N38T (p.Asn38Thr) variant of MYD88 (Q99836)
N38T (p.Asn38Thr) in MYD88 (Q99836) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
N38T (p.Asn38Thr) variant details
- p.Asn38Thr
- ExAC rs748676192
- TOPMed rs748676192
- gnomAD rs748676192
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available