NM_001927.4(DES):c.*662G>A AND Myofibrillar Myopathy, Dominant
- Germline classification:
- Likely 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:
- RCV000322638.12
Allele description [Variation Report for NM_001927.4(DES):c.*662G>A]
NM_001927.4(DES):c.*662G>A
Condition(s)
- Name:
- Myofibrillar Myopathy, Dominant
- Identifiers:
- MedGen: CN239446
-
Caenorhabditis elegans RNA interference defective protein 10 (rde-10), partial m...
Caenorhabditis elegans RNA interference defective protein 10 (rde-10), partial mRNAgi|392885167|ref|NM_058777.6|Nucleotide
-
starch synthase IIa-3 [Triticum aestivum]
starch synthase IIa-3 [Triticum aestivum]gi|8953573|emb|CAB96627.1|Protein
-
Left ventricular systolic dysfunction
Left ventricular systolic dysfunctionMedGen
-
C1277187[conceptid] (1)
MedGen
-
GPR37 G protein-coupled receptor 37 [Pan troglodytes]
GPR37 G protein-coupled receptor 37 [Pan troglodytes]Gene ID:738926Gene
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Last Updated: Sep 16, 2024