WormBase Tree Display for Variation: WBVar02129859

WBVar02129859 Evidence: Paper_evidence: WBPaper00045317
  Name: Public_name: h16468
    Other_name: CE04807:p.Pro47Ser
      R05F9.5.1:c.139C>T
    HGVSg: CHROMOSOME_II:g.4893003C>T
  Sequence_details: SMap: S_parent: Sequence: R05F9
    Flanking_sequences: AACATAAATATTTCTTATCTTAATATAATTTTCAGTGACC CATTTGGACAAGTTCCAGTTCTAGAAGTTGATGGAAGACA
    Mapping_target: CHROMOSOME_II
    Source_location: 200 CHROMOSOME_II 4892990 4892990
    Type_of_mutation: Substitution: C T
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023756
    Laboratory: KR
    Analysis: WGS_Rose
    Status: Live
  Affects: Gene: WBGene00001757
    Transcript: R05F9.5.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: R05F9.5.1:c.139C>T
        HGVSp: CE04807:p.Pro47Ser
        cDNA_position: 142
        CDS_position: 139
        Protein_position: 47
        Exon_number: 3/4
        Codon_change: Cca/Tca
        Amino_acid_change: P/S
  Reference: WBPaper00040589
    WBPaper00000975
    WBPaper00003985
    WBPaper00000699
    WBPaper00045317
  Method: WGS_Rose