NM_007327.4(GRIN1):c.2718C>T (p.Arg906=) AND Intellectual disability, autosomal dominant 8
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 13, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001504127.6
Allele description [Variation Report for NM_007327.4(GRIN1):c.2718C>T (p.Arg906=)]
NM_007327.4(GRIN1):c.2718C>T (p.Arg906=)
Condition(s)
Assertion and evidence details
Last Updated: Feb 20, 2024