NM_001242896.3(DEPDC5):c.2241C>G (p.Leu747=) AND Familial focal epilepsy with variable foci
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Feb 1, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000463725.18
Allele description [Variation Report for NM_001242896.3(DEPDC5):c.2241C>G (p.Leu747=)]
NM_001242896.3(DEPDC5):c.2241C>G (p.Leu747=)
Condition(s)
Assertion and evidence details
Last Updated: Jun 9, 2024