N27D (p.Asn27Asp) variant of SLC34A3 (Q8N130)
N27D (p.Asn27Asp) 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.
N27D (p.Asn27Asp) variant details
- p.Asn27Asp
- Ensembl rs750540324
- Missense
- Variant Prioritization Score for Impact Estimate 0.15
- MetaLR 0.05
- MetaSVM -0.99
- CADD 7.26
- PolyPhen-2 0.00
- SIFT 0.38
- Most common in the Non-Finnish European population (allele frequency 5.4e-06)
- Structural context available