NM_001165963.4(SCN1A):c.5992G>C (p.Glu1998Gln) AND Generalized epilepsy with febrile seizures plus, type 2
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 12, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001133022.5
Allele description [Variation Report for NM_001165963.4(SCN1A):c.5992G>C (p.Glu1998Gln)]
NM_001165963.4(SCN1A):c.5992G>C (p.Glu1998Gln)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024