V38G (p.Val38Gly) variant of AXL (P30530)
V38G (p.Val38Gly) in AXL (P30530) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.35 / 1. The record also includes population frequency data and structural context.
V38G (p.Val38Gly) variant details
- p.Val38Gly
- ExAC rs747638130
- gnomAD rs747638130
- Missense
- Variant Prioritization Score for Impact Estimate 0.352
- REVEL 0.28
- CADD 21.80
- PolyPhen-2 0.25
- SIFT 0.28
- Most common in the Non-Finnish European population (allele frequency 5.4e-06)
- Structural context available