WormBase Tree Display for Variation: WBVar01471303

WBVar01471303 Evidence: Paper_evidence: WBPaper00040707
  Name: Public_name: WBVar01471303
    Other_name: C44C10.9c.1:c.260+160C>T
      C44C10.9a.1:c.455+160C>T
      C44C10.9e.1:c.140+160C>T
      C44C10.9b.1:c.*532+160C>T
    HGVSg: CHROMOSOME_X:g.11714452G>A
  Sequence_details: SMap: S_parent: Sequence: C44C10
    Flanking_sequences: GAGACTTGAGTTCGAAACCTGTTGATTATT GTTGTTAATTCACTCGATAATTTTGATTAC
    Mapping_target: C44C10
    Type_of_mutation: Substitution: g a
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00006698 From_analysis: WGS_Andersen
    Laboratory: QX
    Person: WBPerson1730
    Analysis: WGS_Andersen
    DB_info: Database: dbSNP_rs rs 193356605
        dbSNP_ss ss 295532524
    Status: Live
  Affects: Gene: WBGene00008089
    Transcript: C44C10.9e.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C44C10.9e.1:c.140+160C>T
        Intron_number: 1/2
      C44C10.9c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C44C10.9c.1:c.260+160C>T
        Intron_number: 2/3
      C44C10.9b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C44C10.9b.1:c.*532+160C>T
        Intron_number: 6/7
      C44C10.9a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C44C10.9a.1:c.455+160C>T
        Intron_number: 5/7
  Reference: WBPaper00040707
  Method: WGS_Andersen