S3N (p.Ser3Asn) variant of MOG (Q16653)
S3N (p.Ser3Asn) in MOG (Q16653) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.12 / 1. The record also includes population frequency data and structural context.
S3N (p.Ser3Asn) variant details
- p.Ser3Asn
- ExAC rs775400607
- gnomAD rs775400607
- Missense
- Variant Prioritization Score for Impact Estimate 0.121
- REVEL 0.03
- MetaLR 0.02
- MetaSVM -0.97
- CADD 7.34
- PolyPhen-2 0.00
- SIFT 0.58
- Most common in the South Asian population (allele frequency 2.3e-05)
- Structural context available