P25A (p.Pro25Ala) variant of DES (Desmin)
P25A (p.Pro25Ala) in DES (Desmin) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Desmin-related myofibrillar myopathy. The available variant effect predictions contribute to a CATVariant prioritization score of 0.38 / 1. The record also includes published literature and structural context.
P25A (p.Pro25Ala) variant details
- p.Pro25Ala
- rs1485482974
- ClinGen CA350682640
- ClinVar RCV003804546
- Uncertain significance
- Desmin-related myofibrillar myopathy
- Missense
- Variant Prioritization Score for Impact Estimate 0.384
- AlphaMissense 0.05
- MetaLR 0.26
- MetaSVM -0.79
- PolyPhen-2 0.00
- SIFT 1.00
- MutPred 0.31
- ClinVar: Uncertain significance (Desmin-related myofibrillar myopathy)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available
- Cited in: Dilated Cardiomyopathy Overview. (PMID 20301486)
- Cited in: Evidence-based guideline summary: diagnosis and treatment of limb-girdle and distal dystrophies [RETIRED]: report of… (PMID 25313375)