F9V (p.Phe9Val) variant of CHM (P24386)
F9V (p.Phe9Val) in CHM (P24386) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes variant effect predictions and structural context.
F9V (p.Phe9Val) variant details
- p.Phe9Val
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- MetaLR 0.70
- MetaSVM 0.35
- SIFT 0.06
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available