D19G (p.Asp19Gly) variant of SLC34A3 (Q8N130)
D19G (p.Asp19Gly) in SLC34A3 (Q8N130) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.53 / 1. The record also includes population frequency data and structural context.
D19G (p.Asp19Gly) variant details
- p.Asp19Gly
- ExAC rs753533178
- TOPMed rs753533178
- gnomAD rs753533178
- Missense
- Variant Prioritization Score for Impact Estimate 0.527
- MetaLR 0.03
- MetaSVM -1.00
- CADD 5.96
- PolyPhen-2 0.00
- SIFT 0.67
- Most common in the Latino/Admixed American population (allele frequency 0.00013)
- Structural context available