P47T (p.Pro47Thr) variant of TNFRSF9 (Q07011)
P47T (p.Pro47Thr) in TNFRSF9 (Q07011) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.31 / 1. The record also includes population frequency data and structural context.
P47T (p.Pro47Thr) variant details
- p.Pro47Thr
- TOPMed rs1182809399
- Missense
- Variant Prioritization Score for Impact Estimate 0.309
- REVEL 0.28
- CADD 17.10
- PolyPhen-2 0.44
- SIFT 0.04
- Most common in the South Asian population (allele frequency 1.2e-05)
- Structural context available