WormBase Tree Display for Variation: WBVar00266513

WBVar00266513 Evidence: Paper_evidence: WBPaper00003969
  Name: Public_name: u46
    Other_name: T01C8.7.1:c.1013G>A
      CE39109:p.Trp338Ter
    HGVSg: CHROMOSOME_X:g.16805427C>T
  Sequence_details: SMap: S_parent: Sequence: F41G4
    Flanking_sequences: atgcgtggccctgttttctgaacggaacct ggaaaccaccgaatgtgatacttgcaatga
    Mapping_target: F41G4
    Type_of_mutation: Substitution: g a Paper_evidence: WBPaper00003969
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Laboratory: TU
    Status: Live
  Affects: Gene: WBGene00003168
    Transcript: T01C8.7.1 VEP_consequence: stop_gained
        VEP_impact: HIGH
        HGVSc: T01C8.7.1:c.1013G>A
        HGVSp: CE39109:p.Trp338Ter
        cDNA_position: 1014
        CDS_position: 1013
        Protein_position: 338
        Exon_number: 6/17
        Codon_change: tGg/tAg
        Amino_acid_change: W/*
  Isolation: Mutagen: EMS Paper_evidence: WBPaper00003969
  Genetics: Interpolated_map_position: X 24.0629
  Reference: WBPaper00003969
  Method: Substitution_allele