A35G (p.Ala35Gly) variant of CDKN2A (Tumor suppressor ARF)
A35G (p.Ala35Gly) 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.
A35G (p.Ala35Gly) variant details
- p.Ala35Gly
- Ensembl rs2131148491
- 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