ttype patient gene classification type chr pos ref_allele newbase context65 cons46 HNSC HN_00190 AGPAT1 SNP Missense 6 32138735 G C 47 91 LUAD LUAD-E01278 AGPAT1 SNP Nonsense_Mutation 6 32137073 T A 62 63 MEL MEL-JWCI-WGS-11 AGPAT1 SNP Missense_Mutation 6 32138018 G A 35 93 NB NB-2074 AGPAT1 SNP Missense_Mutation 6 32137139 G A 46 79 LUAD TCGA-05-4396 AGPAT1 SNP Missense_Mutation 6 32138807 C A 23 90 GBM TCGA-06-0154 AGPAT1 SNP Missense_Mutation 6 32138354 G A 39 93 GBM TCGA-06-0192 AGPAT1 SNP Missense_Mutation 6 32139093 G A 40 72 LUSC TCGA-33-6737 AGPAT1 SNP Silent 6 32138256 C T 23 43 LUSC TCGA-56-5897 AGPAT1 SNP Silent 6 32137188 C A 23 55 BRCA TCGA-A7-A0CJ AGPAT1 SNP Splice_Site 6 32138201 C T 19 92 CRC TCGA-AA-3864 AGPAT1 SNP Missense_Mutation 6 32137758 G A 38 67 CRC TCGA-AA-A00E AGPAT1 SNP Silent 6 32137083 G A 36 64 CRC TCGA-AG-3574 AGPAT1 SNP Missense_Mutation 6 32137800 T C 51 67 HNSC TCGA-CR-7395 AGPAT1 SNP Silent 6 32138238 G A 45 80 HNSC TCGA-CV-7095 AGPAT1 SNP Missense_Mutation 6 32137994 C G 26 80 HNSC TCGA-CV-7255 AGPAT1 SNP Missense_Mutation 6 32138309 C T 25 92