ttype patient gene classification type chr pos ref_allele newbase context65 cons46 BRCA BR-0022 NSMCE1 SNP Missense_Mutation 16 27244392 C A 26 65 CRC CRC-0002 NSMCE1 SNP Missense 16 27268789 G A 38 74 MM MM-0535 NSMCE1 SNP Missense_Mutation 16 27238085 C T 31 86 NB NB-1092 NSMCE1 SNP Splice_Site_SNP 16 27246498 C G 18 88 LUSC TCGA-22-1012 NSMCE1 SNP Missense_Mutation 16 27268767 T C 56 52 LUSC TCGA-22-5489 NSMCE1 SNP Silent 16 27238086 G A 39 30 LUAD TCGA-35-3621 NSMCE1 SNP Nonsense_Mutation 16 27244449 G C 45 73 LUSC TCGA-37-5819 NSMCE1 SNP Nonsense_Mutation 16 27246603 T A 61 57 LUAD TCGA-44-3919 NSMCE1 SNP Missense_Mutation 16 27245538 C G 32 73 CRC TCGA-AG-A002 NSMCE1 SNP Missense_Mutation 16 27236549 C T 31 50 UCEC TCGA-AP-A051 NSMCE1 SNP Silent 16 27268865 G A 38 53 UCEC TCGA-AP-A0LM NSMCE1 SNP Missense_Mutation 16 27236512 G A 37 71 UCEC TCGA-AP-A0LM NSMCE1 SNP Missense_Mutation 16 27236549 C T 31 50 UCEC TCGA-AX-A0J0 NSMCE1 SNP Missense_Mutation 16 27236549 C T 31 50 UCEC TCGA-B5-A0JY NSMCE1 SNP Missense_Mutation 16 27236549 C T 31 50 UCEC TCGA-B5-A0JZ NSMCE1 SNP Missense_Mutation 16 27238129 C T 23 86 UCEC TCGA-B5-A11N NSMCE1 SNP Missense_Mutation 16 27236549 C T 31 50 BRCA TCGA-BH-A0W7 NSMCE1 SNP Silent 16 27238139 G A 35 54 HNSC TCGA-CV-7177 NSMCE1 SNP Silent 16 27237111 G A 36 44 UCEC TCGA-D1-A103 NSMCE1 SNP Missense_Mutation 16 27238085 C T 31 86 UCEC TCGA-D1-A167 NSMCE1 SNP Missense_Mutation 16 27268779 G A 40 50 BRCA TCGA-D8-A1J9 NSMCE1 SNP Silent 16 27238062 G A 33 72 BLCA TCGA-FD-A3B7 NSMCE1 SNP Missense_Mutation 16 27268804 C T 30 63 BLCA TCGA-G2-A2EC NSMCE1 SNP Missense_Mutation 16 27246536 C T 30 89