V76G (p.Val76Gly) variant of NOS1AP (O75052)
V76G (p.Val76Gly) 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.
V76G (p.Val76Gly) variant details
- p.Val76Gly
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- MetaLR 0.16
- MetaSVM -0.62
- SIFT 0.00
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available