WormBase Tree Display for Variation: WBVar01264316

WBVar01264316 Evidence: Paper_evidence: WBPaper00037807
  Name: Public_name: WBVar01264316
    Other_name: cewivar00387603
      F47D12.1c.1:c.734+1052T>A
      F47D12.1b.1:c.734+1052T>A
      F47D12.1a.1:c.734+1052T>A
    HGVSg: CHROMOSOME_III:g.6316471T>A
  Sequence_details: SMap: S_parent: Sequence: F47D12
    Flanking_sequences: AGTCGTAGGCTCTATTTCGTTGATAATGACTCATTCACATAGATTTCTTG ATTGCAAAATATAAAAAAAGTTAAATTTAAAAACGTGCAATTTCTCTTCC
    Mapping_target: F47D12
    Type_of_mutation: Substitution: t A 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 539099829
    Status: Live
  Affects: Gene: WBGene00001518
    Transcript: F47D12.1b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F47D12.1b.1:c.734+1052T>A
        Intron_number: 6/12
      F47D12.1a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F47D12.1a.1:c.734+1052T>A
        Intron_number: 6/13
      F47D12.1c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F47D12.1c.1:c.734+1052T>A
        Intron_number: 6/12
  Reference: WBPaper00037807
  Method: WGS_De_Bono