S81T (p.Ser81Thr) variant of ATP7B (Copper-transporting ATPase 2)
S81T (p.Ser81Thr) 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 0.37 / 1. The record also includes population frequency data, published literature, and structural context.
S81T (p.Ser81Thr) variant details
- p.Ser81Thr
- rs1952034021
- ClinGen CA388044799
- ClinVar RCV001238407
- Ensembl rs1952034021
- Uncertain significance
- Wilson disease
- Missense
- Variant Prioritization Score for Impact Estimate 0.365
- REVEL 0.41
- ESM-1b 0.00
- AlphaMissense 0.10
- CADD 18.90
- PolyPhen-2 0.85
- SIFT 0.29
- ClinVar: Uncertain significance (Wilson disease)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Most common in the HGDP:SARDINIAN population (allele frequency 0.056)
- Structural context available
- Cited in: Diagnosis and treatment of Wilson disease: an update. (PMID 18506894)
- Cited in: Wilson Disease. (PMID 20301685)