G4A (p.Gly4Ala) variant of TNFRSF4 (P43489)
G4A (p.Gly4Ala) in TNFRSF4 (P43489) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The available variant effect predictions contribute to a CATVariant prioritization score of 0.15 / 1. The record also includes population frequency data.
G4A (p.Gly4Ala) variant details
- p.Gly4Ala
- TOPMed rs1295347453
- gnomAD rs1295347453
- Uncertain significance
- Missense
- Variant Prioritization Score for Impact Estimate 0.149
- REVEL 0.05
- CADD 15.10
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)