V33G (p.Val33Gly) variant of ABCC2 (Q92887)
V33G (p.Val33Gly) in ABCC2 (Q92887) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.56 / 1. The record also includes population frequency data, published literature, and structural context.
V33G (p.Val33Gly) variant details
- p.Val33Gly
- gnomAD 10-99784672-T-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.559
- CADD 27.20
- PolyPhen-2 1.00
- SIFT 0.00
- Most common in the South Asian population (allele frequency 1.2e-05)
- Structural context available
- Literature evidence available