H36R (p.His36Arg) variant of F12 (Coagulation factor XII)
H36R (p.His36Arg) in F12 (Coagulation factor XII) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.32 / 1. The record also includes population frequency data and structural context.
H36R (p.His36Arg) variant details
- p.His36Arg
- gnomAD rs1763348878
- Missense
- Variant Prioritization Score for Impact Estimate 0.322
- REVEL 0.23
- CADD 3.88
- PolyPhen-2 0.01
- SIFT 0.24
- Most common in the Finnish in Finland (FIN) population (allele frequency 9.4e-05)
- Structural context available