M67R (p.Met67Arg) variant of CD79B (P40259)
M67R (p.Met67Arg) in CD79B (P40259) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.19 / 1. The record also includes population frequency data, published literature, and structural context.
M67R (p.Met67Arg) variant details
- p.Met67Arg
- gnomAD 17-63930304-A-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.189
- REVEL 0.26
- CADD 5.36
- PolyPhen-2 0.00
- SIFT 0.22
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available