A33T (p.Ala33Thr) variant of IL7R (P16871)
A33T (p.Ala33Thr) in IL7R (P16871) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.40 / 1. The record also includes population frequency data and structural context.
A33T (p.Ala33Thr) variant details
- p.Ala33Thr
- ESP rs140673282
- ExAC rs140673282
- TOPMed rs140673282
- gnomAD rs140673282
- Missense
- Variant Prioritization Score for Impact Estimate 0.396
- REVEL 0.33
- CADD 23.20
- PolyPhen-2 0.52
- SIFT 0.09
- Most common in the African/African-American population (allele frequency 4.8e-05)
- Structural context available