Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Ce |
RCV000761630 | SCV000891800 | uncertain significance | not provided | 2018-05-01 | criteria provided, single submitter | clinical testing | |
Invitae | RCV000823148 | SCV000963996 | uncertain significance | Neuronopathy, distal hereditary motor, autosomal recessive 4; Charcot-Marie-Tooth disease recessive intermediate C | 2020-02-29 | 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 for this variant, and the functional significance of the affected amino acid(s) is currently unknown. This variant has not been reported in the literature in individuals with PLEKHG5-related conditions. This variant is not present in population databases (ExAC no frequency). This variant, c.1598_1612del, results in the deletion of 5 amino acid(s) of the PLEKHG5 protein (p.Gln533_Arg537del), but otherwise preserves the integrity of the reading frame. |