WormBase Tree Display for Variation: WBVar01795267

WBVar01795267 Name: Public_name: WBVar01795267
    Other_name (23)
    HGVSg: CHROMOSOME_IV:g.10326096T>A
  Sequence_details: SMap: S_parent: Sequence: K11E8
    Flanking_sequences: TTTTTCCGATTTCCTAAACAAAAATTCCCA TTTTCGAGTATTTCAAATTCCAAAGTTGGT
    Mapping_target: K11E8
    Source_location: 225 CHROMOSOME_IV 10326074 10326074 From_analysis: Million_mutation_project_reanalysis
    Type_of_mutation: Substitution: T A
    SeqStatus: Sequenced
  Variation_type: Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023286 From_analysis: Million_mutation_project_reanalysis
    Laboratory: VC
    Analysis: Million_mutation_project_reanalysis
    Status: Live
  Affects: Gene: WBGene00006779
    Transcript: K11E8.1f.2 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: K11E8.1f.2:c.1319-18A>T
        Intron_number: 15/17
      K11E8.1e.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: K11E8.1e.1:c.1364-18A>T
        Intron_number: 16/18
      K11E8.1t.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: K11E8.1t.1:c.659-18A>T
        Intron_number: 5/6
      K11E8.1s.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: K11E8.1s.1:c.563-18A>T
        Intron_number: 6/7
      K11E8.1g.2 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: K11E8.1g.2:c.1325-18A>T
        Intron_number: 15/17
      K11E8.1p.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: K11E8.1p.1:c.413-18A>T
        Intron_number: 5/6
      K11E8.1o.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: K11E8.1o.1:c.572-18A>T
        Intron_number: 5/7
      K11E8.1h.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: K11E8.1h.1:c.1478-18A>T
        Intron_number: 17/19
      K11E8.1m.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: K11E8.1m.1:c.692-18A>T
        Intron_number: 6/8
      K11E8.1d.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: K11E8.1d.1:c.1211-18A>T
        Intron_number: 14/16
      K11E8.1h.2 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: K11E8.1h.2:c.1478-18A>T
        Intron_number: 16/18
      K11E8.1a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: K11E8.1a.1:c.455-18A>T
        Intron_number: 5/7
      K11E8.1q.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: K11E8.1q.1:c.74-18A>T
        Intron_number: 1/2
      K11E8.1f.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: K11E8.1f.1:c.1319-18A>T
        Intron_number: 16/18
      K11E8.1n.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: K11E8.1n.1:c.410-18A>T
        Intron_number: 6/8
      K11E8.1g.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: K11E8.1g.1:c.1325-18A>T
        Intron_number: 16/18
      K11E8.1e.2 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: K11E8.1e.2:c.1364-18A>T
        Intron_number: 15/17
      K11E8.1d.2 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: K11E8.1d.2:c.1211-18A>T
        Intron_number: 15/17
      K11E8.1i.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: K11E8.1i.1:c.*2610-18A>T
        Intron_number: 14/15
      K11E8.1k.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: K11E8.1k.1:c.*268-18A>T
        Intron_number: 12/13
      K11E8.1r.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: K11E8.1r.1:c.1808-18A>T
        Intron_number: 17/18
      K11E8.1l.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: K11E8.1l.1:c.*253-18A>T
        Intron_number: 12/13
  Method: WGS_Flibotte