S29W (p.Ser29Trp) variant of MCM5 (P33992)
S29W (p.Ser29Trp) 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.
S29W (p.Ser29Trp) variant details
- p.Ser29Trp
- NCI-TCGA Cosmic COSV9933
- cosmic curated COSV99331
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available