G57D (p.Gly57Asp) variant of TNFRSF9 (Q07011)
G57D (p.Gly57Asp) in TNFRSF9 (Q07011) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.30 / 1. The record also includes population frequency data and structural context.
G57D (p.Gly57Asp) variant details
- p.Gly57Asp
- TOPMed rs1639858469
- Missense
- Variant Prioritization Score for Impact Estimate 0.305
- REVEL 0.29
- CADD 15.80
- PolyPhen-2 0.25
- SIFT 0.04
- Most common in the REMAINING population (allele frequency 1.7e-05)
- Structural context available