NM_000834.5(GRIN2B):c.1559C>T (p.Ser520Leu) AND multiple conditions
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 22, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002032787.6
Allele description [Variation Report for NM_000834.5(GRIN2B):c.1559C>T (p.Ser520Leu)]
NM_000834.5(GRIN2B):c.1559C>T (p.Ser520Leu)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024