NM_017534.6(MYH2):c.3709C>T (p.Leu1237Phe) 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:
- RCV000352017.5
Allele description [Variation Report for NM_017534.6(MYH2):c.3709C>T (p.Leu1237Phe)]
NM_017534.6(MYH2):c.3709C>T (p.Leu1237Phe)
Condition(s)
- Name:
- Inclusion Body Myopathy, Dominant
- Identifiers:
- MedGen: CN239244
-
hypothetical protein RirG_222780 [Rhizophagus irregularis DAOM 197198w]
hypothetical protein RirG_222780 [Rhizophagus irregularis DAOM 197198w]gi|595444788|gb|EXX55729.1||gnl|WGS |RirT_222780Protein
-
THRAP3 [Theropithecus gelada]
THRAP3 [Theropithecus gelada]Gene ID:112622872Gene
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024