P15T (p.Pro15Thr) variant of SLC2A4 (P14672)
P15T (p.Pro15Thr) in SLC2A4 (P14672) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.18 / 1. The record also includes population frequency data and structural context.
P15T (p.Pro15Thr) variant details
- p.Pro15Thr
- ExAC rs763807880
- TOPMed rs763807880
- gnomAD rs763807880
- Missense
- Variant Prioritization Score for Impact Estimate 0.18
- REVEL 0.05
- MetaLR 0.26
- MetaSVM -0.87
- CADD 9.31
- PolyPhen-2 0.01
- SIFT 0.30
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.00032)
- Structural context available