NM_001124759.5(FRG2C):c.359A>G (p.Asn120Ser) AND not specified
- Germline classification:
- Benign (1 submission)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001261636.1
Allele description [Variation Report for NM_001124759.5(FRG2C):c.359A>G (p.Asn120Ser)]
NM_001124759.5(FRG2C):c.359A>G (p.Asn120Ser)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Apr 23, 2022