WormBase Tree Display for Variation: WBVar01454596

WBVar01454596 Evidence: Paper_evidence: WBPaper00040707
  Name: Public_name: WBVar01454596
    Other_name: cewivar00155883
      T04A11.14:n.38A>G
    HGVSg: CHROMOSOME_IV:g.12507446A>G
  Sequence_details: SMap: S_parent: Sequence: T04A11
    Flanking_sequences: CGTATCACAGGAAAGCCAATTGTCAGTGGAGGAATTCACG ACGTGCTTCCGCCACCGGACGTGGAGTGTG
    Mapping_target: T04A11
    Type_of_mutation: Substitution: a g
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00004600 From_analysis: Million_mutation_project_reanalysis
          WGS_Andersen
      WBStrain00005835 From_analysis: WGS_Andersen
      WBStrain00023072 From_analysis: Million_mutation_project_reanalysis
          WGS_Andersen
      WBStrain00023075 From_analysis: WGS_Andersen
      WBStrain00023079 From_analysis: WGS_Andersen
      WBStrain00023084 From_analysis: WGS_Andersen
      WBStrain00031115 From_analysis: WGS_Andersen
      WBStrain00031116 From_analysis: WGS_Andersen
      WBStrain00031279 From_analysis: WGS_Andersen
      WBStrain00031284 From_analysis: WGS_Andersen
    Laboratory: QX
    Person: WBPerson1730
    Analysis: Million_mutation_project_reanalysis
      WGS_Andersen
    DB_info: Database: dbSNP_rs rs 193340253
        dbSNP_ss ss 295516172
    Status: Live
  Affects: Gene: WBGene00045131
    Pseudogene: T04A11.14 VEP_consequence: non_coding_transcript_exon_variant
        VEP_impact: MODIFIER
        HGVSc: T04A11.14:n.38A>G
        cDNA_position: 38
        Exon_number: 1/1
  Reference: WBPaper00040707
  Method: WGS_Andersen