G37W (p.Gly37Trp) variant of NPHS2 (Podocin)
G37W (p.Gly37Trp) in NPHS2 (Podocin) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.36 / 1. The record also includes population frequency data and structural context.
G37W (p.Gly37Trp) variant details
- p.Gly37Trp
- ExAC rs756683527
- gnomAD rs756683527
- Missense
- Variant Prioritization Score for Impact Estimate 0.361
- REVEL 0.33
- CADD 17.50
- PolyPhen-2 0.37
- SIFT 0.01
- Population evidence available
- Structural context available