ttype patient gene classification type chr pos ref_allele newbase context65 cons46 BRCA BR-0004 NOC2L SNP Missense 1 889206 G A 42 95 LUAD LUAD-B00731 NOC2L SNP Silent 1 886549 C A 30 61 LUAD LUAD-D02185 NOC2L SNP Silent 1 889237 C A 23 16 LUAD LUAD-S01357 NOC2L SNP Missense_Mutation 1 881822 C A 27 97 LUAD LUAD-S01404 NOC2L SNP Missense_Mutation 1 886530 G C 43 90 MEL ME018 NOC2L SNP Silent 1 886612 G A 41 39 MEL MEL-JWCI-WGS-25 NOC2L SNP Silent 1 892641 G A 42 50 MEL MEL-JWCI-WGS-31 NOC2L SNP Silent 1 883516 G A 35 48 MEL MEL-Ma-Mel-76 NOC2L SNP Silent 1 889237 C T 23 16 MEL MEL-Ma-Mel-85 NOC2L SNP Silent 1 886573 G A 41 47 MM MM-0489 NOC2L SNP Missense_Mutation 1 880445 T C 60 40 GBM TCGA-06-5858 NOC2L SNP Missense_Mutation 1 887446 G A 38 62 OV TCGA-13-0760 NOC2L SNP Missense_Mutation 1 881892 T G 63 89 LUAD TCGA-17-Z026 NOC2L SNP Missense_Mutation 1 892383 C G 30 58 LUSC TCGA-18-3409 NOC2L SNP Missense_Mutation 1 891504 G A 42 51 LUSC TCGA-37-5819 NOC2L SNP Splice_site 1 880525 C A 30 45 LUAD TCGA-38-4631 NOC2L SNP Silent 1 880905 C A 23 48 LUAD TCGA-38-4631 NOC2L SNP Missense_Mutation 1 889421 C A 19 72 OV TCGA-61-2111 NOC2L SNP Missense_Mutation 1 892634 A G 11 67 LUAD TCGA-73-4668 NOC2L SNP Silent 1 887454 C G 29 49 CRC TCGA-AA-3811 NOC2L SNP Splice_site 1 883871 C T 23 70 CRC TCGA-AG-A002 NOC2L SNP Missense_Mutation 1 892306 C T 27 53 UCEC TCGA-AP-A056 NOC2L SNP Missense_Mutation 1 891523 C T 30 90 UCEC TCGA-AP-A059 NOC2L SNP Missense_Mutation 1 892328 C A 32 54 UCEC TCGA-AX-A05Z NOC2L SNP Missense_Mutation 1 881002 C T 31 89 KIRC TCGA-B0-5705 NOC2L SNP Missense_Mutation 1 888619 G T 34 94 UCEC TCGA-B5-A0JY NOC2L SNP Missense_Mutation 1 891361 C T 32 74 UCEC TCGA-B5-A0JY NOC2L SNP Missense_Mutation 1 892595 C A 32 96 UCEC TCGA-B5-A11Y NOC2L SNP Missense_Mutation 1 892309 C T 19 50 HNSC TCGA-BA-4077 NOC2L SNP Missense_Mutation 1 892498 G A 41 52 BLCA TCGA-CF-A1HR NOC2L SNP Missense_Mutation 1 880485 C T 31 69 HNSC TCGA-CN-4731 NOC2L SNP Silent 1 891548 T A 54 49 HNSC TCGA-CV-5432 NOC2L SNP Missense_Mutation 1 880925 C A 30 87 HNSC TCGA-CV-7099 NOC2L SNP Missense_Mutation 1 886571 C A 19 89 UCEC TCGA-D1-A0ZS NOC2L SNP Silent 1 881643 C T 22 50 UCEC TCGA-D1-A0ZS NOC2L SNP Missense_Mutation 1 887838 C T 27 96 UCEC TCGA-D1-A17Q NOC2L SNP Missense_Mutation 1 887795 C A 32 63 BLCA TCGA-DK-A2I6 NOC2L SNP Missense_Mutation 1 880925 C T 30 87 BLCA TCGA-G2-A2EF NOC2L SNP Missense_Mutation 1 892328 C G 32 54