WormBase Tree Display for Variation: WBVar01677933

WBVar01677933 Name: Public_name: WBVar01677933
    Other_name (19)
    HGVSg: CHROMOSOME_V:g.4510617T>G
  Sequence_details: SMap: S_parent: Sequence: T28F12
    Flanking_sequences: TAAGGCTAAACCTAAGCCTAGGCCTAAGCG ACACCTAGGCCTAAATCTGAAGCTAAGTCT
    Mapping_target: T28F12
    Source_location: 225 CHROMOSOME_V 4510603 4510603 From_analysis: Million_mutation_project_reanalysis
    Type_of_mutation: Substitution: T G
    SeqStatus: Sequenced
  Variation_type: Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00006637 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023072 From_analysis: Million_mutation_project_reanalysis
    Laboratory: VC
    Analysis: Million_mutation_project_reanalysis
    Status: Live
  Affects: Gene: WBGene00006796
    Transcript: T28F12.2d.7 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T28F12.2d.7:c.237-175T>G
        Intron_number: 6/7
      T28F12.2a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T28F12.2a.1:c.1596-175T>G
        Intron_number: 10/11
      T28F12.2b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T28F12.2b.1:c.1485-175T>G
        Intron_number: 10/11
      T28F12.2d.2 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T28F12.2d.2:c.237-175T>G
        Intron_number: 10/11
      T28F12.2d.3 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T28F12.2d.3:c.237-175T>G
        Intron_number: 10/11
      T28F12.2d.8 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T28F12.2d.8:c.237-175T>G
        Intron_number: 5/6
      T28F12.2c.2 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T28F12.2c.2:c.363-175T>G
        Intron_number: 9/10
      T28F12.2d.9 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T28F12.2d.9:c.237-175T>G
        Intron_number: 4/5
      T28F12.2d.10 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T28F12.2d.10:c.237-175T>G
        Intron_number: 2/3
      T28F12.2h.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T28F12.2h.1:c.1362-175T>G
        Intron_number: 8/8
      T28F12.2d.4 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T28F12.2d.4:c.237-175T>G
        Intron_number: 10/11
      T28F12.2e.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T28F12.2e.1:c.1473-175T>G
        Intron_number: 9/9
      T28F12.2d.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T28F12.2d.1:c.237-175T>G
        Intron_number: 10/11
      T28F12.2c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T28F12.2c.1:c.363-175T>G
        Intron_number: 9/10
      T28F12.2d.5 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T28F12.2d.5:c.237-175T>G
        Intron_number: 9/10
      T28F12.2d.6 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T28F12.2d.6:c.237-175T>G
        Intron_number: 7/8
      T28F12.2g.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T28F12.2g.1:c.1374-175T>G
        Intron_number: 8/8
      T28F12.2f.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T28F12.2f.1:c.1584-175T>G
        Intron_number: 10/10
  Method: WGS_Flibotte