WormBase Tree Display for Variation: WBVar01626908

WBVar01626908 Name: Public_name: WBVar01626908
    Other_name: cewivar00307086
      C41C4.5a.1:c.457+54G>A
      C41C4.5d.1:c.715+54G>A
      C41C4.5e.1:c.715+54G>A
      C41C4.4a.1:c.801+3339C>T
      C41C4.5c.2:c.397+54G>A
      C41C4.5b.1:c.571+54G>A
      C41C4.5h.1:c.715+54G>A
      C41C4.5c.1:c.397+54G>A
    HGVSg: CHROMOSOME_II:g.8119572G>A
  Sequence_details: SMap: S_parent: Sequence: C41C4
    Flanking_sequences: TGACAAATTGTTTTAAAAAACCTTTCACAG GTAAAGATTTTTGAAATTCTAAATATAAAA
    Mapping_target: C41C4
    Source_location: 225 CHROMOSOME_II 8119520 8119520 From_analysis: Million_mutation_project_reanalysis
    Type_of_mutation: Substitution: G A
    SeqStatus: Sequenced
  Variation_type: Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00006625 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023139 From_analysis: Million_mutation_project_reanalysis
      WBStrain00027648 From_analysis: Million_mutation_project_reanalysis
      WBStrain00027652 From_analysis: Million_mutation_project_reanalysis
      WBStrain00027660 From_analysis: Million_mutation_project_reanalysis
      WBStrain00027662 From_analysis: Million_mutation_project_reanalysis
    Laboratory: VC
    Analysis: Million_mutation_project_reanalysis
    Status: Live
  Affects: Gene: WBGene00002147
      WBGene00006832
    Transcript: C41C4.5e.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C41C4.5e.1:c.715+54G>A
        Intron_number: 6/15
      C41C4.4a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C41C4.4a.1:c.801+3339C>T
        Intron_number: 6/11
      C41C4.5c.2 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C41C4.5c.2:c.397+54G>A
        Intron_number: 7/14
      C41C4.5c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C41C4.5c.1:c.397+54G>A
        Intron_number: 6/15
      C41C4.5d.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C41C4.5d.1:c.715+54G>A
        Intron_number: 6/13
      C41C4.5a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C41C4.5a.1:c.457+54G>A
        Intron_number: 5/14
      C41C4.5h.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C41C4.5h.1:c.715+54G>A
        Intron_number: 5/14
      C41C4.5b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C41C4.5b.1:c.571+54G>A
        Intron_number: 5/14
  Method: WGS_Flibotte