WormBase Tree Display for Variation: WBVar01435868

WBVar01435868 Evidence: Paper_evidence: WBPaper00040707
  Name: Public_name: WBVar01435868
    Other_name: cewivar00079321
      F47F6.9b.1:c.195-13G>T
      F47F6.9a.1:c.1194-13G>T
    HGVSg: CHROMOSOME_II:g.1262355G>T
  Sequence_details: SMap: S_parent: Sequence: F47F6
    Flanking_sequences: TGGGTCTTAAAATCGGCCAAATGAACTATA CACAAATTACAGAGGAAGCCTGTCGAATTC
    Mapping_target: F47F6
    Type_of_mutation: Substitution: g t
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain (45)
    Laboratory: QX
    Person: WBPerson1730
    Analysis: Million_mutation_project_reanalysis
      WGS_Andersen
    DB_info: Database: dbSNP_rs rs 193323930
        dbSNP_ss ss 295499848
    Status: Live
  Affects: Gene: WBGene00305421
      WBGene00023410
    Transcript: F47F6.16
      F47F6.9b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F47F6.9b.1:c.195-13G>T
        Intron_number: 1/2
      F47F6.9a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F47F6.9a.1:c.1194-13G>T
        Intron_number: 9/11
  Reference: WBPaper00040707
  Method: WGS_Andersen