R9G (p.Arg9Gly) variant of IDH2 (P48735)
R9G (p.Arg9Gly) in IDH2 (P48735) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.35 / 1. The record also includes population frequency data and structural context.
R9G (p.Arg9Gly) variant details
- p.Arg9Gly
- Ensembl rs1596083346
- Missense
- Variant Prioritization Score for Impact Estimate 0.354
- REVEL 0.30
- CADD 23.00
- PolyPhen-2 0.00
- SIFT 0.05
- Most common in the Non-Finnish European population (allele frequency 2e-06)
- Structural context available