WormBase Tree Display for Variation: WBVar01310149

WBVar01310149 Evidence: Paper_evidence: WBPaper00037807
  Name: Public_name: WBVar01310149
    Other_name: cewivar00509059
      F26C11.2.1:c.399+129T>C
    HGVSg: CHROMOSOME_II:g.9899187A>G
  Sequence_details: SMap: S_parent: Sequence: F26C11
    Flanking_sequences: CTACTTGTTTGCTATTAGACGCGGGATACGGTAGTCTATGTTGGAGATTC TGGTGAGAACGAGCAGTTCTTTCTAGCATTGATTATCAAAAAGTGGAGCA
    Mapping_target: F26C11
    Type_of_mutation: Substitution: a G 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
    Laboratory: AX
      QX
    Person: WBPerson1730
    Analysis: WGS_De_Bono
      Million_mutation_project_reanalysis
      WGS_Andersen
    DB_info: Database: dbSNP_ss ss 539167414
    History: Acquires_merge: WBVar01439259
    Status: Live
  Affects: Gene: WBGene00006744
    Transcript: F26C11.2.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F26C11.2.1:c.399+129T>C
        Intron_number: 4/7
  Reference: WBPaper00040707
    WBPaper00037807
  Method: WGS_De_Bono