V38F (p.Val38Phe) variant of CD79A (P11912)
V38F (p.Val38Phe) in CD79A (P11912) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.20 / 1. The record also includes population frequency data, published literature, and structural context.
V38F (p.Val38Phe) variant details
- p.Val38Phe
- gnomAD 19-41879022-G-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.201
- REVEL 0.09
- MetaLR 0.16
- MetaSVM -0.97
- CADD 21.90
- PolyPhen-2 0.67
- SIFT 0.06
- Most common in the Non-Finnish European population (allele frequency 5.4e-06)
- Structural context available
- Literature evidence available