WormBase Tree Display for Variation: WBVar01445591

WBVar01445591 Evidence: Paper_evidence: WBPaper00040707
  Name: Public_name: WBVar01445591
    Other_name: F54D8.6.1:c.783+17A>G
    HGVSg: CHROMOSOME_III:g.5104277A>G
  Sequence_details: SMap: S_parent: Sequence: F54D8
    Flanking_sequences: CTGCGCCACCGATTGTGAGTTTTTTTTTCT AAAATGTTTTTTTTTCGAATTCTCAAATTT
    Mapping_target: F54D8
    Type_of_mutation: Substitution: a g
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00004602 From_analysis: WGS_Andersen
      WBStrain00023139 From_analysis: WGS_Andersen
      WBStrain00027648 From_analysis: WGS_Andersen
      WBStrain00027660 From_analysis: WGS_Andersen
      WBStrain00027661 From_analysis: WGS_Andersen
      WBStrain00027662 From_analysis: WGS_Andersen
      WBStrain00027669 From_analysis: WGS_Andersen
    Laboratory: QX
    Person: WBPerson1730
    Analysis: WGS_Andersen
    DB_info: Database: dbSNP_rs rs 193332627
        dbSNP_ss ss 295508546
    Status: Live
  Affects: Gene: WBGene00018802
    Transcript: F54D8.6.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F54D8.6.1:c.783+17A>G
        Intron_number: 4/14
  Reference: WBPaper00040707
  Method: WGS_Andersen