W37S (p.Trp37Ser) variant of CFH (Complement factor H)
W37S (p.Trp37Ser) in CFH (Complement factor H) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.50 / 1. The record also includes population frequency data, published literature, and structural context.
W37S (p.Trp37Ser) variant details
- p.Trp37Ser
- gnomAD 1-196673029-G-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.501
- REVEL 0.30
- CADD 25.00
- PolyPhen-2 0.98
- SIFT 0.00
- Population evidence available
- Structural context available
- Literature evidence available