I18T (p.Ile18Thr) variant of NOS1AP (O75052)
I18T (p.Ile18Thr) in NOS1AP (O75052) 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.
I18T (p.Ile18Thr) variant details
- p.Ile18Thr
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- MetaLR 0.03
- MetaSVM -1.08
- SIFT 0.01
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available