I17N (p.Ile17Asn) variant of RAD21 (O60216)
I17N (p.Ile17Asn) in RAD21 (O60216) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
I17N (p.Ile17Asn) variant details
- p.Ile17Asn
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available