ttype patient gene classification type chr pos ref_allele newbase context65 cons46 DLBCL DLBCL-Ls148 FBXO11 SNP Missense_Mutation 2 48040962 C T 30 100 DLBCL DLBCL-Ls2245 FBXO11 SNP Splice_site 2 48059488 C T 21 100 DLBCL DLBCL-Ls843 FBXO11 SNP Missense_Mutation 2 48037482 T A 64 94 DLBCL DLBCL-Ls843 FBXO11 SNP Nonsense_Mutation 2 48046184 C A 29 100 ESO ESO-0059 FBXO11 SNP Missense_Mutation 2 48066092 G T 33 67 ESO ESO-887 FBXO11 SNP Missense_Mutation 2 48045924 T A 55 93 HNSC HN_62417 FBXO11 SNP Missense 2 48035313 C A 32 100 LUAD LUAD-NYU847 FBXO11 SNP Splice_site 2 48059908 C A 24 100 MEL MEL-JWCI-27 FBXO11 SNP Missense_Mutation 2 48050376 G T 47 100 MEL MEL-JWCI-WGS-1 FBXO11 SNP Silent 2 48059756 G A 45 80 MEL MEL-JWCI-WGS-24 FBXO11 SNP Missense_Mutation 2 48063042 G A 47 99 MEL MEL-JWCI-WGS-26 FBXO11 SNP Silent 2 48046127 G A 36 62 MEL MEL-Ma-Mel-107 FBXO11 SNP Missense_Mutation 2 48059591 G A 38 100 MEL MEL-Ma-Mel-119 FBXO11 SNP Missense_Mutation 2 48059516 A G 2 93 MM MM-0297 FBXO11 SNP Silent 2 48040449 A G 16 52 MM MM-0636 FBXO11 SNP Missense_Mutation 2 48045942 T C 51 93 LUAD TCGA-05-4382 FBXO11 SNP Silent 2 48059590 C A 19 45 LUAD TCGA-17-Z055 FBXO11 SNP Missense_Mutation 2 48060016 T A 61 94 LUSC TCGA-18-3416 FBXO11 SNP Missense_Mutation 2 48040932 G A 33 100 LUSC TCGA-18-3417 FBXO11 SNP Missense_Mutation 2 48059965 T A 50 94 LUSC TCGA-21-1070 FBXO11 SNP Missense_Mutation 2 48066854 T C 52 90 LUSC TCGA-37-4141 FBXO11 SNP Missense_Mutation 2 48063100 T C 49 91 LUAD TCGA-50-6593 FBXO11 SNP Missense_Mutation 2 48066010 T A 50 92 LUSC TCGA-60-2698 FBXO11 SNP Missense_Mutation 2 48059968 C T 32 100 LUSC TCGA-60-2719 FBXO11 SNP Missense_Mutation 2 48035532 T C 51 93 BRCA TCGA-A2-A04X FBXO11 SNP Missense_Mutation 2 48047527 C T 29 100 CRC TCGA-AA-3667 FBXO11 SNP Missense_Mutation 2 48046168 G C 36 100 CRC TCGA-AA-3845 FBXO11 SNP Missense_Mutation 2 48036826 C T 27 100 CRC TCGA-AA-3845 FBXO11 SNP Missense_Mutation 2 48059591 G A 38 100 CRC TCGA-AA-3864 FBXO11 SNP Silent 2 48066030 G T 34 64 CRC TCGA-AA-A00A FBXO11 SNP Missense_Mutation 2 48059591 G A 38 100 AML TCGA-AB-2806 FBXO11 INS Frame_Shift_Ins 2 48036754 - GA 61 92 CRC TCGA-AG-3892 FBXO11 SNP Missense_Mutation 2 48036302 G T 33 66 UCEC TCGA-AP-A059 FBXO11 SNP Missense_Mutation 2 48036378 G T 42 100 UCEC TCGA-AP-A0LM FBXO11 SNP Missense_Mutation 2 48035348 G T 35 100 UCEC TCGA-AX-A05Z FBXO11 SNP Missense_Mutation 2 48035337 C A 28 100 UCEC TCGA-AX-A05Z FBXO11 SNP Missense_Mutation 2 48036770 A T 1 79 UCEC TCGA-AX-A060 FBXO11 SNP Missense_Mutation 2 48063064 T C 61 77 UCEC TCGA-AX-A060 FBXO11 SNP Silent 2 48066805 C T 19 70 KIRC TCGA-B0-5702 FBXO11 SNP Silent 2 48050392 A T 7 51 UCEC TCGA-B5-A0K2 FBXO11 SNP Missense_Mutation 2 48066602 C G 19 100 UCEC TCGA-B5-A11E FBXO11 SNP Missense_Mutation 2 48060162 A C 9 92 HNSC TCGA-BA-5152 FBXO11 SNP Missense_Mutation 2 48063095 C T 25 99 HNSC TCGA-BB-7871 FBXO11 SNP Missense_Mutation 2 48066599 G A 46 100 KIRC TCGA-BP-4787 FBXO11 DEL Silent 2 48040362 AAC - 13 60 UCEC TCGA-BS-A0UF FBXO11 SNP Missense_Mutation 2 48045990 A C 1 93 KIRC TCGA-CJ-4916 FBXO11 SNP Missense_Mutation 2 48066061 T C 50 92 HNSC TCGA-CN-5364 FBXO11 INS Frame_Shift_Ins 2 48035326 - GG 15 53 HNSC TCGA-CR-7395 FBXO11 SNP Missense_Mutation 2 48035487 C G 32 100 HNSC TCGA-CV-5441 FBXO11 INS Frame_Shift_Ins 2 48059803 - T 8 94 HNSC TCGA-CV-7416 FBXO11 SNP Missense_Mutation 2 48066041 C T 17 100 BRCA TCGA-D8-A27P FBXO11 SNP Missense_Mutation 2 48049368 T C 52 91 BLCA TCGA-FD-A3N5 FBXO11 SNP Missense_Mutation 2 48061799 C T 29 100