S11N (p.Ser11Asn) variant of MOG (Q16653)
S11N (p.Ser11Asn) in MOG (Q16653) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.15 / 1. The record also includes population frequency data and structural context.
S11N (p.Ser11Asn) variant details
- p.Ser11Asn
- NCI-TCGA Cosmic COSV1009
- cosmic curated COSV10097
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.152
- REVEL 0.04
- MetaLR 0.04
- MetaSVM -1.11
- CADD 19.40
- PolyPhen-2 0.03
- SIFT 0.50
- UniProt: Variant assessed as somatic; moderate impact.
- Population evidence available
- Structural context available