ttype patient gene classification type chr pos ref_allele newbase context65 cons46 HNSC HN_62699 HSDL1 SNP Missense 16 84164850 G A 34 98 LUAD LUAD-B02077 HSDL1 SNP Missense_Mutation 16 84163196 C G 22 97 LUAD LUAD-S01315 HSDL1 SNP Silent 16 84164783 G A 45 63 MEL MEL-JWCI-27 HSDL1 SNP Silent 16 84163306 G A 41 48 MEL MEL-JWCI-WGS-7 HSDL1 SNP Silent 16 84164903 G A 44 75 MM MM-0553 HSDL1 SNP Missense_Mutation 16 84164790 C G 28 67 LUAD TCGA-05-4396 HSDL1 SNP Missense_Mutation 16 84164764 G T 39 64 LUAD TCGA-05-4396 HSDL1 SNP Missense_Mutation 16 84164892 C A 24 99 LUAD TCGA-05-4403 HSDL1 INS Frame_Shift_Ins 16 84164817 - T 28 83 LUAD TCGA-50-5930 HSDL1 SNP Silent 16 84163918 G A 48 52 CRC TCGA-AA-3672 HSDL1 SNP Nonsense_Mutation 16 84163352 A T 5 87 CRC TCGA-AA-3877 HSDL1 SNP Missense_Mutation 16 84163250 G A 37 51 UCEC TCGA-AP-A059 HSDL1 SNP Missense_Mutation 16 84163765 C A 28 58 UCEC TCGA-B5-A11Y HSDL1 SNP Missense_Mutation 16 84163994 G A 46 97 HNSC TCGA-CN-6995 HSDL1 SNP Nonsense_Mutation 16 84163848 G A 37 54 UCEC TCGA-D1-A17Q HSDL1 SNP Silent 16 84163651 C T 31 46