NM_005097.4(LGI1):c.261T>C (p.Phe87=) AND Autosomal dominant epilepsy with auditory features
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 16, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002139290.5
Allele description [Variation Report for NM_005097.4(LGI1):c.261T>C (p.Phe87=)]
NM_005097.4(LGI1):c.261T>C (p.Phe87=)
Condition(s)
- Name:
- Autosomal dominant epilepsy with auditory features
- Identifiers:
- MONDO: MONDO:0010898; MedGen: C1838062
Assertion and evidence details
Last Updated: Feb 28, 2024