WormBase Tree Display for Variation: WBVar01408476

WBVar01408476 Evidence: Paper_evidence: WBPaper00037807
  Name: Public_name: WBVar01408476
    Other_name: cewivar00738540
      T08A11.1d.1:c.*251dup
      T08A11.1c.1:c.*251dup
      T08A11.1g.1:c.*251dup
      T08A11.1a.1:c.*251dup
      T08A11.1h.1:c.*251dup
      T08A11.1b.1:c.*251dup
      T08A11.1f.1:c.*251dup
      T08A11.1e.1:c.*251dup
    HGVSg: CHROMOSOME_III:g.4248418_4248419insA
  Sequence_details: SMap: S_parent: Sequence: Y44F5A
    Flanking_sequences: GACCGGTGTGTGGGGGGAAATAAGGTTGCTTAGAAAATGTTTAAAGCAAC AAAAAAACATAGAATGAGAGTAATAAGAGATAAAAATAAATTAATACACT
    Mapping_target: Y44F5A
    Type_of_mutation: Insertion: A Paper_evidence: WBPaper00037807
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00006642 From_analysis: WGS_De_Bono
      WBStrain00006643 From_analysis: Million_mutation_project_reanalysis
      WBStrain00006645 From_analysis: Million_mutation_project_reanalysis
    Laboratory: AX
    Analysis: WGS_De_Bono
      Million_mutation_project_reanalysis
    DB_info: Database: dbSNP_ss ss 539122949
    History: Acquires_merge: WBVar02010413
    Status: Live
  Affects: Gene: WBGene00011604
    Transcript: T08A11.1e.1 VEP_consequence: 3_prime_UTR_variant
        VEP_impact: MODIFIER
        HGVSc: T08A11.1e.1:c.*251dup
        cDNA_position: 5396-5397
        Exon_number: 18/18
      T08A11.1g.1 VEP_consequence: 3_prime_UTR_variant
        VEP_impact: MODIFIER
        HGVSc: T08A11.1g.1:c.*251dup
        cDNA_position: 5498-5499
        Exon_number: 19/19
      T08A11.1h.1 VEP_consequence: 3_prime_UTR_variant
        VEP_impact: MODIFIER
        HGVSc: T08A11.1h.1:c.*251dup
        cDNA_position: 5504-5505
        Exon_number: 19/19
      T08A11.1d.1 VEP_consequence: 3_prime_UTR_variant
        VEP_impact: MODIFIER
        HGVSc: T08A11.1d.1:c.*251dup
        cDNA_position: 5498-5499
        Exon_number: 19/19
      T08A11.1f.1 VEP_consequence: 3_prime_UTR_variant
        VEP_impact: MODIFIER
        HGVSc: T08A11.1f.1:c.*251dup
        cDNA_position: 5402-5403
        Exon_number: 18/18
      T08A11.1c.1 VEP_consequence: 3_prime_UTR_variant
        VEP_impact: MODIFIER
        HGVSc: T08A11.1c.1:c.*251dup
        cDNA_position: 5396-5397
        Exon_number: 18/18
      T08A11.1b.1 VEP_consequence: 3_prime_UTR_variant
        VEP_impact: MODIFIER
        HGVSc: T08A11.1b.1:c.*251dup
        cDNA_position: 5492-5493
        Exon_number: 19/19
      T08A11.1a.1 VEP_consequence: 3_prime_UTR_variant
        VEP_impact: MODIFIER
        HGVSc: T08A11.1a.1:c.*251dup
        cDNA_position: 5490-5491
        Exon_number: 19/19
  Reference: WBPaper00037807
  Method: WGS_De_Bono