M33V (p.Met33Val) variant of FBXW7 (Q969H0)
M33V (p.Met33Val) in FBXW7 (Q969H0) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
M33V (p.Met33Val) variant details
- p.Met33Val
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available