NM_017534.6(MYH2):c.3358C>T (p.Arg1120Cys) AND Inclusion Body Myopathy, Dominant
- Germline classification:
- Uncertain significance (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:
- RCV000347813.5
Allele description [Variation Report for NM_017534.6(MYH2):c.3358C>T (p.Arg1120Cys)]
NM_017534.6(MYH2):c.3358C>T (p.Arg1120Cys)
Condition(s)
- Name:
- Inclusion Body Myopathy, Dominant
- Identifiers:
- MedGen: CN239244
Assertion and evidence details
Last Updated: Aug 5, 2023