G57A (p.Gly57Ala) variant of ERCC3 (P19447)
G57A (p.Gly57Ala) in ERCC3 (P19447) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
G57A (p.Gly57Ala) variant details
- p.Gly57Ala
- NCI-TCGA Cosmic COSV5342
- cosmic curated COSV53426
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available