WormBase Tree Display for Variation: WBVar02137303

WBVar02137303 Evidence: Paper_evidence: WBPaper00045317
  Name: Public_name: h12651
    Other_name: C14C10.5a.1:c.4378C>T
      C14C10.5b.1:c.4330C>T
      CE05284:p.Pro1460Ser
      CE48360:p.Pro1444Ser
    HGVSg: CHROMOSOME_V:g.12605386C>T
  Sequence_details: SMap: S_parent: Sequence: C14C10
    Flanking_sequences: GAGGTACGAAAAGCAGAGAAAAATGTGGAATTGGCTCGAC CGATGCTCACGAAAACATTTGAACTGATGAAAGAAGACGG
    Mapping_target: CHROMOSOME_V
    Source_location: 200 CHROMOSOME_V 12605365 12605365
    Type_of_mutation: Substitution: C T
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023858
    Laboratory: KR
    Analysis: WGS_Rose
    Status: Live
  Affects: Gene: WBGene00007588
    Transcript: C14C10.5b.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: C14C10.5b.1:c.4330C>T
        HGVSp: CE48360:p.Pro1444Ser
        cDNA_position: 4424
        CDS_position: 4330
        Protein_position: 1444
        Exon_number: 7/11
        Codon_change: Ccg/Tcg
        Amino_acid_change: P/S
      C14C10.5a.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: C14C10.5a.1:c.4378C>T
        HGVSp: CE05284:p.Pro1460Ser
        cDNA_position: 4472
        CDS_position: 4378
        Protein_position: 1460
        Exon_number: 6/10
        Codon_change: Ccg/Tcg
        Amino_acid_change: P/S
  Reference: WBPaper00040589
    WBPaper00000975
    WBPaper00003985
    WBPaper00000699
    WBPaper00045317
  Method: WGS_Rose