NM_005359.6(SMAD4):c.1632G>A (p.Pro544=) AND Myhre syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 13, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001124521.11
Allele description [Variation Report for NM_005359.6(SMAD4):c.1632G>A (p.Pro544=)]
NM_005359.6(SMAD4):c.1632G>A (p.Pro544=)
Condition(s)
Assertion and evidence details
Last Updated: May 19, 2024