[{"start":6524705,"seq_region_name":"1","allele_string":"C/T","assembly_name":"GRCh38","strand":1,"end":6524705,"id":"1_6524705_C/T","transcript_consequences":[{"hgnc_id":"HGNC:26265","gene_symbol_source":"HGNC","gene_id":"ENSG00000162408","strand":-1,"transcript_id":"ENST00000377705","consequence_terms":["3_prime_UTR_variant"],"variant_allele":"T","cdna_end":3269,"cdna_start":3269,"biotype":"protein_coding","impact":"MODIFIER","gene_symbol":"NOL9"},{"gene_id":"ENSG00000171680","gene_symbol_source":"HGNC","hgnc_id":"HGNC:29105","impact":"MODIFIER","gene_symbol":"PLEKHG5","biotype":"protein_coding","variant_allele":"T","transcript_id":"ENST00000377740","strand":-1,"distance":4696,"consequence_terms":["upstream_gene_variant"]},{"flags":["cds_end_NF"],"hgnc_id":"HGNC:29105","gene_symbol_source":"HGNC","gene_id":"ENSG00000171680","consequence_terms":["upstream_gene_variant"],"distance":4631,"transcript_id":"ENST00000675812","strand":-1,"variant_allele":"T","biotype":"protein_coding","gene_symbol":"PLEKHG5","impact":"MODIFIER"},{"hgnc_id":"HGNC:26265","gene_symbol_source":"HGNC","gene_id":"ENSG00000162408","cdna_end":3373,"variant_allele":"T","consequence_terms":["3_prime_UTR_variant"],"transcript_id":"ENST00000870262","strand":-1,"gene_symbol":"NOL9","impact":"MODIFIER","biotype":"protein_coding","cdna_start":3373},{"gene_symbol_source":"HGNC","gene_id":"ENSG00000162408","hgnc_id":"HGNC:26265","gene_symbol":"NOL9","impact":"MODIFIER","biotype":"protein_coding","cdna_start":3289,"variant_allele":"T","cdna_end":3289,"consequence_terms":["3_prime_UTR_variant"],"transcript_id":"ENST00000870263","strand":-1},{"variant_allele":"T","cdna_end":2833,"transcript_id":"ENST00000870264","strand":-1,"consequence_terms":["3_prime_UTR_variant"],"impact":"MODIFIER","gene_symbol":"NOL9","cdna_start":2833,"biotype":"protein_coding","hgnc_id":"HGNC:26265","gene_symbol_source":"HGNC","gene_id":"ENSG00000162408"},{"cdna_start":3328,"biotype":"protein_coding","impact":"MODIFIER","gene_symbol":"NOL9","strand":-1,"transcript_id":"ENST00000870265","consequence_terms":["3_prime_UTR_variant"],"cdna_end":3328,"variant_allele":"T","gene_id":"ENSG00000162408","gene_symbol_source":"HGNC","hgnc_id":"HGNC:26265"},{"hgnc_id":"HGNC:26265","gene_id":"ENSG00000162408","gene_symbol_source":"HGNC","consequence_terms":["3_prime_UTR_variant"],"transcript_id":"ENST00000925477","strand":-1,"cdna_end":3283,"variant_allele":"T","biotype":"protein_coding","cdna_start":3283,"gene_symbol":"NOL9","impact":"MODIFIER"},{"gene_id":"ENSG00000162408","gene_symbol_source":"HGNC","hgnc_id":"HGNC:26265","gene_symbol":"NOL9","impact":"MODIFIER","biotype":"protein_coding","cdna_start":3046,"cdna_end":3046,"variant_allele":"T","consequence_terms":["3_prime_UTR_variant"],"transcript_id":"ENST00000925478","strand":-1},{"hgnc_id":"HGNC:29105","gene_symbol_source":"HGNC","gene_id":"ENSG00000171680","variant_allele":"T","transcript_id":"ENST00000934259","strand":-1,"consequence_terms":["upstream_gene_variant"],"distance":4703,"impact":"MODIFIER","gene_symbol":"PLEKHG5","biotype":"protein_coding"},{"hgnc_id":"HGNC:29105","gene_symbol_source":"HGNC","gene_id":"ENSG00000171680","variant_allele":"T","transcript_id":"ENST00000948663","strand":-1,"distance":4637,"consequence_terms":["upstream_gene_variant"],"impact":"MODIFIER","gene_symbol":"PLEKHG5","biotype":"protein_coding"},{"variant_allele":"T","transcript_id":"ENST00001008552","strand":-1,"consequence_terms":["downstream_gene_variant"],"distance":40,"impact":"MODIFIER","gene_symbol":"NOL9","biotype":"nonsense_mediated_decay","hgnc_id":"HGNC:26265","gene_symbol_source":"HGNC","gene_id":"ENSG00000162408"},{"consequence_terms":["downstream_gene_variant"],"distance":211,"transcript_id":"ENST00001008553","strand":-1,"variant_allele":"T","biotype":"nonsense_mediated_decay","gene_symbol":"NOL9","impact":"MODIFIER","hgnc_id":"HGNC:26265","gene_id":"ENSG00000162408","gene_symbol_source":"HGNC"},{"gene_symbol_source":"HGNC","gene_id":"ENSG00000162408","hgnc_id":"HGNC:26265","biotype":"nonsense_mediated_decay","gene_symbol":"NOL9","impact":"MODIFIER","distance":966,"consequence_terms":["downstream_gene_variant"],"transcript_id":"ENST00001008554","strand":-1,"variant_allele":"T"},{"impact":"MODIFIER","gene_symbol":"NOL9","biotype":"nonsense_mediated_decay","variant_allele":"T","transcript_id":"ENST00001065564","strand":-1,"consequence_terms":["downstream_gene_variant"],"distance":440,"gene_symbol_source":"HGNC","gene_id":"ENSG00000162408","hgnc_id":"HGNC:26265"},{"variant_allele":"T","cdna_end":3292,"strand":-1,"transcript_id":"ENST00001145126","consequence_terms":["3_prime_UTR_variant"],"impact":"MODIFIER","gene_symbol":"NOL9","cdna_start":3292,"biotype":"protein_coding","hgnc_id":"HGNC:26265","gene_id":"ENSG00000162408","gene_symbol_source":"HGNC"}],"input":"1 6524705 6524705 C/T 1","most_severe_consequence":"3_prime_UTR_variant"}]