WormBase Tree Display for Variation: WBVar02139660

WBVar02139660 Evidence: Paper_evidence: WBPaper00045317
  Name: Public_name: h7902
    Other_name: C34D10.1.1:c.286C>T
      CE02532:p.Pro96Ser
    HGVSg: CHROMOSOME_X:g.8030481C>T
  Sequence_details: SMap: S_parent: Sequence: C34D10
    Flanking_sequences: CGTCGACAAGTTGAAAATTGAGATTAGCAAAAAAGGATCG CGACGGTAAATCTCAAAATTTAATTTCAAATTAAACAAAA
    Mapping_target: CHROMOSOME_X
    Source_location: 200 CHROMOSOME_X 8030425 8030425
    Type_of_mutation: Substitution: C T
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023705
    Laboratory: KR
    Analysis: WGS_Rose
    Status: Live
  Affects: Gene: WBGene00016406
    Transcript: C34D10.1.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: C34D10.1.1:c.286C>T
        HGVSp: CE02532:p.Pro96Ser
        cDNA_position: 306
        CDS_position: 286
        Protein_position: 96
        Exon_number: 5/8
        Codon_change: Ccg/Tcg
        Amino_acid_change: P/S
  Reference: WBPaper00040589
    WBPaper00000975
    WBPaper00003985
    WBPaper00000699
    WBPaper00045317
  Method: WGS_Rose