WormBase Tree Display for Variation: WBVar01729846

WBVar01729846 Name: Public_name: WBVar01729846
    Other_name (11)
    HGVSg: CHROMOSOME_IV:g.7437893T>C
  Sequence_details: SMap: S_parent: Sequence: B0496
    Flanking_sequences: AGTATATCTCATTGATCCTTCTGTGCATCT ACTTCTTGTCTCTGAACTCTAACCCATTTG
    Mapping_target: B0496
    Source_location: 225 CHROMOSOME_IV 7437882 7437882 From_analysis: Million_mutation_project_reanalysis
    Type_of_mutation: Substitution: T C
    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
      WBStrain00027662 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.2773+34T>C
        Intron_number: 13/27
      B0496.3a.2 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: B0496.3a.2:c.2650+34T>C
        Intron_number: 13/27
      B0496.3b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: B0496.3b.1:c.2773+34T>C
        Intron_number: 13/30
      B0496.3i.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: B0496.3i.1:c.2824+34T>C
        Intron_number: 13/29
      B0496.3g.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: B0496.3g.1:c.2773+34T>C
        Intron_number: 16/31
      B0496.3a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: B0496.3a.1:c.2650+34T>C
        Intron_number: 18/32
      B0496.3e.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: B0496.3e.1:c.3490+34T>C
        Intron_number: 19/34
      B0496.3f.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: B0496.3f.1:c.2773+34T>C
        Intron_number: 13/28
      B0496.3h.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: B0496.3h.1:c.2773+34T>C
        Intron_number: 16/30
      B0496.3d.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: B0496.3d.1:c.2773+34T>C
        Intron_number: 16/32
  Method: WGS_Flibotte