I11L (p.Ile11Leu) variant of CDKN2A (Tumor suppressor ARF)
I11L (p.Ile11Leu) in CDKN2A (Tumor suppressor ARF) is a missense change. Clinical records from ClinVar and UniProt describe it as uncertain significance in the context of Hereditary cancer-predisposing syndrome. The record also includes structural context.
I11L (p.Ile11Leu) variant details
- p.Ile11Leu
- Ensembl rs1820535855
- Uncertain significance
- Hereditary cancer-predisposing syndrome
- Missense
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome)
- UniProt: Uncertain significance
- Structural context available