NM_005120.3(MED12):c.5266C>T (p.Leu1756=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 18, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000504418.6
Allele description [Variation Report for NM_005120.3(MED12):c.5266C>T (p.Leu1756=)]
NM_005120.3(MED12):c.5266C>T (p.Leu1756=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Apr 9, 2023