WormBase Tree Display for Variation: WBVar02127908

WBVar02127908 Evidence: Paper_evidence: WBPaper00045317
  Name: Public_name: h8867
    Other_name: F30F8.2.1:c.1142+126A>T
    HGVSg: CHROMOSOME_I:g.7827724T>A
  Sequence_details: SMap: S_parent: Sequence: F30F8
    Flanking_sequences: GGCTGTGCCTAGAAGGGAAGATGGTCTCAAACGCAAAAAA GCAGACCTCATGTCTACCGTGTACCTACAGGCATTTGTAC
    Mapping_target: CHROMOSOME_I
    Source_location: 200 CHROMOSOME_I 7827718 7827718
    Type_of_mutation: Substitution: T A
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023693
    Laboratory: KR
    Analysis: WGS_Rose
    Status: Live
  Affects: Gene: WBGene00009271
    Transcript: F30F8.2.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F30F8.2.1:c.1142+126A>T
        Intron_number: 6/8
  Reference: WBPaper00040589
    WBPaper00000975
    WBPaper00003985
    WBPaper00000699
    WBPaper00045317
  Method: WGS_Rose