WormBase Tree Display for Variation: WBVar01794825

WBVar01794825 Name: Public_name: WBVar01794825
    Other_name: cewivar00497200
      B0496.3b.1:c.112+120C>T
      B0496.3d.1:c.112+120C>T
      B0496.3a.2:c.112+120C>T
      B0496.3h.1:c.112+120C>T
      B0496.3e.1:c.829+120C>T
      B0496.3f.1:c.112+120C>T
      B0496.3g.1:c.112+120C>T
      B0496.3h.2:c.112+120C>T
      B0496.3a.1:c.112+120C>T
    HGVSg: CHROMOSOME_IV:g.7429165C>T
  Sequence_details: SMap: S_parent: Sequence: B0496
    Flanking_sequences: AGAGAGAGAGAGAGAAGATCTACGAAAGTT TAAAGAGAAAGAGATAAATCAATGGATACG
    Mapping_target: B0496
    Source_location: 225 CHROMOSOME_IV 7429154 7429154 From_analysis: Million_mutation_project_reanalysis
    Type_of_mutation: Substitution: C T
    SeqStatus: Sequenced
  Variation_type: Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00022899 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023286 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+120C>T
        Intron_number: 1/27
      B0496.3a.2 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: B0496.3a.2:c.112+120C>T
        Intron_number: 2/27
      B0496.3b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: B0496.3b.1:c.112+120C>T
        Intron_number: 1/30
      B0496.3g.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: B0496.3g.1:c.112+120C>T
        Intron_number: 4/31
      B0496.3a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: B0496.3a.1:c.112+120C>T
        Intron_number: 7/32
      B0496.3e.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: B0496.3e.1:c.829+120C>T
        Intron_number: 7/34
      B0496.3f.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: B0496.3f.1:c.112+120C>T
        Intron_number: 1/28
      B0496.3h.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: B0496.3h.1:c.112+120C>T
        Intron_number: 4/30
      B0496.3d.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: B0496.3d.1:c.112+120C>T
        Intron_number: 4/32
  Method: WGS_Flibotte