M18T (p.Met18Thr) variant of CLDN14 (Claudin-14)
M18T (p.Met18Thr) in CLDN14 (Claudin-14) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.40 / 1. The record also includes population frequency data and structural context.
M18T (p.Met18Thr) variant details
- p.Met18Thr
- gnomAD rs1435667810
- Missense
- Variant Prioritization Score for Impact Estimate 0.401
- REVEL 0.41
- CADD 23.20
- PolyPhen-2 0.14
- SIFT 0.05
- Population evidence available
- Structural context available