Annotation Detail
Information
- Associated Genes
- MYH7
- Associated Variants
-
MYH7 p.Val606Met (p.V606M)
(
ENST00000355349.4,
ENST00000713768.1,
ENST00000713769.1 )
MYH7 p.Val606Met (p.V606M) ( ENST00000355349.4, ENST00000713768.1, ENST00000713769.1 ) - Associated Disease
- hypertrophic cardiomyopathy 1
- Source Database
- ClinVar
- Description
- NM_000257.4(MYH7):c.1816G>A (p.Val606Met) AND Hypertrophic cardiomyopathy 1
- ClinVar Allele ID
- 29130
- ClinVar RefSeq Alternation Syntax
- NM_000257.4:c.1816G>A
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2022-04-27
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000015147
- ClinVar Disease
- Hypertrophic cardiomyopathy 1
- Observed Origin Sample
- germline
- Observed Origin Sample
- unknown
- Pubmed
- 11424919
- Pubmed
- 1552912
Drugs