ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-122 HTR1D SNP Missense_Mutation 1 23520208 T G 51 90 HNSC HN_63081 HTR1D SNP Missense 1 23520183 C T 23 85 LUAD LUAD-CHTN-3090415 HTR1D SNP Missense_Mutation 1 23519850 C A 27 74 LUAD LUAD-NYU1219 HTR1D SNP Missense_Mutation 1 23519733 C A 25 98 LUAD LUAD-RT-S01702 HTR1D SNP Missense_Mutation 1 23519767 G T 42 98 MEL MEL-13473 HTR1D SNP Nonsense_Mutation 1 23520401 C T 30 99 MEL MEL-Ma-Mel-102 HTR1D SNP Silent 1 23519822 C T 30 69 MEL MEL-Ma-Mel-102 HTR1D SNP Missense_Mutation 1 23520239 C T 29 99 MEL MEL-Ma-Mel-119 HTR1D SNP Missense_Mutation 1 23519802 C T 26 98 MM MM-0546 HTR1D SNP Silent 1 23520335 G A 41 84 LUAD TCGA-05-4427 HTR1D SNP Nonsense_Mutation 1 23520676 G A 47 57 GBM TCGA-06-6391 HTR1D SNP Missense_Mutation 1 23520158 C T 17 58 GBM TCGA-27-1831 HTR1D SNP Silent 1 23520071 G A 45 51 LUAD TCGA-44-6147 HTR1D SNP Silent 1 23520467 G T 47 51 CRC TCGA-A6-2676 HTR1D SNP Missense_Mutation 1 23520463 C T 31 99 CRC TCGA-AA-3710 HTR1D SNP Silent 1 23520215 G T 47 51 CRC TCGA-AA-A03F HTR1D SNP Missense_Mutation 1 23519913 G A 37 55 UCEC TCGA-AP-A059 HTR1D SNP Missense_Mutation 1 23520033 C T 27 98 UCEC TCGA-AP-A0LM HTR1D SNP Missense_Mutation 1 23520289 C A 32 77 UCEC TCGA-B5-A0JY HTR1D SNP Silent 1 23520425 G A 37 34 UCEC TCGA-B5-A11E HTR1D SNP Missense_Mutation 1 23519776 A G 7 90 UCEC TCGA-B5-A11E HTR1D SNP Silent 1 23520605 C T 27 39 HNSC TCGA-BA-5149 HTR1D SNP Silent 1 23520575 G A 39 52 UCEC TCGA-BS-A0UF HTR1D SNP Missense_Mutation 1 23520161 C A 32 68 UCEC TCGA-BS-A0UJ HTR1D SNP Missense_Mutation 1 23520303 T G 57 91 HNSC TCGA-CN-5358 HTR1D SNP Silent 1 23520602 G C 45 55 UCEC TCGA-D1-A167 HTR1D SNP Missense_Mutation 1 23520393 C T 26 99 HNSC TCGA-DQ-7590 HTR1D SNP Silent 1 23519918 C T 27 42 BRCA TCGA-E2-A10C HTR1D SNP Silent 1 23519996 G A 45 60 BLCA TCGA-G2-A3IB HTR1D SNP Missense_Mutation 1 23519904 G A 41 84