L91M (p.Leu91Met) variant of CSF1R (P07333)
L91M (p.Leu91Met) in CSF1R (P07333) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
L91M (p.Leu91Met) variant details
- p.Leu91Met
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.