Q39R (p.Gln39Arg) variant of F2 (Prothrombin)
Q39R (p.Gln39Arg) in F2 (Prothrombin) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.22 / 1. The record also includes population frequency data, published literature, and structural context.
Q39R (p.Gln39Arg) variant details
- p.Gln39Arg
- gnomAD 11-46719738-A-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.22
- REVEL 0.23
- CADD 11.00
- PolyPhen-2 0.00
- SIFT 0.47
- Population evidence available
- Structural context available
- Literature evidence available