WormBase Tree Display for Variation: WBVar01310015

WBVar01310015 Evidence: Paper_evidence: WBPaper00037807
  Name: Public_name: WBVar01310015
    Other_name: cewivar00508979
      CE01659:p.Pro512=
      T10B9.7.1:c.1536G>A
    HGVSg: CHROMOSOME_II:g.9783830C>T
  Sequence_details: SMap: S_parent: Sequence: T10B9
    Flanking_sequences: GTTCCAAAATTAAAGTAAATAGACAATAATACTGAAATTTACCAAATTCT GGTCTCAAGTGCACGAAAACATCTTCAGGCGATGTAGTAGCACTTCCCAC
    Mapping_target: T10B9
    Type_of_mutation: Substitution: c T Paper_evidence: WBPaper00037807
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00022850 From_analysis: WGS_De_Bono
          Million_mutation_project_reanalysis
          WGS_Andersen
      WBStrain00031279 From_analysis: WGS_Andersen
      WBStrain00031284 From_analysis: WGS_Andersen
    Laboratory: AX
      QX
    Person: WBPerson1730
    Analysis: WGS_De_Bono
      Million_mutation_project_reanalysis
      WGS_Andersen
    DB_info: Database: dbSNP_ss ss 539167294
    History: Acquires_merge: WBVar01439208
    Status: Live
  Affects: Gene: WBGene00011676
    Transcript: T10B9.7.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: T10B9.7.1:c.1536G>A
        HGVSp: CE01659:p.Pro512=
        cDNA_position: 1812
        CDS_position: 1536
        Protein_position: 512
        Exon_number: 6/7
        Codon_change: ccG/ccA
        Amino_acid_change: P
  Reference: WBPaper00040707
    WBPaper00037807
  Method: WGS_De_Bono