NM_012186.3(FOXE3):c.587G>C (p.Gly196Ala) AND not specified
- Germline classification:
- Likely benign (3 submissions)
- Last evaluated:
- Jul 21, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000600499.6
Allele description [Variation Report for NM_012186.3(FOXE3):c.587G>C (p.Gly196Ala)]
NM_012186.3(FOXE3):c.587G>C (p.Gly196Ala)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: May 12, 2024