WormBase Tree Display for Variation: WBVar01981378

WBVar01981378 Name: Public_name: WBVar01981378
    Other_name: cewivar00707464
      C34E11.2d.1:c.714+161del
      C34E11.2c.1:c.615+161del
      C34E11.2f.1:c.714+161del
      C34E11.2e.1:c.714+161del
      C34E11.2a.1:c.714+161del
      C34E11.2g.1:c.714+161del
      C34E11.2b.1:c.447+161del
    HGVSg: CHROMOSOME_X:g.11810812del
  Sequence_details: SMap: S_parent: Sequence: C34E11
    Flanking_sequences: GAAAATCTATAATATAAATTGCTTGTTTTC AAAAAAAAAAACAGAAATAATTCAAATAAG
    Mapping_target: C34E11
    Source_location: 225 CHROMOSOME_X 11810744 11810744 From_analysis: Million_mutation_project_reanalysis
    Type_of_mutation: Deletion
    SeqStatus: Sequenced
  Variation_type: Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00004602 From_analysis: Million_mutation_project_reanalysis
      WBStrain00006640 From_analysis: Million_mutation_project_reanalysis
      WBStrain00022850 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023072 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023139 From_analysis: Million_mutation_project_reanalysis
      WBStrain00024204 From_analysis: Million_mutation_project_reanalysis
      WBStrain00027647 From_analysis: Million_mutation_project_reanalysis
      WBStrain00027648 From_analysis: Million_mutation_project_reanalysis
      WBStrain00027660 From_analysis: Million_mutation_project_reanalysis
    Laboratory: VC
    Analysis: Million_mutation_project_reanalysis
    Status: Live
  Affects: Gene: WBGene00007935
    Transcript: C34E11.2c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C34E11.2c.1:c.615+161del
        Intron_number: 3/13
      C34E11.2g.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C34E11.2g.1:c.714+161del
        Intron_number: 4/12
      C34E11.2b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C34E11.2b.1:c.447+161del
        Intron_number: 2/12
      C34E11.2a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C34E11.2a.1:c.714+161del
        Intron_number: 4/15
      C34E11.2f.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C34E11.2f.1:c.714+161del
        Intron_number: 5/15
      C34E11.2e.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C34E11.2e.1:c.714+161del
        Intron_number: 4/15
      C34E11.2d.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C34E11.2d.1:c.714+161del
        Intron_number: 4/14
  Method: WGS_Flibotte