[{"allele_string":"-/C","end":22125502,"id":"9_22125503_-/C","seq_region_name":"9","strand":1,"start":22125503,"most_severe_consequence":"intron_variant","transcript_consequences":[{"gene_symbol_source":"HGNC","transcript_id":"ENST00000421632","gene_symbol":"CDKN2B-AS1","biotype":"lncRNA","variant_allele":"C","hgnc_id":"HGNC:34341","strand":1,"impact":"MODIFIER","distance":4813,"gene_id":"ENSG00000240498","consequence_terms":["downstream_gene_variant"]},{"biotype":"lncRNA","variant_allele":"C","hgnc_id":"HGNC:34341","gene_symbol_source":"HGNC","transcript_id":"ENST00000422420","gene_symbol":"CDKN2B-AS1","distance":4405,"consequence_terms":["downstream_gene_variant"],"gene_id":"ENSG00000240498","strand":1,"impact":"MODIFIER"},{"transcript_id":"ENST00000428597","gene_symbol_source":"HGNC","gene_symbol":"CDKN2B-AS1","biotype":"lncRNA","hgnc_id":"HGNC:34341","variant_allele":"C","strand":1,"impact":"MODIFIER","distance":4789,"consequence_terms":["downstream_gene_variant"],"gene_id":"ENSG00000240498"},{"gene_symbol":"CDKN2B-AS1","transcript_id":"ENST00000577551","gene_symbol_source":"HGNC","biotype":"lncRNA","variant_allele":"C","hgnc_id":"HGNC:34341","impact":"MODIFIER","strand":1,"distance":4930,"gene_id":"ENSG00000240498","consequence_terms":["downstream_gene_variant"]},{"biotype":"lncRNA","hgnc_id":"HGNC:34341","variant_allele":"C","gene_symbol_source":"HGNC","transcript_id":"ENST00000580576","gene_symbol":"CDKN2B-AS1","distance":4865,"consequence_terms":["downstream_gene_variant"],"gene_id":"ENSG00000240498","strand":1,"impact":"MODIFIER"},{"gene_id":"ENSG00000240498","consequence_terms":["downstream_gene_variant"],"distance":4930,"strand":1,"impact":"MODIFIER","hgnc_id":"HGNC:34341","variant_allele":"C","biotype":"lncRNA","transcript_id":"ENST00000581051","gene_symbol_source":"HGNC","gene_symbol":"CDKN2B-AS1"},{"variant_allele":"C","hgnc_id":"HGNC:34341","biotype":"lncRNA","gene_symbol":"CDKN2B-AS1","transcript_id":"ENST00000582072","gene_symbol_source":"HGNC","consequence_terms":["downstream_gene_variant"],"gene_id":"ENSG00000240498","distance":4930,"impact":"MODIFIER","strand":1},{"impact":"MODIFIER","strand":1,"distance":4930,"gene_id":"ENSG00000240498","consequence_terms":["downstream_gene_variant"],"gene_symbol":"CDKN2B-AS1","transcript_id":"ENST00000584020","gene_symbol_source":"HGNC","biotype":"lncRNA","variant_allele":"C","hgnc_id":"HGNC:34341"},{"hgnc_id":"HGNC:34341","variant_allele":"C","biotype":"lncRNA","gene_symbol":"CDKN2B-AS1","transcript_id":"ENST00000584637","gene_symbol_source":"HGNC","consequence_terms":["downstream_gene_variant"],"gene_id":"ENSG00000240498","distance":4930,"impact":"MODIFIER","strand":1},{"biotype":"lncRNA","variant_allele":"C","hgnc_id":"HGNC:34341","gene_symbol_source":"HGNC","transcript_id":"ENST00000584816","gene_symbol":"CDKN2B-AS1","distance":4930,"gene_id":"ENSG00000240498","consequence_terms":["downstream_gene_variant"],"strand":1,"impact":"MODIFIER"},{"strand":1,"impact":"MODIFIER","distance":4791,"gene_id":"ENSG00000240498","consequence_terms":["downstream_gene_variant"],"transcript_id":"ENST00000585267","gene_symbol_source":"HGNC","gene_symbol":"CDKN2B-AS1","biotype":"lncRNA","hgnc_id":"HGNC:34341","variant_allele":"C"},{"impact":"MODIFIER","strand":1,"gene_id":"ENSG00000240498","consequence_terms":["downstream_gene_variant"],"distance":4789,"gene_symbol":"CDKN2B-AS1","gene_symbol_source":"HGNC","transcript_id":"ENST00000643286","hgnc_id":"HGNC:34341","variant_allele":"C","biotype":"lncRNA"},{"impact":"MODIFIER","strand":1,"consequence_terms":["downstream_gene_variant"],"gene_id":"ENSG00000240498","distance":4791,"gene_symbol":"CDKN2B-AS1","gene_symbol_source":"HGNC","transcript_id":"ENST00000644233","variant_allele":"C","hgnc_id":"HGNC:34341","biotype":"lncRNA"},{"impact":"MODIFIER","strand":1,"distance":4793,"consequence_terms":["downstream_gene_variant"],"gene_id":"ENSG00000240498","gene_symbol":"CDKN2B-AS1","gene_symbol_source":"HGNC","transcript_id":"ENST00000645223","biotype":"lncRNA","variant_allele":"C","hgnc_id":"HGNC:34341"},{"consequence_terms":["intron_variant","non_coding_transcript_variant"],"gene_id":"ENSG00000240498","impact":"MODIFIER","strand":1,"biotype":"lncRNA","variant_allele":"C","hgnc_id":"HGNC:34341","gene_symbol":"CDKN2B-AS1","gene_symbol_source":"HGNC","transcript_id":"ENST00000650946"},{"transcript_id":"ENST00000658981","gene_symbol_source":"HGNC","gene_symbol":"CDKN2B-AS1","hgnc_id":"HGNC:34341","variant_allele":"C","biotype":"lncRNA","strand":1,"impact":"MODIFIER","consequence_terms":["downstream_gene_variant"],"gene_id":"ENSG00000240498","distance":4789},{"strand":1,"impact":"MODIFIER","distance":1598,"consequence_terms":["upstream_gene_variant"],"gene_id":"ENSG00000240498","gene_symbol_source":"HGNC","transcript_id":"ENST00000755351","gene_symbol":"CDKN2B-AS1","biotype":"lncRNA","hgnc_id":"HGNC:34341","variant_allele":"C"},{"biotype":"lncRNA","hgnc_id":"HGNC:34341","variant_allele":"C","gene_symbol":"CDKN2B-AS1","gene_symbol_source":"HGNC","transcript_id":"ENST00000806148","distance":4789,"consequence_terms":["downstream_gene_variant"],"gene_id":"ENSG00000240498","impact":"MODIFIER","strand":1},{"variant_allele":"C","hgnc_id":"HGNC:34341","biotype":"lncRNA","gene_symbol":"CDKN2B-AS1","transcript_id":"ENST00000806149","gene_symbol_source":"HGNC","gene_id":"ENSG00000240498","consequence_terms":["downstream_gene_variant"],"distance":4791,"impact":"MODIFIER","strand":1},{"gene_symbol":"CDKN2B-AS1","gene_symbol_source":"HGNC","transcript_id":"ENST00000806151","variant_allele":"C","hgnc_id":"HGNC:34341","biotype":"lncRNA","impact":"MODIFIER","strand":1,"gene_id":"ENSG00000240498","consequence_terms":["downstream_gene_variant"],"distance":4783},{"gene_symbol_source":"HGNC","transcript_id":"ENST00000806152","gene_symbol":"CDKN2B-AS1","hgnc_id":"HGNC:34341","variant_allele":"C","biotype":"lncRNA","strand":1,"impact":"MODIFIER","gene_id":"ENSG00000240498","consequence_terms":["downstream_gene_variant"],"distance":4789},{"gene_symbol":"CDKN2B-AS1","transcript_id":"ENST00000806153","gene_symbol_source":"HGNC","biotype":"lncRNA","hgnc_id":"HGNC:34341","variant_allele":"C","impact":"MODIFIER","strand":1,"distance":4792,"consequence_terms":["downstream_gene_variant"],"gene_id":"ENSG00000240498"}],"input":"9 22125503 22125502 -/C 1","assembly_name":"GRCh38"}]