WormBase Tree Display for Variation: WBVar01451752

WBVar01451752 Evidence: Paper_evidence: WBPaper00040707
  Name: Public_name: WBVar01451752
    Other_name: Y37E11C.1b.1:c.1971C>T
      Y37E11C.1c.1:c.1503C>T
      CE31638:p.Ile657=
      CE31639:p.Ile501=
      Y37E11C.1a.1:c.2496C>T
      CE21557:p.Ile832=
    HGVSg: CHROMOSOME_IV:g.3525503C>T
  Sequence_details: SMap: S_parent: Sequence: M57
    Flanking_sequences: AAATCGCACCAAAGTAATGGAATCTTCCAT GATTTTGGCGGCTCCGCGGCGAATCGGCCC
    Mapping_target: M57
    Type_of_mutation: Substitution: c t
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00005305 From_analysis: WGS_Andersen
      WBStrain00005315 From_analysis: WGS_Andersen
    Laboratory: QX
    Person: WBPerson1730
    Analysis: WGS_Andersen
    DB_info: Database: dbSNP_rs rs 193337409
        dbSNP_ss ss 295513328
    Status: Live
  Affects: Gene: WBGene00006769
    Transcript: Y37E11C.1c.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: Y37E11C.1c.1:c.1503C>T
        HGVSp: CE31639:p.Ile501=
        cDNA_position: 1503
        CDS_position: 1503
        Protein_position: 501
        Exon_number: 4/4
        Codon_change: atC/atT
        Amino_acid_change: I
      Y37E11C.1b.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: Y37E11C.1b.1:c.1971C>T
        HGVSp: CE31638:p.Ile657=
        cDNA_position: 1971
        CDS_position: 1971
        Protein_position: 657
        Exon_number: 6/6
        Codon_change: atC/atT
        Amino_acid_change: I
      Y37E11C.1a.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: Y37E11C.1a.1:c.2496C>T
        HGVSp: CE21557:p.Ile832=
        cDNA_position: 2496
        CDS_position: 2496
        Protein_position: 832
        Exon_number: 10/11
        Codon_change: atC/atT
        Amino_acid_change: I
  Reference: WBPaper00040707
  Method: WGS_Andersen