NM_005120.3(MED12):c.5316G>A (p.Pro1772=) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jul 31, 2013
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000081266.7
Allele description [Variation Report for NM_005120.3(MED12):c.5316G>A (p.Pro1772=)]
NM_005120.3(MED12):c.5316G>A (p.Pro1772=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: May 1, 2024