WormBase Tree Display for Variation: WBVar00089165

WBVar00089165 Evidence: Paper_evidence: WBPaper00003663
  Name: Public_name: mn450
    Other_name: F46A9.6.2:c.289C>T
      CE08260:p.Arg97Ter
      F46A9.6.1:c.289C>T
    HGVSg: CHROMOSOME_I:g.9443379G>A
  Sequence_details: SMap: S_parent: Sequence: F46A9
    Flanking_sequences: acaacgaaattcttcaaattttcaggtgtc gattcgatccggaatgtgcacaggtacttc
    Mapping_target: F46A9
    Type_of_mutation: Substitution: c t Paper_evidence: WBPaper00003663
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Laboratory: SP
    Status: Live
  Affects: Gene: WBGene00003172
    Transcript: F46A9.6.2 VEP_consequence: stop_gained
        VEP_impact: HIGH
        HGVSc: F46A9.6.2:c.289C>T
        HGVSp: CE08260:p.Arg97Ter
        cDNA_position: 321
        CDS_position: 289
        Protein_position: 97
        Exon_number: 3/5
        Codon_change: Cga/Tga
        Amino_acid_change: R/*
      F46A9.6.1 VEP_consequence: stop_gained
        VEP_impact: HIGH
        HGVSc: F46A9.6.1:c.289C>T
        HGVSp: CE08260:p.Arg97Ter
        cDNA_position: 321
        CDS_position: 289
        Protein_position: 97
        Exon_number: 3/6
        Codon_change: Cga/Tga
        Amino_acid_change: R/*
  Genetics: Interpolated_map_position: I 3.76437
  Reference: WBPaper00003663
  Method: Substitution_allele