D36G (p.Asp36Gly) variant of IL7R (P16871)
D36G (p.Asp36Gly) in IL7R (P16871) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.64 / 1. The record also includes population frequency data, published literature, and structural context.
D36G (p.Asp36Gly) variant details
- p.Asp36Gly
- gnomAD 5-35860876-A-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.638
- REVEL 0.66
- CADD 25.90
- PolyPhen-2 0.95
- SIFT 0.03
- Most common in the Non-Finnish European population (allele frequency 3.6e-06)
- Structural context available
- Literature evidence available