C26S (p.Cys26Ser) variant of ABCC2 (Q92887)
C26S (p.Cys26Ser) in ABCC2 (Q92887) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.80 / 1. The record also includes population frequency data, published literature, and structural context.
C26S (p.Cys26Ser) variant details
- p.Cys26Ser
- gnomAD 10-99784651-G-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.797
- CADD 28.10
- PolyPhen-2 1.00
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available