S3L (p.Ser3Leu) variant of SLC2A4 (P14672)
S3L (p.Ser3Leu) in SLC2A4 (P14672) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.43 / 1. The record also includes population frequency data and structural context.
S3L (p.Ser3Leu) variant details
- p.Ser3Leu
- gnomAD rs1227450234
- Missense
- Variant Prioritization Score for Impact Estimate 0.431
- REVEL 0.25
- MetaLR 0.28
- MetaSVM -0.78
- CADD 24.30
- PolyPhen-2 0.01
- SIFT 0.01
- Most common in the Non-Finnish European population (allele frequency 1e-06)
- Structural context available