WormBase Tree Display for Variation: WBVar01446575

WBVar01446575 Evidence: Paper_evidence: WBPaper00040707
  Name: Public_name: WBVar01446575
    Other_name: R151.9.1:c.417G>A
      CE00827:p.Gln139=
    HGVSg: CHROMOSOME_III:g.7198324C>T
  Sequence_details: SMap: S_parent: Sequence: R151
    Flanking_sequences: CATCGTGGCGAGTTGAGACTGAACCTTGGT TGGAATGCGTCCGAAATATAGGCCCGAGTT
    Mapping_target: R151
    Type_of_mutation: Substitution: c t
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00005835 From_analysis: WGS_Andersen
      WBStrain00022928 From_analysis: WGS_Andersen
      WBStrain00022930 From_analysis: WGS_Andersen
          Million_mutation_project_reanalysis
      WBStrain00023150 From_analysis: WGS_Andersen
      WBStrain00023180 From_analysis: WGS_Andersen
      WBStrain00023211 From_analysis: WGS_Andersen
      WBStrain00023279 From_analysis: WGS_Andersen
      WBStrain00023665 From_analysis: WGS_Andersen
          Million_mutation_project_reanalysis
    Laboratory: QX
    Person: WBPerson1730
    Analysis: WGS_Andersen
    DB_info: Database: dbSNP_rs rs 193333313
        dbSNP_ss ss 295509232
    Status: Live
  Affects: Gene: WBGene00020112
    Transcript: R151.9.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: R151.9.1:c.417G>A
        HGVSp: CE00827:p.Gln139=
        cDNA_position: 418
        CDS_position: 417
        Protein_position: 139
        Exon_number: 5/6
        Codon_change: caG/caA
        Amino_acid_change: Q
  Reference: WBPaper00040707
  Method: WGS_Andersen