V41F (p.Val41Phe) variant of F2 (Prothrombin)
V41F (p.Val41Phe) in F2 (Prothrombin) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.35 / 1. The record also includes population frequency data, published literature, and structural context.
V41F (p.Val41Phe) variant details
- p.Val41Phe
- gnomAD 11-46719743-G-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.352
- REVEL 0.35
- CADD 14.50
- PolyPhen-2 0.21
- SIFT 0.62
- Population evidence available
- Structural context available
- Literature evidence available