Annotation Detail
Information
- Associated Genes
- TPM3
- Associated Variants
-
TPM3 p.Met9Arg (p.M9R)
(
ENST00000651641.1,
ENST00000368530.7,
ENST00000271850.11 )
TPM3 p.Met9Arg (p.M9R) ( ENST00000271850.11, ENST00000368530.7, ENST00000651641.1 ) - Associated Disease
- Congenital myopathy 4A, autosomal dominant
- Source Database
- ClinVar
- Description
- NM_152263.4(TPM3):c.26T>G (p.Met9Arg) AND Congenital myopathy 4A, autosomal dominant
- ClinVar Allele ID
- 27485
- ClinVar RefSeq Alternation Syntax
- NR_103460.2:n.108T>G
- ClinVar RefSeq Alternation Syntax
- NM_001364679.2:c.26T>G
- ClinVar RefSeq Alternation Syntax
- NM_152263.4:c.26T>G
- ClinVar RefSeq Alternation Syntax
- NM_001364681.2:c.26T>G
- ClinVar RefSeq Alternation Syntax
- NM_001364682.1:c.26T>G
- ClinVar RefSeq Alternation Syntax
- NM_001364680.2:c.26T>G
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2005-01-01
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV003151723
- ClinVar Disease
- Congenital myopathy 4A, autosomal dominant
- Observed Origin Sample
- germline
- Pubmed
- 10587521
- Pubmed
- 7704029
- Pubmed
- 15562513
Drugs