G13G (p.Gly13Gly) variant of ALDH2 (P05091)
G13G (p.Gly13Gly) in ALDH2 (P05091) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.30 / 1. The record also includes population frequency data, published literature, and structural context.
G13G (p.Gly13Gly) variant details
- p.Gly13Gly
- rs1064903
- gnomAD 12-111767021-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.296
- CADD 11.30
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available
- Literature evidence available