T8I (p.Thr8Ile) variant of CDKN2A (Tumor suppressor ARF)
T8I (p.Thr8Ile) 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.
T8I (p.Thr8Ile) variant details
- p.Thr8Ile
- cosmic curated COSV10606
- TOPMed rs1820536698
- 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