NM_006772.3(SYNGAP1):c.886T>G (p.Ser296Ala) AND Intellectual disability, autosomal dominant 5
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jul 27, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000527897.7
Allele description [Variation Report for NM_006772.3(SYNGAP1):c.886T>G (p.Ser296Ala)]
NM_006772.3(SYNGAP1):c.886T>G (p.Ser296Ala)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024