ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-0013 HARS2 SNP Missense_Mutation 5 140076579 A C 2 50 ESO ESO-077 HARS2 SNP Missense_Mutation 5 140075746 A G 3 81 LUAD LUAD-S01306 HARS2 SNP Silent 5 140077555 C T 22 45 LUAD TCGA-05-4396 HARS2 SNP Missense_Mutation 5 140075203 G T 43 50 LUAD TCGA-05-4397 HARS2 SNP Missense_Mutation 5 140076603 G A 41 50 LUSC TCGA-18-3409 HARS2 SNP Silent 5 140075750 C T 30 81 LUSC TCGA-34-5232 HARS2 SNP Missense_Mutation 5 140073533 T G 56 58 LUAD TCGA-44-3918 HARS2 SNP Missense_Mutation 5 140076891 G T 43 61 LUAD TCGA-50-5946 HARS2 SNP Silent 5 140076793 A G 7 46 LUSC TCGA-85-6561 HARS2 SNP Missense_Mutation 5 140073541 C A 29 66 CRC TCGA-A6-2672 HARS2 SNP Silent 5 140075140 A G 2 59 CRC TCGA-AA-3516 HARS2 SNP Missense_Mutation 5 140075196 G A 40 100 CRC TCGA-AA-3984 HARS2 SNP Missense_Mutation 5 140076627 A G 14 90 CRC TCGA-AG-A002 HARS2 SNP Missense_Mutation 5 140077256 G A 41 60 CRC TCGA-AG-A01L HARS2 SNP Missense_Mutation 5 140075196 G A 40 100 UCEC TCGA-AX-A05Z HARS2 SNP Missense_Mutation 5 140078096 A C 1 50 UCEC TCGA-AX-A060 HARS2 SNP Missense_Mutation 5 140076881 C T 27 78 UCEC TCGA-AX-A0J0 HARS2 SNP Silent 5 140075702 G A 41 51 UCEC TCGA-B5-A11Y HARS2 SNP Missense_Mutation 5 140077641 G A 40 100 HNSC TCGA-BA-5556 HARS2 SNP Missense_Mutation 5 140073602 G A 41 99 UCEC TCGA-BG-A0M4 HARS2 SNP Missense_Mutation 5 140073860 C A 24 87 KIRC TCGA-BP-4768 HARS2 SNP Missense_Mutation 5 140076951 G A 43 100 UCEC TCGA-BS-A0UF HARS2 SNP Nonsense_Mutation 5 140073220 G T 33 48 UCEC TCGA-D1-A163 HARS2 SNP Missense_Mutation 5 140076933 G A 48 100 UCEC TCGA-D1-A167 HARS2 SNP Missense_Mutation 5 140075141 C T 19 90