D29G (p.Asp29Gly) variant of IL7R (P16871)
D29G (p.Asp29Gly) 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, published literature, and structural context.
D29G (p.Asp29Gly) variant details
- p.Asp29Gly
- gnomAD 5-35860855-A-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.391
- REVEL 0.31
- CADD 22.80
- PolyPhen-2 0.16
- SIFT 0.13
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available