W18G (p.Trp18Gly) variant of CLDN10 (Claudin-10)
W18G (p.Trp18Gly) in CLDN10 (Claudin-10) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.79 / 1. The record also includes population frequency data, published literature, and structural context.
W18G (p.Trp18Gly) variant details
- p.Trp18Gly
- gnomAD 13-95552805-T-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.792
- REVEL 0.84
- MetaLR 0.84
- MetaSVM 0.86
- CADD 32.00
- PolyPhen-2 0.98
- SIFT 0.04
- Population evidence available
- Structural context available
- Literature evidence available