Description
The p.Arg498Leu variant in SMPD1 (also known as p.Arg496Leu due to a difference in cDNA numbering) has been reported in at least 5 individuals with Niemann-Pick disease (PMID: 2023926, 29995201, 15221801, 18815062) and has been identified in 0.280% (29/10346) of Ashkenazi Jewish chromosomes and 0.005% (6/128826) of European (non-Finnish) chromosomes by the Genome Aggregation Database (gnomAD, http://gnomad.broadinstitute.org; dbSNP rs120074117). Although this variant has been seen in the general population, its frequency is not high enough to rule out a pathogenic role due to the increased carrier frequency of this variant in the Ashkenazi Jewish population. This variant has also been reported in ClinVar (VariationID: 2980) as pathogenic by 8 submitters. Animal models in mice have shown that this variant causes Niemann-Pick disease (PMID: 18815062). In vitro functional studies provide additional evidence that the p.Arg498Leu variant may impact protein function (PMID: 18815062). However, these types of assays may not accurately represent biological function. Computational prediction tools and conservation analyses suggest that this variant may impact the protein, though this information is not predictive enough to determine pathogenicity. The presence of this variant in 3 affected homozygotes and in combination with a reported pathogenic variant in 2 individuals with Niemann-Pick disease increases the likelihood that the p.Arg498Leu variant is pathogenic (VariationID: 198093; PMID: 2023926, 29995201, 15221801, 18815062). The phenotype of an individual homozygous for this variant is highly specific for Niemann-Pick disease based on acid sphingomyelinase activity being <10% of normal, consistent with disease (PMID: 18815062). Multiple variants in the same region as p.Arg498Cys have been reported in association with disease in ClinVar and the literature and the variant is located in a region of SMPD1 that is essential to protein folding and stability, suggesting that this variant is in a hot spot and functional domain and supports pathogenicity (VariationID: 167712, 198095; PMID: 18815062, 27725636; DOI: 10.1111/febs.13655). In summary, this variant meets criteria to be classified as pathogenic for Niemann-Pick disease in an autosomal recessive manner based on mouse models, the presence of the variant in affected homozygotes and compound heterozygotes, and the phenotype of individuals with the variant being highly specific for severe disease. ACMG/AMP Criteria applied: PM3_strong, PS3, PP3, PP4, PM1 (Richards 2015).
| # | Sample | Method | Observation |
|---|
| Origin | Affected | Number tested | Tissue | Purpose | Method | Individuals | Allele frequency | Families | Co-occurrences |
|---|
| 1 | germline | unknown | not provided | not provided | not provided | | not provided | not provided | not provided | not provided |
