ttype patient gene classification type chr pos ref_allele newbase context65 cons46 HNSC HN_62298 BRI3BP SNP Missense 12 125509768 A G 2 52 OV TCGA-10-0930 BRI3BP SNP Missense_Mutation 12 125497110 C A 28 41 LUSC TCGA-33-4586 BRI3BP SNP Missense_Mutation 12 125509875 A T 7 60 LUSC TCGA-39-5016 BRI3BP SNP Missense_Mutation 12 125497114 G T 41 82 LUSC TCGA-43-2578 BRI3BP SNP Missense_Mutation 12 125509609 G C 42 73 LUAD TCGA-75-6211 BRI3BP SNP Missense_Mutation 12 125509731 G A 40 52 BRCA TCGA-A8-A09E BRI3BP INS Frame_Shift_Ins 12 125509844 - G 58 53 CRC TCGA-AG-3892 BRI3BP SNP Missense_Mutation 12 125509608 G A 39 97 UCEC TCGA-BS-A0TC BRI3BP SNP Missense_Mutation 12 125509878 G A 40 60 BLCA TCGA-DK-A3IN BRI3BP SNP Missense_Mutation 12 125509837 G A 37 97 BLCA TCGA-FD-A3N5 BRI3BP SNP Splice_site 12 125497182 G A 39 81