ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-0590 ALKBH4 SNP Missense_Mutation 7 102097846 C T 19 51 LUAD LUAD-B00523 ALKBH4 SNP Missense_Mutation 7 102098337 C T 24 73 MM MM-0546 ALKBH4 SNP Missense_Mutation 7 102098269 C T 31 61 MM MM-0591 ALKBH4 SNP Missense_Mutation 7 102098354 G T 42 62 LUSC TCGA-22-4591 ALKBH4 SNP Silent 7 102098135 C T 23 29 LUSC TCGA-34-2608 ALKBH4 SNP Silent 7 102098423 A G 8 48 LUAD TCGA-44-3398 ALKBH4 SNP Missense_Mutation 7 102100065 C G 21 87 LUAD TCGA-44-3918 ALKBH4 SNP Missense_Mutation 7 102097954 C A 19 72 LUAD TCGA-49-6767 ALKBH4 SNP Silent 7 102097955 G A 38 44 UCEC TCGA-AP-A051 ALKBH4 SNP Missense_Mutation 7 102097870 C T 27 60 UCEC TCGA-AP-A059 ALKBH4 SNP Missense_Mutation 7 102097848 G A 43 92 UCEC TCGA-AX-A063 ALKBH4 SNP Missense_Mutation 7 102098034 C T 27 81 KIRC TCGA-B0-5699 ALKBH4 SNP Missense_Mutation 7 102098340 C T 23 53 UCEC TCGA-B5-A11H ALKBH4 SNP Silent 7 102100135 A G 5 47 HNSC TCGA-BA-5152 ALKBH4 SNP Nonsense_Mutation 7 102100194 C A 30 55 HNSC TCGA-CN-5373 ALKBH4 SNP Nonstop_Mutation 7 102097843 A T 6 85 HNSC TCGA-CN-6022 ALKBH4 SNP Silent 7 102098318 C G 26 48 UCEC TCGA-D1-A160 ALKBH4 SNP Missense_Mutation 7 102100199 G T 48 74