R197T (p.Arg197Thr) variant of MAOB (P27338)
R197T (p.Arg197Thr) in MAOB (P27338) 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.
R197T (p.Arg197Thr) variant details
- p.Arg197Thr
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- MetaLR 0.85
- MetaSVM 0.73
- SIFT 0.00
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available