ClinVar Miner

Submissions for variant NM_000027.4(AGA):c.1000G>T (p.Glu334Ter)

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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 RCV002664353 SCV003525717 uncertain significance Aspartylglucosaminuria 2022-09-13 criteria provided, single submitter clinical testing This sequence change creates a premature translational stop signal (p.Glu334*) in the AGA gene. While this is not anticipated to result in nonsense mediated decay, it is expected to disrupt the last 13 amino acid(s) of the AGA protein. This variant is not present in population databases (gnomAD no frequency). This premature translational stop signal has been observed in individual(s) with clinical features of AGA-related conditions (PMID: 11309371). Experimental studies and prediction algorithms are not available or were not evaluated, and the functional significance of this variant is currently unknown. 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.

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