ttype patient gene classification type chr pos ref_allele newbase context65 cons46 LUAD TCGA-17-Z026 HDHD3 SNP Missense_Mutation 9 116136292 C G 30 69 GBM TCGA-32-1979 HDHD3 SNP Missense_Mutation 9 116136378 G A 38 81 CRC TCGA-AA-3845 HDHD3 SNP Missense_Mutation 9 116136478 A G 16 59 CRC TCGA-AA-3966 HDHD3 SNP Missense_Mutation 9 116136612 C T 31 69 HNSC TCGA-CV-5430 HDHD3 SNP Silent 9 116136274 G A 35 75 HNSC TCGA-CV-6961 HDHD3 SNP Missense_Mutation 9 116136231 G C 41 97 HNSC TCGA-CV-7235 HDHD3 SNP Silent 9 116136605 C T 29 61