G16= variant of MAOB (P27338)
G16= in MAOB (P27338) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; low impact. The record also includes structural context.
G16= variant details
- NCI-TCGA Cosmic COSV1009
- Variant assessed as somatic; low impact.
- Missense
- UniProt: Variant assessed as somatic; low impact.
- Structural context available