Annotation Detail
Information
- Associated Genes
- CAPN3
- Associated Variants
-
CAPN3 p.Arg769Gln (p.R769Q)
(
ENST00000337571.9,
ENST00000357568.8,
ENST00000397163.8,
ENST00000397200.8,
ENST00000397204.9,
ENST00000349748.8,
ENST00000569136.6,
ENST00000561817.5,
ENST00000318023.11,
ENST00000673743.1,
ENST00000673771.1,
ENST00000674093.1,
ENST00000674119.1,
ENST00000673692.1,
ENST00000674018.1,
ENST00000673936.1,
ENST00000674139.1,
ENST00000674146.1,
ENST00000674149.1,
ENST00000673978.1,
ENST00000673750.1,
ENST00000673890.1,
ENST00000674052.1,
ENST00000673886.1,
ENST00000673928.1,
ENST00000673851.1 )
CAPN3 p.Arg769Gln (p.R769Q) ( ENST00000318023.11, ENST00000337571.9, ENST00000349748.8, ENST00000357568.8, ENST00000397163.8, ENST00000397200.8, ENST00000397204.9, ENST00000561817.5, ENST00000569136.6, ENST00000673692.1, ENST00000673743.1, ENST00000673750.1, ENST00000673771.1, ENST00000673851.1, ENST00000673886.1, ENST00000673890.1, ENST00000673928.1, ENST00000673936.1, ENST00000673978.1, ENST00000674018.1, ENST00000674052.1, ENST00000674093.1, ENST00000674119.1, ENST00000674139.1, ENST00000674146.1, ENST00000674149.1 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_000070.3(CAPN3):c.2306G>A (p.Arg769Gln) AND not provided
- ClinVar Allele ID
- 32652
- ClinVar RefSeq Alternation Syntax
- NM_173089.2:c.311G>A
- ClinVar RefSeq Alternation Syntax
- NM_173088.2:c.770G>A
- ClinVar RefSeq Alternation Syntax
- NM_024344.2:c.2288G>A
- ClinVar RefSeq Alternation Syntax
- NM_173090.2:c.311G>A
- ClinVar RefSeq Alternation Syntax
- NM_000070.3:c.2306G>A
- ClinVar RefSeq Alternation Syntax
- NM_173087.2:c.2030G>A
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2022-12-08
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000711017
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs