T42M (p.Thr42Met) variant of CLDN14 (Claudin-14)
T42M (p.Thr42Met) in CLDN14 (Claudin-14) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.81 / 1. The record also includes population frequency data and structural context.
T42M (p.Thr42Met) variant details
- p.Thr42Met
- ExAC rs533194857
- TOPMed rs533194857
- gnomAD rs533194857
- Missense
- Variant Prioritization Score for Impact Estimate 0.807
- REVEL 0.82
- CADD 26.70
- PolyPhen-2 1.00
- SIFT 0.01
- Population evidence available
- Structural context available