R21W (p.Arg21Trp) variant of CDKN2A (Tumor suppressor ARF)
R21W (p.Arg21Trp) in CDKN2A (Tumor suppressor ARF) 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.
R21W (p.Arg21Trp) variant details
- p.Arg21Trp
- TOPMed rs1397255688
- gnomAD rs1397255688
- 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