NM_138690.3(GRIN3B):c.1811C>T (p.Thr604Met) AND Neurodevelopmental disorder
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 1, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001262994.1
Allele description [Variation Report for NM_138690.3(GRIN3B):c.1811C>T (p.Thr604Met)]
NM_138690.3(GRIN3B):c.1811C>T (p.Thr604Met)
Condition(s)
- Name:
- Neurodevelopmental disorder
- Identifiers:
- MONDO: MONDO:0700092; MeSH: D065886; MedGen: C1535926
Assertion and evidence details
Last Updated: Apr 23, 2022