L13F (p.Leu13Phe) variant of CLDN14 (Claudin-14)
L13F (p.Leu13Phe) in CLDN14 (Claudin-14) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.59 / 1. The record also includes population frequency data, published literature, and structural context.
L13F (p.Leu13Phe) variant details
- p.Leu13Phe
- gnomAD 21-36461659-G-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.588
- REVEL 0.67
- CADD 23.40
- PolyPhen-2 0.68
- SIFT 0.08
- Population evidence available
- Structural context available
- Literature evidence available