ttype patient gene classification type chr pos ref_allele newbase context65 cons46 CLL CW244 NCF1 SNP Missense_Mutation 7 74197939 C T 30 75 ESO ESO-175 NCF1 SNP Missense_Mutation 7 74193626 C T 27 68 ESO ESO-408 NCF1 SNP Silent 7 74191648 G A 39 7 LUAD LUAD_E00522 NCF1 SNP Silent 7 74197944 C T 19 48 LUAD LUAD_E00623 NCF1 SNP Missense_Mutation 7 74193740 G A 45 67 MEL MEL-JWCI-WGS-1 NCF1 SNP Silent 7 74191624 C T 30 52 MEL MEL-Ma-Mel-114 NCF1 SNP Silent 7 74193754 C T 30 44 MM MM-0638 NCF1 SNP Missense_Mutation 7 74197913 C T 27 89 GBM TCGA-14-1829 NCF1 SNP Missense_Mutation 7 74193497 C T 24 54 LUSC TCGA-18-3409 NCF1 SNP Silent 7 74197370 G A 43 33 LUAD TCGA-49-4514 NCF1 SNP Missense_Mutation 7 74193606 C A 22 86 BRCA TCGA-A8-A09I NCF1 SNP Missense_Mutation 7 74193727 C G 29 61 CRC TCGA-AA-3947 NCF1 SNP Missense_Mutation 7 74193734 C T 27 58 BRCA TCGA-AQ-A1H3 NCF1 SNP Missense_Mutation 7 74193672 C T 19 66 UCEC TCGA-AX-A05S NCF1 SNP Splice_site 7 74197403 C T 27 39 UCEC TCGA-AX-A0J1 NCF1 SNP Missense_Mutation 7 74197317 G A 38 74 UCEC TCGA-B5-A0JY NCF1 SNP Splice_Site 7 74197281 G T 33 86 UCEC TCGA-B5-A11H NCF1 SNP Silent 7 74197397 C T 27 55 UCEC TCGA-BK-A0CC NCF1 SNP Silent 7 74193718 C T 31 50 KIRC TCGA-BP-4770 NCF1 SNP Missense_Mutation 7 74191683 A G 14 73 HNSC TCGA-D6-6516 NCF1 SNP Silent 7 74193715 C T 30 47 BRCA TCGA-E2-A1LL NCF1 SNP Missense_Mutation 7 74197317 G A 38 74