ClinVar Miner

Submissions for variant NM_000268.4(NF2):c.1745T>C (p.Leu582Ser)

dbSNP: rs2067498896
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001071119 SCV001236407 uncertain significance Neurofibromatosis, type 2 2019-03-12 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 (SIFT, PolyPhen-2, Align-GVGD) all suggest that this variant is likely to be tolerated, but these predictions have not been confirmed by published functional studies and their clinical significance is uncertain. This variant has not been reported in the literature in individuals with NF2-related conditions. This variant is not present in population databases (ExAC no frequency). This sequence change replaces leucine with serine at codon 582 of the NF2 protein (p.Leu582Ser). The leucine residue is moderately conserved and there is a large physicochemical difference between leucine and serine.

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