NM_001242896.3(DEPDC5):c.3272C>T (p.Ala1091Val) AND Familial focal epilepsy with variable foci
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 13, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000456738.7
Allele description [Variation Report for NM_001242896.3(DEPDC5):c.3272C>T (p.Ala1091Val)]
NM_001242896.3(DEPDC5):c.3272C>T (p.Ala1091Val)
Condition(s)
Assertion and evidence details
Last Updated: May 1, 2024