S19I (p.Ser19Ile) variant of PDGFRA (P16234)
S19I (p.Ser19Ile) in PDGFRA (P16234) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes variant effect predictions and structural context.
S19I (p.Ser19Ile) variant details
- p.Ser19Ile
- NCI-TCGA Cosmic COSV5726
- cosmic curated COSV57264
- Variant assessed as somatic; moderate impact.
- Missense
- MetaLR 0.22
- MetaSVM -0.94
- SIFT 0.40
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available