NM_007126.5(VCP):c.*885G>A AND Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 12, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001167478.4
Allele description [Variation Report for NM_007126.5(VCP):c.*885G>A]
NM_007126.5(VCP):c.*885G>A
Condition(s)
- Name:
- Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1
- Synonyms:
- MULTISYSTEM PROTEINOPATHY 1; Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 1; Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia 1
- Identifiers:
- MONDO: MONDO:0008178; MedGen: C4551951; OMIM: 167320
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Taxonomy Links for GEO Profiles (Select 119830572) (1)
Taxonomy
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PMC Links for GEO Profiles (Select 119830572) (18)
PMC
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Homo sapiens clone HCG IV.9 unknown mRNA
Homo sapiens clone HCG IV.9 unknown mRNAgi|4104614|gb|AF036977.1|Nucleotide
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Taxonomy Links for GEO Profiles (Select 27104616) (1)
Taxonomy
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PMC Links for GEO Profiles (Select 27104616) (2)
PMC
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Last Updated: Aug 5, 2023