F111S (p.Phe111Ser) variant of KRIT1 (O00522)
F111S (p.Phe111Ser) in KRIT1 (O00522) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
F111S (p.Phe111Ser) variant details
- p.Phe111Ser
- NCI-TCGA Cosmic COSV6066
- cosmic curated COSV60666
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available