NM_201596.3(CACNB2):c.1122C>T (p.Asp374=) AND Brugada syndrome 4
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 5, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000865431.9
Allele description [Variation Report for NM_201596.3(CACNB2):c.1122C>T (p.Asp374=)]
NM_201596.3(CACNB2):c.1122C>T (p.Asp374=)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024