WormBase Tree Display for Variation: WBVar01419520

WBVar01419520 Evidence: Paper_evidence: WBPaper00037807
  Name: Public_name: WBVar01419520
    Other_name: cewivar00384471
      F12B6.2c.1:c.908-43C>T
      F12B6.2a.1:c.1034-43C>T
    HGVSg: CHROMOSOME_I:g.2253654C>T
  Sequence_details: SMap: S_parent: Sequence: F12B6
    Flanking_sequences: GTCATTTTTAACCGAACTCTTTACGTTTCAAAGTACTCTAACCCACACCA TTGGATGTGACGTCACCGGTGGCCTAACTTTCCCATTTTCAGCCAGTTTT
    Mapping_target: F12B6
    Type_of_mutation: Substitution: c T Paper_evidence: WBPaper00037807
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00006642 From_analysis: WGS_De_Bono
      WBStrain00006643 From_analysis: Million_mutation_project_reanalysis
      WBStrain00006645 From_analysis: Million_mutation_project_reanalysis
    Laboratory: AX
    Analysis: WGS_De_Bono
      Million_mutation_project_reanalysis
    DB_info: Database: dbSNP_ss ss 539127020
    Status: Live
  Affects: Gene: WBGene00017398
    Transcript: F12B6.2c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F12B6.2c.1:c.908-43C>T
        Intron_number: 6/10
      F12B6.2a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F12B6.2a.1:c.1034-43C>T
        Intron_number: 8/13
  Reference: WBPaper00037807
  Method: WGS_De_Bono