S15R (p.Ser15Arg) variant of CHEK2 (O96017)
S15R (p.Ser15Arg) in CHEK2 (O96017) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Hereditary cancer-predisposing syndrome. The record also includes structural context.
S15R (p.Ser15Arg) variant details
- p.Ser15Arg
- Ensembl rs2146155168
- Uncertain significance
- Hereditary cancer-predisposing syndrome
- Missense
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available