ttype patient gene classification type chr pos ref_allele newbase context65 cons46 LUAD LUAD-B00731 KCNRG SNP Missense_Mutation 13 50589903 C T 31 56 MEL ME014 KCNRG SNP Missense_Mutation 13 50589708 C T 30 87 GBM TCGA-06-0686 KCNRG SNP Silent 13 50589662 G C 47 52 LUAD TCGA-17-Z057 KCNRG SNP Silent 13 50589843 T C 52 51 LUSC TCGA-18-3415 KCNRG SNP Silent 13 50590025 A G 5 53 GBM TCGA-32-2634 KCNRG SNP Missense_Mutation 13 50589726 C T 19 49 LUSC TCGA-33-4582 KCNRG SNP Missense_Mutation 13 50589841 T C 61 62 KIRC TCGA-A3-3380 KCNRG SNP Missense_Mutation 13 50594550 A G 11 65 UCEC TCGA-A5-A0GP KCNRG SNP Silent 13 50589732 T C 60 47 CRC TCGA-AA-3530 KCNRG SNP Missense_Mutation 13 50589660 G A 48 66 CRC TCGA-AA-3530 KCNRG SNP Missense_Mutation 13 50589805 G T 36 66 CRC TCGA-AA-3984 KCNRG SNP Missense_Mutation 13 50594584 G T 33 54 CRC TCGA-AA-A00N KCNRG SNP Splice_site 13 50594589 G T 45 59 UCEC TCGA-AP-A0LM KCNRG SNP Missense_Mutation 13 50589751 A C 9 81 UCEC TCGA-B5-A11E KCNRG SNP Missense_Mutation 13 50589840 T G 64 51 UCEC TCGA-BS-A0UJ KCNRG SNP Missense_Mutation 13 50590137 A G 3 82 UCEC TCGA-D1-A17Q KCNRG SNP Missense_Mutation 13 50589903 C T 31 56 UCEC TCGA-D1-A17Q KCNRG SNP Missense_Mutation 13 50590112 G T 45 54