NM_001134407.3(GRIN2A):c.4250G>A (p.Arg1417Gln) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 24, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003258841.3
Allele description [Variation Report for NM_001134407.3(GRIN2A):c.4250G>A (p.Arg1417Gln)]
NM_001134407.3(GRIN2A):c.4250G>A (p.Arg1417Gln)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: May 12, 2024