R36Q (p.Arg36Gln) variant of CD79B (P40259)
R36Q (p.Arg36Gln) in CD79B (P40259) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.10 / 1. The record also includes population frequency data and structural context.
R36Q (p.Arg36Gln) variant details
- p.Arg36Gln
- ESP rs148536804
- ExAC rs148536804
- TOPMed rs148536804
- gnomAD rs148536804
- Missense
- Variant Prioritization Score for Impact Estimate 0.101
- REVEL 0.12
- CADD 0.00
- PolyPhen-2 0.00
- SIFT 0.65
- Most common in the South Asian population (allele frequency 0.00024)
- Structural context available