NM_001134407.3(GRIN2A):c.2694C>T (p.Leu898=) AND not specified
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Apr 11, 2014
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000125315.9
Allele description [Variation Report for NM_001134407.3(GRIN2A):c.2694C>T (p.Leu898=)]
NM_001134407.3(GRIN2A):c.2694C>T (p.Leu898=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Oct 8, 2024