G37V (p.Gly37Val) variant of CLDN14 (Claudin-14)
G37V (p.Gly37Val) 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.
G37V (p.Gly37Val) variant details
- p.Gly37Val
- gnomAD 21-36461586-C-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.774
- REVEL 0.77
- CADD 24.60
- PolyPhen-2 1.00
- SIFT 0.00
- Population evidence available
- Structural context available
- Literature evidence available