A21P (p.Ala21Pro) variant of ABCC2 (Q92887)
A21P (p.Ala21Pro) in ABCC2 (Q92887) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.46 / 1. The record also includes population frequency data, published literature, and structural context.
A21P (p.Ala21Pro) variant details
- p.Ala21Pro
- gnomAD 10-99784635-G-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.459
- CADD 15.30
- PolyPhen-2 0.00
- SIFT 0.88
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available
- Literature evidence available