S59T (p.Ser59Thr) variant of ABCC2 (Q92887)
S59T (p.Ser59Thr) in ABCC2 (Q92887) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.38 / 1. The record also includes population frequency data, published literature, and structural context.
S59T (p.Ser59Thr) variant details
- p.Ser59Thr
- gnomAD 10-99784749-T-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.38
- CADD 15.30
- PolyPhen-2 0.07
- SIFT 0.07
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available
- Literature evidence available