P3S (p.Pro3Ser) variant of SLC2A1 (P11166)
P3S (p.Pro3Ser) in SLC2A1 (P11166) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.26 / 1. The record also includes population frequency data and structural context.
P3S (p.Pro3Ser) variant details
- p.Pro3Ser
- gnomAD rs1232724729
- Missense
- Variant Prioritization Score for Impact Estimate 0.263
- REVEL 0.21
- CADD 17.90
- PolyPhen-2 0.00
- SIFT 0.58
- Most common in the Latino/Admixed American population (allele frequency 2.8e-05)
- Structural context available