NM_032380.5(GFM2):c.1671C>T (p.Leu557=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 17, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003091784.2
Allele description [Variation Report for NM_032380.5(GFM2):c.1671C>T (p.Leu557=)]
NM_032380.5(GFM2):c.1671C>T (p.Leu557=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 20, 2024