ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-752 NUDT22 SNP Missense_Mutation 11 63996795 C T 26 80 MEL MEL-JWCI-WGS-24 NUDT22 SNP Silent 11 63997004 G A 35 53 MM MM-0427 NUDT22 SNP Splice_site 11 63997461 G A 45 54 MM MM-0624 NUDT22 SNP Silent 11 63994346 G A 43 42 LUAD TCGA-05-4396 NUDT22 SNP Missense_Mutation 11 63994191 G C 42 90 LUSC TCGA-18-3419 NUDT22 SNP Nonsense_Mutation 11 63997406 C T 29 60 LUSC TCGA-22-4595 NUDT22 SNP Missense_Mutation 11 63996966 G C 45 79 LUSC TCGA-39-5031 NUDT22 SNP Silent 11 63997459 C T 32 54 CRC TCGA-AG-3598 NUDT22 SNP Silent 11 63995078 C G 31 48 CRC TCGA-AG-A002 NUDT22 SNP Silent 11 63995105 C A 32 56 UCEC TCGA-AX-A0J1 NUDT22 SNP Missense_Mutation 11 63997325 G A 40 52 UCEC TCGA-B5-A11E NUDT22 SNP Missense_Mutation 11 63994315 A G 6 83 UCEC TCGA-B5-A11U NUDT22 SNP Missense_Mutation 11 63996741 T C 55 74 UCEC TCGA-B5-A11Z NUDT22 SNP Silent 11 63994220 C T 26 58 BRCA TCGA-BH-A1FN NUDT22 SNP Silent 11 63995111 C T 21 61 HNSC TCGA-CV-6934 NUDT22 SNP Missense_Mutation 11 63994371 G T 43 96 BRCA TCGA-E2-A10A NUDT22 SNP Missense_Mutation 11 63994510 C G 17 73