A101V (p.Ala101Val) variant of IDH2 (P48735)
A101V (p.Ala101Val) in IDH2 (P48735) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.65 / 1. The record also includes population frequency data and structural context.
A101V (p.Ala101Val) variant details
- p.Ala101Val
- Ensembl rs2151551271
- Missense
- Variant Prioritization Score for Impact Estimate 0.65
- REVEL 0.55
- CADD 28.30
- PolyPhen-2 0.55
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available