WormBase Tree Display for Variation: WBVar01290865

WBVar01290865 Evidence: Paper_evidence: WBPaper00037807
  Name: Public_name: WBVar01290865
    Other_name: cewivar00506213
      F31C3.3.1:c.126T>C
      CE42847:p.Val42=
      F31C3.17:n.61T>C
    HGVSg: CHROMOSOME_I:g.15050344A>G
  Sequence_details: SMap: S_parent: Sequence: F31C3
    Flanking_sequences: TCAATGTGAATGGAGAGCCACGAGATTTTGATGGTGACGTCACGCAACTG ACGAATCCCACACCTCCGATGCGAACATGAGATTTTGTAACGAATGAGAA
    Mapping_target: F31C3
    Type_of_mutation: Substitution: a G Paper_evidence: WBPaper00037807
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00022850 From_analysis: Million_mutation_project_reanalysis
          WGS_De_Bono
      WBStrain00023018 From_analysis: Million_mutation_project_reanalysis
    Laboratory: AX
    Analysis: WGS_De_Bono
      Million_mutation_project_reanalysis
    DB_info: Database: dbSNP_ss ss 539150058
    Status: Live
  Affects: Gene: WBGene00219927
      WBGene00009285
    Transcript: F31C3.17 VEP_consequence: non_coding_transcript_exon_variant
        VEP_impact: MODIFIER
        HGVSc: F31C3.17:n.61T>C
        cDNA_position: 61
        Exon_number: 1/1
      F31C3.3.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: F31C3.3.1:c.126T>C
        HGVSp: CE42847:p.Val42=
        cDNA_position: 147
        CDS_position: 126
        Protein_position: 42
        Exon_number: 3/12
        Codon_change: gtT/gtC
        Amino_acid_change: V
  Reference: WBPaper00037807
  Method: WGS_De_Bono