NM_000059.4(BRCA2):c.7992T>A (p.Ile2664=) AND not specified
- Germline classification:
- Conflicting interpretations of pathogenicity (2 submissions)
- Last evaluated:
- Feb 6, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000045376.19
Allele description [Variation Report for NM_000059.4(BRCA2):c.7992T>A (p.Ile2664=)]
NM_000059.4(BRCA2):c.7992T>A (p.Ile2664=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Mar 30, 2024