NM_007327.4(GRIN1):c.1044C>T (p.Phe348=) AND Intellectual disability, autosomal dominant 8
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Dec 27, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000649666.17
Allele description [Variation Report for NM_007327.4(GRIN1):c.1044C>T (p.Phe348=)]
NM_007327.4(GRIN1):c.1044C>T (p.Phe348=)
Condition(s)
Assertion and evidence details
Last Updated: Nov 3, 2024