P7T (p.Pro7Thr) variant of ITGA2B (Integrin alpha-IIb)
P7T (p.Pro7Thr) in ITGA2B (Integrin alpha-IIb) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.20 / 1. The record also includes population frequency data and structural context.
P7T (p.Pro7Thr) variant details
- p.Pro7Thr
- gnomAD rs2048679771
- Missense
- Variant Prioritization Score for Impact Estimate 0.203
- REVEL 0.14
- MetaLR 0.62
- MetaSVM -0.44
- CADD 2.37
- SIFT 0.59
- Most common in the Finnish in Finland (FIN) population (allele frequency 9.4e-05)
- Structural context available