NM_006514.4(SCN10A):c.5682T>C (p.Phe1894=) AND Brugada syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 29, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002219331.5
Allele description [Variation Report for NM_006514.4(SCN10A):c.5682T>C (p.Phe1894=)]
NM_006514.4(SCN10A):c.5682T>C (p.Phe1894=)
Condition(s)
- Name:
- Brugada syndrome
- Synonyms:
- Sudden unexpected nocturnal death syndrome; Sudden unexplained nocturnal death syndrome; Sudden Unexplained Death Syndrome; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0015263; MedGen: C1142166; OMIM: PS601144
Assertion and evidence details
Last Updated: May 1, 2024