P86R (p.Pro86Arg) variant of DPYD (Q12882)
P86R (p.Pro86Arg) in DPYD (Q12882) is a missense change. Clinical records from EBI and UniProt describe it as pathogenic. The record also includes variant effect predictions and structural context.
P86R (p.Pro86Arg) variant details
- p.Pro86Arg
- 1000Genomes rs568132506
- ExAC rs568132506
- TOPMed rs568132506
- gnomAD rs568132506
- Pathogenic
- Missense
- MetaLR 0.70
- MetaSVM 0.42
- SIFT 0.00
- EBI: Pathogenic
- UniProt: Pathogenic
- Structural context available