P29A (p.Pro29Ala) variant of IDH2 (P48735)
P29A (p.Pro29Ala) in IDH2 (P48735) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.16 / 1. The record also includes population frequency data and structural context.
P29A (p.Pro29Ala) variant details
- p.Pro29Ala
- Ensembl rs1431694926
- Missense
- Variant Prioritization Score for Impact Estimate 0.163
- REVEL 0.05
- CADD 10.90
- PolyPhen-2 0.00
- SIFT 0.66
- Most common in the Non-Finnish European population (allele frequency 1e-06)
- Structural context available