NM_007327.4(GRIN1):c.352G>A (p.Val118Met) AND GRIN1-related disorder
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 11, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004528329.1
Allele description [Variation Report for NM_007327.4(GRIN1):c.352G>A (p.Val118Met)]
NM_007327.4(GRIN1):c.352G>A (p.Val118Met)
Condition(s)
- Name:
- GRIN1-related disorder
- Synonyms:
- GRIN1-related condition
- Identifiers:
Assertion and evidence details
Last Updated: Sep 16, 2024