D26E (p.Asp26Glu) variant of TNFRSF9 (Q07011)
D26E (p.Asp26Glu) in TNFRSF9 (Q07011) is a missense change. Clinical records from EBI and UniProt describe it as likely benign. The available variant effect predictions contribute to a CATVariant prioritization score of 0.11 / 1. The record also includes population frequency data and structural context.
D26E (p.Asp26Glu) variant details
- p.Asp26Glu
- TOPMed rs914264787
- gnomAD rs914264787
- Likely benign
- Missense
- Variant Prioritization Score for Impact Estimate 0.109
- REVEL 0.12
- CADD 1.31
- EBI: Likely benign
- UniProt: Likely benign
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available