WormBase Tree Display for Variation: WBVar02128555

WBVar02128555 Evidence: Paper_evidence: WBPaper00045317
  Name: Public_name: h11878
    Other_name: F15D3.1a.1:c.3622-106G>A
      F15D3.1j.1:c.145-106G>A
      F15D3.1c.1:c.2944-106G>A
      F15D3.1d.1:c.145-106G>A
      F15D3.1h.1:c.3622-106G>A
      F15D3.1i.1:c.2944-106G>A
    HGVSg: CHROMOSOME_I:g.11546307C>T
  Sequence_details: SMap: S_parent: Sequence: F15D3
    Flanking_sequences: TAGAACTTTCCTAGGCCACCAATTTCAAATGTTTGTAACT TGCCTAAAATTGAGATTTCTGACTGTTTCAAAACGCGTCA
    Mapping_target: CHROMOSOME_I
    Source_location: 200 CHROMOSOME_I 11546297 11546297
    Type_of_mutation: Substitution: C T
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023743
    Laboratory: KR
    Analysis: WGS_Rose
    Status: Live
  Affects: Gene: WBGene00001131
    Transcript: F15D3.1j.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F15D3.1j.1:c.145-106G>A
        Intron_number: 10/39
      F15D3.1a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F15D3.1a.1:c.3622-106G>A
        Intron_number: 17/48
      F15D3.1d.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F15D3.1d.1:c.145-106G>A
        Intron_number: 1/31
      F15D3.1i.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F15D3.1i.1:c.2944-106G>A
        Intron_number: 12/41
      F15D3.1c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F15D3.1c.1:c.2944-106G>A
        Intron_number: 12/42
      F15D3.1h.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F15D3.1h.1:c.3622-106G>A
        Intron_number: 16/46
  Reference: WBPaper00040589
    WBPaper00000975
    WBPaper00003985
    WBPaper00000699
    WBPaper00045317
  Method: WGS_Rose