[{"transcript_consequences":[{"gene_symbol":"NOL9","impact":"MODIFIER","transcript_id":"ENST00000377705","variant_allele":"T","strand":-1,"cdna_start":3269,"cdna_end":3269,"hgnc_id":"HGNC:26265","gene_id":"ENSG00000162408","biotype":"protein_coding","gene_symbol_source":"HGNC","consequence_terms":["3_prime_UTR_variant"]},{"gene_symbol":"PLEKHG5","impact":"MODIFIER","distance":4696,"strand":-1,"transcript_id":"ENST00000377740","variant_allele":"T","gene_id":"ENSG00000171680","hgnc_id":"HGNC:29105","gene_symbol_source":"HGNC","biotype":"protein_coding","consequence_terms":["upstream_gene_variant"]},{"impact":"MODIFIER","distance":4631,"gene_symbol":"PLEKHG5","hgnc_id":"HGNC:29105","gene_id":"ENSG00000171680","transcript_id":"ENST00000675812","variant_allele":"T","strand":-1,"flags":["cds_end_NF"],"gene_symbol_source":"HGNC","biotype":"protein_coding","consequence_terms":["upstream_gene_variant"]},{"gene_symbol_source":"HGNC","biotype":"protein_coding","consequence_terms":["downstream_gene_variant"],"impact":"MODIFIER","distance":40,"gene_symbol":"NOL9","gene_id":"ENSG00000162408","hgnc_id":"HGNC:26265","transcript_id":"ENST00000870262","variant_allele":"T","strand":-1},{"consequence_terms":["downstream_gene_variant"],"biotype":"protein_coding","gene_symbol_source":"HGNC","gene_id":"ENSG00000162408","hgnc_id":"HGNC:26265","variant_allele":"T","strand":-1,"transcript_id":"ENST00000870263","impact":"MODIFIER","distance":440,"gene_symbol":"NOL9"},{"gene_symbol_source":"HGNC","biotype":"protein_coding","consequence_terms":["downstream_gene_variant"],"distance":440,"impact":"MODIFIER","gene_symbol":"NOL9","hgnc_id":"HGNC:26265","gene_id":"ENSG00000162408","strand":-1,"variant_allele":"T","transcript_id":"ENST00000870264"},{"consequence_terms":["downstream_gene_variant"],"gene_symbol_source":"HGNC","biotype":"protein_coding","transcript_id":"ENST00000870265","variant_allele":"T","strand":-1,"hgnc_id":"HGNC:26265","gene_id":"ENSG00000162408","gene_symbol":"NOL9","distance":1007,"impact":"MODIFIER"},{"hgnc_id":"HGNC:26265","gene_id":"ENSG00000162408","variant_allele":"T","strand":-1,"transcript_id":"ENST00000925477","distance":862,"impact":"MODIFIER","gene_symbol":"NOL9","consequence_terms":["downstream_gene_variant"],"gene_symbol_source":"HGNC","biotype":"protein_coding"},{"distance":965,"impact":"MODIFIER","gene_symbol":"NOL9","hgnc_id":"HGNC:26265","gene_id":"ENSG00000162408","transcript_id":"ENST00000925478","strand":-1,"variant_allele":"T","gene_symbol_source":"HGNC","biotype":"protein_coding","consequence_terms":["downstream_gene_variant"]},{"gene_symbol":"PLEKHG5","distance":4703,"impact":"MODIFIER","variant_allele":"T","transcript_id":"ENST00000934259","strand":-1,"hgnc_id":"HGNC:29105","gene_id":"ENSG00000171680","gene_symbol_source":"HGNC","biotype":"protein_coding","consequence_terms":["upstream_gene_variant"]},{"gene_symbol":"PLEKHG5","distance":4637,"impact":"MODIFIER","strand":-1,"transcript_id":"ENST00000948663","variant_allele":"T","gene_id":"ENSG00000171680","hgnc_id":"HGNC:29105","biotype":"protein_coding","gene_symbol_source":"HGNC","consequence_terms":["upstream_gene_variant"]}],"most_severe_consequence":"3_prime_UTR_variant","strand":1,"input":"1 6524705 6524705 C/T 1","allele_string":"C/T","assembly_name":"GRCh38","start":6524705,"end":6524705,"id":"1_6524705_C/T","seq_region_name":"1"}]