Annotation Detail
Information
- Associated Genes
- TNNI3
- Associated Variants
-
TNNI3 p.Arg170Trp (p.R170W)
(
ENST00000344887.10,
ENST00000588882.1,
ENST00000665070.1,
ENST00000714236.1,
ENST00000714237.1,
ENST00000714238.1,
ENST00000714240.1 )
TNNI3 p.Arg170Trp (p.R170W) ( ENST00000344887.10, ENST00000588882.1, ENST00000665070.1, ENST00000714236.1, ENST00000714237.1, ENST00000714238.1, ENST00000714240.1 ) - Associated Disease
- Cardiomyopathy, familial restrictive, 1
- Source Database
- ClinVar
- Description
- NM_000363.5(TNNI3):c.508C>T (p.Arg170Trp) AND Cardiomyopathy, familial restrictive, 1
- ClinVar Allele ID
- 176073
- ClinVar RefSeq Alternation Syntax
- NM_000363.5:c.508C>T
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2020-07-21
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001254049
- ClinVar Disease
- Cardiomyopathy, familial restrictive, 1
- Observed Origin Sample
- de novo
Drugs