C56R (p.Cys56Arg) variant of TNFRSF4 (P43489)
C56R (p.Cys56Arg) in TNFRSF4 (P43489) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.74 / 1. The record also includes population frequency data and structural context.
C56R (p.Cys56Arg) variant details
- p.Cys56Arg
- gnomAD rs1460774660
- Missense
- Variant Prioritization Score for Impact Estimate 0.742
- REVEL 0.83
- CADD 25.40
- PolyPhen-2 1.00
- SIFT 0.00
- Most common in the Latino/Admixed American population (allele frequency 2.3e-05)
- Structural context available