WormBase Tree Display for Variation: WBVar01459634

WBVar01459634 Evidence: Paper_evidence: WBPaper00040707
  Name: Public_name: WBVar01459634
    Other_name: CE38548:p.Phe322=
      T19H12.11.1:c.966T>C
    HGVSg: CHROMOSOME_V:g.4898912A>G
  Sequence_details: SMap: S_parent: Sequence: T19H12
    Flanking_sequences: TGACTCGAACATTTTGATAAGTCCTGCTTT AAATTATCCGGCATCTCATAGGATCGAATA
    Mapping_target: T19H12
    Type_of_mutation: Substitution: a g
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00031279 From_analysis: WGS_Andersen
      WBStrain00031284 From_analysis: WGS_Andersen
    Laboratory: QX
    Person: WBPerson1730
    Analysis: WGS_Andersen
    DB_info: Database: dbSNP_rs rs 193345291
        dbSNP_ss ss 295521210
    Status: Live
  Affects: Gene: WBGene00020594
    Transcript: T19H12.11.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: T19H12.11.1:c.966T>C
        HGVSp: CE38548:p.Phe322=
        cDNA_position: 1004
        CDS_position: 966
        Protein_position: 322
        Exon_number: 6/8
        Codon_change: ttT/ttC
        Amino_acid_change: F
  Reference: WBPaper00040707
  Method: WGS_Andersen