WormBase Tree Display for Variation: WBVar01279187

WBVar01279187 Evidence: Paper_evidence: WBPaper00037807
  Name: Public_name: WBVar01279187
    Other_name: cewivar00391199
      F12B6.3a.1:c.844-142A>T
      F12B6.3b.1:c.766-142A>T
    HGVSg: CHROMOSOME_I:g.2245998A>T
  Sequence_details: SMap: S_parent: Sequence: F12B6
    Flanking_sequences: GCCTAAGACTAACCCTTAACCTAAGCCTAAGTCCAAGCATAATTCTAAAT TTAGCTTAAGACTAAGCCTAAGCCCAAGCCTAAGCCTAAGCCTAAGCCTA
    Mapping_target: F12B6
    Type_of_mutation: Substitution: a 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
      WBStrain00022852 From_analysis: Million_mutation_project_reanalysis
      WBStrain00022856 From_analysis: Million_mutation_project_reanalysis
      WBStrain00022930 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023018 From_analysis: Million_mutation_project_reanalysis
      WBStrain00027652 From_analysis: Million_mutation_project_reanalysis
    Laboratory: AX
    Analysis: WGS_De_Bono
      Million_mutation_project_reanalysis
    DB_info: Database: dbSNP_ss ss 539139548
    Status: Live
  Affects: Gene: WBGene00017399
    Transcript: F12B6.3b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F12B6.3b.1:c.766-142A>T
        Intron_number: 5/6
      F12B6.3a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F12B6.3a.1:c.844-142A>T
        Intron_number: 6/7
  Reference: WBPaper00037807
  Method: WGS_De_Bono