ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-S41 NSL1 SNP Missense_Mutation 1 212912929 T A 64 50 HNSC HN_62739 NSL1 SNP Synonymous 1 212960962 C A 25 59 HNSC HN_62996 NSL1 SNP Nonsense 1 212960969 G C 45 65 LUAD LUAD-YINHD NSL1 SNP Missense_Mutation 1 212964922 C T 30 75 MEL MEL-Ma-Mel-122 NSL1 SNP Nonsense_Mutation 1 212911944 G A 47 68 LUAD TCGA-50-5930 NSL1 SNP Silent 1 212964938 G A 37 45 LUAD TCGA-64-5781 NSL1 SNP Silent 1 212911978 C T 30 60 CRC TCGA-AA-3955 NSL1 SNP Splice_site 1 212912877 T G 56 64 UCEC TCGA-B5-A0JY NSL1 SNP Missense_Mutation 1 212957757 C A 32 81 BRCA TCGA-BH-A0C0 NSL1 SNP Missense_Mutation 1 212911865 G C 48 63 BRCA TCGA-BH-A0DK NSL1 SNP Missense_Mutation 1 212911824 T C 56 64 UCEC TCGA-BS-A0UV NSL1 SNP Nonsense_Mutation 1 212965006 C A 32 57 HNSC TCGA-CR-6472 NSL1 SNP Missense_Mutation 1 212964964 C T 31 75 HNSC TCGA-CR-7365 NSL1 SNP Missense_Mutation 1 212965008 C A 31 50 BRCA TCGA-E9-A1RF NSL1 SNP Missense_Mutation 1 212912896 C G 30 56 BLCA TCGA-GV-A3JX NSL1 SNP Silent 1 212911828 C T 29 62