T46I (p.Thr46Ile) variant of ERCC2 (P18074)
T46I (p.Thr46Ile) in ERCC2 (P18074) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
T46I (p.Thr46Ile) variant details
- p.Thr46Ile
- NCI-TCGA Cosmic COSV5553
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available