D47N (p.Asp47Asn) variant of MOG (Q16653)
D47N (p.Asp47Asn) in MOG (Q16653) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.24 / 1. The record also includes population frequency data and structural context.
D47N (p.Asp47Asn) variant details
- p.Asp47Asn
- TOPMed rs1365254099
- gnomAD rs1365254099
- Missense
- Variant Prioritization Score for Impact Estimate 0.242
- REVEL 0.05
- CADD 21.20
- PolyPhen-2 0.69
- SIFT 0.11
- Most common in the Non-Finnish European population (allele frequency 7.2e-06)
- Structural context available