ClinVar Miner

Submissions for variant NM_003664.5(AP3B1):c.2673G>C (p.Gln891His)

dbSNP: rs770455413
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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 RCV000688317 SCV000815923 uncertain significance Hermansky-Pudlak syndrome 2 2023-07-07 criteria provided, single submitter clinical testing 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. An algorithm developed to predict the effect of missense changes on protein structure and function (PolyPhen-2) suggests that this variant is likely to be tolerated. ClinVar contains an entry for this variant (Variation ID: 568074). This variant has not been reported in the literature in individuals affected with AP3B1-related conditions. This variant is present in population databases (rs770455413, gnomAD 0.003%). This sequence change replaces glutamine, which is neutral and polar, with histidine, which is basic and polar, at codon 891 of the AP3B1 protein (p.Gln891His).

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