G111R (p.Gly111Arg) variant of CARD9 (Q9H257)
G111R (p.Gly111Arg) in CARD9 (Q9H257) 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 0.56 / 1. The record also includes population frequency data.
G111R (p.Gly111Arg) variant details
- p.Gly111Arg
- rs769183409
- NCI-TCGA Cosmic COSV5373
- cosmic curated COSV53731
- ExAC rs769183409
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.555
- REVEL 0.40
- CADD 24.50
- PolyPhen-2 1.00
- SIFT 0.00
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the East Asian population (allele frequency 5e-05)