NM_000335.5(SCN5A):c.3033G>C (p.Pro1011=) AND not provided
- Germline classification:
- Likely benign (2 submissions)
- Last evaluated:
- May 2, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000829591.10
Allele description [Variation Report for NM_000335.5(SCN5A):c.3033G>C (p.Pro1011=)]
NM_000335.5(SCN5A):c.3033G>C (p.Pro1011=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Jun 2, 2024