ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-838 FAM181B SNP Missense_Mutation 11 82443837 G A 39 62 LUAD TCGA-17-Z049 FAM181B SNP Missense_Mutation 11 82443607 G A 47 72 LUSC TCGA-22-5473 FAM181B SNP Nonsense_Mutation 11 82443575 G T 48 66 LUAD TCGA-64-1678 FAM181B SNP Missense_Mutation 11 82444630 C T 22 63 GBM TCGA-76-6664 FAM181B SNP Silent 11 82443599 C T 17 59 HNSC TCGA-CQ-6220 FAM181B SNP Missense_Mutation 11 82444469 G C 45 60 HNSC TCGA-CV-5434 FAM181B SNP Silent 11 82444616 C A 23 48