S59Y (p.Ser59Tyr) variant of ABCC2 (Q92887)
S59Y (p.Ser59Tyr) in ABCC2 (Q92887) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.29 / 1. The record also includes population frequency data, published literature, and structural context.
S59Y (p.Ser59Tyr) variant details
- p.Ser59Tyr
- gnomAD 10-99784750-C-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.289
- CADD 9.15
- PolyPhen-2 0.00
- SIFT 0.06
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available