ttype patient gene classification type chr pos ref_allele newbase context65 cons46 BRCA BR-MEX-189 FAM69B SNP Missense_Mutation 9 139612054 G T 38 58 ESO ESO-0103 FAM69B SNP Silent 9 139617440 G T 46 51 LUAD LUAD-RT-S01702 FAM69B SNP Missense_Mutation 9 139617537 C T 27 63 LUAD LUAD_E00565 FAM69B SNP Silent 9 139618007 C T 27 42 LUSC TCGA-22-5473 FAM69B SNP Silent 9 139616741 C T 29 54 LUSC TCGA-51-4080 FAM69B INS Frame_Shift_Ins 9 139616693 - A 17 70 CRC TCGA-AA-3678 FAM69B INS Frame_Shift_Ins 9 139617732 - G 59 90 CRC TCGA-AA-3864 FAM69B SNP Missense_Mutation 9 139616674 G A 39 54 AML TCGA-AB-2808 FAM69B SNP Missense_Mutation 9 139612080 G A 40 45 UCEC TCGA-AP-A059 FAM69B SNP Missense_Mutation 9 139616614 T C 50 74 UCEC TCGA-AP-A0LM FAM69B SNP Missense_Mutation 9 139617873 G A 37 59 UCEC TCGA-BG-A18B FAM69B SNP Silent 9 139617828 C T 20 57 UCEC TCGA-BS-A0TJ FAM69B SNP Missense_Mutation 9 139617657 G A 38 58 UCEC TCGA-BS-A0UF FAM69B SNP Silent 9 139617773 C T 31 47 HNSC TCGA-CR-7373 FAM69B SNP Silent 9 139617956 C T 19 47 UCEC TCGA-D1-A15X FAM69B SNP Missense_Mutation 9 139617906 C T 27 68 UCEC TCGA-D1-A17D FAM69B SNP Missense_Mutation 9 139617928 G A 38 47