NM_000335.5(SCN5A):c.1066G>T (p.Asp356Tyr) AND Brugada syndrome 1
- Germline classification:
- Likely pathogenic (1 submission)
- Last evaluated:
- Nov 2, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000790455.2
Allele description [Variation Report for NM_000335.5(SCN5A):c.1066G>T (p.Asp356Tyr)]
NM_000335.5(SCN5A):c.1066G>T (p.Asp356Tyr)
Condition(s)
Assertion and evidence details
Last Updated: Feb 4, 2024