S135P (p.Ser135Pro) variant of SLC2A2 (P11168)
S135P (p.Ser135Pro) in SLC2A2 (P11168) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.52 / 1. The record also includes population frequency data and structural context.
S135P (p.Ser135Pro) variant details
- p.Ser135Pro
- ExAC rs771843187
- gnomAD rs771843187
- Missense
- Variant Prioritization Score for Impact Estimate 0.518
- REVEL 0.55
- CADD 24.20
- PolyPhen-2 0.82
- SIFT 0.01
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available