WormBase Tree Display for Variation: WBVar00305457

WBVar00305457 Evidence: Paper_evidence: WBPaper00036201
  Name: Public_name: otn8636
    Other_name: OH7677_73010
      Y41C4A.4e.1:c.186+1326C>T
      Y41C4A.4c.1:c.210+1326C>T
      Y41C4A.4a.1:c.243+1326C>T
      Y41C4A.4g.1:c.561+1326C>T
      Y41C4A.4b.1:c.243+1326C>T
      Y41C4A.4d.1:c.261+1326C>T
    HGVSg: CHROMOSOME_III:g.11686629C>T
  Sequence_details: SMap: S_parent: Sequence: Y41C4A
    Flanking_sequences: ATTTTTTGAGTCGTCATAACTTTTTTCTGGAAAGTTTTCAAGAAGTTTCA TATGAAATTCGATGTTTTCAGGCAATTTGGGCCTAATAAGGCAATTTTAA
    Mapping_target: Y41C4A
    Type_of_mutation: Substitution: C T
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00029537
    Laboratory: OTN
    Analysis: WGS_Hobert
    Status: Live
  Affects: Gene: WBGene00000793
    Transcript: Y41C4A.4e.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y41C4A.4e.1:c.186+1326C>T
        Intron_number: 4/8
      Y41C4A.4g.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y41C4A.4g.1:c.561+1326C>T
        Intron_number: 2/6
      Y41C4A.4b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y41C4A.4b.1:c.243+1326C>T
        Intron_number: 3/6
      Y41C4A.4a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y41C4A.4a.1:c.243+1326C>T
        Intron_number: 4/8
      Y41C4A.4d.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y41C4A.4d.1:c.261+1326C>T
        Intron_number: 4/8
      Y41C4A.4c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y41C4A.4c.1:c.210+1326C>T
        Intron_number: 3/6
  Genetics: Map: III
  Reference: WBPaper00036201
  Method: WGS_Hobert