WormBase Tree Display for Variation: WBVar01621000

WBVar01621000 Name: Public_name: WBVar01621000
    Other_name: cewivar00300721
      C34E11.3g.1:c.345+41T>A
      C34E11.3a.1:c.306+41T>A
      C34E11.3c.1:c.-3235+41T>A
      C34E11.3e.1:c.345+41T>A
      C34E11.3f.1:c.345+41T>A
      C34E11.3b.1:c.306+41T>A
      C34E11.3d.1:c.-3235+41T>A
    HGVSg: CHROMOSOME_X:g.11826823T>A
  Sequence_details: SMap: S_parent: Sequence: C34E11
    Flanking_sequences: CGGATATTACGAATATTGCTCTTGTTTTCC AGGACATTTAGAGTTGTATTCAAGTTTATT
    Mapping_target: C34E11
    Source_location: 225 CHROMOSOME_X 11826755 11826755 From_analysis: Million_mutation_project_reanalysis
    Type_of_mutation: Substitution: T A
    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: WBGene00044079
    Transcript: C34E11.3f.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C34E11.3f.1:c.345+41T>A
        Intron_number: 3/27
      C34E11.3b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C34E11.3b.1:c.306+41T>A
        Intron_number: 2/24
      C34E11.3g.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C34E11.3g.1:c.345+41T>A
        Intron_number: 3/25
      C34E11.3d.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C34E11.3d.1:c.-3235+41T>A
        Intron_number: 2/26
      C34E11.3e.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C34E11.3e.1:c.345+41T>A
        Intron_number: 4/27
      C34E11.3c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C34E11.3c.1:c.-3235+41T>A
        Intron_number: 3/28
      C34E11.3a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C34E11.3a.1:c.306+41T>A
        Intron_number: 4/28
  Method: WGS_Flibotte