NM_006772.3(SYNGAP1):c.804C>T (p.Ile268=) AND Intellectual disability, autosomal dominant 5
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 14, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003820318.1
Allele description [Variation Report for NM_006772.3(SYNGAP1):c.804C>T (p.Ile268=)]
NM_006772.3(SYNGAP1):c.804C>T (p.Ile268=)
Condition(s)
Assertion and evidence details
Last Updated: Mar 5, 2024