P19S (p.Pro19Ser) variant of CHM (P24386)
P19S (p.Pro19Ser) 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.
P19S (p.Pro19Ser) variant details
- p.Pro19Ser
- NCI-TCGA TCGA novel
- Ensembl rs1933881041
- Variant assessed as somatic; moderate impact.
- Missense
- MetaLR 0.37
- MetaSVM -0.28
- SIFT 0.01
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available