NM_000059.4(BRCA2):c.4670C>G (p.Thr1557Ser) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 7, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000442303.5
Allele description
NM_000059.4(BRCA2):c.4670C>G (p.Thr1557Ser)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Aug 11, 2021