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