WormBase Tree Display for Variation: WBVar01439144

WBVar01439144 Evidence: Paper_evidence: WBPaper00040707
  Name: Public_name: WBVar01439144
    Other_name: F35H8.5a.1:c.60+13T>C
    HGVSg: CHROMOSOME_II:g.9576380T>C
  Sequence_details: SMap: S_parent: Sequence: F35H8
    Flanking_sequences: CCGACGAGTCCCGTTCAGGTAATTTTTTTT TCAATTTTTATTAGGAAAGATCTATATGAA
    Mapping_target: F35H8
    Type_of_mutation: Substitution: t c
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00006635 From_analysis: WGS_Andersen
      WBStrain00006637 From_analysis: WGS_Andersen
      WBStrain00022850 From_analysis: WGS_Andersen
      WBStrain00022958 From_analysis: WGS_Andersen
      WBStrain00022960 From_analysis: WGS_Andersen
      WBStrain00027653 From_analysis: WGS_Andersen
      WBStrain00027656 From_analysis: WGS_Andersen
      WBStrain00031279 From_analysis: WGS_Andersen
      WBStrain00031284 From_analysis: WGS_Andersen
    Laboratory: QX
    Person: WBPerson1730
    Analysis: WGS_Andersen
    DB_info: Database: dbSNP_rs rs 193327205
        dbSNP_ss ss 295503124
    Status: Live
  Affects: Gene: WBGene00001368
    Transcript: F35H8.5a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F35H8.5a.1:c.60+13T>C
        Intron_number: 2/8
  Reference: WBPaper00040707
  Method: WGS_Andersen