Annotation Detail
Information
- Associated Genes
- TNNI3
- Associated Variants
-
TNNI3 p.Arg170Gly (p.R170G)
(
ENST00000344887.10,
ENST00000588882.1,
ENST00000665070.1,
ENST00000714236.1,
ENST00000714237.1,
ENST00000714238.1,
ENST00000714240.1 )
TNNI3 p.Arg170Gly (p.R170G) ( ENST00000344887.10, ENST00000588882.1, ENST00000665070.1, ENST00000714236.1, ENST00000714237.1, ENST00000714238.1, ENST00000714240.1 ) - Associated Disease
- Cardiomyopathy, familial restrictive, 1 hypertrophic cardiomyopathy 7 dilated cardiomyopathy 1FF
- Source Database
- ClinVar
- Description
- NM_000363.5(TNNI3):c.508C>G (p.Arg170Gly) AND multiple conditions
- ClinVar Allele ID
- 176215
- ClinVar RefSeq Alternation Syntax
- NM_000363.5:c.508C>G
- Clinical Significance Description
- Likely pathogenic
- Clinical Significance Last Update
- 2013-02-19
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000197009
- ClinVar Disease
- Cardiomyopathy, familial restrictive, 1
- ClinVar Disease
- Hypertrophic cardiomyopathy 7
- ClinVar Disease
- Dilated cardiomyopathy 1FF
- Observed Origin Sample
- germline
Drugs