NM_006772.3(SYNGAP1):c.3100C>G (p.Pro1034Ala) AND Intellectual disability, autosomal dominant 5
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jul 17, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002576760.2
Allele description [Variation Report for NM_006772.3(SYNGAP1):c.3100C>G (p.Pro1034Ala)]
NM_006772.3(SYNGAP1):c.3100C>G (p.Pro1034Ala)
Condition(s)
Assertion and evidence details
Last Updated: Mar 5, 2024