Y97N (p.Tyr97Asn) variant of NOD1 (Q9Y239)
Y97N (p.Tyr97Asn) 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.
Y97N (p.Tyr97Asn) variant details
- p.Tyr97Asn
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available