WormBase Tree Display for Variation: WBVar01447851

WBVar01447851 Evidence: Paper_evidence: WBPaper00040707
  Name: Public_name: WBVar01447851
    Other_name: CE00582:p.Arg199=
      T16G12.12.1:c.-14+4686C>G
      T16G12.4.1:c.597C>G
    HGVSg: CHROMOSOME_III:g.10058548C>G
  Sequence_details: SMap: S_parent: Sequence: T16G12
    Flanking_sequences: TCTCAACGCCAAACTTGATCATTCGACGCG CAGAAGCAAGTCAGAGAGAAGAGAAACTCA
    Mapping_target: T16G12
    Type_of_mutation: Substitution: c g
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00031279 From_analysis: WGS_Andersen
      WBStrain00031284 From_analysis: WGS_Andersen
    Laboratory: QX
    Person: WBPerson1730
    Analysis: WGS_Andersen
    DB_info: Database: dbSNP_rs rs 193334196
        dbSNP_ss ss 295510115
    Status: Live
  Affects: Gene: WBGene00011805
      WBGene00269433
    Transcript: T16G12.4.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: T16G12.4.1:c.597C>G
        HGVSp: CE00582:p.Arg199=
        cDNA_position: 624
        CDS_position: 597
        Protein_position: 199
        Exon_number: 4/5
        Codon_change: cgC/cgG
        Amino_acid_change: R
      T16G12.12.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T16G12.12.1:c.-14+4686C>G
        Intron_number: 1/5
  Reference: WBPaper00040707
  Method: WGS_Andersen