Description
The p.Arg476Gln variant in SMPD1 (also known as p.Arg474Gln due to a difference in cDNA numbering) has been reported in 1 individual with Niemann-Pick disease (PMID: 264991070) and has been identified in 0.016% (5/30616) of South Asian chromosomes and 0.003% (3/113764) of European (non-Finnish) chromosomes by the Genome Aggregation Database (gnomAD, http://gnomad.broadinstitute.org; dbSNP rs763566905). Although this variant has been seen in the general population, its frequency is low enough to be consistent with a recessive carrier frequency. This variant has also been reported in ClinVar (VariationID: 285606) as likely pathogenic by GeneDx. 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 combination with reported pathogenic variant and in an individual with Niemann-Pick disease increases the likelihood that the p.Arg476Gln variant is pathogenic (VariationID: 592260; VariationID: 264991070). One additional pathogenic variant, resulting in a different amino acid change at the same position, p.Arg476Trp, has been reported in association with disease in the literature and ClinVar, supporting that a change at this position may not be tolerated (VariationID: 93315; PMID: 31122880, 12712061, 23252888, 19405096, 29995201, 12369017). In summary, although additional studies are required to fully establish its clinical significance, this variant is likely pathogenic. ACMG/AMP Criteria applied: PM5, PM3, PM2_supporting, PP3 (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 |
