F138L (p.Phe138Leu) variant of CHM (P24386)
F138L (p.Phe138Leu) 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.
F138L (p.Phe138Leu) variant details
- p.Phe138Leu
- NCI-TCGA Cosmic COSV1007
- Variant assessed as somatic; moderate impact.
- Missense
- MetaLR 0.07
- MetaSVM -1.05
- SIFT 0.64
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available