H39Y (p.His39Tyr) variant of TNFAIP3 (P21580)
H39Y (p.His39Tyr) in TNFAIP3 (P21580) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.61 / 1. The record also includes population frequency data and structural context.
H39Y (p.His39Tyr) variant details
- p.His39Tyr
- ExAC rs778400121
- gnomAD rs778400121
- Missense
- Variant Prioritization Score for Impact Estimate 0.613
- MetaLR 0.08
- MetaSVM -1.09
- CADD 26.00
- PolyPhen-2 1.00
- SIFT 0.16
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available