K22N (p.Lys22Asn) variant of FHL1 (Q13642)
K22N (p.Lys22Asn) in FHL1 (Q13642) is a missense change. Clinical records from EBI and UniProt describe it as benign. The record also includes experimental measurements and structural context.
K22N (p.Lys22Asn) variant details
- p.Lys22Asn
- NCI-TCGA TCGA novel
- 1000Genomes rs140149764
- ESP rs140149764
- ExAC rs140149764
- Benign
- Missense
- EBI: Benign
- UniProt: Benign
- Structural context available
- FHL1 Zinc finger, LIM-type domain domainome 1.0: score -0.201