ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-0103 DHRS9 SNP Silent 2 169938361 C T 29 54 HNSC HN_00313 DHRS9 SNP Missense 2 169939872 C A 22 57 LUAD LUAD-NYU669 DHRS9 SNP Missense_Mutation 2 169938278 G C 45 98 LUAD LUAD-S01315 DHRS9 SNP Silent 2 169939852 G C 45 71 LUAD LUAD-S01473 DHRS9 SNP Missense_Mutation 2 169948388 G A 45 58 MEL ME029 DHRS9 SNP Silent 2 169940038 C T 31 38 MEL MEL-JWCI-WGS-18 DHRS9 SNP Missense_Mutation 2 169938387 A G 2 52 MEL MEL-Ma-Mel-105 DHRS9 SNP Missense_Mutation 2 169948421 C T 30 59 MEL MEL-Ma-Mel-54a DHRS9 SNP Silent 2 169948399 C T 31 41 MEL MEL-Ma-Mel-86 DHRS9 SNP Missense_Mutation 2 169938239 G A 45 100 MEL MEL-Ma-Mel-86 DHRS9 SNP Missense_Mutation 2 169948421 C T 30 59 LUAD TCGA-05-4396 DHRS9 SNP Silent 2 169939948 C A 29 67 LUAD TCGA-05-4396 DHRS9 SNP Missense_Mutation 2 169948302 G T 39 61 GBM TCGA-06-6697 DHRS9 SNP Silent 2 169939876 C T 27 20 LUAD TCGA-17-Z018 DHRS9 SNP Silent 2 169938310 C A 24 46 LUAD TCGA-17-Z046 DHRS9 SNP Silent 2 169952148 T A 53 50 LUAD TCGA-44-2662 DHRS9 SNP Missense_Mutation 2 169938312 C T 29 98 LUAD TCGA-64-5781 DHRS9 DEL Frame_Shift_Del 2 169939978 G - 47 57 BRCA TCGA-A2-A0YJ DHRS9 SNP Silent 2 169939876 C T 27 20 CRC TCGA-A6-2676 DHRS9 SNP Silent 2 169948417 G A 48 50 BRCA TCGA-A8-A08G DHRS9 SNP Missense_Mutation 2 169938396 G A 43 78 CRC TCGA-AA-3864 DHRS9 SNP Missense_Mutation 2 169939950 T C 50 93 UCEC TCGA-AP-A056 DHRS9 SNP Missense_Mutation 2 169938167 G T 33 57 UCEC TCGA-B5-A0JY DHRS9 SNP Missense_Mutation 2 169938231 G T 33 51 UCEC TCGA-B5-A0JY DHRS9 SNP Missense_Mutation 2 169952140 C A 32 60 UCEC TCGA-B5-A0K2 DHRS9 SNP Missense_Mutation 2 169939953 G A 36 52 UCEC TCGA-B5-A0K6 DHRS9 SNP Nonsense_Mutation 2 169938248 G T 43 100 BRCA TCGA-B6-A0RL DHRS9 DEL Frame_Shift_Del 2 169948337 A - 8 90 HNSC TCGA-BB-7863 DHRS9 SNP Missense_Mutation 2 169948429 C G 29 61 BLCA TCGA-BT-A20R DHRS9 SNP Silent 2 169939948 C T 29 67 BLCA TCGA-BT-A3PK DHRS9 SNP Missense_Mutation 2 169948457 G A 45 60 HNSC TCGA-CR-7364 DHRS9 SNP Missense_Mutation 2 169938164 G A 45 48