Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV001008424 | SCV001168193 | likely pathogenic | not provided | 2018-10-25 | criteria provided, single submitter | clinical testing | A variant that is likely pathogenic has been identified in the DEPDC5 gene. The c.944_945delAT variant has not been published as a pathogenic variant, nor has it been reported as a benign variant to our knowledge. The c.944_945delAT variant is not observed in large population cohorts (Lek et al., 2016). The c.944_945delAT variant in the DEPDC5 gene causes a frameshift starting with codon Asparagine 315, changes this amino acid to a Serine residue and creates a premature Stop codon at position 3 of the new reading frame, denoted p.Asn315SerfsX3. This variant is predicted to cause loss of normal protein function either through protein truncation or nonsense-mediated mRNA decay. Therefore, this variant is likely pathogenic; however, the possibility that it is benign cannot be excluded. |