WormBase Tree Display for Variation: WBVar00276179

WBVar00276179 Evidence: Paper_evidence: WBPaper00036200
  Name: Public_name: gk2292
    Other_name: D1007.15b.1:c.1099+48A>G
      D1007.15c.1:c.1121-24A>G
      D1007.15a.1:c.1120+48A>G
    HGVSg: CHROMOSOME_I:g.4559741A>G
  Sequence_details: SMap: S_parent: Sequence: D1007
    Flanking_sequences: GGCAAACTAGAGAAATAGTAAATAATTTTT GTATTAGATAGGGTATTTTTCAGGTTACAC
    Mapping_target: D1007
    Type_of_mutation: Substitution: A G
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00037339
    Laboratory: VC
    Person: WBPerson427
    Analysis: Million_Mutation_Pilot_Project
    KO_consortium_allele
    Status: Live
  Affects: Gene: WBGene00017010
    Transcript: D1007.15b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: D1007.15b.1:c.1099+48A>G
        Intron_number: 7/17
      D1007.15c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: D1007.15c.1:c.1121-24A>G
        Intron_number: 6/6
      D1007.15a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: D1007.15a.1:c.1120+48A>G
        Intron_number: 7/17
  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