NM_000334.4(SCN4A):c.2722G>A (p.Glu908Lys) AND not specified
- Germline classification:
- Benign/Likely benign (3 submissions)
- Last evaluated:
- Mar 27, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000241827.14
Allele description [Variation Report for NM_000334.4(SCN4A):c.2722G>A (p.Glu908Lys)]
NM_000334.4(SCN4A):c.2722G>A (p.Glu908Lys)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 29, 2024