G37D (p.Gly37Asp) variant of PRMT5 (O14744)
G37D (p.Gly37Asp) in PRMT5 (O14744) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.24 / 1. The record also includes population frequency data, published literature, and structural context.
G37D (p.Gly37Asp) variant details
- p.Gly37Asp
- gnomAD 14-22920730-C-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.24
- CADD 10.20
- Population evidence available
- Structural context available
- Literature evidence available