D26N (p.Asp26Asn) variant of FLG (Filaggrin)
D26N (p.Asp26Asn) in FLG (Filaggrin) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as benign in the context of not provided. The record also includes variant effect predictions and population frequency data.
D26N (p.Asp26Asn) variant details
- p.Asp26Asn
- rs73007748
- ClinGen CA1108111
- ClinVar RCV000886323
- 1000Genomes rs73007748
- Benign
- not provided
- Missense
- AlphaMissense 0.20
- MetaLR 0.03
- MetaSVM -1.08
- PolyPhen-2 0.99
- SIFT 0.05
- ClinVar: Benign (not provided)
- EBI: Benign
- UniProt: Benign
- Population evidence available