S38F (p.Ser38Phe) variant of IRAG1 (Q9Y6F6)
S38F (p.Ser38Phe) in IRAG1 (Q9Y6F6) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.33 / 1. The record also includes population frequency data and structural context.
S38F (p.Ser38Phe) variant details
- p.Ser38Phe
- rs1282735373
- NCI-TCGA Cosmic COSV7021
- cosmic curated COSV70211
- gnomAD rs1282735373
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.325
- AlphaMissense 0.13
- MetaLR 0.08
- MetaSVM -1.07
- SIFT 0.00
- MutPred 0.17
- UniProt: Variant assessed as somatic; moderate impact.
- Population evidence available
- Structural context available