ttype patient gene classification type chr pos ref_allele newbase context65 cons46 LUAD LUAD_E00565 GMNN SNP Missense_Mutation 6 24780958 G A 33 85 MEL ME032 GMNN SNP Nonsense_Mutation 6 24784759 C T 17 98 LUAD TCGA-05-4396 GMNN SNP Missense_Mutation 6 24784711 C A 23 63 OV TCGA-13-0751 GMNN SNP Missense_Mutation 6 24781746 C A 20 55 OV TCGA-13-2060 GMNN SNP Missense_Mutation 6 24784337 G T 41 84 LUSC TCGA-21-1070 GMNN SNP Missense_Mutation 6 24786002 C T 32 60 LUSC TCGA-22-1002 GMNN SNP Missense_Mutation 6 24781805 A G 4 50 CRC TCGA-AA-A010 GMNN SNP Silent 6 24777492 G A 34 59 CRC TCGA-AA-A010 GMNN SNP Splice_Site 6 24785865 G T 33 89 CRC TCGA-AA-A010 GMNN SNP Silent 6 24786006 G A 39 42 UCEC TCGA-B5-A0K4 GMNN SNP Missense_Mutation 6 24784350 G C 33 98 UCEC TCGA-B5-A11E GMNN SNP Missense_Mutation 6 24785876 G A 44 51 UCEC TCGA-D1-A16F GMNN SNP Silent 6 24785955 G T 47 48 HNSC TCGA-D6-6516 GMNN SNP Missense_Mutation 6 24781768 C T 22 47