WormBase Tree Display for Variation: WBVar01254910

WBVar01254910 Evidence: Paper_evidence: WBPaper00037807
  Name: Public_name: WBVar01254910
    Other_name: cewivar00283657
      C09F5.1a.1:c.1554-32C>G
      C09F5.1b.1:c.975-32C>G
    HGVSg: CHROMOSOME_III:g.662322C>G
  Sequence_details: SMap: S_parent: Sequence: C09F5
    Flanking_sequences: TGAGATCGATTTTTTTGAAATTTTTGTCAAGTTATTAATCAAATGCCATG AAATCAAATTGAATACATTTCCATTTTTCAGAGTGGAAACCGACATCGGC
    Mapping_target: C09F5
    Type_of_mutation: Substitution: c G Paper_evidence: WBPaper00037807
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00006622 From_analysis: Million_mutation_project_reanalysis
      WBStrain00006640 From_analysis: Million_mutation_project_reanalysis
      WBStrain00006642 From_analysis: WGS_De_Bono
      WBStrain00006643 From_analysis: Million_mutation_project_reanalysis
      WBStrain00006645 From_analysis: Million_mutation_project_reanalysis
      WBStrain00022852 From_analysis: Million_mutation_project_reanalysis
      WBStrain00022856 From_analysis: Million_mutation_project_reanalysis
      WBStrain00022878 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023286 From_analysis: Million_mutation_project_reanalysis
    Laboratory: AX
    Analysis: WGS_De_Bono
      Million_mutation_project_reanalysis
    DB_info: Database: dbSNP_ss ss 539091363
    Status: Live
  Affects: Gene: WBGene00015647
    Transcript: C09F5.1a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C09F5.1a.1:c.1554-32C>G
        Intron_number: 9/10
      C09F5.1b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C09F5.1b.1:c.975-32C>G
        Intron_number: 7/8
  Reference: WBPaper00037807
  Method: WGS_De_Bono