WormBase Tree Display for Variation: WBVar01446912

WBVar01446912 Evidence: Paper_evidence: WBPaper00040707
  Name: Public_name: WBVar01446912
    Other_name: C02C2.3.1:c.112+14T>A
    HGVSg: CHROMOSOME_III:g.7866694T>A
  Sequence_details: SMap: S_parent: Sequence: C02C2
    Flanking_sequences: TGATGGAGATGCTGAGTGTAAGTTTTTTTT ATTGAAAATATTTTTTCACGAAACTTCCAA
    Mapping_target: C02C2
    Type_of_mutation: Substitution: t a
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00005835 From_analysis: WGS_Andersen
      WBStrain00022928 From_analysis: WGS_Andersen
      WBStrain00022930 From_analysis: WGS_Andersen
          Million_mutation_project_reanalysis
      WBStrain00023150 From_analysis: WGS_Andersen
      WBStrain00023180 From_analysis: WGS_Andersen
      WBStrain00023211 From_analysis: WGS_Andersen
      WBStrain00023279 From_analysis: WGS_Andersen
      WBStrain00031279 From_analysis: WGS_Andersen
      WBStrain00031284 From_analysis: WGS_Andersen
    Laboratory: QX
    Person: WBPerson1730
    Analysis: WGS_Andersen
    DB_info: Database: dbSNP_rs rs 193333547
        dbSNP_ss ss 295509466
    Status: Live
  Affects: Gene: WBGene00000845
    Transcript: C02C2.3.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C02C2.3.1:c.112+14T>A
        Intron_number: 2/8
  Reference: WBPaper00040707
  Method: WGS_Andersen