NM_000335.5(SCN5A):c.1820G>T (p.Gly607Val) AND Brugada syndrome 1
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 5, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001729437.9
Allele description [Variation Report for NM_000335.5(SCN5A):c.1820G>T (p.Gly607Val)]
NM_000335.5(SCN5A):c.1820G>T (p.Gly607Val)
Condition(s)
Assertion and evidence details
Last Updated: Jun 9, 2024