Q4W (p.Gln4Trp) variant of KMT2D (O14686)
Q4W (p.Gln4Trp) in KMT2D (O14686) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes structural context.
Q4W (p.Gln4Trp) variant details
- p.Gln4Trp
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available