R16R (p.Arg16Arg) variant of TNFAIP3 (P21580)
R16R (p.Arg16Arg) in TNFAIP3 (P21580) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.25 / 1. The record also includes population frequency data, published literature, and structural context.
R16R (p.Arg16Arg) variant details
- p.Arg16Arg
- rs1295337888
- gnomAD 6-137871275-G-A
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.245
- CADD 13.10
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available