WormBase Tree Display for Variation: WBVar01546927

WBVar01546927 Name: Public_name: WBVar01546927
    Other_name: cewivar00121607
      F45E10.1d.1:c.711+149T>C
      F45E10.1h.1:c.1113+149T>C
      F45E10.1g.1:c.1113+149T>C
      F45E10.1f.1:c.189+149T>C
      F45E10.1c.1:c.1113+149T>C
      F45E10.1a.1:c.1113+149T>C
      F45E10.1b.1:c.1113+149T>C
    HGVSg: CHROMOSOME_II:g.11070566A>G
  Sequence_details: SMap: S_parent: Sequence: F45E10
    Flanking_sequences: AAATATTTTTTATTTCTTTTTCTATATCTG TATCTTCAATATGAACCAAGATATAAATCT
    Mapping_target: F45E10
    Source_location: 225 CHROMOSOME_II 11070508 11070508 From_analysis: Million_mutation_project_reanalysis
    Type_of_mutation: Substitution: A G
    SeqStatus: Sequenced
  Variation_type: Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00004599 From_analysis: Million_mutation_project_reanalysis
      WBStrain00004600 From_analysis: Million_mutation_project_reanalysis
      WBStrain00006629 From_analysis: Million_mutation_project_reanalysis
      WBStrain00006631 From_analysis: Million_mutation_project_reanalysis
      WBStrain00006640 From_analysis: Million_mutation_project_reanalysis
      WBStrain00022878 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023138 From_analysis: Million_mutation_project_reanalysis
      WBStrain00027647 From_analysis: Million_mutation_project_reanalysis
    Laboratory: VC
    Analysis: Million_mutation_project_reanalysis
    Status: Live
  Affects: Gene: WBGene00006788
    Transcript: F45E10.1c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F45E10.1c.1:c.1113+149T>C
        Intron_number: 8/23
      F45E10.1b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F45E10.1b.1:c.1113+149T>C
        Intron_number: 8/22
      F45E10.1d.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F45E10.1d.1:c.711+149T>C
        Intron_number: 6/20
      F45E10.1g.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F45E10.1g.1:c.1113+149T>C
        Intron_number: 8/21
      F45E10.1a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F45E10.1a.1:c.1113+149T>C
        Intron_number: 9/23
      F45E10.1h.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F45E10.1h.1:c.1113+149T>C
        Intron_number: 8/21
      F45E10.1f.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F45E10.1f.1:c.189+149T>C
        Intron_number: 1/15
  Method: WGS_Flibotte