R137G (p.Arg137Gly) variant of ABCG2 (Q9UNQ0)
R137G (p.Arg137Gly) in ABCG2 (Q9UNQ0) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.75 / 1. The record also includes population frequency data and structural context.
R137G (p.Arg137Gly) variant details
- p.Arg137Gly
- gnomAD rs1724845435
- Missense
- Variant Prioritization Score for Impact Estimate 0.754
- REVEL 0.95
- CADD 27.40
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available