WormBase Tree Display for Variation: WBVar01469818

WBVar01469818 Evidence: Paper_evidence: WBPaper00040707
  Name: Public_name: WBVar01469818
    Other_name: cewivar00531962
      CE30092:p.Tyr49=
      K09F5.6b.1:c.147T>C
      K09F5.6a.1:c.147T>C
      CE53611:p.Tyr49=
    HGVSg: CHROMOSOME_X:g.7720169T>C
  Sequence_details: SMap: S_parent: Sequence: K09F5
    Flanking_sequences: CAACGAAATCAAATGGCCAACCGGAGGATA CCTTATGGCTACCTCATGGCATATGCCACT
    Mapping_target: K09F5
    Type_of_mutation: Substitution: t c
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain (33)
    Laboratory: QX
    Person: WBPerson1730
    Analysis: Million_mutation_project_reanalysis
      WGS_Andersen
    DB_info: Database: dbSNP_rs rs 193355120
        dbSNP_ss ss 295531039
    Status: Live
  Affects: Gene: WBGene00044698
    Transcript: K09F5.6b.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: K09F5.6b.1:c.147T>C
        HGVSp: CE53611:p.Tyr49=
        cDNA_position: 283
        CDS_position: 147
        Protein_position: 49
        Exon_number: 4/15
        Codon_change: taT/taC
        Amino_acid_change: Y
      K09F5.6a.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: K09F5.6a.1:c.147T>C
        HGVSp: CE30092:p.Tyr49=
        cDNA_position: 283
        CDS_position: 147
        Protein_position: 49
        Exon_number: 4/14
        Codon_change: taT/taC
        Amino_acid_change: Y
  Reference: WBPaper00040707
  Method: WGS_Andersen