NM_000335.5(SCN5A):c.3781G>A (p.Gly1261Ser) AND Cardiovascular phenotype
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 7, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004018613.1
Allele description [Variation Report for NM_000335.5(SCN5A):c.3781G>A (p.Gly1261Ser)]
NM_000335.5(SCN5A):c.3781G>A (p.Gly1261Ser)
Condition(s)
- Name:
- Cardiovascular phenotype
- Identifiers:
- MedGen: CN230736
Assertion and evidence details
Last Updated: Sep 29, 2024