D17G (p.Asp17Gly) variant of ABCC2 (Q92887)
D17G (p.Asp17Gly) in ABCC2 (Q92887) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.52 / 1. The record also includes population frequency data, published literature, and structural context.
D17G (p.Asp17Gly) variant details
- p.Asp17Gly
- gnomAD 10-99784624-A-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.516
- CADD 25.20
- PolyPhen-2 0.12
- SIFT 0.03
- Most common in the African/African-American population (allele frequency 3e-05)
- Structural context available
- Literature evidence available