WormBase Tree Display for Variation: WBVar01472571

WBVar01472571 Evidence: Paper_evidence: WBPaper00040707
  Name: Public_name: WBVar01472571
    Other_name: cewivar00460135
      C44H4.4.1:c.2215+3904C>T
      CE43213:p.Ala668Thr
      C44H4.2.1:c.2002G>A
    HGVSg: CHROMOSOME_X:g.14580451G>A
  Sequence_details: SMap: S_parent: Sequence: C44H4
    Flanking_sequences: AAGAGTGAGCACATTGACGAATTCGCTCTA CTTCTTCAAATTCCAATGAGCCAACTCTCC
    Mapping_target: C44H4
    Type_of_mutation: Substitution: g a
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00005305 From_analysis: WGS_Andersen
      WBStrain00005315 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
      WBStrain00027669 From_analysis: WGS_Andersen
      WBStrain00030851 From_analysis: WGS_Andersen
    Laboratory: QX
    Person: WBPerson1730
    Analysis: Million_mutation_project_reanalysis
      WGS_Andersen
    DB_info: Database: dbSNP_rs rs 193357873
        dbSNP_ss ss 295533792
    Status: Live
  Affects: Gene: WBGene00002282
      WBGene00008094
    Transcript: C44H4.4.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C44H4.4.1:c.2215+3904C>T
        Intron_number: 15/20
      C44H4.2.1 (12)
  Reference: WBPaper00040707
  Method: WGS_Andersen