WormBase Tree Display for Variation: WBVar01280827

WBVar01280827 Evidence: Paper_evidence: WBPaper00037807
  Name: Public_name: WBVar01280827
    Other_name: cewivar00504823
      F21A9.2.1:c.145-11T>A
    HGVSg: CHROMOSOME_I:g.3708502A>T
  Sequence_details: SMap: S_parent: Sequence: F21A9
    Flanking_sequences: CCATCTCGAAACCCATCGATTCACCGGTGAAGTTGGAGAGCTGGAAATTA GGAGGTTCTACGGTGCATTTGTGCGGGGAATATGGTGTATTGTGTCTGTC
    Mapping_target: F21A9
    Type_of_mutation: Substitution: a T Paper_evidence: WBPaper00037807
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00022850 From_analysis: WGS_De_Bono
          Million_mutation_project_reanalysis
          WGS_Andersen
      WBStrain00023224 From_analysis: WGS_Andersen
      WBStrain00023234 From_analysis: WGS_Andersen
      WBStrain00023280 From_analysis: WGS_Andersen
      WBStrain00023281 From_analysis: WGS_Andersen
      WBStrain00023311 From_analysis: WGS_Andersen
      WBStrain00031279 From_analysis: WGS_Andersen
      WBStrain00031284 From_analysis: WGS_Andersen
    Laboratory: AX
      QX
    Person: WBPerson1730
    Analysis: WGS_De_Bono
      Million_mutation_project_reanalysis
      WGS_Andersen
    DB_info: Database: dbSNP_ss ss 539141024
    History: Acquires_merge: WBVar01431170
    Status: Live
  Affects: Gene: WBGene00017651
    Transcript: F21A9.2.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F21A9.2.1:c.145-11T>A
        Intron_number: 3/10
  Reference: WBPaper00040707
    WBPaper00037807
  Method: WGS_De_Bono