WormBase Tree Display for Variation: WBVar02031153

WBVar02031153 Name: Public_name: WBVar02031153
    Other_name: cewivar00759735
      B0496.3f.1:c.112+324_112+325del
      B0496.3h.1:c.112+324_112+325del
      B0496.3b.1:c.112+324_112+325del
      B0496.3h.2:c.112+324_112+325del
      B0496.3d.1:c.112+324_112+325del
      B0496.3e.1:c.829+324_829+325del
      B0496.3g.1:c.112+324_112+325del
      B0496.3a.1:c.112+324_112+325del
      B0496.3a.2:c.112+324_112+325del
    HGVSg: CHROMOSOME_IV:g.7429369_7429370del
  Sequence_details: SMap: S_parent: Sequence: B0496
    Flanking_sequences: TGAAAGTCAATTGATTATATAGATTAAGGT ATGACAATTTGAAAATTGAAGAAACATTGG
    Mapping_target: B0496
    Source_location: 225 CHROMOSOME_IV 7429358 7429359 From_analysis: Million_mutation_project_reanalysis
    Type_of_mutation: Deletion
    SeqStatus: Sequenced
  Variation_type: Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023191 From_analysis: Million_mutation_project_reanalysis
    Laboratory: VC
    Analysis: Million_mutation_project_reanalysis
    Status: Live
  Affects: Gene: WBGene00006814
    Transcript: B0496.3h.2 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: B0496.3h.2:c.112+324_112+325del
        Intron_number: 1/27
      B0496.3a.2 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: B0496.3a.2:c.112+324_112+325del
        Intron_number: 2/27
      B0496.3b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: B0496.3b.1:c.112+324_112+325del
        Intron_number: 1/30
      B0496.3g.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: B0496.3g.1:c.112+324_112+325del
        Intron_number: 4/31
      B0496.3a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: B0496.3a.1:c.112+324_112+325del
        Intron_number: 7/32
      B0496.3e.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: B0496.3e.1:c.829+324_829+325del
        Intron_number: 7/34
      B0496.3f.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: B0496.3f.1:c.112+324_112+325del
        Intron_number: 1/28
      B0496.3h.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: B0496.3h.1:c.112+324_112+325del
        Intron_number: 4/30
      B0496.3d.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: B0496.3d.1:c.112+324_112+325del
        Intron_number: 4/32
  Method: WGS_Flibotte