ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-107 LMO2 SNP Silent 11 33886234 G A 38 50 LUAD LUAD-B02050 LMO2 SNP Silent 11 33886228 G A 33 51 LUAD LUAD-NYU1051S LMO2 DNP Missense_Mutation 11 33880984 CC AA 18 100 MEL MEL-JWCI-WGS-13 LMO2 SNP Missense_Mutation 11 33881113 C T 22 100 MM MM-0335 LMO2 SNP Missense 11 33886207 C A 24 71 PRAD P09-1580 LMO2 SNP Missense_Mutation 11 33881018 T C 63 91 LUAD TCGA-05-4382 LMO2 SNP Missense_Mutation 11 33881003 G C 45 100 LUAD TCGA-17-Z046 LMO2 SNP Missense_Mutation 11 33886287 G T 39 76 LUSC TCGA-37-5819 LMO2 SNP Missense_Mutation 11 33886199 C A 23 100 LUAD TCGA-50-6591 LMO2 SNP Missense_Mutation 11 33880984 C G 18 100 LUAD TCGA-64-1676 LMO2 SNP Silent 11 33886333 G A 43 46 BRCA TCGA-A2-A0EY LMO2 SNP Missense_Mutation 11 33886164 G A 39 56 CRC TCGA-AG-A002 LMO2 SNP Missense_Mutation 11 33880946 C T 31 100 UCEC TCGA-AP-A0LM LMO2 SNP Missense_Mutation 11 33881064 C A 32 71 UCEC TCGA-B5-A11E LMO2 SNP Missense_Mutation 11 33881076 A C 9 71 BLCA TCGA-BT-A20O LMO2 SNP Nonsense_Mutation 11 33886306 G T 42 75 UCEC TCGA-D1-A103 LMO2 SNP Missense_Mutation 11 33886300 C A 32 87 UCEC TCGA-DI-A0WH LMO2 SNP Missense_Mutation 11 33880985 C A 24 100