T14N (p.Thr14Asn) variant of SLC34A3 (Q8N130)
T14N (p.Thr14Asn) in SLC34A3 (Q8N130) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.31 / 1. The record also includes population frequency data and structural context.
T14N (p.Thr14Asn) variant details
- p.Thr14Asn
- TOPMed rs1410537698
- gnomAD rs1410537698
- Missense
- Variant Prioritization Score for Impact Estimate 0.307
- MetaLR 0.05
- MetaSVM -1.06
- CADD 8.85
- SIFT 0.09
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available