ttype patient gene classification type chr pos ref_allele newbase context65 cons46 GBM TCGA-41-3393 NCBP2 SNP Missense_Mutation 3 196664454 C T 31 98 LUAD TCGA-67-6217 NCBP2 SNP Missense_Mutation 3 196664485 G A 38 58 CRC TCGA-AA-3524 NCBP2 SNP Missense_Mutation 3 196664484 C T 23 98 CRC TCGA-AA-3864 NCBP2 SNP Silent 3 196664498 C T 23 48 UCEC TCGA-AP-A056 NCBP2 SNP Missense_Mutation 3 196664404 C T 23 98 UCEC TCGA-AP-A0LM NCBP2 SNP Silent 3 196664432 G A 40 43 UCEC TCGA-AP-A0LM NCBP2 SNP Missense_Mutation 3 196666168 C T 22 100 UCEC TCGA-B5-A11J NCBP2 SNP Missense_Mutation 3 196669272 C T 23 53 UCEC TCGA-BS-A0U7 NCBP2 SNP Missense_Mutation 3 196669358 A T 7 68 HNSC TCGA-CQ-5327 NCBP2 SNP Missense_Mutation 3 196664450 G C 45 67 HNSC TCGA-CQ-5330 NCBP2 SNP Missense_Mutation 3 196669371 A T 10 69 HNSC TCGA-CV-7104 NCBP2 SNP Splice_Site 3 196664503 C G 32 97 UCEC TCGA-D1-A17Q NCBP2 SNP Missense_Mutation 3 196663950 G A 37 67