WormBase Tree Display for Variation: WBVar01853477

WBVar01853477 Name: Public_name: WBVar01853477
    Other_name: cewivar00566585
      F57H12.4.3:c.257+159T>C
      F57H12.4.1:c.257+159T>C
      F57H12.4.4:c.257+159T>C
      F57H12.4.2:c.257+159T>C
    HGVSg: CHROMOSOME_IV:g.7971710T>C
  Sequence_details: SMap: S_parent: Sequence: F57H12
    Flanking_sequences: CTAGCAGTGAAAGCCGTTGCTCATTATTTC AAATTATGACTGTTCTAGATGTCTTGTCTC
    Mapping_target: F57H12
    Source_location: 225 CHROMOSOME_IV 7971698 7971698 From_analysis: Million_mutation_project_reanalysis
    Type_of_mutation: Substitution: T C
    SeqStatus: Sequenced
  Variation_type: Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023072 From_analysis: Million_mutation_project_reanalysis
    Laboratory: VC
    Analysis: Million_mutation_project_reanalysis
    Status: Live
  Affects: Gene: WBGene00019019
    Transcript: F57H12.4.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F57H12.4.1:c.257+159T>C
        Intron_number: 4/8
      F57H12.4.3 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F57H12.4.3:c.257+159T>C
        Intron_number: 5/9
      F57H12.4.2 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F57H12.4.2:c.257+159T>C
        Intron_number: 5/9
      F57H12.4.4 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F57H12.4.4:c.257+159T>C
        Intron_number: 4/8
  Method: WGS_Flibotte