D5028H (p.Asp5028His) variant of KMT2D (O14686)
D5028H (p.Asp5028His) in KMT2D (O14686) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as likely pathogenic in the context of Kabuki syndrome 1. The record also includes structural context.
D5028H (p.Asp5028His) variant details
- p.Asp5028His
- Ensembl rs2120364170
- Likely pathogenic
- Kabuki syndrome 1
- Missense
- ClinVar: Likely pathogenic (Kabuki syndrome 1)
- EBI: uncertain significance (in KABUK1)
- UniProt: Uncertain significance (in KABUK1)
- Structural context available