G9G (p.Gly9Gly) variant of ALDH2 (P05091)
G9G (p.Gly9Gly) in ALDH2 (P05091) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.35 / 1. The record also includes population frequency data, published literature, and structural context.
G9G (p.Gly9Gly) variant details
- p.Gly9Gly
- gnomAD 12-111767009-G-A
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.351
- CADD 8.82
- Most common in the Non-Finnish European population (allele frequency 9.3e-07)
- Structural context available
- Literature evidence available