NM_207305.5(FOXD4):c.477C>A (p.Asn159Lys) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 3, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004189079.1
Allele description [Variation Report for NM_207305.5(FOXD4):c.477C>A (p.Asn159Lys)]
NM_207305.5(FOXD4):c.477C>A (p.Asn159Lys)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Nov 24, 2024