WormBase Tree Display for Variation: WBVar00272344

WBVar00272344 Evidence: Paper_evidence: WBPaper00005369
  Name: Public_name: WBVar00272344
    Other_name: uCE5-1708
      C37C3.6c.1:c.468-12del
      C37C3.6b.1:c.468-12del
      C37C3.6a.1:c.468-12del
      C37C3.6a.2:c.468-12del
    HGVSg: CHROMOSOME_V:g.7828358del
  Sequence_details: SMap: S_parent: Sequence: C37C3
    Flanking_sequences: AAATTCAACGATGAGGCTCTTGATGGAAACTACCACAAGTGGACTCCATACAAGGGAAAGAACAAGTAAGTTAACTTTCTTCAAGATGTTTTTCTAATTT CGAGTTTTCAGGTGCGAGCTCGTCTGTAAGCCAGAATCTGGAAACTTCTACTACAAGTGGGCTGATAAGGTTGTTGATGGAACCAAGTGCGACTCCAAGA
    Mapping_target: C37C3
    Type_of_mutation: Deletion: T
    SeqStatus: Sequenced
  Variation_type: SNP
    Predicted_SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00004602 From_analysis: SNP_Swan
    Analysis: SNP_Swan
    Status: Live
  Affects: Gene: WBGene00003242
    Transcript: C37C3.6b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C37C3.6b.1:c.468-12del
        Intron_number: 4/19
      C37C3.6a.2 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C37C3.6a.2:c.468-12del
        Intron_number: 4/17
      C37C3.6a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C37C3.6a.1:c.468-12del
        Intron_number: 4/17
      C37C3.6c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C37C3.6c.1:c.468-12del
        Intron_number: 4/11
  Reference: WBPaper00005369
  Method: SNP_Swan