G7R (p.Gly7Arg) variant of PRMT5 (O14744)
G7R (p.Gly7Arg) in PRMT5 (O14744) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.28 / 1. The record also includes population frequency data and structural context.
G7R (p.Gly7Arg) variant details
- p.Gly7Arg
- gnomAD rs1402305196
- Missense
- Variant Prioritization Score for Impact Estimate 0.284
- CADD 16.30
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available