P68T (p.Pro68Thr) variant of SLC2A2 (P11168)
P68T (p.Pro68Thr) in SLC2A2 (P11168) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.30 / 1. The record also includes population frequency data and structural context.
P68T (p.Pro68Thr) variant details
- p.Pro68Thr
- gnomAD rs1391257598
- Missense
- Variant Prioritization Score for Impact Estimate 0.303
- REVEL 0.20
- CADD 11.80
- PolyPhen-2 0.01
- SIFT 0.02
- Most common in the East Asian population (allele frequency 2.5e-05)
- Structural context available