Annotation Detail
Information
- Associated Genes
- MYBPC3
- Associated Variants
-
MYBPC3 p.Val771Met (p.V771M)
(
ENST00000399249.6,
ENST00000545968.6 )
MYBPC3 p.Val771Met (p.V771M) ( ENST00000399249.6, ENST00000545968.6 ) - Associated Disease
- Left ventricular noncompaction 10 hypertrophic cardiomyopathy 4
- Source Database
- ClinVar
- Description
- NM_000256.3(MYBPC3):c.2311G>A (p.Val771Met) AND multiple conditions
- ClinVar Allele ID
- 171136
- ClinVar RefSeq Alternation Syntax
- NM_000256.3:c.2311G>A
- Clinical Significance Description
- Likely pathogenic
- Clinical Significance Last Update
- 2018-10-31
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000763242
- ClinVar Disease
- Hypertrophic cardiomyopathy 4
- ClinVar Disease
- Left ventricular noncompaction 10
- Observed Origin Sample
- unknown
Drugs