G29S (p.Gly29Ser) variant of NOS1AP (O75052)
G29S (p.Gly29Ser) in NOS1AP (O75052) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
G29S (p.Gly29Ser) variant details
- p.Gly29Ser
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available