NM_001165963.4(SCN1A):c.3723T>C (p.Tyr1241=) AND Generalized epilepsy with febrile seizures plus, type 2
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 13, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001134604.12
Allele description [Variation Report for NM_001165963.4(SCN1A):c.3723T>C (p.Tyr1241=)]
NM_001165963.4(SCN1A):c.3723T>C (p.Tyr1241=)
Condition(s)
Assertion and evidence details
Last Updated: Apr 15, 2024