NM_000335.5(SCN5A):c.5382T>C (p.Tyr1794=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 9, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003658895.2
Allele description [Variation Report for NM_000335.5(SCN5A):c.5382T>C (p.Tyr1794=)]
NM_000335.5(SCN5A):c.5382T>C (p.Tyr1794=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Oct 8, 2024