ClinVar Miner

Submissions for variant NM_198586.3(NHLRC1):c.1039G>A (p.Gly347Arg)

dbSNP: rs1783733675
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001202489 SCV001373602 uncertain significance Lafora disease 2021-01-16 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 are either unavailable or do not agree on the potential impact of this missense change (SIFT: "Deleterious"; PolyPhen-2: "Possibly Damaging"; Align-GVGD: "Class C0"). This variant has not been reported in the literature in individuals with NHLRC1-related conditions. This variant is not present in population databases (ExAC no frequency). This sequence change replaces glycine with arginine at codon 347 of the NHLRC1 protein (p.Gly347Arg). The glycine residue is highly conserved and there is a moderate physicochemical difference between glycine and arginine.

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