F52I (p.Phe52Ile) variant of CHM (P24386)
F52I (p.Phe52Ile) 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.
F52I (p.Phe52Ile) variant details
- p.Phe52Ile
- NCI-TCGA Cosmic COSV6256
- cosmic curated COSV62565
- Variant assessed as somatic; moderate impact.
- Missense
- MetaLR 0.36
- MetaSVM -0.56
- SIFT 0.16
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available