ttype patient gene classification type chr pos ref_allele newbase context65 cons46 CLL CW219 SNX3 SNP Silent 6 108533362 T C 58 67 BRCA TCGA-A2-A0EX SNX3 SNP Missense_Mutation 6 108581992 C A 27 69 UCEC TCGA-A5-A0GP SNX3 SNP Nonsense_Mutation 6 108544222 C A 32 100 BRCA TCGA-A8-A08L SNX3 SNP Missense_Mutation 6 108544177 T G 56 79 CRC TCGA-AG-A002 SNX3 SNP Missense_Mutation 6 108535732 C A 32 87 UCEC TCGA-AP-A051 SNX3 SNP Missense_Mutation 6 108533357 G A 42 100 UCEC TCGA-AP-A051 SNX3 SNP Nonsense_Mutation 6 108544180 G A 38 53 UCEC TCGA-AP-A0LM SNX3 SNP Missense_Mutation 6 108581976 T G 64 49 KIRC TCGA-B0-4841 SNX3 SNP Missense_Mutation 6 108533446 A T 12 54 HNSC TCGA-CR-7390 SNX3 SNP Missense_Mutation 6 108533400 C T 29 80