G37C (p.Gly37Cys) variant of CLDN10 (Claudin-10)
G37C (p.Gly37Cys) in CLDN10 (Claudin-10) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.81 / 1. The record also includes population frequency data and structural context.
G37C (p.Gly37Cys) variant details
- p.Gly37Cys
- TOPMed rs1405417875
- gnomAD rs1405417875
- Missense
- Variant Prioritization Score for Impact Estimate 0.81
- REVEL 0.88
- CADD 32.00
- Population evidence available
- Structural context available