WormBase Tree Display for Variation: WBVar02126959

WBVar02126959 Evidence: Paper_evidence: WBPaper00045317
  Name: Public_name: h13663
    Other_name: CE39788:p.Arg148=
      T28F2.5.1:c.444G>A
    HGVSg: CHROMOSOME_I:g.3644930C>T
  Sequence_details: SMap: S_parent: Sequence: T28F2
    Flanking_sequences: AAATAACAAAAACCCTACCAGGCGTCGGAGGAGTCGAACC CGTGATCCACTTCTTGGCATCATGTTATCCAGTGCTCCGA
    Mapping_target: CHROMOSOME_I
    Source_location: 200 CHROMOSOME_I 3644932 3644932
    Type_of_mutation: Substitution: C T
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023809
    Laboratory: KR
    Analysis: WGS_Rose
    Status: Live
  Affects: Gene: WBGene00000368
    Transcript: T28F2.5.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: T28F2.5.1:c.444G>A
        HGVSp: CE39788:p.Arg148=
        cDNA_position: 645
        CDS_position: 444
        Protein_position: 148
        Exon_number: 6/11
        Codon_change: cgG/cgA
        Amino_acid_change: R
  Reference: WBPaper00040589
    WBPaper00000975
    WBPaper00003985
    WBPaper00000699
    WBPaper00045317
  Method: WGS_Rose