G39D (p.Gly39Asp) variant of AXL (P30530)
G39D (p.Gly39Asp) in AXL (P30530) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.09 / 1. The record also includes population frequency data and structural context.
G39D (p.Gly39Asp) variant details
- p.Gly39Asp
- gnomAD rs1354956512
- Missense
- Variant Prioritization Score for Impact Estimate 0.0861
- REVEL 0.03
- CADD 12.60
- PolyPhen-2 0.17
- SIFT 0.54
- Most common in the East Asian population (allele frequency 2.6e-05)
- Structural context available