WormBase Tree Display for Variation: WBVar00275922

WBVar00275922 Evidence: Paper_evidence: WBPaper00036200
  Name: Public_name: ok5368
    Other_name: C26H9A.2d.1:c.3525-23T>A
      C26H9A.2a.1:c.3525-23T>A
      C26H9A.2c.1:c.3525-23T>A
      C26H9A.2b.1:c.3525-23T>A
    HGVSg: CHROMOSOME_IV:g.12661586T>A
  Sequence_details: SMap: S_parent: Sequence: C26H9A
    Flanking_sequences: ACGGACAGATTATAAAATTCTGTAATTCTA TCACTAAAATTAATTCTTGCAGATTCCGCC
    Mapping_target: C26H9A
    Type_of_mutation: Substitution: T A
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00033305
    Laboratory: RB
    Person: WBPerson46
    Analysis: Million_Mutation_Pilot_Project
    KO_consortium_allele
    Status: Live
  Affects: Gene: WBGene00007752
    Transcript: C26H9A.2b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C26H9A.2b.1:c.3525-23T>A
        Intron_number: 19/37
      C26H9A.2c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C26H9A.2c.1:c.3525-23T>A
        Intron_number: 19/37
      C26H9A.2d.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C26H9A.2d.1:c.3525-23T>A
        Intron_number: 18/35
      C26H9A.2a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C26H9A.2a.1:c.3525-23T>A
        Intron_number: 19/37
  Isolation: Mutagen: ENU
  Reference: WBPaper00036200
  Remark: Allele identified through whole-genome sequencing by the Gene Knockout Consortium Paper_evidence: WBPaper00036200
    Sequenced by the C. elegans Gene Knockout Consortium Paper_evidence: WBPaper00041807
  Method: KO_consortium_allele