NM_005120.3(MED12):c.1738A>G (p.Met580Val) AND FG syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Sep 26, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003762202.1
Allele description [Variation Report for NM_005120.3(MED12):c.1738A>G (p.Met580Val)]
NM_005120.3(MED12):c.1738A>G (p.Met580Val)
Condition(s)
Assertion and evidence details
Last Updated: Jun 9, 2024