WormBase Tree Display for Variation: WBVar00095126

WBVar00095126 Evidence: Paper_evidence: WBPaper00024501
  Name: Public_name: p802
    Other_name: CE31568:p.Gln346Ter
      M02B7.3a.3:c.952C>T
      CE31567:p.Gln318Ter
      M02B7.3b.1:c.1036C>T
      M02B7.3a.2:c.952C>T
      M02B7.3a.1:c.952C>T
    HGVSg: CHROMOSOME_IV:g.3797722G>A
  Sequence_details: SMap: S_parent: Sequence: M02B7
    Flanking_sequences: gatccaaaggatgctcttcttcgagagtac aggaggaaatcgctcggctcaagtctatgg
    Mapping_target: M02B7
    Type_of_mutation: Substitution: c t Paper_evidence: WBPaper00024501
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00030794
      WBStrain00049023
    Laboratory: PR
    Status: Live
  Affects: Gene: WBGene00003884
    Transcript: M02B7.3a.3 VEP_consequence: stop_gained
        VEP_impact: HIGH
        HGVSc: M02B7.3a.3:c.952C>T
        HGVSp: CE31567:p.Gln318Ter
        cDNA_position: 1196
        CDS_position: 952
        Protein_position: 318
        Exon_number: 6/11
        Codon_change: Cag/Tag
        Amino_acid_change: Q/*
      M02B7.3a.1 VEP_consequence: stop_gained
        VEP_impact: HIGH
        HGVSc: M02B7.3a.1:c.952C>T
        HGVSp: CE31567:p.Gln318Ter
        cDNA_position: 1050
        CDS_position: 952
        Protein_position: 318
        Exon_number: 7/12
        Codon_change: Cag/Tag
        Amino_acid_change: Q/*
      M02B7.3a.2 VEP_consequence: stop_gained
        VEP_impact: HIGH
        HGVSc: M02B7.3a.2:c.952C>T
        HGVSp: CE31567:p.Gln318Ter
        cDNA_position: 1641
        CDS_position: 952
        Protein_position: 318
        Exon_number: 7/12
        Codon_change: Cag/Tag
        Amino_acid_change: Q/*
      M02B7.3b.1 VEP_consequence: stop_gained
        VEP_impact: HIGH
        HGVSc: M02B7.3b.1:c.1036C>T
        HGVSp: CE31568:p.Gln346Ter
        cDNA_position: 1036
        CDS_position: 1036
        Protein_position: 346
        Exon_number: 6/10
        Codon_change: Cag/Tag
        Amino_acid_change: Q/*
    Interactor: WBInteraction000521350
  Genetics: Interpolated_map_position: IV -2.21234
    Mapping_data: In_2_point: 364
        365
      In_multi_point: 900
        903
        906
        962
      In_pos_neg_data: 1630
        1631
  Description: Phenotype (33)
    Phenotype_not_observed (13)
  Reference (38)
  Remark: Variation stub/paper connection generated from the May 2021 NN VFP dataset.
    Created by WBPerson51134 from the NN_VFP_triage_pipeline
  Method: Substitution_allele