S49N (p.Ser49Asn) variant of IL2RB (P14784)
S49N (p.Ser49Asn) in IL2RB (P14784) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.31 / 1. The record also includes population frequency data.
S49N (p.Ser49Asn) variant details
- p.Ser49Asn
- ExAC rs781374102
- TOPMed rs781374102
- gnomAD rs781374102
- Missense
- Variant Prioritization Score for Impact Estimate 0.305
- REVEL 0.28
- CADD 12.30
- PolyPhen-2 0.01
- SIFT 0.18
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)