WormBase Tree Display for Variation: WBVar02140652

WBVar02140652 Evidence: Paper_evidence: WBPaper00045317
  Name: Public_name: h7905
    Other_name: T10B10.8.1:c.294+172G>A
    HGVSg: CHROMOSOME_X:g.15165522C>T
  Sequence_details: SMap: S_parent: Sequence: T10B10
    Flanking_sequences: AAACCAAGAAACAGAAACTGGACTCTTAGCAGCGGATCAA ACTCCTTGATTTTTGAAACTTGATTTTGCGGCTCATGGCG
    Mapping_target: CHROMOSOME_X
    Source_location: 200 CHROMOSOME_X 15165442 15165442
    Type_of_mutation: Substitution: C T
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023705
    Laboratory: KR
    Analysis: WGS_Rose
    Status: Live
  Affects: Gene: WBGene00011684
    Transcript: T10B10.8.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T10B10.8.1:c.294+172G>A
        Intron_number: 3/8
  Reference: WBPaper00040589
    WBPaper00000975
    WBPaper00003985
    WBPaper00000699
    WBPaper00045317
  Method: WGS_Rose