WormBase Tree Display for Variation: WBVar01435661

WBVar01435661 Evidence: Paper_evidence: WBPaper00040707
  Name: Public_name: WBVar01435661
    Other_name: cewivar00303741
      T07D3.9b.1:c.471+11G>A
      T07D3.9a.1:c.606+11G>A
      T07D3.9a.2:c.606+11G>A
    HGVSg: CHROMOSOME_II:g.899582C>T
  Sequence_details: SMap: S_parent: Sequence: T07D3
    Flanking_sequences: AAAACTTACATAAAGCTTGTGAGATTTTTG AGAAGCTCACCATAATGAATTCCGCTTTGA
    Mapping_target: T07D3
    Type_of_mutation: Substitution: c t
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00005305 From_analysis: WGS_Andersen
      WBStrain00005315 From_analysis: WGS_Andersen
      WBStrain00005834 From_analysis: WGS_Andersen
      WBStrain00006616 From_analysis: WGS_Andersen
      WBStrain00006618 From_analysis: WGS_Andersen
      WBStrain00006625 From_analysis: Million_mutation_project_reanalysis
          WGS_Andersen
      WBStrain00023065 From_analysis: WGS_Andersen
      WBStrain00023665 From_analysis: Million_mutation_project_reanalysis
          WGS_Andersen
      WBStrain00027652 From_analysis: Million_mutation_project_reanalysis
          WGS_Andersen
      WBStrain00027664 From_analysis: WGS_Andersen
    Laboratory: QX
    Person: WBPerson1730
    Analysis: Million_mutation_project_reanalysis
      WGS_Andersen
    DB_info: Database: dbSNP_rs rs 193323723
        dbSNP_ss ss 295499641
    Status: Live
  Affects: Gene: WBGene00020311
    Transcript: T07D3.9a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T07D3.9a.1:c.606+11G>A
        Intron_number: 5/8
      T07D3.9b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T07D3.9b.1:c.471+11G>A
        Intron_number: 5/7
      T07D3.9a.2 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T07D3.9a.2:c.606+11G>A
        Intron_number: 6/9
  Reference: WBPaper00040707
  Method: WGS_Andersen