ttype patient gene classification type chr pos ref_allele newbase context65 cons46 LUAD LUAD-NYU627 NXNL2 SNP Missense_Mutation 9 91150648 G A 39 60 MEL MEL-JWCI-WGS-1 NXNL2 SNP Missense_Mutation 9 91150635 C T 21 70 LUAD TCGA-05-4390 NXNL2 SNP Missense_Mutation 9 91150599 C A 27 81 GBM TCGA-06-0154 NXNL2 SNP Silent 9 91150637 C T 19 50 LUSC TCGA-22-4613 NXNL2 SNP Missense_Mutation 9 91150497 G C 37 82 LUSC TCGA-33-4566 NXNL2 SNP Silent 9 91150625 G C 38 51 LUAD TCGA-50-5946 NXNL2 SNP Silent 9 91150523 G A 35 62 UCEC TCGA-B5-A11Y NXNL2 SNP Missense_Mutation 9 91150414 C A 27 54 BRCA TCGA-BH-A0DX NXNL2 SNP Silent 9 91159324 C G 21 56 BLCA TCGA-BT-A3PJ NXNL2 SNP Nonsense_Mutation 9 91150578 C T 21 57 HNSC TCGA-CN-6013 NXNL2 SNP Missense_Mutation 9 91150602 G A 37 67 KIRC TCGA-CZ-5463 NXNL2 SNP Missense_Mutation 9 91159434 C A 26 83 UCEC TCGA-D1-A15X NXNL2 SNP Missense_Mutation 9 91159310 T A 57 90