WormBase Tree Display for Variation: WBVar02127363

WBVar02127363 Evidence: Paper_evidence: WBPaper00045317
  Name: Public_name: h11632
    Other_name: C01G8.9c.1:c.1499-892T>C
      C01G8.9a.1:c.1256-892T>C
      C01G8.9d.1:c.1418-892T>C
      C01G8.9a.2:c.1256-892T>C
    HGVSg: CHROMOSOME_I:g.5307339A>G
  Sequence_details: SMap: S_parent: Sequence: C01G8
    Flanking_sequences: GAAGGAAAAAAGATAGAGGAGAGGAAGGAATATCGGCTGG GGCGTGGCTTGTTGTTGTAGAAGAGCGACAGCACCTCGAG
    Mapping_target: CHROMOSOME_I
    Source_location: 200 CHROMOSOME_I 5307342 5307342
    Type_of_mutation: Substitution: A G
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023706
    Laboratory: KR
    Analysis: WGS_Rose
    Status: Live
  Affects: Gene: WBGene00002717
    Transcript: C01G8.9d.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C01G8.9d.1:c.1418-892T>C
        Intron_number: 8/14
      C01G8.9a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C01G8.9a.1:c.1256-892T>C
        Intron_number: 8/15
      C01G8.9c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C01G8.9c.1:c.1499-892T>C
        Intron_number: 7/13
      C01G8.9a.2 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C01G8.9a.2:c.1256-892T>C
        Intron_number: 7/14
  Reference: WBPaper00040589
    WBPaper00000975
    WBPaper00003985
    WBPaper00000699
    WBPaper00045317
  Method: WGS_Rose