NM_006950.3(SYN1):c.1107C>T (p.Ile369=) AND Epilepsy, X-linked, with variable learning disabilities and behavior disorders
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Nov 6, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000544246.2
Assertion and evidence details
Last Updated: Nov 2, 2019