WormBase Tree Display for Variation: WBVar01447847

WBVar01447847 Evidence: Paper_evidence: WBPaper00040707
  Name: Public_name: WBVar01447847
    Other_name: T16G12.1.1:c.1947C>T
      CE36716:p.Ile649=
    HGVSg: CHROMOSOME_III:g.10045752G>A
  Sequence_details: SMap: S_parent: Sequence: T16G12
    Flanking_sequences: CTTGATTAATTTCAGAATTCGATCAAAACC ATGTCGTCGTAGATGATTCTGAAGTGGTCA
    Mapping_target: T16G12
    Type_of_mutation: Substitution: g a
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023139 From_analysis: WGS_Andersen
          Million_mutation_project_reanalysis
      WBStrain00023665 From_analysis: WGS_Andersen
          Million_mutation_project_reanalysis
      WBStrain00027648 From_analysis: WGS_Andersen
          Million_mutation_project_reanalysis
      WBStrain00027660 From_analysis: WGS_Andersen
          Million_mutation_project_reanalysis
      WBStrain00027661 From_analysis: WGS_Andersen
      WBStrain00027662 From_analysis: WGS_Andersen
          Million_mutation_project_reanalysis
      WBStrain00027669 From_analysis: WGS_Andersen
    Laboratory: QX
    Person: WBPerson1730
    Analysis: WGS_Andersen
    DB_info: Database: dbSNP_rs rs 193334193
        dbSNP_ss ss 295510112
    Status: Live
  Affects: Gene: WBGene00011803
    Transcript: T16G12.1.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: T16G12.1.1:c.1947C>T
        HGVSp: CE36716:p.Ile649=
        cDNA_position: 2061
        CDS_position: 1947
        Protein_position: 649
        Exon_number: 13/32
        Codon_change: atC/atT
        Amino_acid_change: I
  Reference: WBPaper00040707
  Method: WGS_Andersen