WormBase Tree Display for Variation: WBVar01451962

WBVar01451962 Evidence: Paper_evidence: WBPaper00040707
  Name: Public_name: WBVar01451962
    Other_name: F56D6.2.1:c.1370+22T>C
      F56D6.2.2:c.1370+22T>C
    HGVSg: CHROMOSOME_IV:g.3924364T>C
  Sequence_details: SMap: S_parent: Sequence: F56D6
    Flanking_sequences: CAGCCCATAGTGAGTAGTTTATTTGATGAA ATAGTTCTAAAAAGCCTTTTTTCAGCGCCACAACCTATTGGTTGCCGTATTCTGATTAAGGACATTGTAA
    Mapping_target: F56D6
    Type_of_mutation: Substitution: t c
    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 193337619
        dbSNP_ss ss 295513538
    Status: Live
  Affects: Gene: WBGene00018971
    Transcript: F56D6.2.2 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F56D6.2.2:c.1370+22T>C
        Intron_number: 9/10
      F56D6.2.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F56D6.2.1:c.1370+22T>C
        Intron_number: 9/10
  Reference: WBPaper00040707
  Method: WGS_Andersen