ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-0029 CIR1 SNP Missense_Mutation 2 175215449 C G 32 96 ESO ESO-177 CIR1 SNP Missense_Mutation 2 175213257 C A 24 64 MED MD-074 CIR1 SNP Missense_Mutation 2 175213553 T C 54 70 MEL MEL-Ma-Mel-36 CIR1 SNP Missense_Mutation 2 175213693 C A 32 62 MM MM-0383 CIR1 SNP Missense 2 175213535 C T 28 60 MM MM-0497 CIR1 SNP Missense_Mutation 2 175252495 C T 32 100 LUAD TCGA-05-4396 CIR1 SNP Missense_Mutation 2 175243704 G T 35 100 LUAD TCGA-05-4396 CIR1 SNP Missense_Mutation 2 175246450 G T 43 87 LUAD TCGA-17-Z023 CIR1 SNP Missense_Mutation 2 175252428 T C 62 92 LUSC TCGA-39-5037 CIR1 SNP Missense_Mutation 2 175213308 G A 47 62 BRCA TCGA-A8-A08Z CIR1 SNP Missense_Mutation 2 175213880 T C 56 69 CRC TCGA-AA-3870 CIR1 SNP Missense_Mutation 2 175213362 G A 40 46 CRC TCGA-AA-3984 CIR1 SNP Missense_Mutation 2 175243671 G A 37 100 CRC TCGA-AA-A00N CIR1 SNP Missense_Mutation 2 175260282 T G 64 49 CRC TCGA-AA-A010 CIR1 SNP Nonsense_Mutation 2 175213353 G A 38 62 UCEC TCGA-AP-A0LM CIR1 SNP Missense_Mutation 2 175213808 G A 41 66 UCEC TCGA-AP-A0LM CIR1 SNP Missense_Mutation 2 175216390 C T 31 77 UCEC TCGA-B5-A11M CIR1 SNP Missense_Mutation 2 175213407 G A 39 53 UCEC TCGA-BS-A0UF CIR1 SNP Missense_Mutation 2 175245447 A C 1 52 UCEC TCGA-BS-A0UV CIR1 SNP Nonsense_Mutation 2 175243714 G A 37 67 BLCA TCGA-G2-A2EF CIR1 SNP Missense_Mutation 2 175213677 C T 24 52 BLCA TCGA-G2-A2EO CIR1 SNP Missense_Mutation 2 175213338 C T 32 63 HNSC TCGA-H7-7774 CIR1 SNP Nonsense_Mutation 2 175252492 G A 48 100