WormBase Tree Display for Variation: WBVar01264910

WBVar01264910 Evidence: Paper_evidence: WBPaper00037807
  Name: Public_name: WBVar01264910
    Other_name: cewivar00387791
      F31E3.2c.1:c.144+167C>T
      F31E3.2a.1:c.144+167C>T
      F31E3.2b.1:c.144+167C>T
    HGVSg: CHROMOSOME_III:g.6974772C>T
  Sequence_details: SMap: S_parent: Sequence: F31E3
    Flanking_sequences: TACATAATGGTAAAGCACACTAACCGCAGTTCGGTGCAAGTGTGGTTTTA TCGGAGTAACCACGCTTTACTATGCCTAGCTCATTCCTAGATCTGCCTAA
    Mapping_target: F31E3
    Type_of_mutation: Substitution: c T Paper_evidence: WBPaper00037807
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00006642 From_analysis: WGS_De_Bono
      WBStrain00006643 From_analysis: Million_mutation_project_reanalysis
      WBStrain00006645 From_analysis: Million_mutation_project_reanalysis
      WBStrain00027647 From_analysis: Million_mutation_project_reanalysis
      WBStrain00031113 From_analysis: Million_mutation_project_reanalysis
    Laboratory: AX
    Analysis: WGS_De_Bono
      Million_mutation_project_reanalysis
    DB_info: Database: dbSNP_ss ss 539100364
    Status: Live
  Affects: Gene: WBGene00017950
    Transcript: F31E3.2b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F31E3.2b.1:c.144+167C>T
        Intron_number: 2/11
      F31E3.2a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F31E3.2a.1:c.144+167C>T
        Intron_number: 2/10
      F31E3.2c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F31E3.2c.1:c.144+167C>T
        Intron_number: 2/10
  Reference: WBPaper00037807
  Method: WGS_De_Bono