Q 8124G>A LUSC-US 11 118374740 118374740 single base substitution G A synonymous_variant Q2711Q 8133G>A LUSC-US 11 118374740 118374740 single base substitution G A upstream_gene_variant LUSC-US 11 118376003 118376003 single base substitution C G downstream_gene_variant LUSC-US 11 118376003 118376003 single base substitution C G synonymous_variant L3091L 9273C>G LUSC-US 11 118376003 118376003 single base substitution C G synonymous_variant L3129L 9387C>G LUSC-US 11 118376003 118376003 single base substitution C G synonymous_variant L3132L 9396C>G LUSC-US 11 118376003 118376003 single base substitution C G upstream_gene_variant LUSC-US 11 118376731 118376731 single base substitution C G downstream_gene_variant LUSC-US 11 118376731 118376731 single base substitution C G missense_variant T3334S 10001C>G LUSC-US 11 118376731 118376731 single base substitution C G missense_variant T3372S 10115C>G LUSC-US 11 118376731 118376731 single base substitution C G missense_variant T3375S 10124C>G LUSC-US 11 118376731 118376731 single base substitution C G upstream_gene_variant LUSC-US 11 118376855 118376855 single base substitution G A downstream_gene_variant LUSC-US 11 118376855 118376855 single base substitution G A synonymous_variant Q3375Q 10125G>A LUSC-US 11 118376855 118376855 single base substitution G A synonymous_variant Q3413Q 10239G>A LUSC-US 11 118376855 118376855 single base substitution G A synonymous_variant Q3416Q 10248G>A LUSC-US 11 118376855 118376855 single base substitution G A upstream_gene_variant LUSC-US 11 118390362 118390362 single base substitution C G exon_variant LUSC-US 11 118390362 118390362 single base substitution C G missense_variant L3685V 11053C>G LUSC-US 11 118390362 118390362 single base substitution C G missense_variant L3723V 11167C>G LUSC-US 11 118390362 118390362 single base substitution C G missense_variant L3726V 11176C>G LUSC-US 11 118390362 118390362 single base substitution C G upstream_gene_variant LUSC-US 11 118398237 118398237 single base substitution C T downstream_gene_variant MALY-DE 11 118302360 118302360 deletion of <=200bp A - upstream_gene_variant MALY-DE 11 118305886 118305886 single base substitution A G upstream_gene_variant MALY-DE 11 118306341 118306341 single base substitution G T upstream_gene_variant MALY-DE 11 118306345 118306345 single base substitution G C upstream_gene_variant MALY-DE 11 118308450 118308450 single base substitution C G intron_variant MALY-DE 11 118313802 118313802 single base substitution A G intron_variant MALY-DE 11 118315775 118315775 insertion of <=200bp - T intron_variant MALY-DE 11 118322239 118322239 single base substitution A T downstream_gene_variant MALY-DE 11 118322239 118322239 single base substitution A T intron_variant MALY-DE 11 118326385 118326385 single base substitution A T downstream_gene_variant MALY-DE 11 118326385 118326385 single base substitution A T intron_variant MALY-DE 11 118345510 118345510 single base substitution T C downstream_gene_variant MALY-DE 11 118345510 118345510 single base substitution T C intron_variant MALY-DE 11 118347863 118347863 single base substitution G C downstream_gene_variant MALY-DE 11 118347863 118347863 single base substitution G C intron_variant MALY-DE 11 118347863 118347863 single base substitution G C upstream_gene_variant MALY-DE 11 118349530 118349530 insertion of <=200bp - TGAT downstream_gene_variant MALY-DE 11 118349530 118349530 insertion of <=200bp - TGAT intron_variant MALY-DE 11 118349530 118349530 insertion of <=200bp - TGAT upstream_gene_variant MALY-DE 11 118349533 118349534 deletion of <=200bp TG - downstream_gene_variant MALY-DE 11 118349533 118349534 deletion of <=200bp TG - intron_variant MALY-DE 11 118349533 118349534 deletion of <=200bp TG - upstream_gene_variant MALY-DE 11 118358771 118358771 single base substitution T C downstream_gene_variant MALY-DE 11 118358771 118358771 single base substitution T C intron_variant MALY-DE 11 118359610 118359610 single base substitution T A downstream_gene_variant MALY-DE 11 118359610 118359610 single base substitution T A intron_variant MALY-DE 11 118366880 118366880 single base substitution T G downstream_gene_variant MALY-DE 11 118366880 118366880 single base substitution T G intron_variant MALY-DE 11 118366880 118366880 single base substitution T G upstream_gene_variant MALY-DE 11 118373699 118373699 single base substitution T G exon_variant MALY-DE 11 118373699 118373699 single base substitution T G synonymous_variant S2323S 6969T>G MALY-DE 11 118373699 118373699 single base substitution T G synonymous_variant S2361S 7083T>G MALY-DE 11 118373699 118373699 single base substitution T G synonymous_variant S2364S 7092T>G MALY-DE 11 118373699 118373699 single base substitution T G upstream_gene_variant MALY-DE 11 118375395 118375395 single base substitution C A downstream_gene_variant MALY-DE 11 118375395 118375395 single base substitution C A missense_variant L2889I 8665C>A MALY-DE 11 118375395 118375395 single base substitution C A missense_variant L2927I 8779C>A MALY-DE 11 118375395 118375395 single base substitution C A missense_variant L2930I 8788C>A MALY-DE 11 118375395 118375395 single base substitution C A upstream_gene_variant MALY-DE 11 118391374 118391374 single base substitution A G exon_variant MALY-DE 11 118391374 118391374 single base substitution A G intron_variant MALY-DE 11 118392813 118392813 single base substitution T C exon_variant MALY-DE 11 118392813 118392813 single base substitution T C missense_variant F3908L 11722T>C MALY-DE 11 118392813 118392813 single base substitution T C missense_variant F3946L 11836T>C MALY-DE 11 118392813 118392813 single base substitution T C missense_variant F3949L 11845T>C MELA-AU 11 118302230 118302230 single base substitution C T upstream_gene_variant MELA-AU 11 118302369 118302369 single base substitution A C upstream_gene_variant MELA-AU 11 118302474 118302474 single base substitution A T upstream_gene_variant MELA-AU 11 118302559 118302559 single base substitution A C upstream_gene_variant MELA-AU 11 118302717 118302717 single base substitution C T upstream_gene_variant MELA-AU 11 118302790 118302790 single base substitution C T upstream_gene_variant MELA-AU 11 118303261 118303261 single base substitution C T upstream_gene_variant MELA-AU 11 118303976 118303976 single base substitution G A upstream_gene_variant MELA-AU 11 118304543 118304543 single base substitution G A upstream_gene_variant MELA-AU 11 118304786 118304786 single base substitution A G upstream_gene_variant MELA-AU 11 118304849 118304849 single base substitution G A upstream_gene_variant MELA-AU 11 118304935 118304935 single base substitution C T upstream_gene_variant MELA-AU 11 118305019 118305019 single base substitution C T upstream_gene_variant MELA-AU 11 118305857 118305857 single base substitution G A upstream_gene_variant MELA-AU 11 118306130 118306130 single base substitution G A upstream_gene_variant MELA-AU 11 118306513 118306513 single base substitution C T upstream_gene_variant MELA-AU 11 118306759 118306759 single base substitution G A upstream_gene_variant MELA-AU 11 118307038 118307038 single base substitution G A upstream_gene_variant MELA-AU 11 118307052 118307052 single base substitution G A upstream_gene_variant MELA-AU 11 118307178 118307178 single base substitution C T upstream_gene_variant MELA-AU 11 118307717 118307717 single base substitution C T intron_variant MELA-AU 11 118307745 118307745 single base substitution C T intron_variant MELA-AU 11 118311059 118311059 single base substitution T G intron_variant MELA-AU 11 118312494 118312494 single base substitution T C intron_variant MELA-AU 11 118312628 118312628 single base substitution C T intron_variant MELA-AU 11 118312877 118312877 single base substitution C T intron_variant MELA-AU 11 118313415 118313415 single base substitution A G intron_variant MELA-AU 11 118314680 118314680 single base substitution T C intron_variant MELA-AU 11 118314914 118314914 single base substitution C G intron_variant MELA-AU 11 118315241 118315241 single base substitution C T intron_variant MELA-AU 11 118315610 118315610 single base substitution C T intron_variant MELA-AU 11 118317400 118317400 single base substitution G A intron_variant MELA-AU 11 118317436 118317436 single base substitution C T intron_variant MELA-AU 11 118317898 118317898 single base substitution A G intron_variant MELA-AU 11 118318158 118318158 single base substitution A G intron_variant MELA-AU 11 118319203 118319203 single base substitution C T 3_prime_UTR_variant MELA-AU 11 118319203 118319203 single base substitution C T intron_variant MELA-AU 11 118321967 118321967 single base substitution C T downstream_gene_variant MELA-AU 11 118321967 118321967 single base substitution C T intron_variant MELA-AU 11 118323264 118323264 single base substitution C T downstream_gene_variant MELA-AU 11 118323264 118323264 single base substitution C T intron_variant MELA-AU 11 118323563 118323563 single base substitution G T downstream_gene_variant MELA-AU 11 118323563 118323563 single base substitution G T intron_variant MELA-AU 11 118324196 118324196 single base substitution C T downstream_gene_variant MELA-AU 11 118324196 118324196 single base substitution C T intron_variant MELA-AU 11 118326153 118326153 single base substitution G A downstream_gene_variant MELA-AU 11 118326153 118326153 single base substitution G A intron_variant MELA-AU 11 118326361 118326361 single base substitution C T downstream_gene_variant MELA-AU 11 118326361 118326361 single base substitution C T intron_variant MELA-AU 11 118326415 118326415 single base substitution T G downstream_gene_variant MELA-AU 11 118326415 118326415 single base substitution T G intron_variant MELA-AU 11 118327911 118327911 single base substitution C T intron_variant MELA-AU 11 118327997 118327997 single base substitution T C intron_variant MELA-AU 11 118328296 118328296 single base substitution C T intron_variant MELA-AU 11 118328463 118328463 single base substitution C T intron_variant MELA-AU 11 118328489 118328489 single base substitution C T intron_variant MELA-AU 11 118328742 118328742 single base substitution C T intron_variant MELA-AU 11 118328954 118328954 single base substitution C T intron_variant MELA-AU 11 118329828 118329828 single base substitution C T intron_variant MELA-AU 11 118330138 118330138 single base substitution C T intron_variant MELA-AU 11 118330524 118330525 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 11 118330635 118330635 single base substitution C T intron_variant MELA-AU 11 118331888 118331888 single base substitution C T intron_variant MELA-AU 11 118332432 118332432 single base substitution T A intron_variant MELA-AU 11 118332471 118332471 single base substitution T G intron_variant MELA-AU 11 118333852 118333852 deletion of <=200bp A - intron_variant MELA-AU 11 118334297 118334297 single base substitution C T intron_variant MELA-AU 11 118334971 118334971 single base substitution C T intron_variant MELA-AU 11 118335164 118335164 single base substitution C T intron_variant MELA-AU 11 118336672 118336672 single base substitution C T intron_variant MELA-AU 11 118338227 118338227 single base substitution C T intron_variant MELA-AU 11 118339392 118339392 single base substitution T A intron_variant MELA-AU 11 118339395 118339395 single base substitution C T intron_variant MELA-AU 11 118339563 118339563 single base substitution C T splice_region_variant MELA-AU 11 118340760 118340760 single base substitution C T intron_variant MELA-AU 11 118341134 118341134 single base substitution C T intron_variant MELA-AU 11 118341609 118341609 single base substitution C T intron_variant MELA-AU 11 118342427 118342427 single base substitution C T intron_variant MELA-AU 11 118342427 118342427 single base substitution C T stop_gained R185* 553C>T MELA-AU 11 118342427 118342427 single base substitution C T stop_gained R218* 652C>T MELA-AU 11 118342465 118342465 single base substitution C T intron_variant MELA-AU 11 118342465 118342465 single base substitution C T synonymous_variant S197S 591C>T MELA-AU 11 118342465 118342465 single base substitution C T synonymous_variant S230S 690C>T MELA-AU 11 118343121 118343121 single base substitution C T intron_variant MELA-AU 11 118343121 118343121 single base substitution C T missense_variant A416V 1247C>T MELA-AU 11 118343121 118343121 single base substitution C T missense_variant A449V 1346C>T MELA-AU 11 118343564 118343564 single base substitution C T intron_variant MELA-AU 11 118343564 118343564 single base substitution C T missense_variant P564S 1690C>T MELA-AU 11 118343564 118343564 single base substitution C T missense_variant P597S 1789C>T MELA-AU 11 118343658 118343658 single base substitution C T intron_variant MELA-AU 11 118343658 118343658 single base substitution C T missense_variant P595L 1784C>T MELA-AU 11 118343658 118343658 single base substitution C T missense_variant P628L 1883C>T MELA-AU 11 118344438 118344438 single base substitution C T intron_variant MELA-AU 11 118344438 118344438 single base substitution C T missense_variant P855L 2564C>T MELA-AU 11 118344438 118344438 single base substitution C T missense_variant P888L 2663C>T MELA-AU 11 118344523 118344523 single base substitution G A intron_variant MELA-AU 11 118344523 118344523 single base substitution G A synonymous_variant E883E 2649G>A MELA-AU 11 118344523 118344523 single base substitution G A synonymous_variant E916E 2748G>A MELA-AU 11 118344609 118344609 single base substitution C T intron_variant MELA-AU 11 118344609 118344609 single base substitution C T missense_variant S912F 2735C>T MELA-AU 11 118344609 118344609 single base substitution C T missense_variant S945F 2834C>T MELA-AU 11 118345802 118345802 single base substitution C T downstream_gene_variant MELA-AU 11 118345802 118345802 single base substitution C T intron_variant MELA-AU 11 118346035 118346035 single base substitution C T downstream_gene_variant MELA-AU 11 118346035 118346035 single base substitution C T intron_variant MELA-AU 11 118347243 118347243 single base substitution G A downstream_gene_variant MELA-AU 11 118347243 118347243 single base substitution G A intron_variant MELA-AU 11 118348253 118348253 single base substitution C T downstream_gene_variant MELA-AU 11 118348253 118348253 single base substitution C T intron_variant MELA-AU 11 118348253 118348253 single base substitution C T upstream_gene_variant MELA-AU 11 118348780 118348780 single base substitution C T downstream_gene_variant MELA-AU 11 118348780 118348780 single base substitution C T missense_variant P1145S 3433C>T MELA-AU 11 118348780 118348780 single base substitution C T missense_variant P1178S 3532C>T MELA-AU 11 118348780 118348780 single base substitution C T missense_variant P223S 667C>T MELA-AU 11 118348780 118348780 single base substitution C T upstream_gene_variant MELA-AU 11 118348802 118348802 single base substitution C T downstream_gene_variant MELA-AU 11 118348802 118348802 single base substitution C T missense_variant S1152L 3455C>T MELA-AU 11 118348802 118348802 single base substitution C T missense_variant S1185L 3554C>T MELA-AU 11 118348802 118348802 single base substitution C T missense_variant S230L 689C>T MELA-AU 11 118348802 118348802 single base substitution C T upstream_gene_variant MELA-AU 11 118348876 118348876 single base substitution C T downstream_gene_variant MELA-AU 11 118348876 118348876 single base substitution C T missense_variant P1177S 3529C>T MELA-AU 11 118348876 118348876 single base substitution C T missense_variant P1210S 3628C>T MELA-AU 11 118348876 118348876 single base substitution C T missense_variant P255S 763C>T MELA-AU 11 118348876 118348876 single base substitution C T upstream_gene_variant MELA-AU 11 118349927 118349927 single base substitution T C downstream_gene_variant MELA-AU 11 118349927 118349927 single base substitution T C intron_variant MELA-AU 11 118349927 118349927 single base substitution T C upstream_gene_variant MELA-AU 11 118350223 118350223 single base substitution A G downstream_gene_variant MELA-AU 11 118350223 118350223 single base substitution A G intron_variant MELA-AU 11 118350223 118350223 single base substitution A G upstream_gene_variant MELA-AU 11 118351120 118351120 single base substitution C T downstream_gene_variant MELA-AU 11 118351120 118351120 single base substitution C T intron_variant MELA-AU 11 118351120 118351120 single base substitution C T upstream_gene_variant MELA-AU 11 118351181 118351181 single base substitution C T downstream_gene_variant MELA-AU 11 118351181 118351181 single base substitution C T intron_variant MELA-AU 11 118351181 118351181 single base substitution C T upstream_gene_variant MELA-AU 11 118352310 118352310 single base substitution C T downstream_gene_variant MELA-AU 11 118352310 118352310 single base substitution C T intron_variant MELA-AU 11 118352310 118352310 single base substitution C T upstream_gene_variant MELA-AU 11 118352311 118352311 single base substitution C T downstream_gene_variant MELA-AU 11 118352311 118352311 single base substitution C T intron_variant MELA-AU 11 118352311 118352311 single base substitution C T upstream_gene_variant MELA-AU 11 118352647 118352647 single base substitution A C downstream_gene_variant MELA-AU 11 118352647 118352647 single base substitution A C missense_variant K1284N 3852A>C MELA-AU 11 118352647 118352647 single base substitution A C missense_variant K1317N 3951A>C MELA-AU 11 118352647 118352647 single base substitution A C missense_variant K34N 102A>C MELA-AU 11 118352647 118352647 single base substitution A C upstream_gene_variant MELA-AU 11 118352747 118352747 single base substitution G T downstream_gene_variant MELA-AU 11 118352747 118352747 single base substitution G T exon_variant MELA-AU 11 118352747 118352747 single base substitution G T stop_gained E1318* 3952G>T MELA-AU 11 118352747 118352747 single base substitution G T stop_gained E1351* 4051G>T MELA-AU 11 118352747 118352747 single base substitution G T stop_gained E68* 202G>T MELA-AU 11 118352920 118352920 single base substitution A G downstream_gene_variant MELA-AU 11 118352920 118352920 single base substitution A G intron_variant MELA-AU 11 118353804 118353804 single base substitution C T downstream_gene_variant MELA-AU 11 118353804 118353804 single base substitution C T intron_variant MELA-AU 11 118354239 118354239 single base substitution C T intron_variant MELA-AU 11 118355145 118355145 single base substitution G A downstream_gene_variant MELA-AU 11 118355145 118355145 single base substitution G A intron_variant MELA-AU 11 118355303 118355303 single base substitution C T downstream_gene_variant MELA-AU 11 118355303 118355303 single base substitution C T intron_variant MELA-AU 11 118355609 118355609 single base substitution G A downstream_gene_variant MELA-AU 11 118355609 118355609 single base substitution G A intron_variant MELA-AU 11 118355609 118355609 single base substitution G A missense_variant M1417I 4251G>A MELA-AU 11 118356379 118356379 single base substitution G A downstream_gene_variant MELA-AU 11 118356379 118356379 single base substitution G A intron_variant MELA-AU 11 118356792 118356792 single base substitution C T downstream_gene_variant MELA-AU 11 118356792 118356792 single base substitution C T intron_variant MELA-AU 11 118360575 118360575 single base substitution C T synonymous_variant T1478T 4434C>T MELA-AU 11 118360575 118360575 single base substitution C T synonymous_variant T1516T 4548C>T MELA-AU 11 118360575 118360575 single base substitution C T synonymous_variant T228T 684C>T MELA-AU 11 118360743 118360743 single base substitution G A intron_variant MELA-AU 11 118360827 118360827 single base substitution C A intron_variant MELA-AU 11 118361077 118361077 single base substitution C T intron_variant MELA-AU 11 118361208 118361208 single base substitution C T intron_variant MELA-AU 11 118361991 118361991 single base substitution C T missense_variant R1555C 4663C>T MELA-AU 11 118361991 118361991 single base substitution C T missense_variant R1593C 4777C>T MELA-AU 11 118361991 118361991 single base substitution C T missense_variant R305C 913C>T MELA-AU 11 118362046 118362046 single base substitution T C intron_variant MELA-AU 11 118362956 118362956 single base substitution C T downstream_gene_variant MELA-AU 11 118362956 118362956 single base substitution C T intron_variant MELA-AU 11 118363473 118363473 single base substitution C T downstream_gene_variant MELA-AU 11 118363473 118363473 single base substitution C T intron_variant MELA-AU 11 118365133 118365133 single base substitution C T downstream_gene_variant MELA-AU 11 118365133 118365133 single base substitution C T intron_variant MELA-AU 11 118365450 118365450 single base substitution C T downstream_gene_variant MELA-AU 11 118365450 118365450 single base substitution C T synonymous_variant S1736S 5208C>T MELA-AU 11 118365450 118365450 single base substitution C T synonymous_variant S1774S 5322C>T MELA-AU 11 118365450 118365450 single base substitution C T synonymous_variant S1777S 5331C>T MELA-AU 11 118365905 118365905 single base substitution C T downstream_gene_variant MELA-AU 11 118365905 118365905 single base substitution C T intron_variant MELA-AU 11 118365959 118365959 single base substitution C T downstream_gene_variant MELA-AU 11 118365959 118365959 single base substitution C T intron_variant MELA-AU 11 118367393 118367393 deletion of <=200bp T - downstream_gene_variant MELA-AU 11 118367393 118367393 deletion of <=200bp T - intron_variant MELA-AU 11 118367393 118367393 deletion of <=200bp T - upstream_gene_variant MELA-AU 11 118368478 118368478 single base substitution G A intron_variant MELA-AU 11 118368478 118368478 single base substitution G A upstream_gene_variant MELA-AU 11 118368576 118368576 single base substitution G A intron_variant MELA-AU 11 118368576 118368576 single base substitution G A upstream_gene_variant MELA-AU 11 118368620 118368620 single base substitution T G intron_variant MELA-AU 11 118368620 118368620 single base substitution T G upstream_gene_variant MELA-AU 11 118368764 118368764 single base substitution G A missense_variant M1885I 5655G>A MELA-AU 11 118368764 118368764 single base substitution G A missense_variant M1923I 5769G>A MELA-AU 11 118368764 118368764 single base substitution G A missense_variant M1926I 5778G>A MELA-AU 11 118368764 118368764 single base substitution G A upstream_gene_variant MELA-AU 11 118369357 118369357 single base substitution C T intron_variant MELA-AU 11 118369357 118369357 single base substitution C T upstream_gene_variant MELA-AU 11 118370248 118370248 single base substitution C T intron_variant MELA-AU 11 118370248 118370248 single base substitution C T upstream_gene_variant MELA-AU 11 118370715 118370715 single base substitution C T intron_variant MELA-AU 11 118370715 118370715 single base substitution C T upstream_gene_variant MELA-AU 11 118370903 118370903 single base substitution C T intron_variant MELA-AU 11 118370903 118370903 single base substitution C T upstream_gene_variant MELA-AU 11 118372850 118372850 single base substitution C T intron_variant MELA-AU 11 118372850 118372850 single base substitution C T upstream_gene_variant MELA-AU 11 118372882 118372882 single base substitution C T intron_variant MELA-AU 11 118372882 118372882 single base substitution C T upstream_gene_variant MELA-AU 11 118374290 118374290 single base substitution A G downstream_gene_variant MELA-AU 11 118374290 118374290 single base substitution A G synonymous_variant P2520P 7560A>G MELA-AU 11 118374290 118374290 single base substitution A G synonymous_variant P2558P 7674A>G MELA-AU 11 118374290 118374290 single base substitution A G synonymous_variant P2561P 7683A>G MELA-AU 11 118374290 118374290 single base substitution A G upstream_gene_variant MELA-AU 11 118374553 118374553 single base substitution C T downstream_gene_variant MELA-AU 11 118374553 118374553 single base substitution C T missense_variant P2608L 7823C>T MELA-AU 11 118374553 118374553 single base substitution C T missense_variant P2646L 7937C>T MELA-AU 11 118374553 118374553 single base substitution C T missense_variant P2649L 7946C>T MELA-AU 11 118374553 118374553 single base substitution C T upstream_gene_variant MELA-AU 11 118375097 118375097 single base substitution G A downstream_gene_variant MELA-AU 11 118375097 118375097 single base substitution G A synonymous_variant E2789E 8367G>A MELA-AU 11 118375097 118375097 single base substitution G A synonymous_variant E2827E 8481G>A MELA-AU 11 118375097 118375097 single base substitution G A synonymous_variant E2830E 8490G>A MELA-AU 11 118375097 118375097 single base substitution G A upstream_gene_variant MELA-AU 11 118375913 118375913 single base substitution C T downstream_gene_variant MELA-AU 11 118375913 118375913 single base substitution C T synonymous_variant T3061T 9183C>T MELA-AU 11 118375913 118375913 single base substitution C T synonymous_variant T3099T 9297C>T MELA-AU 11 118375913 118375913 single base substitution C T synonymous_variant T3102T 9306C>T MELA-AU 11 118375913 118375913 single base substitution C T upstream_gene_variant MELA-AU 11 118376107 118376107 single base substitution C T downstream_gene_variant MELA-AU 11 118376107 118376107 single base substitution C T missense_variant S3126F 9377C>T MELA-AU 11 118376107 118376107 single base substitution C T missense_variant S3164F 9491C>T MELA-AU 11 118376107 118376107 single base substitution C T missense_variant S3167F 9500C>T MELA-AU 11 118376107 118376107 single base substitution C T upstream_gene_variant MELA-AU 11 118377324 118377324 single base substitution C T downstream_gene_variant MELA-AU 11 118377324 118377324 single base substitution C T exon_variant MELA-AU 11 118377324 118377324 single base substitution C T missense_variant P3532S 10594C>T MELA-AU 11 118377324 118377324 single base substitution C T missense_variant P3570S 10708C>T MELA-AU 11 118377324 118377324 single base substitution C T missense_variant P3573S 10717C>T MELA-AU 11 118377324 118377324 single base substitution C T upstream_gene_variant MELA-AU 11 118379326 118379326 single base substitution C T downstream_gene_variant MELA-AU 11 118379326 118379326 single base substitution C T intron_variant MELA-AU 11 118379326 118379326 single base substitution C T upstream_gene_variant MELA-AU 11 118379562 118379562 single base substitution C T downstream_gene_variant MELA-AU 11 118379562 118379562 single base substitution C T intron_variant MELA-AU 11 118379562 118379562 single base substitution C T upstream_gene_variant MELA-AU 11 118380060 118380060 single base substitution C T downstream_gene_variant MELA-AU 11 118380060 118380060 single base substitution C T intron_variant MELA-AU 11 118380060 118380060 single base substitution C T upstream_gene_variant MELA-AU 11 118380307 118380307 single base substitution C T downstream_gene_variant MELA-AU 11 118380307 118380307 single base substitution C T intron_variant MELA-AU 11 118380307 118380307 single base substitution C T upstream_gene_variant MELA-AU 11 118381086 118381086 single base substitution C T downstream_gene_variant MELA-AU 11 118381086 118381086 single base substitution C T intron_variant MELA-AU 11 118381094 118381094 single base substitution C T downstream_gene_variant MELA-AU 11 118381094 118381094 single base substitution C T intron_variant MELA-AU 11 118381124 118381124 single base substitution A G downstream_gene_variant MELA-AU 11 118381124 118381124 single base substitution A G intron_variant MELA-AU 11 118381227 118381227 single base substitution T C downstream_gene_variant MELA-AU 11 118381227 118381227 single base substitution T C intron_variant MELA-AU 11 118381264 118381264 single base substitution C T downstream_gene_variant MELA-AU 11 118381264 118381264 single base substitution C T intron_variant MELA-AU 11 118382155 118382155 single base substitution C T downstream_gene_variant MELA-AU 11 118382155 118382155 single base substitution C T intron_variant MELA-AU 11 118382979 118382979 single base substitution C T downstream_gene_variant MELA-AU 11 118382979 118382979 single base substitution C T exon_variant MELA-AU 11 118382979 118382979 single base substitution C T intron_variant MELA-AU 11 118382992 118382992 single base substitution C T downstream_gene_variant MELA-AU 11 118382992 118382992 single base substitution C T exon_variant MELA-AU 11 118382992 118382992 single base substitution C T intron_variant MELA-AU 11 118383672 118383672 single base substitution C T downstream_gene_variant MELA-AU 11 118383672 118383672 single base substitution C T intron_variant MELA-AU 11 118383694 118383694 single base substitution C A downstream_gene_variant MELA-AU 11 118383694 118383694 single base substitution C A intron_variant MELA-AU 11 118383779 118383779 single base substitution A G downstream_gene_variant MELA-AU 11 118383779 118383779 single base substitution A G intron_variant MELA-AU 11 118384032 118384032 single base substitution C T downstream_gene_variant MELA-AU 11 118384032 118384032 single base substitution C T intron_variant MELA-AU 11 118385254 118385254 single base substitution C T downstream_gene_variant MELA-AU 11 118385254 118385254 single base substitution C T intron_variant MELA-AU 11 118385378 118385378 single base substitution C T downstream_gene_variant MELA-AU 11 118385378 118385378 single base substitution C T intron_variant MELA-AU 11 118385378 118385378 single base substitution C T upstream_gene_variant MELA-AU 11 118385830 118385830 single base substitution G A downstream_gene_variant MELA-AU 11 118385830 118385830 single base substitution G A intron_variant MELA-AU 11 118385830 118385830 single base substitution G A upstream_gene_variant MELA-AU 11 118388380 118388380 single base substitution C T intron_variant MELA-AU 11 118388380 118388380 single base substitution C T upstream_gene_variant MELA-AU 11 118388634 118388634 single base substitution C T intron_variant MELA-AU 11 118388634 118388634 single base substitution C T upstream_gene_variant MELA-AU 11 118389189 118389189 single base substitution A G intron_variant MELA-AU 11 118389189 118389189 single base substitution A G upstream_gene_variant MELA-AU 11 118389235 118389236 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 11 118389235 118389236 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 11 118389618 118389618 single base substitution C T intron_variant MELA-AU 11 118389618 118389618 single base substitution C T upstream_gene_variant MELA-AU 11 118389718 118389718 single base substitution G A intron_variant MELA-AU 11 118389718 118389718 single base substitution G A upstream_gene_variant MELA-AU 11 118390430 118390430 single base substitution C T exon_variant MELA-AU 11 118390430 118390430 single base substitution C T synonymous_variant F3707F 11121C>T MELA-AU 11 118390430 118390430 single base substitution C T synonymous_variant F3745F 11235C>T MELA-AU 11 118390430 118390430 single base substitution C T synonymous_variant F3748F 11244C>T MELA-AU 11 118390430 118390430 single base substitution C T upstream_gene_variant MELA-AU 11 118390465 118390466 multiple base substitution (>=2bp and <=200bp) CC TT exon_variant MELA-AU 11 118390465 118390466 multiple base substitution (>=2bp and <=200bp) CC TT missense_variant P3719L 11156CC>TT MELA-AU 11 118390465 118390466 multiple base substitution (>=2bp and <=200bp) CC TT missense_variant P3757L 11270CC>TT MELA-AU 11 118390465 118390466 multiple base substitution (>=2bp and <=200bp) CC TT missense_variant P3760L 11279CC>TT MELA-AU 11 118390465 118390466 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 11 118390472 118390472 single base substitution C T exon_variant MELA-AU 11 118390472 118390472 single base substitution C T synonymous_variant N3721N 11163C>T MELA-AU 11 118390472 118390472 single base substitution C T synonymous_variant N3759N 11277C>T MELA-AU 11 118390472 118390472 single base substitution C T synonymous_variant N3762N 11286C>T MELA-AU 11 118390472 118390472 single base substitution C T upstream_gene_variant MELA-AU 11 118391132 118391132 single base substitution C T exon_variant MELA-AU 11 118391132 118391132 single base substitution C T intron_variant MELA-AU 11 118391900 118391900 single base substitution C T exon_variant MELA-AU 11 118391900 118391900 single base substitution C T intron_variant MELA-AU 11 118392474 118392474 single base substitution A T intron_variant MELA-AU 11 118392632 118392632 single base substitution C T exon_variant MELA-AU 11 118392632 118392632 single base substitution C T synonymous_variant F3847F 11541C>T MELA-AU 11 118392632 118392632 single base substitution C T synonymous_variant F3885F 11655C>T MELA-AU 11 118392632 118392632 single base substitution C T synonymous_variant F3888F 11664C>T MELA-AU 11 118392657 118392657 single base substitution G A exon_variant MELA-AU 11 118392657 118392657 single base substitution G A missense_variant D3856N 11566G>A MELA-AU 11 118392657 118392657 single base substitution G A missense_variant D3894N 11680G>A MELA-AU 11 118392657 118392657 single base substitution G A missense_variant D3897N 11689G>A MELA-AU 11 118392955 118392955 single base substitution T C 3_prime_UTR_variant MELA-AU 11 118392955 118392955 single base substitution T C downstream_gene_variant MELA-AU 11 118392955 118392955 single base substitution T C exon_variant MELA-AU 11 118393932 118393932 single base substitution G A 3_prime_UTR_variant MELA-AU 11 118393932 118393932 single base substitution G A downstream_gene_variant MELA-AU 11 118396244 118396244 single base substitution G A 3_prime_UTR_variant MELA-AU 11 118396244 118396244 single base substitution G A downstream_gene_variant MELA-AU 11 118398129 118398129 single base substitution C T downstream_gene_variant MELA-AU 11 118398674 118398674 single base substitution A G downstream_gene_variant MELA-AU 11 118399049 118399049 single base substitution C T downstream_gene_variant MELA-AU 11 118399352 118399352 single base substitution C T downstream_gene_variant MELA-AU 11 118400534 118400534 single base substitution G A downstream_gene_variant ORCA-IN 11 118326437 118326437 single base substitution G T downstream_gene_variant ORCA-IN 11 118326437 118326437 single base substitution G T intron_variant ORCA-IN 11 118353467 118353467 deletion of <=200bp C - downstream_gene_variant ORCA-IN 11 118353467 118353467 deletion of <=200bp C - intron_variant ORCA-IN 11 118360860 118360860 single base substitution T C missense_variant V1493A 4478T>C ORCA-IN 11 118360860 118360860 single base substitution T C missense_variant V1531A 4592T>C ORCA-IN 11 118360860 118360860 single base substitution T C missense_variant V243A 728T>C ORCA-IN 11 118362613 118362613 single base substitution G A downstream_gene_variant ORCA-IN 11 118362613 118362613 single base substitution G A synonymous_variant R1617R 4851G>A ORCA-IN 11 118362613 118362613 single base substitution G A synonymous_variant R1655R 4965G>A ORCA-IN 11 118362613 118362613 single base substitution G A synonymous_variant R1658R 4974G>A ORCA-IN 11 118365879 118365879 deletion of <=200bp A - downstream_gene_variant ORCA-IN 11 118365879 118365879 deletion of <=200bp A - intron_variant ORCA-IN 11 118375299 118375299 single base substitution G T downstream_gene_variant ORCA-IN 11 118375299 118375299 single base substitution G T stop_gained E2857* 8569G>T ORCA-IN 11 118375299 118375299 single base substitution G T stop_gained E2895* 8683G>T ORCA-IN 11 118375299 118375299 single base substitution G T stop_gained E2898* 8692G>T ORCA-IN 11 118375299 118375299 single base substitution G T upstream_gene_variant ORCA-IN 11 118383805 118383805 single base substitution T C downstream_gene_variant ORCA-IN 11 118383805 118383805 single base substitution T C intron_variant ORCA-IN 11 118392791 118392791 single base substitution G T exon_variant ORCA-IN 11 118392791 118392791 single base substitution G T missense_variant E3900D 11700G>T ORCA-IN 11 118392791 118392791 single base substitution G T missense_variant E3938D 11814G>T ORCA-IN 11 118392791 118392791 single base substitution G T missense_variant E3941D 11823G>T ORCA-IN 11 118399386 118399386 single base substitution G A downstream_gene_variant OV-AU 11 118306394 118306394 single base substitution C A upstream_gene_variant OV-AU 11 118307578 118307578 single base substitution G A synonymous_variant Q117Q 351G>A OV-AU 11 118307578 118307578 single base substitution G A synonymous_variant Q34Q 102G>A OV-AU 11 118307578 118307578 single base substitution G A synonymous_variant Q40Q 120G>A OV-AU 11 118319763 118319763 single base substitution A T 3_prime_UTR_variant OV-AU 11 118319763 118319763 single base substitution A T intron_variant OV-AU 11 118321820 118321820 single base substitution T A downstream_gene_variant OV-AU 11 118321820 118321820 single base substitution T A intron_variant OV-AU 11 118328243 118328243 single base substitution C G intron_variant OV-AU 11 118330006 118330006 single base substitution C G intron_variant OV-AU 11 118333148 118333148 single base substitution G A intron_variant OV-AU 11 118333489 118333489 single base substitution G C intron_variant OV-AU 11 118340026 118340026 single base substitution A C intron_variant OV-AU 11 118354723 118354723 single base substitution G T intron_variant OV-AU 11 118357924 118357924 single base substitution A G downstream_gene_variant OV-AU 11 118357924 118357924 single base substitution A G intron_variant OV-AU 11 118364585 118364585 single base substitution C A downstream_gene_variant OV-AU 11 118364585 118364585 single base substitution C A intron_variant OV-AU 11 118380007 118380007 single base substitution T A downstream_gene_variant OV-AU 11 118380007 118380007 single base substitution T A intron_variant OV-AU 11 118380007 118380007 single base substitution T A upstream_gene_variant OV-AU 11 118394384 118394384 single base substitution G C 3_prime_UTR_variant OV-AU 11 118394384 118394384 single base substitution G C downstream_gene_variant OV-AU 11 118399547 118399547 single base substitution G C downstream_gene_variant OV-US 11 118363844 118363844 single base substitution G C downstream_gene_variant OV-US 11 118363844 118363844 single base substitution G C missense_variant D1652H 4954G>C OV-US 11 118363844 118363844 single base substitution G C missense_variant D1690H 5068G>C OV-US 11 118363844 118363844 single base substitution G C missense_variant D1693H 5077G>C OV-US 11 118373604 118373604 single base substitution A G exon_variant OV-US 11 118373604 118373604 single base substitution A G missense_variant K2292E 6874A>G OV-US 11 118373604 118373604 single base substitution A G missense_variant K2330E 6988A>G OV-US 11 118373604 118373604 single base substitution A G missense_variant K2333E 6997A>G OV-US 11 118373604 118373604 single base substitution A G upstream_gene_variant PACA-AU 11 118307161 118307161 single base substitution C T upstream_gene_variant PACA-AU 11 118309622 118309622 single base substitution C T intron_variant PACA-AU 11 118316445 118316445 single base substitution C T intron_variant PACA-AU 11 118318794 118318794 single base substitution G A 3_prime_UTR_variant PACA-AU 11 118318794 118318794 single base substitution G A intron_variant PACA-AU 11 118320193 118320193 single base substitution C T 3_prime_UTR_variant PACA-AU 11 118320193 118320193 single base substitution C T intron_variant PACA-AU 11 118323569 118323569 single base substitution G A downstream_gene_variant PACA-AU 11 118323569 118323569 single base substitution G A intron_variant PACA-AU 11 118326849 118326849 single base substitution C T intron_variant PACA-AU 11 118335406 118335406 single base substitution T C intron_variant PACA-AU 11 118339013 118339013 single base substitution T C intron_variant PACA-AU 11 118341158 118341158 single base substitution G T intron_variant PACA-AU 11 118343199 118343199 single base substitution G A intron_variant PACA-AU 11 118343199 118343199 single base substitution G A missense_variant R442Q 1325G>A PACA-AU 11 118343199 118343199 single base substitution G A missense_variant R475Q 1424G>A PACA-AU 11 118346961 118346961 single base substitution A G downstream_gene_variant PACA-AU 11 118346961 118346961 single base substitution A G intron_variant PACA-AU 11 118348645 118348645 single base substitution G C downstream_gene_variant PACA-AU 11 118348645 118348645 single base substitution G C intron_variant PACA-AU 11 118348645 118348645 single base substitution G C upstream_gene_variant PACA-AU 11 118364933 118364933 single base substitution G T downstream_gene_variant PACA-AU 11 118364933 118364933 single base substitution G T intron_variant PACA-AU 11 118370445 118370464 deletion of <=200bp AGATTGCGCCACTGCATTCC - intron_variant PACA-AU 11 118370445 118370464 deletion of <=200bp AGATTGCGCCACTGCATTCC - upstream_gene_variant PACA-AU 11 118376511 118376511 single base substitution G A downstream_gene_variant PACA-AU 11 118376511 118376511 single base substitution G A missense_variant A3261T 9781G>A PACA-AU 11 118376511 118376511 single base substitution G A missense_variant A3299T 9895G>A PACA-AU 11 118376511 118376511 single base substitution G A missense_variant A3302T 9904G>A PACA-AU 11 118376511 118376511 single base substitution G A upstream_gene_variant PACA-AU 11 118389685 118389685 single base substitution C T intron_variant PACA-AU 11 118389685 118389685 single base substitution C T upstream_gene_variant PACA-AU 11 118392464 118392471 deletion of <=200bp GAAAGATA - intron_variant PACA-CA 11 118303479 118303479 single base substitution G A upstream_gene_variant PACA-CA 11 118304889 118304889 single base substitution G A upstream_gene_variant PACA-CA 11 118305674 118305674 single base substitution G A upstream_gene_variant PACA-CA 11 118305839 118305839 single base substitution C G upstream_gene_variant PACA-CA 11 118309239 118309239 single base substitution C G intron_variant PACA-CA 11 118316455 118316455 single base substitution C T intron_variant PACA-CA 11 118320941 118320941 single base substitution A T 3_prime_UTR_variant PACA-CA 11 118320941 118320941 single base substitution A T downstream_gene_variant PACA-CA 11 118320941 118320941 single base substitution A T intron_variant PACA-CA 11 118325014 118325015 deletion of <=200bp TT - downstream_gene_variant PACA-CA 11 118325014 118325015 deletion of <=200bp TT - intron_variant PACA-CA 11 118325510 118325510 single base substitution G C downstream_gene_variant PACA-CA 11 118325510 118325510 single base substitution G C intron_variant PACA-CA 11 118325570 118325570 single base substitution T A downstream_gene_variant PACA-CA 11 118325570 118325570 single base substitution T A intron_variant PACA-CA 11 118325957 118325957 single base substitution G C downstream_gene_variant PACA-CA 11 118325957 118325957 single base substitution G C intron_variant PACA-CA 11 118334547 118334547 single base substitution A T intron_variant PACA-CA 11 118334570 118334570 single base substitution T C intron_variant PACA-CA 11 118335049 118335049 single base substitution G A intron_variant PACA-CA 11 118336617 118336617 single base substitution G C intron_variant PACA-CA 11 118339449 118339449 single base substitution G A intron_variant PACA-CA 11 118340964 118340964 single base substitution A G intron_variant PACA-CA 11 118342717 118342717 single base substitution C T intron_variant PACA-CA 11 118342717 118342717 single base substitution C T synonymous_variant L281L 843C>T PACA-CA 11 118342717 118342717 single base substitution C T synonymous_variant L314L 942C>T PACA-CA 11 118344185 118344185 insertion of <=200bp - C frameshift_variant T771H? PACA-CA 11 118344185 118344185 insertion of <=200bp - C frameshift_variant T804H? PACA-CA 11 118344185 118344185 insertion of <=200bp - C intron_variant PACA-CA 11 118344783 118344783 deletion of <=200bp A - frameshift_variant E1003 PACA-CA 11 118344783 118344783 deletion of <=200bp A - frameshift_variant E970 PACA-CA 11 118344783 118344783 deletion of <=200bp A - intron_variant PACA-CA 11 118345842 118345842 single base substitution C G downstream_gene_variant PACA-CA 11 118345842 118345842 single base substitution C G intron_variant PACA-CA 11 118346630 118346630 deletion of <=200bp T - downstream_gene_variant PACA-CA 11 118346630 118346630 deletion of <=200bp T - intron_variant PACA-CA 11 118347309 118347309 single base substitution T G downstream_gene_variant PACA-CA 11 118347309 118347309 single base substitution T G intron_variant PACA-CA 11 118349527 118349527 single base substitution G A downstream_gene_variant PACA-CA 11 118349527 118349527 single base substitution G A intron_variant PACA-CA 11 118349527 118349527 single base substitution G A upstream_gene_variant PACA-CA 11 118352973 118352973 insertion of <=200bp - A downstream_gene_variant PACA-CA 11 118352973 118352973 insertion of <=200bp - A intron_variant PACA-CA 11 118356345 118356345 single base substitution C G downstream_gene_variant PACA-CA 11 118356345 118356345 single base substitution C G intron_variant PACA-CA 11 118371707 118371707 deletion of <=200bp C - exon_variant PACA-CA 11 118371707 118371707 deletion of <=200bp C - frameshift_variant S2014 PACA-CA 11 118371707 118371707 deletion of <=200bp C - frameshift_variant S2052 PACA-CA 11 118371707 118371707 deletion of <=200bp C - frameshift_variant S2055 PACA-CA 11 118373224 118373224 single base substitution A T exon_variant PACA-CA 11 118373224 118373224 single base substitution A T missense_variant Q2165L 6494A>T PACA-CA 11 118373224 118373224 single base substitution A T missense_variant Q2203L 6608A>T PACA-CA 11 118373224 118373224 single base substitution A T missense_variant Q2206L 6617A>T PACA-CA 11 118373224 118373224 single base substitution A T upstream_gene_variant PACA-CA 11 118373864 118373864 single base substitution A G exon_variant PACA-CA 11 118373864 118373864 single base substitution A G synonymous_variant E2378E 7134A>G PACA-CA 11 118373864 118373864 single base substitution A G synonymous_variant E2416E 7248A>G PACA-CA 11 118373864 118373864 single base substitution A G synonymous_variant E2419E 7257A>G PACA-CA 11 118373864 118373864 single base substitution A G upstream_gene_variant PACA-CA 11 118373907 118373907 single base substitution A G exon_variant PACA-CA 11 118373907 118373907 single base substitution A G missense_variant K2393E 7177A>G PACA-CA 11 118373907 118373907 single base substitution A G missense_variant K2431E 7291A>G PACA-CA 11 118373907 118373907 single base substitution A G missense_variant K2434E 7300A>G PACA-CA 11 118373907 118373907 single base substitution A G upstream_gene_variant PACA-CA 11 118377151 118377151 single base substitution C T downstream_gene_variant PACA-CA 11 118377151 118377151 single base substitution C T missense_variant P3474L 10421C>T PACA-CA 11 118377151 118377151 single base substitution C T missense_variant P3512L 10535C>T PACA-CA 11 118377151 118377151 single base substitution C T missense_variant P3515L 10544C>T PACA-CA 11 118377151 118377151 single base substitution C T upstream_gene_variant PACA-CA 11 118378738 118378738 insertion of <=200bp - T downstream_gene_variant PACA-CA 11 118378738 118378738 insertion of <=200bp - T intron_variant PACA-CA 11 118378738 118378738 insertion of <=200bp - T upstream_gene_variant PACA-CA 11 118381344 118381344 single base substitution T C downstream_gene_variant PACA-CA 11 118381344 118381344 single base substitution T C intron_variant PACA-CA 11 118383345 118383345 insertion of <=200bp - T downstream_gene_variant PACA-CA 11 118383345 118383345 insertion of <=200bp - T intron_variant PACA-CA 11 118383529 118383529 single base substitution T A downstream_gene_variant PACA-CA 11 118383529 118383529 single base substitution T A intron_variant PACA-CA 11 118395156 118395156 single base substitution C G 3_prime_UTR_variant PACA-CA 11 118395156 118395156 single base substitution C G downstream_gene_variant PACA-CA 11 118397940 118397940 single base substitution C G downstream_gene_variant PACA-CA 11 118399698 118399698 deletion of <=200bp T - downstream_gene_variant PACA-CA 11 118401094 118401094 single base substitution G A downstream_gene_variant PAEN-AU 11 118308244 118308244 single base substitution A C intron_variant PAEN-AU 11 118373054 118373054 single base substitution G A intron_variant PAEN-AU 11 118373054 118373054 single base substitution G A upstream_gene_variant PAEN-AU 11 118393601 118393601 single base substitution A C 3_prime_UTR_variant PAEN-AU 11 118393601 118393601 single base substitution A C downstream_gene_variant PAEN-IT 11 118302773 118302773 single base substitution C G upstream_gene_variant PAEN-IT 11 118312062 118312062 single base substitution G C intron_variant PAEN-IT 11 118323744 118323744 single base substitution C G downstream_gene_variant PAEN-IT 11 118323744 118323744 single base substitution C G intron_variant PAEN-IT 11 118371110 118371110 single base substitution A G intron_variant PAEN-IT 11 118371110 118371110 single base substitution A G upstream_gene_variant PAEN-IT 11 118373007 118373007 single base substitution A C intron_variant PAEN-IT 11 118373007 118373007 single base substitution A C upstream_gene_variant PAEN-IT 11 118379233 118379233 single base substitution C G downstream_gene_variant PAEN-IT 11 118379233 118379233 single base substitution C G intron_variant PAEN-IT 11 118379233 118379233 single base substitution C G upstream_gene_variant PAEN-IT 11 118389882 118389882 single base substitution G T intron_variant PAEN-IT 11 118389882 118389882 single base substitution G T upstream_gene_variant PBCA-DE 11 118328770 118328770 insertion of <=200bp - T intron_variant PBCA-DE 11 118336889 118336889 single base substitution A G intron_variant PBCA-DE 11 118338723 118338723 deletion of <=200bp T - intron_variant PBCA-DE 11 118340215 118340215 single base substitution T A intron_variant PBCA-DE 11 118348808 118348808 single base substitution G A downstream_gene_variant PBCA-DE 11 118348808 118348808 single base substitution G A missense_variant R1154Q 3461G>A PBCA-DE 11 118348808 118348808 single base substitution G A missense_variant R1187Q 3560G>A PBCA-DE 11 118348808 118348808 single base substitution G A missense_variant R232Q 695G>A PBCA-DE 11 118348808 118348808 single base substitution G A upstream_gene_variant PBCA-DE 11 118354246 118354246 insertion of <=200bp - A intron_variant PBCA-DE 11 118359161 118359161 single base substitution G A downstream_gene_variant PBCA-DE 11 118359161 118359161 single base substitution G A intron_variant PBCA-DE 11 118360866 118360866 insertion of <=200bp - A frameshift_variant C1495*? PBCA-DE 11 118360866 118360866 insertion of <=200bp - A frameshift_variant C1533*? PBCA-DE 11 118360866 118360866 insertion of <=200bp - A frameshift_variant C245*? PBCA-DE 11 118364203 118364203 single base substitution T A downstream_gene_variant PBCA-DE 11 118364203 118364203 single base substitution T A intron_variant PBCA-DE 11 118367237 118367237 single base substitution A T downstream_gene_variant PBCA-DE 11 118367237 118367237 single base substitution A T intron_variant PBCA-DE 11 118367237 118367237 single base substitution A T upstream_gene_variant PBCA-DE 11 118381207 118381207 single base substitution A G downstream_gene_variant PBCA-DE 11 118381207 118381207 single base substitution A G intron_variant PBCA-DE 11 118391491 118391491 single base substitution C T exon_variant PBCA-DE 11 118391491 118391491 single base substitution C T intron_variant PRAD-CA 11 118303943 118303943 single base substitution C T upstream_gene_variant PRAD-CA 11 118307606 118307606 single base substitution C T missense_variant R127C 379C>T PRAD-CA 11 118307606 118307606 single base substitution C T missense_variant R44C 130C>T PRAD-CA 11 118307606 118307606 single base substitution C T missense_variant R50C 148C>T PRAD-CA 11 118353268 118353268 single base substitution A G downstream_gene_variant PRAD-CA 11 118353268 118353268 single base substitution A G intron_variant PRAD-CA 11 118353482 118353482 single base substitution G A downstream_gene_variant PRAD-CA 11 118353482 118353482 single base substitution G A intron_variant PRAD-CA 11 118361211 118361211 single base substitution A G intron_variant PRAD-CA 11 118370456 118370456 single base substitution C G intron_variant PRAD-CA 11 118370456 118370456 single base substitution C G upstream_gene_variant PRAD-CA 11 118370473 118370473 single base substitution C T intron_variant PRAD-CA 11 118370473 118370473 single base substitution C T upstream_gene_variant PRAD-UK 11 118316170 118316170 single base substitution C T intron_variant PRAD-UK 11 118316590 118316590 single base substitution G A intron_variant PRAD-UK 11 118326422 118326422 insertion of <=200bp - T downstream_gene_variant PRAD-UK 11 118326422 118326422 insertion of <=200bp - T intron_variant PRAD-UK 11 118336876 118336876 single base substitution G A intron_variant PRAD-UK 11 118358618 118358618 single base substitution G T downstream_gene_variant PRAD-UK 11 118358618 118358618 single base substitution G T intron_variant PRAD-UK 11 118362839 118362839 single base substitution T G downstream_gene_variant PRAD-UK 11 118362839 118362839 single base substitution T G intron_variant PRAD-UK 11 118397303 118397303 single base substitution A G 3_prime_UTR_variant PRAD-UK 11 118397303 118397303 single base substitution A G downstream_gene_variant PRAD-UK 11 118401881 118401881 single base substitution C T downstream_gene_variant PRAD-US 11 118307279 118307281 deletion of <=200bp GGC - inframe_deletion G18 PRAD-US 11 118307279 118307281 deletion of <=200bp GGC - upstream_gene_variant PRAD-US 11 118343036 118343036 insertion of <=200bp - A frameshift_variant E388R? PRAD-US 11 118343036 118343036 insertion of <=200bp - A frameshift_variant E421R? PRAD-US 11 118343036 118343036 insertion of <=200bp - A intron_variant PRAD-US 11 118343381 118343381 single base substitution C T intron_variant PRAD-US 11 118343381 118343381 single base substitution C T missense_variant R503W 1507C>T PRAD-US 11 118343381 118343381 single base substitution C T missense_variant R536W 1606C>T PRAD-US 11 118343971 118343971 single base substitution T C intron_variant PRAD-US 11 118343971 118343971 single base substitution T C synonymous_variant A699A 2097T>C PRAD-US 11 118343971 118343971 single base substitution T C synonymous_variant A732A 2196T>C READ-US 11 118343503 118343503 single base substitution G A intron_variant READ-US 11 118343503 118343503 single base substitution G A synonymous_variant T543T 1629G>A READ-US 11 118343503 118343503 single base substitution G A synonymous_variant T576T 1728G>A RECA-EU 11 118312227 118312227 single base substitution T G intron_variant RECA-EU 11 118312716 118312716 single base substitution A G intron_variant RECA-EU 11 118313302 118313302 single base substitution T A intron_variant RECA-EU 11 118335604 118335604 single base substitution G A intron_variant RECA-EU 11 118357270 118357270 single base substitution A G downstream_gene_variant RECA-EU 11 118357270 118357270 single base substitution A G intron_variant RECA-EU 11 118386843 118386843 single base substitution C G downstream_gene_variant RECA-EU 11 118386843 118386843 single base substitution C G intron_variant RECA-EU 11 118386843 118386843 single base substitution C G upstream_gene_variant SKCA-BR 11 118302715 118302715 single base substitution C T upstream_gene_variant SKCA-BR 11 118302901 118302901 single base substitution T C upstream_gene_variant SKCA-BR 11 118303994 118303994 single base substitution A C upstream_gene_variant SKCA-BR 11 118306249 118306249 single base substitution C T upstream_gene_variant SKCA-BR 11 118306250 118306250 single base substitution C T upstream_gene_variant SKCA-BR 11 118306290 118306290 single base substitution C T upstream_gene_variant SKCA-BR 11 118307143 118307143 single base substitution C T upstream_gene_variant SKCA-BR 11 118307393 118307393 single base substitution T C missense_variant S56P 166T>C SKCA-BR 11 118307393 118307393 single base substitution T C upstream_gene_variant SKCA-BR 11 118307644 118307644 single base substitution A G synonymous_variant G139G 417A>G SKCA-BR 11 118307644 118307644 single base substitution A G synonymous_variant G56G 168A>G SKCA-BR 11 118307644 118307644 single base substitution A G synonymous_variant G62G 186A>G SKCA-BR 11 118316927 118316927 single base substitution C T intron_variant SKCA-BR 11 118319656 118319660 deletion of <=200bp TCATA - 3_prime_UTR_variant SKCA-BR 11 118319656 118319660 deletion of <=200bp TCATA - intron_variant SKCA-BR 11 118322968 118322968 single base substitution C T downstream_gene_variant SKCA-BR 11 118322968 118322968 single base substitution C T intron_variant SKCA-BR 11 118328850 118328850 single base substitution G T intron_variant SKCA-BR 11 118330482 118330482 single base substitution A C intron_variant SKCA-BR 11 118330483 118330483 single base substitution A C intron_variant SKCA-BR 11 118331426 118331426 single base substitution G A intron_variant SKCA-BR 11 118333415 118333415 single base substitution A G intron_variant SKCA-BR 11 118344814 118344814 single base substitution C T intron_variant SKCA-BR 11 118344814 118344814 single base substitution C T synonymous_variant A1013A 3039C>T SKCA-BR 11 118344814 118344814 single base substitution C T synonymous_variant A980A 2940C>T SKCA-BR 11 118346157 118346157 single base substitution G A downstream_gene_variant SKCA-BR 11 118346157 118346157 single base substitution G A intron_variant SKCA-BR 11 118346983 118346983 single base substitution T C downstream_gene_variant SKCA-BR 11 118346983 118346983 single base substitution T C intron_variant SKCA-BR 11 118353768 118353768 single base substitution T C downstream_gene_variant SKCA-BR 11 118353768 118353768 single base substitution T C intron_variant SKCA-BR 11 118353921 118353921 single base substitution C T intron_variant SKCA-BR 11 118355521 118355521 single base substitution C T downstream_gene_variant SKCA-BR 11 118355521 118355521 single base substitution C T intron_variant SKCA-BR 11 118360171 118360171 single base substitution C T intron_variant SKCA-BR 11 118365177 118365177 single base substitution A G downstream_gene_variant SKCA-BR 11 118365177 118365177 single base substitution A G intron_variant SKCA-BR 11 118365883 118365883 single base substitution T A downstream_gene_variant SKCA-BR 11 118365883 118365883 single base substitution T A intron_variant SKCA-BR 11 118367588 118367588 single base substitution G A downstream_gene_variant SKCA-BR 11 118367588 118367588 single base substitution G A intron_variant SKCA-BR 11 118367588 118367588 single base substitution G A upstream_gene_variant SKCA-BR 11 118373018 118373018 insertion of <=200bp - AAT intron_variant SKCA-BR 11 118373018 118373018 insertion of <=200bp - AAT upstream_gene_variant SKCA-BR 11 118374432 118374432 single base substitution C T downstream_gene_variant SKCA-BR 11 118374432 118374432 single base substitution C T missense_variant P2568S 7702C>T SKCA-BR 11 118374432 118374432 single base substitution C T missense_variant P2606S 7816C>T SKCA-BR 11 118374432 118374432 single base substitution C T missense_variant P2609S 7825C>T SKCA-BR 11 118374432 118374432 single base substitution C T upstream_gene_variant SKCA-BR 11 118376990 118376990 single base substitution C A downstream_gene_variant SKCA-BR 11 118376990 118376990 single base substitution C A synonymous_variant L3420L 10260C>A SKCA-BR 11 118376990 118376990 single base substitution C A synonymous_variant L3458L 10374C>A SKCA-BR 11 118376990 118376990 single base substitution C A synonymous_variant L3461L 10383C>A SKCA-BR 11 118376990 118376990 single base substitution C A upstream_gene_variant SKCA-BR 11 118376991 118376991 single base substitution C T downstream_gene_variant SKCA-BR 11 118376991 118376991 single base substitution C T missense_variant L3421F 10261C>T SKCA-BR 11 118376991 118376991 single base substitution C T missense_variant L3459F 10375C>T SKCA-BR 11 118376991 118376991 single base substitution C T missense_variant L3462F 10384C>T SKCA-BR 11 118376991 118376991 single base substitution C T upstream_gene_variant SKCA-BR 11 118377696 118377696 single base substitution C T downstream_gene_variant SKCA-BR 11 118377696 118377696 single base substitution C T intron_variant SKCA-BR 11 118377696 118377696 single base substitution C T upstream_gene_variant SKCA-BR 11 118379435 118379436 deletion of <=200bp CA - downstream_gene_variant SKCA-BR 11 118379435 118379436 deletion of <=200bp CA - intron_variant SKCA-BR 11 118379435 118379436 deletion of <=200bp CA - upstream_gene_variant SKCA-BR 11 118383928 118383928 single base substitution C T downstream_gene_variant SKCA-BR 11 118383928 118383928 single base substitution C T intron_variant SKCA-BR 11 118384680 118384680 single base substitution G A downstream_gene_variant SKCA-BR 11 118384680 118384680 single base substitution G A intron_variant SKCA-BR 11 118386161 118386161 single base substitution C T downstream_gene_variant SKCA-BR 11 118386161 118386161 single base substitution C T intron_variant SKCA-BR 11 118386161 118386161 single base substitution C T upstream_gene_variant SKCA-BR 11 118399328 118399328 single base substitution C A downstream_gene_variant SKCA-BR 11 118399499 118399499 single base substitution C T downstream_gene_variant SKCM-US 11 118342713 118342713 single base substitution C T intron_variant SKCM-US 11 118342713 118342713 single base substitution C T missense_variant P280L 839C>T SKCM-US 11 118342713 118342713 single base substitution C T missense_variant P313L 938C>T SKCM-US 11 118343024 118343024 single base substitution C T intron_variant SKCM-US 11 118343024 118343024 single base substitution C T stop_gained Q384* 1150C>T SKCM-US 11 118343024 118343024 single base substitution C T stop_gained Q417* 1249C>T SKCM-US 11 118343602 118343602 single base substitution C T intron_variant SKCM-US 11 118343602 118343602 single base substitution C T synonymous_variant S576S 1728C>T SKCM-US 11 118343602 118343602 single base substitution C T synonymous_variant S609S 1827C>T SKCM-US 11 118343772 118343772 single base substitution C T intron_variant SKCM-US 11 118343772 118343772 single base substitution C T missense_variant S633F 1898C>T SKCM-US 11 118343772 118343772 single base substitution C T missense_variant S666F 1997C>T SKCM-US 11 118343788 118343788 single base substitution C T intron_variant SKCM-US 11 118343788 118343788 single base substitution C T synonymous_variant A638A 1914C>T SKCM-US 11 118343788 118343788 single base substitution C T synonymous_variant A671A 2013C>T SKCM-US 11 118343920 118343920 single base substitution C T intron_variant SKCM-US 11 118343920 118343920 single base substitution C T synonymous_variant L682L 2046C>T SKCM-US 11 118343920 118343920 single base substitution C T synonymous_variant L715L 2145C>T SKCM-US 11 118344107 118344107 single base substitution C T intron_variant SKCM-US 11 118344107 118344107 single base substitution C T stop_gained R745* 2233C>T SKCM-US 11 118344107 118344107 single base substitution C T stop_gained R778* 2332C>T SKCM-US 11 118344279 118344279 single base substitution C T intron_variant SKCM-US 11 118344279 118344279 single base substitution C T missense_variant S802F 2405C>T SKCM-US 11 118344279 118344279 single base substitution C T missense_variant S835F 2504C>T SKCM-US 11 118344383 118344383 single base substitution C T intron_variant SKCM-US 11 118344383 118344383 single base substitution C T missense_variant P837S 2509C>T SKCM-US 11 118344383 118344383 single base substitution C T missense_variant P870S 2608C>T SKCM-US 11 118344458 118344458 single base substitution C T intron_variant SKCM-US 11 118344458 118344458 single base substitution C T stop_gained R862* 2584C>T SKCM-US 11 118344458 118344458 single base substitution C T stop_gained R895* 2683C>T SKCM-US 11 118344497 118344497 single base substitution G A intron_variant SKCM-US 11 118344497 118344497 single base substitution G A missense_variant E875K 2623G>A SKCM-US 11 118344497 118344497 single base substitution G A missense_variant E908K 2722G>A SKCM-US 11 118344687 118344687 single base substitution C T intron_variant SKCM-US 11 118344687 118344687 single base substitution C T missense_variant S938L 2813C>T SKCM-US 11 118344687 118344687 single base substitution C T missense_variant S971L 2912C>T SKCM-US 11 118344861 118344861 single base substitution C T intron_variant SKCM-US 11 118344861 118344861 single base substitution C T missense_variant S1029F 3086C>T SKCM-US 11 118344861 118344861 single base substitution C T missense_variant S996F 2987C>T SKCM-US 11 118344862 118344877 deletion of <=200bp TAGCACTGTTAAACAT - frameshift_variant SSTVKH1029 SKCM-US 11 118344862 118344877 deletion of <=200bp TAGCACTGTTAAACAT - frameshift_variant SSTVKH996 SKCM-US 11 118344862 118344877 deletion of <=200bp TAGCACTGTTAAACAT - intron_variant SKCM-US 11 118353184 118353184 single base substitution C T downstream_gene_variant SKCM-US 11 118353184 118353184 single base substitution C T intron_variant SKCM-US 11 118353184 118353184 single base substitution C T missense_variant P104S 310C>T SKCM-US 11 118353184 118353184 single base substitution C T missense_variant P1354S 4060C>T SKCM-US 11 118353184 118353184 single base substitution C T missense_variant P1387S 4159C>T SKCM-US 11 118355575 118355575 single base substitution A G downstream_gene_variant SKCM-US 11 118355575 118355575 single base substitution A G intron_variant SKCM-US 11 118355575 118355575 single base substitution A G splice_acceptor_variant SKCM-US 11 118359392 118359392 single base substitution C T downstream_gene_variant SKCM-US 11 118359392 118359392 single base substitution C T missense_variant P1428S 4282C>T SKCM-US 11 118359392 118359392 single base substitution C T missense_variant P1466S 4396C>T SKCM-US 11 118359392 118359392 single base substitution C T missense_variant P178S 532C>T SKCM-US 11 118360862 118360862 single base substitution C T missense_variant R1494C 4480C>T SKCM-US 11 118360862 118360862 single base substitution C T missense_variant R1532C 4594C>T SKCM-US 11 118360862 118360862 single base substitution C T missense_variant R244C 730C>T SKCM-US 11 118362000 118362000 single base substitution C T missense_variant H1558Y 4672C>T SKCM-US 11 118362000 118362000 single base substitution C T missense_variant H1596Y 4786C>T SKCM-US 11 118362000 118362000 single base substitution C T missense_variant H308Y 922C>T SKCM-US 11 118362005 118362005 single base substitution C T synonymous_variant S1559S 4677C>T SKCM-US 11 118362005 118362005 single base substitution C T synonymous_variant S1597S 4791C>T SKCM-US 11 118362005 118362005 single base substitution C T synonymous_variant S309S 927C>T SKCM-US 11 118362611 118362611 single base substitution C T downstream_gene_variant SKCM-US 11 118362611 118362611 single base substitution C T missense_variant R1617W 4849C>T SKCM-US 11 118362611 118362611 single base substitution C T missense_variant R1655W 4963C>T SKCM-US 11 118362611 118362611 single base substitution C T missense_variant R1658W 4972C>T SKCM-US 11 118363900 118363900 single base substitution A G downstream_gene_variant SKCM-US 11 118363900 118363900 single base substitution A G synonymous_variant L1670L 5010A>G SKCM-US 11 118363900 118363900 single base substitution A G synonymous_variant L1708L 5124A>G SKCM-US 11 118363900 118363900 single base substitution A G synonymous_variant L1711L 5133A>G SKCM-US 11 118365427 118365427 single base substitution C T downstream_gene_variant SKCM-US 11 118365427 118365427 single base substitution C T missense_variant P1729S 5185C>T SKCM-US 11 118365427 118365427 single base substitution C T missense_variant P1767S 5299C>T SKCM-US 11 118365427 118365427 single base substitution C T missense_variant P1770S 5308C>T SKCM-US 11 118365449 118365449 single base substitution C T downstream_gene_variant SKCM-US 11 118365449 118365449 single base substitution C T missense_variant S1736F 5207C>T SKCM-US 11 118365449 118365449 single base substitution C T missense_variant S1774F 5321C>T SKCM-US 11 118365449 118365449 single base substitution C T missense_variant S1777F 5330C>T SKCM-US 11 118365450 118365450 single base substitution C T downstream_gene_variant SKCM-US 11 118365450 118365450 single base substitution C T synonymous_variant S1736S 5208C>T SKCM-US 11 118365450 118365450 single base substitution C T synonymous_variant S1774S 5322C>T SKCM-US 11 118365450 118365450 single base substitution C T synonymous_variant S1777S 5331C>T SKCM-US 11 118366446 118366446 single base substitution C T downstream_gene_variant SKCM-US 11 118366446 118366446 single base substitution C T missense_variant P1758S 5272C>T SKCM-US 11 118366446 118366446 single base substitution C T missense_variant P1796S 5386C>T SKCM-US 11 118366446 118366446 single base substitution C T missense_variant P1799S 5395C>T SKCM-US 11 118366446 118366446 single base substitution C T upstream_gene_variant SKCM-US 11 118366464 118366464 single base substitution T A downstream_gene_variant SKCM-US 11 118366464 118366464 single base substitution T A missense_variant Y1764N 5290T>A SKCM-US 11 118366464 118366464 single base substitution T A missense_variant Y1802N 5404T>A SKCM-US 11 118366464 118366464 single base substitution T A missense_variant Y1805N 5413T>A SKCM-US 11 118366464 118366464 single base substitution T A upstream_gene_variant SKCM-US 11 118372446 118372446 single base substitution C T exon_variant SKCM-US 11 118372446 118372446 single base substitution C T stop_gained R2086* 6256C>T SKCM-US 11 118372446 118372446 single base substitution C T stop_gained R2124* 6370C>T SKCM-US 11 118372446 118372446 single base substitution C T stop_gained R2127* 6379C>T SKCM-US 11 118372446 118372446 single base substitution C T upstream_gene_variant SKCM-US 11 118372518 118372518 single base substitution C T exon_variant SKCM-US 11 118372518 118372518 single base substitution C T missense_variant P2110S 6328C>T SKCM-US 11 118372518 118372518 single base substitution C T missense_variant P2148S 6442C>T SKCM-US 11 118372518 118372518 single base substitution C T missense_variant P2151S 6451C>T SKCM-US 11 118372518 118372518 single base substitution C T upstream_gene_variant SKCM-US 11 118373178 118373178 single base substitution C T exon_variant SKCM-US 11 118373178 118373178 single base substitution C T stop_gained R2150* 6448C>T SKCM-US 11 118373178 118373178 single base substitution C T stop_gained R2188* 6562C>T SKCM-US 11 118373178 118373178 single base substitution C T stop_gained R2191* 6571C>T SKCM-US 11 118373178 118373178 single base substitution C T upstream_gene_variant SKCM-US 11 118373240 118373240 single base substitution G A exon_variant SKCM-US 11 118373240 118373240 single base substitution G A synonymous_variant R2170R 6510G>A SKCM-US 11 118373240 118373240 single base substitution G A synonymous_variant R2208R 6624G>A SKCM-US 11 118373240 118373240 single base substitution G A synonymous_variant R2211R 6633G>A SKCM-US 11 118373240 118373240 single base substitution G A upstream_gene_variant SKCM-US 11 118373290 118373290 single base substitution C T exon_variant SKCM-US 11 118373290 118373290 single base substitution C T missense_variant S2187F 6560C>T SKCM-US 11 118373290 118373290 single base substitution C T missense_variant S2225F 6674C>T SKCM-US 11 118373290 118373290 single base substitution C T missense_variant S2228F 6683C>T SKCM-US 11 118373290 118373290 single base substitution C T upstream_gene_variant SKCM-US 11 118373344 118373344 single base substitution T C exon_variant SKCM-US 11 118373344 118373344 single base substitution T C missense_variant V2205A 6614T>C SKCM-US 11 118373344 118373344 single base substitution T C missense_variant V2243A 6728T>C SKCM-US 11 118373344 118373344 single base substitution T C missense_variant V2246A 6737T>C SKCM-US 11 118373344 118373344 single base substitution T C upstream_gene_variant SKCM-US 11 118373601 118373601 single base substitution C T exon_variant SKCM-US 11 118373601 118373601 single base substitution C T missense_variant P2291S 6871C>T SKCM-US 11 118373601 118373601 single base substitution C T missense_variant P2329S 6985C>T SKCM-US 11 118373601 118373601 single base substitution C T missense_variant P2332S 6994C>T SKCM-US 11 118373601 118373601 single base substitution C T upstream_gene_variant SKCM-US 11 118373665 118373665 single base substitution C T exon_variant SKCM-US 11 118373665 118373665 single base substitution C T missense_variant S2312F 6935C>T SKCM-US 11 118373665 118373665 single base substitution C T missense_variant S2350F 7049C>T SKCM-US 11 118373665 118373665 single base substitution C T missense_variant S2353F 7058C>T SKCM-US 11 118373665 118373665 single base substitution C T upstream_gene_variant SKCM-US 11 118373727 118373727 single base substitution C T exon_variant SKCM-US 11 118373727 118373727 single base substitution C T missense_variant H2333Y 6997C>T SKCM-US 11 118373727 118373727 single base substitution C T missense_variant H2371Y 7111C>T SKCM-US 11 118373727 118373727 single base substitution C T missense_variant H2374Y 7120C>T SKCM-US 11 118373727 118373727 single base substitution C T upstream_gene_variant SKCM-US 11 118373881 118373881 single base substitution C T exon_variant SKCM-US 11 118373881 118373881 single base substitution C T missense_variant S2384F 7151C>T SKCM-US 11 118373881 118373881 single base substitution C T missense_variant S2422F 7265C>T SKCM-US 11 118373881 118373881 single base substitution C T missense_variant S2425F 7274C>T SKCM-US 11 118373881 118373881 single base substitution C T upstream_gene_variant SKCM-US 11 118374107 118374107 single base substitution C T exon_variant SKCM-US 11 118374107 118374107 single base substitution C T synonymous_variant V2459V 7377C>T SKCM-US 11 118374107 118374107 single base substitution C T synonymous_variant V2497V 7491C>T SKCM-US 11 118374107 118374107 single base substitution C T synonymous_variant V2500V 7500C>T SKCM-US 11 118374107 118374107 single base substitution C T upstream_gene_variant SKCM-US 11 118374290 118374290 single base substitution A G downstream_gene_variant SKCM-US 11 118374290 118374290 single base substitution A G synonymous_variant P2520P 7560A>G SKCM-US 11 118374290 118374290 single base substitution A G synonymous_variant P2558P 7674A>G SKCM-US 11 118374290 118374290 single base substitution A G synonymous_variant P2561P 7683A>G SKCM-US 11 118374290 118374290 single base substitution A G upstream_gene_variant SKCM-US 11 118374328 118374328 single base substitution C T downstream_gene_variant SKCM-US 11 118374328 118374328 single base substitution C T missense_variant A2533V 7598C>T SKCM-US 11 118374328 118374328 single base substitution C T missense_variant A2571V 7712C>T SKCM-US 11 118374328 118374328 single base substitution C T missense_variant A2574V 7721C>T SKCM-US 11 118374328 118374328 single base substitution C T upstream_gene_variant SKCM-US 11 118374333 118374333 single base substitution C T downstream_gene_variant SKCM-US 11 118374333 118374333 single base substitution C T missense_variant P2535S 7603C>T SKCM-US 11 118374333 118374333 single base substitution C T missense_variant P2573S 7717C>T SKCM-US 11 118374333 118374333 single base substitution C T missense_variant P2576S 7726C>T SKCM-US 11 118374333 118374333 single base substitution C T upstream_gene_variant SKCM-US 11 118374553 118374553 single base substitution C T downstream_gene_variant SKCM-US 11 118374553 118374553 single base substitution C T missense_variant P2608L 7823C>T SKCM-US 11 118374553 118374553 single base substitution C T missense_variant P2646L 7937C>T SKCM-US 11 118374553 118374553 single base substitution C T missense_variant P2649L 7946C>T SKCM-US 11 118374553 118374553 single base substitution C T upstream_gene_variant SKCM-US 11 118375064 118375064 single base substitution C T downstream_gene_variant SKCM-US 11 118375064 118375064 single base substitution C T synonymous_variant S2778S 8334C>T SKCM-US 11 118375064 118375064 single base substitution C T synonymous_variant S2816S 8448C>T SKCM-US 11 118375064 118375064 single base substitution C T synonymous_variant S2819S 8457C>T SKCM-US 11 118375064 118375064 single base substitution C T upstream_gene_variant SKCM-US 11 118375153 118375153 single base substitution C A downstream_gene_variant SKCM-US 11 118375153 118375153 single base substitution C A missense_variant P2808H 8423C>A SKCM-US 11 118375153 118375153 single base substitution C A missense_variant P2846H 8537C>A SKCM-US 11 118375153 118375153 single base substitution C A missense_variant P2849H 8546C>A SKCM-US 11 118375153 118375153 single base substitution C A upstream_gene_variant SKCM-US 11 118375357 118375357 single base substitution C T downstream_gene_variant SKCM-US 11 118375357 118375357 single base substitution C T missense_variant S2876F 8627C>T SKCM-US 11 118375357 118375357 single base substitution C T missense_variant S2914F 8741C>T SKCM-US 11 118375357 118375357 single base substitution C T missense_variant S2917F 8750C>T SKCM-US 11 118375357 118375357 single base substitution C T upstream_gene_variant SKCM-US 11 118375399 118375399 single base substitution C T downstream_gene_variant SKCM-US 11 118375399 118375399 single base substitution C T missense_variant P2890L 8669C>T SKCM-US 11 118375399 118375399 single base substitution C T missense_variant P2928L 8783C>T SKCM-US 11 118375399 118375399 single base substitution C T missense_variant P2931L 8792C>T SKCM-US 11 118375399 118375399 single base substitution C T upstream_gene_variant SKCM-US 11 118375417 118375417 single base substitution T A downstream_gene_variant SKCM-US 11 118375417 118375417 single base substitution T A stop_gained L2896* 8687T>A SKCM-US 11 118375417 118375417 single base substitution T A stop_gained L2934* 8801T>A SKCM-US 11 118375417 118375417 single base substitution T A stop_gained L2937* 8810T>A SKCM-US 11 118375417 118375417 single base substitution T A upstream_gene_variant SKCM-US 11 118375435 118375435 single base substitution C T downstream_gene_variant SKCM-US 11 118375435 118375435 single base substitution C T missense_variant T2902I 8705C>T SKCM-US 11 118375435 118375435 single base substitution C T missense_variant T2940I 8819C>T SKCM-US 11 118375435 118375435 single base substitution C T missense_variant T2943I 8828C>T SKCM-US 11 118375435 118375435 single base substitution C T upstream_gene_variant SKCM-US 11 118375900 118375900 single base substitution C T downstream_gene_variant SKCM-US 11 118375900 118375900 single base substitution C T missense_variant P3057L 9170C>T SKCM-US 11 118375900 118375900 single base substitution C T missense_variant P3095L 9284C>T SKCM-US 11 118375900 118375900 single base substitution C T missense_variant P3098L 9293C>T SKCM-US 11 118375900 118375900 single base substitution C T upstream_gene_variant SKCM-US 11 118375975 118375975 single base substitution C T downstream_gene_variant SKCM-US 11 118375975 118375975 single base substitution C T missense_variant S3082L 9245C>T SKCM-US 11 118375975 118375975 single base substitution C T missense_variant S3120L 9359C>T SKCM-US 11 118375975 118375975 single base substitution C T missense_variant S3123L 9368C>T SKCM-US 11 118375975 118375975 single base substitution C T upstream_gene_variant SKCM-US 11 118376065 118376065 single base substitution G A downstream_gene_variant SKCM-US 11 118376065 118376065 single base substitution G A missense_variant S3112N 9335G>A SKCM-US 11 118376065 118376065 single base substitution G A missense_variant S3150N 9449G>A SKCM-US 11 118376065 118376065 single base substitution G A missense_variant S3153N 9458G>A SKCM-US 11 118376065 118376065 single base substitution G A upstream_gene_variant SKCM-US 11 118376241 118376241 single base substitution A G downstream_gene_variant SKCM-US 11 118376241 118376241 single base substitution A G missense_variant T3171A 9511A>G SKCM-US 11 118376241 118376241 single base substitution A G missense_variant T3209A 9625A>G SKCM-US 11 118376241 118376241 single base substitution A G missense_variant T3212A 9634A>G SKCM-US 11 118376241 118376241 single base substitution A G upstream_gene_variant SKCM-US 11 118390453 118390453 single base substitution C T exon_variant SKCM-US 11 118390453 118390453 single base substitution C T missense_variant A3715V 11144C>T SKCM-US 11 118390453 118390453 single base substitution C T missense_variant A3753V 11258C>T SKCM-US 11 118390453 118390453 single base substitution C T missense_variant A3756V 11267C>T SKCM-US 11 118390453 118390453 single base substitution C T upstream_gene_variant SKCM-US 11 118399448 118399448 single base substitution G A downstream_gene_variant SKCM-US 11 118399470 118399470 single base substitution C T downstream_gene_variant STAD-US 11 118343010 118343010 single base substitution C T intron_variant STAD-US 11 118343010 118343010 single base substitution C T missense_variant A379V 1136C>T STAD-US 11 118343010 118343010 single base substitution C T missense_variant A412V 1235C>T STAD-US 11 118343133 118343133 single base substitution G A intron_variant STAD-US 11 118343133 118343133 single base substitution G A missense_variant R420Q 1259G>A STAD-US 11 118343133 118343133 single base substitution G A missense_variant R453Q 1358G>A STAD-US 11 118343628 118343628 single base substitution T G intron_variant STAD-US 11 118343628 118343628 single base substitution T G missense_variant L585R 1754T>G STAD-US 11 118343628 118343628 single base substitution T G missense_variant L618R 1853T>G STAD-US 11 118343719 118343719 single base substitution G A intron_variant STAD-US 11 118343719 118343719 single base substitution G A synonymous_variant P615P 1845G>A STAD-US 11 118343719 118343719 single base substitution G A synonymous_variant P648P 1944G>A STAD-US 11 118343854 118343854 single base substitution C T intron_variant STAD-US 11 118343854 118343854 single base substitution C T synonymous_variant D660D 1980C>T STAD-US 11 118343854 118343854 single base substitution C T synonymous_variant D693D 2079C>T STAD-US 11 118344186 118344186 deletion of <=200bp C - frameshift_variant T771 STAD-US 11 118344186 118344186 deletion of <=200bp C - frameshift_variant T804 STAD-US 11 118344186 118344186 deletion of <=200bp C - intron_variant STAD-US 11 118344186 118344186 insertion of <=200bp - C frameshift_variant T771T? STAD-US 11 118344186 118344186 insertion of <=200bp - C frameshift_variant T804T? STAD-US 11 118344186 118344186 insertion of <=200bp - C intron_variant STAD-US 11 118344459 118344459 single base substitution G A intron_variant STAD-US 11 118344459 118344459 single base substitution G A missense_variant R862Q 2585G>A STAD-US 11 118344459 118344459 single base substitution G A missense_variant R895Q 2684G>A STAD-US 11 118344530 118344530 single base substitution C T intron_variant STAD-US 11 118344530 118344530 single base substitution C T missense_variant R886W 2656C>T STAD-US 11 118344530 118344530 single base substitution C T missense_variant R919W 2755C>T STAD-US 11 118347547 118347547 single base substitution T C downstream_gene_variant STAD-US 11 118347547 118347547 single base substitution T C missense_variant S1062P 3184T>C STAD-US 11 118347547 118347547 single base substitution T C missense_variant S1095P 3283T>C STAD-US 11 118347547 118347547 single base substitution T C missense_variant S140P 418T>C STAD-US 11 118347547 118347547 single base substitution T C upstream_gene_variant STAD-US 11 118352503 118352503 single base substitution C T downstream_gene_variant STAD-US 11 118352503 118352503 single base substitution C T synonymous_variant N1236N 3708C>T STAD-US 11 118352503 118352503 single base substitution C T synonymous_variant N1269N 3807C>T STAD-US 11 118352503 118352503 single base substitution C T upstream_gene_variant STAD-US 11 118352757 118352757 single base substitution A C downstream_gene_variant STAD-US 11 118352757 118352757 single base substitution A C exon_variant STAD-US 11 118352757 118352757 single base substitution A C missense_variant K1321T 3962A>C STAD-US 11 118352757 118352757 single base substitution A C missense_variant K1354T 4061A>C STAD-US 11 118352757 118352757 single base substitution A C missense_variant K71T 212A>C STAD-US 11 118354898 118354898 single base substitution G A missense_variant E113K 337G>A STAD-US 11 118354898 118354898 single base substitution G A missense_variant E1363K 4087G>A STAD-US 11 118354898 118354898 single base substitution G A missense_variant E1396K 4186G>A STAD-US 11 118354898 118354898 single base substitution G A splice_region_variant STAD-US 11 118359351 118359351 single base substitution G T downstream_gene_variant STAD-US 11 118359351 118359351 single base substitution G T missense_variant C1414F 4241G>T STAD-US 11 118359351 118359351 single base substitution G T missense_variant C1452F 4355G>T STAD-US 11 118359351 118359351 single base substitution G T missense_variant C164F 491G>T STAD-US 11 118359369 118359369 single base substitution T C downstream_gene_variant STAD-US 11 118359369 118359369 single base substitution T C missense_variant F1420S 4259T>C STAD-US 11 118359369 118359369 single base substitution T C missense_variant F1458S 4373T>C STAD-US 11 118359369 118359369 single base substitution T C missense_variant F170S 509T>C STAD-US 11 118359442 118359442 single base substitution T C downstream_gene_variant STAD-US 11 118359442 118359442 single base substitution T C synonymous_variant C1444C 4332T>C STAD-US 11 118359442 118359442 single base substitution T C synonymous_variant C1482C 4446T>C STAD-US 11 118359442 118359442 single base substitution T C synonymous_variant C194C 582T>C STAD-US 11 118361992 118361992 single base substitution G A missense_variant R1555H 4664G>A STAD-US 11 118361992 118361992 single base substitution G A missense_variant R1593H 4778G>A STAD-US 11 118361992 118361992 single base substitution G A missense_variant R305H 914G>A STAD-US 11 118362626 118362626 single base substitution T C downstream_gene_variant STAD-US 11 118362626 118362626 single base substitution T C synonymous_variant L1622L 4864T>C STAD-US 11 118362626 118362626 single base substitution T C synonymous_variant L1660L 4978T>C STAD-US 11 118362626 118362626 single base substitution T C synonymous_variant L1663L 4987T>C STAD-US 11 118363776 118363776 single base substitution C T downstream_gene_variant STAD-US 11 118363776 118363776 single base substitution C T missense_variant A1629V 4886C>T STAD-US 11 118363776 118363776 single base substitution C T missense_variant A1667V 5000C>T STAD-US 11 118363776 118363776 single base substitution C T missense_variant A1670V 5009C>T STAD-US 11 118363823 118363823 single base substitution C T downstream_gene_variant STAD-US 11 118363823 118363823 single base substitution C T missense_variant R1645C 4933C>T STAD-US 11 118363823 118363823 single base substitution C T missense_variant R1683C 5047C>T STAD-US 11 118363823 118363823 single base substitution C T missense_variant R1686C 5056C>T STAD-US 11 118365419 118365419 single base substitution G A downstream_gene_variant STAD-US 11 118365419 118365419 single base substitution G A missense_variant R1726H 5177G>A STAD-US 11 118365419 118365419 single base substitution G A missense_variant R1764H 5291G>A STAD-US 11 118365419 118365419 single base substitution G A missense_variant R1767H 5300G>A STAD-US 11 118369241 118369241 single base substitution G A missense_variant E1946K 5836G>A STAD-US 11 118369241 118369241 single base substitution G A missense_variant E1984K 5950G>A STAD-US 11 118369241 118369241 single base substitution G A missense_variant E1987K 5959G>A STAD-US 11 118369241 118369241 single base substitution G A upstream_gene_variant STAD-US 11 118371787 118371787 single base substitution G A exon_variant STAD-US 11 118371787 118371787 single base substitution G A missense_variant V2041I 6121G>A STAD-US 11 118371787 118371787 single base substitution G A missense_variant V2079I 6235G>A STAD-US 11 118371787 118371787 single base substitution G A missense_variant V2082I 6244G>A STAD-US 11 118371815 118371815 single base substitution A G exon_variant STAD-US 11 118371815 118371815 single base substitution A G missense_variant E2050G 6149A>G STAD-US 11 118371815 118371815 single base substitution A G missense_variant E2088G 6263A>G STAD-US 11 118371815 118371815 single base substitution A G missense_variant E2091G 6272A>G STAD-US 11 118373253 118373253 single base substitution A G exon_variant STAD-US 11 118373253 118373253 single base substitution A G missense_variant M2175V 6523A>G STAD-US 11 118373253 118373253 single base substitution A G missense_variant M2213V 6637A>G STAD-US 11 118373253 118373253 single base substitution A G missense_variant M2216V 6646A>G STAD-US 11 118373253 118373253 single base substitution A G upstream_gene_variant STAD-US 11 118373724 118373724 single base substitution C A exon_variant STAD-US 11 118373724 118373724 single base substitution C A missense_variant L2332I 6994C>A STAD-US 11 118373724 118373724 single base substitution C A missense_variant L2370I 7108C>A STAD-US 11 118373724 118373724 single base substitution C A missense_variant L2373I 7117C>A STAD-US 11 118373724 118373724 single base substitution C A upstream_gene_variant STAD-US 11 118374582 118374582 single base substitution C T downstream_gene_variant STAD-US 11 118374582 118374582 single base substitution C T stop_gained R2618* 7852C>T STAD-US 11 118374582 118374582 single base substitution C T stop_gained R2656* 7966C>T STAD-US 11 118374582 118374582 single base substitution C T stop_gained R2659* 7975C>T STAD-US 11 118374582 118374582 single base substitution C T upstream_gene_variant STAD-US 11 118374596 118374596 single base substitution A G downstream_gene_variant STAD-US 11 118374596 118374596 single base substitution A G synonymous_variant S2622S 7866A>G STAD-US 11 118374596 118374596 single base substitution A G synonymous_variant S2660S 7980A>G STAD-US 11 118374596 118374596 single base substitution A G synonymous_variant S2663S 7989A>G STAD-US 11 118374596 118374596 single base substitution A G upstream_gene_variant STAD-US 11 118374689 118374689 single base substitution A G downstream_gene_variant STAD-US 11 118374689 118374689 single base substitution A G synonymous_variant S2653S 7959A>G STAD-US 11 118374689 118374689 single base substitution A G synonymous_variant S2691S 8073A>G STAD-US 11 118374689 118374689 single base substitution A G synonymous_variant S2694S 8082A>G STAD-US 11 118374689 118374689 single base substitution A G upstream_gene_variant STAD-US 11 118375019 118375019 single base substitution C T downstream_gene_variant STAD-US 11 118375019 118375019 single base substitution C T synonymous_variant L2763L 8289C>T STAD-US 11 118375019 118375019 single base substitution C T synonymous_variant L2801L 8403C>T STAD-US 11 118375019 118375019 single base substitution C T synonymous_variant L2804L 8412C>T STAD-US 11 118375019 118375019 single base substitution C T upstream_gene_variant STAD-US 11 118375060 118375060 single base substitution C T downstream_gene_variant STAD-US 11 118375060 118375060 single base substitution C T missense_variant P2777L 8330C>T STAD-US 11 118375060 118375060 single base substitution C T missense_variant P2815L 8444C>T STAD-US 11 118375060 118375060 single base substitution C T missense_variant P2818L 8453C>T STAD-US 11 118375060 118375060 single base substitution C T upstream_gene_variant STAD-US 11 118375821 118375821 single base substitution C T downstream_gene_variant STAD-US 11 118375821 118375821 single base substitution C T missense_variant P3031S 9091C>T STAD-US 11 118375821 118375821 single base substitution C T missense_variant P3069S 9205C>T STAD-US 11 118375821 118375821 single base substitution C T missense_variant P3072S 9214C>T STAD-US 11 118375821 118375821 single base substitution C T upstream_gene_variant STAD-US 11 118375915 118375915 deletion of <=200bp A - downstream_gene_variant STAD-US 11 118375915 118375915 deletion of <=200bp A - frameshift_variant Q3062 STAD-US 11 118375915 118375915 deletion of <=200bp A - frameshift_variant Q3100 STAD-US 11 118375915 118375915 deletion of <=200bp A - frameshift_variant Q3103 STAD-US 11 118375915 118375915 deletion of <=200bp A - upstream_gene_variant STAD-US 11 118375926 118375926 single base substitution T C downstream_gene_variant STAD-US 11 118375926 118375926 single base substitution T C synonymous_variant L3066L 9196T>C STAD-US 11 118375926 118375926 single base substitution T C synonymous_variant L3104L 9310T>C STAD-US 11 118375926 118375926 single base substitution T C synonymous_variant L3107L 9319T>C STAD-US 11 118375926 118375926 single base substitution T C upstream_gene_variant STAD-US 11 118376657 118376657 single base substitution A G downstream_gene_variant STAD-US 11 118376657 118376657 single base substitution A G synonymous_variant Q3309Q 9927A>G STAD-US 11 118376657 118376657 single base substitution A G synonymous_variant Q3347Q 10041A>G STAD-US 11 118376657 118376657 single base substitution A G synonymous_variant Q3350Q 10050A>G STAD-US 11 118376657 118376657 single base substitution A G upstream_gene_variant STAD-US 11 118376815 118376815 single base substitution C T downstream_gene_variant STAD-US 11 118376815 118376815 single base substitution C T missense_variant P3362L 10085C>T STAD-US 11 118376815 118376815 single base substitution C T missense_variant P3400L 10199C>T STAD-US 11 118376815 118376815 single base substitution C T missense_variant P3403L 10208C>T STAD-US 11 118376815 118376815 single base substitution C T upstream_gene_variant STAD-US 11 118376836 118376836 single base substitution C T downstream_gene_variant STAD-US 11 118376836 118376836 single base substitution C T missense_variant P3369L 10106C>T STAD-US 11 118376836 118376836 single base substitution C T missense_variant P3407L 10220C>T STAD-US 11 118376836 118376836 single base substitution C T missense_variant P3410L 10229C>T STAD-US 11 118376836 118376836 single base substitution C T upstream_gene_variant STAD-US 11 118379858 118379858 single base substitution G A downstream_gene_variant STAD-US 11 118379858 118379858 single base substitution G A missense_variant A3574T 10720G>A STAD-US 11 118379858 118379858 single base substitution G A missense_variant A3612T 10834G>A STAD-US 11 118379858 118379858 single base substitution G A missense_variant A3615T 10843G>A STAD-US 11 118379858 118379858 single base substitution G A upstream_gene_variant STAD-US 11 118379895 118379895 single base substitution C T downstream_gene_variant STAD-US 11 118379895 118379895 single base substitution C T missense_variant A3586V 10757C>T STAD-US 11 118379895 118379895 single base substitution C T missense_variant A3624V 10871C>T STAD-US 11 118379895 118379895 single base substitution C T missense_variant A3627V 10880C>T STAD-US 11 118379895 118379895 single base substitution C T upstream_gene_variant STAD-US 11 118390341 118390341 single base substitution G A exon_variant STAD-US 11 118390341 118390341 single base substitution G A missense_variant G3678S 11032G>A STAD-US 11 118390341 118390341 single base substitution G A missense_variant G3716S 11146G>A STAD-US 11 118390341 118390341 single base substitution G A missense_variant G3719S 11155G>A STAD-US 11 118390341 118390341 single base substitution G A upstream_gene_variant STAD-US 11 118391558 118391558 single base substitution G A exon_variant STAD-US 11 118391558 118391558 single base substitution G A missense_variant R3783Q 11348G>A STAD-US 11 118391558 118391558 single base substitution G A missense_variant R3821Q 11462G>A STAD-US 11 118391558 118391558 single base substitution G A missense_variant R3824Q 11471G>A STAD-US 11 118391565 118391565 deletion of <=200bp A - exon_variant STAD-US 11 118391565 118391565 deletion of <=200bp A - frameshift_variant L3785 STAD-US 11 118391565 118391565 deletion of <=200bp A - frameshift_variant L3823 STAD-US 11 118391565 118391565 deletion of <=200bp A - frameshift_variant L3826 STAD-US 11 118392022 118392022 single base substitution G A exon_variant STAD-US 11 118392022 118392022 single base substitution G A missense_variant G3804S 11410G>A STAD-US 11 118392022 118392022 single base substitution G A missense_variant G3842S 11524G>A STAD-US 11 118392022 118392022 single base substitution G A missense_variant G3845S 11533G>A STAD-US 11 118392684 118392684 single base substitution C T exon_variant STAD-US 11 118392684 118392684 single base substitution C T missense_variant R3865C 11593C>T STAD-US 11 118392684 118392684 single base substitution C T missense_variant R3903C 11707C>T STAD-US 11 118392684 118392684 single base substitution C T missense_variant R3906C 11716C>T STAD-US 11 118392870 118392870 single base substitution C T exon_variant STAD-US 11 118392870 118392870 single base substitution C T missense_variant R3927W 11779C>T STAD-US 11 118392870 118392870 single base substitution C T missense_variant R3965W 11893C>T STAD-US 11 118392870 118392870 single base substitution C T missense_variant R3968W 11902C>T STAD-US 11 118398293 118398293 single base substitution C T downstream_gene_variant STAD-US 11 118399370 118399370 deletion of <=200bp G - downstream_gene_variant STAD-US 11 118399486 118399486 single base substitution G A downstream_gene_variant STAD-US 11 118399499 118399499 single base substitution C T downstream_gene_variant THCA-SA 11 118355642 118355642 single base substitution A C downstream_gene_variant THCA-SA 11 118355642 118355642 single base substitution A C intron_variant THCA-SA 11 118355642 118355642 single base substitution A C synonymous_variant I1428I 4284A>C THCA-SA 11 118368665 118368665 single base substitution A G synonymous_variant L1852L 5556A>G THCA-SA 11 118368665 118368665 single base substitution A G synonymous_variant L1890L 5670A>G THCA-SA 11 118368665 118368665 single base substitution A G synonymous_variant L1893L 5679A>G THCA-SA 11 118368665 118368665 single base substitution A G upstream_gene_variant THCA-SA 11 118373861 118373861 single base substitution C T exon_variant THCA-SA 11 118373861 118373861 single base substitution C T synonymous_variant N2377N 7131C>T THCA-SA 11 118373861 118373861 single base substitution C T synonymous_variant N2415N 7245C>T THCA-SA 11 118373861 118373861 single base substitution C T synonymous_variant N2418N 7254C>T THCA-SA 11 118373861 118373861 single base substitution C T upstream_gene_variant THCA-SA 11 118376831 118376831 single base substitution G T downstream_gene_variant THCA-SA 11 118376831 118376831 single base substitution G T missense_variant M3367I 10101G>T THCA-SA 11 118376831 118376831 single base substitution G T missense_variant M3405I 10215G>T THCA-SA 11 118376831 118376831 single base substitution G T missense_variant M3408I 10224G>T THCA-SA 11 118376831 118376831 single base substitution G T upstream_gene_variant THCA-SA 11 118376925 118376925 single base substitution A G downstream_gene_variant THCA-SA 11 118376925 118376925 single base substitution A G missense_variant I3399V 10195A>G THCA-SA 11 118376925 118376925 single base substitution A G missense_variant I3437V 10309A>G THCA-SA 11 118376925 118376925 single base substitution A G missense_variant I3440V 10318A>G THCA-SA 11 118376925 118376925 single base substitution A G upstream_gene_variant THCA-SA 11 118393856 118393856 single base substitution G T 3_prime_UTR_variant THCA-SA 11 118393856 118393856 single base substitution G T downstream_gene_variant THCA-US 11 118361935 118361935 single base substitution A G missense_variant K1536R 4607A>G THCA-US 11 118361935 118361935 single base substitution A G missense_variant K1574R 4721A>G THCA-US 11 118361935 118361935 single base substitution A G missense_variant K286R 857A>G THCA-US 11 118362606 118362606 single base substitution A C missense_variant N1615T 4844A>C THCA-US 11 118362606 118362606 single base substitution A C missense_variant N1653T 4958A>C THCA-US 11 118362606 118362606 single base substitution A C missense_variant N1656T 4967A>C THCA-US 11 118362606 118362606 single base substitution A C missense_variant N365T 1094A>C THCA-US 11 118374769 118374769 single base substitution A T downstream_gene_variant THCA-US 11 118374769 118374769 single base substitution A T missense_variant D2680V 8039A>T THCA-US 11 118374769 118374769 single base substitution A T missense_variant D2718V 8153A>T THCA-US 11 118374769 118374769 single base substitution A T missense_variant D2721V 8162A>T THCA-US 11 118374769 118374769 single base substitution A T upstream_gene_variant THCA-US 11 118374951 118374951 single base substitution A G downstream_gene_variant THCA-US 11 118374951 118374951 single base substitution A G missense_variant K2741E 8221A>G THCA-US 11 118374951 118374951 single base substitution A G missense_variant K2779E 8335A>G THCA-US 11 118374951 118374951 single base substitution A G missense_variant K2782E 8344A>G THCA-US 11 118374951 118374951 single base substitution A G upstream_gene_variant THCA-US 11 118375798 118375798 single base substitution A G downstream_gene_variant THCA-US 11 118375798 118375798 single base substitution A G missense_variant N3023S 9068A>G THCA-US 11 118375798 118375798 single base substitution A G missense_variant N3061S 9182A>G THCA-US 11 118375798 118375798 single base substitution A G missense_variant N3064S 9191A>G THCA-US 11 118375798 118375798 single base substitution A G upstream_gene_variant THCA-US 11 118379887 118379887 single base substitution A C downstream_gene_variant THCA-US 11 118379887 118379887 single base substitution A C missense_variant Q3583H 10749A>C THCA-US 11 118379887 118379887 single base substitution A C missense_variant Q3621H 10863A>C THCA-US 11 118379887 118379887 single base substitution A C missense_variant Q3624H 10872A>C THCA-US 11 118379887 118379887 single base substitution A C upstream_gene_variant THCA-US 11 118398234 118398234 single base substitution G A downstream_gene_variant UCEC-US 11 118342585 118342585 single base substitution T C intron_variant UCEC-US 11 118342585 118342585 single base substitution T C synonymous_variant H237H 711T>C UCEC-US 11 118342585 118342585 single base substitution T C synonymous_variant H270H 810T>C UCEC-US 11 118342612 118342612 single base substitution G T intron_variant UCEC-US 11 118342612 118342612 single base substitution G T missense_variant K246N 738G>T UCEC-US 11 118342612 118342612 single base substitution G T missense_variant K279N 837G>T UCEC-US 11 118342634 118342634 single base substitution A C intron_variant UCEC-US 11 118342634 118342634 single base substitution A C missense_variant K254Q 760A>C UCEC-US 11 118342634 118342634 single base substitution A C missense_variant K287Q 859A>C UCEC-US 11 118343056 118343056 single base substitution G A intron_variant UCEC-US 11 118343056 118343056 single base substitution G A synonymous_variant L394L 1182G>A UCEC-US 11 118343056 118343056 single base substitution G A synonymous_variant L427L 1281G>A UCEC-US 11 118343093 118343093 single base substitution C T intron_variant UCEC-US 11 118343093 118343093 single base substitution C T stop_gained R407* 1219C>T UCEC-US 11 118343093 118343093 single base substitution C T stop_gained R440* 1318C>T UCEC-US 11 118343153 118343153 single base substitution C T intron_variant UCEC-US 11 118343153 118343153 single base substitution C T missense_variant R427W 1279C>T UCEC-US 11 118343153 118343153 single base substitution C T missense_variant R460W 1378C>T UCEC-US 11 118347553 118347553 single base substitution C T downstream_gene_variant UCEC-US 11 118347553 118347553 single base substitution C T stop_gained R1064* 3190C>T UCEC-US 11 118347553 118347553 single base substitution C T stop_gained R1097* 3289C>T UCEC-US 11 118347553 118347553 single base substitution C T stop_gained R142* 424C>T UCEC-US 11 118347553 118347553 single base substitution C T upstream_gene_variant UCEC-US 11 118347672 118347672 single base substitution G T downstream_gene_variant UCEC-US 11 118347672 118347672 single base substitution G T missense_variant K1103N 3309G>T UCEC-US 11 118347672 118347672 single base substitution G T missense_variant K1136N 3408G>T UCEC-US 11 118347672 118347672 single base substitution G T missense_variant K181N 543G>T UCEC-US 11 118347672 118347672 single base substitution G T upstream_gene_variant UCEC-US 11 118348798 118348798 single base substitution C T downstream_gene_variant UCEC-US 11 118348798 118348798 single base substitution C T stop_gained R1151* 3451C>T UCEC-US 11 118348798 118348798 single base substitution C T stop_gained R1184* 3550C>T UCEC-US 11 118348798 118348798 single base substitution C T stop_gained R229* 685C>T UCEC-US 11 118348798 118348798 single base substitution C T upstream_gene_variant UCEC-US 11 118348802 118348802 single base substitution C T downstream_gene_variant UCEC-US 11 118348802 118348802 single base substitution C T missense_variant S1152L 3455C>T UCEC-US 11 118348802 118348802 single base substitution C T missense_variant S1185L 3554C>T UCEC-US 11 118348802 118348802 single base substitution C T missense_variant S230L 689C>T UCEC-US 11 118348802 118348802 single base substitution C T upstream_gene_variant UCEC-US 11 118348864 118348864 single base substitution T C downstream_gene_variant UCEC-US 11 118348864 118348864 single base substitution T C missense_variant C1173R 3517T>C UCEC-US 11 118348864 118348864 single base substitution T C missense_variant C1206R 3616T>C UCEC-US 11 118348864 118348864 single base substitution T C missense_variant C251R 751T>C UCEC-US 11 118348864 118348864 single base substitution T C upstream_gene_variant UCEC-US 11 118350938 118350938 single base substitution C T downstream_gene_variant UCEC-US 11 118350938 118350938 single base substitution C T stop_gained Q1207* 3619C>T UCEC-US 11 118350938 118350938 single base substitution C T stop_gained Q1240* 3718C>T UCEC-US 11 118350938 118350938 single base substitution C T upstream_gene_variant UCEC-US 11 118352561 118352561 single base substitution A C downstream_gene_variant UCEC-US 11 118352561 118352561 single base substitution A C missense_variant K1256Q 3766A>C UCEC-US 11 118352561 118352561 single base substitution A C missense_variant K1289Q 3865A>C UCEC-US 11 118352561 118352561 single base substitution A C missense_variant K6Q 16A>C UCEC-US 11 118352561 118352561 single base substitution A C upstream_gene_variant UCEC-US 11 118359367 118359367 single base substitution G T downstream_gene_variant UCEC-US 11 118359367 118359367 single base substitution G T missense_variant K1419N 4257G>T UCEC-US 11 118359367 118359367 single base substitution G T missense_variant K1457N 4371G>T UCEC-US 11 118359367 118359367 single base substitution G T missense_variant K169N 507G>T UCEC-US 11 118359428 118359428 single base substitution C T downstream_gene_variant UCEC-US 11 118359428 118359428 single base substitution C T missense_variant R1440C 4318C>T UCEC-US 11 118359428 118359428 single base substitution C T missense_variant R1478C 4432C>T UCEC-US 11 118359428 118359428 single base substitution C T missense_variant R190C 568C>T UCEC-US 11 118362576 118362576 single base substitution C A missense_variant S1605Y 4814C>A UCEC-US 11 118362576 118362576 single base substitution C A missense_variant S1643Y 4928C>A UCEC-US 11 118362576 118362576 single base substitution C A missense_variant S1646Y 4937C>A UCEC-US 11 118362576 118362576 single base substitution C A missense_variant S355Y 1064C>A UCEC-US 11 118362640 118362640 single base substitution G A downstream_gene_variant UCEC-US 11 118362640 118362640 single base substitution G A synonymous_variant R1626R 4878G>A UCEC-US 11 118362640 118362640 single base substitution G A synonymous_variant R1664R 4992G>A UCEC-US 11 118362640 118362640 single base substitution G A synonymous_variant R1667R 5001G>A UCEC-US 11 118363798 118363798 single base substitution C T downstream_gene_variant UCEC-US 11 118363798 118363798 single base substitution C T synonymous_variant P1636P 4908C>T UCEC-US 11 118363798 118363798 single base substitution C T synonymous_variant P1674P 5022C>T UCEC-US 11 118363798 118363798 single base substitution C T synonymous_variant P1677P 5031C>T UCEC-US 11 118371776 118371776 single base substitution G A exon_variant UCEC-US 11 118371776 118371776 single base substitution G A missense_variant R2037H 6110G>A UCEC-US 11 118371776 118371776 single base substitution G A missense_variant R2075H 6224G>A UCEC-US 11 118371776 118371776 single base substitution G A missense_variant R2078H 6233G>A UCEC-US 11 118371830 118371830 single base substitution G T exon_variant UCEC-US 11 118371830 118371830 single base substitution G T missense_variant R2055M 6164G>T UCEC-US 11 118371830 118371830 single base substitution G T missense_variant R2093M 6278G>T UCEC-US 11 118371830 118371830 single base substitution G T missense_variant R2096M 6287G>T UCEC-US 11 118373178 118373178 single base substitution C T exon_variant UCEC-US 11 118373178 118373178 single base substitution C T stop_gained R2150* 6448C>T UCEC-US 11 118373178 118373178 single base substitution C T stop_gained R2188* 6562C>T UCEC-US 11 118373178 118373178 single base substitution C T stop_gained R2191* 6571C>T UCEC-US 11 118373178 118373178 single base substitution C T upstream_gene_variant UCEC-US 11 118373353 118373353 single base substitution T G exon_variant UCEC-US 11 118373353 118373353 single base substitution T G missense_variant V2208G 6623T>G UCEC-US 11 118373353 118373353 single base substitution T G missense_variant V2246G 6737T>G UCEC-US 11 118373353 118373353 single base substitution T G missense_variant V2249G 6746T>G UCEC-US 11 118373353 118373353 single base substitution T G upstream_gene_variant UCEC-US 11 118373443 118373443 single base substitution A C exon_variant UCEC-US 11 118373443 118373443 single base substitution A C missense_variant K2238T 6713A>C UCEC-US 11 118373443 118373443 single base substitution A C missense_variant K2276T 6827A>C UCEC-US 11 118373443 118373443 single base substitution A C missense_variant K2279T 6836A>C UCEC-US 11 118373443 118373443 single base substitution A C upstream_gene_variant UCEC-US 11 118373690 118373690 single base substitution G A exon_variant UCEC-US 11 118373690 118373690 single base substitution G A synonymous_variant S2320S 6960G>A UCEC-US 11 118373690 118373690 single base substitution G A synonymous_variant S2358S 7074G>A UCEC-US 11 118373690 118373690 single base substitution G A synonymous_variant S2361S 7083G>A UCEC-US 11 118373690 118373690 single base substitution G A upstream_gene_variant UCEC-US 11 118373751 118373751 single base substitution C T exon_variant UCEC-US 11 118373751 118373751 single base substitution C T stop_gained R2341* 7021C>T UCEC-US 11 118373751 118373751 single base substitution C T stop_gained R2379* 7135C>T UCEC-US 11 118373751 118373751 single base substitution C T stop_gained R2382* 7144C>T UCEC-US 11 118373751 118373751 single base substitution C T upstream_gene_variant UCEC-US 11 118374094 118374094 single base substitution C T exon_variant UCEC-US 11 118374094 118374094 single base substitution C T missense_variant S2455F 7364C>T UCEC-US 11 118374094 118374094 single base substitution C T missense_variant S2493F 7478C>T UCEC-US 11 118374094 118374094 single base substitution C T missense_variant S2496F 7487C>T UCEC-US 11 118374094 118374094 single base substitution C T upstream_gene_variant UCEC-US 11 118374445 118374445 single base substitution G A downstream_gene_variant UCEC-US 11 118374445 118374445 single base substitution G A missense_variant G2572D 7715G>A UCEC-US 11 118374445 118374445 single base substitution G A missense_variant G2610D 7829G>A UCEC-US 11 118374445 118374445 single base substitution G A missense_variant G2613D 7838G>A UCEC-US 11 118374445 118374445 single base substitution G A upstream_gene_variant UCEC-US 11 118374685 118374685 single base substitution C A downstream_gene_variant UCEC-US 11 118374685 118374685 single base substitution C A missense_variant S2652Y 7955C>A UCEC-US 11 118374685 118374685 single base substitution C A missense_variant S2690Y 8069C>A UCEC-US 11 118374685 118374685 single base substitution C A missense_variant S2693Y 8078C>A UCEC-US 11 118374685 118374685 single base substitution C A upstream_gene_variant UCEC-US 11 118374928 118374928 single base substitution C A downstream_gene_variant UCEC-US 11 118374928 118374928 single base substitution C A missense_variant S2733Y 8198C>A UCEC-US 11 118374928 118374928 single base substitution C A missense_variant S2771Y 8312C>A UCEC-US 11 118374928 118374928 single base substitution C A missense_variant S2774Y 8321C>A UCEC-US 11 118374928 118374928 single base substitution C A upstream_gene_variant UCEC-US 11 118374970 118374970 single base substitution C A downstream_gene_variant UCEC-US 11 118374970 118374970 single base substitution C A missense_variant S2747Y 8240C>A UCEC-US 11 118374970 118374970 single base substitution C A missense_variant S2785Y 8354C>A UCEC-US 11 118374970 118374970 single base substitution C A missense_variant S2788Y 8363C>A UCEC-US 11 118374970 118374970 single base substitution C A upstream_gene_variant UCEC-US 11 118374995 118374995 single base substitution A G downstream_gene_variant UCEC-US 11 118374995 118374995 single base substitution A G synonymous_variant G2755G 8265A>G UCEC-US 11 118374995 118374995 single base substitution A G synonymous_variant G2793G 8379A>G UCEC-US 11 118374995 118374995 single base substitution A G synonymous_variant G2796G 8388A>G UCEC-US 11 118374995 118374995 single base substitution A G upstream_gene_variant UCEC-US 11 118375452 118375452 single base substitution C T downstream_gene_variant UCEC-US 11 118375452 118375452 single base substitution C T missense_variant P2908S 8722C>T UCEC-US 11 118375452 118375452 single base substitution C T missense_variant P2946S 8836C>T UCEC-US 11 118375452 118375452 single base substitution C T missense_variant P2949S 8845C>T UCEC-US 11 118375452 118375452 single base substitution C T upstream_gene_variant UCEC-US 11 118375755 118375755 single base substitution G A downstream_gene_variant UCEC-US 11 118375755 118375755 single base substitution G A missense_variant V3009M 9025G>A UCEC-US 11 118375755 118375755 single base substitution G A missense_variant V3047M 9139G>A UCEC-US 11 118375755 118375755 single base substitution G A missense_variant V3050M 9148G>A UCEC-US 11 118375755 118375755 single base substitution G A upstream_gene_variant UCEC-US 11 118376962 118376962 single base substitution A C downstream_gene_variant UCEC-US 11 118376962 118376962 single base substitution A C missense_variant H3411P 10232A>C UCEC-US 11 118376962 118376962 single base substitution A C missense_variant H3449P 10346A>C UCEC-US 11 118376962 118376962 single base substitution A C missense_variant H3452P 10355A>C UCEC-US 11 118376962 118376962 single base substitution A C upstream_gene_variant UCEC-US 11 118378313 118378313 single base substitution G A downstream_gene_variant UCEC-US 11 118378313 118378313 single base substitution G A exon_variant UCEC-US 11 118378313 118378313 single base substitution G A synonymous_variant G3567G 10701G>A UCEC-US 11 118378313 118378313 single base substitution G A synonymous_variant G3605G 10815G>A UCEC-US 11 118378313 118378313 single base substitution G A synonymous_variant G3608G 10824G>A UCEC-US 11 118378313 118378313 single base substitution G A upstream_gene_variant UCEC-US 11 118380737 118380737 single base substitution C T downstream_gene_variant UCEC-US 11 118380737 118380737 single base substitution C T exon_variant UCEC-US 11 118380737 118380737 single base substitution C T missense_variant R3618W 10852C>T UCEC-US 11 118380737 118380737 single base substitution C T missense_variant R3656W 10966C>T UCEC-US 11 118380737 118380737 single base substitution C T missense_variant R3659W 10975C>T UCEC-US 11 118390405 118390405 single base substitution C T exon_variant UCEC-US 11 118390405 118390405 single base substitution C T missense_variant A3699V 11096C>T UCEC-US 11 118390405 118390405 single base substitution C T missense_variant A3737V 11210C>T UCEC-US 11 118390405 118390405 single base substitution C T missense_variant A3740V 11219C>T UCEC-US 11 118390405 118390405 single base substitution C T upstream_gene_variant UCEC-US 11 118392101 118392101 single base substitution C A exon_variant UCEC-US 11 118392101 118392101 single base substitution C A missense_variant T3830N 11489C>A UCEC-US 11 118392101 118392101 single base substitution C A missense_variant T3868N 11603C>A UCEC-US 11 118392101 118392101 single base substitution C A missense_variant T3871N 11612C>A UCEC-US 11 118392633 118392633 single base substitution C T exon_variant UCEC-US 11 118392633 118392633 single base substitution C T stop_gained R3848* 11542C>T UCEC-US 11 118392633 118392633 single base substitution C T stop_gained R3886* 11656C>T UCEC-US 11 118392633 118392633 single base substitution C T stop_gained R3889* 11665C>T

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand TCGA-B5-A11E-01 COSM923604 c.11603C>A p.T3868N Substitution - Missense 11:118521386-118521386 + DM2 COSM5609410 c.6467C>T p.S2156F Substitution - Missense 11:118501828-118501828 + pfg006T COSM1638752 c.1507C>T p.R503W Substitution - Missense 11:118472666-118472666 + TCGA-UC-A7PF-01 COSM4830006 c.3742G>T p.A1248S Substitution - Missense 11:118481822-118481822 + 2492723 COSM245704 c.6222C>T p.C2074C Substitution - coding silent 11:118501059-118501059 + SH-4885 COSM1351609 c.2312delC p.P773fs*8 Deletion - Frameshift 11:118473471-118473471 + TCGA-B7-5816-01 COSM4018337 c.10041A>G p.Q3347Q Substitution - coding silent 11:118505942-118505942 + PD2148a COSM28468 c.1264delA p.I422fs*8 Deletion - Frameshift 11:118472423-118472423 + 2492706 COSM5716812 c.16C>T p.R6W Substitution - Missense 11:118436528-118436528 + ccRCC-90 COSM1662782 c.3139G>T p.D1047Y Substitution - Missense 11:118474298-118474298 + PD6318a COSM4384620 c.9674G>A p.R3225H Substitution - Missense 11:118505575-118505575 + 389 COSM4427543 c.198G>A p.A66A Substitution - coding silent 11:118436710-118436710 + LP6005334-DNA_F03 COSM4409809 c.11894G>A p.R3965Q Substitution - Missense 11:118522156-118522156 + TCGA-IR-A3LA-01 COSM4845519 c.4822G>A p.E1608K Substitution - Missense 11:118491755-118491755 + OSCC-GB_00270111 COSM3710009 c.8683G>T p.E2895* Substitution - Nonsense 11:118504584-118504584 + TCGA-12-0707 COSM2154532 c.9909A>G p.P3303P Substitution - coding silent 11:118505810-118505810 + TCGA-DK-A3X1-01 COSM3791224 c.5841C>T p.L1947L Substitution - coding silent 11:118498417-118498417 + YULAN COSM1704632 c.5519C>T p.P1840L Substitution - Missense 11:118495864-118495864 + RK048_C01 COSM1627818 c.7752A>G p.Q2584Q Substitution - coding silent 11:118503653-118503653 + HCC81 COSM1604165 c.4131G>A p.L1377L Substitution - coding silent 11:118484227-118484227 + TCGA-CC-A5UE-01 COSM415319 c.9838C>T p.R3280* Substitution - Nonsense 11:118505739-118505739 + ESO-051 COSM1257772 c.448G>C p.G150R Substitution - Missense 11:118468790-118468790 + SWE-2B COSM1178233 c.8969C>A p.T2990N Substitution - Missense 11:118504870-118504870 + TCGA-CG-4442-01 COSM4018314 c.5047C>T p.R1683C Substitution - Missense 11:118493108-118493108 + DM4 COSM5609416 c.10374C>T p.L3458L Substitution - coding silent 11:118506275-118506275 + HF-19967 COSM1192974 c.703_704insA p.I235fs*18 Insertion - Frameshift 11:118471862-118471863 + PD6080a COSM4384624 c.11214G>C p.K3738N Substitution - Missense 11:118519694-118519694 + TCGA-FS-A1ZS-06 COSM3443979 c.6370C>T p.R2124* Substitution - Nonsense 11:118501731-118501731 + TCGA-CM-6162-01 COSM1351615 c.3799G>A p.V1267I Substitution - Missense 11:118481879-118481879 + TCGA-24-1614-01 COSM78093 c.10648G>C p.G3550R Substitution - Missense 11:118506549-118506549 + TCGA-BR-8591-01 COSM4018349 c.11462G>A p.R3821Q Substitution - Missense 11:118520843-118520843 + 9642_PT COSM5753609 c.11522G>A p.R3841Q Substitution - Missense 11:118521305-118521305 + PD2164a COSM28466 c.7012A>T p.T2338S Substitution - Missense 11:118502913-118502913 + TCGA-G4-6309-01 COSM1351611 c.2584C>T p.R862* Substitution - Nonsense 11:118473743-118473743 + TCGA-A2-A25E-01 COSM1475077 c.2700_2701insTAAA p.S901fs*1 Insertion - Frameshift 11:118473859-118473860 + YUSCA COSM5371771 c.3146C>T p.P1049L Substitution - Missense 11:118474305-118474305 + 9642_CLM COSM5753609 c.11522G>A p.R3841Q Substitution - Missense 11:118521305-118521305 + T2269 COSM282814 c.7044C>T p.I2348I Substitution - coding silent 11:118502945-118502945 + 274T COSM1725054 c.10240_10241insC p.S3416fs*10 Insertion - Frameshift 11:118506141-118506142 + OSCC-GB_00070111 COSM3710007 c.4965G>A p.R1655R Substitution - coding silent 11:118491898-118491898 + I2L-P19Tb-Tumor-Biopsy COSM5360766 c.5878C>T p.R1960* Substitution - Nonsense 11:118498454-118498454 + 2492721 COSM5721817 c.4522G>A p.E1508K Substitution - Missense 11:118489834-118489834 + 76 COSM3732778 c.4650delT p.H1551fs*35 Deletion - Frameshift 11:118490203-118490203 + YUDUTY COSM1704636 c.6782C>T p.S2261F Substitution - Missense 11:118502683-118502683 + PD11773a COSM5024904 c.8011T>G p.L2671V Substitution - Missense 11:118503912-118503912 + TCGA-FP-A4BE-01 COSM4018345 c.10871C>T p.A3624V Substitution - Missense 11:118509180-118509180 + 2492721 COSM5724107 c.34C>T p.R12* Substitution - Nonsense 11:118436546-118436546 + TCGA-A6-5666-01 COSM1351613 c.3460C>T p.R1154W Substitution - Missense 11:118478092-118478092 + TCGA-BH-A0DE-01 COSM428499 c.6150-1G>A p.? Unknown 11:118500986-118500986 + MM1S COSM1235526 c.10318G>A p.A3440T Substitution - Missense 11:118506219-118506219 + TCGA-EE-A2GN-06 COSM3443985 c.6985C>T p.P2329S Substitution - Missense 11:118502886-118502886 + LUAD-S01345 COSM396841 c.5631G>C p.L1877F Substitution - Missense 11:118496343-118496343 + LUAD-CHTN-MAD08-00104 COSM361130 c.6445A>G p.S2149G Substitution - Missense 11:118501806-118501806 + TCGA-FW-A3R5-06 COSM3868521 c.1728C>T p.S576S Substitution - coding silent 11:118472887-118472887 + T3724 COSM4702383 c.2992A>G p.T998A Substitution - Missense 11:118474151-118474151 + 2293782 COSM4608349 c.500C>A p.S167* Substitution - Nonsense 11:118468842-118468842 + HCC81T COSM1604165 c.4131G>A p.L1377L Substitution - coding silent 11:118484227-118484227 + TCGA-B5-A11O-01 COSM923593 c.7864C>T p.R2622C Substitution - Missense 11:118503765-118503765 + 587376 COSM1215182 c.4081G>T p.E1361* Substitution - Nonsense 11:118482490-118482490 + MOLT-4 COSM1676466 c.4234G>A p.E1412K Substitution - Missense 11:118484877-118484877 + TCGA-D8-A27G-01 COSM3808493 c.9855C>T p.I3285I Substitution - coding silent 11:118505756-118505756 + TCGA-AG-A002-01 COSM262033 c.2207G>T p.R736M Substitution - Missense 11:118473366-118473366 + CSCC-27-T COSM4492295 c.3958C>T p.P1320S Substitution - Missense 11:118482038-118482038 + ESCC_118 COSM5640159 c.9154G>A p.D3052N Substitution - Missense 11:118505055-118505055 + OSCC-GB_00670111 COSM4883814 c.4592T>C p.V1531A Substitution - Missense 11:118490145-118490145 + HCC147 COSM3666007 c.6800A>G p.Q2267R Substitution - Missense 11:118502701-118502701 + AOCS-112-1-2 COSM2105312 c.351G>A p.Q117Q Substitution - coding silent 11:118436863-118436863 + MOLT-4 COSM1676472 c.7383G>T p.K2461N Substitution - Missense 11:118503284-118503284 + TCGA-AC-A23H-01 COSM3808495 c.10130C>T p.S3377L Substitution - Missense 11:118506031-118506031 + TCGA-DM-A1D4-01 COSM1351605 c.1442G>A p.S481N Substitution - Missense 11:118472601-118472601 + TCGA-A8-A0A6-01 COSM3808489 c.9476A>C p.H3159P Substitution - Missense 11:118505377-118505377 + Pat_76_A COSM5837927 c.3842C>T p.P1281L Substitution - Missense 11:118481922-118481922 + B35 COSM254812 c.11348C>G p.S3783C Substitution - Missense 11:118519992-118519992 + TCGA-FW-A3R5-06 COSM3868523 c.6442C>T p.P2148S Substitution - Missense 11:118501803-118501803 + TARGET-30-PAPYNZ COSM1286205 c.6772C>A p.Q2258K Substitution - Missense 11:118502673-118502673 + TCGA-37-3783-01 COSM686164 c.8124G>A p.Q2708Q Substitution - coding silent 11:118504025-118504025 + LUAD-B01811 COSM333792 c.329C>A p.P110Q Substitution - Missense 11:118436841-118436841 + 169 COSM1215168 c.3941C>T p.P1314L Substitution - Missense 11:118482021-118482021 + TCGA-CD-A4MI-01 COSM4018284 c.1259G>A p.R420Q Substitution - Missense 11:118472418-118472418 + TCGA-FD-A3N5-01 COSM1297696 c.5676T>G p.Y1892* Substitution - Nonsense 11:118497956-118497956 + TCGA-CG-4465-01 COSM4018304 c.4355G>T p.C1452F Substitution - Missense 11:118488636-118488636 + 2492730 COSM5729064 c.2796G>A p.G932G Substitution - coding silent 11:118473955-118473955 + TCGA-BT-A20Q-01 COSM415325 c.7516G>A p.E2506K Substitution - Missense 11:118503417-118503417 + HCC2998 COSM1676474 c.9457T>G p.L3153V Substitution - Missense 11:118505358-118505358 + PT52 COSM5940145 c.5960C>T p.P1987L Substitution - Missense 11:118499310-118499310 + TCGA-A5-A0GP-01 COSM923591 c.7478C>T p.S2493F Substitution - Missense 11:118503379-118503379 + TCGA-E8-A419-01 COSM3368243 c.10863A>C p.Q3621H Substitution - Missense 11:118509172-118509172 + DM45 COSM3443947 c.2233C>T p.R745* Substitution - Nonsense 11:118473392-118473392 + PD5727a COSM2105558 c.7795A>G p.M2599V Substitution - Missense 11:118503696-118503696 + HCT15 COSM1351607 c.2311_2312insC p.S774fs*12 Insertion - Frameshift 11:118473470-118473471 + TCGA-BR-8485-01 COSM4018355 c.11893C>T p.R3965W Substitution - Missense 11:118522155-118522155 + TCGA-CJ-4912-01 COSM466400 c.6138T>A p.P2046P Substitution - coding silent 11:118499902-118499902 + TCGA-AZ-6598-01 COSM1351640 c.5736A>G p.E1912E Substitution - coding silent 11:118498016-118498016 + TCGA-AX-A0J0-01 COSM923594 c.8069C>A p.S2690Y Substitution - Missense 11:118503970-118503970 + Pat_32_A COSM282816 c.10342G>A p.E3448K Substitution - Missense 11:118506243-118506243 + B9 COSM253764 c.4437C>A p.C1479* Substitution - Nonsense 11:118488718-118488718 + LB831-BLC COSM25626 c.7062delC p.S2355fs*18 Deletion - Frameshift 11:118502961-118502961 + TCGA-B8-5159-01 COSM466402 c.7544C>A p.P2515Q Substitution - Missense 11:118503445-118503445 + 2492720 COSM245704 c.6222C>T p.C2074C Substitution - coding silent 11:118501059-118501059 + TCGA-FW-A3R5-06 COSM3868529 c.8783C>T p.P2928L Substitution - Missense 11:118504684-118504684 + PR-2916 COSM245705 c.5820A>T p.G1940G Substitution - coding silent 11:118498396-118498396 + HCC61T COSM1604167 c.7093C>G p.L2365V Substitution - Missense 11:118502994-118502994 + PD6944a COSM4384600 c.5414G>A p.W1805* Substitution - Nonsense 11:118495759-118495759 + TCGA-AN-A0FW-01 COSM2105509 c.5590delC p.P1865fs*3 Deletion - Frameshift 11:118496302-118496302 + TCGA-AA-A010-01 COSM282815 c.7989A>G p.G2663G Substitution - coding silent 11:118503890-118503890 + TCGA-FW-A3R5-06 COSM3868525 c.7712C>T p.A2571V Substitution - Missense 11:118503613-118503613 + SH-7329 COSM5020622 c.5670A>G p.L1890L Substitution - coding silent 11:118497950-118497950 + TCGA-G4-6588-01 COSM1351619 c.3948delA p.E1318fs*38 Deletion - Frameshift 11:118482028-118482028 + TCGA-JW-A852-01 COSM4823785 c.10317C>T p.A3439A Substitution - coding silent 11:118506218-118506218 + HCT15 COSM1676464 c.3185C>A p.S1062Y Substitution - Missense 11:118476833-118476833 + ESCC-F83 COSM5048801 c.1948A>C p.N650H Substitution - Missense 11:118473107-118473107 + DLD1 COSM2105644 c.11271C>A p.P3757P Substitution - coding silent 11:118519751-118519751 + PD7379a COSM1351675 c.11456G>A p.R3819H Substitution - Missense 11:118520837-118520837 + TCGA-AX-A05Z-01 COSM923579 c.3766A>C p.K1256Q Substitution - Missense 11:118481846-118481846 + TCGA-AZ-6598-01 COSM1351661 c.9587delT p.L3197fs*15 Deletion - Frameshift 11:118505488-118505488 + TCGA-AR-A1AT-01 COSM1475082 c.4101G>A p.P1367P Substitution - coding silent 11:118484197-118484197 + B112 COSM254811 c.4437C>G p.C1479W Substitution - Missense 11:118488718-118488718 + T613 COSM4702395 c.6714A>G p.S2238S Substitution - coding silent 11:118502615-118502615 + SH-7329 COSM5020616 c.4284A>C p.I1428I Substitution - coding silent 11:118484927-118484927 + YUKAT COSM5371769 c.3081A>G p.L1027L Substitution - coding silent 11:118474240-118474240 + PD18749a COSM5780602 c.4909G>A p.E1637K Substitution - Missense 11:118491842-118491842 + DM77 COSM5609422 c.8485C>T p.L2829L Substitution - coding silent 11:118504386-118504386 + 100912 COSM96030 c.1281G>T p.R427R Substitution - coding silent 11:118472440-118472440 + TCGA-DK-A1A3-01 COSM415327 c.2637G>A p.E879E Substitution - coding silent 11:118473796-118473796 + TCGA-CA-6718-01 COSM1351663 c.9863G>T p.R3288I Substitution - Missense 11:118505764-118505764 + ESO-0079 COSM1257770 c.11719C>G p.H3907D Substitution - Missense 11:118521981-118521981 + BD191T COSM5490586 c.11480C>G p.S3827C Substitution - Missense 11:118520861-118520861 + 2492724 COSM5724942 c.6783C>T p.S2261S Substitution - coding silent 11:118502684-118502684 + BON-1 COSM5368386 c.10011T>A p.S3337R Substitution - Missense 11:118505912-118505912 + 587332 COSM1215172 c.2858C>T p.T953I Substitution - Missense 11:118474017-118474017 + BD189T COSM5490632 c.5549-1G>A p.? Unknown 11:118496260-118496260 + 387 COSM4427220 c.7171T>C p.S2391P Substitution - Missense 11:118503072-118503072 + ME050T COSM230690 c.4961C>T p.S1654F Substitution - Missense 11:118491894-118491894 + TCGA-CF-A1HR-01 COSM415324 c.7516G>C p.E2506Q Substitution - Missense 11:118503417-118503417 + TCGA-BP-5170-01 COSM3359031 c.6485T>A p.L2162* Substitution - Nonsense 11:118501846-118501846 + S00933 COSM317632 c.4268T>C p.L1423S Substitution - Missense 11:118484911-118484911 + TCGA-BG-A0VW-01 COSM923600 c.10346A>C p.H3449P Substitution - Missense 11:118506247-118506247 + TCGA-AA-A010-01 COSM282813 c.5927G>A p.R1976Q Substitution - Missense 11:118498503-118498503 + TCGA-AA-3672-01 COSM266934 c.11708G>A p.R3903H Substitution - Missense 11:118521970-118521970 + TCGA-AP-A051-01 COSM923573 c.3190C>T p.R1064* Substitution - Nonsense 11:118476838-118476838 + CRC-03T COSM5451120 c.5447A>T p.Q1816L Substitution - Missense 11:118495792-118495792 + 2492720 COSM5721820 c.11236C>T p.R3746C Substitution - Missense 11:118519716-118519716 + PD6503a COSM4384626 c.11283C>A p.H3761Q Substitution - Missense 11:118519763-118519763 + CHC1738T COSM4805288 c.10244C>T p.P3415L Substitution - Missense 11:118506145-118506145 + 587342 COSM1215178 c.11626G>A p.D3876N Substitution - Missense 11:118521409-118521409 + ACINAR28 COSM1732942 c.10570C>T p.R3524W Substitution - Missense 11:118506471-118506471 + ccRCC-24 COSM1662778 c.770A>G p.K257R Substitution - Missense 11:118471929-118471929 + TCGA-A8-A0A6-01 COSM3808473 c.1782A>C p.S594S Substitution - coding silent 11:118472941-118472941 + 392 COSM4428051 c.5332G>A p.E1778K Substitution - Missense 11:118494745-118494745 + TCGA-DA-A3F8-06 COSM1704638 c.7111C>T p.H2371Y Substitution - Missense 11:118503012-118503012 + 42 COSM1676466 c.4234G>A p.E1412K Substitution - Missense 11:118484877-118484877 + PD6985a COSM4384610 c.7664C>T p.P2555L Substitution - Missense 11:118503565-118503565 + 09-341 COSM1645515 c.4897C>T p.R1633* Substitution - Nonsense 11:118491830-118491830 + LUAD-NYU408 COSM374076 c.7098C>T p.S2366S Substitution - coding silent 11:118502999-118502999 + 40M COSM5585777 c.5527C>T p.P1843S Substitution - Missense 11:118495872-118495872 + ESCC_63 COSM5633274 c.35G>T p.R12L Substitution - Missense 11:118436547-118436547 + TCGA-BT-A20N-01 COSM415322 c.8293G>C p.E2765Q Substitution - Missense 11:118504194-118504194 + CSCC-27-T COSM4497834 c.5054C>T p.S1685F Substitution - Missense 11:118493115-118493115 + TCGA-D5-6930-01 COSM1351609 c.2312delC p.P773fs*8 Deletion - Frameshift 11:118473471-118473471 + B35-Tumor COSM254812 c.11348C>G p.S3783C Substitution - Missense 11:118519992-118519992 + TCGA-BR-4362-01 COSM4018327 c.7980A>G p.S2660S Substitution - coding silent 11:118503881-118503881 + HCC13T COSM1604173 c.10485delG p.E3496fs*52 Deletion - Frameshift 11:118506386-118506386 + HCT15 COSM2105644 c.11271C>A p.P3757P Substitution - coding silent 11:118519751-118519751 + PD4937a COSM162498 c.1291G>A p.D431N Substitution - Missense 11:118472450-118472450 + TCGA-EI-6917-01 COSM2105358 c.1629G>A p.T543T Substitution - coding silent 11:118472788-118472788 + CSB34 COSM5027498 c.9871T>C p.S3291P Substitution - Missense 11:118505772-118505772 + YUMOKI COSM5371781 c.11340C>T p.F3780F Substitution - coding silent 11:118519984-118519984 + B112 COSM254811 c.4437C>G p.C1479W Substitution - Missense 11:118488718-118488718 + PD6125a COSM4384602 c.6364C>T p.P2122S Substitution - Missense 11:118501725-118501725 + pfg043T COSM4760544 c.6447T>G p.S2149R Substitution - Missense 11:118501808-118501808 + TCGA-A8-A0A6-01 COSM3808477 c.3733A>C p.T1245P Substitution - Missense 11:118481813-118481813 + I2L-P19Ta-Tumor-Organoid COSM5360576 c.10511C>A p.A3504D Substitution - Missense 11:118506412-118506412 + PD6081a COSM4384594 c.4738G>A p.D1580N Substitution - Missense 11:118491237-118491237 + TCGA-A2-A3Y0-01 COSM5831667 c.6800delA p.R2268fs*6 Deletion - Frameshift 11:118502701-118502701 + TCGA-AP-A056-01 COSM923582 c.4928C>A p.S1643Y Substitution - Missense 11:118491861-118491861 + TCGA-06-2565-01 COSM3397448 c.9575C>T p.P3192L Substitution - Missense 11:118505476-118505476 + CHC1616T COSM4803638 c.4111C>T p.Q1371* Substitution - Nonsense 11:118484207-118484207 + RKO COSM1351609 c.2312delC p.P773fs*8 Deletion - Frameshift 11:118473471-118473471 + 8053106 COSM3808471 c.1325G>A p.R442Q Substitution - Missense 11:118472484-118472484 + LIM1215 COSM4184876 c.2720C>A p.P907H Substitution - Missense 11:118473879-118473879 + 2492705 COSM5716812 c.16C>T p.R6W Substitution - Missense 11:118436528-118436528 + TCGA-24-1553-01 COSM79384 c.1504G>T p.E502* Substitution - Nonsense 11:118472663-118472663 + TCGA-CM-6171-01 COSM1351642 c.5810delA p.K1938fs*43 Deletion - Frameshift 11:118498386-118498386 + 970010 COSM1582078 c.11546T>G p.I3849S Substitution - Missense 11:118521329-118521329 + STC246 COSM4018294 c.2656C>T p.R886W Substitution - Missense 11:118473815-118473815 + 193 COSM3722541 c.5655T>A p.N1885K Substitution - Missense 11:118496367-118496367 + SWE-26 COSM1179221 c.5698C>T p.H1900Y Substitution - Missense 11:118497978-118497978 + PD8028a COSM5945210 c.5718G>A p.W1906* Substitution - Nonsense 11:118497998-118497998 + TCGA-ER-A3ET-06 COSM3443989 c.7265C>T p.S2422F Substitution - Missense 11:118503166-118503166 + CSCC-6-T COSM4514623 c.981C>T p.P327P Substitution - coding silent 11:118472140-118472140 + TCGA-CG-5721-01 COSM4018325 c.7966C>T p.R2656* Substitution - Nonsense 11:118503867-118503867 + ESCC_31 COSM5627760 c.8743A>G p.I2915V Substitution - Missense 11:118504644-118504644 + TCGA-43-2578-01 COSM686167 c.5745C>A p.D1915E Substitution - Missense 11:118498025-118498025 + PT33 COSM5894938 c.3570-5C>T p.? Unknown 11:118480169-118480169 + B9 COSM253764 c.4437C>A p.C1479* Substitution - Nonsense 11:118488718-118488718 + ID01 COSM1166675 c.7384C>A p.P2462T Substitution - Missense 11:118503285-118503285 + I2L-P19Ta-Tumor-Biopsy COSM5360576 c.10511C>A p.A3504D Substitution - Missense 11:118506412-118506412 + TCGA-BC-A10Q-01 COSM4927676 c.6891G>A p.V2297V Substitution - coding silent 11:118502792-118502792 + TCGA-EK-A3GK-01 COSM4854511 c.9598G>C p.E3200Q Substitution - Missense 11:118505499-118505499 + 587342 COSM1215176 c.2798G>A p.R933Q Substitution - Missense 11:118473957-118473957 + HCT15 COSM2105414 c.2817T>C p.H939H Substitution - coding silent 11:118473976-118473976 + CSCC-44-T COSM4529345 c.1603G>A p.E535K Substitution - Missense 11:118472762-118472762 + PDA_043 COSM5000374 c.10666_10667delAA p.K3556fs*10 Deletion - Frameshift 11:118506567-118506568 + TCGA-EE-A3AF-06 COSM3444003 c.8801T>A p.L2934* Substitution - Nonsense 11:118504702-118504702 + HDC90 COSM4637253 c.5388T>G p.P1796P Substitution - coding silent 11:118495733-118495733 + DM93 COSM5609430 c.7822G>A p.E2608K Substitution - Missense 11:118503723-118503723 + TCGA-FS-A1Z3-06 COSM3444005 c.8819C>T p.T2940I Substitution - Missense 11:118504720-118504720 + TCGA-D7-6528-01 COSM4018331 c.8403C>T p.L2801L Substitution - coding silent 11:118504304-118504304 + 587284 COSM1215174 c.2797C>T p.R933W Substitution - Missense 11:118473956-118473956 + BD124T COSM2105341 c.1137delA p.K381fs*19 Deletion - Frameshift 11:118472296-118472296 + ESO-141 COSM1257774 c.8591G>A p.G2864D Substitution - Missense 11:118504492-118504492 + CSCC-19-T COSM4500168 c.5581C>T p.L1861L Substitution - coding silent 11:118496293-118496293 + 2318496 COSM4777306 c.3542G>T p.G1181V Substitution - Missense 11:118478174-118478174 + PD1768a COSM27618 c.5711C>T p.A1904V Substitution - Missense 11:118497991-118497991 + ICGC_MB66 COSM3764282 c.3461G>A p.R1154Q Substitution - Missense 11:118478093-118478093 + TCGA-AZ-4315-01 COSM1351626 c.4594C>T p.R1532C Substitution - Missense 11:118490147-118490147 + TCGA-DK-A1AC-01 COSM1297692 c.3493G>A p.E1165K Substitution - Missense 11:118478125-118478125 + sysucc-311T COSM5477439 c.2234G>A p.R745Q Substitution - Missense 11:118473393-118473393 + S03-26121-TP COSM4990126 c.5138G>A p.R1713K Substitution - Missense 11:118493199-118493199 + CSCC-62-T COSM4456419 c.10088C>T p.T3363I Substitution - Missense 11:118505989-118505989 + PD6113a COSM4384582 c.455G>A p.G152D Substitution - Missense 11:118468797-118468797 + TCGA-AX-A0J1-01 COSM923570 c.1182G>A p.L394L Substitution - coding silent 11:118472341-118472341 + 1517_PT COSM5753605 c.1482G>T p.E494D Substitution - Missense 11:118472641-118472641 + TCGA-FW-A3R5-06 COSM3868527 c.8537C>A p.P2846H Substitution - Missense 11:118504438-118504438 + E18 COSM1666193 c.8873A>C p.K2958T Substitution - Missense 11:118504774-118504774 + cSCCP1 COSM136035 c.11594C>T p.S3865F Substitution - Missense 11:118521377-118521377 + 27T COSM3710009 c.8683G>T p.E2895* Substitution - Nonsense 11:118504584-118504584 + B103 COSM254810 c.4368C>A p.H1456Q Substitution - Missense 11:118488649-118488649 + TCGA-BR-6452-01 COSM4018341 c.10220C>T p.P3407L Substitution - Missense 11:118506121-118506121 + PD6235a COSM1732940 c.8449G>A p.D2817N Substitution - Missense 11:118504350-118504350 + 16638 COSM48570 c.6611G>A p.R2204Q Substitution - Missense 11:118502512-118502512 + PD6810a COSM2105392 c.2684A>G p.K895R Substitution - Missense 11:118473843-118473843 + C086 COSM5534582 c.9409C>T p.P3137S Substitution - Missense 11:118505310-118505310 + EOPC-022_tumor COSM5950624 c.6486G>C p.L2162F Substitution - Missense 11:118501847-118501847 + TCGA-AP-A051-01 COSM923568 c.738G>T p.K246N Substitution - Missense 11:118471897-118471897 + PD6120a COSM4384612 c.8221C>G p.P2741A Substitution - Missense 11:118504122-118504122 + HCT-15 COSM1676464 c.3185C>A p.S1062Y Substitution - Missense 11:118476833-118476833 + Pat_53_A COSM1351607 c.2311_2312insC p.S774fs*12 Insertion - Frameshift 11:118473470-118473471 + TCGA-FS-A1YW-06 COSM3444011 c.9449G>A p.S3150N Substitution - Missense 11:118505350-118505350 + SNUH_G15_S1 COSM3675996 c.2331T>C p.S777S Substitution - coding silent 11:118473490-118473490 + 169 COSM3729846 c.11265_11266insC p.N3759fs*9 Insertion - Frameshift 11:118519745-118519746 + S00472 COSM317631 c.9479A>G p.Q3160R Substitution - Missense 11:118505380-118505380 + TCGA-CG-5726-01 COSM4018302 c.4087G>A p.E1363K Substitution - Missense 11:118484183-118484183 + CHC889T COSM4954414 c.3235C>T p.L1079F Substitution - Missense 11:118476883-118476883 + SH-7329 COSM5020404 c.7245C>T p.N2415N Substitution - coding silent 11:118503146-118503146 + KM12 COSM2105618 c.10528A>G p.T3510A Substitution - Missense 11:118506429-118506429 + LUAD-NYU796 COSM376340 c.4739A>T p.D1580V Substitution - Missense 11:118491238-118491238 + LUAD-E00897 COSM364311 c.1280_1281GG>TT p.R427>? Complex 11:118472439-118472440 + TCGA-60-2726-01 COSM686166 c.6375T>A p.P2125P Substitution - coding silent 11:118501736-118501736 + DM10 COSM5609394 c.4709C>A p.P1570H Substitution - Missense 11:118491208-118491208 + YUBER COSM1704628 c.4060C>T p.P1354S Substitution - Missense 11:118482469-118482469 + B69 COSM255058 c.4427_4429delGTC p.R1478delR Deletion - In frame 11:118488708-118488710 + PT09_2 COSM5894938 c.3570-5C>T p.? Unknown 11:118480169-118480169 + DM51 COSM5609418 c.7277G>A p.R2426K Substitution - Missense 11:118503178-118503178 + TCGA-D1-A15X-01 COSM923567 c.711T>C p.H237H Substitution - coding silent 11:118471870-118471870 + TCGA-CZ-5465-01 COSM466406 c.11261A>G p.N3754S Substitution - Missense 11:118519741-118519741 + 2492722 COSM245704 c.6222C>T p.C2074C Substitution - coding silent 11:118501059-118501059 + B34 COSM1745549 c.8333_8334insA p.M2780fs*3 Insertion - Frameshift 11:118504234-118504235 + HCC2998 COSM1676474 c.9457T>G p.L3153V Substitution - Missense 11:118505358-118505358 + HCC147T COSM3666007 c.6800A>G p.Q2267R Substitution - Missense 11:118502701-118502701 + PD6861a COSM4384630 c.11792T>C p.M3931T Substitution - Missense 11:118522054-118522054 + SH-4435 COSM5020167 c.3291A>G p.P1097P Substitution - coding silent 11:118476939-118476939 + TCGA-F1-6874-01 COSM4018329 c.8073A>G p.S2691S Substitution - coding silent 11:118503974-118503974 + 19 COSM5747332 c.1320T>G p.I440M Substitution - Missense 11:118472479-118472479 + T3535 COSM1351607 c.2311_2312insC p.S774fs*12 Insertion - Frameshift 11:118473470-118473471 + HCT-15 COSM1676470 c.6533T>C p.V2178A Substitution - Missense 11:118502434-118502434 + TCGA-MK-A4N6-01 COSM3368241 c.8335A>G p.K2779E Substitution - Missense 11:118504236-118504236 + TCGA-AZ-6598-01 COSM1351624 c.4400T>C p.L1467P Substitution - Missense 11:118488681-118488681 + PD11741a COSM5801687 c.1379delA p.K461fs*106 Deletion - Frameshift 11:118472538-118472538 + 2557_CLM COSM5753607 c.9718C>G p.P3240A Substitution - Missense 11:118505619-118505619 + TCGA-BR-8680-01 COSM4018300 c.3962A>C p.K1321T Substitution - Missense 11:118482042-118482042 + TCGA-BR-A4CS-01 COSM4018335 c.9205C>T p.P3069S Substitution - Missense 11:118505106-118505106 + TCGA-EB-A553-01 COSM3443999 c.8448C>T p.S2816S Substitution - coding silent 11:118504349-118504349 + TCGA-F1-6177-01 COSM4018294 c.2656C>T p.R886W Substitution - Missense 11:118473815-118473815 + PT42 COSM5925589 c.2252C>T p.P751L Substitution - Missense 11:118473411-118473411 + YUKAT COSM5371777 c.6392C>T p.S2131F Substitution - Missense 11:118501753-118501753 + PD9577a COSM5785981 c.4642C>T p.Q1548* Substitution - Nonsense 11:118490195-118490195 + TCGA-EE-A181-06 COSM1704628 c.4060C>T p.P1354S Substitution - Missense 11:118482469-118482469 + CN-AML-NR-36-Dx COSM5427115 c.4186G>A p.D1396N Substitution - Missense 11:118484282-118484282 + ccRCC-64 COSM1659800 c.3495G>A p.E1165E Substitution - coding silent 11:118478127-118478127 + ESCC_134 COSM5642704 c.11744C>G p.S3915C Substitution - Missense 11:118522006-118522006 + TCGA-27-2524-01 COSM3397450 c.11095G>C p.E3699Q Substitution - Missense 11:118511983-118511983 + TCGA-D1-A101-01 COSM923581 c.4432C>T p.R1478C Substitution - Missense 11:118488713-118488713 + TCGA-EJ-7782-01 COSM1638752 c.1507C>T p.R503W Substitution - Missense 11:118472666-118472666 + MZ7-mel COSM25628 c.6508C>T p.P2170S Substitution - Missense 11:118502409-118502409 + PD6914a COSM4384618 c.9224C>G p.T3075S Substitution - Missense 11:118505125-118505125 + CHC889T COSM4954414 c.3235C>T p.L1079F Substitution - Missense 11:118476883-118476883 + CHC892T COSM4959895 c.391G>A p.A131T Substitution - Missense 11:118436903-118436903 + GBM_IV-21 COSM4967092 c.7290A>C p.K2430N Substitution - Missense 11:118503191-118503191 + PD5734a COSM4384606 c.7223G>A p.S2408N Substitution - Missense 11:118503124-118503124 + TCGA-DU-5853-01 COSM3967346 c.2427T>A p.S809S Substitution - coding silent 11:118473586-118473586 + TCGA-AN-A046-01 COSM3808497 c.11222G>A p.R3741Q Substitution - Missense 11:118519702-118519702 + TCGA-A6-6142-01 COSM1351649 c.7444G>A p.V2482I Substitution - Missense 11:118503345-118503345 + TCGA-EB-A3XD-01 COSM3443971 c.5321C>T p.S1774F Substitution - Missense 11:118494734-118494734 + PCSI_0468_Pa_P_526 COSM4809344 c.843C>T p.L281L Substitution - coding silent 11:118472002-118472002 + TCGA-AX-A05Z-01 COSM923598 c.8836C>T p.P2946S Substitution - Missense 11:118504737-118504737 + B103 COSM254810 c.4368C>A p.H1456Q Substitution - Missense 11:118488649-118488649 + CSCC-31-T COSM4486120 c.3014C>T p.S1005F Substitution - Missense 11:118474173-118474173 + TCGA-AZ-4615-01 COSM3687109 c.11880C>T p.G3960G Substitution - coding silent 11:118522142-118522142 + TCGA-AA-3492-01 COSM1351607 c.2311_2312insC p.S774fs*12 Insertion - Frameshift 11:118473470-118473471 + DLD1 COSM2105414 c.2817T>C p.H939H Substitution - coding silent 11:118473976-118473976 + XHDG53C COSM4767756 c.9933C>A p.A3311A Substitution - coding silent 11:118505834-118505834 + TCGA-D3-A1QA-06 COSM3443969 c.5299C>T p.P1767S Substitution - Missense 11:118494712-118494712 + YUSCA COSM5371775 c.5224G>A p.G1742R Substitution - Missense 11:118494342-118494342 + PCSI_0528_Pa_P_526 COSM5032100 c.7248A>G p.E2416E Substitution - coding silent 11:118503149-118503149 + TCGA-A2-A0EY-01 COSM428500 c.8606C>T p.S2869L Substitution - Missense 11:118504507-118504507 + DM10 COSM5609398 c.11113C>A p.R3705S Substitution - Missense 11:118512001-118512001 + B73 COSM254815 c.7556C>T p.T2519I Substitution - Missense 11:118503457-118503457 + TCGA-EE-A2GC-06 COSM1351611 c.2584C>T p.R862* Substitution - Nonsense 11:118473743-118473743 + HCC56 COSM1604163 c.3216C>T p.C1072C Substitution - coding silent 11:118476864-118476864 + TCGA-CZ-4865-01 COSM3359033 c.8435C>A p.T2812K Substitution - Missense 11:118504336-118504336 + B73 COSM254815 c.7556C>T p.T2519I Substitution - Missense 11:118503457-118503457 + B73-Tumor COSM254815 c.7556C>T p.T2519I Substitution - Missense 11:118503457-118503457 + TCGA-DA-A1I7-06 COSM3443951 c.2623G>A p.E875K Substitution - Missense 11:118473782-118473782 + TCGA-29-1771-01 COSM1321879 c.9959G>A p.S3320N Substitution - Missense 11:118505860-118505860 + 2290930 COSM1351657 c.9299delA p.I3102fs*3 Deletion - Frameshift 11:118505200-118505200 + PD6041a COSM5768776 c.1732A>G p.I578V Substitution - Missense 11:118472891-118472891 + TCGA-AA-A010-01 COSM282811 c.1601C>T p.S534L Substitution - Missense 11:118472760-118472760 + I2L-P19Tb-Tumor-Organoid COSM5360762 c.5281-1G>A p.? Unknown 11:118494693-118494693 + TCGA-BR-6452-01 COSM4018306 c.4373T>C p.F1458S Substitution - Missense 11:118488654-118488654 + PCSI_0135_Pa_X COSM3375669 c.8056A>G p.R2686G Substitution - Missense 11:118503957-118503957 + BD182T COSM5490615 c.3310A>G p.I1104V Substitution - Missense 11:118476958-118476958 + TCGA-AA-A010-01 COSM282812 c.3180G>T p.E1060D Substitution - Missense 11:118476828-118476828 + DM58 COSM5609420 c.1485G>A p.E495E Substitution - coding silent 11:118472644-118472644 + TCGA-CG-4438-01 COSM4018347 c.11146G>A p.G3716S Substitution - Missense 11:118519626-118519626 + 88 COSM5015050 c.518G>A p.R173Q Substitution - Missense 11:118471677-118471677 + TCGA-CG-5721-01 COSM4018308 c.4446T>C p.C1482C Substitution - coding silent 11:118488727-118488727 + SJDES014-R2 COSM4574086 c.10135A>G p.S3379G Substitution - Missense 11:118506036-118506036 + OSCC-GB_01060111 COSM4882920 c.11814G>T p.E3938D Substitution - Missense 11:118522076-118522076 + B103-Tumor COSM254810 c.4368C>A p.H1456Q Substitution - Missense 11:118488649-118488649 + TCGA-AP-A0LM-01 COSM923597 c.8379A>G p.G2793G Substitution - coding silent 11:118504280-118504280 + S00-35182-TP COSM4990132 c.7411C>T p.P2471S Substitution - Missense 11:118503312-118503312 + TCGA-A2-A0YJ-01 COSM428501 c.9134A>C p.K3045T Substitution - Missense 11:118505035-118505035 + PD3391a COSM30375 c.3960C>T p.P1320P Substitution - coding silent 11:118482040-118482040 + YUZINO COSM1704630 c.4622C>T p.P1541L Substitution - Missense 11:118490175-118490175 + TCGA-AO-A03M-01 COSM3808481 c.5011G>C p.D1671H Substitution - Missense 11:118493072-118493072 + TCGA-D7-A4YY-01 COSM4018351 c.11524G>A p.G3842S Substitution - Missense 11:118521307-118521307 + PD6889a COSM4384590 c.3810G>C p.K1270N Substitution - Missense 11:118481890-118481890 + TCGA-EE-A2A2-06 COSM3443981 c.6674C>T p.S2225F Substitution - Missense 11:118502575-118502575 + YUKAT COSM5371779 c.9547G>A p.G3183S Substitution - Missense 11:118505448-118505448 + TCGA-29-1778-01 COSM1321881 c.4438A>G p.K1480E Substitution - Missense 11:118488719-118488719 + T3498 COSM4702404 c.10752A>G p.P3584P Substitution - coding silent 11:118507535-118507535 + PD6177a COSM4384608 c.7537C>A p.Q2513K Substitution - Missense 11:118503438-118503438 + TCGA-AG-A002-01 COSM262034 c.10127G>A p.G3376D Substitution - Missense 11:118506028-118506028 + MEL-Ma-Mel-55 COSM1167725 c.1806delT p.P603fs*20 Deletion - Frameshift 11:118472965-118472965 + SNUH_G76_S1 COSM4418310 c.11504+7C>T p.? Unknown 11:118520892-118520892 + T1154 COSM4702400 c.10265C>T p.A3422V Substitution - Missense 11:118506166-118506166 + SH-7166 COSM5020622 c.5670A>G p.L1890L Substitution - coding silent 11:118497950-118497950 + PD23560a COSM5768134 c.5602G>C p.E1868Q Substitution - Missense 11:118496314-118496314 + B85-0 COSM1756743 c.5154G>T p.G1718G Substitution - coding silent 11:118493215-118493215 + TCGA-Q1-A5R3-01 COSM4834020 c.10688G>T p.S3563I Substitution - Missense 11:118506589-118506589 + TCGA-AX-A05Z-01 COSM923603 c.11210C>T p.A3737V Substitution - Missense 11:118519690-118519690 + S00472 COSM317631 c.9479A>G p.Q3160R Substitution - Missense 11:118505380-118505380 + TCGA-AP-A059-01 COSM923572 c.1279C>T p.R427W Substitution - Missense 11:118472438-118472438 + CSCC-40-T COSM4485538 c.2946C>T p.S982S Substitution - coding silent 11:118474105-118474105 + TCGA-22-5473-01 COSM686163 c.9387C>G p.L3129L Substitution - coding silent 11:118505288-118505288 + CSCC-27-T COSM4520239 c.10486G>A p.E3496K Substitution - Missense 11:118506387-118506387 + TCGA-FW-A5DX-01 COSM3443955 c.2987C>T p.S996F Substitution - Missense 11:118474146-118474146 + TCGA-BR-8590-01 COSM4018333 c.8444C>T p.P2815L Substitution - Missense 11:118504345-118504345 + SA237 COSM212842 c.2348C>A p.S783Y Substitution - Missense 11:118473507-118473507 + Pat_66_A COSM5837919 c.590C>T p.S197F Substitution - Missense 11:118471749-118471749 + TCGA-D3-A3C3-06 COSM3443961 c.4786C>T p.H1596Y Substitution - Missense 11:118491285-118491285 + ESCC_52 COSM5631131 c.2328C>T p.V776V Substitution - coding silent 11:118473487-118473487 + Au1 COSM5597089 c.3332A>T p.D1111V Substitution - Missense 11:118476980-118476980 + TCGA-BS-A0TC-01 COSM923587 c.6562C>T p.R2188* Substitution - Nonsense 11:118502463-118502463 + RKO COSM4647262 c.4095A>G p.P1365P Substitution - coding silent 11:118484191-118484191 + 71 COSM5015052 c.2221T>C p.F741L Substitution - Missense 11:118473380-118473380 + 38 COSM5762892 c.2131A>G p.I711V Substitution - Missense 11:118473290-118473290 + MEL-JWCI-WGS-38 COSM1167604 c.10201delC p.P3401fs*20 Deletion - Frameshift 11:118506102-118506102 + PD3298a COSM30372 c.1058G>A p.R353Q Substitution - Missense 11:118472217-118472217 + T2197 COSM4702387 c.4178T>A p.I1393N Substitution - Missense 11:118484274-118484274 + CHC1616T COSM4803638 c.4111C>T p.Q1371* Substitution - Nonsense 11:118484207-118484207 + TCGA-EL-A3ZH-01 COSM3368237 c.4958A>C p.N1653T Substitution - Missense 11:118491891-118491891 + YUZINO COSM1704626 c.3196C>T p.P1066S Substitution - Missense 11:118476844-118476844 + DM31 COSM202117 c.11577C>T p.A3859A Substitution - coding silent 11:118521360-118521360 + CSCC-31-T COSM3710007 c.4965G>A p.R1655R Substitution - coding silent 11:118491898-118491898 + TCGA-BR-7958-01 COSM4018312 c.5000C>T p.A1667V Substitution - Missense 11:118493061-118493061 + SH-6055 COSM5020490 c.1810A>G p.M604V Substitution - Missense 11:118472969-118472969 + Pat_76_B COSM5837927 c.3842C>T p.P1281L Substitution - Missense 11:118481922-118481922 + SH-9248 COSM5020404 c.7245C>T p.N2415N Substitution - coding silent 11:118503146-118503146 + DM12 COSM5609404 c.5982C>T p.F1994F Substitution - coding silent 11:118499332-118499332 + TCGA-C8-A27B-01 COSM1475079 c.3005C>G p.S1002C Substitution - Missense 11:118474164-118474164 + ESCC_17 COSM5625891 c.1706C>T p.P569L Substitution - Missense 11:118472865-118472865 + T3503 COSM4702402 c.10592C>T p.P3531L Substitution - Missense 11:118506493-118506493 + TCGA-CM-6171-01 COSM1351634 c.5291G>A p.R1764H Substitution - Missense 11:118494704-118494704 + TCGA-G4-6588-01 COSM1351657 c.9299delA p.I3102fs*3 Deletion - Frameshift 11:118505200-118505200 + 451 COSM1742455 c.5835C>G p.C1945W Substitution - Missense 11:118498411-118498411 + S00-35182-TP COSM4990124 c.3923A>G p.Q1308R Substitution - Missense 11:118482003-118482003 + Pat_41_B COSM5837929 c.6956C>T p.S2319F Substitution - Missense 11:118502857-118502857 + LUAD-RT-S01831 COSM384248 c.6696C>T p.T2232T Substitution - coding silent 11:118502597-118502597 + TCGA-DA-A1I0-06 COSM3443937 c.839C>T p.P280L Substitution - Missense 11:118471998-118471998 + HCC42 COSM1604171 c.9182A>G p.N3061S Substitution - Missense 11:118505083-118505083 + TCGA-BR-6566-01 COSM4018292 c.2585G>A p.R862Q Substitution - Missense 11:118473744-118473744 + PD23559a COSM5784431 c.928G>A p.E310K Substitution - Missense 11:118472087-118472087 + SC_9081 COSM5550933 c.4715G>A p.C1572Y Substitution - Missense 11:118491214-118491214 + CN-AML-CR-54-Dx COSM5427115 c.4186G>A p.D1396N Substitution - Missense 11:118484282-118484282 + 38 COSM5762896 c.6691G>A p.G2231R Substitution - Missense 11:118502592-118502592 + B71 COSM254814 c.8647C>G p.L2883V Substitution - Missense 11:118504548-118504548 + ME011T COSM224409 c.10375C>T p.L3459F Substitution - Missense 11:118506276-118506276 + 86797 COSM94708 c.7748C>T p.S2583F Substitution - Missense 11:118503649-118503649 + TCGA-AN-A0FD-01 COSM428503 c.11868C>G p.P3956P Substitution - coding silent 11:118522130-118522130 + YUCHIME COSM1704624 c.905G>A p.R302Q Substitution - Missense 11:118472064-118472064 + sysucc-880T COSM5461922 c.6367G>A p.D2123N Substitution - Missense 11:118501728-118501728 + HCC61T COSM1604169 c.7094T>C p.L2365P Substitution - Missense 11:118502995-118502995 + HCC083T COSM5816392 c.5287G>T p.E1763* Substitution - Nonsense 11:118494700-118494700 + PD6236a COSM4384586 c.2557A>C p.K853Q Substitution - Missense 11:118473716-118473716 + TCGA-EE-A3AA-06 COSM3443997 c.7937C>T p.P2646L Substitution - Missense 11:118503838-118503838 + CSCC-10-T COSM4518663 c.72_73CC>TT p.R25W Substitution - Missense 11:118436584-118436585 + B71 COSM254814 c.8647C>G p.L2883V Substitution - Missense 11:118504548-118504548 + TCGA-AP-A059-01 COSM172385 c.7074G>A p.S2358S Substitution - coding silent 11:118502975-118502975 + ESO-005 COSM1257768 c.2039C>T p.S680L Substitution - Missense 11:118473198-118473198 + CLN2 COSM5024815 c.2993C>A p.T998N Substitution - Missense 11:118474152-118474152 + TCGA-EE-A2GR-06 COSM3443943 c.1914C>T p.A638A Substitution - coding silent 11:118473073-118473073 + 90226 COSM330230 c.203delG p.G68fs*82 Deletion - Frameshift 11:118436715-118436715 + T2940 COSM4384620 c.9674G>A p.R3225H Substitution - Missense 11:118505575-118505575 + XHDG50C COSM4767617 c.4891G>C p.E1631Q Substitution - Missense 11:118491824-118491824 + SH-9248 COSM5020622 c.5670A>G p.L1890L Substitution - coding silent 11:118497950-118497950 + LP6005409-DNA_A01 COSM5951965 c.4686C>T p.L1562L Substitution - coding silent 11:118490239-118490239 + HCC82 COSM3666011 c.11441T>C p.L3814P Substitution - Missense 11:118520822-118520822 + PD7016a COSM4384622 c.10487A>G p.E3496G Substitution - Missense 11:118506388-118506388 + 46M COSM5588296 c.10840C>T p.L3614F Substitution - Missense 11:118509149-118509149 + TCGA-AR-A0TX-01 COSM428496 c.2698C>T p.Q900* Substitution - Nonsense 11:118473857-118473857 + SWE-10 COSM1178772 c.10224A>G p.Q3408Q Substitution - coding silent 11:118506125-118506125 + 58 COSM4169983 c.2713T>A p.L905M Substitution - Missense 11:118473872-118473872 + I2L-P7-Tumor-Organoid COSM3808471 c.1325G>A p.R442Q Substitution - Missense 11:118472484-118472484 + TCGA-AP-A0LM-01 COSM923590 c.7135C>T p.R2379* Substitution - Nonsense 11:118503036-118503036 + 2492723 COSM5721820 c.11236C>T p.R3746C Substitution - Missense 11:118519716-118519716 + CSCC-27-T COSM4490553 c.3659C>T p.S1220F Substitution - Missense 11:118481739-118481739 + PT52 COSM5940147 c.7564G>A p.V2522M Substitution - Missense 11:118503465-118503465 + WA28 COSM240677 c.5447_5449delAGC p.Q1816delQ Deletion - In frame 11:118495792-118495794 + DM16 COSM5609406 c.5720C>T p.S1907L Substitution - Missense 11:118498000-118498000 + 2521252 COSM5889151 c.9733C>T p.P3245S Substitution - Missense 11:118505634-118505634 + BD57T COSM1215174 c.2797C>T p.R933W Substitution - Missense 11:118473956-118473956 + TCGA-CG-5728-01 COSM4018343 c.10834G>A p.A3612T Substitution - Missense 11:118509143-118509143 + PDA_086 COSM5002821 c.3105C>A p.C1035* Substitution - Nonsense 11:118474264-118474264 + TCGA-AA-A010-01 COSM282817 c.10727C>T p.S3576F Substitution - Missense 11:118506628-118506628 + PD7374a COSM4384614 c.9037G>C p.E3013Q Substitution - Missense 11:118504938-118504938 + HCC109T COSM5816802 c.2371G>T p.A791S Substitution - Missense 11:118473530-118473530 + TCGA-GF-A6C9-06 COSM4903487 c.2405C>T p.S802F Substitution - Missense 11:118473564-118473564 + BD87T COSM5020616 c.4284A>C p.I1428I Substitution - coding silent 11:118484927-118484927 + TCGA-AA-A010-01 COSM282816 c.10342G>A p.E3448K Substitution - Missense 11:118506243-118506243 + KM12 COSM2105648 c.11469delA p.K3825fs*31 Deletion - Frameshift 11:118520850-118520850 + TCGA-13-0912-01 COSM75424 c.6988A>G p.K2330E Substitution - Missense 11:118502889-118502889 + TCGA-CM-5349-01 COSM1351647 c.6661A>G p.R2221G Substitution - Missense 11:118502562-118502562 + 2492723 COSM5724107 c.34C>T p.R12* Substitution - Nonsense 11:118436546-118436546 + TCGA-DD-A3A9-01 COSM4920392 c.8173G>A p.E2725K Substitution - Missense 11:118504074-118504074 + TCGA-AN-A046-01 COSM3808475 c.1954C>T p.R652* Substitution - Nonsense 11:118473113-118473113 + B69 COSM254813 c.3173C>G p.S1058* Substitution - Nonsense 11:118476821-118476821 + TCGA-AX-A0J0-01 COSM923569 c.760A>C p.K254Q Substitution - Missense 11:118471919-118471919 + TCGA-EE-A2GI-06 COSM3443939 c.1150C>T p.Q384* Substitution - Nonsense 11:118472309-118472309 + TCGA-EE-A3JB-06 COSM4898318 c.6624G>A p.R2208R Substitution - coding silent 11:118502525-118502525 + TCGA-ER-A19S-06 COSM3443941 c.1898C>T p.S633F Substitution - Missense 11:118473057-118473057 + PD8614a COSM5793343 c.4366C>G p.H1456D Substitution - Missense 11:118488647-118488647 + DM10 COSM5609400 c.10833C>A p.V3611V Substitution - coding silent 11:118509142-118509142 + S00-28455-TP COSM4990128 c.6462G>A p.Q2154Q Substitution - coding silent 11:118501823-118501823 + 2492725 COSM5724942 c.6783C>T p.S2261S Substitution - coding silent 11:118502684-118502684 + PT32 COSM5907567 c.1960C>T p.P654S Substitution - Missense 11:118473119-118473119 + TCGA-CD-A48A-01 COSM4018288 c.1845G>A p.P615P Substitution - coding silent 11:118473004-118473004 + CSCC-11-T COSM4467576 c.1498C>A p.P500T Substitution - Missense 11:118472657-118472657 + CN-AML-08-T COSM5425984 c.7061C>G p.P2354R Substitution - Missense 11:118502962-118502962 + 2492704 COSM5716812 c.16C>T p.R6W Substitution - Missense 11:118436528-118436528 + S03-45671-TP COSM4990122 c.681C>G p.T227T Substitution - coding silent 11:118471840-118471840 + PD11355a COSM5801822 c.9864_9865delAT p.R3288fs*2 Deletion - Frameshift 11:118505765-118505766 + CSCC-38-T COSM4513509 c.9403C>T p.L3135L Substitution - coding silent 11:118505304-118505304 + DM79 COSM5609424 c.6073T>C p.S2025P Substitution - Missense 11:118499837-118499837 + HCC83T COSM3666009 c.7676T>A p.I2559N Substitution - Missense 11:118503577-118503577 + TCGA-AA-3492-01 COSM1351667 c.10200G>A p.P3400P Substitution - coding silent 11:118506101-118506101 + RK187_C01 COSM1627816 c.6070+3A>G p.? Unknown 11:118499423-118499423 + TCGA-EE-A29L-06 COSM3443973 c.5322C>T p.S1774S Substitution - coding silent 11:118494735-118494735 + C058 COSM4853865 c.11356C>T p.R3786C Substitution - Missense 11:118520000-118520000 + PTC_301 COSM5959613 c.10215G>T p.M3405I Substitution - Missense 11:118506116-118506116 + TCGA-18-3409-01 COSM686160 c.10239G>A p.Q3413Q Substitution - coding silent 11:118506140-118506140 + CN-AML-NR-08-Dx COSM5425984 c.7061C>G p.P2354R Substitution - Missense 11:118502962-118502962 + TCGA-D3-A3C7-06 COSM923587 c.6562C>T p.R2188* Substitution - Nonsense 11:118502463-118502463 + PD6098a COSM4384592 c.4291delA p.R1431fs*13 Deletion - Frameshift 11:118484934-118484934 + ccRCC-41 COSM1662780 c.1623A>T p.R541S Substitution - Missense 11:118472782-118472782 + B112-Tumor COSM254811 c.4437C>G p.C1479W Substitution - Missense 11:118488718-118488718 + TCGA-CH-5744-01 COSM1127893 c.2097T>C p.A699A Substitution - coding silent 11:118473256-118473256 + PD6982a COSM4384598 c.5149C>T p.Q1717* Substitution - Nonsense 11:118493210-118493210 + DM26 COSM5609412 c.8447C>G p.S2816C Substitution - Missense 11:118504348-118504348 + 3N01-VS-3T01 COSM4978255 c.11056A>T p.I3686F Substitution - Missense 11:118510112-118510112 + 7T COSM3710007 c.4965G>A p.R1655R Substitution - coding silent 11:118491898-118491898 + S0080 COSM5882020 c.5758A>T p.N1920Y Substitution - Missense 11:118498038-118498038 + T2197 COSM4702393 c.6535G>T p.G2179C Substitution - Missense 11:118502436-118502436 + SH-7166 COSM5020404 c.7245C>T p.N2415N Substitution - coding silent 11:118503146-118503146 + PT14_1 COSM5897016 c.11085T>A p.D3695E Substitution - Missense 11:118511973-118511973 + TCGA-D5-6928-01 COSM1351671 c.10817A>G p.Q3606R Substitution - Missense 11:118507600-118507600 + 88 COSM5015054 c.7439A>T p.N2480I Substitution - Missense 11:118503340-118503340 + T3535 COSM4702377 c.1894delT p.S633fs*24 Deletion - Frameshift 11:118473053-118473053 + Au3 COSM5601815 c.167delC p.P58fs*92 Deletion - Frameshift 11:118436679-118436679 + TCGA-Q2-A5QZ-01 COSM3985965 c.7316A>C p.E2439A Substitution - Missense 11:118503217-118503217 + TCGA-AP-A056-01 COSM923575 c.3451C>T p.R1151* Substitution - Nonsense 11:118478083-118478083 + CSCC-7-T COSM4522571 c.1168G>C p.E390Q Substitution - Missense 11:118472327-118472327 + TCGA-BT-A20Q-01 COSM415320 c.8515G>A p.D2839N Substitution - Missense 11:118504416-118504416 + TCGA-EE-A29V-06 COSM3443987 c.7049C>T p.S2350F Substitution - Missense 11:118502950-118502950 + TCGA-AP-A056-01 COSM923574 c.3309G>T p.K1103N Substitution - Missense 11:118476957-118476957 + BD62T COSM5498670 c.9648T>C p.S3216S Substitution - coding silent 11:118505549-118505549 + TCGA-B5-A11E-01 COSM923596 c.8354C>A p.S2785Y Substitution - Missense 11:118504255-118504255 + TCGA-A6-6654-01 COSM1351677 c.11794C>T p.R3932C Substitution - Missense 11:118522056-118522056 + TCGA-EE-A3JA-06 COSM3444001 c.8741C>T p.S2914F Substitution - Missense 11:118504642-118504642 + CHC433T COSM3666856 c.7335T>A p.S2445S Substitution - coding silent 11:118503236-118503236 + SH-9248 COSM5020616 c.4284A>C p.I1428I Substitution - coding silent 11:118484927-118484927 + ESCC_156 COSM5645967 c.9344T>C p.M3115T Substitution - Missense 11:118505245-118505245 + TCGA-DA-A1I5-06 COSM3444015 c.11258C>T p.A3753V Substitution - Missense 11:118519738-118519738 + RK184_C01 COSM1627814 c.2599A>G p.S867G Substitution - Missense 11:118473758-118473758 + TCGA-AP-A051-01 COSM923577 c.3517T>C p.C1173R Substitution - Missense 11:118478149-118478149 + TCGA-A6-6781-01 COSM1351669 c.10266G>A p.A3422A Substitution - coding silent 11:118506167-118506167 + TCGA-EP-A2KA-01 COSM4917486 c.10709C>T p.P3570L Substitution - Missense 11:118506610-118506610 + MOLT-4 COSM1676468 c.4678G>A p.A1560T Substitution - Missense 11:118490231-118490231 + S01861 COSM5670971 c.3220A>G p.R1074G Substitution - Missense 11:118476868-118476868 + C391 COSM2105524 c.6610C>T p.R2204W Substitution - Missense 11:118502511-118502511 + TCGA-66-2786-01 COSM686161 c.10115C>G p.T3372S Substitution - Missense 11:118506016-118506016 + EGC15 COSM5050562 c.8961C>T p.G2987G Substitution - coding silent 11:118504862-118504862 + HCT8 COSM2105414 c.2817T>C p.H939H Substitution - coding silent 11:118473976-118473976 + ESCC_BICR_039T COSM5429524 c.6581G>A p.R2194H Substitution - Missense 11:118502482-118502482 + S02322 COSM5691145 c.5962G>C p.E1988Q Substitution - Missense 11:118499312-118499312 + TCGA-63-6202-01 COSM686165 c.7838A>G p.K2613R Substitution - Missense 11:118503739-118503739 + 35M COSM5581667 c.2111C>T p.P704L Substitution - Missense 11:118473270-118473270 + TCGA-EE-A3J4-06 COSM1351611 c.2584C>T p.R862* Substitution - Nonsense 11:118473743-118473743 + 2492720 COSM5721817 c.4522G>A p.E1508K Substitution - Missense 11:118489834-118489834 + MB130PT COSM88007 c.4995+1G>A p.? Unknown 11:118491929-118491929 + T2197 COSM1351609 c.2312delC p.P773fs*8 Deletion - Frameshift 11:118473471-118473471 + 2246945 COSM4413481 c.9338G>A p.S3113N Substitution - Missense 11:118505239-118505239 + PR-2682 COSM242569 c.4219G>T p.E1407* Substitution - Nonsense 11:118484862-118484862 + PCSI_0303_Pa_P_526 COSM3786987 c.10535C>T p.P3512L Substitution - Missense 11:118506436-118506436 + PD6869a COSM4384604 c.7128G>C p.R2376S Substitution - Missense 11:118503029-118503029 + CPCG0238-F1 COSM4880698 c.379C>T p.R127C Substitution - Missense 11:118436891-118436891 + HCC067T COSM5824086 c.4854C>T p.A1618A Substitution - coding silent 11:118491787-118491787 + HCC56T COSM1604163 c.3216C>T p.C1072C Substitution - coding silent 11:118476864-118476864 + PD7384a COSM4384628 c.11584G>A p.V3862I Substitution - Missense 11:118521367-118521367 + HCC61 COSM1604169 c.7094T>C p.L2365P Substitution - Missense 11:118502995-118502995 + 578 COSM3722543 c.8733C>A p.V2911V Substitution - coding silent 11:118504634-118504634 + S02162 COSM4386857 c.1000A>G p.R334G Substitution - Missense 11:118472159-118472159 + 8016470 COSM3383233 c.9895G>A p.A3299T Substitution - Missense 11:118505796-118505796 + pfg068T COSM4760546 c.10969A>G p.K3657E Substitution - Missense 11:118510025-118510025 + B35 COSM254812 c.11348C>G p.S3783C Substitution - Missense 11:118519992-118519992 + C086 COSM5534580 c.10208C>T p.S3403L Substitution - Missense 11:118506109-118506109 + DM102 COSM5609402 c.8570C>T p.T2857I Substitution - Missense 11:118504471-118504471 + HT115 COSM2105372 c.2162G>A p.R721Q Substitution - Missense 11:118473321-118473321 + WA22 COSM237738 c.834C>G p.L278L Substitution - coding silent 11:118471993-118471993 + T3724 COSM4702391 c.6150-1G>T p.? Unknown 11:118500986-118500986 + BD114T COSM5503828 c.8811G>T p.R2937R Substitution - coding silent 11:118504712-118504712 + 112377 COSM94709 c.8598C>G p.S2866R Substitution - Missense 11:118504499-118504499 + 2492722 COSM5721817 c.4522G>A p.E1508K Substitution - Missense 11:118489834-118489834 + TCGA-F4-6570-01 COSM1351655 c.9255G>A p.M3085I Substitution - Missense 11:118505156-118505156 + TCGA-AX-A0J1-01 COSM923592 c.7829G>A p.G2610D Substitution - Missense 11:118503730-118503730 + ESO-859 COSM1239439 c.6185G>A p.R2062H Substitution - Missense 11:118501022-118501022 + T3080 COSM4702398 c.7581delA p.M2529fs*11 Deletion - Frameshift 11:118503482-118503482 + PD13802a COSM5025052 c.7136G>A p.R2379Q Substitution - Missense 11:118503037-118503037 + LIM1215 COSM4184874 c.2632C>T p.R878W Substitution - Missense 11:118473791-118473791 + NB-3538 COSM1286203 c.3435A>C p.P1145P Substitution - coding silent 11:118478067-118478067 + C058 COSM3443947 c.2233C>T p.R745* Substitution - Nonsense 11:118473392-118473392 + CHC892T COSM4959895 c.391G>A p.A131T Substitution - Missense 11:118436903-118436903 + TCGA-D8-A1Y1-01 COSM2105648 c.11469delA p.K3825fs*31 Deletion - Frameshift 11:118520850-118520850 + 2492720 COSM5724107 c.34C>T p.R12* Substitution - Nonsense 11:118436546-118436546 + DLD1 COSM1676464 c.3185C>A p.S1062Y Substitution - Missense 11:118476833-118476833 + TCGA-B5-A11J-01 COSM923599 c.9139G>A p.V3047M Substitution - Missense 11:118505040-118505040 + TCGA-JW-A5VL-01 COSM4846694 c.6136C>T p.P2046S Substitution - Missense 11:118499900-118499900 + TCGA-A8-A0A6-01 COSM3808491 c.9522A>C p.P3174P Substitution - coding silent 11:118505423-118505423 + TCGA-AG-4015-01 COSM289591 c.2016C>T p.T672T Substitution - coding silent 11:118473175-118473175 + Pat_26_A COSM1351609 c.2312delC p.P773fs*8 Deletion - Frameshift 11:118473471-118473471 + 2530678 COSM5885865 c.7341delG p.E2448fs*5 Deletion - Frameshift 11:118503242-118503242 + TCGA-13-0885-01 COSM75423 c.5068G>C p.D1690H Substitution - Missense 11:118493129-118493129 + TCGA-BS-A0UV-01 COSM923580 c.4371G>T p.K1457N Substitution - Missense 11:118488652-118488652 + 107597 COSM94711 c.9577G>A p.D3193N Substitution - Missense 11:118505478-118505478 + tumor_4184094 COSM3356166 c.7083T>G p.S2361S Substitution - coding silent 11:118502984-118502984 + C0045T COSM4165663 c.393C>A p.A131A Substitution - coding silent 11:118436905-118436905 + RK223_C01 COSM4943644 c.7212A>G p.L2404L Substitution - coding silent 11:118503113-118503113 + I2L-P19Tb-Tumor-Organoid COSM5360766 c.5878C>T p.R1960* Substitution - Nonsense 11:118498454-118498454 + TCGA-18-3410-01 COSM686170 c.2364C>A p.A788A Substitution - coding silent 11:118473523-118473523 + PT09_1 COSM5894938 c.3570-5C>T p.? Unknown 11:118480169-118480169 + TCGA-CS-5390-01 COSM3967350 c.10939A>G p.M3647V Substitution - Missense 11:118509995-118509995 + TCGA-D1-A103-01 COSM923576 c.3455C>T p.S1152L Substitution - Missense 11:118478087-118478087 + CCK81 COSM2105650 c.11512A>G p.I3838V Substitution - Missense 11:118521295-118521295 + H292 COSM1197296 c.10721C>A p.T3574K Substitution - Missense 11:118506622-118506622 + 2492721 COSM245704 c.6222C>T p.C2074C Substitution - coding silent 11:118501059-118501059 + IGROV-1 COSM1676476 c.11795G>A p.R3932H Substitution - Missense 11:118522057-118522057 + PT49 COSM5935743 c.3011C>T p.S1004F Substitution - Missense 11:118474170-118474170 + TCGA-GN-A26D-06 COSM3444013 c.9625A>G p.T3209A Substitution - Missense 11:118505526-118505526 + 103595 COSM94710 c.9126G>T p.Q3042H Substitution - Missense 11:118505027-118505027 + DM17 COSM5609408 c.6479G>A p.R2160Q Substitution - Missense 11:118501840-118501840 + TCGA-AA-3510-01 COSM923587 c.6562C>T p.R2188* Substitution - Nonsense 11:118502463-118502463 + TCGA-B0-5812-01 COSM466404 c.9468G>C p.M3156I Substitution - Missense 11:118505369-118505369 + 2293762 COSM4606976 c.2887A>T p.K963* Substitution - Nonsense 11:118474046-118474046 + C086 COSM3808475 c.1954C>T p.R652* Substitution - Nonsense 11:118473113-118473113 + DM8 COSM5609426 c.9897A>C p.A3299A Substitution - coding silent 11:118505798-118505798 + DM28 COSM5609414 c.990C>T p.S330S Substitution - coding silent 11:118472149-118472149 + T3225 COSM4702385 c.4016C>A p.P1339Q Substitution - Missense 11:118482425-118482425 + 59T COSM5575853 c.1885C>T p.P629S Substitution - Missense 11:118473044-118473044 + 2492726 COSM5724942 c.6783C>T p.S2261S Substitution - coding silent 11:118502684-118502684 + LS411 COSM2105648 c.11469delA p.K3825fs*31 Deletion - Frameshift 11:118520850-118520850 + S01563 COSM25627 c.2880A>G p.I960M Substitution - Missense 11:118474039-118474039 + TCGA-A8-A07P-01 COSM428497 c.3583C>T p.Q1195* Substitution - Nonsense 11:118480187-118480187 + PD6847a COSM1351665 c.10067C>T p.A3356V Substitution - Missense 11:118505968-118505968 + J15_T COSM3979168 c.4332+8A>C p.? Unknown 11:118484983-118484983 + TCGA-HU-A4GH-01 COSM4018286 c.1754T>G p.L585R Substitution - Missense 11:118472913-118472913 + S00501 COSM308680 c.1378_1379insA p.S462fs*19 Insertion - Frameshift 11:118472537-118472538 + BD242T COSM5490530 c.1430C>T p.S477F Substitution - Missense 11:118472589-118472589 + S00933 COSM317632 c.4268T>C p.L1423S Substitution - Missense 11:118484911-118484911 + TCGA-AZ-4315-01 COSM1351659 c.9301A>C p.K3101Q Substitution - Missense 11:118505202-118505202 + Pat_41_B COSM5837925 c.3350C>T p.A1117V Substitution - Missense 11:118477982-118477982 + LS411 COSM1351609 c.2312delC p.P773fs*8 Deletion - Frameshift 11:118473471-118473471 + TCGA-D3-A3C7-06 COSM3444007 c.9284C>T p.P3095L Substitution - Missense 11:118505185-118505185 + TCGA-AG-A002-01 COSM262032 c.1341G>A p.P447P Substitution - coding silent 11:118472500-118472500 + 2197 COSM5017225 c.6911A>T p.K2304M Substitution - Missense 11:118502812-118502812 + TCGA-DJ-A13P-01 COSM3368239 c.8153A>T p.D2718V Substitution - Missense 11:118504054-118504054 + LUAD-LIP77 COSM342097 c.4115A>C p.E1372A Substitution - Missense 11:118484211-118484211 + 360_T COSM3979166 c.4246G>T p.E1416* Substitution - Nonsense 11:118484889-118484889 + DLD1 COSM4621979 c.11780T>A p.V3927D Substitution - Missense 11:118522042-118522042 + TCGA-BS-A0UV-01 COSM923605 c.11656C>T p.R3886* Substitution - Nonsense 11:118521918-118521918 + GHE0536 COSM5713821 c.374A>C p.N125T Substitution - Missense 11:118436886-118436886 + BD35T COSM5490684 c.9475C>T p.H3159Y Substitution - Missense 11:118505376-118505376 + sysucc-1370T COSM5469511 c.10464C>T p.D3488D Substitution - coding silent 11:118506365-118506365 + TCGA-C4-A0F1-01 COSM415319 c.9838C>T p.R3280* Substitution - Nonsense 11:118505739-118505739 + TCGA-66-2759-01 COSM686158 c.11167C>G p.L3723V Substitution - Missense 11:118519647-118519647 + CSCC-10-T COSM4482126 c.2576C>T p.S859F Substitution - Missense 11:118473735-118473735 + TCGA-28-5213-01 COSM3397446 c.9033A>C p.S3011S Substitution - coding silent 11:118504934-118504934 + TCGA-AD-6889-01 COSM266934 c.11708G>A p.R3903H Substitution - Missense 11:118521970-118521970 + TCGA-D3-A2JO-06 COSM3443945 c.2046C>T p.L682L Substitution - coding silent 11:118473205-118473205 + Au1 COSM5597091 c.1432C>T p.R478* Substitution - Nonsense 11:118472591-118472591 + TCGA-E2-A574-01 COSM3808471 c.1325G>A p.R442Q Substitution - Missense 11:118472484-118472484 + ESCC_94 COSM5637350 c.9870A>T p.K3290N Substitution - Missense 11:118505771-118505771 + RK041_C01 COSM1627816 c.6070+3A>G p.? Unknown 11:118499423-118499423 + sysucc-1315T COSM5480081 c.5443G>A p.E1815K Substitution - Missense 11:118495788-118495788 + B66 COSM255057 c.5972_5991del20 p.E1992fs*4 Deletion - Frameshift 11:118499322-118499341 + T3094 COSM4702381 c.2947C>A p.L983M Substitution - Missense 11:118474106-118474106 + B66 COSM255057 c.5972_5991del20 p.E1992fs*4 Deletion - Frameshift 11:118499322-118499341 + CHC433T COSM3666856 c.7335T>A p.S2445S Substitution - coding silent 11:118503236-118503236 + CHC805T COSM4954307 c.3755C>G p.P1252R Substitution - Missense 11:118481835-118481835 + TCGA-41-4097-01 COSM1351624 c.4400T>C p.L1467P Substitution - Missense 11:118488681-118488681 + TCGA-HF-7132-01 COSM2105485 c.4778G>A p.R1593H Substitution - Missense 11:118491277-118491277 + TCGA-CG-5721-01 COSM4018310 c.4978T>C p.L1660L Substitution - coding silent 11:118491911-118491911 + HX13T COSM1351609 c.2312delC p.P773fs*8 Deletion - Frameshift 11:118473471-118473471 + 24T COSM5575717 c.8717C>A p.P2906H Substitution - Missense 11:118504618-118504618 + TCGA-D5-6529-01 COSM1351665 c.10067C>T p.A3356V Substitution - Missense 11:118505968-118505968 + TCGA-A2-A3Y0-01 COSM3808487 c.7208A>G p.K2403R Substitution - Missense 11:118503109-118503109 + P149 COSM1737319 c.514C>T p.P172S Substitution - Missense 11:118471673-118471673 + CHC1747T COSM4788109 c.2863G>A p.A955T Substitution - Missense 11:118474022-118474022 + GC_296T1-GC_296N COSM4772180 c.7455_7456insT p.K2486fs*1 Insertion - Frameshift 11:118503356-118503357 + TCGA-AP-A056-01 COSM923588 c.6737T>G p.V2246G Substitution - Missense 11:118502638-118502638 + TCGA-BR-6852-01 COSM4018323 c.7108C>A p.L2370I Substitution - Missense 11:118503009-118503009 + Gp5D COSM2105632 c.10938G>T p.L3646L Substitution - coding silent 11:118509994-118509994 + DM8 COSM5609428 c.7041A>T p.K2347N Substitution - Missense 11:118502942-118502942 + TCGA-EB-A430-01 COSM3443995 c.7717C>T p.P2573S Substitution - Missense 11:118503618-118503618 + TCGA-HU-8602-01 COSM268500 c.6235G>A p.V2079I Substitution - Missense 11:118501072-118501072 + TCGA-AZ-4315-01 COSM1257768 c.2039C>T p.S680L Substitution - Missense 11:118473198-118473198 + BD124T COSM5494360 c.2312_2313insC p.S774fs*12 Insertion - Frameshift 11:118473471-118473472 + TCGA-BP-5168-01 COSM466399 c.3918G>A p.P1306P Substitution - coding silent 11:118481998-118481998 + TCGA-FP-A4BE-01 COSM4018290 c.1980C>T p.D660D Substitution - coding silent 11:118473139-118473139 + 2492722 COSM5721820 c.11236C>T p.R3746C Substitution - Missense 11:118519716-118519716 + 83 COSM3732819 c.9678_9679insA p.Q3227fs*6 Insertion - Frameshift 11:118505579-118505580 + TCGA-23-1114-01 COSM1321887 c.526C>A p.R176S Substitution - Missense 11:118471685-118471685 + TCGA-A8-A0A6-01 COSM3808485 c.6441A>C p.T2147T Substitution - coding silent 11:118501802-118501802 + TCGA-HT-7469-01 COSM3967348 c.7724C>T p.P2575L Substitution - Missense 11:118503625-118503625 + TCGA-HU-A4H4-01 COSM4018319 c.6263A>G p.E2088G Substitution - Missense 11:118501100-118501100 + TCGA-D3-A51T-06 COSM3443949 c.2509C>T p.P837S Substitution - Missense 11:118473668-118473668 + 587334 COSM1215170 c.6825T>A p.N2275K Substitution - Missense 11:118502726-118502726 + C086 COSM5534578 c.10673C>T p.S3558F Substitution - Missense 11:118506574-118506574 + TCGA-B5-A11E-01 COSM923584 c.5022C>T p.P1674P Substitution - coding silent 11:118493083-118493083 + 587376 COSM1215184 c.7855C>T p.R2619C Substitution - Missense 11:118503756-118503756 + TCGA-FG-8186-01 COSM466406 c.11261A>G p.N3754S Substitution - Missense 11:118519741-118519741 + HCT8 COSM2105644 c.11271C>A p.P3757P Substitution - coding silent 11:118519751-118519751 + TCGA-ER-A193-06 COSM3443977 c.5404T>A p.Y1802N Substitution - Missense 11:118495749-118495749 + RKO COSM2105384 c.2620_2621delAG p.D877fs*8 Deletion - Frameshift 11:118473779-118473780 + TCGA-AP-A059-01 COSM923586 c.6278G>T p.R2093M Substitution - Missense 11:118501115-118501115 + TCGA-EE-A2MR-06 COSM3444009 c.9359C>T p.S3120L Substitution - Missense 11:118505260-118505260 + 587376 COSM1215186 c.9251A>G p.N3084S Substitution - Missense 11:118505152-118505152 + TCGA-FK-A3SD-01 COSM3368235 c.4721A>G p.K1574R Substitution - Missense 11:118491220-118491220 + EGC15 COSM1351665 c.10067C>T p.A3356V Substitution - Missense 11:118505968-118505968 + TCGA-EK-A3GK-01 COSM4853865 c.11356C>T p.R3786C Substitution - Missense 11:118520000-118520000 + MB116PT COSM88008 c.2319G>A p.P773P Substitution - coding silent 11:118473478-118473478 + YUWIA COSM5371765 c.1187G>A p.G396E Substitution - Missense 11:118472346-118472346 + CN-AML-36-T COSM5427115 c.4186G>A p.D1396N Substitution - Missense 11:118484282-118484282 + TCGA-AP-A056-01 COSM923589 c.6827A>C p.K2276T Substitution - Missense 11:118502728-118502728 + B71-Tumor COSM254814 c.8647C>G p.L2883V Substitution - Missense 11:118504548-118504548 + DM29 COSM2105339 c.947C>T p.S316L Substitution - Missense 11:118472106-118472106 + TCGA-BS-A0V7-01 COSM923601 c.10815G>A p.G3605G Substitution - coding silent 11:118507598-118507598 + TCGA-F4-6856-01 COSM1351675 c.11456G>A p.R3819H Substitution - Missense 11:118520837-118520837 + Pat_41_B COSM5837923 c.2932C>T p.P978S Substitution - Missense 11:118474091-118474091 + TCGA-AD-6964-01 COSM1351603 c.1362G>A p.P454P Substitution - coding silent 11:118472521-118472521 + PD6977a COSM4384588 c.3755C>A p.P1252H Substitution - Missense 11:118481835-118481835 + TCGA-AP-A059-01 COSM923583 c.4992G>A p.R1664R Substitution - coding silent 11:118491925-118491925 + TCGA-BR-A4QL-01 COSM1351634 c.5291G>A p.R1764H Substitution - Missense 11:118494704-118494704 + 39 COSM5762898 c.8956G>A p.E2986K Substitution - Missense 11:118504857-118504857 + TCGA-BR-8487-01 COSM4018353 c.11707C>T p.R3903C Substitution - Missense 11:118521969-118521969 + GB02 COSM1743791 c.4662A>T p.S1554S Substitution - coding silent 11:118490215-118490215 + TCGA-G3-A25T-01 COSM4941516 c.1542C>T p.P514P Substitution - coding silent 11:118472701-118472701 + HCC118T COSM5813530 c.2943A>T p.P981P Substitution - coding silent 11:118474102-118474102 + PD4937a COSM162499 c.1566G>C p.E522D Substitution - Missense 11:118472725-118472725 + TCGA-BR-4184-01 COSM4018321 c.6637A>G p.M2213V Substitution - Missense 11:118502538-118502538 + ESCC_11 COSM5624219 c.8136A>G p.P2712P Substitution - coding silent 11:118504037-118504037 + ACINAR01 COSM1732940 c.8449G>A p.D2817N Substitution - Missense 11:118504350-118504350 + PD5748a COSM4384584 c.1402C>A p.H468N Substitution - Missense 11:118472561-118472561 + TCGA-CJ-5672-01 COSM466405 c.10841T>C p.L3614P Substitution - Missense 11:118509150-118509150 + T2940 COSM4702389 c.4677C>T p.C1559C Substitution - coding silent 11:118490230-118490230 + TCGA-EE-A3J8-06 COSM3443965 c.4963C>T p.R1655W Substitution - Missense 11:118491896-118491896 + 3N35-VS-3T35 COSM4018355 c.11893C>T p.R3965W Substitution - Missense 11:118522155-118522155 + B85-0-Tumor COSM1756743 c.5154G>T p.G1718G Substitution - coding silent 11:118493215-118493215 + 16668 COSM48571 c.8017A>T p.T2673S Substitution - Missense 11:118503918-118503918 + 081T COSM1731568 c.6596delC p.L2200fs*10 Deletion - Frameshift 11:118502497-118502497 + 33T COSM255058 c.4427_4429delGTC p.R1478delR Deletion - In frame 11:118488708-118488710 + TCGA-A5-A0GW-01 COSM923585 c.6224G>A p.R2075H Substitution - Missense 11:118501061-118501061 + 61 COSM923585 c.6224G>A p.R2075H Substitution - Missense 11:118501061-118501061 + SC_9076 COSM5568099 c.9950C>G p.S3317* Substitution - Nonsense 11:118505851-118505851 + cSCCP4 COSM138846 c.3493G>C p.E1165Q Substitution - Missense 11:118478125-118478125 + TCGA-DK-A3X1-01 COSM3791226 c.11163G>A p.G3721G Substitution - coding silent 11:118519643-118519643 + TCGA-BT-A0YX-01 COSM415326 c.4697G>A p.G1566E Substitution - Missense 11:118491196-118491196 + sysucc-1317T COSM5448093 c.9827C>A p.T3276N Substitution - Missense 11:118505728-118505728 + TCGA-G3-A5SJ-01 COSM4914896 c.572C>G p.S191* Substitution - Nonsense 11:118471731-118471731 + YUKAT COSM5371767 c.1838G>A p.R613Q Substitution - Missense 11:118472997-118472997 + HCC83 COSM3666009 c.7676T>A p.I2559N Substitution - Missense 11:118503577-118503577 + TCGA-22-5491-01 COSM686168 c.4006G>T p.E1336* Substitution - Nonsense 11:118482086-118482086 + TCGA-BT-A20Q-01 COSM415323 c.7974G>C p.K2658N Substitution - Missense 11:118503875-118503875 + TCGA-AA-3696-01 COSM268500 c.6235G>A p.V2079I Substitution - Missense 11:118501072-118501072 + TCGA-CK-5913-01 COSM1351653 c.8818A>G p.T2940A Substitution - Missense 11:118504719-118504719 + TCGA-BR-8369-01 COSM4018296 c.3184T>C p.S1062P Substitution - Missense 11:118476832-118476832 + 2492721 COSM5721820 c.11236C>T p.R3746C Substitution - Missense 11:118519716-118519716 + HCC42T COSM1604171 c.9182A>G p.N3061S Substitution - Missense 11:118505083-118505083 + 55 COSM4777717 c.6399_6400insC p.C2134fs*41 Insertion - Frameshift 11:118501760-118501761 + Pa02C COSM84115 c.6820G>C p.G2274R Substitution - Missense 11:118502721-118502721 + 131 COSM3732918 c.2495C>G p.P832R Substitution - Missense 11:118473654-118473654 + IPMN21 COSM248850 c.5953-2A>G p.? Unknown 11:118499301-118499301 + TCGA-D8-A1XK-01 COSM3808483 c.5515A>G p.T1839A Substitution - Missense 11:118495860-118495860 + ESCC_3 COSM5622546 c.4914A>G p.K1638K Substitution - coding silent 11:118491847-118491847 + TCGA-D3-A51T-06 COSM3443963 c.4791C>T p.S1597S Substitution - coding silent 11:118491290-118491290 + TCGA-ER-A193-06 COSM3443959 c.4396C>T p.P1466S Substitution - Missense 11:118488677-118488677 + YUSWI COSM1704640 c.9722C>T p.S3241L Substitution - Missense 11:118505623-118505623 + TCGA-24-2288-01 COSM116715 c.9606C>A p.S3202R Substitution - Missense 11:118505507-118505507 + CSCC-7-T COSM4514519 c.9776C>T p.P3259L Substitution - Missense 11:118505677-118505677 + CHC805T COSM4954307 c.3755C>G p.P1252R Substitution - Missense 11:118481835-118481835 + TCGA-BL-A3JM-01 COSM1297694 c.4330G>C p.E1444Q Substitution - Missense 11:118484973-118484973 + PCSI_0060_Pa_X COSM3375602 c.7291A>G p.K2431E Substitution - Missense 11:118503192-118503192 + ME043T COSM228564 c.6905C>T p.S2302F Substitution - Missense 11:118502806-118502806 + HCC82T COSM3666011 c.11441T>C p.L3814P Substitution - Missense 11:118520822-118520822 + RK046_C02 COSM1627812 c.536C>G p.P179R Substitution - Missense 11:118471695-118471695 + 587228 COSM1215168 c.3941C>T p.P1314L Substitution - Missense 11:118482021-118482021 + 103T COSM1237852 c.11801T>A p.I3934N Substitution - Missense 11:118522063-118522063 + S12-23181-TP COSM4529345 c.1603G>A p.E535K Substitution - Missense 11:118472762-118472762 + SH-7166 COSM5020616 c.4284A>C p.I1428I Substitution - coding silent 11:118484927-118484927 + TCGA-61-1737-01 COSM1321885 c.3127C>G p.L1043V Substitution - Missense 11:118474286-118474286 + TCGA-EE-A3J5-06 COSM3443981 c.6674C>T p.S2225F Substitution - Missense 11:118502575-118502575 + TCGA-HU-A4GQ-01 COSM4018298 c.3708C>T p.N1236N Substitution - coding silent 11:118481788-118481788 + T3174 COSM4702379 c.2809_2811delTCA p.S938delS Deletion - In frame 11:118473968-118473970 + HCC58 COSM3666005 c.4702T>G p.F1568V Substitution - Missense 11:118491201-118491201 + DM58 COSM3443939 c.1150C>T p.Q384* Substitution - Nonsense 11:118472309-118472309 + sysucc-1247T COSM3443947 c.2233C>T p.R745* Substitution - Nonsense 11:118473392-118473392 + TCGA-FW-A3R5-06 COSM1351626 c.4594C>T p.R1532C Substitution - Missense 11:118490147-118490147 + TCGA-D1-A103-01 COSM923571 c.1219C>T p.R407* Substitution - Nonsense 11:118472378-118472378 + A4 COSM5349624 c.8793G>T p.L2931L Substitution - coding silent 11:118504694-118504694 + DM10 COSM5609396 c.4594C>A p.R1532S Substitution - Missense 11:118490147-118490147 + CAL33 COSM2105463 c.3858C>T p.A1286A Substitution - coding silent 11:118481938-118481938 + CSCC-20-T COSM4514889 c.9900C>A p.P3300P Substitution - coding silent 11:118505801-118505801 + TCGA-23-1122-01 COSM71655 c.4391A>G p.E1464G Substitution - Missense 11:118488672-118488672 + TCGA-FS-A1ZZ-06 COSM3443947 c.2233C>T p.R745* Substitution - Nonsense 11:118473392-118473392 + YUTUR COSM5371763 c.864G>A p.G288G Substitution - coding silent 11:118472023-118472023 + PR-05-3595 COSM245704 c.6222C>T p.C2074C Substitution - coding silent 11:118501059-118501059 + CSCC-60-T COSM4494741 c.4395C>T p.R1465R Substitution - coding silent 11:118488676-118488676 + I2L-P19Tb-Tumor-Biopsy COSM5360762 c.5281-1G>A p.? Unknown 11:118494693-118494693 + TCGA-CU-A0YO-01 COSM415321 c.8408C>T p.S2803L Substitution - Missense 11:118504309-118504309 + DLBCL-PatientI COSM220404 c.1223A>T p.Q408L Substitution - Missense 11:118472382-118472382 + TCGA-FS-A1ZC-06 COSM3443959 c.4396C>T p.P1466S Substitution - Missense 11:118488677-118488677 + MEL-JWCI-WGS-7 COSM1167631 c.11612delG p.E3872fs*21 Deletion - Frameshift 11:118521395-118521395 + TCGA-EE-A2GC-06 COSM3443975 c.5386C>T p.P1796S Substitution - Missense 11:118495731-118495731 + HCC58T COSM3666005 c.4702T>G p.F1568V Substitution - Missense 11:118491201-118491201 + CSCC-31-T COSM4467584 c.1498C>T p.P500S Substitution - Missense 11:118472657-118472657 + TCGA-FY-A3BL-01 COSM1604171 c.9182A>G p.N3061S Substitution - Missense 11:118505083-118505083 + TCGA-24-1844-01 COSM1321883 c.3634G>C p.A1212P Substitution - Missense 11:118480238-118480238 + ESCC_BICR_021T COSM5434258 c.3462G>T p.R1154R Substitution - coding silent 11:118478094-118478094 + TCGA-BH-A18U-01 COSM428502 c.9168G>A p.P3056P Substitution - coding silent 11:118505069-118505069 + TCGA-Q1-A73S-01 COSM4836675 c.6254G>A p.S2085N Substitution - Missense 11:118501091-118501091 + YUSCA COSM923571 c.1219C>T p.R407* Substitution - Nonsense 11:118472378-118472378 + T3091 COSM4702398 c.7581delA p.M2529fs*11 Deletion - Frameshift 11:118503482-118503482 + 234 COSM3731364 c.1655delC p.Q554fs*13 Deletion - Frameshift 11:118472814-118472814 + pfg068T COSM4747798 c.2886_2889delAAAG p.K964fs*42 Deletion - Frameshift 11:118474045-118474048 + Br27P COSM40331 c.6473G>A p.G2158D Substitution - Missense 11:118501834-118501834 + TCGA-BP-5182-01 COSM466403 c.8662G>T p.E2888* Substitution - Nonsense 11:118504563-118504563 + SH-5693 COSM5020404 c.7245C>T p.N2415N Substitution - coding silent 11:118503146-118503146 + Pat_24_A COSM1351611 c.2584C>T p.R862* Substitution - Nonsense 11:118473743-118473743 + CSCC-49-T COSM4506593 c.7236C>T p.S2412S Substitution - coding silent 11:118503137-118503137 + S0080 COSM5882018 c.5756A>C p.K1919T Substitution - Missense 11:118498036-118498036 + S01563 COSM25627 c.2880A>G p.I960M Substitution - Missense 11:118474039-118474039 + TCGA-F4-6569-01 COSM1351673 c.11102G>A p.R3701Q Substitution - Missense 11:118511990-118511990 + DM8 COSM5611333 c.8221_8222CC>TT p.P2741L Substitution - Missense 11:118504122-118504123 + CSCC-7-T COSM4449881 c.3634+2T>G p.? Unknown 11:118480240-118480240 + CHC1738T COSM4805288 c.10244C>T p.P3415L Substitution - Missense 11:118506145-118506145 + TCGA-CZ-5470-01 COSM466401 c.7203C>A p.T2401T Substitution - coding silent 11:118503104-118503104 + PD8734a COSM4384596 c.4769A>G p.K1590R Substitution - Missense 11:118491268-118491268 + SS6003109 COSM5036317 c.5794-10G>C p.? Unknown 11:118498360-118498360 + YUSPO COSM5371773 c.4357G>T p.E1453* Substitution - Nonsense 11:118488638-118488638 + YUGAFFE COSM1704638 c.7111C>T p.H2371Y Substitution - Missense 11:118503012-118503012 + P02-2035 COSM245706 c.7332A>G p.K2444K Substitution - coding silent 11:118503233-118503233 + Pa02C COSM84116 c.7770T>G p.N2590K Substitution - Missense 11:118503671-118503671 + TCGA-A5-A0VP-01 COSM923578 c.3619C>T p.Q1207* Substitution - Nonsense 11:118480223-118480223 + LUAD-VUMN6 COSM347790 c.2854G>C p.D952H Substitution - Missense 11:118474013-118474013 + HX27T COSM3746236 c.11171A>C p.H3724P Substitution - Missense 11:118519651-118519651 + TCGA-EE-A29X-06 COSM3443993 c.7674A>G p.P2558P Substitution - coding silent 11:118503575-118503575 + 1 COSM5762894 c.3770G>T p.S1257I Substitution - Missense 11:118481850-118481850 + LIM1899 COSM1351607 c.2311_2312insC p.S774fs*12 Insertion - Frameshift 11:118473470-118473471 + TCGA-FS-A1ZA-06 COSM3443983 c.6728T>C p.V2243A Substitution - Missense 11:118502629-118502629 + 2492723 COSM5721817 c.4522G>A p.E1508K Substitution - Missense 11:118489834-118489834 + ESCC_81 COSM5635845 c.11611C>T p.R3871W Substitution - Missense 11:118521394-118521394 + PD6894a COSM4384616 c.9107C>A p.S3036Y Substitution - Missense 11:118505008-118505008 + TCGA-D9-A3Z1-06 COSM3443953 c.2813C>T p.S938L Substitution - Missense 11:118473972-118473972 + CSCC-15-T COSM3443959 c.4396C>T p.P1466S Substitution - Missense 11:118488677-118488677 + 2521259 COSM5890609 c.5863C>T p.H1955Y Substitution - Missense 11:118498439-118498439 + LUAD-RT-S01699 COSM378134 c.1200G>C p.K400N Substitution - Missense 11:118472359-118472359 + LUAD-F00018 COSM338947 c.4282A>G p.I1428V Substitution - Missense 11:118484925-118484925 + ESO-1670 COSM1257776 c.7612G>T p.A2538S Substitution - Missense 11:118503513-118503513 + S0029 COSM5882016 c.1817G>A p.G606E Substitution - Missense 11:118472976-118472976 + NCI-H128 COSM25627 c.2880A>G p.I960M Substitution - Missense 11:118474039-118474039 + SWE-46 COSM1180079 c.4087-1G>A p.? Unknown 11:118484182-118484182 + CRC-19T COSM5480825 c.1264A>G p.I422V Substitution - Missense 11:118472423-118472423 + TCGA-DA-A1HY-06 COSM3443957 c.4219-2A>G p.? Unknown 11:118484860-118484860 + TCGA-BR-4184-01 COSM4018316 c.5950G>A p.E1984K Substitution - Missense 11:118498526-118498526 + CSCC-55-T COSM4512202 c.8948C>T p.P2983L Substitution - Missense 11:118504849-118504849 + T3174 COSM4702375 c.1277G>A p.R426Q Substitution - Missense 11:118472436-118472436 + CSCC-38-T COSM4505036 c.681C>T p.T227T Substitution - coding silent 11:118471840-118471840 + RK048_C COSM1627818 c.7752A>G p.Q2584Q Substitution - coding silent 11:118503653-118503653 + TCGA-DK-A2I6-01 COSM1297690 c.517C>T p.R173* Substitution - Nonsense 11:118471676-118471676 + YUAKER COSM1704634 c.5563C>T p.R1855* Substitution - Nonsense 11:118496275-118496275 + 2492722 COSM5724107 c.34C>T p.R12* Substitution - Nonsense 11:118436546-118436546 + 587234 COSM1215180 c.7852C>T p.R2618C Substitution - Missense 11:118503753-118503753 + Pat_45_B COSM5837921 c.1294G>A p.E432K Substitution - Missense 11:118472453-118472453 + TCGA-BR-8487-01 COSM4018339 c.10199C>T p.P3400L Substitution - Missense 11:118506100-118506100 + PD8979a COSM5792373 c.11631C>A p.S3877R Substitution - Missense 11:118521414-118521414 + TCGA-AA-A010-01 COSM282814 c.7044C>T p.I2348I Substitution - coding silent 11:118502945-118502945 + TCGA-D1-A17Q-01 COSM923595 c.8312C>A p.S2771Y Substitution - Missense 11:118504213-118504213 + PR-00-1165 COSM245703 c.11521C>T p.R3841W Substitution - Missense 11:118521304-118521304 + TCGA-CG-5728-01 COSM2105598 c.9310T>C p.L3104L Substitution - coding silent 11:118505211-118505211 + TCGA-AG-3892-01 COSM257414 c.9886T>C p.F3296L Substitution - Missense 11:118505787-118505787 + TCGA-E9-A54Y-01 COSM3808479 c.4390G>T p.E1464* Substitution - Nonsense 11:118488671-118488671 + S09-2518-TP COSM4990130 c.6854C>T p.S2285F Substitution - Missense 11:118502755-118502755 + T3174 COSM1351609 c.2312delC p.P773fs*8 Deletion - Frameshift 11:118473471-118473471 + TCGA-AP-A056-01 COSM923602 c.10966C>T p.R3656W Substitution - Missense 11:118510022-118510022 + HCC61 COSM1604167 c.7093C>G p.L2365V Substitution - Missense 11:118502994-118502994 + TCGA-EE-A3AC-06 COSM3443991 c.7491C>T p.V2497V Substitution - coding silent 11:118503392-118503392 + CHC1747T COSM4788109 c.2863G>A p.A955T Substitution - Missense 11:118474022-118474022 + 260211 COSM3725925 c.545G>T p.G182V Substitution - Missense 11:118471704-118471704 + SJHGG024_R COSM4969518 c.10917_10918delAA p.S3640fs*1 Deletion - Frameshift 11:118509973-118509974 + TCGA-FS-A1ZS-06 COSM3443967 c.5124A>G p.L1708L Substitution - coding silent 11:118493185-118493185 + CSCC-31-T COSM4545139 c.3711G>T p.V1237V Substitution - coding silent 11:118481791-118481791 + sysucc-311T COSM1351663 c.9863G>T p.R3288I Substitution - Missense 11:118505764-118505764 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.258855 11q23 159555

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C Missense p.H3452P c.10355A>C 11 118376962 UCEC A C Missense p.K3048T c.9143A>C 11 118375750 BRCA A C Synonymous p.P1145P c.3435A>C 11 118348782 NB A C Synonymous p.S3014S c.9042A>C 11 118375649 GBM A - Frameshift p.D1710Ifs*2 c.5127delA 11 118363894 LUAD - A Frameshift p.E390Rfs*34 c.1167dupA 11 118343037 PRAD A - Frameshift p.N1473Ifs*113 c.4418delA 11 118359411 BLCA - A Frameshift p.P3668Tfs*8 c.11001dupA 11 118380758 LUAD - A Frameshift p.S462Ifs*19 c.1383dupA 11 118343254 SCLC AGCCTTTAGATCTAGAAGGAGTCAAG - Frameshift p.P1708Efs*15 c.5122_5147delCCTTTAGATCTAGAAGGAGTCAAGAG 11 118363887 BRCA A G IntronicSNV . c.11146+121A>G 11 118382861 HC A G IntronicSNV . c.432+11269A>G 11 118318928 HC A G Missense p.E1464G c.4391A>G 11 118359387 OV A G Missense p.I960M c.2880A>G 11 118344754 SCLC A G Missense p.K1574R c.4721A>G 11 118361935 THCA A G Missense p.K2333E c.6997A>G 11 118373604 OV A G Missense p.K2616R c.7847A>G 11 118374454 LUSC A G Missense p.M3650V c.10948A>G 11 118380710 LGG A G Missense p.N2579S c.7736A>G 11 118374343 LUAD A G Missense p.N3064S c.9191A>G 11 118375798 THCA A G Missense p.N3757S c.11270A>G 11 118390456 LGG A G Missense p.N3757S c.11270A>G 11 118390456 RCCC A G Missense p.Q3163R c.9488A>G 11 118376095 SCLC A G Missense p.T3212A c.9634A>G 11 118376241 CM A G SpliceAcceptorSNV . c.4219-2A>G 11 118355575 CM A G Synonymous p.L1711L c.5133A>G 11 118363900 CM A G Synonymous p.P2561P c.7683A>G 11 118374290 CM A G Synonymous p.P3410P c.10230A>G 11 118376837 LUAD A G Synonymous p.Q2587Q c.7761A>G 11 118374368 HC A G Synonymous p.Q3350Q c.10050A>G 11 118376657 STAD A G Synonymous p.S2694S c.8082A>G 11 118374689 STAD A T Missense p.D2721V c.8162A>T 11 118374769 THCA C A Missense p.D1918E c.5754C>A 11 118368740 LUSC C A Missense p.L1602I c.4804C>A 11 118362018 LUAD C A Missense p.L2373I c.7117C>A 11 118373724 STAD C A Missense p.P3183T c.9547C>A 11 118376154 LUAD C A Missense p.Q2261K c.6781C>A 11 118373388 NB C A Missense p.S3205R c.9615C>A 11 118376222 OV C A Missense p.S783Y c.2348C>A 11 118344222 BRCA C A Missense p.T2815K c.8444C>A 11 118375051 RCCC C A Synonymous p.A788A c.2364C>A 11 118344238 LUSC C A Synonymous p.P1159P c.3477C>A 11 118348824 CM C A Synonymous p.V2914V c.8742C>A 11 118375349 HNSC - CCTC Frameshift p.S2565Lfs*3 c.7692_7693insCTCC 11 118374298 BLCA CCTCTGG - Frameshift p.P1466Rfs*118 c.4396_4402delCCTCTGG 11 118359392 BRCA C - Frameshift p.P3404Qfs*20 c.10211delC 11 118376817 CM C G Missense p.H3910D c.11728C>G 11 118392696 ESCA C G Missense p.L2886V c.8656C>G 11 118375263 CLL C G Missense p.L3726V c.11176C>G 11 118390362 LUSC C G Missense p.P179R c.536C>G 11 118342410 HC C G Missense p.P3140A c.9418C>G 11 118376025 HNSC C G Missense p.S1002C c.3005C>G 11 118344879 BRCA C G Missense p.S2935C c.8804C>G 11 118375411 HNSC C G Missense p.S3786C c.11357C>G 11 118390707 CLL C G Missense p.T3375S c.10124C>G 11 118376731 LUSC C G Synonymous p.G2660G c.7980C>G 11 118374587 STAD C G Synonymous p.L3132L c.9396C>G 11 118376003 LUSC C G Synonymous p.P3115P c.9345C>G 11 118375952 CM C G Synonymous p.P3959P c.11877C>G 11 118392845 BRCA C G Synonymous p.T124T c.372C>G 11 118307599 CLL C T IntronicSNV . c.11430-26C>T 11 118391491 MB C T Missense p.A3756V c.11267C>T 11 118390453 CM C T Missense p.H1596Y c.4786C>T 11 118362000 CM C T Missense p.H1958Y c.5872C>T 11 118369154 BRCA C T Missense p.H2374Y c.7120C>T 11 118373727 CM C T Missense p.H708Y c.2122C>T 11 118343996 CM C T Missense p.L3462F c.10384C>T 11 118376991 CM C T Missense p.P1354S c.4060C>T 11 118353184 CM C T Missense p.P1466S c.4396C>T 11 118359392 CM C T Missense p.P1799S c.5395C>T 11 118366446 CM C T Missense p.P2332S c.6994C>T 11 118373601 CM C T Missense p.P2578L c.7733C>T 11 118374340 LGG C T Missense p.P2649L c.7946C>T 11 118374553 CM C T Missense p.P280L c.839C>T 11 118342713 CM C T Missense p.P3090S c.9268C>T 11 118375875 HNSC C T Missense p.P3098L c.9293C>T 11 118375900 CM C T Missense p.P3195L c.9584C>T 11 118376191 GBM C T Missense p.P603S c.1807C>T 11 118343681 CM C T Missense p.R1350C c.4048C>T 11 118353172 STAD C T Missense p.R1478C c.4432C>T 11 118359428 UCEC C T Missense p.R1658W c.4972C>T 11 118362611 CM C T Missense p.R503W c.1507C>T 11 118343381 STAD C T Missense p.R886W c.2656C>T 11 118344530 STAD C T Missense p.S1657F c.4970C>T 11 118362609 CM C T Missense p.S2228F c.6683C>T 11 118373290 CM C T Missense p.S2255L c.6764C>T 11 118373371 CM C T Missense p.S2305F c.6914C>T 11 118373521 CM C T Missense p.S2353F c.7058C>T 11 118373665 CM C T Missense p.S2425F c.7274C>T 11 118373881 CM C T Missense p.S2496F c.7487C>T 11 118374094 UCEC C T Missense p.S2806L c.8417C>T 11 118375024 BLCA C T Missense p.S2872L c.8615C>T 11 118375222 BRCA C T Missense p.S2917F c.8750C>T 11 118375357 CM C T Missense p.S3204F c.9611C>T 11 118376218 CM C T Missense p.S633F c.1898C>T 11 118343772 CM C T Missense p.S680L c.2039C>T 11 118343913 ESCA C T Missense p.S859F c.2576C>T 11 118344450 CM C T Missense p.T2943I c.8828C>T 11 118375435 CM C T Nonsense p.Q1195* c.3583C>T 11 118350902 BRCA C T Nonsense p.Q1207* c.3619C>T 11 118350938 UCEC C T Nonsense p.Q2902* c.8704C>T 11 118375311 CM C T Nonsense p.Q384* c.1150C>T 11 118343024 CM C T Nonsense p.R1264* c.3790C>T 11 118352585 HNSC C T Nonsense p.R1636* c.4906C>T 11 118362545 HNSC C T Nonsense p.R173* c.517C>T 11 118342391 BLCA C T Nonsense p.R2127* c.6379C>T 11 118372446 CM C T Nonsense p.R2191* c.6571C>T 11 118373178 CM C T Nonsense p.R2191* c.6571C>T 11 118373178 UCEC C T Nonsense p.R3283* c.9847C>T 11 118376454 BLCA C T Nonsense p.R745* c.2233C>T 11 118344107 CM C T Nonsense p.R862* c.2584C>T 11 118344458 CM C T Synonymous p.A2243A c.6729C>T 11 118373336 MM C T Synonymous p.A638A c.1914C>T 11 118343788 CM C T Synonymous p.F1455F c.4365C>T 11 118359361 LUAD C T Synonymous p.I3105I c.9315C>T 11 118375922 CM C T Synonymous p.I3180I c.9540C>T 11 118376147 HNSC C T Synonymous p.L278L c.834C>T 11 118342708 CM C T Synonymous p.L682L c.2046C>T 11 118343920 CM C T Synonymous p.S1777S c.5331C>T 11 118365450 CM C T Synonymous p.T672T c.2016C>T 11 118343890 COREAD C T Synonymous p.V2500V c.7500C>T 11 118374107 CM G A Missense p.A3615T c.10843G>A 11 118379858 STAD G A Missense p.D2842N c.8524G>A 11 118375131 BLCA G A Missense p.D431N c.1291G>A 11 118343165 BRCA G A Missense p.E1363K c.4087G>A 11 118354898 STAD G A Missense p.E2475K c.7423G>A 11 118374030 HNSC G A Missense p.E2509K c.7525G>A 11 118374132 BLCA G A Missense p.E3941K c.11821G>A 11 118392789 HNSC G A Missense p.E875K c.2623G>A 11 118344497 CM G A Missense p.G1566E c.4697G>A 11 118361911 BLCA G A Missense p.G2161D c.6482G>A 11 118372549 GBM G A Missense p.G2606S c.7816G>A 11 118374423 MM G A Missense p.G2867D c.8600G>A 11 118375207 ESCA G A Missense p.G3719S c.11155G>A 11 118390341 STAD G A Missense p.M1585I c.4755G>A 11 118361969 HNSC G A Missense p.R1154Q c.3461G>A 11 118348808 MB G A Missense p.R1665H c.4994G>A 11 118362633 COREAD G A Missense p.R2065H c.6194G>A 11 118371737 ESCA G A Missense p.R2078H c.6233G>A 11 118371776 UCEC G A Missense p.R2207Q c.6620G>A 11 118373227 LUAD G A Missense p.R3789H c.11366G>A 11 118390716 COREAD G A Missense p.R530K c.1589G>A 11 118343463 HNSC G A Missense p.S3153N c.9458G>A 11 118376065 CM G A Missense p.V157I c.469G>A 11 118339526 HNSC G A Missense p.V2082I c.6244G>A 11 118371787 COREAD G A Missense p.V3050M c.9148G>A 11 118375755 UCEC G A SpliceAcceptorSNV . c.6159-1G>A 11 118371701 BRCA G A Synonymous p.E879E c.2637G>A 11 118344511 BLCA G A Synonymous p.G3608G c.10824G>A 11 118378313 UCEC G A Synonymous p.P1306P c.3918G>A 11 118352713 RCCC G A Synonymous p.P1367P c.4101G>A 11 118354912 BRCA G A Synonymous p.P3059P c.9177G>A 11 118375784 BRCA G A Synonymous p.Q2711Q c.8133G>A 11 118374740 LUSC G A Synonymous p.R2211R c.6633G>A 11 118373240 CM G C Missense p.A3463P c.10387G>C 11 118376994 LUAD G C Missense p.D1693H c.5077G>C 11 118363844 OV G C Missense p.E1444Q c.4330G>C 11 118355688 BLCA G C Missense p.E2509Q c.7525G>C 11 118374132 BLCA G C Missense p.E2768Q c.8302G>C 11 118374909 BLCA G C Missense p.E3702Q c.11104G>C 11 118382698 GBM G C Missense p.E522D c.1566G>C 11 118343440 BRCA G C Missense p.G150R c.448G>C 11 118339505 ESCA G C Missense p.G2277R c.6829G>C 11 118373436 PAAD G C Missense p.G3553R c.10657G>C 11 118377264 OV G C Missense p.K2661N c.7983G>C 11 118374590 BLCA G C Missense p.L2472F c.7416G>C 11 118374023 HNSC G C Missense p.R1686P c.5057G>C 11 118363824 LUAD GGAACCTGGTCAG - Frameshift p.E2451*fs*1 c.7351_7363delGAACCTGGTCAGG 11 118373957 BLCA GG AA MultiAAMissense p.M1926_A1927delinsIT c.5778_5779delinsAA 11 118368764 CM GGACCAGCTGGAAAATTG - InFrameDeletion p.D1469_W1474delDQLENW c.4405_4422delGACCAGCTGGAAAATTGG 11 118359400 BRCA G T Missense p.A2541S c.7621G>T 11 118374228 ESCA G T Missense p.C1170F c.3509G>T 11 118348856 BRCA G T Missense p.C1452F c.4355G>T 11 118359351 STAD G T Missense p.D920Y c.2758G>T 11 118344632 LUAD G T Missense p.R2096S c.6288G>T 11 118371831 COREAD G T Missense p.R3659L c.10976G>T 11 118380738 STAD G T Missense p.V3731L c.11191G>T 11 118390377 HNSC G T Nonsense p.E1336* c.4006G>T 11 118352801 LUSC G T Nonsense p.E2891* c.8671G>T 11 118375278 RCCC G T Nonsense p.E502* c.1504G>T 11 118343378 OV G T SpliceDonorSNV . c.10754+1G>T 11 118377362 HNSC - TAAA Frameshift p.S901Ifs*3 c.2701_2702insTAAA 11 118344575 BRCA TAGCACTGTTAAACAT - Frameshift p.S997Pfs*5 c.2989_3004delAGCACTGTTAAACATT 11 118344862 CM T A Nonsense p.L2165* c.6494T>A 11 118372561 RCCC T A Nonsense p.L2937* c.8810T>A 11 118375417 CM T A Synonymous p.P2049P c.6147T>A 11 118370617 RCCC T A Synonymous p.P2128P c.6384T>A 11 118372451 LUSC T A Synonymous p.S809S c.2427T>A 11 118344301 LGG T C Missense p.L1423S c.4268T>C 11 118355626 SCLC T C Missense p.L1467P c.4400T>C 11 118359396 GBM T C Missense p.S3294P c.9880T>C 11 118376487 BRCA T C Missense p.V2246A c.6737T>C 11 118373344 CM T C Synonymous p.A699A c.2097T>C 11 118343971 PRAD T C Synonymous p.L3107L c.9319T>C 11 118375926 STAD - T Frameshift p.I1184Yfs*28 c.3549dupT 11 118348896 RCCC - T Frameshift p.M1926Ifs*12 c.5777dupT 11 118368763 HNSC T - Frameshift p.P603Lfs*20 c.1806delT 11 118343680 CM T G 3-UTRSNV . c.11916+3948T>G 11 118396832 HC TG - Frameshift p.V3930Hfs*6 c.11788_11789delGT 11 118392755 BLCA T G Missense p.N2593K c.7779T>G 11 118374386 PAAD T G Nonsense p.Y1895* c.5685T>G 11 118368671 BLCA - T IntronicInsertion . c.3634+92dupT 11 118351036 ESCA