Annotation Detail
Information
- Associated Genes
- TNNC1
- Associated Variants
-
TNNC1 p.Asp145Glu (p.D145E)
(
ENST00000232975.8 )
TNNC1 p.Asp145Glu (p.D145E) ( ENST00000232975.8 ) - Associated Disease
- cardiomyopathy
- Source Database
- ClinVar
- Description
- NM_003280.3(TNNC1):c.435C>A (p.Asp145Glu) AND Cardiomyopathy
- ClinVar Allele ID
- 27484
- ClinVar RefSeq Alternation Syntax
- NM_003280.3:c.435C>A
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Last Update
- 2021-12-22
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV003149570
- ClinVar Disease
- Cardiomyopathy
- Observed Origin Sample
- germline
Drugs