NM_001130987.2(DYSF):c.4026C>T (p.Asn1342=) AND Miyoshi myopathy
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jun 14, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000331227.6
Allele description [Variation Report for NM_001130987.2(DYSF):c.4026C>T (p.Asn1342=)]
NM_001130987.2(DYSF):c.4026C>T (p.Asn1342=)
Condition(s)
Assertion and evidence details
Last Updated: Jun 29, 2024