WormBase Tree Display for Variation: WBVar01533979

WBVar01533979 Name: Public_name: WBVar01533979
    Other_name: cewivar00080100
      F56D12.1b.1:c.498C>T
      CE37118:p.Leu166=
      CE33403:p.Leu166=
      F56D12.1d.1:c.78C>T
      F56D12.1a.2:c.498C>T
      CE40074:p.Leu26=
      F56D12.1a.1:c.498C>T
      CE29047:p.Leu166=
      F56D12.1c.1:c.498C>T
    HGVSg: CHROMOSOME_II:g.1308925G>A
  Sequence_details: SMap: S_parent: Sequence: F56D12
    Flanking_sequences: GAAAACCGCGTTGAATCGGAAGAAATCGAT AGCTCACAGGCGGCGTCAATTTCAGCCTGA
    Mapping_target: F56D12
    Source_location: 225 CHROMOSOME_II 1308932 1308932 From_analysis: Million_mutation_project_reanalysis
    Type_of_mutation: Substitution: G A
    SeqStatus: Sequenced
  Variation_type: Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00000034 From_analysis: Million_mutation_project_reanalysis
      WBStrain00004599 From_analysis: Million_mutation_project_reanalysis
      WBStrain00006625 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023665 From_analysis: Million_mutation_project_reanalysis
      WBStrain00027652 From_analysis: Million_mutation_project_reanalysis
    Laboratory: VC
    Analysis: Million_mutation_project_reanalysis
    Status: Live
  Affects: Gene: WBGene00000112
    Transcript: F56D12.1b.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: F56D12.1b.1:c.498C>T
        HGVSp: CE33403:p.Leu166=
        cDNA_position: 500
        CDS_position: 498
        Protein_position: 166
        Exon_number: 5/8
        Codon_change: ctC/ctT
        Amino_acid_change: L
      F56D12.1a.2 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: F56D12.1a.2:c.498C>T
        HGVSp: CE29047:p.Leu166=
        cDNA_position: 597
        CDS_position: 498
        Protein_position: 166
        Exon_number: 6/10
        Codon_change: ctC/ctT
        Amino_acid_change: L
      F56D12.1a.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: F56D12.1a.1:c.498C>T
        HGVSp: CE29047:p.Leu166=
        cDNA_position: 501
        CDS_position: 498
        Protein_position: 166
        Exon_number: 5/9
        Codon_change: ctC/ctT
        Amino_acid_change: L
      F56D12.1d.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: F56D12.1d.1:c.78C>T
        HGVSp: CE40074:p.Leu26=
        cDNA_position: 78
        CDS_position: 78
        Protein_position: 26
        Exon_number: 1/4
        Codon_change: ctC/ctT
        Amino_acid_change: L
      F56D12.1c.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: F56D12.1c.1:c.498C>T
        HGVSp: CE37118:p.Leu166=
        cDNA_position: 498
        CDS_position: 498
        Protein_position: 166
        Exon_number: 4/6
        Codon_change: ctC/ctT
        Amino_acid_change: L
  Method: WGS_Flibotte