Annotation Detail
Information
- Associated Genes
- MYBPC3
- Associated Variants
-
MYBPC3 p.Arg177Cys (p.R177C)
(
ENST00000399249.6,
ENST00000545968.6 )
MYBPC3 p.Arg177Cys (p.R177C) ( ENST00000399249.6, ENST00000545968.6 ) - Associated Disease
- not specified
- Source Database
- ClinVar
- Description
- NM_000256.3(MYBPC3):c.529C>T (p.Arg177Cys) AND not specified
- ClinVar Allele ID
- 45275
- ClinVar RefSeq Alternation Syntax
- NM_000256.3:c.529C>T
- Clinical Significance Description
- Conflicting interpretations of pathogenicity
- Clinical Significance Last Update
- 2023-04-11
- Clinical Significance Review Status
- criteria provided, conflicting interpretations
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000151166
- ClinVar Disease
- not specified
- Observed Origin Sample
- germline
Drugs