P7T (p.Pro7Thr) variant of TNFRSF1A (P19438)
P7T (p.Pro7Thr) in TNFRSF1A (P19438) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.51 / 1. The record also includes population frequency data and structural context.
P7T (p.Pro7Thr) variant details
- p.Pro7Thr
- ExAC rs200727600
- TOPMed rs200727600
- gnomAD rs200727600
- Missense
- Variant Prioritization Score for Impact Estimate 0.511
- REVEL 0.57
- CADD 22.40
- PolyPhen-2 0.01
- SIFT 0.03
- Most common in the Non-Finnish European population (allele frequency 2.9e-05)
- Structural context available