WormBase Tree Display for Variation: WBVar01459713

WBVar01459713 Evidence: Paper_evidence: WBPaper00040707
  Name: Public_name: WBVar01459713
    Other_name: cewivar00554491
      CE30386:p.Val6=
      K11D12.3a.1:c.18G>T
    HGVSg: CHROMOSOME_V:g.5019266G>T
  Sequence_details: SMap: S_parent: Sequence: K11D12
    Flanking_sequences: GTTCATGAACGGAATGAAAACTGACGAGGT CATCAAACGGAGGAGCTTGTCGACGGCTCA
    Mapping_target: K11D12
    Type_of_mutation: Substitution: g t
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00006649 From_analysis: WGS_Andersen
      WBStrain00022928 From_analysis: WGS_Andersen
      WBStrain00022930 From_analysis: Million_mutation_project_reanalysis
          WGS_Andersen
      WBStrain00023144 From_analysis: WGS_Andersen
      WBStrain00023149 From_analysis: WGS_Andersen
      WBStrain00023150 From_analysis: WGS_Andersen
      WBStrain00023151 From_analysis: WGS_Andersen
      WBStrain00023211 From_analysis: WGS_Andersen
      WBStrain00023279 From_analysis: WGS_Andersen
    Laboratory: QX
    Person: WBPerson1730
    Analysis: Million_mutation_project_reanalysis
      WGS_Andersen
    DB_info: Database: dbSNP_rs rs 193345370
        dbSNP_ss ss 295521289
    Status: Live
  Affects: Gene: WBGene00005655
    Transcript: K11D12.3a.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: K11D12.3a.1:c.18G>T
        HGVSp: CE30386:p.Val6=
        cDNA_position: 43
        CDS_position: 18
        Protein_position: 6
        Exon_number: 2/8
        Codon_change: gtG/gtT
        Amino_acid_change: V
  Reference: WBPaper00040707
  Method: WGS_Andersen