WormBase Tree Display for Variation: WBVar02139902

WBVar02139902 Evidence: Paper_evidence: WBPaper00045317
  Name: Public_name: h14290
    Other_name: T09B9.2.1:c.429-42G>A
    HGVSg: CHROMOSOME_X:g.9763697C>T
  Sequence_details: SMap: S_parent: Sequence: T09B9
    Flanking_sequences: TGAAAGTTGATGAGAATAAGTGAGGTTCTAAGATGAAGGT TAAGGGGAATTGAGTTCATTGAACTGAATTTCATCTTTCT
    Mapping_target: CHROMOSOME_X
    Source_location: 200 CHROMOSOME_X 9763631 9763631
    Type_of_mutation: Substitution: C T
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023854
    Laboratory: KR
    Analysis: WGS_Rose
    Status: Live
  Affects: Gene: WBGene00011643
    Transcript: T09B9.2.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T09B9.2.1:c.429-42G>A
        Intron_number: 3/10
  Reference: WBPaper00040589
    WBPaper00000975
    WBPaper00003985
    WBPaper00000699
    WBPaper00045317
  Method: WGS_Rose