NM_000834.5(GRIN2B):c.1539C>T (p.Leu513=) AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 5, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001391911.6
Allele description [Variation Report for NM_000834.5(GRIN2B):c.1539C>T (p.Leu513=)]
NM_000834.5(GRIN2B):c.1539C>T (p.Leu513=)
Condition(s)
Assertion and evidence details
Last Updated: Mar 5, 2024