NM_005120.3(MED12):c.1363C>T (p.Arg455Trp) AND FG syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 7, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003597218.1
Allele description [Variation Report for NM_005120.3(MED12):c.1363C>T (p.Arg455Trp)]
NM_005120.3(MED12):c.1363C>T (p.Arg455Trp)
Condition(s)
Assertion and evidence details
Last Updated: Jul 29, 2024