NM_001242896.3(DEPDC5):c.3330+8C>T AND Familial focal epilepsy with variable foci
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 8, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002110698.4
Allele description [Variation Report for NM_001242896.3(DEPDC5):c.3330+8C>T]
NM_001242896.3(DEPDC5):c.3330+8C>T
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024