E138Q (p.Glu138Gln) variant of ABCG2 (Q9UNQ0)
E138Q (p.Glu138Gln) in ABCG2 (Q9UNQ0) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
E138Q (p.Glu138Gln) variant details
- p.Glu138Gln
- NCI-TCGA Cosmic COSV5294
- cosmic curated COSV52945
- NCI-TCGA Cosmic COSV9941
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available