S41L (p.Ser41Leu) variant of IL7R (P16871)
S41L (p.Ser41Leu) in IL7R (P16871) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.39 / 1. The record also includes population frequency data and structural context.
S41L (p.Ser41Leu) variant details
- p.Ser41Leu
- gnomAD rs1759788104
- Missense
- Variant Prioritization Score for Impact Estimate 0.393
- REVEL 0.32
- CADD 24.80
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available