R38G (p.Arg38Gly) variant of RRAD (GTP-binding protein RAD)
R38G (p.Arg38Gly) in RRAD (GTP-binding protein RAD) 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.
R38G (p.Arg38Gly) variant details
- p.Arg38Gly
- TOPMed rs1267935196
- gnomAD rs1267935196
- Missense
- Variant Prioritization Score for Impact Estimate 0.355
- REVEL 0.27
- ESM-1b 0.14
- AlphaMissense 0.28
- CADD 24.50
- PolyPhen-2 0.63
- SIFT 0.23
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available