NM_001164508.2(NEB):c.13275C>T (p.Arg4425=) AND Nemaline myopathy 2
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 3, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001393139.13
Allele description [Variation Report for NM_001164508.2(NEB):c.13275C>T (p.Arg4425=)]
NM_001164508.2(NEB):c.13275C>T (p.Arg4425=)
Condition(s)
Assertion and evidence details
Last Updated: Apr 20, 2024