Q56H (p.Gln56His) variant of PRMT5 (O14744)
Q56H (p.Gln56His) in PRMT5 (O14744) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.32 / 1. The record also includes population frequency data and structural context.
Q56H (p.Gln56His) variant details
- p.Gln56His
- gnomAD rs1308506118
- Missense
- Variant Prioritization Score for Impact Estimate 0.323
- REVEL 0.03
- CADD 22.40
- PolyPhen-2 0.00
- SIFT 0.14
- Most common in the REMAINING population (allele frequency 1.7e-05)
- Structural context available