Annotation Detail
Information
- Associated Genes
- TNNI3
- Associated Variants
-
TNNI3 p.Val176Met (p.V176M)
(
ENST00000344887.10,
ENST00000588882.1,
ENST00000665070.1,
ENST00000714236.1,
ENST00000714237.1,
ENST00000714238.1,
ENST00000714240.1 )
TNNI3 p.Val176Met (p.V176M) ( ENST00000344887.10, ENST00000588882.1, ENST00000665070.1, ENST00000714236.1, ENST00000714237.1, ENST00000714238.1, ENST00000714240.1 ) - Associated Disease
- Primary familial hypertrophic cardiomyopathy
- Source Database
- ClinVar
- Description
- NM_000363.5(TNNI3):c.526G>A (p.Val176Met) AND Primary familial hypertrophic cardiomyopathy
- ClinVar Allele ID
- 176213
- ClinVar RefSeq Alternation Syntax
- NM_000363.5:c.526G>A
- Clinical Significance Description
- Likely pathogenic
- Clinical Significance Last Update
- 2014-05-05
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000157532
- ClinVar Disease
- Primary familial hypertrophic cardiomyopathy
- Observed Origin Sample
- germline
Drugs