H38Y (p.His38Tyr) variant of TNFAIP3 (P21580)
H38Y (p.His38Tyr) in TNFAIP3 (P21580) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.34 / 1. The record also includes population frequency data and structural context.
H38Y (p.His38Tyr) variant details
- p.His38Tyr
- Ensembl rs2114458898
- Missense
- Variant Prioritization Score for Impact Estimate 0.339
- MetaLR 0.01
- MetaSVM -1.02
- CADD 22.70
- PolyPhen-2 0.01
- SIFT 0.13
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available