WormBase Tree Display for Variation: WBVar00270166

WBVar00270166 Name: Public_name: WBVar00270166
    Other_name: uCE3-1379
      cewivar00153706
      Y37D8A.13.1:c.2301T>C
      CE20217:p.Leu767=
    HGVSg: CHROMOSOME_III:g.12883463A>G
  Sequence_details: SMap: S_parent: Sequence: Y37D8A
    Flanking_sequences: ACGATGGCATATTGCCGAATTTGATCTGCCGATCTGGGGATTCCTCGTCCTTCTCATCGCTGGGCTTCGGGATCTCCACCACCGAACGTCGCCGATAGCA AGCATCAGACAGACCAGGCATAGGAGTAGGAAGACTCCGAATCCGAGAAGAATCGCGAAAAGGGTAGCAGTCTCCAGGGTGGTTCCAATGTTCAGGTGAG
    Mapping_target: Y37D8A
    Type_of_mutation: Substitution: A G
    SeqStatus: Sequenced
  Variation_type: SNP
    Predicted_SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00004600 From_analysis: Million_mutation_project_reanalysis
      WBStrain00004602 From_analysis: SNP_Swan
          Million_mutation_project_reanalysis
      WBStrain00022850 From_analysis: WGS_De_Bono
          Million_mutation_project_reanalysis
      WBStrain00022899 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023286 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023665 From_analysis: Million_mutation_project_reanalysis
    Laboratory: AX
    Analysis: SNP_Swan
      WGS_De_Bono
      Million_mutation_project_reanalysis
    History: Acquires_merge: WBVar01338832
    Status: Live
  Affects: Gene: WBGene00006804
    Transcript: Y37D8A.13.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: Y37D8A.13.1:c.2301T>C
        HGVSp: CE20217:p.Leu767=
        cDNA_position: 2432
        CDS_position: 2301
        Protein_position: 767
        Exon_number: 6/8
        Codon_change: ctT/ctC
        Amino_acid_change: L
  Reference: WBPaper00037807
    WBPaper00005369
  Method: SNP_Swan