P41T (p.Pro41Thr) variant of AXL (P30530)
P41T (p.Pro41Thr) in AXL (P30530) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.55 / 1. The record also includes population frequency data and structural context.
P41T (p.Pro41Thr) variant details
- p.Pro41Thr
- gnomAD rs2033773715
- Missense
- Variant Prioritization Score for Impact Estimate 0.545
- REVEL 0.39
- CADD 22.70
- PolyPhen-2 0.92
- SIFT 0.07
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available