WormBase Tree Display for Variation: WBVar01470382

WBVar01470382 Evidence: Paper_evidence: WBPaper00040707
  Name: Public_name: WBVar01470382
    Other_name: cewivar00060189
      C25A11.4c.1:c.456+191G>A
      C25A11.4a.1:c.-820+191G>A
      C25A11.4b.1:c.456+191G>A
      C25A11.4d.1:c.456+191G>A
      C25A11.4f.1:c.456+191G>A
    HGVSg: CHROMOSOME_X:g.9088900G>A
  Sequence_details: SMap: S_parent: Sequence: H08J11
    Flanking_sequences: TAGGCGGAAGGAGGATTGTTAGGTGTAAAT TCTTTGAAGACAATGGAGACAGTCCCGAAT
    Mapping_target: H08J11
    Type_of_mutation: Substitution: g a
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain (76)
    Laboratory: QX
    Person: WBPerson1730
    Analysis: Million_mutation_project_reanalysis
      WGS_Andersen
    DB_info: Database: dbSNP_rs rs 193355684
        dbSNP_ss ss 295531603
    Status: Live
  Affects: Gene: WBGene00000100
    Transcript: C25A11.4d.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C25A11.4d.1:c.456+191G>A
        Intron_number: 5/29
      C25A11.4a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C25A11.4a.1:c.-820+191G>A
        Intron_number: 4/30
      C25A11.4f.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C25A11.4f.1:c.456+191G>A
        Intron_number: 4/28
      C25A11.4c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C25A11.4c.1:c.456+191G>A
        Intron_number: 5/23
      C25A11.4b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C25A11.4b.1:c.456+191G>A
        Intron_number: 4/18
  Reference: WBPaper00040707
  Method: WGS_Andersen