T38M (p.Thr38Met) variant of CLDN10 (Claudin-10)
T38M (p.Thr38Met) in CLDN10 (Claudin-10) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.75 / 1. The record also includes population frequency data and structural context.
T38M (p.Thr38Met) variant details
- p.Thr38Met
- gnomAD rs1280008667
- Missense
- Variant Prioritization Score for Impact Estimate 0.749
- REVEL 0.79
- CADD 26.90
- PolyPhen-2 0.87
- SIFT 0.02
- Population evidence available
- Structural context available