P56S (p.Pro56Ser) variant of CSF1R (P07333)
P56S (p.Pro56Ser) in CSF1R (P07333) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
P56S (p.Pro56Ser) variant details
- p.Pro56Ser
- cosmic curated COSV10458
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.