Annotation Detail
Information
- Associated Genes
- MYH7
- Associated Variants
-
MYH7 p.Asn444Ser (p.N444S)
(
ENST00000713768.1,
ENST00000355349.4,
ENST00000713769.1 )
MYH7 p.Asn444Ser (p.N444S) ( ENST00000355349.4, ENST00000713768.1, ENST00000713769.1 ) - Associated Disease
- Primary familial hypertrophic cardiomyopathy
- Source Database
- ClinVar
- Description
- NM_000257.4(MYH7):c.1331A>G (p.Asn444Ser) AND Primary familial hypertrophic cardiomyopathy
- ClinVar Allele ID
- 179652
- ClinVar RefSeq Alternation Syntax
- NM_000257.4:c.1331A>G
- Clinical Significance Description
- Likely pathogenic
- Clinical Significance Last Update
- 2015-04-07
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000208202
- ClinVar Disease
- Primary familial hypertrophic cardiomyopathy
- Observed Origin Sample
- germline
Drugs