H39H (p.His39His) variant of MOG (Q16653)
H39H (p.His39His) in MOG (Q16653) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.08 / 1. The record also includes population frequency data, published literature, and structural context.
H39H (p.His39His) variant details
- p.His39His
- gnomAD 6-29659347-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.0824
- CADD 0.28
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available
- Literature evidence available