L69F (p.Leu69Phe) variant of TNFRSF13B (O14836)
L69F (p.Leu69Phe) in TNFRSF13B (O14836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.42 / 1. The record also includes population frequency data.
L69F (p.Leu69Phe) variant details
- p.Leu69Phe
- 1000Genomes rs562284274
- ExAC rs562284274
- gnomAD rs562284274
- Missense
- Variant Prioritization Score for Impact Estimate 0.42
- REVEL 0.47
- CADD 22.40
- PolyPhen-2 1.00
- SIFT 0.04
- Most common in the Non-Finnish European population (allele frequency 2.9e-05)