H38R (p.His38Arg) variant of TNFAIP3 (P21580)
H38R (p.His38Arg) in TNFAIP3 (P21580) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.37 / 1. The record also includes population frequency data and structural context.
H38R (p.His38Arg) variant details
- p.His38Arg
- cosmic curated COSV52801
- Missense
- Variant Prioritization Score for Impact Estimate 0.373
- MetaLR 0.06
- MetaSVM -1.10
- CADD 26.00
- PolyPhen-2 0.89
- SIFT 0.01
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available