G52D (p.Gly52Asp) variant of CSF1R (P07333)
G52D (p.Gly52Asp) in CSF1R (P07333) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
G52D (p.Gly52Asp) variant details
- p.Gly52Asp
- NCI-TCGA Cosmic COSV9964
- cosmic curated COSV99643
- ESP rs144261133
- ExAC rs144261133
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.