ttype patient gene classification type chr pos ref_allele newbase context65 cons46 LUAD LUAD_E01147 HMGN4 SNP Splice_site 6 26545433 C T 18 56 MEL ME002 HMGN4 SNP Missense_Mutation 6 26545483 G T 44 56 LUAD TCGA-17-Z040 HMGN4 SNP Missense_Mutation 6 26545565 C T 26 52 LUAD TCGA-67-3771 HMGN4 SNP Silent 6 26545530 A G 7 38 UCEC TCGA-AP-A0LM HMGN4 SNP Missense_Mutation 6 26545568 C A 32 72 UCEC TCGA-AX-A0J0 HMGN4 SNP Missense_Mutation 6 26545601 G T 33 49 UCEC TCGA-BS-A0UF HMGN4 SNP Splice_Site 6 26545354 G T 33 50 HNSC TCGA-CN-4736 HMGN4 SNP Missense_Mutation 6 26545528 C T 18 72