WormBase Tree Display for Variation: WBVar00276302

WBVar00276302 Evidence: Paper_evidence: WBPaper00036200
  Name: Public_name: gk2925
    Other_name: F11F1.1b.1:c.1322-324C>T
      F11F1.9.1:c.44C>T
      F11F1.1a.1:c.1322-926C>T
      CE15803:p.Ala15Val
    HGVSg: CHROMOSOME_III:g.13398942C>T
  Sequence_details: SMap: S_parent: Sequence: F11F1
    Flanking_sequences: AAGTTGCTTTCACACTTGTTGTTTCAATTG AATTGTAACAGCAGTTCCTCTCGGAGGGAT
    Mapping_target: F11F1
    Type_of_mutation: Substitution: C T
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00005866
    Laboratory: VC
    Person: WBPerson427
    Analysis: Million_Mutation_Pilot_Project
    KO_consortium_allele
    Status: Live
  Affects: Gene: WBGene00008714
      WBGene00306134
    Transcript: F11F1.1a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F11F1.1a.1:c.1322-926C>T
        Intron_number: 6/8
      F11F1.9.1 (12)
      F11F1.1b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F11F1.1b.1:c.1322-324C>T
        Intron_number: 5/8
  Isolation: Mutagen: EMS
  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