P56H (p.Pro56His) variant of CSF1R (P07333)
P56H (p.Pro56His) in CSF1R (P07333) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
P56H (p.Pro56His) variant details
- p.Pro56His
- NCI-TCGA Cosmic COSV5382
- NCI-TCGA Cosmic COSV5384
- cosmic curated COSV53841
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.