I12T (p.Ile12Thr) variant of NOD1 (Q9Y239)
I12T (p.Ile12Thr) 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.
I12T (p.Ile12Thr) variant details
- p.Ile12Thr
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available