A26T (p.Ala26Thr) variant of MCM5 (P33992)
A26T (p.Ala26Thr) in MCM5 (P33992) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
A26T (p.Ala26Thr) variant details
- p.Ala26Thr
- NCI-TCGA Cosmic COSV5334
- cosmic curated COSV53346
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available