NM_007327.4(GRIN1):c.802G>A (p.Gly268Arg) AND Intellectual disability, autosomal dominant 8
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 24, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001034474.7
Allele description [Variation Report for NM_007327.4(GRIN1):c.802G>A (p.Gly268Arg)]
NM_007327.4(GRIN1):c.802G>A (p.Gly268Arg)
Condition(s)
Assertion and evidence details
Last Updated: Feb 20, 2024