V11I (p.Val11Ile) variant of IL7R (P16871)
V11I (p.Val11Ile) in IL7R (P16871) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.14 / 1. The record also includes population frequency data and structural context.
V11I (p.Val11Ile) variant details
- p.Val11Ile
- cosmic curated COSV57413
- TOPMed rs1759660556
- gnomAD rs1759660556
- Missense
- Variant Prioritization Score for Impact Estimate 0.136
- REVEL 0.10
- CADD 0.14
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available