P91S (p.Pro91Ser) variant of F12 (Coagulation factor XII)
P91S (p.Pro91Ser) in F12 (Coagulation factor XII) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.28 / 1. The record also includes population frequency data and structural context.
P91S (p.Pro91Ser) variant details
- p.Pro91Ser
- ExAC rs763794408
- gnomAD rs763794408
- Missense
- Variant Prioritization Score for Impact Estimate 0.281
- REVEL 0.21
- CADD 17.40
- PolyPhen-2 0.01
- SIFT 0.15
- Most common in the East Asian population (allele frequency 0.00015)
- Structural context available