WormBase Tree Display for Variation: WBVar01465856

WBVar01465856 Evidence: Paper_evidence: WBPaper00040707
  Name: Public_name: WBVar01465856
    Other_name: cewivar00590505
      Y39B6A.13.1:c.123G>A
      CE21694:p.Arg41=
    HGVSg: CHROMOSOME_V:g.19119195C>T
  Sequence_details: SMap: S_parent: Sequence: Y39B6A
    Flanking_sequences: AAGTTTTTGCATCGAAATCTTCACAATCAA CGGAAAACGCGCTCTTTTTCATCGCCGCTT
    Mapping_target: Y39B6A
    Type_of_mutation: Substitution: c t
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00006697 From_analysis: WGS_Andersen
      WBStrain00006698 From_analysis: WGS_Andersen
      WBStrain00023072 From_analysis: Million_mutation_project_reanalysis
          WGS_Andersen
      WBStrain00023079 From_analysis: WGS_Andersen
      WBStrain00023084 From_analysis: WGS_Andersen
    Laboratory: QX
    Person: WBPerson1730
    Analysis: Million_mutation_project_reanalysis
      WGS_Andersen
    DB_info: Database: dbSNP_rs rs 193351512
        dbSNP_ss ss 295527431
    Status: Live
  Affects: Gene: WBGene00012675
    Transcript: Y39B6A.13.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: Y39B6A.13.1:c.123G>A
        HGVSp: CE21694:p.Arg41=
        cDNA_position: 188
        CDS_position: 123
        Protein_position: 41
        Exon_number: 3/7
        Codon_change: cgG/cgA
        Amino_acid_change: R
  Reference: WBPaper00040707
  Method: WGS_Andersen