ttype patient gene classification type chr pos ref_allele newbase context65 cons46 DLBCL DLBCL-Ls1065 HOXD12 SNP Missense_Mutation 2 176964634 G C 36 62 LUAD LUAD-S01409 HOXD12 SNP Missense_Mutation 2 176965472 C G 27 85 MM MM-0457 HOXD12 SNP Silent 2 176964712 G T 38 49 OV TCGA-10-0931 HOXD12 SNP Missense_Mutation 2 176964687 C A 26 62 LUAD TCGA-17-Z008 HOXD12 SNP Silent 2 176964979 G C 37 50 LUAD TCGA-17-Z022 HOXD12 SNP Silent 2 176965452 C G 27 45 LUSC TCGA-33-4566 HOXD12 SNP Missense_Mutation 2 176965022 G T 37 71 LUSC TCGA-43-5668 HOXD12 SNP Missense_Mutation 2 176964863 C T 27 57 LUAD TCGA-44-2668 HOXD12 SNP Nonsense_Mutation 2 176965302 C A 17 72 LUSC TCGA-46-6026 HOXD12 SNP Silent 2 176964967 G T 38 54 LUSC TCGA-66-2793 HOXD12 SNP Missense_Mutation 2 176964762 C T 28 76 LUAD TCGA-91-6829 HOXD12 SNP Missense_Mutation 2 176964621 C G 23 76 CRC TCGA-AG-3727 HOXD12 SNP Missense_Mutation 2 176965450 C T 27 56 UCEC TCGA-AP-A059 HOXD12 SNP Missense_Mutation 2 176965007 C T 22 49 UCEC TCGA-AX-A05Z HOXD12 SNP Missense_Mutation 2 176965305 G A 37 40 HNSC TCGA-BB-7862 HOXD12 SNP Missense_Mutation 2 176964836 C T 26 54 HNSC TCGA-BB-7871 HOXD12 SNP Missense_Mutation 2 176965471 G A 42 76 UCEC TCGA-BS-A0UF HOXD12 SNP Missense_Mutation 2 176964887 G A 38 54 UCEC TCGA-BS-A0UV HOXD12 SNP Missense_Mutation 2 176965333 G A 37 100 HNSC TCGA-CR-7402 HOXD12 SNP Missense_Mutation 2 176964737 G T 39 55 HNSC TCGA-CV-6954 HOXD12 SNP Silent 2 176964535 T C 59 55 HNSC TCGA-DQ-7595 HOXD12 SNP Missense_Mutation 2 176964665 C A 27 74