D19N (p.Asp19Asn) variant of SLC40A1 (Ferroportin)
D19N (p.Asp19Asn) in SLC40A1 (Ferroportin) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.26 / 1. The record also includes population frequency data and structural context.
D19N (p.Asp19Asn) variant details
- p.Asp19Asn
- gnomAD rs1421189425
- Missense
- Variant Prioritization Score for Impact Estimate 0.26
- REVEL 0.24
- CADD 18.00
- PolyPhen-2 0.00
- SIFT 0.82
- Most common in the Middle Eastern population (allele frequency 0.0007)
- Structural context available