ttype patient gene classification type chr pos ref_allele newbase context65 cons46 HNSC HN_62814 SCRT1 SNP Missense 8 145559791 G A 38 60 LUAD LUAD-B01246 SCRT1 SNP Missense_Mutation 8 145559816 G T 35 55 LUAD LUAD-E01317 SCRT1 SNP Missense_Mutation 8 145557001 T C 51 78 BRCA TCGA-A8-A075 SCRT1 SNP Missense_Mutation 8 145559756 G A 40 69