G9C (p.Gly9Cys) variant of TNFRSF4 (P43489)
G9C (p.Gly9Cys) in TNFRSF4 (P43489) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.13 / 1. The record also includes population frequency data and structural context.
G9C (p.Gly9Cys) variant details
- p.Gly9Cys
- gnomAD rs1396484290
- Missense
- Variant Prioritization Score for Impact Estimate 0.133
- REVEL 0.16
- CADD 4.47
- PolyPhen-2 0.17
- SIFT 0.20
- Most common in the Finnish in Finland (FIN) population (allele frequency 9.4e-05)
- Structural context available