R26G (p.Arg26Gly) variant of RAI1 (Retinoic acid-induced protein 1)
R26G (p.Arg26Gly) in RAI1 (Retinoic acid-induced protein 1) is a missense change. Clinical records from EBI and UniProt describe it as likely benign. The available variant effect predictions contribute to a CATVariant prioritization score of 0.60 / 1. The record also includes population frequency data and structural context.
R26G (p.Arg26Gly) variant details
- p.Arg26Gly
- ESP rs376964045
- ExAC rs376964045
- TOPMed rs376964045
- gnomAD rs376964045
- Likely benign
- Missense
- Variant Prioritization Score for Impact Estimate 0.597
- REVEL 0.59
- ESM-1b 0.00
- AlphaMissense 0.68
- CADD 26.40
- EBI: Likely benign
- UniProt: Likely benign
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available