Annotation Detail
Information
- Associated Genes
- CAPN3
- Associated Variants
-
CAPN3 p.Arg493Trp (p.R493W)
(
ENST00000349748.8,
ENST00000357568.8,
ENST00000318023.11,
ENST00000397163.8 )
CAPN3 p.Arg493Trp (p.R493W) ( ENST00000357568.8, ENST00000318023.11, ENST00000349748.8, ENST00000397163.8 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_000070.3(CAPN3):c.1477C>T (p.Arg493Trp) AND not provided
- ClinVar Allele ID
- 190955
- ClinVar RefSeq Alternation Syntax
- NM_024344.2:c.1477C>T
- ClinVar RefSeq Alternation Syntax
- NM_173087.2:c.1333C>T
- ClinVar RefSeq Alternation Syntax
- NM_000070.3:c.1477C>T
- Clinical Significance Description
- Pathogenic/Likely pathogenic
- Clinical Significance Last Update
- 2022-08-02
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000173976
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
- Observed Origin Sample
- unknown
Drugs