ClinVar Miner

Submissions for variant NM_000268.4(NF2):c.1685A>G (p.His562Arg)

dbSNP: rs878853926
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001369166 SCV001565596 uncertain significance Neurofibromatosis, type 2 2021-08-19 criteria provided, single submitter clinical testing This sequence change replaces histidine with arginine at codon 562 of the NF2 protein (p.His562Arg). The histidine residue is moderately conserved and there is a small physicochemical difference between histidine and arginine. This variant is not present in population databases (ExAC no frequency). This variant has not been reported in the literature in individuals with NF2-related conditions. 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: "Tolerated"; PolyPhen-2: "Possibly Damaging"; Align-GVGD: "Class C0"). 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.

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