G18R (p.Gly18Arg) variant of ABCC9 (O60706)
G18R (p.Gly18Arg) in ABCC9 (O60706) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
G18R (p.Gly18Arg) variant details
- p.Gly18Arg
- NCI-TCGA Cosmic COSV5396
- cosmic curated COSV53964
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available