NM_005097.4(LGI1):c.46C>G (p.Leu16Val) AND Autosomal dominant epilepsy with auditory features
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 9, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002231765.15
Allele description [Variation Report for NM_005097.4(LGI1):c.46C>G (p.Leu16Val)]
NM_005097.4(LGI1):c.46C>G (p.Leu16Val)
Condition(s)
- Name:
- Autosomal dominant epilepsy with auditory features
- Identifiers:
- MONDO: MONDO:0010898; MedGen: C1838062
Assertion and evidence details
Last Updated: Oct 8, 2024