WormBase Tree Display for Variation: WBVar02133014

WBVar02133014 Evidence: Paper_evidence: WBPaper00045317
  Name: Public_name: h4681
    Other_name: Y39E4B.3c.1:c.594+72G>A
      Y39E4B.3b.1:c.594+72G>A
      Y39E4B.3a.1:c.594+72G>A
    HGVSg: CHROMOSOME_III:g.13096604C>T
  Sequence_details: SMap: S_parent: Sequence: Y39E4B
    Flanking_sequences: CCGACAAATCGGCAAATTGCCGGAACTGAAATTTCTGACAAATCGGCAAATTGCCAGAATTAAAATTTCCGGCAAATCGG AAACTGCCGGAATTGAAATTTCCGGCAAACCGGCAAATTT
    Mapping_target: CHROMOSOME_III
    Source_location: 200 CHROMOSOME_III 13096485 13096485
    Type_of_mutation: Substitution: C T
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023661
    Laboratory: KR
    Analysis: WGS_Rose
    Status: Live
  Affects: Gene: WBGene00004164
    Transcript: Y39E4B.3b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y39E4B.3b.1:c.594+72G>A
        Intron_number: 3/8
      Y39E4B.3c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y39E4B.3c.1:c.594+72G>A
        Intron_number: 3/5
      Y39E4B.3a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y39E4B.3a.1:c.594+72G>A
        Intron_number: 2/6
  Reference: WBPaper00040589
    WBPaper00000975
    WBPaper00003985
    WBPaper00000699
    WBPaper00045317
  Method: WGS_Rose