S4G (p.Ser4Gly) variant of TNFRSF9 (Q07011)
S4G (p.Ser4Gly) 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.
S4G (p.Ser4Gly) variant details
- p.Ser4Gly
- TOPMed rs921425538
- gnomAD rs921425538
- Missense
- Variant Prioritization Score for Impact Estimate 0.0454
- REVEL 0.02
- CADD 0.06
- PolyPhen-2 0.00
- SIFT 1.00
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available