T39T (p.Thr39Thr) variant of ITGB4 (Integrin beta-4)
T39T (p.Thr39Thr) in ITGB4 (Integrin beta-4) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.10 / 1. The record also includes population frequency data, published literature, and structural context.
T39T (p.Thr39Thr) variant details
- p.Thr39Thr
- rs760303034
- gnomAD 17-75727232-G-A
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.099
- CADD 2.59
- Most common in the 1KG:CLM population (allele frequency 0.0053)
- Structural context available
- Literature evidence available