S49T (p.Ser49Thr) variant of CD79B (P40259)
S49T (p.Ser49Thr) in CD79B (P40259) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.06 / 1. The record also includes population frequency data and structural context.
S49T (p.Ser49Thr) variant details
- p.Ser49Thr
- ESP rs371066461
- ExAC rs371066461
- TOPMed rs371066461
- gnomAD rs371066461
- Missense
- Variant Prioritization Score for Impact Estimate 0.0639
- REVEL 0.07
- CADD 1.53
- PolyPhen-2 0.00
- SIFT 0.02
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available