S25F (p.Ser25Phe) variant of ABCG2 (Q9UNQ0)
S25F (p.Ser25Phe) in ABCG2 (Q9UNQ0) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.29 / 1. The record also includes population frequency data and structural context.
S25F (p.Ser25Phe) variant details
- p.Ser25Phe
- Ensembl rs911128576
- Missense
- Variant Prioritization Score for Impact Estimate 0.288
- REVEL 0.15
- CADD 15.20
- PolyPhen-2 0.00
- SIFT 0.12
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available