W37C (p.Trp37Cys) variant of CFH (Complement factor H)
W37C (p.Trp37Cys) in CFH (Complement factor H) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.53 / 1. The record also includes population frequency data, published literature, and structural context.
W37C (p.Trp37Cys) variant details
- p.Trp37Cys
- gnomAD 1-196673030-G-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.53
- REVEL 0.35
- CADD 25.40
- PolyPhen-2 1.00
- SIFT 0.00
- Population evidence available
- Structural context available
- Literature evidence available