P49S (p.Pro49Ser) variant of SLC2A2 (P11168)
P49S (p.Pro49Ser) in SLC2A2 (P11168) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.17 / 1. The record also includes population frequency data and structural context.
P49S (p.Pro49Ser) variant details
- p.Pro49Ser
- TOPMed rs983907950
- gnomAD rs983907950
- Missense
- Variant Prioritization Score for Impact Estimate 0.171
- REVEL 0.12
- CADD 4.57
- PolyPhen-2 0.00
- SIFT 0.96
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available