NM_005120.3(MED12):c.1011A>C (p.Pro337=) AND FG syndrome
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Oct 28, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003596173.2
Allele description [Variation Report for NM_005120.3(MED12):c.1011A>C (p.Pro337=)]
NM_005120.3(MED12):c.1011A>C (p.Pro337=)
Condition(s)
Assertion and evidence details
Last Updated: Nov 3, 2024