T26I (p.Thr26Ile) variant of ATP7B (Copper-transporting ATPase 2)
T26I (p.Thr26Ile) 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 0.27 / 1. The record also includes population frequency data, published literature, and structural context.
T26I (p.Thr26Ile) variant details
- p.Thr26Ile
- rs1360917706
- ClinGen CA388045380
- ClinVar RCV004014146
- TOPMed rs1360917706
- Uncertain significance
- Wilson disease
- Missense
- Variant Prioritization Score for Impact Estimate 0.273
- REVEL 0.25
- ESM-1b 0.00
- AlphaMissense 0.09
- CADD 15.90
- PolyPhen-2 0.02
- SIFT 0.02
- ClinVar: Uncertain significance (Wilson disease)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Most common in the HGDP:SAN population (allele frequency 1)
- Structural context available
- Cited in: Diagnosis and treatment of Wilson disease: an update. (PMID 18506894)
- Cited in: Wilson Disease. (PMID 20301685)