P9Q (p.Pro9Gln) variant of ITGB3 (Integrin beta-3)
P9Q (p.Pro9Gln) in ITGB3 (Integrin beta-3) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.14 / 1. The record also includes population frequency data, published literature, and structural context.
P9Q (p.Pro9Gln) variant details
- p.Pro9Gln
- gnomAD 17-47253887-C-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.136
- MetaLR 0.04
- MetaSVM -1.00
- CADD 3.81
- PolyPhen-2 0.00
- SIFT 0.68
- Most common in the REMAINING population (allele frequency 2.2e-05)
- Structural context available
- Literature evidence available