N68I (p.Asn68Ile) variant of CD79B (P40259)
N68I (p.Asn68Ile) in CD79B (P40259) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.18 / 1. The record also includes population frequency data, published literature, and structural context.
N68I (p.Asn68Ile) variant details
- p.Asn68Ile
- gnomAD 17-63930301-T-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.182
- REVEL 0.21
- CADD 10.20
- PolyPhen-2 0.60
- SIFT 0.10
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available