NM_000059.4(BRCA2):c.5244C>A (p.Ser1748Arg) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 4, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000160084.5
Allele description [Variation Report for NM_000059.4(BRCA2):c.5244C>A (p.Ser1748Arg)]
NM_000059.4(BRCA2):c.5244C>A (p.Ser1748Arg)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 29, 2024