WormBase Tree Display for Variation: WBVar01465501

WBVar01465501 Evidence: Paper_evidence: WBPaper00040707
  Name: Public_name: WBVar01465501
    Other_name: cewivar00449556
      Y69H2.7b.1:c.279+245A>G
      Y69H2.7a.1:c.279+245A>G
    HGVSg: CHROMOSOME_V:g.18690867A>G
  Sequence_details: SMap: S_parent: Sequence: Y69H2
    Flanking_sequences: AAAAATTTGGTATTAATCGCTAAAACTTTG AAATTATTTTAAAAAAAGTGAATTTCAGAC
    Mapping_target: Y69H2
    Type_of_mutation: Substitution: a g
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023139 From_analysis: Million_mutation_project_reanalysis
          WGS_Andersen
      WBStrain00027648 From_analysis: Million_mutation_project_reanalysis
          WGS_Andersen
      WBStrain00027660 From_analysis: Million_mutation_project_reanalysis
          WGS_Andersen
      WBStrain00027661 From_analysis: WGS_Andersen
      WBStrain00027662 From_analysis: Million_mutation_project_reanalysis
          WGS_Andersen
      WBStrain00027669 From_analysis: WGS_Andersen
    Laboratory: QX
    Person: WBPerson1730
    Analysis: Million_mutation_project_reanalysis
      WGS_Andersen
    DB_info: Database: dbSNP_rs rs 193351157
        dbSNP_ss ss 295527076
    Status: Live
  Affects: Gene: WBGene00013482
    Transcript: Y69H2.7b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y69H2.7b.1:c.279+245A>G
        Intron_number: 4/8
      Y69H2.7a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y69H2.7a.1:c.279+245A>G
        Intron_number: 4/8
  Reference: WBPaper00040707
  Method: WGS_Andersen