N40D (p.Asn40Asp) variant of AXL (P30530)
N40D (p.Asn40Asp) in AXL (P30530) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.19 / 1. The record also includes population frequency data, published literature, and structural context.
N40D (p.Asn40Asp) variant details
- p.Asn40Asp
- gnomAD 19-41220668-A-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.186
- REVEL 0.07
- CADD 17.60
- PolyPhen-2 0.01
- SIFT 0.13
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available