N37H (p.Asn37His) variant of CD79B (P40259)
N37H (p.Asn37His) in CD79B (P40259) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.25 / 1. The record also includes population frequency data, published literature, and structural context.
N37H (p.Asn37His) variant details
- p.Asn37His
- gnomAD 17-63931344-T-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.247
- REVEL 0.24
- CADD 16.40
- PolyPhen-2 0.36
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available