WormBase Tree Display for Variation: WBVar01286379

WBVar01286379 Evidence: Paper_evidence: WBPaper00037807
  Name: Public_name: WBVar01286379
    Other_name: cewivar00324522
      CE23872:p.Phe849=
      M01G12.12.1:c.2547T>C
      M01G12.12.2:c.2547T>C
    HGVSg: CHROMOSOME_I:g.12102128A>G
  Sequence_details: SMap: S_parent: Sequence: Y47H10A
    Flanking_sequences: TTGGAATCTCGAGGTGGGAGTATGTTCCTGTGATTTTTCGTGTATTGAAC AAGACCTGTCCGTATTGTAGAATCCCAGTCTCGTCGACAACGCCAAGCAT
    Mapping_target: Y47H10A
    Type_of_mutation: Substitution: a G Paper_evidence: WBPaper00037807
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain (17)
    Laboratory: AX
    Analysis: WGS_De_Bono
      Million_mutation_project_reanalysis
    DB_info: Database: dbSNP_ss ss 539146021
    History: Acquires_merge: WBVar01425259
    Status: Live
  Affects: Gene: WBGene00004509
    Transcript: M01G12.12.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: M01G12.12.1:c.2547T>C
        HGVSp: CE23872:p.Phe849=
        cDNA_position: 2606
        CDS_position: 2547
        Protein_position: 849
        Exon_number: 14/23
        Codon_change: ttT/ttC
        Amino_acid_change: F
      M01G12.12.2 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: M01G12.12.2:c.2547T>C
        HGVSp: CE23872:p.Phe849=
        cDNA_position: 2566
        CDS_position: 2547
        Protein_position: 849
        Exon_number: 13/22
        Codon_change: ttT/ttC
        Amino_acid_change: F
  Reference: WBPaper00037807
  Method: WGS_De_Bono