ClinVar Miner

Submissions for variant NM_003190.5(TAPBP):c.1069G>A (p.Asp357Asn)

gnomAD frequency: 0.00007  dbSNP: rs376210117
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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 RCV000698594 SCV000827267 uncertain significance MHC class I deficiency 2023-06-05 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 disruptive. ClinVar contains an entry for this variant (Variation ID: 576167). This variant has not been reported in the literature in individuals affected with TAPBP-related conditions. This variant is present in population databases (rs376210117, gnomAD 0.008%). This sequence change replaces aspartic acid, which is acidic and polar, with asparagine, which is neutral and polar, at codon 357 of the TAPBP protein (p.Asp357Asn).

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