NM_001349338.3(FOXP1):c.1702C>T (p.Pro568Ser) AND Inborn genetic diseases
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Apr 5, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002311531.9
Allele description [Variation Report for NM_001349338.3(FOXP1):c.1702C>T (p.Pro568Ser)]
NM_001349338.3(FOXP1):c.1702C>T (p.Pro568Ser)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: Nov 3, 2024