Submissions for variant NM_001242896.3(DEPDC5):c.4747del (p.Arg1583fs)

Total submissions: 1

Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
Labcorp Genetics (formerly Invitae), Labcorp	RCV002852865	SCV003228196	uncertain significance	Familial focal epilepsy with variable foci	2025-01-30	criteria provided, single submitter	clinical testing	This sequence change results in a frameshift in the DEPDC5 gene (p.Arg1583Valfs*49). While this is not anticipated to result in nonsense mediated decay, it is expected to disrupt the last 21 amino acid(s) of the DEPDC5 protein and extend the protein by 27 additional amino acid residues. This variant is not present in population databases (gnomAD no frequency). This frameshift has been observed in individual(s) with clinical features of familial focal epilepsy with variable foci (internal data). ClinVar contains an entry for this variant (Variation ID: 2022943). Experimental studies and prediction algorithms are not available or were not evaluated, and the functional significance of this variant is currently unknown. This variant results in an extension of the DEPDC5 protein. Other variant(s) that result in a similarly extended protein product (p.Arg1583Profs*36) have been observed in individuals with DEPDC5-related disease (internal data). This suggests that these extensions may be clinically significant. 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.