NM_001134407.3(GRIN2A):c.2664G>A (p.Thr888=) AND not specified
- Germline classification:
- Conflicting interpretations of pathogenicity (2 submissions)
- Last evaluated:
- Apr 25, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000427722.9
Allele description [Variation Report for NM_001134407.3(GRIN2A):c.2664G>A (p.Thr888=)]
NM_001134407.3(GRIN2A):c.2664G>A (p.Thr888=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: May 12, 2024