R41K (p.Arg41Lys) variant of TNFRSF9 (Q07011)
R41K (p.Arg41Lys) in TNFRSF9 (Q07011) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.04 / 1. The record also includes population frequency data and structural context.
R41K (p.Arg41Lys) variant details
- p.Arg41Lys
- ExAC rs774199690
- TOPMed rs774199690
- gnomAD rs774199690
- Missense
- Variant Prioritization Score for Impact Estimate 0.0361
- REVEL 0.01
- CADD 0.01
- PolyPhen-2 0.00
- SIFT 1.00
- Most common in the South Asian population (allele frequency 1.2e-05)
- Structural context available