WormBase Tree Display for Variation: WBVar01749217

WBVar01749217 Name: Public_name: WBVar01749217
    Other_name: cewivar00448678
      E01B7.1.1:c.2277+419T>C
      E01B7.1.2:c.2277+419T>C
    HGVSg: CHROMOSOME_V:g.17933021T>C
  Sequence_details: SMap: S_parent: Sequence: Y59A8B
    Flanking_sequences: ATTTTCTCAAGTTTCCTGTAAAATTTCATT TGATTCGAGTTTTTTCCGCAAACATTTTTT
    Mapping_target: Y59A8B
    Source_location: 225 CHROMOSOME_V 17932995 17932995 From_analysis: Million_mutation_project_reanalysis
    Type_of_mutation: Substitution: T C
    SeqStatus: Sequenced
  Variation_type: Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00022868 From_analysis: Million_mutation_project_reanalysis
      WBStrain00022878 From_analysis: Million_mutation_project_reanalysis
      WBStrain00022930 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023139 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023192 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: WBGene00008441
    Transcript: E01B7.1.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: E01B7.1.1:c.2277+419T>C
        Intron_number: 16/18
      E01B7.1.2 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: E01B7.1.2:c.2277+419T>C
        Intron_number: 17/19
  Method: WGS_Flibotte