WormBase Tree Display for Variation: WBVar01289812

WBVar01289812 Evidence: Paper_evidence: WBPaper00037807
  Name: Public_name: WBVar01289812
    Other_name: cewivar00326043
      F49B2.6.1:c.1052+85T>C
    HGVSg: CHROMOSOME_I:g.14333550T>C
  Sequence_details: SMap: S_parent: Sequence: Y105E8A
    Flanking_sequences: TAGCAACAGCTAAATTGCTGTGGCAGACCAGAAAAATCAGAAATTTGAAA TCTAAATTCTCTGCTATTTGGCGCTACATAGTCAATTTTGACTATGAGAG
    Mapping_target: Y105E8A
    Type_of_mutation: Substitution: t C Paper_evidence: WBPaper00037807
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00006629 From_analysis: Million_mutation_project_reanalysis
      WBStrain00006642 From_analysis: WGS_De_Bono
      WBStrain00006643 From_analysis: Million_mutation_project_reanalysis
      WBStrain00006645 From_analysis: Million_mutation_project_reanalysis
      WBStrain00022850 From_analysis: WGS_De_Bono
          Million_mutation_project_reanalysis
      WBStrain00023018 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023191 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 539149110
    History: Acquires_merge: WBVar01428560
    Status: Live
  Affects: Gene: WBGene00009865
    Transcript: F49B2.6.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F49B2.6.1:c.1052+85T>C
        Intron_number: 6/18
  Reference: WBPaper00037807
  Method: WGS_De_Bono