P16S (p.Pro16Ser) variant of SLC2A4 (P14672)
P16S (p.Pro16Ser) in SLC2A4 (P14672) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.34 / 1. The record also includes population frequency data and structural context.
P16S (p.Pro16Ser) variant details
- p.Pro16Ser
- TOPMed rs1170001111
- gnomAD rs1170001111
- Missense
- Variant Prioritization Score for Impact Estimate 0.337
- REVEL 0.26
- MetaLR 0.24
- MetaSVM -0.75
- CADD 8.93
- PolyPhen-2 0.00
- SIFT 0.46
- Most common in the East Asian population (allele frequency 2.5e-05)
- Structural context available