V37G (p.Val37Gly) variant of ASXL1 (Polycomb group protein ASXL1)
V37G (p.Val37Gly) in ASXL1 (Polycomb group protein ASXL1) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes structural context.
V37G (p.Val37Gly) variant details
- p.Val37Gly
- NCI-TCGA TCGA novel
- Ensembl rs2122811410
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available