V33M (p.Val33Met) variant of ABCC2 (Q92887)
V33M (p.Val33Met) in ABCC2 (Q92887) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.48 / 1. The record also includes population frequency data and structural context.
V33M (p.Val33Met) variant details
- p.Val33Met
- ESP rs139131305
- ExAC rs139131305
- TOPMed rs139131305
- gnomAD rs139131305
- Missense
- Variant Prioritization Score for Impact Estimate 0.479
- CADD 26.30
- PolyPhen-2 1.00
- SIFT 0.01
- Most common in the Non-Finnish European population (allele frequency 2.7e-06)
- Structural context available