WormBase Tree Display for Variation: WBVar00089160

WBVar00089160 Name: Public_name: mn416
    Other_name: Y49F6B.4.1:c.18-1G>A
    HGVSg: CHROMOSOME_II:g.3482582G>A
  Sequence_details: SMap: S_parent: Sequence: Y49F6B
    Flanking_sequences: atagctattttccataacccaaaccttcca aaacctgcgaaacgccgattttcgaaagct
    Mapping_target: Y49F6B
    Type_of_mutation: Substitution: g a Paper_evidence: WBPaper00023890
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00034394
      WBStrain00034411
      WBStrain00034413
      WBStrain00034415
    Laboratory: SP
    Status: Live
  Affects: Gene: WBGene00004896
    Transcript: Y49F6B.4.1 VEP_consequence: splice_acceptor_variant
        VEP_impact: HIGH
        HGVSc: Y49F6B.4.1:c.18-1G>A
        Intron_number: 2/8
    Interactor: WBInteraction000501527
      WBInteraction000501528
      WBInteraction000519064
      WBInteraction000519076
      WBInteraction000519077
      WBInteraction000519078
      WBInteraction000519079
      WBInteraction000519080
      WBInteraction000519081
  Genetics: Interpolated_map_position: II -6.26161
    Mapping_data: In_multi_point: 2771
        2772
        2773
        2774
  Description: Phenotype_not_observed: WBPhenotype:0000886 Person_evidence: WBPerson261
        Curator_confirmed: WBPerson712
        Remark: Essentially WT alone. Person_evidence: WBPerson261
            Curator_confirmed: WBPerson712
  Reference: WBPaper00014786
    WBPaper00014522
    WBPaper00015748
  Method: Substitution_allele