P42T (p.Pro42Thr) variant of TNFRSF13B (O14836)
P42T (p.Pro42Thr) in TNFRSF13B (O14836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.23 / 1. The record also includes population frequency data.
P42T (p.Pro42Thr) variant details
- p.Pro42Thr
- 1000Genomes rs531640813
- ExAC rs531640813
- TOPMed rs531640813
- gnomAD rs531640813
- Missense
- Variant Prioritization Score for Impact Estimate 0.229
- REVEL 0.35
- CADD 1.32
- PolyPhen-2 0.06
- SIFT 0.15
- Most common in the HGDP:MAKRANI population (allele frequency 0.023)