WormBase Tree Display for Variation: WBVar01470599

WBVar01470599 Evidence: Paper_evidence: WBPaper00040707
  Name: Public_name: WBVar01470599
    Other_name: cewivar00602781
      F15G9.2.1:c.894+229G>T
      F15G9.6.1:c.73+88C>A
    HGVSg: CHROMOSOME_X:g.9709996C>A
  Sequence_details: SMap: S_parent: Sequence: F15G9
    Flanking_sequences: AACGCATTGCAAATGAGCAAACAGTTTAAG TGATTTTCAAAAACTAATAAAGACTTTAAA
    Mapping_target: F15G9
    Type_of_mutation: Substitution: c a
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023072 From_analysis: Million_mutation_project_reanalysis
          WGS_Andersen
      WBStrain00023084 From_analysis: WGS_Andersen
    Laboratory: QX
    Person: WBPerson1730
    Analysis: Million_mutation_project_reanalysis
      WGS_Andersen
    DB_info: Database: dbSNP_rs rs 193355901
        dbSNP_ss ss 295531820
    Status: Live
  Affects: Gene: WBGene00008866
      WBGene00008869
    Transcript: F15G9.2.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F15G9.2.1:c.894+229G>T
        Intron_number: 10/11
      F15G9.6.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F15G9.6.1:c.73+88C>A
        Intron_number: 2/4
  Reference: WBPaper00040707
  Method: WGS_Andersen