C34F (p.Cys34Phe) variant of TNFRSF13B (O14836)
C34F (p.Cys34Phe) in TNFRSF13B (O14836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.75 / 1. The record also includes population frequency data.
C34F (p.Cys34Phe) variant details
- p.Cys34Phe
- ExAC rs778477333
- gnomAD rs778477333
- Missense
- Variant Prioritization Score for Impact Estimate 0.751
- REVEL 0.74
- CADD 24.20
- PolyPhen-2 1.00
- SIFT 0.00
- Most common in the South Asian population (allele frequency 1.2e-05)