E59V (p.Glu59Val) variant of SLC34A3 (Q8N130)
E59V (p.Glu59Val) in SLC34A3 (Q8N130) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.49 / 1. The record also includes population frequency data and structural context.
E59V (p.Glu59Val) variant details
- p.Glu59Val
- ExAC rs761399770
- TOPMed rs761399770
- gnomAD rs761399770
- Missense
- Variant Prioritization Score for Impact Estimate 0.493
- MetaLR 0.09
- MetaSVM -1.06
- CADD 23.40
- SIFT 0.01
- Most common in the Latino/Admixed American population (allele frequency 6.5e-05)
- Structural context available