WormBase Tree Display for Variation: WBVar01458981

WBVar01458981 Evidence: Paper_evidence: WBPaper00040707
  Name: Public_name: WBVar01458981
    Other_name: T27C4.4a.1:c.2919-12A>T
      T27C4.4d.1:c.*885-12A>T
      T27C4.4b.2:c.2608-12A>T
      T27C4.4b.1:c.2608-12A>T
      T27C4.4e.1:c.2203-12A>T
    HGVSg: CHROMOSOME_V:g.3712341A>T
  Sequence_details: SMap: S_parent: Sequence: T27C4
    Flanking_sequences: TTCTGATTTCAGATAAAGTAAAAAAAACAC TTTTTTTGCAGAACTAAACGACGGAACCTA
    Mapping_target: T27C4
    Type_of_mutation: Substitution: a t
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00031279 From_analysis: WGS_Andersen
      WBStrain00031284 From_analysis: WGS_Andersen
    Laboratory: QX
    Person: WBPerson1730
    Analysis: WGS_Andersen
    DB_info: Database: dbSNP_rs rs 193344638
        dbSNP_ss ss 295520557
    Status: Live
  Affects: Gene: WBGene00003025
    Transcript: T27C4.4d.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T27C4.4d.1:c.*885-12A>T
        Intron_number: 8/8
      T27C4.4b.2 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T27C4.4b.2:c.2608-12A>T
        Intron_number: 7/8
      T27C4.4a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T27C4.4a.1:c.2919-12A>T
        Intron_number: 8/9
      T27C4.4e.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T27C4.4e.1:c.2203-12A>T
        Intron_number: 4/4
      T27C4.4b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T27C4.4b.1:c.2608-12A>T
        Intron_number: 7/8
  Reference: WBPaper00040707
  Method: WGS_Andersen