ttype patient gene classification type chr pos ref_allele newbase context65 cons46 MEL ME009 LCN2 SNP Silent 9 130911927 C T 20 59 MEL MEL-JWCI-WGS-7 LCN2 SNP Silent 9 130913944 G A 41 51 MEL MEL-JWCI-WGS-7 LCN2 SNP Splice_Site 9 130915406 G A 36 69 LUAD TCGA-44-2655 LCN2 SNP Missense_Mutation 9 130911883 C A 24 58 LUSC TCGA-70-6723 LCN2 SNP Missense_Mutation 9 130911868 G T 41 48 UCEC TCGA-AP-A054 LCN2 SNP Missense_Mutation 9 130914298 C A 24 71 BLCA TCGA-BT-A0YX LCN2 SNP Missense_Mutation 9 130914288 C G 29 71 HNSC TCGA-CV-7406 LCN2 SNP Missense_Mutation 9 130914289 A C 5 67 BRCA TCGA-E9-A1R2 LCN2 SNP Silent 9 130913971 C G 27 62 BLCA TCGA-G2-A2EO LCN2 SNP Silent 9 130914210 C T 31 19