G23W (p.Gly23Trp) variant of ATP6V1A (P38606)
G23W (p.Gly23Trp) in ATP6V1A (P38606) 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 0.85 / 1. The record also includes population frequency data and structural context.
G23W (p.Gly23Trp) variant details
- p.Gly23Trp
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.846
- REVEL 0.86
- CADD 32.00
- PolyPhen-2 0.96
- SIFT 0.01
- UniProt: Variant assessed as somatic; moderate impact.
- Population evidence available
- Structural context available