Y39G (p.Tyr39Gly) variant of ABCC2 (Q92887)
Y39G (p.Tyr39Gly) in ABCC2 (Q92887) is a protein-truncating change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.39 / 1. The record also includes population frequency data, published literature, and structural context.
Y39G (p.Tyr39Gly) variant details
- p.Tyr39Gly
- gnomAD 10-99784688-C-CGG
- Frameshift
- Variant Prioritization Score for Impact Estimate 0.388
- CADD 29.80
- Most common in the African/African-American population (allele frequency 3e-05)
- Structural context available
- Literature evidence available