Annotation Detail
Information
- Associated Genes
- CAPN3
- Associated Variants
-
CAPN3 p.Leu189Pro (p.L189P)
(
ENST00000357568.8,
ENST00000318023.11,
ENST00000349748.8,
ENST00000397163.8 )
CAPN3 p.Leu189Pro (p.L189P) ( ENST00000318023.11, ENST00000349748.8, ENST00000357568.8, ENST00000397163.8 ) - Associated Disease
- autosomal recessive limb-girdle muscular dystrophy type 2A
- Source Database
- ClinVar
- Description
- NM_000070.3(CAPN3):c.566T>C (p.Leu189Pro) AND Autosomal recessive limb-girdle muscular dystrophy type 2A
- ClinVar Allele ID
- 213823
- ClinVar RefSeq Alternation Syntax
- NM_024344.2:c.566T>C
- ClinVar RefSeq Alternation Syntax
- NM_173087.2:c.566T>C
- ClinVar RefSeq Alternation Syntax
- NM_000070.3:c.566T>C
- Clinical Significance Description
- Conflicting interpretations of pathogenicity
- Clinical Significance Last Update
- 2021-08-26
- Clinical Significance Review Status
- criteria provided, conflicting interpretations
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000201041
- ClinVar Disease
- Autosomal recessive limb-girdle muscular dystrophy type 2A
- Observed Origin Sample
- germline
Drugs