Y11N (p.Tyr11Asn) variant of TNFAIP3 (P21580)
Y11N (p.Tyr11Asn) in TNFAIP3 (P21580) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.51 / 1. The record also includes population frequency data and structural context.
Y11N (p.Tyr11Asn) variant details
- p.Tyr11Asn
- TOPMed rs900039415
- Missense
- Variant Prioritization Score for Impact Estimate 0.511
- MetaLR 0.08
- MetaSVM -1.04
- CADD 25.40
- PolyPhen-2 0.97
- SIFT 0.09
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available