V19M (p.Val19Met) variant of CLDN14 (Claudin-14)
V19M (p.Val19Met) in CLDN14 (Claudin-14) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.42 / 1. The record also includes population frequency data, published literature, and structural context.
V19M (p.Val19Met) variant details
- p.Val19Met
- gnomAD 21-36461641-C-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.42
- REVEL 0.43
- CADD 22.90
- PolyPhen-2 0.89
- SIFT 0.05
- Population evidence available
- Structural context available
- Literature evidence available