R1151P (p.Arg1151Pro) variant of ATP7B (Copper-transporting ATPase 2)
R1151P (p.Arg1151Pro) 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 0.87 / 1. The record also includes population frequency data, published literature, and structural context.
R1151P (p.Arg1151Pro) variant details
- p.Arg1151Pro
- rs377297166
- ClinGen CA388026612
- ClinVar RCV002227383
- ESP rs377297166
- Uncertain significance
- Wilson disease
- Missense
- Variant Prioritization Score for Impact Estimate 0.873
- REVEL 0.89
- ESM-1b 1.00
- AlphaMissense 0.93
- CADD 27.40
- PolyPhen-2 1.00
- SIFT 0.00
- ClinVar: Uncertain significance (Wilson disease)
- EBI: Variant of uncertain significance (in WD)
- UniProt: Uncertain significance (in WD)
- Most common in the 1KG:ACB population (allele frequency 0.0054)
- Structural context available
- Cited in: Diagnosis and treatment of Wilson disease: an update. (PMID 18506894)
- Cited in: Wilson Disease. (PMID 20301685)