NM_138690.3(GRIN3B):c.826C>T (p.Pro276Ser) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 10, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004272346.1
Allele description [Variation Report for NM_138690.3(GRIN3B):c.826C>T (p.Pro276Ser)]
NM_138690.3(GRIN3B):c.826C>T (p.Pro276Ser)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 1, 2024