ttype patient gene classification type chr pos ref_allele newbase context65 cons46 LUAD TCGA-05-4396 FAM168B SNP Missense_Mutation 2 131812893 C A 23 80 LUAD TCGA-05-4397 FAM168B SNP Missense_Mutation 2 131829459 C A 17 86 LUAD TCGA-17-Z048 FAM168B SNP Silent 2 131829435 G A 41 69 LUAD TCGA-50-5941 FAM168B DEL Frame_Shift_Del 2 131813266 A - 13 85 UCEC TCGA-AP-A059 FAM168B SNP Missense_Mutation 2 131812989 C A 28 92 UCEC TCGA-BG-A0MI FAM168B SNP Silent 2 131812927 C T 17 66 UCEC TCGA-BG-A0RY FAM168B SNP Missense_Mutation 2 131813155 C A 25 69 BRCA TCGA-BH-A1EX FAM168B SNP Missense_Mutation 2 131810522 C T 23 95 UCEC TCGA-BS-A0UV FAM168B SNP Missense_Mutation 2 131812883 A G 8 86 BLCA TCGA-BT-A3PJ FAM168B SNP Splice_site 2 131810476 T C 50 88 BLCA TCGA-DK-A1AD FAM168B SNP Missense_Mutation 2 131812980 G A 45 92