WormBase Tree Display for Variation: WBVar00276320

WBVar00276320 Evidence: Paper_evidence: WBPaper00036200
  Name: Public_name: gk2098
    Other_name: F13D2.1a.1:c.813+4279G>A
      F13D2.1b.1:c.813+4279G>A
    HGVSg: CHROMOSOME_X:g.11183367C>T
  Sequence_details: SMap: S_parent: Sequence: F13D2
    Flanking_sequences: GTTTTGTTCGTGAATTAACCTAGTTAATCC GTCACATCACGAGAAAAAAACGAAACATTC
    Mapping_target: F13D2
    Type_of_mutation: Substitution: C T
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00036970
    Laboratory: VC
    Person: WBPerson427
    Analysis: Million_Mutation_Pilot_Project
    KO_consortium_allele
    Status: Live
  Affects: Gene: WBGene00008735
    Transcript: F13D2.1b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F13D2.1b.1:c.813+4279G>A
        Intron_number: 9/38
      F13D2.1a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F13D2.1a.1:c.813+4279G>A
        Intron_number: 8/37
  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