A34V (p.Ala34Val) variant of SLC34A3 (Q8N130)
A34V (p.Ala34Val) in SLC34A3 (Q8N130) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.15 / 1. The record also includes population frequency data and structural context.
A34V (p.Ala34Val) variant details
- p.Ala34Val
- TOPMed rs1284104939
- gnomAD rs1284104939
- Missense
- Variant Prioritization Score for Impact Estimate 0.146
- MetaLR 0.06
- MetaSVM -1.01
- CADD 6.68
- PolyPhen-2 0.00
- SIFT 0.24
- Most common in the REMAINING population (allele frequency 1.7e-05)
- Structural context available