H39Y (p.His39Tyr) variant of MOG (Q16653)
H39Y (p.His39Tyr) in MOG (Q16653) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.26 / 1. The record also includes population frequency data and structural context.
H39Y (p.His39Tyr) variant details
- p.His39Tyr
- ExAC rs776745318
- gnomAD rs776745318
- Missense
- Variant Prioritization Score for Impact Estimate 0.258
- REVEL 0.05
- CADD 9.46
- PolyPhen-2 0.01
- SIFT 0.18
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available