WormBase Tree Display for Variation: WBVar01720160

WBVar01720160 Name: Public_name: WBVar01720160
    Other_name: cewivar00418315
      C52E12.2a.1:c.599+1278C>T
      C52E12.2a.2:c.599+1278C>T
      C52E12.2b.1:c.599+1278C>T
    HGVSg: CHROMOSOME_II:g.6998431C>T
  Sequence_details: SMap: S_parent: Sequence: C52E12
    Flanking_sequences: CCAATTTTGAAATTCGAATCATAAGGGTCC CCTTATGGTTGAAAAAATTTTTCACCTAAA
    Mapping_target: C52E12
    Source_location: 225 CHROMOSOME_II 6998389 6998389 From_analysis: Million_mutation_project_reanalysis
    Type_of_mutation: Substitution: C T
    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: WBGene00006831
    Transcript: C52E12.2a.2 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C52E12.2a.2:c.599+1278C>T
        Intron_number: 5/23
      C52E12.2b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C52E12.2b.1:c.599+1278C>T
        Intron_number: 5/24
      C52E12.2a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C52E12.2a.1:c.599+1278C>T
        Intron_number: 5/23
  Method: WGS_Flibotte