L262P (p.Leu262Pro) variant of PKP2 (Plakophilin-2)
L262P (p.Leu262Pro) in PKP2 (Plakophilin-2) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Arrhythmogenic right ventricular dysplasia 9. The record also includes published literature and structural context.
L262P (p.Leu262Pro) variant details
- p.Leu262Pro
- rs2541339735
- ClinGen CA384362507
- ClinVar RCV002300261
- Uncertain significance
- Arrhythmogenic right ventricular dysplasia 9
- Missense
- ClinVar: Uncertain significance (Arrhythmogenic right ventricular dysplasia 9)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available
- Cited in: Arrhythmogenic Right Ventricular Cardiomyopathy Overview. (PMID 20301310)
- Cited in: ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing. (PMID 23788249)