ttype patient gene classification type chr pos ref_allele newbase context65 cons46 LUSC TCGA-21-5787 UBE2V2 SNP Missense_Mutation 8 48955617 G T 38 87 LUAD TCGA-64-5815 UBE2V2 SNP Missense_Mutation 8 48921025 C T 30 75 CRC TCGA-AA-3864 UBE2V2 SNP Silent 8 48955657 C T 27 48 UCEC TCGA-AP-A059 UBE2V2 SNP Missense_Mutation 8 48955608 G A 40 87 UCEC TCGA-AP-A0LM UBE2V2 SNP Nonsense_Mutation 8 48955714 G A 41 100 UCEC TCGA-B5-A0JY UBE2V2 SNP Nonsense_Mutation 8 48973338 G T 33 97 UCEC TCGA-B5-A11E UBE2V2 SNP Missense_Mutation 8 48955700 A G 10 93 UCEC TCGA-B5-A11E UBE2V2 SNP Silent 8 48962499 A G 5 58 BRCA TCGA-E2-A1IN UBE2V2 SNP Missense_Mutation 8 48962528 C G 30 99