D38E (p.Asp38Glu) variant of TNFRSF9 (Q07011)
D38E (p.Asp38Glu) in TNFRSF9 (Q07011) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.05 / 1. The record also includes population frequency data and structural context.
D38E (p.Asp38Glu) variant details
- p.Asp38Glu
- TOPMed rs1639859707
- gnomAD rs1639859707
- Missense
- Variant Prioritization Score for Impact Estimate 0.0466
- REVEL 0.01
- CADD 4.72
- PolyPhen-2 0.00
- SIFT 0.43
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available