WormBase Tree Display for Variation: WBVar02138712

WBVar02138712 Evidence: Paper_evidence: WBPaper00045317
  Name: Public_name: h7682
    Other_name: D1005.2.1:c.1028-161C>T
    HGVSg: CHROMOSOME_X:g.1462165C>T
  Sequence_details: SMap: S_parent: Sequence: D1005
    Flanking_sequences: CATTTTGAAACGATTAGATTAGTTTTTATCATTTTCCCCA TGGCGCTACTCTGCTTTTAAAACTAATACTATGTGTAAAA
    Mapping_target: CHROMOSOME_X
    Source_location: 200 CHROMOSOME_X 1462161 1462161
    Type_of_mutation: Substitution: C T
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023700
    Laboratory: KR
    Analysis: WGS_Rose
    Status: Live
  Affects: Gene: WBGene00016996
    Transcript: D1005.2.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: D1005.2.1:c.1028-161C>T
        Intron_number: 7/8
  Reference: WBPaper00040589
    WBPaper00000975
    WBPaper00003985
    WBPaper00000699
    WBPaper00045317
  Method: WGS_Rose