S3T (p.Ser3Thr) variant of KMT2D (O14686)
S3T (p.Ser3Thr) 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.
S3T (p.Ser3Thr) variant details
- p.Ser3Thr
- TOPMed rs1451360303
- gnomAD rs1451360303
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available