T26A (p.Thr26Ala) variant of ATP7B (Copper-transporting ATPase 2)
T26A (p.Thr26Ala) 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 0.17 / 1. The record also includes population frequency data, published literature, and structural context.
T26A (p.Thr26Ala) variant details
- p.Thr26Ala
- rs1334967662
- ClinGen CA388045383
- ClinVar RCV003068422
- TOPMed rs1334967662
- Uncertain significance
- Wilson disease
- Missense
- Variant Prioritization Score for Impact Estimate 0.168
- REVEL 0.23
- ESM-1b 0.00
- AlphaMissense 0.05
- CADD 0.24
- PolyPhen-2 0.00
- SIFT 1.00
- ClinVar: Uncertain significance (Wilson disease)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Most common in the 1KG:ACB population (allele frequency 0.038)
- Structural context available
- Cited in: Diagnosis and treatment of Wilson disease: an update. (PMID 18506894)
- Cited in: Wilson Disease. (PMID 20301685)