WormBase Tree Display for Variation: WBVar01679022

WBVar01679022 Name: Public_name: WBVar01679022
    Other_name (13)
    HGVSg: CHROMOSOME_X:g.10802430G>A
  Sequence_details: SMap: S_parent: Sequence: F31B12
    Flanking_sequences: ATATTTGTTTGCTGGTGGAAACAAGAAGAC TGTTGGGAATAGACAAGACGGAAACAAAAA
    Mapping_target: F31B12
    Source_location: 225 CHROMOSOME_X 10802365 10802365 From_analysis: Million_mutation_project_reanalysis
    Type_of_mutation: Substitution: G A
    SeqStatus: Sequenced
  Variation_type: Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00006637 From_analysis: Million_mutation_project_reanalysis
    Laboratory: VC
    Analysis: Million_mutation_project_reanalysis
    Status: Live
  Affects: Gene: WBGene00004036
    Transcript: F31B12.1j.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F31B12.1j.1:c.7692+493C>T
        Intron_number: 49/63
      F31B12.1f.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F31B12.1f.1:c.2889+493C>T
        Intron_number: 17/31
      F31B12.1h.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F31B12.1h.1:c.7743+493C>T
        Intron_number: 49/63
      F31B12.1c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F31B12.1c.1:c.2835+493C>T
        Intron_number: 16/32
      F31B12.1d.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F31B12.1d.1:c.7884+493C>T
        Intron_number: 50/64
      F31B12.1g.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F31B12.1g.1:c.7713+493C>T
        Intron_number: 49/63
      F31B12.1b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F31B12.1b.1:c.2835+493C>T
        Intron_number: 16/31
      F31B12.1a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F31B12.1a.1:c.2835+493C>T
        Intron_number: 17/33
      F31B12.1e.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F31B12.1e.1:c.2865+493C>T
        Intron_number: 16/30
      F31B12.1l.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F31B12.1l.1:c.7722+493C>T
        Intron_number: 49/63
      F31B12.1i.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F31B12.1i.1:c.7863+493C>T
        Intron_number: 50/64
      F31B12.1k.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F31B12.1k.1:c.7893+493C>T
        Intron_number: 50/64
  Method: WGS_Flibotte