ClinVar Miner

Submissions for variant NM_000268.4(NF2):c.1770CTT[1] (p.Phe592del)

dbSNP: rs2067500115
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001306432 SCV001495804 uncertain significance Neurofibromatosis, type 2 2022-07-01 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. Experimental studies and prediction algorithms are not available or were not evaluated, and the functional significance of this variant is currently unknown. This variant has not been reported in the literature in individuals affected with NF2-related conditions. This variant is not present in population databases (gnomAD no frequency). This variant, c.1773_1775del, results in the deletion of 1 amino acid(s) of the NF2 protein (p.Phe592del), but otherwise preserves the integrity of the reading frame.

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