NM_207361.6(FREM2):c.3830T>G (p.Phe1277Cys) AND multiple conditions
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 31, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002488582.1
Allele description [Variation Report for NM_207361.6(FREM2):c.3830T>G (p.Phe1277Cys)]
NM_207361.6(FREM2):c.3830T>G (p.Phe1277Cys)
Condition(s)
Assertion and evidence details
Last Updated: Dec 24, 2023