ttype patient gene classification type chr pos ref_allele newbase context65 cons46 BRCA BR-MEX-166 WDR37 SNP Missense_Mutation 10 1151123 C G 18 100 DLBCL DLBCL-MAYO_DLBCL_234 WDR37 SNP Silent 10 1118203 G A 39 36 ESO ESO-167 WDR37 SNP Missense_Mutation 10 1118138 A C 1 89 LUAD LUAD-S00488 WDR37 SNP Nonsense_Mutation 10 1123931 G T 37 87 LUAD LUAD-S01356 WDR37 DNP Missense_Mutation 10 1149659 GG TT 43 100 MEL ME009 WDR37 SNP Missense_Mutation 10 1130415 G A 41 100 MEL ME048 WDR37 SNP Splice_Site 10 1132224 A C 7 77 MEL MEL-JWCI-WGS-12 WDR37 SNP Missense_Mutation 10 1170250 G A 33 100 MEL MEL-Ma-Mel-114 WDR37 SNP Missense_Mutation 10 1175199 C T 22 76 PRAD PR-P559 WDR37 SNP Splice_site 10 1139434 C T 20 100 LUAD TCGA-05-4382 WDR37 SNP Missense_Mutation 10 1170222 G T 44 100 LUAD TCGA-50-6592 WDR37 SNP Silent 10 1126036 C G 29 57 UCEC TCGA-A5-A0GH WDR37 SNP Missense_Mutation 10 1175180 G A 42 78 UCEC TCGA-A5-A0GP WDR37 SNP Nonsense_Mutation 10 1123910 G T 33 100 BRCA TCGA-AO-A03N WDR37 SNP Missense_Mutation 10 1118202 C T 19 72 UCEC TCGA-AP-A056 WDR37 SNP Missense_Mutation 10 1149581 G A 37 100 UCEC TCGA-AP-A056 WDR37 SNP Missense_Mutation 10 1170271 G A 38 100 KIRC TCGA-B0-5107 WDR37 SNP Splice_site 10 1149775 A C 7 64 BRCA TCGA-BH-A0WA WDR37 SNP Silent 10 1123883 C T 32 58 UCEC TCGA-BS-A0UF WDR37 SNP Nonsense_Mutation 10 1123904 G T 33 100 UCEC TCGA-BS-A0UV WDR37 SNP Missense_Mutation 10 1118121 C T 31 98 HNSC TCGA-CV-7427 WDR37 SNP Missense_Mutation 10 1123898 C G 29 100 UCEC TCGA-D1-A163 WDR37 SNP Missense_Mutation 10 1130353 G A 34 100 UCEC TCGA-D1-A16F WDR37 SNP Splice_Site 10 1123944 G A 48 100 BRCA TCGA-EW-A1IZ WDR37 SNP Missense_Mutation 10 1151084 C T 19 87