WormBase Tree Display for Variation: WBVar01551592

WBVar01551592 Name: Public_name: WBVar01551592
    Other_name: cewivar00128649
      T06H11.1f.1:c.693-46G>T
      T06H11.1b.1:c.543-46G>T
      T06H11.1g.1:c.417-46G>T
      T06H11.1a.1:c.657-46G>T
      T06H11.1c.1:c.429-46G>T
      T06H11.1e.1:c.348-46G>T
      T06H11.1d.1:c.573-46G>T
    HGVSg: CHROMOSOME_X:g.10107516C>A
  Sequence_details: SMap: S_parent: Sequence: T06H11
    Flanking_sequences: TTTGAAAATAATTCAGGTAAAAGAATGTTA TATAAGATGTTTCCCTGAAAGAAATCAAAC
    Mapping_target: T06H11
    Source_location: 225 CHROMOSOME_X 10107457 10107457 From_analysis: Million_mutation_project_reanalysis
    Type_of_mutation: Substitution: C A
    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
      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.543-46G>T
        Intron_number: 5/12
      T06H11.1g.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T06H11.1g.1:c.417-46G>T
        Intron_number: 4/12
      T06H11.1f.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T06H11.1f.1:c.693-46G>T
        Intron_number: 6/14
      T06H11.1e.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T06H11.1e.1:c.348-46G>T
        Intron_number: 4/13
      T06H11.1d.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T06H11.1d.1:c.573-46G>T
        Intron_number: 3/11
      T06H11.1a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T06H11.1a.1:c.657-46G>T
        Intron_number: 3/11
      T06H11.1c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T06H11.1c.1:c.429-46G>T
        Intron_number: 4/13
  Method: WGS_Flibotte