NM_001164508.2(NEB):c.4938C>T (p.Asn1646=) AND Nemaline myopathy 2
- Germline classification:
- Likely benign (2 submissions)
- Last evaluated:
- Dec 19, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000873515.11
Allele description [Variation Report for NM_001164508.2(NEB):c.4938C>T (p.Asn1646=)]
NM_001164508.2(NEB):c.4938C>T (p.Asn1646=)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024