WormBase Tree Display for Variation: WBVar01546124

WBVar01546124 Name: Public_name: WBVar01546124
    Other_name: cewivar00120252
      F56D12.1d.1:c.258+42C>T
      F56D12.1a.2:c.678+42C>T
      F56D12.1a.1:c.678+42C>T
      F56D12.1c.1:c.678+42C>T
      F56D12.1b.1:c.678+42C>T
    HGVSg: CHROMOSOME_II:g.1308703G>A
  Sequence_details: SMap: S_parent: Sequence: F56D12
    Flanking_sequences: TTTTCTCGGAAATTTTCAAATTTTCATCAC AATTTCGGCTTTTCAAGGCTATTTCTAGTT
    Mapping_target: F56D12
    Source_location: 225 CHROMOSOME_II 1308710 1308710 From_analysis: Million_mutation_project_reanalysis
    Type_of_mutation: Substitution: G A
    SeqStatus: Sequenced
  Variation_type: Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00004599 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023665 From_analysis: Million_mutation_project_reanalysis
      WBStrain00027652 From_analysis: Million_mutation_project_reanalysis
    Laboratory: VC
    Analysis: Million_mutation_project_reanalysis
    Status: Live
  Affects: Gene: WBGene00000112
    Transcript: F56D12.1b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F56D12.1b.1:c.678+42C>T
        Intron_number: 5/7
      F56D12.1a.2 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F56D12.1a.2:c.678+42C>T
        Intron_number: 6/9
      F56D12.1a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F56D12.1a.1:c.678+42C>T
        Intron_number: 5/8
      F56D12.1d.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F56D12.1d.1:c.258+42C>T
        Intron_number: 1/3
      F56D12.1c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F56D12.1c.1:c.678+42C>T
        Intron_number: 4/5
  Method: WGS_Flibotte