WormBase Tree Display for Variation: WBVar01305644

WBVar01305644 Evidence: Paper_evidence: WBPaper00037807
  Name: Public_name: WBVar01305644
    Other_name: cewivar00184258
      CE02859:p.Val232=
      T05C1.1.1:c.696T>C
    HGVSg: CHROMOSOME_II:g.4480612T>C
  Sequence_details: SMap: S_parent: Sequence: T05C1
    Flanking_sequences: TAAACTAGTCCTATTTCCAGCTTCACACCCGGCCACGGAAGCGTCGAAGT ACCAAGGTCACCCAAGAAGCCTCACCACCAAAGTTGAACCCATCGAACAG
    Mapping_target: T05C1
    Type_of_mutation: Substitution: t C Paper_evidence: WBPaper00037807
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00004602 From_analysis: WGS_De_Bono
          Million_mutation_project_reanalysis
          WGS_Andersen
      WBStrain00022850 From_analysis: WGS_De_Bono
          Million_mutation_project_reanalysis
          WGS_Andersen
      WBStrain00023191 From_analysis: Million_mutation_project_reanalysis
          WGS_Andersen
      WBStrain00031279 From_analysis: WGS_Andersen
      WBStrain00031284 From_analysis: WGS_Andersen
    Laboratory: AX
      QX
    Person: WBPerson1730
    Analysis: WGS_De_Bono
      Million_mutation_project_reanalysis
      WGS_Andersen
    DB_info: Database: dbSNP_ss ss 539163360
    History: Acquires_merge: WBVar01371031
        WBVar01437499
    Status: Live
  Affects: Gene: WBGene00020248
    Transcript: T05C1.1.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: T05C1.1.1:c.696T>C
        HGVSp: CE02859:p.Val232=
        cDNA_position: 721
        CDS_position: 696
        Protein_position: 232
        Exon_number: 7/8
        Codon_change: gtT/gtC
        Amino_acid_change: V
  Reference: WBPaper00040707
    WBPaper00037807
  Method: WGS_De_Bono