NM_005120.3(MED12):c.1167G>A (p.Lys389=) AND not specified
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Nov 18, 2015
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000432789.1
Allele description [Variation Report for NM_005120.3(MED12):c.1167G>A (p.Lys389=)]
NM_005120.3(MED12):c.1167G>A (p.Lys389=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Apr 20, 2024