L116Q (p.Leu116Gln) variant of TNFRSF4 (P43489)
L116Q (p.Leu116Gln) in TNFRSF4 (P43489) 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.
L116Q (p.Leu116Gln) variant details
- p.Leu116Gln
- ExAC rs753682470
- TOPMed rs753682470
- gnomAD rs753682470
- Missense
- Variant Prioritization Score for Impact Estimate 0.0378
- REVEL 0.01
- CADD 1.87
- PolyPhen-2 0.00
- SIFT 0.35
- Most common in the Non-Finnish European population (allele frequency 6.3e-06)