P186S (p.Pro186Ser) variant of MSI1 (O43347)
P186S (p.Pro186Ser) in MSI1 (O43347) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
P186S (p.Pro186Ser) variant details
- p.Pro186Ser
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available