S2I (p.Ser2Ile) variant of WRN (Q14191)
S2I (p.Ser2Ile) in WRN (Q14191) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
S2I (p.Ser2Ile) variant details
- p.Ser2Ile
- NCI-TCGA Cosmic COSV9998
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available