R65G (p.Arg65Gly) variant of SLC34A3 (Q8N130)
R65G (p.Arg65Gly) in SLC34A3 (Q8N130) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.30 / 1. The record also includes population frequency data and structural context.
R65G (p.Arg65Gly) variant details
- p.Arg65Gly
- TOPMed rs1836287619
- Missense
- Variant Prioritization Score for Impact Estimate 0.297
- MetaLR 0.07
- MetaSVM -1.01
- CADD 22.20
- PolyPhen-2 0.25
- SIFT 0.05
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available