NM_000843.4(GRM6):c.2397C>T (p.Phe799=) AND not provided
- Germline classification:
- Benign (3 submissions)
- Last evaluated:
- Jan 31, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000086048.8
Allele description [Variation Report for NM_000843.4(GRM6):c.2397C>T (p.Phe799=)]
NM_000843.4(GRM6):c.2397C>T (p.Phe799=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 28, 2024
SCV000118192