WormBase Tree Display for Variation: WBVar01662229

WBVar01662229 Name: Public_name: WBVar01662229
    Other_name: cewivar00350282
      F12B6.2c.1:c.307+171A>G
      F12B6.2a.1:c.433+171A>G
    HGVSg: CHROMOSOME_I:g.2251774A>G
  Sequence_details: SMap: S_parent: Sequence: F12B6
    Flanking_sequences: CTAAAACTCGAATAAAATAAAAAAAAACAT TATGAAATAGCTTTCTAAAACTTTGGAAAA
    Mapping_target: F12B6
    Source_location: 225 CHROMOSOME_I 2251776 2251776 From_analysis: Million_mutation_project_reanalysis
    Type_of_mutation: Substitution: A G
    SeqStatus: Sequenced
  Variation_type: Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00006637 From_analysis: Million_mutation_project_reanalysis
      WBStrain00022868 From_analysis: Million_mutation_project_reanalysis
      WBStrain00022886 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023072 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023191 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023192 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023286 From_analysis: Million_mutation_project_reanalysis
      WBStrain00027662 From_analysis: Million_mutation_project_reanalysis
    Laboratory: VC
    Analysis: Million_mutation_project_reanalysis
    Status: Live
  Affects: Gene: WBGene00017398
    Transcript: F12B6.2c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F12B6.2c.1:c.307+171A>G
        Intron_number: 3/10
      F12B6.2a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F12B6.2a.1:c.433+171A>G
        Intron_number: 5/13
  Method: WGS_Flibotte