ClinVar Miner

Submissions for variant NM_003664.5(AP3B1):c.1034G>A (p.Ser345Asn)

gnomAD frequency: 0.00001  dbSNP: rs750036781
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001307170 SCV001496568 uncertain significance Hermansky-Pudlak syndrome 2 2022-02-10 criteria provided, single submitter clinical testing ClinVar contains an entry for this variant (Variation ID: 1009652). 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. Algorithms developed to predict the effect of missense changes on protein structure and function (SIFT, PolyPhen-2, Align-GVGD) all suggest that this variant is likely to be tolerated. This variant has not been reported in the literature in individuals affected with AP3B1-related conditions. This variant is present in population databases (rs750036781, gnomAD 0.01%). This sequence change replaces serine, which is neutral and polar, with asparagine, which is neutral and polar, at codon 345 of the AP3B1 protein (p.Ser345Asn).

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