G27R (p.Gly27Arg) variant of ABCG5 (Q9H222)
G27R (p.Gly27Arg) in ABCG5 (Q9H222) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.44 / 1. The record also includes population frequency data and structural context.
G27R (p.Gly27Arg) variant details
- p.Gly27Arg
- NCI-TCGA Cosmic COSV5321
- cosmic curated COSV53210
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.436
- CADD 11.30
- UniProt: Variant assessed as somatic; moderate impact.
- Population evidence available
- Structural context available