WormBase Tree Display for Variation: WBVar01407112

WBVar01407112 Evidence: Paper_evidence: WBPaper00037807
  Name: Public_name: WBVar01407112
    Other_name: cewivar00686725
      R05H10.5a.1:c.*473_*474insCTG
      R05H10.5b.1:c.*473_*474insCTG
    HGVSg: CHROMOSOME_II:g.14869501_14869502insCTG
  Sequence_details: SMap: S_parent: Sequence: R05H10
    Flanking_sequences: TTAAATTTTCCGGTTTTCTAAGCTTTTTTTTCGAGAATTTCACTAAAAAT CGAATTTTCCAGATTTTCAATTTTTTTCCCTCATTTTCACTCAATTTTCT
    Mapping_target: R05H10
    Type_of_mutation: Insertion: CTG Paper_evidence: WBPaper00037807
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00004602 From_analysis: Million_mutation_project_reanalysis
      WBStrain00006642 From_analysis: WGS_De_Bono
      WBStrain00022850 From_analysis: WGS_De_Bono
    Laboratory: AX
    Analysis: WGS_De_Bono
      Million_mutation_project_reanalysis
    DB_info: Database: dbSNP_ss ss 539121722
    History: Acquires_merge: WBVar01415020
        WBVar01961186
    Status: Live
  Affects: Gene: WBGene00011045
    Transcript: R05H10.5a.1 VEP_consequence: 3_prime_UTR_variant
        VEP_impact: MODIFIER
        HGVSc: R05H10.5a.1:c.*473_*474insCTG
        cDNA_position: 977-978
        Exon_number: 5/5
      R05H10.5b.1 VEP_consequence: 3_prime_UTR_variant
        VEP_impact: MODIFIER
        HGVSc: R05H10.5b.1:c.*473_*474insCTG
        cDNA_position: 1013-1014
        Exon_number: 5/5
  Reference: WBPaper00037807
  Method: WGS_De_Bono