NM_005120.3(MED12):c.1640C>T (p.Ala547Val) AND FG syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 28, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003776592.1
Allele description [Variation Report for NM_005120.3(MED12):c.1640C>T (p.Ala547Val)]
NM_005120.3(MED12):c.1640C>T (p.Ala547Val)
Condition(s)
Assertion and evidence details
Last Updated: Sep 8, 2024