WormBase Tree Display for Variation: WBVar00089166

WBVar00089166 Evidence: Paper_evidence: WBPaper00003663
  Name: Public_name: mn455
    Other_name: F46A9.6.1:c.529C>T
      CE08260:p.Gln177Ter
      F46A9.6.2:c.529C>T
    HGVSg: CHROMOSOME_I:g.9443139G>A
  Sequence_details: SMap: S_parent: Sequence: F46A9
    Flanking_sequences: gctctttcacttccacatttacatgctgca aggcacttcaagcagcctatatgccagctt
    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.529C>T
        HGVSp: CE08260:p.Gln177Ter
        cDNA_position: 561
        CDS_position: 529
        Protein_position: 177
        Exon_number: 3/5
        Codon_change: Cag/Tag
        Amino_acid_change: Q/*
      F46A9.6.1 VEP_consequence: stop_gained
        VEP_impact: HIGH
        HGVSc: F46A9.6.1:c.529C>T
        HGVSp: CE08260:p.Gln177Ter
        cDNA_position: 561
        CDS_position: 529
        Protein_position: 177
        Exon_number: 3/6
        Codon_change: Cag/Tag
        Amino_acid_change: Q/*
  Genetics: Interpolated_map_position: I 3.76437
  Reference: WBPaper00003663
  Method: Substitution_allele