G37D (p.Gly37Asp) variant of CLDN10 (Claudin-10)
G37D (p.Gly37Asp) in CLDN10 (Claudin-10) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.83 / 1. The record also includes population frequency data and structural context.
G37D (p.Gly37Asp) variant details
- p.Gly37Asp
- rs1371711623
- NCI-TCGA Cosmic COSV5482
- gnomAD rs1371711623
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.831
- REVEL 0.85
- CADD 29.70
- PolyPhen-2 0.69
- SIFT 0.01
- UniProt: Variant assessed as somatic; moderate impact.
- Population evidence available
- Structural context available