WormBase Tree Display for Variation: WBVar01686389

WBVar01686389 Name: Public_name: WBVar01686389
    Other_name: cewivar00377830
      F53A3.4c.1:c.3196-4693T>C
      F53A3.4a.1:c.3196-4693T>C
      F53A3.4b.1:c.3196-4693T>C
      F53A3.4d.1:c.-1672+3084T>C
    HGVSg: CHROMOSOME_III:g.1922984T>C
  Sequence_details: SMap: S_parent: Sequence: B0524
    Flanking_sequences: GCGGATTTGAGAAAATTTGGAGTAATTCAG CAGACCAAATATTCCTTGAAAATTCTCAAG
    Mapping_target: B0524
    Source_location: 225 CHROMOSOME_III 1922975 1922975 From_analysis: Million_mutation_project_reanalysis
    Type_of_mutation: Substitution: T C
    SeqStatus: Sequenced
  Variation_type: Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00006640 From_analysis: Million_mutation_project_reanalysis
      WBStrain00008273 From_analysis: Million_mutation_project_reanalysis
    Laboratory: VC
    Analysis: Million_mutation_project_reanalysis
    Status: Live
  Affects: Gene: WBGene00004128
    Transcript: F53A3.4d.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F53A3.4d.1:c.-1672+3084T>C
        Intron_number: 1/11
      F53A3.4c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F53A3.4c.1:c.3196-4693T>C
        Intron_number: 14/16
      F53A3.4b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F53A3.4b.1:c.3196-4693T>C
        Intron_number: 14/23
      F53A3.4a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F53A3.4a.1:c.3196-4693T>C
        Intron_number: 15/23
  Method: WGS_Flibotte