Annotation Detail
Information
- Associated Genes
- CAPN3
- Associated Variants
-
CAPN3 p.Gly124Ala (p.G124A)
(
ENST00000349748.8,
ENST00000357568.8,
ENST00000318023.11,
ENST00000397163.8 )
CAPN3 p.Gly124Ala (p.G124A) ( ENST00000318023.11, ENST00000349748.8, ENST00000357568.8, ENST00000397163.8 ) - Associated Disease
- Inborn genetic diseases
- Source Database
- ClinVar
- Description
- NM_000070.3(CAPN3):c.371G>C (p.Gly124Ala) AND Inborn genetic diseases
- ClinVar Allele ID
- 134020
- ClinVar RefSeq Alternation Syntax
- NM_000070.3:c.371G>C
- ClinVar RefSeq Alternation Syntax
- NM_024344.2:c.371G>C
- ClinVar RefSeq Alternation Syntax
- NM_173087.2:c.371G>C
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Last Update
- 2022-02-10
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV002528206
- ClinVar Disease
- Inborn genetic diseases
- Observed Origin Sample
- germline
Drugs