L18F (p.Leu18Phe) variant of TNFRSF4 (P43489)
L18F (p.Leu18Phe) in TNFRSF4 (P43489) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.21 / 1. The record also includes population frequency data.
L18F (p.Leu18Phe) variant details
- p.Leu18Phe
- gnomAD rs1278868135
- Missense
- Variant Prioritization Score for Impact Estimate 0.207
- REVEL 0.13
- CADD 16.10
- PolyPhen-2 0.05
- SIFT 0.14
- Most common in the Latino/Admixed American population (allele frequency 4.7e-05)