S39S (p.Ser39Ser) variant of IL7R (P16871)
S39S (p.Ser39Ser) in IL7R (P16871) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.08 / 1. The record also includes population frequency data, published literature, and structural context.
S39S (p.Ser39Ser) variant details
- p.Ser39Ser
- rs1349991152
- gnomAD 5-35860886-A-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.0845
- CADD 0.59
- Most common in the South Asian population (allele frequency 2.3e-05)
- Structural context available
- Literature evidence available