WormBase Tree Display for Variation: WBVar01393731

WBVar01393731 Evidence: Paper_evidence: WBPaper00037807
  Name: Public_name: WBVar01393731
    Other_name: cewivar00670967
      F22D3.2d.1:c.1167+279del
      F22D3.2g.1:c.1167+279del
      F22D3.2e.1:c.1158+279del
      F22D3.2j.1:c.1158+279del
    HGVSg: CHROMOSOME_II:g.6943056del
  Sequence_details: SMap: S_parent: Sequence: F22D3
    Flanking_sequences: TCTGATCCATAATTTATTGTTCTCTGAACTTTGAATCTCTTTTTTGGTTA TTTTTGATTCTCAAGTCGTCTATATTTAGCTTCAATATGACTGAATGGTT
    Mapping_target: F22D3
    Type_of_mutation: Deletion: T Paper_evidence: WBPaper00037807
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain (17)
    Laboratory: AX
    Analysis: WGS_De_Bono
      Million_mutation_project_reanalysis
    DB_info: Database: dbSNP_ss ss 539113154
    Status: Live
  Affects: Gene: WBGene00017699
    Transcript: F22D3.2g.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F22D3.2g.1:c.1167+279del
        Intron_number: 14/18
      F22D3.2e.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F22D3.2e.1:c.1158+279del
        Intron_number: 14/18
      F22D3.2d.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F22D3.2d.1:c.1167+279del
        Intron_number: 14/18
      F22D3.2j.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F22D3.2j.1:c.1158+279del
        Intron_number: 14/18
  Reference: WBPaper00037807
  Method: WGS_De_Bono