A16G (p.Ala16Gly) variant of ASXL3 (Q9C0F0)
A16G (p.Ala16Gly) in ASXL3 (Q9C0F0) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
A16G (p.Ala16Gly) variant details
- p.Ala16Gly
- NCI-TCGA Cosmic COSV5247
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available