A37T (p.Ala37Thr) variant of FHL1 (Q13642)
A37T (p.Ala37Thr) in FHL1 (Q13642) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.17 / 1. The record also includes population frequency data, experimental measurements, published literature, and structural context.
A37T (p.Ala37Thr) variant details
- p.Ala37Thr
- rs192893870
- gnomAD X-136196860-G-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.173
- CADD 13.10
- Population evidence available
- Structural context available
- FHL1 Zinc finger, LIM-type domain domainome 1.0: score -0.0816
- Literature evidence available