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

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