S3T (p.Ser3Thr) variant of SLC34A3 (Q8N130)
S3T (p.Ser3Thr) in SLC34A3 (Q8N130) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.13 / 1. The record also includes population frequency data, published literature, and structural context.
S3T (p.Ser3Thr) variant details
- p.Ser3Thr
- gnomAD 9-137231710-G-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.128
- MetaLR 0.04
- MetaSVM -1.02
- CADD 4.04
- PolyPhen-2 0.00
- SIFT 0.24
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available