WormBase Tree Display for Variation: WBVar00305170

WBVar00305170 Evidence: Paper_evidence: WBPaper00036201
  Name: Public_name: otn8349
    Other_name: OH7677_38771
      F22D3.2d.1:c.1102-92G>T
      F22D3.2j.1:c.1093-92G>T
      F22D3.2g.1:c.1102-92G>T
      F22D3.2e.1:c.1093-92G>T
    HGVSg: CHROMOSOME_II:g.6942620G>T
  Sequence_details: SMap: S_parent: Sequence: F22D3
    Flanking_sequences: GTTATTTCCCTACGAGACCCAACTGTAGGGGGCGGAGCCTTTTAAATTGG TATTGGTTCCCAAATCGAAAATGTTTCTACGTCCTCATAATAAAATGAAA
    Mapping_target: F22D3
    Type_of_mutation: Substitution: G T
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00029537
    Laboratory: OTN
    Analysis: WGS_Hobert
    Status: Live
  Affects: Gene: WBGene00017699
    Transcript: F22D3.2g.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F22D3.2g.1:c.1102-92G>T
        Intron_number: 13/18
      F22D3.2e.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F22D3.2e.1:c.1093-92G>T
        Intron_number: 13/18
      F22D3.2d.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F22D3.2d.1:c.1102-92G>T
        Intron_number: 13/18
      F22D3.2j.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F22D3.2j.1:c.1093-92G>T
        Intron_number: 13/18
  Genetics: Map: II
  Reference: WBPaper00036201
  Method: WGS_Hobert