W37R (p.Trp37Arg) variant of CFH (Complement factor H)
W37R (p.Trp37Arg) in CFH (Complement factor H) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.42 / 1. The record also includes population frequency data, published literature, and structural context.
W37R (p.Trp37Arg) variant details
- p.Trp37Arg
- gnomAD 1-196673028-T-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.423
- REVEL 0.35
- CADD 23.00
- PolyPhen-2 0.99
- SIFT 0.07
- Population evidence available
- Structural context available
- Literature evidence available