A101T (p.Ala101Thr) variant of IDH2 (P48735)
A101T (p.Ala101Thr) in IDH2 (P48735) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.74 / 1. The record also includes population frequency data and structural context.
A101T (p.Ala101Thr) variant details
- p.Ala101Thr
- Ensembl rs2151551274
- Missense
- Variant Prioritization Score for Impact Estimate 0.737
- REVEL 0.70
- CADD 26.80
- PolyPhen-2 0.97
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available