NM_001242896.3(DEPDC5):c.3311C>T (p.Ser1104Leu) AND Epilepsy, familial focal, with variable foci 1
- Germline classification:
- Uncertain significance (5 submissions)
- Last evaluated:
- May 28, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000254574.21
Allele description [Variation Report for NM_001242896.3(DEPDC5):c.3311C>T (p.Ser1104Leu)]
NM_001242896.3(DEPDC5):c.3311C>T (p.Ser1104Leu)
Condition(s)
Assertion and evidence details
Last Updated: Mar 23, 2024