WormBase Tree Display for Variation: WBVar02135838

WBVar02135838 Evidence: Paper_evidence: WBPaper00045317
  Name: Public_name: h16393
    Other_name: F44C8.5b.1:c.660+101C>T
      F44C8.5b.2:c.660+101C>T
    HGVSg: CHROMOSOME_V:g.2223028C>T
  Sequence_details: SMap: S_parent: Sequence: F44C8
    Flanking_sequences: TGGCAATTTGTCGATTTTCCGTTTGCCGAACATCAATTTG CGAAAGTTTTTAGAGTGATTTTTCATAAGACGGAAACACT
    Mapping_target: CHROMOSOME_V
    Source_location: 200 CHROMOSOME_V 2223028 2223028
    Type_of_mutation: Substitution: C T
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023752
    Laboratory: KR
    Analysis: WGS_Rose
    Status: Live
  Affects: Gene: WBGene00003718
    Transcript: F44C8.5b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F44C8.5b.1:c.660+101C>T
        Intron_number: 6/9
      F44C8.5b.2 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F44C8.5b.2:c.660+101C>T
        Intron_number: 5/7
  Reference: WBPaper00040589
    WBPaper00000975
    WBPaper00003985
    WBPaper00000699
    WBPaper00045317
  Method: WGS_Rose