WormBase Tree Display for Variation: WBVar01259625

WBVar01259625 Evidence: Paper_evidence: WBPaper00037807
  Name: Public_name: WBVar01259625
    Other_name: cewivar00285320
      W04B5.3a.1:c.904-35C>T
      W04B5.3b.1:c.904-35C>T
      W04B5.3c.1:c.904-35C>T
    HGVSg: CHROMOSOME_III:g.2422416C>T
  Sequence_details: SMap: S_parent: Sequence: W04B5
    Flanking_sequences: GCTCTCCACGAGCAAAATTCAAATTTTTAGCTTAAAAGTCTATAACTGAG TCCTAGAAAAAATTAAGGTTCATGAAATTTCCAGACCTACCCCCAATCGG
    Mapping_target: W04B5
    Type_of_mutation: Substitution: c T Paper_evidence: WBPaper00037807
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain (16)
    Laboratory: AX
      QX
    Person: WBPerson1730
    Analysis: WGS_De_Bono
      Million_mutation_project_reanalysis
      WGS_Andersen
    DB_info: Database: dbSNP_ss ss 539095606
    History: Acquires_merge: WBVar01444355
    Status: Live
  Affects: Gene: WBGene00021020
    Transcript: W04B5.3a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: W04B5.3a.1:c.904-35C>T
        Intron_number: 9/13
      W04B5.3c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: W04B5.3c.1:c.904-35C>T
        Intron_number: 9/12
      W04B5.3b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: W04B5.3b.1:c.904-35C>T
        Intron_number: 8/11
  Reference: WBPaper00040707
    WBPaper00037807
  Method: WGS_De_Bono