G13W (p.Gly13Trp) variant of CR1 (Complement receptor type 1)
G13W (p.Gly13Trp) in CR1 (Complement receptor type 1) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.10 / 1. The record also includes population frequency data, published literature, and structural context.
G13W (p.Gly13Trp) variant details
- p.Gly13Trp
- gnomAD 1-207496304-G-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.102
- REVEL 0.02
- MetaLR 0.04
- MetaSVM -0.99
- CADD 6.90
- PolyPhen-2 0.00
- SIFT 0.11
- Population evidence available
- Structural context available
- Literature evidence available