G37D (p.Gly37Asp) variant of CLDN14 (Claudin-14)
G37D (p.Gly37Asp) in CLDN14 (Claudin-14) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.77 / 1. The record also includes population frequency data, published literature, and structural context.
G37D (p.Gly37Asp) variant details
- p.Gly37Asp
- gnomAD 21-36461586-C-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.766
- REVEL 0.76
- CADD 24.60
- PolyPhen-2 0.86
- SIFT 0.02
- Population evidence available
- Structural context available
- Literature evidence available