T59A (p.Thr59Ala) variant of FANCC (Fanconi anemia group C protein)
T59A (p.Thr59Ala) in FANCC (Fanconi anemia group C protein) 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.
T59A (p.Thr59Ala) variant details
- p.Thr59Ala
- NCI-TCGA Cosmic COSV5666
- cosmic curated COSV56662
- Uncertain significance
- Hereditary cancer-predisposing syndrome
- Missense
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome)
- UniProt: Uncertain significance
- Structural context available