ClinVar Miner

Submissions for variant NM_006158.5(NEFL):c.1544AAG[1] (p.Glu516del)

dbSNP: rs758240691
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001327016 SCV001518074 uncertain significance Charcot-Marie-Tooth disease type 2E 2023-03-27 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 NEFL-related conditions. This variant is present in population databases (rs758240691, gnomAD 0.006%). This variant, c.1547_1549del, results in the deletion of 1 amino acid(s) of the NEFL protein (p.Glu516del), but otherwise preserves the integrity of the reading frame.

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