WormBase Tree Display for Variation: WBVar01759291

WBVar01759291 Name: Public_name: WBVar01759291
    Other_name: cewivar00459014
      F11A1.3g.1:c.718-33G>A
      F11A1.3e.1:c.541-33G>A
      F11A1.3e.4:c.541-33G>A
      F11A1.3b.1:c.541-33G>A
      F11A1.3f.1:c.616-33G>A
      F11A1.3a.1:c.718-33G>A
      F11A1.3d.1:c.616-33G>A
      F11A1.3e.3:c.541-33G>A
      F11A1.3e.2:c.541-33G>A
    HGVSg: CHROMOSOME_X:g.10661901G>A
  Sequence_details: SMap: S_parent: Sequence: F11A1
    Flanking_sequences: AGTTCCCCTATAATTTGCTATGTTTCTTAA AGAATTTAGACAATACAATATTATATTTTC
    Mapping_target: F11A1
    Source_location: 225 CHROMOSOME_X 10661838 10661838 From_analysis: Million_mutation_project_reanalysis
    Type_of_mutation: Substitution: G A
    SeqStatus: Sequenced
  Variation_type: Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023139 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: WBGene00000908
    Transcript: F11A1.3b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F11A1.3b.1:c.541-33G>A
        Intron_number: 4/14
      F11A1.3e.2 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F11A1.3e.2:c.541-33G>A
        Intron_number: 6/18
      F11A1.3e.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F11A1.3e.1:c.541-33G>A
        Intron_number: 7/19
      F11A1.3e.4 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F11A1.3e.4:c.541-33G>A
        Intron_number: 6/18
      F11A1.3f.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F11A1.3f.1:c.616-33G>A
        Intron_number: 6/17
      F11A1.3a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F11A1.3a.1:c.718-33G>A
        Intron_number: 6/17
      F11A1.3g.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F11A1.3g.1:c.718-33G>A
        Intron_number: 7/18
      F11A1.3e.3 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F11A1.3e.3:c.541-33G>A
        Intron_number: 8/20
      F11A1.3d.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F11A1.3d.1:c.616-33G>A
        Intron_number: 5/15
  Method: WGS_Flibotte