G56R (p.Gly56Arg) variant of HNRNPU (Q00839)
G56R (p.Gly56Arg) in HNRNPU (Q00839) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.26 / 1. The record also includes population frequency data and structural context.
G56R (p.Gly56Arg) variant details
- p.Gly56Arg
- gnomAD rs1201749229
- Missense
- Variant Prioritization Score for Impact Estimate 0.258
- REVEL 0.08
- ESM-1b 0.00
- AlphaMissense 0.32
- CADD 22.10
- PolyPhen-2 0.00
- SIFT 0.41
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available