NM_000465.4(BARD1):c.1311T>C (p.Ile437=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 13, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003987455.1
Allele description [Variation Report for NM_000465.4(BARD1):c.1311T>C (p.Ile437=)]
NM_000465.4(BARD1):c.1311T>C (p.Ile437=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 8, 2024