Annotation Detail
Information
- Associated Genes
- CAV3 OXTR
- Associated Variants
-
CAV3 p.Leu79Arg (p.L79R)
(
ENST00000343849.3,
ENST00000397368.2 )
CAV3 p.Leu79Arg (p.L79R) ( ENST00000343849.3, ENST00000397368.2 ) - Associated Disease
- long QT syndrome
- Source Database
- ClinVar
- Description
- NM_033337.3(CAV3):c.236T>G (p.Leu79Arg) AND Long QT syndrome
- ClinVar Allele ID
- 23335
- ClinVar RefSeq Alternation Syntax
- NM_001234.5:c.236T>G
- ClinVar RefSeq Alternation Syntax
- NM_033337.3:c.236T>G
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Last Update
- 2019-11-08
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001246513
- ClinVar Disease
- Long QT syndrome
- Observed Origin Sample
- germline
Drugs