WormBase Tree Display for Variation: WBVar00276606

WBVar00276606 Evidence: Paper_evidence: WBPaper00036200
  Name: Public_name: gk1461
    Other_name: F47D12.9a.2:c.377-156T>A
      F47D12.9b.2:c.-23-156T>A
      F47D12.9a.1:c.377-156T>A
    HGVSg: CHROMOSOME_III:g.6301705A>T
  Sequence_details: SMap: S_parent: Sequence: F47D12
    Flanking_sequences: GGTGCGTCCATAGTCTGCGGAAAACGGGAA TTCCGCGTGCGGAAGCGTCCATAGTCTGCG
    Mapping_target: F47D12
    Type_of_mutation: Substitution: A T
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00036969
    Laboratory: VC
    Person: WBPerson427
    Analysis: Million_Mutation_Pilot_Project
    KO_consortium_allele
    Status: Live
  Affects: Gene: WBGene00018564
    Transcript: F47D12.9b.2 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F47D12.9b.2:c.-23-156T>A
        Intron_number: 1/6
      F47D12.9a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F47D12.9a.1:c.377-156T>A
        Intron_number: 3/7
      F47D12.9a.2 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F47D12.9a.2:c.377-156T>A
        Intron_number: 4/8
  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