NM_032380.5(GFM2):c.2178T>A (p.Val726=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 20, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002696254.2
Allele description [Variation Report for NM_032380.5(GFM2):c.2178T>A (p.Val726=)]
NM_032380.5(GFM2):c.2178T>A (p.Val726=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 28, 2024