P9T (p.Pro9Thr) variant of ITGB3 (Integrin beta-3)
P9T (p.Pro9Thr) in ITGB3 (Integrin beta-3) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.24 / 1. The record also includes population frequency data, published literature, and structural context.
P9T (p.Pro9Thr) variant details
- p.Pro9Thr
- gnomAD 17-47253886-C-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.24
- MetaLR 0.06
- MetaSVM -1.03
- CADD 6.39
- PolyPhen-2 0.01
- SIFT 0.63
- Most common in the Latino/Admixed American population (allele frequency 8e-05)
- Structural context available
- Literature evidence available