WormBase Tree Display for Variation: WBVar01307292

WBVar01307292 Evidence: Paper_evidence: WBPaper00037807
  Name: Public_name: WBVar01307292
    Other_name: cewivar00355781
      F22D3.2f.1:c.1019+608C>T
      F22D3.2j.1:c.1010+608C>T
      F22D3.2d.1:c.1019+608C>T
      F22D3.2g.1:c.1019+608C>T
      F22D3.2e.1:c.1010+608C>T
    HGVSg: CHROMOSOME_II:g.6934763C>T
  Sequence_details: SMap: S_parent: Sequence: F22D3
    Flanking_sequences: CACAATTGACTCGTTTTTTCGGTATAATTAAAACTAATTGATTACTTTTG TCCTTGTAGGCAATTTATGTGCAGGATATTAGCGTTGATCTTATTTCGAT
    Mapping_target: F22D3
    Type_of_mutation: Substitution: c T Paper_evidence: WBPaper00037807
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00006637 From_analysis: Million_mutation_project_reanalysis
      WBStrain00022850 From_analysis: Million_mutation_project_reanalysis
          WGS_De_Bono
      WBStrain00023286 From_analysis: Million_mutation_project_reanalysis
    Laboratory: AX
    Analysis: WGS_De_Bono
      Million_mutation_project_reanalysis
    DB_info: Database: dbSNP_ss ss 539164843
    Status: Live
  Affects: Gene: WBGene00017699
    Transcript: F22D3.2g.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F22D3.2g.1:c.1019+608C>T
        Intron_number: 12/18
      F22D3.2e.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F22D3.2e.1:c.1010+608C>T
        Intron_number: 12/18
      F22D3.2d.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F22D3.2d.1:c.1019+608C>T
        Intron_number: 12/18
      F22D3.2f.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F22D3.2f.1:c.1019+608C>T
        Intron_number: 10/10
      F22D3.2j.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F22D3.2j.1:c.1010+608C>T
        Intron_number: 12/18
  Reference: WBPaper00037807
  Method: WGS_De_Bono