R18Q (p.Arg18Gln) variant of PIK3CG (P48736)
R18Q (p.Arg18Gln) in PIK3CG (P48736) 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.
R18Q (p.Arg18Gln) variant details
- p.Arg18Gln
- rs142380460
- NCI-TCGA Cosmic COSV6324
- cosmic curated COSV63248
- 1000Genomes rs142380460
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.335
- REVEL 0.14
- MetaLR 0.31
- MetaSVM -0.69
- CADD 21.50
- PolyPhen-2 0.05
- SIFT 0.01
- UniProt: Variant assessed as somatic; moderate impact.
- Population evidence available
- Structural context available