NM_001369369.1(FOXN1):c.414C>T (p.Ala138=) AND T-cell immunodeficiency, congenital alopecia, and nail dystrophy
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- May 19, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003872978.1
Allele description [Variation Report for NM_001369369.1(FOXN1):c.414C>T (p.Ala138=)]
NM_001369369.1(FOXN1):c.414C>T (p.Ala138=)
Condition(s)
Assertion and evidence details
Last Updated: Mar 5, 2024