p.Arg55 Thr56del variant of ABCC2 (Q92887)
p.Arg55 Thr56del in ABCC2 (Q92887) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.29 / 1. The record also includes population frequency data, published literature, and structural context.
p.Arg55 Thr56del variant details
- rs752853724
- gnomAD 10-99784734-TCCAG
- Inframe Deletion
- Variant Prioritization Score for Impact Estimate 0.291
- CADD 15.00
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available
- Literature evidence available