Total submissions: 1
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. |