NM_001349253.2(SCN11A):c.2799T>C (p.Asn933=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 18, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000980644.3
Allele description
NM_001349253.2(SCN11A):c.2799T>C (p.Asn933=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
Assertion and evidence details
Last Updated: Aug 23, 2022