NM_001040142.2(SCN2A):c.3453C>T (p.Pro1151=) AND not specified
- Germline classification:
- Benign (4 submissions)
- Last evaluated:
- Aug 1, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000175358.22
Allele description [Variation Report for NM_001040142.2(SCN2A):c.3453C>T (p.Pro1151=)]
NM_001040142.2(SCN2A):c.3453C>T (p.Pro1151=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Apr 20, 2024