NM_005097.4(LGI1):c.69A>G (p.Leu23=) AND Autosomal dominant epilepsy with auditory features
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 30, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002072202.5
Allele description [Variation Report for NM_005097.4(LGI1):c.69A>G (p.Leu23=)]
NM_005097.4(LGI1):c.69A>G (p.Leu23=)
Condition(s)
- Name:
- Autosomal dominant epilepsy with auditory features
- Identifiers:
- MONDO: MONDO:0010898; MedGen: C1838062
-
NIMA (never in mitosis gene a)-related kinase 2 variant, partial [Homo sapiens]
NIMA (never in mitosis gene a)-related kinase 2 variant, partial [Homo sapiens]gi|62898267|dbj|BAD97073.1|Protein
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Feb 28, 2024