S50G (p.Ser50Gly) variant of ABCG2 (Q9UNQ0)
S50G (p.Ser50Gly) in ABCG2 (Q9UNQ0) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.28 / 1. The record also includes population frequency data and structural context.
S50G (p.Ser50Gly) variant details
- p.Ser50Gly
- gnomAD rs1171922894
- Missense
- Variant Prioritization Score for Impact Estimate 0.279
- REVEL 0.22
- CADD 21.90
- PolyPhen-2 0.01
- SIFT 0.14
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available