Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV001210203 | SCV001381677 | uncertain significance | Charcot-Marie-Tooth disease axonal type 2P | 2019-06-27 | criteria provided, single submitter | clinical testing | This variant has not been reported in the literature in individuals with LRSAM1-related conditions. This variant is not present in population databases (ExAC no frequency). This variant, c.2161_2163del, results in the deletion of 1 amino acid(s) of the LRSAM1 protein (p.His721del), but otherwise preserves the integrity of the reading frame. Experimental studies and prediction algorithms are not available or were not evaluated for this variant, and the functional significance of the affected amino acid(s) is currently unknown. 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. |