I38K (p.Ile38Lys) variant of SLC2A2 (P11168)
I38K (p.Ile38Lys) in SLC2A2 (P11168) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.71 / 1. The record also includes population frequency data and structural context.
I38K (p.Ile38Lys) variant details
- p.Ile38Lys
- gnomAD rs1360464436
- Missense
- Variant Prioritization Score for Impact Estimate 0.711
- REVEL 0.78
- CADD 23.60
- PolyPhen-2 0.98
- SIFT 0.00
- Most common in the South Asian population (allele frequency 1.2e-05)
- Structural context available