S49N (p.Ser49Asn) variant of CD79B (P40259)
S49N (p.Ser49Asn) in CD79B (P40259) is a missense change. The record also includes structural context.
S49N (p.Ser49Asn) variant details
- p.Ser49Asn
- cosmic curated COSV50080
- ESP rs371066461
- ExAC rs371066461
- TOPMed rs371066461
- Missense
- Structural context available