WormBase Tree Display for Variation: WBVar00274058

WBVar00274058 Evidence: Paper_evidence: WBPaper00005369
  Name: Public_name: WBVar00274058
    Other_name: uCE6-708
      cewivar00269687
      T26C11.6.1:c.1169+263A>G
    HGVSg: CHROMOSOME_X:g.1850814T>C
  Sequence_details: SMap: S_parent: Sequence: T26C11
    Flanking_sequences: CTTAGGCCCTCAAGCGTAGGCCCTCAGGCGTAGGCCCTCAGGCTTAGGCCCACGGCCTAGGCCCACAAGCTTAGGCCATCAGGCTTAGGCCCTCAGGCGT GGCCCTCAGGCTTAAGCCCTCAGGCGTAGGCCCTCAGGCGAAGGCCCTCAGGATTAGCCCCTAAAATCCGGAGCTTAGGCTTAAGCACTTGGGCTTACCT
    Mapping_target: T26C11
    Type_of_mutation: Substitution: T C
    SeqStatus: Sequenced
  Variation_type: SNP
    Predicted_SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00004602 From_analysis: Million_mutation_project_reanalysis
      WBStrain00006640 From_analysis: Million_mutation_project_reanalysis
      WBStrain00022878 From_analysis: Million_mutation_project_reanalysis
    Analysis: SNP_Swan
      Million_mutation_project_reanalysis
    Status: Live
  Affects: Gene: WBGene00000444
    Transcript: T26C11.6.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T26C11.6.1:c.1169+263A>G
        Intron_number: 5/7
  Reference: WBPaper00005369
  Method: SNP_Swan