G9D (p.Gly9Asp) variant of IL7R (P16871)
G9D (p.Gly9Asp) in IL7R (P16871) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
G9D (p.Gly9Asp) variant details
- p.Gly9Asp
- ExAC rs776642878
- gnomAD rs776642878
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available