A26S (p.Ala26Ser) variant of CHM (P24386)
A26S (p.Ala26Ser) 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.
A26S (p.Ala26Ser) variant details
- p.Ala26Ser
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- MetaLR 0.78
- MetaSVM 0.68
- SIFT 0.01
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available