NM_001242896.3(DEPDC5):c.1217+8C>A AND Familial focal epilepsy with variable foci
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Sep 1, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001065851.5
Allele description [Variation Report for NM_001242896.3(DEPDC5):c.1217+8C>A]
NM_001242896.3(DEPDC5):c.1217+8C>A
Condition(s)
Assertion and evidence details
Last Updated: Feb 20, 2024