Q95K (p.Gln95Lys) variant of TNFRSF13B (O14836)
Q95K (p.Gln95Lys) in TNFRSF13B (O14836) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The available variant effect predictions contribute to a CATVariant prioritization score of 0.57 / 1. The record also includes population frequency data.
Q95K (p.Gln95Lys) variant details
- p.Gln95Lys
- ExAC rs549493928
- TOPMed rs549493928
- gnomAD rs549493928
- Uncertain significance
- Missense
- Variant Prioritization Score for Impact Estimate 0.571
- REVEL 0.46
- CADD 22.90
- PolyPhen-2 0.20
- SIFT 0.03
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.00019)