NM_170707.4(LMNA):c.12G>A (p.Pro4=) AND not specified
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Nov 17, 2015
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000422715.1
Allele description [Variation Report for NM_170707.4(LMNA):c.12G>A (p.Pro4=)]
NM_170707.4(LMNA):c.12G>A (p.Pro4=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 29, 2024