WormBase Tree Display for Variation: WBVar02126527

WBVar02126527 Evidence: Paper_evidence: WBPaper00045317
  Name: Public_name: h14774
    Other_name: W03F11.6c.1:c.130-359C>G
      W03F11.6a.1:c.130-359C>G
      W03F11.6f.1:c.130-359C>G
      W03F11.6d.1:c.130-359C>G
    HGVSg: CHROMOSOME_I:g.2162659C>G
  Sequence_details: SMap: S_parent: Sequence: W03F11
    Flanking_sequences: TTTTAGGCCATTTTTTGAGGCGTCATAACTTTTTTTTTGA AAGTTTTCAAAAAGTTTCATTATGAAATTCGGTGTTTTCAGGCAATTTTGAGTCTAATATAAAGCATTTAAAAAAATTCG
    Mapping_target: CHROMOSOME_I
    Source_location: 200 CHROMOSOME_I 2162660 2162660
    Type_of_mutation: Substitution: C G
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023781
    Laboratory: KR
    Analysis: WGS_Rose
    Status: Live
  Affects: Gene: WBGene00021009
    Transcript: W03F11.6f.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: W03F11.6f.1:c.130-359C>G
        Intron_number: 2/21
      W03F11.6a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: W03F11.6a.1:c.130-359C>G
        Intron_number: 2/21
      W03F11.6d.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: W03F11.6d.1:c.130-359C>G
        Intron_number: 2/21
      W03F11.6c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: W03F11.6c.1:c.130-359C>G
        Intron_number: 2/21
  Reference: WBPaper00040589
    WBPaper00000975
    WBPaper00003985
    WBPaper00000699
    WBPaper00045317
  Method: WGS_Rose