I41M (p.Ile41Met) variant of MOG (Q16653)
I41M (p.Ile41Met) in MOG (Q16653) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.48 / 1. The record also includes population frequency data and structural context.
I41M (p.Ile41Met) variant details
- p.Ile41Met
- ExAC rs774206213
- TOPMed rs774206213
- gnomAD rs774206213
- Missense
- Variant Prioritization Score for Impact Estimate 0.478
- REVEL 0.49
- CADD 22.80
- PolyPhen-2 0.71
- SIFT 0.00
- Most common in the South Asian population (allele frequency 0.00013)
- Structural context available