V13M (p.Val13Met) variant of CLDN10 (Claudin-10)
V13M (p.Val13Met) in CLDN10 (Claudin-10) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.58 / 1. The record also includes population frequency data, published literature, and structural context.
V13M (p.Val13Met) variant details
- p.Val13Met
- gnomAD 13-95433861-G-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.576
- CADD 21.80
- Population evidence available
- Structural context available
- Literature evidence available