A177T (p.Ala177Thr) variant of F12 (Coagulation factor XII)
A177T (p.Ala177Thr) in F12 (Coagulation factor XII) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.41 / 1. The record also includes population frequency data and structural context.
A177T (p.Ala177Thr) variant details
- p.Ala177Thr
- ExAC rs776006786
- gnomAD rs776006786
- Missense
- Variant Prioritization Score for Impact Estimate 0.412
- REVEL 0.27
- CADD 27.30
- PolyPhen-2 0.12
- SIFT 0.06
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available