ttype patient gene classification type chr pos ref_allele newbase context65 cons46 MEL MEL-Ma-Mel-67 SCGB1C1 SNP Missense_Mutation 11 193825 G A 37 49 GBM TCGA-14-1034 SCGB1C1 SNP Silent 11 193135 C T 29 49 LUAD TCGA-73-4662 SCGB1C1 SNP Nonsense_Mutation 11 193795 G T 45 65 BRCA TCGA-AO-A0JC SCGB1C1 SNP Missense_Mutation 11 193146 G A 46 60 UCEC TCGA-BG-A0LX SCGB1C1 SNP Missense_Mutation 11 193802 C T 18 76 BRCA TCGA-BH-A1F8 SCGB1C1 SNP Missense_Mutation 11 193718 C T 26 65 HNSC TCGA-CV-7411 SCGB1C1 SNP Missense_Mutation 11 193783 G A 33 64