ttype patient gene classification type chr pos ref_allele newbase context65 cons46 MEL MEL-JWCI-WGS-1 SNCG SNP Missense_Mutation 10 88722364 G A 41 70 LUAD TCGA-17-Z016 SNCG SNP Missense_Mutation 10 88719864 C T 29 52 UCEC TCGA-B5-A11V SNCG SNP Missense_Mutation 10 88722373 C A 26 59 UCEC TCGA-BS-A0UF SNCG SNP Missense_Mutation 10 88718513 A G 9 91 UCEC TCGA-D1-A15X SNCG SNP Missense_Mutation 10 88718570 A G 16 91