R26K (p.Arg26Lys) variant of SLC34A3 (Q8N130)
R26K (p.Arg26Lys) in SLC34A3 (Q8N130) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.20 / 1. The record also includes population frequency data and structural context.
R26K (p.Arg26Lys) variant details
- p.Arg26Lys
- TOPMed rs1206280444
- gnomAD rs1206280444
- Missense
- Variant Prioritization Score for Impact Estimate 0.196
- MetaLR 0.04
- MetaSVM -0.97
- CADD 5.34
- PolyPhen-2 0.00
- SIFT 0.96
- Most common in the REMAINING population (allele frequency 1.7e-05)
- Structural context available