WormBase Tree Display for Variation: WBVar02127772

WBVar02127772 Evidence: Paper_evidence: WBPaper00045317
  Name: Public_name: h3949
    Other_name: F22D6.12.2:c.526C>T
      CE29590:p.Pro176Ser
      F22D6.12.1:c.526C>T
    HGVSg: CHROMOSOME_I:g.7113761C>T
  Sequence_details: SMap: S_parent: Sequence: F22D6
    Flanking_sequences: TTTTGAAAATATTAAATTGCAAAATTTTCAGAAACGTCCA CAATAAGTTGGGGAAGTCATGAAATAATTGATTCGGTGTA
    Mapping_target: CHROMOSOME_I
    Source_location: 200 CHROMOSOME_I 7113760 7113760
    Type_of_mutation: Substitution: C T
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023775
    Laboratory: KR
    Analysis: WGS_Rose
    Status: Live
  Affects: Gene: WBGene00001644
    Transcript: F22D6.12.2 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: F22D6.12.2:c.526C>T
        HGVSp: CE29590:p.Pro176Ser
        cDNA_position: 633
        CDS_position: 526
        Protein_position: 176
        Exon_number: 6/10
        Codon_change: Cca/Tca
        Amino_acid_change: P/S
      F22D6.12.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: F22D6.12.1:c.526C>T
        HGVSp: CE29590:p.Pro176Ser
        cDNA_position: 526
        CDS_position: 526
        Protein_position: 176
        Exon_number: 5/9
        Codon_change: Cca/Tca
        Amino_acid_change: P/S
  Reference: WBPaper00040589
    WBPaper00000975
    WBPaper00003985
    WBPaper00000699
    WBPaper00045317
  Method: WGS_Rose