Q92H (p.Gln92His) variant of NOD1 (Q9Y239)
Q92H (p.Gln92His) in NOD1 (Q9Y239) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
Q92H (p.Gln92His) variant details
- p.Gln92His
- NCI-TCGA Cosmic COSV9976
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available