ClinVar Miner

Submissions for variant NM_000036.3(AMPD1):c.247A>G (p.Asn83Asp)

dbSNP: rs749940824
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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 RCV001949112 SCV002208962 uncertain significance Muscle AMP deaminase deficiency 2022-08-09 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. 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. ClinVar contains an entry for this variant (Variation ID: 1438943). This variant has not been reported in the literature in individuals affected with AMPD1-related conditions. This variant is present in population databases (rs749940824, gnomAD 0.0009%). This sequence change replaces asparagine, which is neutral and polar, with aspartic acid, which is acidic and polar, at codon 116 of the AMPD1 protein (p.Asn116Asp).

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