WormBase Tree Display for Variation: WBVar01620410

WBVar01620410 Name: Public_name: WBVar01620410
    Other_name: cewivar00300090
      F31B12.1j.1:c.4933+326A>G
      F31B12.1k.1:c.5134+326A>G
      F31B12.1g.1:c.4954+326A>G
      F31B12.1l.1:c.4963+326A>G
      F31B12.1h.1:c.4984+326A>G
      F31B12.1d.1:c.5125+326A>G
      F31B12.1i.1:c.5104+326A>G
    HGVSg: CHROMOSOME_X:g.10813722T>C
  Sequence_details: SMap: S_parent: Sequence: F31B12
    Flanking_sequences: TAACCTGGTTTTGCCAAAAAATATACCCAT CAACAACGTCTAAAATTTGAAATGAAGAAC
    Mapping_target: F31B12
    Source_location: 225 CHROMOSOME_X 10813657 10813657 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.4933+326A>G
        Intron_number: 34/63
      F31B12.1g.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F31B12.1g.1:c.4954+326A>G
        Intron_number: 34/63
      F31B12.1d.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F31B12.1d.1:c.5125+326A>G
        Intron_number: 35/64
      F31B12.1h.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F31B12.1h.1:c.4984+326A>G
        Intron_number: 34/63
      F31B12.1l.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F31B12.1l.1:c.4963+326A>G
        Intron_number: 34/63
      F31B12.1i.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F31B12.1i.1:c.5104+326A>G
        Intron_number: 35/64
      F31B12.1k.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F31B12.1k.1:c.5134+326A>G
        Intron_number: 35/64
  Method: WGS_Flibotte