E12Q (p.Glu12Gln) variant of NOD2 (Q9HC29)
E12Q (p.Glu12Gln) in NOD2 (Q9HC29) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes variant effect predictions and structural context.
E12Q (p.Glu12Gln) variant details
- p.Glu12Gln
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- MetaLR 0.08
- MetaSVM -1.02
- SIFT 0.03
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available