WormBase Tree Display for Variation: WBVar01467578

WBVar01467578 Evidence: Paper_evidence: WBPaper00040707
  Name: Public_name: WBVar01467578
    Other_name: W05H7.4e.1:c.182-731C>A
      W05H7.4b.1:c.182-731C>A
      W05H7.4c.1:c.*360C>A
    HGVSg: CHROMOSOME_X:g.1444047G>T
  Sequence_details: SMap: S_parent: Sequence: W05H7
    Flanking_sequences: CTAGTAGTAAGTACAGAAATCAGATTTTTG GAGATCAAAATTTCAAGATTACAACGTTTT
    Mapping_target: W05H7
    Type_of_mutation: Substitution: g 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 193352880
        dbSNP_ss ss 295528799
    Status: Live
  Affects: Gene: WBGene00021047
    Transcript: W05H7.4b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: W05H7.4b.1:c.182-731C>A
        Intron_number: 3/9
      W05H7.4c.1 VEP_consequence: 3_prime_UTR_variant
        VEP_impact: MODIFIER
        HGVSc: W05H7.4c.1:c.*360C>A
        cDNA_position: 1078
        Exon_number: 5/10
      W05H7.4e.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: W05H7.4e.1:c.182-731C>A
        Intron_number: 3/9
  Reference: WBPaper00040707
  Method: WGS_Andersen