E12V (p.Glu12Val) variant of ATP7B (Copper-transporting ATPase 2)
E12V (p.Glu12Val) 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 0.31 / 1. The record also includes population frequency data, published literature, and structural context.
E12V (p.Glu12Val) variant details
- p.Glu12Val
- rs374944498
- ClinGen CA6989713
- ClinVar RCV001280026
- ESP rs374944498
- Uncertain significance
- Wilson disease
- Missense
- Variant Prioritization Score for Impact Estimate 0.314
- REVEL 0.34
- ESM-1b 0.00
- AlphaMissense 0.15
- CADD 22.80
- PolyPhen-2 0.00
- SIFT 0.02
- ClinVar: Uncertain significance (Wilson disease)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Most common in the HGDP:BIAKA population (allele frequency 0.023)
- Structural context available
- Cited in: Diagnosis and treatment of Wilson disease: an update. (PMID 18506894)
- Cited in: Wilson Disease. (PMID 20301685)