P56R (p.Pro56Arg) variant of CSF1R (P07333)
P56R (p.Pro56Arg) in CSF1R (P07333) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
P56R (p.Pro56Arg) variant details
- p.Pro56Arg
- NCI-TCGA Cosmic COSV5382
- cosmic curated COSV53828
- NCI-TCGA Cosmic COSV5384
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.