NM_006772.3(SYNGAP1):c.3662G>A (p.Arg1221Gln) AND Intellectual disability, autosomal dominant 5
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Mar 19, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001522591.6
Allele description [Variation Report for NM_006772.3(SYNGAP1):c.3662G>A (p.Arg1221Gln)]
NM_006772.3(SYNGAP1):c.3662G>A (p.Arg1221Gln)
Condition(s)
Assertion and evidence details
Last Updated: May 7, 2024