ttype patient gene classification type chr pos ref_allele newbase context65 cons46 BRCA BR-MEX-074 WDR53 SNP Missense_Mutation 3 196287976 T G 62 74 BRCA BR-MEX-082 WDR53 SNP Missense 3 196281555 A C 9 91 DLBCL DLBCL-MAYO_DLBCL_234 WDR53 SNP Missense_Mutation 3 196288208 G A 38 62 LUAD LUAD-B00915 WDR53 SNP Missense_Mutation 3 196288223 G C 41 72 LUAD LUAD-E00443 WDR53 SNP Silent 3 196281538 C T 19 32 MEL MEL-Ma-Mel-05 WDR53 DNP Missense_Mutation 3 196281097 GG AA 35 49 MEL MEL-Ma-Mel-102 WDR53 SNP Missense_Mutation 3 196281531 T C 61 70 LUAD TCGA-05-4250 WDR53 SNP Missense_Mutation 3 196281560 G T 42 74 LUAD TCGA-05-4396 WDR53 SNP Missense_Mutation 3 196281604 C A 21 53 LUAD TCGA-05-4396 WDR53 SNP Silent 3 196281651 G T 39 99 LUAD TCGA-05-4424 WDR53 SNP Missense_Mutation 3 196288274 C A 26 99 LUAD TCGA-17-Z018 WDR53 SNP Missense_Mutation 3 196288135 T C 51 89 LUSC TCGA-18-3410 WDR53 SNP Missense_Mutation 3 196281625 C A 24 71 OV TCGA-36-1580 WDR53 SNP Missense_Mutation 3 196281623 T C 54 91 OV TCGA-61-2095 WDR53 SNP Missense 3 196287989 T C 52 61 BRCA TCGA-A8-A09G WDR53 SNP Silent 3 196287993 G A 45 58 CRC TCGA-AG-A002 WDR53 SNP Nonsense_Mutation 3 196288061 C A 32 97 UCEC TCGA-AP-A0LG WDR53 SNP Missense_Mutation 3 196288294 G A 46 58 UCEC TCGA-B5-A11E WDR53 SNP Missense_Mutation 3 196288208 G A 38 62 HNSC TCGA-BB-4225 WDR53 SNP Silent 3 196288329 C T 23 48 KIRC TCGA-BP-4166 WDR53 SNP Missense_Mutation 3 196288045 G A 45 97 UCEC TCGA-BS-A0UF WDR53 SNP Missense_Mutation 3 196287941 A G 9 59 HNSC TCGA-CN-4728 WDR53 SNP Missense_Mutation 3 196281368 T C 56 59 HNSC TCGA-CR-6481 WDR53 SNP Missense_Mutation 3 196288262 C G 32 99 HNSC TCGA-CR-6481 WDR53 SNP Silent 3 196288299 C G 29 52 HNSC TCGA-CV-6933 WDR53 SNP Missense_Mutation 3 196281606 T C 52 53 UCEC TCGA-D1-A103 WDR53 SNP Missense_Mutation 3 196288025 G T 35 67