WormBase Tree Display for Variation: WBVar02012076

WBVar02012076 Name: Public_name: WBVar02012076
    Other_name: cewivar00740484
      F53C3.13f.1:c.962+73_962+78del
      F53C3.13e.1:c.956+73_956+78del
      F53C3.13b.1:c.956+73_956+78del
      F53C3.13a.1:c.956+73_956+78del
      F53C3.13c.1:c.956+73_956+78del
      F53C3.13d.1:c.956+73_956+78del
      F53C3.13d.2:c.956+73_956+78del
    HGVSg: CHROMOSOME_II:g.3924383_3924388del
  Sequence_details: SMap: S_parent: Sequence: F53C3
    Flanking_sequences: GACAATCGGACAAAGCGTGAGAGAGAGGTG GTAGTAGTAGTAGTAGGCTGCCGGCGGAGA
    Mapping_target: F53C3
    Source_location: 225 CHROMOSOME_II 3924385 3924390 From_analysis: Million_mutation_project_reanalysis
    Type_of_mutation: Deletion
    SeqStatus: Sequenced
  Variation_type: Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00008273 From_analysis: Million_mutation_project_reanalysis
      WBStrain00022868 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023018 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023192 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023665 From_analysis: Million_mutation_project_reanalysis
      WBStrain00031113 From_analysis: Million_mutation_project_reanalysis
    Laboratory: VC
    Analysis: Million_mutation_project_reanalysis
    Status: Live
  Affects: Gene: WBGene00018756
    Transcript: F53C3.13e.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F53C3.13e.1:c.956+73_956+78del
        Intron_number: 5/6
      F53C3.13b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F53C3.13b.1:c.956+73_956+78del
        Intron_number: 5/6
      F53C3.13d.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F53C3.13d.1:c.956+73_956+78del
        Intron_number: 5/7
      F53C3.13a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F53C3.13a.1:c.956+73_956+78del
        Intron_number: 5/6
      F53C3.13d.2 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F53C3.13d.2:c.956+73_956+78del
        Intron_number: 5/6
      F53C3.13f.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F53C3.13f.1:c.962+73_962+78del
        Intron_number: 5/6
      F53C3.13c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F53C3.13c.1:c.956+73_956+78del
        Intron_number: 5/6
  Method: WGS_Flibotte