G26R (p.Gly26Arg) variant of SMAD2 (SMAD family member 2)
G26R (p.Gly26Arg) in SMAD2 (SMAD family member 2) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.45 / 1. The record also includes population frequency data and structural context.
G26R (p.Gly26Arg) variant details
- p.Gly26Arg
- gnomAD rs2033451522
- Missense
- Variant Prioritization Score for Impact Estimate 0.45
- REVEL 0.26
- CADD 24.10
- Most common in the Latino/Admixed American population (allele frequency 6.5e-05)
- Structural context available