ClinVar Miner

Submissions for variant NM_000027.4(AGA):c.698+1del

dbSNP: rs2111013273
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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 RCV001389042 SCV001590247 pathogenic Aspartylglucosaminuria 2020-03-08 criteria provided, single submitter clinical testing For these reasons, this variant has been classified as Pathogenic. Loss-of-function variants in AGA are known to be pathogenic (PMID: 7627186, 11309371). This variant has not been reported in the literature in individuals with AGA-related conditions. This variant is not present in population databases (ExAC no frequency). This sequence change creates a premature translational stop signal (p.Gly233Alafs*3) in the AGA gene. It is expected to result in an absent or disrupted protein product.

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