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

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