ClinVar Miner

Submissions for variant NM_000152.5(GAA):c.1629_1630delinsTA (p.Val544Met)

dbSNP: rs1598582152
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000822287 SCV000963082 uncertain significance Glycogen storage disease, type II 2024-01-12 criteria provided, single submitter clinical testing This sequence change replaces valine, which is neutral and non-polar, with methionine, which is neutral and non-polar, at codon 544 of the GAA protein (p.Val544Met). Information on the frequency of this variant in the gnomAD database is not available, as this variant may be reported differently in the database. This variant has not been reported in the literature in individuals affected with GAA-related conditions. ClinVar contains an entry for this variant (Variation ID: 664232). 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.
Fulgent Genetics, Fulgent Genetics RCV000822287 SCV002781530 uncertain significance Glycogen storage disease, type II 2021-10-04 criteria provided, single submitter clinical testing

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