T39N (p.Thr39Asn) variant of FHL1 (Q13642)
T39N (p.Thr39Asn) in FHL1 (Q13642) is a missense change. The record also includes population frequency data, experimental measurements, and structural context.
T39N (p.Thr39Asn) variant details
- p.Thr39Asn
- gnomAD rs1252282869
- Missense
- Population evidence available
- Structural context available
- FHL1 Zinc finger, LIM-type domain domainome 1.0: score -0.177