P21Q (p.Pro21Gln) variant of TNFRSF13C (Q96RJ3)
P21Q (p.Pro21Gln) in TNFRSF13C (Q96RJ3) is a missense change. Clinical records from EBI and UniProt describe it as benign. The available variant effect predictions contribute to a CATVariant prioritization score of 0.05 / 1. The record also includes population frequency data.
P21Q (p.Pro21Gln) variant details
- p.Pro21Gln
- 1000Genomes rs77874543
- ESP rs77874543
- ExAC rs77874543
- TOPMed rs77874543
- Benign
- Missense
- Variant Prioritization Score for Impact Estimate 0.0494
- REVEL 0.02
- CADD 2.06
- PolyPhen-2 0.00
- SIFT 1.00
- EBI: Benign
- UniProt: Benign
- Population evidence available