S13F (p.Ser13Phe) variant of ABCC2 (Q92887)
S13F (p.Ser13Phe) in ABCC2 (Q92887) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.26 / 1. The record also includes population frequency data, published literature, and structural context.
S13F (p.Ser13Phe) variant details
- p.Ser13Phe
- gnomAD 10-99784612-C-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.257
- CADD 17.20
- PolyPhen-2 0.01
- SIFT 0.02
- Population evidence available
- Structural context available
- Literature evidence available