WormBase Tree Display for Variation: WBVar01982514

WBVar01982514 Name: Public_name: WBVar01982514
    Other_name (23)
    HGVSg: CHROMOSOME_II:g.6844590del
  Sequence_details: SMap: S_parent: Sequence: C04A2
    Flanking_sequences: AAAGGAAAACTCGTTTATCGTAGCCCACCA TTTTTTTTTCTTTTTTTTCTATTCATCCAA
    Mapping_target: C04A2
    Source_location: 225 CHROMOSOME_II 6844547 6844547 From_analysis: Million_mutation_project_reanalysis
    Type_of_mutation: Deletion
    SeqStatus: Sequenced
  Variation_type: Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00006622 From_analysis: Million_mutation_project_reanalysis
      WBStrain00022852 From_analysis: Million_mutation_project_reanalysis
      WBStrain00022856 From_analysis: Million_mutation_project_reanalysis
      WBStrain00022886 From_analysis: Million_mutation_project_reanalysis
      WBStrain00022902 From_analysis: Million_mutation_project_reanalysis
      WBStrain00022930 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023018 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023072 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023191 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023192 From_analysis: Million_mutation_project_reanalysis
    Laboratory: VC
    Analysis: Million_mutation_project_reanalysis
    Status: Live
  Affects: Gene: WBGene00001194
    Transcript: C04A2.3c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C04A2.3c.1:c.-13-772del
        Intron_number: 10/14
      C04A2.3h.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C04A2.3h.1:c.1431-772del
        Intron_number: 9/11
      C04A2.3q.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C04A2.3q.1:c.819-772del
        Intron_number: 4/6
      C04A2.3o.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C04A2.3o.1:c.1101-772del
        Intron_number: 7/9
      C04A2.3k.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C04A2.3k.1:c.1422-772del
        Intron_number: 9/11
      C04A2.3f.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C04A2.3f.1:c.1524-772del
        Intron_number: 10/12
      C04A2.3m.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C04A2.3m.1:c.1110-772del
        Intron_number: 7/9
      C04A2.3i.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C04A2.3i.1:c.1431-772del
        Intron_number: 9/11
      C04A2.3g.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C04A2.3g.1:c.1524-772del
        Intron_number: 10/12
      C04A2.3c.2 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C04A2.3c.2:c.-13-772del
        Intron_number: 5/9
      C04A2.3c.5 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C04A2.3c.5:c.-13-772del
        Intron_number: 2/6
      C04A2.3c.3 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C04A2.3c.3:c.-13-772del
        Intron_number: 10/14
      C04A2.3c.4 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C04A2.3c.4:c.-13-772del
        Intron_number: 5/9
      C04A2.3d.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C04A2.3d.1:c.810-772del
        Intron_number: 4/6
      C04A2.3r.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C04A2.3r.1:c.810-772del
        Intron_number: 4/6
      C04A2.3c.6 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C04A2.3c.6:c.-13-772del
        Intron_number: 1/5
      C04A2.3b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C04A2.3b.1:c.1101-772del
        Intron_number: 11/14
      C04A2.3a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C04A2.3a.1:c.1533-772del
        Intron_number: 11/14
      C04A2.3e.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C04A2.3e.1:c.1533-772del
        Intron_number: 10/12
      C04A2.3p.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C04A2.3p.1:c.819-772del
        Intron_number: 5/8
      C04A2.3j.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C04A2.3j.1:c.1422-772del
        Intron_number: 9/11
      C04A2.3n.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C04A2.3n.1:c.1110-772del
        Intron_number: 7/9
  Method: WGS_Flibotte