WormBase Tree Display for Variation: WBVar01433841

WBVar01433841 Evidence: Paper_evidence: WBPaper00040707
  Name: Public_name: WBVar01433841
    Other_name: cewivar00352727
      T27F6.5a.1:c.322-291A>C
      T27F6.5d.1:c.326-291A>C
    HGVSg: CHROMOSOME_I:g.12488578A>C
  Sequence_details: SMap: S_parent: Sequence: T27F6
    Flanking_sequences: TTTTGGGCCAAAAATTCACTTTTTGCCGAA AAATCCACTAAATAGTCAAAACTTCGGAAT
    Mapping_target: T27F6
    Type_of_mutation: Substitution: a c
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00006635 From_analysis: WGS_Andersen
      WBStrain00006637 From_analysis: Million_mutation_project_reanalysis
          WGS_Andersen
      WBStrain00022847 From_analysis: WGS_Andersen
      WBStrain00022848 From_analysis: WGS_Andersen
      WBStrain00022849 From_analysis: WGS_Andersen
    Laboratory: QX
    Person: WBPerson1730
    Analysis: Million_mutation_project_reanalysis
      WGS_Andersen
    DB_info: Database: dbSNP_rs rs 193321903
        dbSNP_ss ss 295497821
    Status: Live
  Affects: Gene: WBGene00004190
    Transcript: T27F6.5a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T27F6.5a.1:c.322-291A>C
        Intron_number: 3/7
      T27F6.5d.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T27F6.5d.1:c.326-291A>C
        Intron_number: 3/7
  Reference: WBPaper00040707
  Method: WGS_Andersen