E98G (p.Glu98Gly) variant of CARD9 (Q9H257)
E98G (p.Glu98Gly) in CARD9 (Q9H257) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.41 / 1. The record also includes population frequency data and structural context.
E98G (p.Glu98Gly) variant details
- p.Glu98Gly
- gnomAD rs1833268163
- Missense
- Variant Prioritization Score for Impact Estimate 0.411
- REVEL 0.23
- CADD 28.60
- PolyPhen-2 1.00
- SIFT 0.01
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available