WormBase Tree Display for Variation: WBVar02130736

WBVar02130736 Evidence: Paper_evidence: WBPaper00045317
  Name: Public_name: h8669
    Other_name: CE18980:p.Ser19Tyr
      VW02B12L.1.1:c.56C>A
    HGVSg: CHROMOSOME_II:g.11438366G>T
  Sequence_details: SMap: S_parent: Sequence: VW02B12L
    Flanking_sequences: CAGCTCTCCCAACTCGGCGACACATTGATAGGCGGACTCG ATTGGAAGAAGATTTGGCACAATTTCATGTGCTCCGATCT
    Mapping_target: CHROMOSOME_II
    Source_location: 200 CHROMOSOME_II 11438283 11438283
    Type_of_mutation: Substitution: G T
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023676
    Laboratory: KR
    Analysis: WGS_Rose
    Status: Live
  Affects: Gene: WBGene00006915
    Transcript: VW02B12L.1.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: VW02B12L.1.1:c.56C>A
        HGVSp: CE18980:p.Ser19Tyr
        cDNA_position: 87
        CDS_position: 56
        Protein_position: 19
        Exon_number: 2/8
        Codon_change: tCc/tAc
        Amino_acid_change: S/Y
  Reference: WBPaper00040589
    WBPaper00000975
    WBPaper00003985
    WBPaper00000699
    WBPaper00045317
  Method: WGS_Rose