V158G (p.Val158Gly) variant of PRMT5 (O14744)
V158G (p.Val158Gly) in PRMT5 (O14744) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.36 / 1. The record also includes population frequency data and structural context.
V158G (p.Val158Gly) variant details
- p.Val158Gly
- gnomAD rs2044430393
- Missense
- Variant Prioritization Score for Impact Estimate 0.362
- REVEL 0.18
- CADD 23.50
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available