G21R (p.Gly21Arg) variant of STK11 (Q15831)
G21R (p.Gly21Arg) in STK11 (Q15831) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Hereditary cancer-predisposing syndrome; Peutz-Jeghers syndrome. The record also includes structural context.
G21R (p.Gly21Arg) variant details
- p.Gly21Arg
- TOPMed rs1064793751
- gnomAD rs1064793751
- Uncertain significance
- Hereditary cancer-predisposing syndrome; Peutz-Jeghers syndrome
- Missense
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome; Peutz-Jeghers syndrome)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available