NM_005120.3(MED12):c.4448C>T (p.Ser1483Leu) AND FG syndrome 1
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 26, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004527549.1
Allele description [Variation Report for NM_005120.3(MED12):c.4448C>T (p.Ser1483Leu)]
NM_005120.3(MED12):c.4448C>T (p.Ser1483Leu)
Condition(s)
Assertion and evidence details
Last Updated: Aug 11, 2024