F111V (p.Phe111Val) variant of KRIT1 (O00522)
F111V (p.Phe111Val) 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.
F111V (p.Phe111Val) variant details
- p.Phe111Val
- NCI-TCGA Cosmic COSV6067
- cosmic curated COSV60670
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available