T47T (p.Thr47Thr) variant of TNFAIP3 (P21580)
T47T (p.Thr47Thr) in TNFAIP3 (P21580) 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.
T47T (p.Thr47Thr) variant details
- p.Thr47Thr
- rs774689592
- gnomAD 6-137871368-A-C
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.0968
- CADD 2.28
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available
- Literature evidence available