WormBase Tree Display for Variation: WBVar01439635

WBVar01439635 Evidence: Paper_evidence: WBPaper00040707
  Name: Public_name: WBVar01439635
    Other_name: C09G5.2a.1:c.797+319T>C
      C09G5.6.1:c.2648-17A>G
    HGVSg: CHROMOSOME_II:g.10711831A>G
  Sequence_details: SMap: S_parent: Sequence: C09G5
    Flanking_sequences: GTAGAATTGTTATGCGGAAATTATCATTAA TTAAATTCAATTGCAGTTGAAACTTCCGTA
    Mapping_target: C09G5
    Type_of_mutation: Substitution: a g
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00005298 From_analysis: WGS_Andersen
      WBStrain00005306 From_analysis: WGS_Andersen
    Laboratory: QX
    Person: WBPerson1730
    Analysis: WGS_Andersen
    DB_info: Database: dbSNP_rs rs 193327696
        dbSNP_ss ss 295503615
    Status: Live
  Affects: Gene: WBGene00007488
      WBGene00000251
    Transcript: C09G5.2a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C09G5.2a.1:c.797+319T>C
        Intron_number: 6/10
      C09G5.6.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C09G5.6.1:c.2648-17A>G
        Intron_number: 5/6
  Reference: WBPaper00040707
  Method: WGS_Andersen