ttype patient gene classification type chr pos ref_allele newbase context65 cons46 CLL CW178_redo PTHLH SNP Missense_Mutation 12 28116380 C T 31 80 DLBCL DLBCL-MAYO_DLBCL_234 PTHLH SNP Missense_Mutation 12 28116480 T C 61 65 LUAD LUAD-B00915 PTHLH SNP Missense_Mutation 12 28116566 G A 35 71 LUAD LUAD-F00162 PTHLH SNP Missense_Mutation 12 28116408 G A 40 80 LUAD LUAD-NYU669 PTHLH SNP Missense_Mutation 12 28116453 G T 42 66 MEL ME016 PTHLH SNP Silent 12 28116412 C T 30 40 MEL ME030 PTHLH SNP Missense_Mutation 12 28116380 C T 31 80 MEL ME033 PTHLH SNP Missense_Mutation 12 28116380 C T 31 80 MEL MEL-Ma-Mel-102 PTHLH SNP Silent 12 28116574 C T 24 59 LUAD TCGA-05-4396 PTHLH SNP Silent 12 28116415 G T 39 42 LUAD TCGA-17-Z042 PTHLH SNP Missense_Mutation 12 28116330 C T 24 72 OV TCGA-24-0975 PTHLH SNP Missense 12 28116348 T C 58 51 LUSC TCGA-46-3769 PTHLH SNP Missense_Mutation 12 28116594 C T 29 76 LUAD TCGA-50-5941 PTHLH SNP Nonsense_Mutation 12 28116578 G T 37 64 LUAD TCGA-91-6836 PTHLH SNP Missense_Mutation 12 28116505 C A 24 82 CRC TCGA-A6-2676 PTHLH SNP Silent 12 28122398 G A 38 59 CRC TCGA-AG-3887 PTHLH SNP Missense_Mutation 12 28116698 C G 32 91 UCEC TCGA-AX-A0J1 PTHLH SNP Missense_Mutation 12 28116302 G A 40 65 UCEC TCGA-B5-A0JV PTHLH SNP Missense_Mutation 12 28116635 C T 31 91 UCEC TCGA-B5-A11J PTHLH SNP Nonsense_Mutation 12 28116381 G A 38 57 BRCA TCGA-BH-A1FD PTHLH SNP Missense_Mutation 12 28116584 G A 34 78 BRCA TCGA-C8-A26V PTHLH SNP Missense_Mutation 12 28116284 G A 45 50 BLCA TCGA-DK-A3IM PTHLH SNP Silent 12 28116292 C T 28 61