S101T (p.Ser101Thr) variant of UMOD (Uromodulin)
S101T (p.Ser101Thr) in UMOD (Uromodulin) is a missense change. Clinical records from ClinVar and UniProt describe it as likely benign in the context of Inborn genetic diseases. The record also includes structural context.
S101T (p.Ser101Thr) variant details
- p.Ser101Thr
- Ensembl rs890891558
- Likely benign
- Inborn genetic diseases
- Missense
- ClinVar: Likely benign (Inborn genetic diseases)
- UniProt: Likely benign
- Structural context available