ttype patient gene classification type chr pos ref_allele newbase context65 cons46 MEL MEL-JWCI-WGS-25 SCGB1D1 SNP Missense_Mutation 11 61960887 A T 1 45 MEL MEL-JWCI-WGS-35 SCGB1D1 SNP Splice_site 11 61960872 G A 41 26 LUAD TCGA-17-Z014 SCGB1D1 SNP Missense_Mutation 11 61957767 C T 31 35 LUSC TCGA-43-6143 SCGB1D1 SNP Missense_Mutation 11 61960877 A G 4 43 LUAD TCGA-50-5935 SCGB1D1 SNP Silent 11 61957768 G A 39 42 CRC TCGA-AA-3710 SCGB1D1 SNP Missense_Mutation 11 61959539 G A 44 39 CRC TCGA-AG-A002 SCGB1D1 SNP Missense_Mutation 11 61960885 G T 33 43 UCEC TCGA-AP-A056 SCGB1D1 SNP Silent 11 61960885 G A 33 43 UCEC TCGA-AP-A059 SCGB1D1 SNP Missense_Mutation 11 61959636 C A 28 42 UCEC TCGA-AX-A1C8 SCGB1D1 SNP Missense_Mutation 11 61959695 G T 36 9 UCEC TCGA-B5-A0JY SCGB1D1 SNP Splice_site 11 61960901 G T 33 48 HNSC TCGA-CV-7089 SCGB1D1 SNP Splice_site 11 61957758 T C 51 59 BLCA TCGA-DK-A3IM SCGB1D1 SNP Silent 11 61959667 C T 27 52