Annotation Detail
Information
- Associated Genes
- MYH7 LOC126861898
- Associated Variants
-
MYH7 p.Phe764Leu (p.F764L)
(
ENST00000713769.1,
ENST00000713768.1,
ENST00000355349.4 )
MYH7 p.Phe764Leu (p.F764L) ( ENST00000355349.4, ENST00000713768.1, ENST00000713769.1 ) - Associated Disease
- hypertrophic cardiomyopathy
- Source Database
- ClinVar
- Description
- NM_000257.4(MYH7):c.2292C>G (p.Phe764Leu) AND Hypertrophic cardiomyopathy
- ClinVar Allele ID
- 29148
- ClinVar RefSeq Alternation Syntax
- NM_000257.4:c.2292C>G
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2021-07-13
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001213330
- ClinVar Disease
- Hypertrophic cardiomyopathy
- Observed Origin Sample
- germline
Drugs