ClinVar Miner

Submissions for variant NM_001371596.2(MFSD8):c.926A>G (p.Asn309Ser)

dbSNP: rs1737983004
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001348605 SCV001542912 uncertain significance Neuronal ceroid lipofuscinosis 7 2024-01-15 criteria provided, single submitter clinical testing This sequence change replaces asparagine, which is neutral and polar, with serine, which is neutral and polar, at codon 309 of the MFSD8 protein (p.Asn309Ser). This variant is not present in population databases (gnomAD no frequency). This variant has not been reported in the literature in individuals affected with MFSD8-related conditions. ClinVar contains an entry for this variant (Variation ID: 1044369). Advanced modeling of protein sequence and biophysical properties (such as structural, functional, and spatial information, amino acid conservation, physicochemical variation, residue mobility, and thermodynamic stability) performed at Invitae indicates that this missense variant is not expected to disrupt MFSD8 protein function with a negative predictive value of 80%. In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance.
Natera, Inc. RCV001831142 SCV002084780 uncertain significance Late-infantile neuronal ceroid lipofuscinosis 2021-03-10 no assertion criteria provided clinical testing

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