ttype patient gene classification type chr pos ref_allele newbase context65 cons46 DLBCL DLBCL-MAYO_DLBCL_234 KRR1 SNP Silent 12 75897765 A G 8 70 ESO ESO-0129 KRR1 DNP Missense_Mutation 12 75897721 TC AA 62 69 LUAD LUAD-LC15C KRR1 SNP Silent 12 75902141 C T 32 49 LUAD LUAD-RT-S01771 KRR1 SNP Missense_Mutation 12 75893615 C T 29 63 MED MD-280 KRR1 SNP Silent 12 75900306 T C 60 69 MEL MEL-JWCI-WGS-1 KRR1 SNP Missense_Mutation 12 75902203 G A 41 100 OV TCGA-13-0724 KRR1 SNP Missense_Mutation 12 75897755 G A 40 76 LUAD TCGA-67-6215 KRR1 SNP Missense_Mutation 12 75897801 A T 2 59 CRC TCGA-AA-3877 KRR1 SNP Silent 12 75902207 C T 23 56 CRC TCGA-AA-A00A KRR1 SNP Silent 12 75893613 T C 64 59 CRC TCGA-AG-A002 KRR1 SNP Missense_Mutation 12 75897824 C A 32 99 CRC TCGA-AG-A011 KRR1 SNP Silent 12 75900604 T C 54 62 UCEC TCGA-AX-A0J0 KRR1 SNP Missense_Mutation 12 75893673 C A 32 66 UCEC TCGA-B5-A11E KRR1 SNP Silent 12 75902207 C T 23 56 BLCA TCGA-BT-A0YX KRR1 SNP Silent 12 75900673 C T 29 73 HNSC TCGA-CR-6478 KRR1 SNP Silent 12 75905362 G A 34 35 HNSC TCGA-CR-7388 KRR1 SNP Missense_Mutation 12 75895584 C T 32 84 UCEC TCGA-D1-A103 KRR1 SNP Splice_site 12 75905293 C A 24 72 BLCA TCGA-DK-A3IK KRR1 SNP Missense_Mutation 12 75905364 G A 37 49 UCEC TCGA-E6-A1LZ KRR1 SNP Missense_Mutation 12 75900572 G A 45 84