NM_000334.4(SCN4A):c.3429C>T (p.Phe1143=) AND not specified
- Germline classification:
- Likely benign (2 submissions)
- Last evaluated:
- Jul 21, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000247115.10
Allele description [Variation Report for NM_000334.4(SCN4A):c.3429C>T (p.Phe1143=)]
NM_000334.4(SCN4A):c.3429C>T (p.Phe1143=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Apr 15, 2024