T17N (p.Thr17Asn) variant of SLC47A1 (Q96FL8)
T17N (p.Thr17Asn) in SLC47A1 (Q96FL8) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.03 / 1. The record also includes population frequency data and structural context.
T17N (p.Thr17Asn) variant details
- p.Thr17Asn
- ExAC rs768787010
- TOPMed rs768787010
- gnomAD rs768787010
- Missense
- Variant Prioritization Score for Impact Estimate 0.0313
- REVEL 0.01
- CADD 0.08
- PolyPhen-2 0.00
- SIFT 0.57
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available