ttype patient gene classification type chr pos ref_allele newbase context65 cons46 BRCA BR-MEX-192 FAM19A4 SNP Missense_Mutation 3 68782298 G A 38 78 ESO ESO-1488 FAM19A4 SNP Missense_Mutation 3 68802091 C T 23 100 ESO ESO-887 FAM19A4 SNP Missense_Mutation 3 68929941 C A 19 59 LUAD LUAD-LIP77 FAM19A4 SNP Missense_Mutation 3 68929950 G C 33 84 MEL MEL-JWCI-27 FAM19A4 SNP Silent 3 68929948 T C 53 71 MEL MEL-JWCI-WGS-6 FAM19A4 SNP Missense_Mutation 3 68802157 A G 12 73 NB NB-1042 FAM19A4 SNP Missense_Mutation 3 68929964 G C 37 65 LUAD TCGA-05-4396 FAM19A4 SNP Silent 3 68802081 C A 23 28 GBM TCGA-06-6694 FAM19A4 SNP Nonsense_Mutation 3 68929927 G T 34 84 LUAD TCGA-44-3918 FAM19A4 SNP Missense_Mutation 3 68802096 T A 56 52 LUSC TCGA-60-2713 FAM19A4 SNP Missense_Mutation 3 68934335 C A 24 58 LUAD TCGA-64-1680 FAM19A4 SNP Silent 3 68802078 G C 45 71 AML TCGA-AB-2905 FAM19A4 SNP Missense_Mutation 3 68802037 C T 23 87 UCEC TCGA-AX-A05Z FAM19A4 SNP Missense_Mutation 3 68802149 C A 24 100 UCEC TCGA-AX-A0J0 FAM19A4 SNP Splice_site 3 68782291 C T 31 55 UCEC TCGA-AX-A0J0 FAM19A4 SNP Missense_Mutation 3 68788316 C A 29 100 UCEC TCGA-AX-A0J1 FAM19A4 SNP Silent 3 68802126 C T 25 56 UCEC TCGA-BS-A0UF FAM19A4 SNP Translation_Start_Site 3 68934364 C T 20 52 KIRC TCGA-CJ-4912 FAM19A4 SNP Missense_Mutation 3 68802104 G A 39 61 KIRC TCGA-CJ-4920 FAM19A4 SNP Silent 3 68788346 G C 47 57 HNSC TCGA-CN-6024 FAM19A4 SNP Missense_Mutation 3 68802098 C T 32 100 BLCA TCGA-CU-A3KJ FAM19A4 SNP Missense_Mutation 3 68802156 G C 45 69