WormBase Tree Display for Variation: WBVar01620421

WBVar01620421 Name: Public_name: WBVar01620421
    Other_name: cewivar00300102
      F31B12.1i.1:c.37-2058A>G
      F31B12.1d.1:c.37-2058A>G
      F31B12.1l.1:c.37-2058A>G
      F31B12.1k.1:c.37-2058A>G
      F31B12.1g.1:c.37-2058A>G
      F31B12.1j.1:c.37-2058A>G
      F31B12.1h.1:c.37-2058A>G
    HGVSg: CHROMOSOME_X:g.10835626T>C
  Sequence_details: SMap: S_parent: Sequence: C05A9
    Flanking_sequences: AGAATAAGTTCAGTTTCAGTTTTTTCCGTT GTTTTCAATGACGCATCAAGGACAATGTTG
    Mapping_target: C05A9
    Source_location: 225 CHROMOSOME_X 10835561 10835561 From_analysis: Million_mutation_project_reanalysis
    Type_of_mutation: Substitution: T C
    SeqStatus: Sequenced
  Variation_type: Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00006622 From_analysis: Million_mutation_project_reanalysis
      WBStrain00006637 From_analysis: Million_mutation_project_reanalysis
      WBStrain00022852 From_analysis: Million_mutation_project_reanalysis
      WBStrain00022856 From_analysis: Million_mutation_project_reanalysis
      WBStrain00022878 From_analysis: Million_mutation_project_reanalysis
      WBStrain00022930 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023191 From_analysis: Million_mutation_project_reanalysis
      WBStrain00027652 From_analysis: Million_mutation_project_reanalysis
      WBStrain00027662 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.37-2058A>G
        Intron_number: 1/63
      F31B12.1g.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F31B12.1g.1:c.37-2058A>G
        Intron_number: 1/63
      F31B12.1d.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F31B12.1d.1:c.37-2058A>G
        Intron_number: 1/64
      F31B12.1h.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F31B12.1h.1:c.37-2058A>G
        Intron_number: 1/63
      F31B12.1l.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F31B12.1l.1:c.37-2058A>G
        Intron_number: 1/63
      F31B12.1i.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F31B12.1i.1:c.37-2058A>G
        Intron_number: 1/64
      F31B12.1k.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F31B12.1k.1:c.37-2058A>G
        Intron_number: 1/64
  Method: WGS_Flibotte