WormBase Tree Display for Variation: WBVar02133119

WBVar02133119 Evidence: Paper_evidence: WBPaper00045317
  Name: Public_name: h16665
    Other_name: B0545.1b.2:c.-133+1461G>A
      B0545.1b.1:c.-133+1461G>A
      B0545.1a.1:c.279+1461G>A
    HGVSg: CHROMOSOME_IV:g.95291G>A
  Sequence_details: SMap: S_parent: Sequence: B0545
    Flanking_sequences: TAAATTTCGGCTCCTAAACTCCATTGCCTCCTAGATTTCT GTTTTCTTTTCGAAGCTCGGTCGGTTGAGCAAATTTTGAA
    Mapping_target: CHROMOSOME_IV
    Source_location: 200 CHROMOSOME_IV 95291 95291
    Type_of_mutation: Substitution: G A
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023759
    Laboratory: KR
    Analysis: WGS_Rose
    Status: Live
  Affects: Gene: WBGene00006599
    Transcript: B0545.1b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: B0545.1b.1:c.-133+1461G>A
        Intron_number: 4/13
      B0545.1a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: B0545.1a.1:c.279+1461G>A
        Intron_number: 4/12
      B0545.1b.2 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: B0545.1b.2:c.-133+1461G>A
        Intron_number: 2/10
  Reference: WBPaper00040589
    WBPaper00000975
    WBPaper00003985
    WBPaper00000699
    WBPaper00045317
  Method: WGS_Rose