WormBase Tree Display for Variation: WBVar02135920

WBVar02135920 Evidence: Paper_evidence: WBPaper00045317
  Name: Public_name: h7819
    Other_name: W02G9.5c.1:c.930C>T
      CE51081:p.Phe449=
      W02G9.5b.1:c.1347C>T
      CE51063:p.Phe515=
      CE51111:p.Phe310=
      W02G9.5a.1:c.1545C>T
    HGVSg: CHROMOSOME_V:g.2662637C>T
  Sequence_details: SMap: S_parent: Sequence: W02G9
    Flanking_sequences: GTGGCCGAACAAGAACGTTCCCAGCGATCATCTTCCAATT TCGCGAAATTCCGTCTAATTCAAGATTCTTCTGTTCTTCA
    Mapping_target: CHROMOSOME_V
    Source_location: 200 CHROMOSOME_V 2662636 2662636
    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: WBGene00020955
    Transcript: W02G9.5a.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: W02G9.5a.1:c.1545C>T
        HGVSp: CE51063:p.Phe515=
        cDNA_position: 1545
        CDS_position: 1545
        Protein_position: 515
        Exon_number: 8/8
        Codon_change: ttC/ttT
        Amino_acid_change: F
      W02G9.5c.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: W02G9.5c.1:c.930C>T
        HGVSp: CE51111:p.Phe310=
        cDNA_position: 930
        CDS_position: 930
        Protein_position: 310
        Exon_number: 4/4
        Codon_change: ttC/ttT
        Amino_acid_change: F
      W02G9.5b.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: W02G9.5b.1:c.1347C>T
        HGVSp: CE51081:p.Phe449=
        cDNA_position: 1347
        CDS_position: 1347
        Protein_position: 449
        Exon_number: 7/7
        Codon_change: ttC/ttT
        Amino_acid_change: F
  Reference: WBPaper00040589
    WBPaper00000975
    WBPaper00003985
    WBPaper00000699
    WBPaper00045317
  Method: WGS_Rose