R9H (p.Arg9His) variant of IDH2 (P48735)
R9H (p.Arg9His) in IDH2 (P48735) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.31 / 1. The record also includes population frequency data and structural context.
R9H (p.Arg9His) variant details
- p.Arg9His
- Ensembl rs2151558074
- Missense
- Variant Prioritization Score for Impact Estimate 0.309
- REVEL 0.15
- CADD 23.20
- PolyPhen-2 0.03
- SIFT 0.03
- Most common in the Latino/Admixed American population (allele frequency 4.3e-05)
- Structural context available