WormBase Tree Display for Variation: WBVar02139051

WBVar02139051 Evidence: Paper_evidence: WBPaper00045317
  Name: Public_name: h7683
    Other_name: C02F12.10a.1:c.293+80T>A
    HGVSg: CHROMOSOME_X:g.3673167A>T
  Sequence_details: SMap: S_parent: Sequence: C02F12
    Flanking_sequences: TTCAAAACTGGGATGTACCAACAATTTTAACATGAAAATT AAAAAAAAAACATTTAAACTTGCTTCGACCATTACTAATA
    Mapping_target: CHROMOSOME_X
    Source_location: 200 CHROMOSOME_X 3673155 3673155
    Type_of_mutation: Substitution: A T
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023700
    Laboratory: KR
    Analysis: WGS_Rose
    Status: Live
  Affects: Gene: WBGene00045215
    Transcript: C02F12.10a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C02F12.10a.1:c.293+80T>A
        Intron_number: 5/6
  Reference: WBPaper00040589
    WBPaper00000975
    WBPaper00003985
    WBPaper00000699
    WBPaper00045317
  Method: WGS_Rose