ClinVar Miner

Submissions for variant NM_025132.4(WDR19):c.2972A>G (p.Asn991Ser)

gnomAD frequency: 0.00003  dbSNP: rs763190830
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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 RCV002034369 SCV002308155 uncertain significance Asphyxiating thoracic dystrophy 5; Senior-Loken syndrome 8 2023-05-15 criteria provided, single submitter clinical testing ClinVar contains an entry for this variant (Variation ID: 1522330). This variant has not been reported in the literature in individuals affected with WDR19-related conditions. This variant is present in population databases (rs763190830, gnomAD 0.06%). This sequence change replaces asparagine, which is neutral and polar, with serine, which is neutral and polar, at codon 991 of the WDR19 protein (p.Asn991Ser). 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 WDR19 protein function. 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.
Fulgent Genetics, Fulgent Genetics RCV005032135 SCV005665243 uncertain significance Asphyxiating thoracic dystrophy 5; Nephronophthisis 13; Cranioectodermal dysplasia 4; Senior-Loken syndrome 8; Spermatogenic failure 72 2024-05-30 criteria provided, single submitter clinical testing

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