WormBase Tree Display for Variation: WBVar01439655

WBVar01439655 Evidence: Paper_evidence: WBPaper00040707
  Name: Public_name: WBVar01439655
    Other_name: cewivar00094616
      C52A11.4g.1:c.6+430C>T
      C52A11.4e.1:c.6+430C>T
      C52A11.4b.1:c.633+430C>T
      C52A11.4f.1:c.633+430C>T
      C52A11.4d.1:c.720+430C>T
      C52A11.4a.1:c.633+430C>T
    HGVSg: CHROMOSOME_II:g.10766206G>A
  Sequence_details: SMap: S_parent: Sequence: T19E10
    Flanking_sequences: TTTAAAAAATTTAAACCAAGACATGGGAGG GTCTATTTTGATATTTTGTTTTACCTCGAA
    Mapping_target: T19E10
    Type_of_mutation: Substitution: g a
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain (26)
    Laboratory: QX
    Person: WBPerson1730
    Analysis: Million_mutation_project_reanalysis
      WGS_Andersen
    DB_info: Database: dbSNP_rs rs 193327716
        dbSNP_ss ss 295503635
    Status: Live
  Affects: Gene: WBGene00003404
    Transcript: C52A11.4b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C52A11.4b.1:c.633+430C>T
        Intron_number: 8/19
      C52A11.4f.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C52A11.4f.1:c.633+430C>T
        Intron_number: 7/42
      C52A11.4g.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C52A11.4g.1:c.6+430C>T
        Intron_number: 6/40
      C52A11.4e.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C52A11.4e.1:c.6+430C>T
        Intron_number: 1/35
      C52A11.4d.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C52A11.4d.1:c.720+430C>T
        Intron_number: 8/42
      C52A11.4a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C52A11.4a.1:c.633+430C>T
        Intron_number: 8/43
  Reference: WBPaper00040707
  Method: WGS_Andersen