ClinVar Miner

Submissions for variant NM_000027.4(AGA):c.308G>A (p.Gly103Glu)

dbSNP: rs1736932419
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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 RCV001248152 SCV001421621 uncertain significance Aspartylglucosaminuria 2022-07-08 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. 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 expected to disrupt AGA protein function. ClinVar contains an entry for this variant (Variation ID: 972180). This variant has not been reported in the literature in individuals affected with AGA-related conditions. This variant is not present in population databases (gnomAD no frequency). This sequence change replaces glycine, which is neutral and non-polar, with glutamic acid, which is acidic and polar, at codon 103 of the AGA protein (p.Gly103Glu).
Natera, Inc. RCV001248152 SCV002084890 uncertain significance Aspartylglucosaminuria 2021-07-29 no assertion criteria provided clinical testing

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