M18V (p.Met18Val) variant of CLDN14 (Claudin-14)
M18V (p.Met18Val) in CLDN14 (Claudin-14) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.24 / 1. The record also includes population frequency data and structural context.
M18V (p.Met18Val) variant details
- p.Met18Val
- 1000Genomes rs369883669
- ExAC rs369883669
- TOPMed rs369883669
- gnomAD rs369883669
- Missense
- Variant Prioritization Score for Impact Estimate 0.236
- REVEL 0.23
- CADD 18.20
- PolyPhen-2 0.02
- SIFT 0.03
- Population evidence available
- Structural context available