WormBase Tree Display for Variation: WBVar02138810

WBVar02138810 Evidence: Paper_evidence: WBPaper00045317
  Name: Public_name: h14273
    Other_name: F49H12.1a.1:c.788+103C>T
      F49H12.1b.1:c.710+103C>T
    HGVSg: CHROMOSOME_X:g.2091496C>T
  Sequence_details: SMap: S_parent: Sequence: F49H12
    Flanking_sequences: AATTCTCAGAATTACGGTACATATTATATACATACCTGCT TCCGTGCGTTTGAGAAAGATTTGACATCAATTCAAATTTT
    Mapping_target: CHROMOSOME_X
    Source_location: 200 CHROMOSOME_X 2091491 2091491
    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: WBGene00003087
    Transcript: F49H12.1b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F49H12.1b.1:c.710+103C>T
        Intron_number: 7/10
      F49H12.1a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F49H12.1a.1:c.788+103C>T
        Intron_number: 8/11
  Reference: WBPaper00040589
    WBPaper00000975
    WBPaper00003985
    WBPaper00000699
    WBPaper00045317
  Method: WGS_Rose