H39R (p.His39Arg) variant of TNFAIP3 (P21580)
H39R (p.His39Arg) in TNFAIP3 (P21580) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.64 / 1. The record also includes population frequency data, published literature, and structural context.
H39R (p.His39Arg) variant details
- p.His39Arg
- gnomAD 6-137871343-A-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.642
- CADD 26.20
- PolyPhen-2 1.00
- SIFT 0.00
- Most common in the East Asian population (allele frequency 2.5e-05)
- Structural context available
- Literature evidence available