W34S (p.Trp34Ser) variant of ABCC2 (Q92887)
W34S (p.Trp34Ser) in ABCC2 (Q92887) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.83 / 1. The record also includes population frequency data and structural context.
W34S (p.Trp34Ser) variant details
- p.Trp34Ser
- ExAC rs766440827
- gnomAD rs766440827
- Missense
- Variant Prioritization Score for Impact Estimate 0.83
- CADD 32.00
- PolyPhen-2 1.00
- SIFT 0.00
- Most common in the South Asian population (allele frequency 0.00021)
- Structural context available