Full data view for gene PIGL

Information The variants shown are described using the NM_004278.3 transcript reference sequence.

2 entries on 1 page. Showing entries 1 - 2.
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AscendingDNA change (cDNA)     

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+/. - c.60G>A r.(?) p.(Trp20*) Unknown - pathogenic g.16120600G>A g.16217286G>A - - PIGL_000015 Compound Heterozygous. Two variants in PIGL gene. This is a nonsense (c.60G > A; p.Trp20Ter; W20X) pathogenic variant. It was interpreted as pathogenic as it causes loss of normal protein function through truncation or nonsense-mediated mRNA decay. - - - Germline/De novo (untested) - - - - - DNA SEQ - Commercially available multigene panel for intellectual disability (GeneDx), Sanger sequencing  HPMRS1;GPIBD2 Patient 1 PubMed: Altassan et al., 2018 Individual presented with the main features of HPMRS; developmental delay, cognitive impairment, seizure disorder, skeletal deformities, and high alkaline phosphatase.  M no - - >10y - - Anti-epileptic medications 1 Philippe Campeau
+/. - c.60G>A r.(?) p.(Trp20*) Unknown - pathogenic g.16120600G>A g.16217286G>A - - PIGL_000015 Compound heterozygous. The first variant (c.60G > A; p.Trp20Ter; W20X) is a nonsense variant and was interpreted as pathogenic as it causes loss of normal protein function through truncation or nonsense-mediated mRNA decay. - - - Germline/De novo (untested) - - - - - DNA SEQ - Commercially available multigene panel for intellectual disability (GeneDx), Sanger sequencing  HPMRS1;GPIBD2 Patient 2 PubMed: Altassan et al., 2018 Patient 1's younger brother M no - - >04y - - Anti-epileptic medications. Surgical correction of strabismus. 1 Philippe Campeau
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