P9T (p.Pro9Thr) variant of WWTR1 (Q9GZV5)
P9T (p.Pro9Thr) in WWTR1 (Q9GZV5) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.19 / 1. The record also includes population frequency data, experimental measurements, and structural context.
P9T (p.Pro9Thr) variant details
- p.Pro9Thr
- TOPMed rs921827996
- gnomAD rs921827996
- Missense
- Variant Prioritization Score for Impact Estimate 0.188
- REVEL 0.06
- CADD 18.70
- PolyPhen-2 0.04
- SIFT 0.41
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- WWTR1 WW domain domainome 1.0: score -0.0347