WormBase Tree Display for Variation: WBVar01385003

WBVar01385003 Evidence: Paper_evidence: WBPaper00037807
  Name: Public_name: WBVar01385003
    Other_name: cewivar00144722
      F19H8.1a.1:c.399C>T
      CE37507:p.Asp133=
    HGVSg: CHROMOSOME_II:g.14601350C>T
  Sequence_details: SMap: S_parent: Sequence: F19H8
    Flanking_sequences: GCCGGTTACATTTTCGACTCGGATCTGGGAAGAGGTACAAAGTTCCGTGA GCGCTTCTCTTCTCCCTTACTCTGTACGACGTCAACACTGGTAAAAATCG
    Mapping_target: F19H8
    Type_of_mutation: Substitution: c T Paper_evidence: WBPaper00037807
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00004600 From_analysis: Million_mutation_project_reanalysis
      WBStrain00004602 From_analysis: Million_mutation_project_reanalysis
          WGS_De_Bono
    Laboratory: AX
    Analysis: WGS_De_Bono
      Million_mutation_project_reanalysis
    DB_info: Database: dbSNP_ss ss 539060454
    Status: Live
  Affects: Gene: WBGene00006603
    Transcript: F19H8.1a.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: F19H8.1a.1:c.399C>T
        HGVSp: CE37507:p.Asp133=
        cDNA_position: 406
        CDS_position: 399
        Protein_position: 133
        Exon_number: 3/16
        Codon_change: gaC/gaT
        Amino_acid_change: D
  Reference: WBPaper00037807
  Method: WGS_De_Bono