WormBase Tree Display for Variation: WBVar02140761

WBVar02140761 Evidence: Paper_evidence: WBPaper00045317
  Name: Public_name: h4841
    Other_name: CE15381:p.Pro1136Ser
      ZK662.4.2:c.3406C>T
      ZK662.4.1:c.3406C>T
    HGVSg: CHROMOSOME_X:g.15730645C>T
  Sequence_details: SMap: S_parent: Sequence: ZK678
    Flanking_sequences: CCCAACTGTCAAACCGTCTGAAAATGAGGAATGCGACAAT CGGGCGTTTGCTGCTTCTGTTCGAAACGTGGCGACCGAGG
    Mapping_target: CHROMOSOME_X
    Source_location: 200 CHROMOSOME_X 15730567 15730567
    Type_of_mutation: Substitution: C T
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023661
    Laboratory: KR
    Analysis: WGS_Rose
    Status: Live
  Affects: Gene: WBGene00023497
    Transcript: ZK662.4.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: ZK662.4.1:c.3406C>T
        HGVSp: CE15381:p.Pro1136Ser
        cDNA_position: 3412
        CDS_position: 3406
        Protein_position: 1136
        Exon_number: 8/10
        Codon_change: Ccg/Tcg
        Amino_acid_change: P/S
      ZK662.4.2 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: ZK662.4.2:c.3406C>T
        HGVSp: CE15381:p.Pro1136Ser
        cDNA_position: 3418
        CDS_position: 3406
        Protein_position: 1136
        Exon_number: 8/11
        Codon_change: Ccg/Tcg
        Amino_acid_change: P/S
  Reference: WBPaper00040589
    WBPaper00000975
    WBPaper00003985
    WBPaper00000699
    WBPaper00045317
  Method: WGS_Rose