NM_001242896.3(DEPDC5):c.3242C>T (p.Thr1081Ile) AND Familial focal epilepsy with variable foci
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 1, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001043771.5
Allele description [Variation Report for NM_001242896.3(DEPDC5):c.3242C>T (p.Thr1081Ile)]
NM_001242896.3(DEPDC5):c.3242C>T (p.Thr1081Ile)
Condition(s)
Assertion and evidence details
Last Updated: Aug 23, 2022