WormBase Tree Display for Variation: WBVar02139893

WBVar02139893 Evidence: Paper_evidence: WBPaper00045317
  Name: Public_name: h7499
    Other_name: F15G9.2.1:c.687+12C>T
      F15G9.6.1:c.73+732G>A
    HGVSg: CHROMOSOME_X:g.9710640G>A
  Sequence_details: SMap: S_parent: Sequence: F15G9
    Flanking_sequences: ATCGAAGGTAGCGAATTGGGTTTCGTGTGATGAATGAATG GTTTTACTTACATACGGTGTCAGTTTATCCTTTATACTGC
    Mapping_target: CHROMOSOME_X
    Source_location: 200 CHROMOSOME_X 9710574 9710574
    Type_of_mutation: Substitution: G A
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023691
    Laboratory: KR
    Analysis: WGS_Rose
    Status: Live
  Affects: Gene: WBGene00008866
      WBGene00008869
    Transcript: F15G9.2.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F15G9.2.1:c.687+12C>T
        Intron_number: 8/11
      F15G9.6.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F15G9.6.1:c.73+732G>A
        Intron_number: 2/4
  Reference: WBPaper00040589
    WBPaper00000975
    WBPaper00003985
    WBPaper00000699
    WBPaper00045317
  Method: WGS_Rose