C77Y (p.Cys77Tyr) variant of UMOD (Uromodulin)
C77Y (p.Cys77Tyr) in UMOD (Uromodulin) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as pathogenic in the context of Familial juvenile hyperuricemic nephropathy type 1. The available variant effect predictions contribute to a CATVariant prioritization score of 0.98 / 1. The record also includes published literature and structural context.
C77Y (p.Cys77Tyr) variant details
- p.Cys77Tyr
- rs121917768
- ClinGen CA256244
- ClinVar RCV002251321
- UniProt VAR 025950
- Pathogenic
- Familial juvenile hyperuricemic nephropathy type 1
- Missense
- Variant Prioritization Score for Impact Estimate 0.977
- AlphaMissense 0.94
- MetaLR 0.99
- MetaSVM 1.00
- PolyPhen-2 1.00
- SIFT 0.00
- MutPred 0.98
- ClinVar: Pathogenic (Familial juvenile hyperuricemic nephropathy type 1)
- EBI: Pathogenic (in ADTKD1)
- UniProt: Pathogenic (in ADTKD1)
- Structural context available
- Cited in: Genetic mapping studies of familial juvenile hyperuricemic nephropathy on chromosome 16p11-p13. (PMID 12519891)
- Cited in: UROMODULIN mutations cause familial juvenile hyperuricemic nephropathy. (PMID 12629136)