Y14C (p.Tyr14Cys) variant of ERCC2 (P18074)
Y14C (p.Tyr14Cys) 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.
Y14C (p.Tyr14Cys) variant details
- p.Tyr14Cys
- NCI-TCGA Cosmic COSV5554
- cosmic curated COSV55540
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available