NM_005076.5(CNTN2):c.1914C>T (p.Ile638=) AND Epilepsy, familial adult myoclonic, 5
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 19, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000917281.8
Allele description [Variation Report for NM_005076.5(CNTN2):c.1914C>T (p.Ile638=)]
NM_005076.5(CNTN2):c.1914C>T (p.Ile638=)
Condition(s)
Assertion and evidence details
Last Updated: Feb 14, 2024