WormBase Tree Display for Variation: WBVar01322562

WBVar01322562 Evidence: Paper_evidence: WBPaper00037807
  Name: Public_name: WBVar01322562
    Other_name: cewivar00397330
      K02F3.12b.1:c.1433-29G>T
      K02F3.12a.1:c.1502-29G>T
    HGVSg: CHROMOSOME_III:g.859625G>T
  Sequence_details: SMap: S_parent: Sequence: Y6D11A
    Flanking_sequences: TTTAATATAAGTATGATGTAATCAGGAAGAGGAAAAAGCGACATTTGATT TCCATGTTTGTGATAAAATATTTTTCAGGATTCGTTGGGACTTCTTCAAA
    Mapping_target: Y6D11A
    Type_of_mutation: Substitution: g T Paper_evidence: WBPaper00037807
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00008273 From_analysis: Million_mutation_project_reanalysis
      WBStrain00022850 From_analysis: Million_mutation_project_reanalysis
          WGS_De_Bono
      WBStrain00023138 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 539178586
    Status: Live
  Affects: Gene: WBGene00019334
    Transcript: K02F3.12a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: K02F3.12a.1:c.1502-29G>T
        Intron_number: 5/6
      K02F3.12b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: K02F3.12b.1:c.1433-29G>T
        Intron_number: 5/5
  Reference: WBPaper00037807
  Method: WGS_De_Bono