NM_170707.4(LMNA):c.1755C>T (p.Thr585=) AND not provided
- Germline classification:
- Likely benign (2 submissions)
- Last evaluated:
- Oct 1, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001540572.22
Allele description [Variation Report for NM_170707.4(LMNA):c.1755C>T (p.Thr585=)]
NM_170707.4(LMNA):c.1755C>T (p.Thr585=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Oct 20, 2024