Histogram views are shown when there are more than 50 features on a single chromosome. Please click on the histogram to view individual features at that position.

{"SNV":[{"chr":"10","remapped_from":null,"start":28879647,"original_position":null,"public":1,"intergenic":0,"inheritance":"De novo constitutive","annotated":1,"ref_allele":"A","pathogenicity":"Pathogenic","validation":"Validated","shared":"public","ensembl_transcript":"ENST00000354911","user_hgvs":null,"feedback":"Yes","end":28879647,"vep_consequence":"splice_acceptor_variant","refseq_transcript":null,"genotype":"Heterozygous","patient_snv_id":24423,"id":24423,"assembly":"GRCh37/hg19","gene_name":"WAC","vep_category":"Likely LOF","alt_allele":"G","created":"2017-02-09 13:54:00","patient_id":259380,"confirmed_by":"Sequencing","user_gene":"WAC","updated":"2017-03-05 02:16:57","user_transcript":"ENST00000354911","pathogenicity_percentage":99,"contribution":"Full","remap_value":null}]}

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