NM_007327.4(GRIN1):c.1044C>T (p.Phe348=) AND not specified
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jun 27, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000433279.8
Allele description [Variation Report for NM_007327.4(GRIN1):c.1044C>T (p.Phe348=)]
NM_007327.4(GRIN1):c.1044C>T (p.Phe348=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Nov 10, 2024