Annotation Detail
Information
- Associated Genes
- MYH7
- Associated Variants
-
MYH7 p.Asn1327Lys (p.N1327K)
(
ENST00000713769.1,
ENST00000355349.4,
ENST00000713768.1 )
MYH7 p.Asn1327Lys (p.N1327K) ( ENST00000355349.4, ENST00000713768.1, ENST00000713769.1 ) - Associated Disease
- Primary familial hypertrophic cardiomyopathy
- Source Database
- ClinVar
- Description
- NM_000257.4(MYH7):c.3981C>A (p.Asn1327Lys) AND Primary familial hypertrophic cardiomyopathy
- ClinVar Allele ID
- 45303
- ClinVar RefSeq Alternation Syntax
- NM_000257.4:c.3981C>A
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Last Update
- 2014-06-01
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000030319
- ClinVar Disease
- Primary familial hypertrophic cardiomyopathy
- Observed Origin Sample
- germline
- Observed Origin Sample
- unknown
Drugs