NM_001349253.2(SCN11A):c.408C>T (p.Ile136=) AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 28, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001078506.7
Allele description [Variation Report for NM_001349253.2(SCN11A):c.408C>T (p.Ile136=)]
NM_001349253.2(SCN11A):c.408C>T (p.Ile136=)
Condition(s)
Assertion and evidence details
Last Updated: Apr 15, 2024