WormBase Tree Display for Variation: WBVar01720509

WBVar01720509 Name: Public_name: WBVar01720509
    Other_name: cewivar00418692
      F52H3.1.3:c.2093-599C>T
      F52H3.1.2:c.2093-599C>T
      F52H3.1.4:c.2093-599C>T
      F52H3.1.1:c.2093-599C>T
    HGVSg: CHROMOSOME_II:g.10034147G>A
  Sequence_details: SMap: S_parent: Sequence: F52H3
    Flanking_sequences: AAACAACCCGAGTGAGCAGCAATTTTCCAA CTGAAGGCAAGTTTCTTTTTGTAGTTTTTT
    Mapping_target: F52H3
    Source_location: 225 CHROMOSOME_II 10034088 10034088 From_analysis: Million_mutation_project_reanalysis
    Type_of_mutation: Substitution: G A
    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: WBGene00002497
    Transcript: F52H3.1.3 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F52H3.1.3:c.2093-599C>T
        Intron_number: 10/11
      F52H3.1.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F52H3.1.1:c.2093-599C>T
        Intron_number: 10/11
      F52H3.1.2 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F52H3.1.2:c.2093-599C>T
        Intron_number: 10/11
      F52H3.1.4 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F52H3.1.4:c.2093-599C>T
        Intron_number: 9/10
  Method: WGS_Flibotte