R26S (p.Arg26Ser) variant of SLC34A3 (Q8N130)
R26S (p.Arg26Ser) in SLC34A3 (Q8N130) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.27 / 1. The record also includes population frequency data and structural context.
R26S (p.Arg26Ser) variant details
- p.Arg26Ser
- ExAC rs771909414
- gnomAD rs771909414
- Missense
- Variant Prioritization Score for Impact Estimate 0.269
- MetaLR 0.04
- MetaSVM -0.99
- CADD 5.54
- PolyPhen-2 0.01
- SIFT 0.73
- Most common in the South Asian population (allele frequency 1.2e-05)
- Structural context available