I105M (p.Ile105Met) variant of TYK2 (P29597)
I105M (p.Ile105Met) in TYK2 (P29597) 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.
I105M (p.Ile105Met) variant details
- p.Ile105Met
- ExAC rs770951647
- TOPMed rs770951647
- gnomAD rs770951647
- Likely benign
- Inborn genetic diseases
- Missense
- ClinVar: Likely benign (Inborn genetic diseases)
- UniProt: Likely benign
- Structural context available