A887P (p.Ala887Pro) variant of ATP7B (Copper-transporting ATPase 2)
A887P (p.Ala887Pro) in ATP7B (Copper-transporting ATPase 2) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Wilson disease. The available variant effect predictions contribute to a CATVariant prioritization score of 0.86 / 1. The record also includes population frequency data, published literature, and structural context.
A887P (p.Ala887Pro) variant details
- p.Ala887Pro
- rs768479687
- ClinGen CA388034478
- ClinVar RCV003079396
- ExAC rs768479687
- Uncertain significance
- Wilson disease
- Missense
- Variant Prioritization Score for Impact Estimate 0.863
- REVEL 0.88
- ESM-1b 1.00
- AlphaMissense 0.94
- CADD 26.10
- PolyPhen-2 0.99
- SIFT 0.00
- ClinVar: Uncertain significance (Wilson disease)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Most common in the 1KG:CHB population (allele frequency 0.015)
- Structural context available
- Cited in: Diagnosis and treatment of Wilson disease: an update. (PMID 18506894)
- Cited in: Wilson Disease. (PMID 20301685)