WormBase Tree Display for Variation: WBVar01256553

WBVar01256553 Evidence: Paper_evidence: WBPaper00037807
  Name: Public_name: WBVar01256553
    Other_name: cewivar00020022
      CE39433:p.Cys249=
      Y119D3B.8.1:c.747C>T
      Y119D3B.8.2:c.747C>T
    HGVSg: CHROMOSOME_III:g.1242564C>T
  Sequence_details: SMap: S_parent: Sequence: Y119D3B
    Flanking_sequences: ATACCTCGACTTTTGCAGAATCTCATGAGAAGAAATGCATTTCAAAGTTG AATATAACTTTTGATAAGTCAACTTCGAATCCAGTGGAAATTGCAAAAGT
    Mapping_target: Y119D3B
    Type_of_mutation: Substitution: c T Paper_evidence: WBPaper00037807
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain (143)
    Laboratory: AX
      QX
    Person: WBPerson1730
    Analysis: WGS_De_Bono
      Million_mutation_project_reanalysis
      WGS_Andersen
    DB_info: Database: dbSNP_ss ss 539092841
    History: Acquires_merge: WBVar01443561
        WBVar01324067
    Status: Live
  Affects: Gene: WBGene00022486
    Transcript: Y119D3B.8.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: Y119D3B.8.1:c.747C>T
        HGVSp: CE39433:p.Cys249=
        cDNA_position: 967
        CDS_position: 747
        Protein_position: 249
        Exon_number: 5/6
        Codon_change: tgC/tgT
        Amino_acid_change: C
      Y119D3B.8.2 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: Y119D3B.8.2:c.747C>T
        HGVSp: CE39433:p.Cys249=
        cDNA_position: 810
        CDS_position: 747
        Protein_position: 249
        Exon_number: 4/5
        Codon_change: tgC/tgT
        Amino_acid_change: C
  Reference: WBPaper00040707
    WBPaper00037807
  Method: WGS_De_Bono