NM_170707.4(LMNA):c.1149G>A (p.Glu383=) AND Congenital muscular dystrophy due to LMNA mutation
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 27, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000327855.5
Allele description [Variation Report for NM_170707.4(LMNA):c.1149G>A (p.Glu383=)]
NM_170707.4(LMNA):c.1149G>A (p.Glu383=)
Condition(s)
Assertion and evidence details
Last Updated: Jun 29, 2024