K38T (p.Lys38Thr) variant of SLC2A1 (P11166)
K38T (p.Lys38Thr) in SLC2A1 (P11166) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.47 / 1. The record also includes population frequency data and structural context.
K38T (p.Lys38Thr) variant details
- p.Lys38Thr
- gnomAD rs1467764389
- Missense
- Variant Prioritization Score for Impact Estimate 0.473
- REVEL 0.38
- CADD 24.10
- PolyPhen-2 0.04
- SIFT 0.20
- Most common in the REMAINING population (allele frequency 1.7e-05)
- Structural context available