D17G (p.Asp17Gly) variant of TYK2 (P29597)
D17G (p.Asp17Gly) in TYK2 (P29597) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.11 / 1. The record also includes population frequency data and structural context.
D17G (p.Asp17Gly) variant details
- p.Asp17Gly
- ExAC rs778732100
- gnomAD rs778732100
- Missense
- Variant Prioritization Score for Impact Estimate 0.107
- REVEL 0.08
- CADD 10.70
- PolyPhen-2 0.03
- SIFT 0.06
- Most common in the Finnish in Finland (FIN) population (allele frequency 1.9e-05)
- Structural context available