NM_000335.5(SCN5A):c.3133G>A (p.Val1045Met) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 21, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001290669.9
Allele description [Variation Report for NM_000335.5(SCN5A):c.3133G>A (p.Val1045Met)]
NM_000335.5(SCN5A):c.3133G>A (p.Val1045Met)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Jun 2, 2024