WormBase Tree Display for Variation: WBVar01551591

WBVar01551591 Name: Public_name: WBVar01551591
    Other_name: cewivar00128648
      T06H11.1d.1:c.829+11T>A
      T06H11.1b.1:c.799+11T>A
      T06H11.1f.1:c.949+11T>A
      T06H11.1a.1:c.913+11T>A
      T06H11.1g.1:c.673+11T>A
      T06H11.1e.1:c.604+11T>A
      T06H11.1c.1:c.685+11T>A
    HGVSg: CHROMOSOME_X:g.10107203A>T
  Sequence_details: SMap: S_parent: Sequence: T06H11
    Flanking_sequences: TAATAAATTTTAATTATTTCTGAATTATGA TCAACAATACCGCAAGTAGTTAACACAGTG
    Mapping_target: T06H11
    Source_location: 225 CHROMOSOME_X 10107144 10107144 From_analysis: Million_mutation_project_reanalysis
    Type_of_mutation: Substitution: A T
    SeqStatus: Sequenced
  Variation_type: Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00004599 From_analysis: Million_mutation_project_reanalysis
      WBStrain00022850 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023072 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023139 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023192 From_analysis: Million_mutation_project_reanalysis
      WBStrain00024204 From_analysis: Million_mutation_project_reanalysis
      WBStrain00027647 From_analysis: Million_mutation_project_reanalysis
      WBStrain00027648 From_analysis: Million_mutation_project_reanalysis
      WBStrain00027660 From_analysis: Million_mutation_project_reanalysis
    Laboratory: VC
    Analysis: Million_mutation_project_reanalysis
    Status: Live
  Affects: Gene: WBGene00006792
    Transcript: T06H11.1b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T06H11.1b.1:c.799+11T>A
        Intron_number: 6/12
      T06H11.1g.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T06H11.1g.1:c.673+11T>A
        Intron_number: 5/12
      T06H11.1f.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T06H11.1f.1:c.949+11T>A
        Intron_number: 7/14
      T06H11.1e.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T06H11.1e.1:c.604+11T>A
        Intron_number: 5/13
      T06H11.1d.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T06H11.1d.1:c.829+11T>A
        Intron_number: 4/11
      T06H11.1a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T06H11.1a.1:c.913+11T>A
        Intron_number: 4/11
      T06H11.1c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T06H11.1c.1:c.685+11T>A
        Intron_number: 5/13
  Method: WGS_Flibotte