S59S (p.Ser59Ser) variant of ABCC2 (Q92887)
S59S (p.Ser59Ser) in ABCC2 (Q92887) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.09 / 1. The record also includes population frequency data, published literature, and structural context.
S59S (p.Ser59Ser) variant details
- p.Ser59Ser
- rs771802870
- gnomAD 10-99784751-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.0875
- CADD 0.97
- Most common in the Latino/Admixed American population (allele frequency 6.5e-05)
- Structural context available
- Literature evidence available