E91Q (p.Glu91Gln) variant of ABCC8 (Q09428)
E91Q (p.Glu91Gln) in ABCC8 (Q09428) 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 0.75 / 1. The record also includes population frequency data and structural context.
E91Q (p.Glu91Gln) variant details
- p.Glu91Gln
- NCI-TCGA Cosmic COSV5685
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.754
- REVEL 0.75
- CADD 25.80
- PolyPhen-2 0.98
- SIFT 0.00
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available