ClinVar Miner

Submissions for variant NM_000268.4(NF2):c.1088T>A (p.Met363Lys)

dbSNP: rs2066804849
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001245353 SCV001418636 uncertain significance Neurofibromatosis, type 2 2019-10-25 criteria provided, single submitter clinical testing This variant is not present in population databases (ExAC no frequency). This sequence change replaces methionine with lysine at codon 363 of the NF2 protein (p.Met363Lys). The methionine residue is weakly conserved and there is a moderate physicochemical difference between methionine and lysine. This variant has not been reported in the literature in individuals with NF2-related conditions. 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: "Benign"; Align-GVGD: "Class C0").

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