WormBase Tree Display for Variation: WBVar01250467

WBVar01250467 Evidence: Paper_evidence: WBPaper00037807
  Name: Public_name: WBVar01250467
    Other_name: cewivar00098732
      F54F11.2b.1:c.1524A>G
      CE11095:p.Lys637=
      CE43217:p.Lys508=
      F54F11.2a.1:c.1911A>G
    HGVSg: CHROMOSOME_II:g.13511270A>G
  Sequence_details: SMap: S_parent: Sequence: F54F11
    Flanking_sequences: TGGTATCAGCCAGAGCTCAACTCGATCACCTTCCCCGCTGGAATTCTTAA AAGCCATTCTACGACTTCAACTGGCCAGCGTCGGTTAACTTCGGAGCAAT
    Mapping_target: F54F11
    Type_of_mutation: Substitution: a G Paper_evidence: WBPaper00037807
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain (111)
    Laboratory: AX
    Analysis: WGS_De_Bono
      Million_mutation_project_reanalysis
      WGS_Andersen
    DB_info: Database: dbSNP_ss ss 539087365
    History: Acquires_merge: WBVar01441598
        WBVar01382068
        WBVar01317137
    Status: Live
  Affects: Gene: WBGene00010070
    Transcript: F54F11.2b.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: F54F11.2b.1:c.1524A>G
        HGVSp: CE43217:p.Lys508=
        cDNA_position: 1524
        CDS_position: 1524
        Protein_position: 508
        Exon_number: 5/11
        Codon_change: aaA/aaG
        Amino_acid_change: K
      F54F11.2a.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: F54F11.2a.1:c.1911A>G
        HGVSp: CE11095:p.Lys637=
        cDNA_position: 1923
        CDS_position: 1911
        Protein_position: 637
        Exon_number: 9/16
        Codon_change: aaA/aaG
        Amino_acid_change: K
  Reference: WBPaper00037807
  Method: WGS_De_Bono