WormBase Tree Display for Variation: WBVar01460261

WBVar01460261 Evidence: Paper_evidence: WBPaper00040707
  Name: Public_name: WBVar01460261
    Other_name: W01A11.3b.2:c.301-216G>A
      W01A11.3a.1:c.499-216G>A
      W01A11.3b.1:c.301-216G>A
    HGVSg: CHROMOSOME_V:g.6476928G>A
  Sequence_details: SMap: S_parent: Sequence: W01A11
    Flanking_sequences: CATTACCCTTATCTTCCTCTTCTTTTTTCA TTCTTCACATATTTCAAACCATTTGATGTT
    Mapping_target: W01A11
    Type_of_mutation: Substitution: g a
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00031279 From_analysis: WGS_Andersen
      WBStrain00031284 From_analysis: WGS_Andersen
    Laboratory: QX
    Person: WBPerson1730
    Analysis: WGS_Andersen
    DB_info: Database: dbSNP_rs rs 193345918
        dbSNP_ss ss 295521837
    Status: Live
  Affects: Gene: WBGene00006815
    Transcript: W01A11.3a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: W01A11.3a.1:c.499-216G>A
        Intron_number: 6/17
      W01A11.3b.2 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: W01A11.3b.2:c.301-216G>A
        Intron_number: 5/16
      W01A11.3b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: W01A11.3b.1:c.301-216G>A
        Intron_number: 4/15
  Reference: WBPaper00040707
  Method: WGS_Andersen