N39K (p.Asn39Lys) variant of IL2RB (P14784)
N39K (p.Asn39Lys) in IL2RB (P14784) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.34 / 1. The record also includes population frequency data.
N39K (p.Asn39Lys) variant details
- p.Asn39Lys
- gnomAD rs1158099571
- Missense
- Variant Prioritization Score for Impact Estimate 0.338
- REVEL 0.26
- CADD 23.70
- PolyPhen-2 1.00
- SIFT 0.00
- Most common in the Finnish in Finland (FIN) population (allele frequency 9.4e-05)