WormBase Tree Display for Variation: WBVar01464942

WBVar01464942 Evidence: Paper_evidence: WBPaper00040707
  Name: Public_name: WBVar01464942
    Other_name: cewivar00448742
      Y59A8B.21a.1:c.318-381A>G
      Y59A8B.21b.1:c.318-381A>G
    HGVSg: CHROMOSOME_V:g.17987862A>G
  Sequence_details: SMap: S_parent: Sequence: Y59A8B
    Flanking_sequences: AACTCGCAGAAAATTCTAATAATTCCAAAT ATTACGGAAGCGCGCGAATTATTGCCTAAA
    Mapping_target: Y59A8B
    Type_of_mutation: Substitution: a g
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00005301 From_analysis: WGS_Andersen
      WBStrain00005311 From_analysis: WGS_Andersen
      WBStrain00005835 From_analysis: WGS_Andersen
      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 193350598
        dbSNP_ss ss 295526517
    Status: Live
  Affects: Gene: WBGene00013353
    Transcript: Y59A8B.21a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y59A8B.21a.1:c.318-381A>G
        Intron_number: 3/11
      Y59A8B.21b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y59A8B.21b.1:c.318-381A>G
        Intron_number: 3/11
  Reference: WBPaper00040707
  Method: WGS_Andersen