L17L (p.Leu17Leu) variant of ALDH2 (P05091)
L17L (p.Leu17Leu) in ALDH2 (P05091) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.34 / 1. The record also includes population frequency data, published literature, and structural context.
L17L (p.Leu17Leu) variant details
- p.Leu17Leu
- gnomAD 12-111767031-T-C
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.343
- CADD 7.42
- Most common in the Non-Finnish European population (allele frequency 6.5e-06)
- Structural context available
- Literature evidence available