WormBase Tree Display for Variation: WBVar01600720

WBVar01600720 Name: Public_name: WBVar01600720
    Other_name: cewivar00269382
      K06A9.1c.1:c.1895-1654T>C
      K06A9.1b.1:c.7208-1654T>C
      K06A9.1e.1:c.4280-1654T>C
      K06A9.1d.1:c.3533-1654T>C
      K06A9.1f.1:c.4826-1654T>C
      K06A9.1g.1:c.5102-1654T>C
      K06A9.1a.1:c.2771-1654T>C
    HGVSg: CHROMOSOME_X:g.1556801T>C
  Sequence_details: SMap: S_parent: Sequence: H02F09
    Flanking_sequences: CATCAAGTATTGATCCCAAGTCAACAGAAA CTATTCCAGTACTACAGTGTCACCCAGCTG
    Mapping_target: H02F09
    Source_location: 225 CHROMOSOME_X 1556796 1556796 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
      WBStrain00006622 From_analysis: Million_mutation_project_reanalysis
      WBStrain00006640 From_analysis: Million_mutation_project_reanalysis
      WBStrain00022850 From_analysis: Million_mutation_project_reanalysis
      WBStrain00022878 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023072 From_analysis: Million_mutation_project_reanalysis
    Laboratory: VC
    Analysis: Million_mutation_project_reanalysis
    Status: Live
  Affects: Gene: WBGene00019435
    Transcript: K06A9.1d.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: K06A9.1d.1:c.3533-1654T>C
        Intron_number: 7/12
      K06A9.1c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: K06A9.1c.1:c.1895-1654T>C
        Intron_number: 8/14
      K06A9.1b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: K06A9.1b.1:c.7208-1654T>C
        Intron_number: 8/13
      K06A9.1g.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: K06A9.1g.1:c.5102-1654T>C
        Intron_number: 7/12
      K06A9.1e.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: K06A9.1e.1:c.4280-1654T>C
        Intron_number: 7/12
      K06A9.1f.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: K06A9.1f.1:c.4826-1654T>C
        Intron_number: 7/12
      K06A9.1a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: K06A9.1a.1:c.2771-1654T>C
        Intron_number: 8/14
  Method: WGS_Flibotte