WormBase Tree Display for Variation: WBVar02139906

WBVar02139906 Evidence: Paper_evidence: WBPaper00045317
  Name: Public_name: h18126
    Other_name: F47A4.2.1:c.108+43G>A
    HGVSg: CHROMOSOME_X:g.9822020C>T
  Sequence_details: SMap: S_parent: Sequence: F47A4
    Flanking_sequences: CAAGCTAATCATCCCCTAGTACCTCCATAGTTACATTGCA TCTGTTTGAGCATCTTTTTCCTCGCCCTGGCACGACACTC
    Mapping_target: CHROMOSOME_X
    Source_location: 200 CHROMOSOME_X 9821954 9821954
    Type_of_mutation: Substitution: C T
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023728
    Laboratory: KR
    Analysis: WGS_Rose
    Status: Live
  Affects: Gene: WBGene00001081
    Transcript: F47A4.2.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F47A4.2.1:c.108+43G>A
        Intron_number: 2/20
  Reference: WBPaper00040589
    WBPaper00000975
    WBPaper00003985
    WBPaper00000699
    WBPaper00045317
  Method: WGS_Rose