P9S (p.Pro9Ser) variant of ITGB3 (Integrin beta-3)
P9S (p.Pro9Ser) 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.
P9S (p.Pro9Ser) variant details
- p.Pro9Ser
- gnomAD 17-47253886-C-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.243
- MetaLR 0.06
- MetaSVM -1.01
- CADD 6.28
- PolyPhen-2 0.01
- SIFT 0.83
- Most common in the South Asian population (allele frequency 3e-05)
- Structural context available
- Literature evidence available