[{"seq_region_name":"9","start":22125503,"strand":1,"end":22125502,"assembly_name":"GRCh37","input":"9 22125503 22125502 -/C 1","transcript_consequences":[{"variant_allele":"C","impact":"MODIFIER","gene_symbol":"CDKN2B-AS1","biotype":"antisense","gene_symbol_source":"HGNC","gene_id":"ENSG00000240498","hgnc_id":34341,"strand":1,"distance":4406,"consequence_terms":["downstream_gene_variant"],"transcript_id":"ENST00000422420"},{"variant_allele":"C","gene_symbol":"CDKN2B-AS1","impact":"MODIFIER","biotype":"antisense","gene_id":"ENSG00000240498","gene_symbol_source":"HGNC","hgnc_id":34341,"distance":4408,"strand":1,"transcript_id":"ENST00000428597","consequence_terms":["downstream_gene_variant"]},{"gene_id":"ENSG00000240498","gene_symbol_source":"HGNC","biotype":"antisense","gene_symbol":"CDKN2B-AS1","impact":"MODIFIER","variant_allele":"C","transcript_id":"ENST00000577551","consequence_terms":["downstream_gene_variant"],"distance":4931,"strand":1,"hgnc_id":34341},{"biotype":"antisense","gene_id":"ENSG00000240498","gene_symbol_source":"HGNC","variant_allele":"C","gene_symbol":"CDKN2B-AS1","impact":"MODIFIER","transcript_id":"ENST00000580576","consequence_terms":["downstream_gene_variant"],"hgnc_id":34341,"distance":4857,"strand":1},{"transcript_id":"ENST00000581051","consequence_terms":["downstream_gene_variant"],"hgnc_id":34341,"distance":4931,"strand":1,"biotype":"antisense","gene_id":"ENSG00000240498","gene_symbol_source":"HGNC","variant_allele":"C","gene_symbol":"CDKN2B-AS1","impact":"MODIFIER"},{"transcript_id":"ENST00000582072","consequence_terms":["downstream_gene_variant"],"distance":4931,"strand":1,"hgnc_id":34341,"gene_id":"ENSG00000240498","gene_symbol_source":"HGNC","biotype":"antisense","gene_symbol":"CDKN2B-AS1","impact":"MODIFIER","variant_allele":"C"},{"variant_allele":"C","gene_symbol":"CDKN2B-AS1","impact":"MODIFIER","biotype":"antisense","gene_id":"ENSG00000240498","gene_symbol_source":"HGNC","hgnc_id":34341,"distance":4931,"strand":1,"transcript_id":"ENST00000584020","consequence_terms":["downstream_gene_variant"]},{"consequence_terms":["downstream_gene_variant"],"transcript_id":"ENST00000584637","strand":1,"distance":4931,"hgnc_id":34341,"gene_symbol_source":"HGNC","gene_id":"ENSG00000240498","biotype":"antisense","impact":"MODIFIER","gene_symbol":"CDKN2B-AS1","variant_allele":"C"},{"variant_allele":"C","impact":"MODIFIER","gene_symbol":"CDKN2B-AS1","biotype":"antisense","gene_symbol_source":"HGNC","gene_id":"ENSG00000240498","hgnc_id":34341,"strand":1,"distance":4931,"consequence_terms":["downstream_gene_variant"],"transcript_id":"ENST00000584816"},{"consequence_terms":["downstream_gene_variant"],"transcript_id":"ENST00000585267","strand":1,"distance":4959,"hgnc_id":34341,"gene_symbol_source":"HGNC","gene_id":"ENSG00000240498","biotype":"antisense","impact":"MODIFIER","gene_symbol":"CDKN2B-AS1","variant_allele":"C"}],"most_severe_consequence":"downstream_gene_variant","id":"9_22125503_-/C","allele_string":"-/C"}]