ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-0067 APOA1 SNP Missense_Mutation 11 116707072 C T 31 84 MEL ME002 APOA1 SNP Missense_Mutation 11 116707738 G A 41 71 MEL ME033 APOA1 SNP Nonsense_Mutation 11 116707817 G A 37 54 MEL ME048 APOA1 SNP Missense_Mutation 11 116707825 G A 43 63 MEL MEL-JWCI-WGS-38 APOA1 SNP Missense_Mutation 11 116707029 T A 62 51 LUAD TCGA-05-4396 APOA1 SNP Silent 11 116707737 G T 39 50 LUAD TCGA-05-4396 APOA1 SNP Missense_Mutation 11 116707809 C A 24 63 UCEC TCGA-AP-A0LG APOA1 SNP Missense_Mutation 11 116707771 C T 28 53 BRCA TCGA-BH-A18F APOA1 SNP Silent 11 116706641 C T 32 58 UCEC TCGA-BS-A0UF APOA1 SNP Nonsense_Mutation 11 116707817 G A 37 54 UCEC TCGA-D1-A16X APOA1 SNP Missense_Mutation 11 116707098 A G 6 67