WormBase Tree Display for Variation: WBVar02136833

WBVar02136833 Evidence: Paper_evidence: WBPaper00045317
  Name: Public_name: h12482
    Other_name: T18H9.1b.1:c.1700+31G>A
      T18H9.1a.1:c.1535+31G>A
      T18H9.1d.1:c.1505+31G>A
      T18H9.1c.1:c.1481+31G>A
      T18H9.1g.1:c.1340+31G>A
      T18H9.1f.1:c.1316+31G>A
    HGVSg: CHROMOSOME_V:g.9224091G>A
  Sequence_details: SMap: S_parent: Sequence: F07C3
    Flanking_sequences: TTGAAGGAAGGTGAGCTTGCGTGTTCATAAATAATATATA AACCCTGCTTGCAATTTTTTTATTTTCTATTTTACAACTT
    Mapping_target: CHROMOSOME_V
    Source_location: 200 CHROMOSOME_V 9224065 9224065
    Type_of_mutation: Substitution: G A
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023780
    Laboratory: KR
    Analysis: WGS_Rose
    Status: Live
  Affects: Gene: WBGene00001695
    Transcript: T18H9.1g.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T18H9.1g.1:c.1340+31G>A
        Intron_number: 8/8
      T18H9.1d.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T18H9.1d.1:c.1505+31G>A
        Intron_number: 9/10
      T18H9.1a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T18H9.1a.1:c.1535+31G>A
        Intron_number: 9/10
      T18H9.1f.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T18H9.1f.1:c.1316+31G>A
        Intron_number: 9/10
      T18H9.1c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T18H9.1c.1:c.1481+31G>A
        Intron_number: 9/10
      T18H9.1b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T18H9.1b.1:c.1700+31G>A
        Intron_number: 9/10
  Reference: WBPaper00040589
    WBPaper00000975
    WBPaper00003985
    WBPaper00000699
    WBPaper00045317
  Method: WGS_Rose