ttype patient gene classification type chr pos ref_allele newbase context65 cons46 HNSC HN_62921 BCL2L13 SNP Missense 22 18185077 G C 45 57 MEL ME009 BCL2L13 SNP Missense_Mutation 22 18210011 C T 20 28 MEL MEL-Ma-Mel-67 BCL2L13 SNP Missense_Mutation 22 18178956 C T 29 83 GBM TCGA-06-0878 BCL2L13 SNP Missense_Mutation 22 18178948 C T 18 71 OV TCGA-13-1494 BCL2L13 SNP Silent 22 18209790 C T 23 21 LUSC TCGA-18-3409 BCL2L13 SNP Missense_Mutation 22 18178929 C T 31 58 BRCA TCGA-A2-A0YT BCL2L13 SNP Missense_Mutation 22 18185061 G A 40 64 CRC TCGA-AA-A00N BCL2L13 SNP Missense_Mutation 22 18166077 A C 1 53 CRC TCGA-AG-A002 BCL2L13 SNP Missense_Mutation 22 18185121 C T 31 71 UCEC TCGA-AP-A0LM BCL2L13 SNP Silent 22 18138483 G A 40 56 KIRC TCGA-B0-4690 BCL2L13 SNP Missense_Mutation 22 18210157 G A 43 50 BRCA TCGA-B6-A0IG BCL2L13 SNP Missense_Mutation 22 18209657 G T 42 99 BLCA TCGA-BT-A20P BCL2L13 SNP Silent 22 18171756 C T 29 52 HNSC TCGA-CV-7254 BCL2L13 SNP Missense_Mutation 22 18210216 G C 36 57 UCEC TCGA-D1-A103 BCL2L13 SNP Silent 22 18210087 C T 19 35 BLCA TCGA-DK-A1A3 BCL2L13 SNP Missense_Mutation 22 18209590 G C 45 73 BLCA TCGA-DK-A2I4 BCL2L13 SNP Missense_Mutation 22 18209803 G A 33 95 BLCA TCGA-DK-A3IV BCL2L13 SNP Silent 22 18210132 G A 33 44 BLCA TCGA-G2-A2ES BCL2L13 SNP Missense_Mutation 22 18185037 A C 5 56