Annotation Detail
Information
- Associated Genes
- PKP2
- Associated Variants
-
PKP2 p.Trp676Ter (p.W676*)
(
ENST00000070846.11,
ENST00000700564.2,
ENST00000549461.3,
ENST00000700562.2,
ENST00000700559.2,
ENST00000700558.2,
ENST00000340811.9,
ENST00000700563.2 )
PKP2 p.Trp676Ter (p.W676*) ( ENST00000070846.11, ENST00000340811.9, ENST00000549461.3, ENST00000700558.2, ENST00000700559.2, ENST00000700562.2, ENST00000700563.2, ENST00000700564.2 ) - Associated Disease
- arrhythmogenic right ventricular dysplasia 9
- Source Database
- ClinVar
- Description
- NM_001005242.3(PKP2):c.1896G>A (p.Trp632Ter) AND Arrhythmogenic right ventricular dysplasia 9
- ClinVar Allele ID
- 45343
- ClinVar RefSeq Alternation Syntax
- NM_001005242.3:c.1896G>A
- ClinVar RefSeq Alternation Syntax
- NM_004572.4:c.2028G>A
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2022-08-12
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000656557
- ClinVar Disease
- Arrhythmogenic right ventricular dysplasia 9
- Observed Origin Sample
- germline
- Observed Origin Sample
- unknown
Drugs