Annotation Detail
Information
- Associated Genes
- MYBPC3
- Associated Variants
-
MYBPC3 p.Thr1046Met (p.T1046M)
(
ENST00000399249.6,
ENST00000545968.6 )
MYBPC3 p.Thr1046Met (p.T1046M) ( ENST00000399249.6, ENST00000545968.6 ) - Associated Disease
- Primary familial hypertrophic cardiomyopathy
- Source Database
- ClinVar
- Description
- NM_000256.3(MYBPC3):c.3137C>T (p.Thr1046Met) AND Primary familial hypertrophic cardiomyopathy
- ClinVar Allele ID
- 171135
- ClinVar RefSeq Alternation Syntax
- NM_000256.3:c.3137C>T
- Clinical Significance Description
- Likely pathogenic
- Clinical Significance Last Update
- 2014-06-01
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000148658
- ClinVar Disease
- Primary familial hypertrophic cardiomyopathy
- Observed Origin Sample
- germline
Drugs