P28H (p.Pro28His) variant of PDGFRA (P16234)
P28H (p.Pro28His) in PDGFRA (P16234) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
P28H (p.Pro28His) variant details
- p.Pro28His
- NCI-TCGA Cosmic COSV9995
- cosmic curated COSV99956
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available