WormBase Tree Display for Variation: WBVar01578590

WBVar01578590 Name: Public_name: WBVar01578590
    Other_name: cewivar00194657
      F53A3.4c.1:c.1770+282T>C
      F53A3.4b.1:c.1770+282T>C
      F53A3.4a.1:c.1770+282T>C
    HGVSg: CHROMOSOME_III:g.1911600T>C
  Sequence_details: SMap: S_parent: Sequence: B0524
    Flanking_sequences: ATTTCATGGCGGAGCTCTAAAAATAGGTTA CAAGGGTAGAAATCCGCGAAAAATTCGAAT
    Mapping_target: B0524
    Source_location: 225 CHROMOSOME_III 1911591 1911591 From_analysis: Million_mutation_project_reanalysis
    Type_of_mutation: Substitution: T C
    SeqStatus: Sequenced
  Variation_type: Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00004602 From_analysis: Million_mutation_project_reanalysis
      WBStrain00006640 From_analysis: Million_mutation_project_reanalysis
      WBStrain00008273 From_analysis: Million_mutation_project_reanalysis
      WBStrain00022930 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023138 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023191 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023192 From_analysis: Million_mutation_project_reanalysis
      WBStrain00031113 From_analysis: Million_mutation_project_reanalysis
    Laboratory: VC
    Analysis: Million_mutation_project_reanalysis
    Status: Live
  Affects: Gene: WBGene00004128
    Transcript: F53A3.4c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F53A3.4c.1:c.1770+282T>C
        Intron_number: 8/16
      F53A3.4b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F53A3.4b.1:c.1770+282T>C
        Intron_number: 8/23
      F53A3.4a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F53A3.4a.1:c.1770+282T>C
        Intron_number: 9/23
  Method: WGS_Flibotte