WormBase Tree Display for Variation: WBVar01448595

WBVar01448595 Evidence: Paper_evidence: WBPaper00040707
  Name: Public_name: WBVar01448595
    Other_name: Y47D3A.29.1:c.2988T>G
      CE32262:p.Val996=
    HGVSg: CHROMOSOME_III:g.11146383T>G
  Sequence_details: SMap: S_parent: Sequence: Y47D3A
    Flanking_sequences: GAAGCTTGGAAATGAGATTAAAAAGGCTGT AACAAGTGTCATCGGCTCTTGGAGCTTGAT
    Mapping_target: Y47D3A
    Type_of_mutation: Substitution: t 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 193334705
        dbSNP_ss ss 295510624
    Status: Live
  Affects: Gene: WBGene00012936
      WBGene00305760
    Transcript: Y48A6C.12
      Y47D3A.29.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: Y47D3A.29.1:c.2988T>G
        HGVSp: CE32262:p.Val996=
        cDNA_position: 2988
        CDS_position: 2988
        Protein_position: 996
        Exon_number: 4/11
        Codon_change: gtT/gtG
        Amino_acid_change: V
  Reference: WBPaper00040707
  Method: WGS_Andersen