A21G (p.Ala21Gly) variant of ABCC2 (Q92887)
A21G (p.Ala21Gly) in ABCC2 (Q92887) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.37 / 1. The record also includes population frequency data and structural context.
A21G (p.Ala21Gly) variant details
- p.Ala21Gly
- ExAC rs747479981
- gnomAD rs747479981
- Missense
- Variant Prioritization Score for Impact Estimate 0.37
- CADD 22.20
- PolyPhen-2 0.43
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 9e-06)
- Structural context available