WormBase Tree Display for Variation: WBVar01471614

WBVar01471614 Evidence: Paper_evidence: WBPaper00040707
  Name: Public_name: WBVar01471614
    Other_name: cewivar00157775
      F17E5.2.1:c.1049-54C>T
      F17E5.2.2:c.1049-54C>T
    HGVSg: CHROMOSOME_X:g.12397575C>T
  Sequence_details: SMap: S_parent: Sequence: F17E5
    Flanking_sequences: TCAATCAGTTCAAGATTTGAGAAGTTTCCG CATTATTAGTGAATAACAATAATGAAAAAA
    Mapping_target: F17E5
    Type_of_mutation: Substitution: c t
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00004600 From_analysis: Million_mutation_project_reanalysis
          WGS_Andersen
      WBStrain00023180 From_analysis: WGS_Andersen
      WBStrain00023224 From_analysis: WGS_Andersen
      WBStrain00023234 From_analysis: WGS_Andersen
      WBStrain00023279 From_analysis: WGS_Andersen
      WBStrain00023280 From_analysis: WGS_Andersen
      WBStrain00023281 From_analysis: WGS_Andersen
    Laboratory: QX
    Person: WBPerson1730
    Analysis: Million_mutation_project_reanalysis
      WGS_Andersen
    DB_info: Database: dbSNP_rs rs 193356916
        dbSNP_ss ss 295532835
    Status: Live
  Affects: Gene: WBGene00008924
    Transcript: F17E5.2.2 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F17E5.2.2:c.1049-54C>T
        Intron_number: 10/14
      F17E5.2.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F17E5.2.1:c.1049-54C>T
        Intron_number: 10/14
  Reference: WBPaper00040707
  Method: WGS_Andersen