WormBase Tree Display for Variation: WBVar01453917

WBVar01453917 Evidence: Paper_evidence: WBPaper00040707
  Name: Public_name: WBVar01453917
    Other_name: cewivar00497703
      K11E8.1r.1:c.25+182A>G
    HGVSg: CHROMOSOME_IV:g.10350011T>C
  Sequence_details: SMap: S_parent: Sequence: Y43C5B
    Flanking_sequences: AATGTACCCCGCATTTCTTATCTTACAAAT AAAAAAAAGTTTCATGATATAAATTTTGTG
    Mapping_target: Y43C5B
    Type_of_mutation: Substitution: t c
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00004597 From_analysis: WGS_Andersen
      WBStrain00006363 From_analysis: WGS_Andersen
      WBStrain00023072 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023286 From_analysis: Million_mutation_project_reanalysis
          WGS_Andersen
      WBStrain00023311 From_analysis: WGS_Andersen
      WBStrain00027653 From_analysis: WGS_Andersen
      WBStrain00027656 From_analysis: WGS_Andersen
      WBStrain00031279 From_analysis: WGS_Andersen
      WBStrain00031284 From_analysis: WGS_Andersen
      WBStrain00033541 From_analysis: WGS_Andersen
    Laboratory: QX
    Person: WBPerson1730
    Analysis: Million_mutation_project_reanalysis
      WGS_Andersen
    DB_info: Database: dbSNP_rs rs 193339574
        dbSNP_ss ss 295515493
    Status: Live
  Affects: Gene: WBGene00006779
    Transcript: K11E8.1r.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: K11E8.1r.1:c.25+182A>G
        Intron_number: 1/18
  Reference: WBPaper00040707
  Method: WGS_Andersen