I67M (p.Ile67Met) variant of ABCG2 (Q9UNQ0)
I67M (p.Ile67Met) 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.
I67M (p.Ile67Met) variant details
- p.Ile67Met
- NCI-TCGA Cosmic COSV9941
- cosmic curated COSV99418
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available