NM_000834.5(GRIN2B):c.681C>A (p.Ile227=) AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Sep 7, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000471946.9
Allele description [Variation Report for NM_000834.5(GRIN2B):c.681C>A (p.Ile227=)]
NM_000834.5(GRIN2B):c.681C>A (p.Ile227=)
Condition(s)
Assertion and evidence details
Last Updated: Feb 28, 2024