WormBase Tree Display for Variation: WBVar00088065

WBVar00088065 Evidence: Person_evidence: WBPerson713
  Name: Public_name: je5
    Other_name: C15F1.5b.1:c.663+157C>A
      C15F1.14:n.159G>T
      C15F1.5a.1:c.873+157C>A
      C15F1.9:n.9C>A
      C15F1.10:n.2C>A
    HGVSg: CHROMOSOME_II:g.6968550G>T
  Sequence_details: SMap: S_parent: Sequence: C15F1
    Flanking_sequences: ggccccccttcactatagctcataaactta ctggctgggggtatctcgtgatcatgaaga
    Mapping_target: C15F1
    Type_of_mutation: Substitution: c a
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023447
      WBStrain00023448
      WBStrain00023449
      WBStrain00023450
      WBStrain00023451
      WBStrain00023452
    Laboratory: JW
    Status: Live
  Affects: Gene: WBGene00077724
      WBGene00198924
      WBGene00006344
      WBGene00015796
    Transcript: C15F1.5a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C15F1.5a.1:c.873+157C>A
        Intron_number: 8/11
      C15F1.14 VEP_consequence: non_coding_transcript_exon_variant
        VEP_impact: MODIFIER
        HGVSc: C15F1.14:n.159G>T
        cDNA_position: 159
        Exon_number: 1/1
      C15F1.5b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C15F1.5b.1:c.663+157C>A
        Intron_number: 5/7
      C15F1.9 VEP_consequence: non_coding_transcript_exon_variant
        VEP_impact: MODIFIER
        HGVSc: C15F1.9:n.9C>A
        cDNA_position: 9
        Exon_number: 1/1
      C15F1.10 VEP_consequence: non_coding_transcript_exon_variant
        VEP_impact: MODIFIER
        HGVSc: C15F1.10:n.2C>A
        cDNA_position: 2
        Exon_number: 1/1
    Interactor: WBInteraction000519035
      WBInteraction000519129
  Genetics: Interpolated_map_position: II 0.198865
    Mapping_data: In_multi_point: 2069
        2070
        2071
        3120
        3347
  Description: Phenotype: WBPhenotype:0000050 Person_evidence: WBPerson261
        Curator_confirmed: WBPerson712
        Remark: Impenetrant embryonic lethal, escapers almost WT, abnormal double row of oocyte nuclei Person_evidence: WBPerson261
            Curator_confirmed: WBPerson712
        Penetrance: Incomplete: Person_evidence: WBPerson261
              Curator_confirmed: WBPerson712
      WBPhenotype:0001924 Person_evidence: WBPerson261
        Curator_confirmed: WBPerson712
        Remark: double row of oocyte nuclei Person_evidence: WBPerson261
            Curator_confirmed: WBPerson712
        Penetrance: Incomplete: Person_evidence: WBPerson261
              Curator_confirmed: WBPerson712
  Reference: WBPaper00010922
    WBPaper00022024
    WBPaper00023829
  Remark: This point mutation is compensatory to 5' splice site mutation in unc-73(e936). Person_evidence: WBPerson713
  Method: Substitution_allele