WormBase Tree Display for Variation: WBVar01232657

WBVar01232657 Evidence: Paper_evidence: WBPaper00037807
  Name: Public_name: WBVar01232657
    Other_name: cewivar00279186
      CE46583:p.Pro138=
      CE20785:p.Pro138=
      F43C11.1b.1:c.414A>T
      F43C11.1a.1:c.414A>T
    HGVSg: CHROMOSOME_II:g.2357969A>T
  Sequence_details: SMap: S_parent: Sequence: F43C11
    Flanking_sequences: CAATTTGGAATTGAATGTGATGGCGATAAGTGGAAGGCCACCAAATATCC TTGGGAATTCATTATCTGACTACAGATTATGAAACAATTAATCTTGGCAT
    Mapping_target: F43C11
    Type_of_mutation: Substitution: a T Paper_evidence: WBPaper00037807
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain (114)
    Laboratory: AX
      QX
    Person: WBPerson1730
    Analysis: WGS_De_Bono
      Million_mutation_project_reanalysis
      WGS_Andersen
    DB_info: Database: dbSNP_ss ss 539071335
    History: Acquires_merge: WBVar01436374
        WBVar01298410
    Status: Live
  Affects: Gene: WBGene00018378
    Transcript: F43C11.1b.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: F43C11.1b.1:c.414A>T
        HGVSp: CE46583:p.Pro138=
        cDNA_position: 414
        CDS_position: 414
        Protein_position: 138
        Exon_number: 4/6
        Codon_change: ccA/ccT
        Amino_acid_change: P
      F43C11.1a.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: F43C11.1a.1:c.414A>T
        HGVSp: CE20785:p.Pro138=
        cDNA_position: 414
        CDS_position: 414
        Protein_position: 138
        Exon_number: 4/4
        Codon_change: ccA/ccT
        Amino_acid_change: P
  Reference: WBPaper00040707
    WBPaper00037807
  Method: WGS_De_Bono