ttype patient gene classification type chr pos ref_allele newbase context65 cons46 LUAD LUAD-NYU259 HPRT1 SNP Missense_Mutation 23 133632704 G T 35 94 MEL ME033 HPRT1 SNP Missense_Mutation 23 133607464 G A 44 94 MEL MEL-JWCI-WGS-6 HPRT1 SNP Splice_site 23 133624219 A G 4 83 MEL MEL-Ma-Mel-65 HPRT1 SNP Missense_Mutation 23 133634078 G A 45 82 LUSC TCGA-60-2713 HPRT1 SNP Missense_Mutation 23 133632689 A G 16 86 LUAD TCGA-73-4658 HPRT1 SNP Missense_Mutation 23 133609244 G T 33 52 CRC TCGA-AA-3947 HPRT1 SNP Missense_Mutation 23 133632688 T A 53 86 CRC TCGA-AA-A01R HPRT1 SNP Missense_Mutation 23 133609219 G A 40 91 CRC TCGA-AG-A002 HPRT1 SNP Silent 23 133627615 C T 31 34 KIRC TCGA-B0-5075 HPRT1 SNP Missense_Mutation 23 133609298 C A 32 56 UCEC TCGA-BS-A0UF HPRT1 SNP Missense_Mutation 23 133609336 G T 33 91 UCEC TCGA-BS-A0UV HPRT1 SNP Missense_Mutation 23 133627595 A C 13 85 HNSC TCGA-CV-7090 HPRT1 SNP Missense_Mutation 23 133609219 G A 40 91