P78R (p.Pro78Arg) variant of CD79A (P11912)
P78R (p.Pro78Arg) in CD79A (P11912) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.16 / 1. The record also includes population frequency data and structural context.
P78R (p.Pro78Arg) variant details
- p.Pro78Arg
- ESP rs372519166
- ExAC rs372519166
- TOPMed rs372519166
- gnomAD rs372519166
- Missense
- Variant Prioritization Score for Impact Estimate 0.164
- REVEL 0.10
- CADD 13.70
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available