S3N (p.Ser3Asn) variant of SLC34A3 (Q8N130)
S3N (p.Ser3Asn) in SLC34A3 (Q8N130) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.12 / 1. The record also includes population frequency data and structural context.
S3N (p.Ser3Asn) variant details
- p.Ser3Asn
- TOPMed rs1836225446
- Missense
- Variant Prioritization Score for Impact Estimate 0.118
- MetaLR 0.02
- MetaSVM -0.98
- CADD 0.50
- PolyPhen-2 0.00
- SIFT 1.00
- Most common in the Non-Finnish European population (allele frequency 2.7e-06)
- Structural context available