S56P (p.Ser56Pro) variant of RAD21 (O60216)
S56P (p.Ser56Pro) in RAD21 (O60216) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
S56P (p.Ser56Pro) variant details
- p.Ser56Pro
- NCI-TCGA Cosmic COSV5206
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.