T46S (p.Thr46Ser) variant of ERCC2 (P18074)
T46S (p.Thr46Ser) 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.
T46S (p.Thr46Ser) variant details
- p.Thr46Ser
- NCI-TCGA Cosmic COSV5553
- cosmic curated COSV55538
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available